Tag | Content |
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EnhancerAtlas ID | HS139-10764 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:113515900-113517530 |
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) |
Six3 | MA0631.1 | chr11:113517500-113517517 | CATGGTGATACCCTGTC | - | 6.11 | TCF7L2 | MA0523.1 | chr11:113516609-113516623 | TTCCTTTGAACTTT | - | 7.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 113516583 | 113516875 | chr11 | 113516970 | 113517112 |
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Enhancer Sequence | AGCATACAAC TCCCTCGAGC CAAAATTCTA TTTATTTATT CTTTCAAGCA CTCACTGTTC 60 ACTTACTCAA TTACTCAACC AATATTTATG GATTGTCAAC TTTACACAAA GAAGACCATT 120 CATGAGATAA ACATGAGTTT GGGAGACAGG TAGACCTGGT TCGAGTCTCT ATTCTGTCAT 180 TAATGTTTAT ATGACTTTGA CAAGTTACCT TGAAGTCTCT GGGCCTCAGT TTCCACATCA 240 TAGAATAGGG TTGTTGTGCA GACCAAATGA GAAAATACCT ACACTGCTTA GTATGGGGTC 300 TAGCACATAG TTTTGCATTA ATTTAAAAAT GTGTCATTGC TGTTATTTTG AAGGCAATGT 360 GCTAAGATCT TAAGATGCTC AAAACATGAG ATTATCCCCT TGTACAATCA GTGCATAAAA 420 TCCACTTTCT ATAAAATTAT GTCCCCAGGG AAGACTGTTC TGTCCTTATT GTTGCCTACA 480 CTATCTGCCA TAGAGTTTTG TACATGATAG GTGCTGTTAG CTATTTGGCA AATGACCAAG 540 GATAAACCAG TGTGAGCCAT TTCAATAATA ATGTAGGAGA TCATAGCCTT ATTTAGGAAC 600 ACTGGGCTGT ACAGATGGCA ATTTAAGCAT GGGCACTGAC ACAGACCCAA ATTTAGCCTA 660 TGTATGAAAT CTAGGACTGG ACACACCCCA GAGATTGCCT TTCTAGTGTT TCCTTTGAAC 720 TTTTCTCAGA TACAGAACAT AAAGTGTTAC ATGTAGGCTG AAAGGTATTC GTAGTATTAC 780 AACGTTCATC TCTTATCTTT TGTGCAATAA ATACTGAATT TCTGTCTGGA GGAAAACTGA 840 CATGCAAAGA AATTCCAGCT TGTGATGAGG AAAGAGAGAT GTTGAGAAGT AGCTGGACTG 900 AATCCATAAA CTGACAGGGC ATGAAACAAG GTTGGACCAT AAGACAGGAA GGGACTTGAG 960 GAATCATCGT CATCCTTCCC ACTCATCTAA CAGATGAGGA CACAAGGTCC AAAGAGGCTC 1020 TGTGATTTGG GATACCAGCT AGTTAGTGAC AGGGCTGCAA CAAAGCATGG TTTCCTGACT 1080 CCATTTCAAT GATCCTTCCA CTACATCCGT CTGTCATCGT CTCTGAACAC AAATTCATCA 1140 GAGGCAAGCA GATGACTGCT TTCCTCCTAA TCAGGCGAGA GGGACTGGAA GAGCATCACT 1200 TAGTAAAAGA CGACCAAGTA CAGCCCCTTA TTAGAAGCCA ACCACTAGAG CATGGCCACC 1260 CTCCAGCAGA TGCCAGTCAA AGCAGCTCTT CCTCAGCCCC TACGATCACC GTCTCTAGGC 1320 TGGCTTTTCG AATGAAACAA TGTTGTCAAG CATGTTGATG TCTGCAATTA AGCCAGCTGG 1380 ACAGGGGAAT TCATCCTGGA GACAATTAGA ACTGACACCT GCTTTTAAAA ATGAAAACAA 1440 TCTGAGGAAT ATTTAAGTGA GTCACAGTTC AGCCGCCACA TTTAAAAAAA AAAAAGAAAG 1500 GCCGGGCACA ACGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCAAG ATGGGTGGAT 1560 CACCTGAGTG AGGTCAGGAG TTTGAGACCA GCTTGGCCAA CATGGTGATA CCCTGTCTCT 1620 ACTAAAAATA 1630
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