| Tag | Content |
|---|
EnhancerAtlas ID | HS050-20919 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:71219470-71220830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr14:71220477-71220492 | AGTTAATAATTAACC | - | 7.21 | | HNF1A | MA0046.2 | chr14:71220477-71220492 | AGTTAATAATTAACC | + | 7.68 | | HNF1B | MA0153.2 | chr14:71220478-71220491 | GTTAATAATTAAC | - | 7.04 | | HNF1B | MA0153.2 | chr14:71220478-71220491 | GTTAATAATTAAC | + | 7.12 | | Nr2f6(var.2) | MA0728.1 | chr14:71220295-71220310 | AAGGTTAAAAGGTCA | + | 7.8 |
|
| | 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 |
| GH14I070752 | chr14 | 71219542 | 71220813 |
|
Enhancer Sequence | AAGATCCAAA TATGTTCTGT TTGTGTCCCT GCATCCCTTC TGTGACAGTT TTCACACTAA 60
GCTCTCAGTG TCCTGTGAAG GTGTCTCAGA CCGCCTGGAA GCATGTCGGG GGTGAGGCAG 120
GGGTGGGGGG TTATGGGACT GGGACTGGCC CCATTAGCTC CAGTCAGGGC AGCTCTGCTC 180
TTACCTGGCT TGTTTCTTTG TTTGTCTGCA TTCTATCCCA CTTCAGGGGT TCTACAGCTA 240
AAAGGAATGT GAGAACTACT GCCCAAGTAG GCAGAATGCT ACCAGAGAAA GATTTAGACA 300
GACTTGGGTC AAATGCCTGT TTTATCACTT AACAGCTATG TGCCTTTAGG AAGCAAGTTC 360
ACCTCTCCAA ACCTCAGTTT CCTCATCCCT ACAGCAAAGA CAGCAATACC GACCTTACAG 420
AAGAGTTACA AGGAATCACT AACACCAACA ACTAACCCTC ATCCAGAAAT TACCATCTAT 480
GGCTAGTAGA CCTGTGGTTT CTCCAAAAGG GCCTGAAATG AGATTGTGTC TGAGGAGGCT 540
TATGTAGAGC TACAGTGTTG GTGAGAGCTT TGCTGAGGGA CACTGGCATT CAGAGAAGAA 600
GTCTTTCTGG GGCTGACTAA ACTAGTTTTC CTCTGCCAAC ATCCCGCTTT ATGTTTACAA 660
TGGAAGGTGG GTGATATAAA TGAAGACTTG GTATTCTGTT GGTGGGAAAA AAGACTGGAG 720
AAATTCAAGA GAAATACAAG TTTACGTGGA TCTGAGCTCA GGGAAAGGCG GGCAGTAGAA 780
GTTGATGTGA TTTACCTCAG GTTTAGTCAA CTTAGTTGCC CTCCCAAGGT TAAAAGGTCA 840
ACAAGTCCTT TGATGACCAT TTGCAAGCAG CCTGGAAGAA CTCGTTCAGC TAAGTCACTG 900
CCTCTGAGTA CCTCCCCGCA ACACAGACCC ACCAGCTCCC ACAGTGCTGC CAGTAATTTC 960
CTAAAAGTCC TCACTGCCTA ACCCAACCCT CACAAAATTT ACTCTTGAGT TAATAATTAA 1020
CCACCTCCCG AGGCTTGGTA ATCCCTTCAA CCATTTCCTA GGATCAGAGG TGGAGGAGGG 1080
GTGTTTGATT TTTTTTTCAA AGTGAGGAAA AGTGGACAGC TACCTTTCTT GACAAAAGGC 1140
ACAGCAACTC CATGCCTGTG CTGGGCCAGA GCTCTATTTT GTAGTAACCT GCACCATCTC 1200
TAGACTGTCA GGTCAGGGTC CATGCTCTGA AAGGAGGTGA CCAGTCTCCC TTGAATGAGG 1260
TGGGCTGGGG AATGTCTTGC ACTTGGTAAT TATCTATGAT TCCACATTCC AGGAACCACA 1320
CTGACTGTTT AATAATCTTT GACAAAGATA ATTGAACTAA 1360
|
