| ID: 127379775 | H3K4me1 hESC enhancer GRCh37_chr7:74203411-74204070 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74789067..74789726) | | |
| ID: 127379774 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74201830-74202532 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74787486..74788188) | | |
| ID: 127379773 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74186639-74187184 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74772292..74772837) | | |
| ID: 127379772 | H3K4me1 hESC enhancer GRCh37_chr7:74181785-74182286 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74767440..74767941) | | |
| ID: 124901673 | uncharacterized LOC124901673 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74875961..74883197) | | |
| ID: 106029312 | Williams-Beuren syndrome medial block B recombination region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74733937..74869227) | | |
| ID: 653361 | neutrophil cytosolic factor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74774011..74789315) | CGD1A, NOXO2, SH3PXD1A, p47phox, NCF1 | 608512 |
| ID: 442582 | STAG3 cohesin complex component like 2 (pseudogene) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74881990..74890612, complement) | STAG3L1P, STAG3L3, STAG3L2 | |
| ID: 84163 | GTF2I repeat domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74796151..74851605, complement) | FP630 alpha, GTF2IRD2A, GTF2IRD2 | 608899 |