Tag | Content |
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EnhancerAtlas ID | HS050-47747 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:72511510-72512620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr3:72512528-72512539 | AAATCTCAGCA | + | 6.32 | ZBTB18 | MA0698.1 | chr3:72511985-72511998 | AAACATCTGGATT | - | 7.12 |
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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 |
GH03I072462 | chr3 | 72511761 | 72511950 |
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Enhancer Sequence | ATGAAACTCA GAAAGTTCAA ACCCCTCGCT CTGTGTACGT GTTTGAGGCA AAGTGTGGGA 60 CTAGGAAAAC TCTAGGAGAA CCGTGCCACT TGGCAAATCC TCCTTTAACA AATGATAGCA 120 GTTGCATTTA AGATTCATTT GGTCATACGG ATCATGTTTG TCAGGGCTGT CATTAAAAGC 180 CTAATATTTC CCCCATTGCA GACTGTCTCC GAGTAATCCA AACGTGGGCA GCAGCTAAGC 240 ACGGTCAATT TCATGACCTC CTTCCTGCTA CCCACCTCCC CCTCCCAGCT ATCTCAACTC 300 CCAAGTGGAT GATCCCTCAT CCCTAGCAAC AACTGCAGCT GCTACTGTTT CTTGACTCTG 360 GCGAAGAAAG TGGGCTTGGG GCCAGGCCTA CTGTCCAGGG CTCCCAGTGG AAGATGCTAG 420 AAGAGGGCAG CGCACACTCT CTCACCGTCA GTGACCCAAG TTCATCACCT TGACCAAACA 480 TCTGGATTAC AACACACAGA GTTCAAAGGT CCAGAGTGTG TGTCTGCACC TGGCCAGGCT 540 GTTTAAACGG AGCTGACTTA AACCAAACAC CAGACCTCGG TGCTGTTATT TATGTGGAAG 600 ATTGGATGCC AAGTATAAAT AATAACTACA GCATCTTCTC TCCACAGGCT TTGTGATTAA 660 AGGATGCATA TAAAGGATGC ATATTCACCA TCTACTGTGC ATGAAGAGCT ACCCACCTCT 720 ACTCTGAGTA CCAGACTCTT CTCCCTAGCA GGCAGATTTC CTTTCTACCA ACCGTTTTTT 780 AATGTTTGTT TGCCTGAATA GTATCGAGAC TCCCTTCTGC TGTGGAGCCC TCACTGGCCT 840 CTTCATTTCA GGTCATCAGG TGGAGAGCAC GCTGCAGAGA GGACTGTTCC CATGCCCAGG 900 AGAGGCTTGC GAGTGAGCTC CGTGTAATCA CTCACTGGCA GAATGCAGTG CAGGGGGCTG 960 GGGTTACAGT CAGCGAGGAG CGAGGCACGA TGATGCTTTG GAGTGGAAGT GAGCTTTCAA 1020 ATCTCAGCAG CCCTGAGTGA TTCCTCCACT TAGGGCCAGT GTGTGTGTGA TGGGTGTGGT 1080 TGAGAGCTGC CAGGGGCACA GCAGGCGTGG 1110
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