Tag | Content |
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EnhancerAtlas ID | HS050-31179 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr18:24337080-24338120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | - | 6.2 | HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | + | 6.4 | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | + | 6.17 | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | - | 6.32 | ZNF263 | MA0528.1 | chr18:24337896-24337917 | TCCCCATTTTCCTTCTCCTTT | - | 6.01 |
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| 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 |
GH18I026757 | chr18 | 24337288 | 24338050 |
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Enhancer Sequence | TGTCACACTG AAAAGAGAAG ACTGCATTGA GGTGATGCTC CAAAAGGAGC AGCTTTGATG 60 CAAAAGAAGC AAAACCCTTT TGTTTCTTGG GCTTATACGA AGGTACTTCC TTTAGATCAG 120 AGTCGGGATG CATACACACT ACAAAAACTG GAATGAAAAA GGCAAACCAT TTTTACTCAA 180 CAGAATTCTC TGTACAGGTC AAGGAAATGC CAAACTTAAC AGATGTCTTA GACTGTGCCC 240 TGCAGGTCAA TAAATTAGAG TTTTGTTGAA CCAGGAAGAG GAAGGAATTC CAGGACTTCA 300 GGTCCCCAAA TGGAAATGCC CCTTAGGACA AGTCTAAACT AGGCAAATAG CACTGGAGCT 360 CCTCCAAGTC AGTTGGCTCA GTCTCGTGTA ACTCATTTCT GGCCCCCCTG AAGCTGTTTG 420 TTCAACTGTG CCTTCTACAA CGCTACAGTG TCAAAGAGAG TTAATCATTA GCAAGTGTGA 480 ATAATGTCAG TGTAACGCAG CATGATTGCA GTTCAGTCTG TTTTGACAAA ATTCTAAGCA 540 TTTGTCAGAG TTTACCAAAA AACAAAAAAC AACATGACCA CAGAATGTTA AAATAGCATG 600 AAGTTTGGGG AGCAGTTAAT TCACTTTCTA GCATTTTACA TCACCATTCT CATCGTTTTC 660 CCAGAGGAGA GTGTTGGGTG AGGCCCTCCA GGTGATGCAG TATTACTGAC TGGCCTGGTA 720 TGGTCTGATT CAGTTCAAGT CAGCTTAATG CAGCTCACCT CCAGAGATCC AGGCTTTGGA 780 GAATGATCTA AAGGTTTAGG TGTAGGGTCC TTAACCTCCC CATTTTCCTT CTCCTTTGTC 840 AGAGCCACCT ACTGCCATAG AATTAATATG GACCCATCTG TGATGCAGAG CCTGTTAGGC 900 CTCCTGCTTG TCCCCTGGGC TGGGGATCAT AATGAGTCCA AGCCCTCCCT TTTGACTGGA 960 ACTGCAGGGG CCCTGGTCCT GGAACTCTGA GGTTGAGAAT GGGATGTAAA GCTATATTCC 1020 AGCAAGCACT GAAGGATGAG 1040
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