Tag | Content |
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EnhancerAtlas ID | HS050-06246 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:229334880-229336260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIC | MA0687.1 | chr1:229335785-229335799 | ATAAACAGGAAGTA | + | 6.43 | Stat6 | MA0520.1 | chr1:229336039-229336054 | TGCTTCCTGAGAAAT | + | 6.78 | TFAP2A | MA0003.3 | chr1:229336001-229336012 | AGCCTCAGGCA | + | 6.32 |
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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 |
GH01I229198 | chr1 | 229334343 | 229336741 |
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Enhancer Sequence | TTGATTTACA CTGTAAGATC CATTTCTTAC TATCGTAGTC TTCAAAAAAG CATGCAAGCT 60 TTCTTAAATT TAGTCCCCAG TTATCTTGGG ACTAAATCTG CAATAAGCGT CATCAATGGA 120 AAGAGAGGTT CTTTATGCAT ACACAAAAGG GGTGCTGTCC AGGTGCCGAC CTGGGGGTGG 180 AAGCAGACAC TGGAATTACC TGGGCAATTT CTGCCACAGG TGAGTTTATC AGAAACTAAC 240 GTGGAAGACT ACAGGTACCT GCAAAACCAG ACGGTCCACT TTTTAGCCTC AGGCCACCAT 300 TGCTGCCTCA CCTGAGGACA TAGCAGTAGT GCCAAGCAAG GACTGGTCCA GCCAGGACCA 360 TCCCAGCTCA GGTCCCCTTG GCCTGGCATC CTCTCCTGGG GACTCAGCCT CCCAAGGATC 420 ACGAGGATAT TAGGTCCTAG GTTCCCTGCA CCTGCCAATG GTAGGAAGAT TCCTGGGCGT 480 TCGTCAGGGG GCCCACTTTC TCCATGTGAT AGAGGACAGG TTCATGGTGT TAGGTTTCAG 540 TTCCTGGAAA CAGGATATCC TCCCTTCCCT TCTCTGGCCT GCCTGGGTGC AGTGGGCTGT 600 GGACAACAAG GATGGTCAGC AATTTTGTGG GTCTTACACA CCTCAAGGGA GCTTCTGCAA 660 AGGGATTTGG TAGAAATATT TCTTGAAGTA AACGGGCCGC TGGCAAGGGC TTGACAGTTA 720 ACCTGGGAAT TTATGCACCG ATGTTACAAT CCCAGAGTAC AAACCTGGGA GAGCCTGGCT 780 AGACCCTCTC AGCCACAAGT CAGCAAACGT GTCTGTAAAG GGTCAGAGAG TAAATGTGGA 840 GGCTTTGCAG GCTATATGAT CCCTGTCACA ACTATTCAAC TCTGCTACTG TAAAGCGAAA 900 ACAACATAAA CAGGAAGTAA GCACACAGGC AGCAGTGTGC CGATCAAACC GCACCCACAG 960 CCACAGGCAG TGGGCCAGAG GTGACCCACT AGCCACAGCC GGCCGACCCT GCTCCAGTAC 1020 AATCCCTTCT TTTTATAGCT TCAGAAGTTG AGACCAAGGA GAGGAAAAGG CAGTCAAGCC 1080 CCCCAAGTAC TCACTGCTGG GCACGAGTTT CTGTTACACG GAGCCTCAGG CAAGAGAACC 1140 CTTTTGCTAA GTAATTTTGT GCTTCCTGAG AAATGGAATT CCTGGCCCCC TCTTGCCCTG 1200 GGCAGCAACT CAAAGTGAAG TTAAATTGCC GGGACCTGGA GTTTGTCACC CTGAGTTCAG 1260 ATTCTGGCTT TGTCACAAGT CGCCTAACAT TTCTAAACTT CAGTTTCCTT TTCTGTAGAA 1320 AATGAACAAT AAAAACGACT TCAGCCGTGA TTGTACTCAA GTATGGAGCA GTAAAGAAAA 1380
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