Tag | Content |
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EnhancerAtlas ID | HS191-12076 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr14:71219790-71220790 |
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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I070752 | chr14 | 71219542 | 71220813 |
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Enhancer Sequence | TTTATCACTT AACAGCTATG TGCCTTTAGG AAGCAAGTTC ACCTCTCCAA ACCTCAGTTT 60 CCTCATCCCT ACAGCAAAGA CAGCAATACC GACCTTACAG AAGAGTTACA AGGAATCACT 120 AACACCAACA ACTAACCCTC ATCCAGAAAT TACCATCTAT GGCTAGTAGA CCTGTGGTTT 180 CTCCAAAAGG GCCTGAAATG AGATTGTGTC TGAGGAGGCT TATGTAGAGC TACAGTGTTG 240 GTGAGAGCTT TGCTGAGGGA CACTGGCATT CAGAGAAGAA GTCTTTCTGG GGCTGACTAA 300 ACTAGTTTTC CTCTGCCAAC ATCCCGCTTT ATGTTTACAA TGGAAGGTGG GTGATATAAA 360 TGAAGACTTG GTATTCTGTT GGTGGGAAAA AAGACTGGAG AAATTCAAGA GAAATACAAG 420 TTTACGTGGA TCTGAGCTCA GGGAAAGGCG GGCAGTAGAA GTTGATGTGA TTTACCTCAG 480 GTTTAGTCAA CTTAGTTGCC CTCCCAAGGT TAAAAGGTCA ACAAGTCCTT TGATGACCAT 540 TTGCAAGCAG CCTGGAAGAA CTCGTTCAGC TAAGTCACTG CCTCTGAGTA CCTCCCCGCA 600 ACACAGACCC ACCAGCTCCC ACAGTGCTGC CAGTAATTTC CTAAAAGTCC TCACTGCCTA 660 ACCCAACCCT CACAAAATTT ACTCTTGAGT TAATAATTAA CCACCTCCCG AGGCTTGGTA 720 ATCCCTTCAA CCATTTCCTA GGATCAGAGG TGGAGGAGGG GTGTTTGATT TTTTTTTCAA 780 AGTGAGGAAA AGTGGACAGC TACCTTTCTT GACAAAAGGC ACAGCAACTC CATGCCTGTG 840 CTGGGCCAGA GCTCTATTTT GTAGTAACCT GCACCATCTC TAGACTGTCA GGTCAGGGTC 900 CATGCTCTGA AAGGAGGTGA CCAGTCTCCC TTGAATGAGG TGGGCTGGGG AATGTCTTGC 960 ACTTGGTAAT TATCTATGAT TCCACATTCC AGGAACCACA 1000
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