| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69883 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:112982590-112983550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr9:112983232-112983247 | TGAACTTTGAACTTG | - | 6.73 | | Hnf4a | MA0114.3 | chr9:112983230-112983246 | CTTGAACTTTGAACTT | - | 6.45 | | Rxra | MA0512.2 | chr9:112983232-112983246 | TGAACTTTGAACTT | - | 6.4 | | ZNF263 | MA0528.1 | chr9:112983113-112983134 | GGAGAAGTAGTGGGAGGGGGG | + | 6.28 |
|
| | 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 |
| GH09I110220 | chr9 | 112982761 | 112984050 |
|
Enhancer Sequence | GAGATCGCAT CACTGCACTT CAGCCTGGGC AACAGAGTGA GACCCTGTTT CAAAACTTGC 60
CAGGGTGCAG CCAAGGTCAA GAACCACTGA GCTATTTAAA CGGTTGCTTG TCAAGCTACC 120
TACTTTCAGA GAAACTTTTT TTTCCTTTTT TTTTTTCTTT TTTCCTTTCT TCTTTTTTTT 180
TGAGACAGAG TCTTGCTTTG TCACCCAGGC TGGAGTGCAG TGGCACGATC TCGGCCACTG 240
CAACCTCTGC CTCCCGGATT CAAGCGATTC TCCTGCCTCA ACCTCCCGAG TAGCTGGGAT 300
TACAGGTGCG CACCACTATG CGCAGCTAAT TTTTGTATTT TTAGTAGAGG CAGGGTTTCA 360
GCATGCTGGC CAGGCTTGTC TCGAACTCCT GACCTCGTGA TCCACCCACC TCGGCCTCCC 420
AAAGTGCTGG GATCACAGGC GTGAGCCACT GCTCCCGGCC CAGAGAAACT TTTTTTTCTG 480
TTCATGGTCC TGGCTGGTCT GTTTGCAGAA ATGCATTTAT ACTGGAGAAG TAGTGGGAGG 540
GGGGAAGGGC TCTGCTTTCA GTCTCCATCT TCCTAGATTC CCGGCTCTGA GTTCTCTGCC 600
CTGTCGTCAC ATAGGTAGAT GTGTACCCTC TGCACTGCTC CTTGAACTTT GAACTTGTCA 660
CACAGATTCA GAAAAGAGTA GTGAATCCAG TTTCACAGAT TTTCAACCTG GACTTTACCC 720
ATAGCTATCT GAACTGTAAA TTTGCCCTGC CTTGTTACTC AGGCTGTGAG CTTCTGCCTA 780
GGCTATTATC CCAGTGTGGG CCTCTGCTCT GTTGCTCACC TACACTGGAC GCATCTGAAG 840
AGCATGTTAA TTTGTGCACA AATCTACATG TGTGCACTAC ACTTCAGAGA AATTAAAAAG 900
TCCTACTAGT TTCCGTTTTG GTTTTTATCA ACGATTTCAG CTGCATCTGT GTCTTTTGGA 960
|
