Tag | Content |
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EnhancerAtlas ID | HS050-13777 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:113315250-113317350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr11:113315844-113315855 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr11:113315845-113315855 | TCAAGGTCAT | + | 6.02 |
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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 |
GH11I113445 | chr11 | 113316422 | 113319671 |
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Enhancer Sequence | ATCAGCTTTT TCTATCTATG TTCAGTCTCT AACGGGGCTG TATGTTCCTT GAGGAAATTA 60 CATGGCTTAC ACATCCACAA CCTGAATGAC TGTCTTTTAC ACTCCATGGG CCATCTATAA 120 ATGGTGGCTG ATGATGACGG TGATTGCTCC TTTATTCACC ACACATTTGC TGAGCCCCTA 180 TTATATGCAG TGCTGATTAG GGACTAAGGG TACAACGTTG AACAAGAGAG GCAAGCTCCA 240 TTGTCCTCAC GGAGGCCACC ATCTGGATAG AGGTACTAGC TCGACAGCTG GGGCTCTGAT 300 ATGAGCACAA GCCAGACCAG TGAGTAGGAA AGAGGGTGCA CATTTTGCAG AGAGGGTAAC 360 GTGGCTAATG TCACACACTA AACAGATGAA CTTCCTGCCA CTTTTGTAGC TGCATGGGAT 420 CTTTCACTGC ACGGGACAGA TTTTTGGCAG AAGCAAAGGC TCTGGGAGTC TAGCAAAAAT 480 AAGACAGCAG AAAAATATTA AAGCAAGACT GCAAAACTCA GTGCTGCACA CTCCATCACA 540 AGTGTGAAAA TAGCTCCACA TTCTGAAAAC ACCTGACCAG CACTCTTCAA AAATCTCAAG 600 GTCATGAAAG ACAAGGAAAG ACTGAGGAGC TGTCACAGAT TACAGGAGAC TCAGATGTGA 660 CAACCAAACC ATGTGGGATC CTGGATTCGA TCCTGGGCCA GGAAAAGGAC ATTAGTGGAA 720 AAACTGGCAA AATGCAAATA AAATCTGTCA TTTAGTTAAT AATATTGAGC CAATGTTATT 780 TTCTTAGTTT TGATCATCAC TCTGTGGTTA TATAAAACGT TCACTTTAGG GGAAGCTGAG 840 TGAAGGGTAT AGGGGAACTC TCTGCACTAC TTTGCTACTC TTCTGCAAGT CTAAAATTAT 900 CTCGAATGGA AAACAGGCAT TCACACAGGC ACCTCCGATA CCCAGGTATC TGTGTGAAGG 960 GGCTGTCCAG GCCTTCCTGA GGCATCGTAT CCTCCTCCCA CCTGCAGGCA AGGATGCAGA 1020 AACTTTTTCC AGGCAAAGGG GAGGGTCCTC TTCTCCTTCA CCCTTGGATG GAGCAAATAT 1080 CAAGTATCTG TCCCACATGG TGCTGACTGC GCATGCAAGG GGCAGGAGGC AGAGAAGCAG 1140 AAAAGGAGGA GAGGGGAATT AATATCTGTC AATTGATCCA TTTTTCGTAG CCATCATTTT 1200 AAGCACCTAC TGTGTTCCAG GCATAGCAAC CCTCCTTATA CATGTGCTCT CCATGAATCC 1260 TCATCACGTC TCCATTTCCC AGGAGACGGA AGCCCAGAGA ACTTCAAAAA TTTATCCACA 1320 GTTCTAGCTG CTAGGTGATA GAGGCAGGAC TCTAACAAGC TCAGCCTGTC TCCAGAGCCA 1380 CTGCTGGCTA CAGAGATGCT GGGGGTGGCC TGGCCTTGGA GGCATTTTCC AGCCTGTTCT 1440 GGAGCATTTC CAGGGGCCTG GGTCCGTGAG TTCCAGTGAG TTGCCTGTTG TCCTGGCCCA 1500 GTAAGTTTTT CTCTGTGTCT GACCTGCAAT TGTCCCCTTG CTTCCTGCCA GACCTCAGCG 1560 GCATGTTTCA CTCCTCCTGG GACACATGGA CCCCACTTCA TGCATGGGAA GTACATGGAG 1620 GGTCTTCAGC TCCCCCTTCC CACTCGCCCC TTTCCAGAAG CCCTGATGAC AGATCTGATA 1680 CAGTCACCCC ACCTCCATGG ATCCCACCCT AGTTCCCCAG GCACTCTCTT CATCCAAACT 1740 CCTTAGAGTC ACGTCTGCTG AAAAGACCAG TTTCTACCCC CGGCGCTGAG TCAGACACAG 1800 AGTTGCTGTC AGAACTGGAG AAAACACAGC AGTCATAGTA ACGGTAGCTC CTGTTTATTG 1860 ACTGTTCACC GTATACTGGA CACTGTCTTG CACACTGTAC ACACCTTTGT CCTAATTCTA 1920 AAAGCAACCT TAAAAGGGAA ACATTACTAA TCCTTTTTCA CAGATAATGC CAATGGGGCC 1980 AAGGGAGTTC CTTTAATAAC CTATGTCAAC TAGGAAGTGG CAGTGGAGGA TGGAAGACTG 2040 GGTTTGTCTA GTTGCAAAAC CTCTGTTTCC ACAGTGGCAA TGAGGCACCC CCTACTAACA 2100
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