| ID: 129999187 | ATAC-STARR-seq lymphoblastoid active region 26545 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117251739..117252008) | | |
| ID: 129999186 | ATAC-STARR-seq lymphoblastoid active region 26544 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117110628..117110847) | | |
| ID: 129999185 | ATAC-STARR-seq lymphoblastoid active region 26543 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117110508..117110587) | | |
| ID: 129999184 | ATAC-STARR-seq lymphoblastoid active region 26542 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117041040..117041359) | | |
| ID: 129999183 | ATAC-STARR-seq lymphoblastoid active region 26541 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117024680..117024769) | | |
| ID: 127457478 | OCT4-NANOG hESC enhancer GRCh37_chr7:116794856-116795649 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117154802..117155595) | | |
| ID: 127457477 | H3K27ac hESC enhancer GRCh37_chr7:116716803-116717302 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117076749..117077248) | | |
| ID: 126860159 | MED14-independent group 3 enhancer GRCh37_chr7:116659304-116660503 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117019250..117020449) | | |
| ID: 124901732 | uncharacterized LOC124901732 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117091432..117100379, complement) | | |
| ID: 113219440 | greater CFTR locus negative regulatory element CR11 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117190018..117190413) | | |
| ID: 113219434 | greater CFTR locus negative regulatory element NR4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117088745..117089385) | | |
| ID: 113219433 | greater CFTR locus negative regulatory element CR10 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117159028..117159408) | | |
| ID: 107161150 | MT-ND2 pseudogene 37 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117263526..117263833) | | |
| ID: 105375466 | uncharacterized LOC105375466 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117232748..117241355) | | |
| ID: 102466616 | microRNA 6132 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117020211..117020319) | hsa-mir-6132 | |
| ID: 100421782 | heterogeneous nuclear ribonucleoprotein A1 like 2 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117262818..117264892, complement) | | |
| ID: 93655 | ST7 overlapping transcript 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117182681..117209937) | NCRNA00026, ST7, ST7OT3 | |
| ID: 93654 | ST7 antisense RNA 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117072072..117145592, complement) | ST7AS2, ST7OT2 | |
| ID: 7982 | suppression of tumorigenicity 7 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953501..117230176) | ETS7q, FAM4A, FAM4A1, HELG, RAY1, SEN4, TSG7 | 600833 |