| Tag | Content |
|---|
EnhancerAtlas ID | HS050-66250 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr8:71717070-71718230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr8:71718136-71718146 | GTGAAAGTGA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH08I070804 | chr8 | 71717167 | 71718381 |
| Enhancer Sequence | CACAGACTTT TGGATTGGTA AAATCAATTC TAGTTTATAT AAAAGAAAAA GAGCATTACA 60
CATTCCTTGA AAGCTGTGGT GACCCTGGGG TCCCTGATTC ATAATTGCTT CACCTTCTAC 120
ACAAATGTTT AAGATACTGG CCAATGGGTG AGGCCAAGAT CGCAGACTAG AAACAGTGGT 180
GATCAGAGGC TTCCATCAAA AAGAACCATA ATAAGCATGT AAATCCTTCA CTGGCAACCA 240
AGGTATCCAG ATTGTCTTAT CAGAACTGAC TAGGAGGCTG GCATGATCTG TGGAGAGGAA 300
GGAAGGGCAG TGCAGCACAG CGGCCCACCT AAGAGCCACA CAGGGCAGGG GAATCTCCAC 360
CCCCCAGCCA AGGGAGGTGG TGAGTGAGTG TGCTACCTGG CCAGGTAAAC CGTGCTTTTT 420
CCATGGAACT GTGCAACCCA TGAATCGAAA GATCACACTC GTGTACCCAC GCCACTGGCG 480
CCTAGTGTCT CACCCCAGAG CTGCGCATAT TCTCAACAGT CTAGCAGCTG GAATCTGCTT 540
AGCCTACCGA GCTCCCGGGG GGAGGGGTGA CCAGCACCAC AGCTGTGGCT GCCTGCTGTC 600
TAAGCCATTT GAGCTCCTTG GGGGAAGGGC AGAAGCCAGC ACCGGGACTC ACAACTGCCT 660
AACACGCTAA GCTCCCTGGG TGGGGGAAGG GCGGCATTCA TCTCTATAGC TCCAGGCTGT 720
GCTTTTACCC TGCTGAAGCC AGGGAGACTG GACAACTTGG TCCCAAGACA TGTTCCCCCA 780
CAGCCCAACA CACTGGCTGT GGCAGACTGG CCAGAGTGCC TCTTCAGGCG TGACCCTGAC 840
TCATCCTTAC TGGGTGAGGC TTCCCTGCAG GAACTCCAAT AACTCCAGCC AGAGGCTCCC 900
GGACAGAACC TGGATCTCCC TGGGCCTGAG CCCCTAGGGG AAGGAGTACC TGCAGTCTTT 960
GCAGAACAGC AGATTTAGCC TTTCCTCCTG GTAGTTCTGA GGAGTATAGA CAGCCCAGAT 1020
GAATGTGCTT CCCCCTAGTG AAGCACACCC CCTCCACCAA GGGGCAGTGA AAGTGATTCA 1080
TTAAATGGGT CCTGTTCCCC GTGCCACCAA ACTGAGTGAG ACCTTCCAAC AGGAGTTGTC 1140
TGTCAGACAC CCTATACAGG 1160
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