| ID: 127398260 | H3K4me1 hESC enhancer GRCh37_chr3:111335851-111336351 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111617004..111617504) | | |
| ID: 127398259 | H3K4me1 hESC enhancer GRCh37_chr3:111335350-111335850 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111616503..111617003) | | |
| ID: 127379749 | NECTIN2 pseudogene 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111570638..111571054, complement) | | |
| ID: 126806769 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr3:111328685-111329884 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111609838..111611037) | | |
| ID: 126806768 | MED14-independent group 3 enhancer GRCh37_chr3:111227353-111228552 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111508506..111509705) | | |
| ID: 123002329 | Sharpr-MPRA regulatory region 10775 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111726982..111727276) | | |
| ID: 106478961 | ATPase H+ transporting V0 subunit c pseudogene 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111478745..111479127) | | |
| ID: 105374039 | uncharacterized LOC105374039 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111364517..111542003) | | |
| ID: 105374038 | uncharacterized LOC105374038 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111269139..111275634) | | |
| ID: 100874115 | PLCXD2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111676266..111677433, complement) | | |
| ID: 100420394 | NT5C3A pseudogene 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111633943..111634490) | | |
| ID: 257068 | phosphatidylinositol specific phospholipase C X domain containing 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111674676..111727007) | | 617015 |
| ID: 79413 | zinc finger BED-type containing 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111592900..111595346, complement) | | 615246 |
| ID: 10225 | CD96 molecule [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (111542197..111665996) | TACTILE | 606037 |