Tag | Content |
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EnhancerAtlas ID | HS050-03773 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:114660090-114661470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr1:114660756-114660771 | ATTTCCCAGGAAGTA | - | 6.25 | ZNF263 | MA0528.1 | chr1:114661357-114661378 | CTCTCACCTCTTCCATCCTCC | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 114660584 | 114660874 | chr1 | 114661068 | 114661341 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I114118 | chr1 | 114661009 | 114661661 |
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Enhancer Sequence | GTTGGAGGAA GAGGCAGCTG CCTTGGAGTT GTTCCTGGGT AGAGGGTGGG AACGACACAT 60 CTTCTAGCCT GGATTTCAGA GGCCCCAGCT CCTGCCTGCA GGGCCCCATG GAAGCTGAGC 120 TGATTTGCTG GCTCTTTCTT CCCTCCCAGC CCTGGGCTTC CCTACCCAGC AGCGCCTTCA 180 ATCAGTAGGA TTGGGGAGGG CATCCTGTGT CTTCTCAGGC TCCAGTTCAG ATGTTCCCAG 240 TAAGAGAACT TAAGGGAAAA ATTAAGCTGG CTCTCAGAGG TCTGGGTTCA AATCCCGGTT 300 CTGCTGCGAA TCAGTAGAAT GATATGGGGC AAGTCACTGT GCCTCCCTGA GCTGTGCATC 360 CTCAGCCGTA AAATGAGAGC ATTGTACCAG ATGACCTCAC CTCCTCATTA GTAAAATAGG 420 GTGAACCGTG AAGCCCAATG AGTGTATGCA CTGAAGACGC CTCACAGGGA TCTAGTGCAG 480 AGCAAACTCT TCAGACACTT TCGGGCCCCT TCCTGTTCCA TCCTGCTGTG GAGCGGCCTC 540 TGGCCGCTAG TGGGTTGGCT TCAGCCATCT CCAAACTGCA TCCTGACAAT GCCTCACTGG 600 AAGGAGAAGC AAGCGGTGTG GGAGAGGGGG ACAGGAAGGA GGGAGCATGG GGCCAGGATC 660 CCAGAGATTT CCCAGGAAGT ACAGAGCTCT TTGCTGGGAG GTTGCTATAA ACCAGGCCCC 720 AGGCCTCCCT TCCCCCTGCT CACCCAGGAG CACGATGATA AAGCGCCAAA TTAGCTCCAT 780 TATTGTAACT CCTCCAAAAA TTACAGGCCG CATGTTCTGC CAGAGCCAGC TAATGTCTCT 840 CATTGGTAAG CAGGTGACAC TAATAGTTAT TTCCTCCCTT CCAGGCACCA AGTGCAGAGT 900 GGCAGAAACA GAGTGAGGCT CAGGCTGGGA GGAGAGAGGC CCAGGGAGAA GCCGAGGCAC 960 TGGACGGCCC TGGTGCCAGG GGTCGCCTGA GTGCCACAGC AGAAGTTTGC AGATCCTCCC 1020 TTTGGCTTAA ACTGCCTCTT TGCACTGTAT GAACCTGGAG ACCTCCCTGC TCAGGAATGG 1080 CGCTGCCTGG CATCTGGGGA GGCCACAGCA CGCAGGCCAT GCCAGGCCCT CCGGCGGGGT 1140 GTCCCTGGGG CTCCTGCTGC TGCTGCAGAG GGGCCTGCTG CTCCCCGGCT GTCCCCGCGG 1200 CTCAGGTTCC TTCTCCCAGG CGATGCCCAG CTTTCTCTGG CTTCCCACAC AGCAGTCAGC 1260 ATTTCCTCTC TCACCTCTTC CATCCTCCCC CACCCCCATC TGCCTCTCCT CTCACACCAG 1320 ACAGAGCCAT CTCCTGTCGG TGTCAGCTGA GGCAACGCTT CCTCAAGGGG GCAGGGTCCC 1380
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