Tag | Content |
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EnhancerAtlas ID | HS098-01706 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:44239120-44240540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:44239427-44239442 | ATTTAATAATTAACT | - | 6.42 | HNF1A | MA0046.2 | chr1:44239427-44239442 | ATTTAATAATTAACT | + | 6.51 | HNF1B | MA0153.2 | chr1:44239428-44239441 | TTTAATAATTAAC | - | 6.14 | MAFK | MA0496.2 | chr1:44240443-44240462 | AATTTCTCACTCAGCAAAT | - | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44240162 | 44240471 | chr1 | 44240027 | 44240440 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043773 | chr1 | 44239553 | 44240767 |
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Enhancer Sequence | AAGCCATTGG AAAAGTTGAA AGAACAAGCT GATGATCATC AAGATCCTGT TAACTAGATT 60 CCCCAGTTTA CATTTTAACA TTTTCCACAT TTGTCCTATC TTTGTAGATG GATAGATAGA 120 TAGATGATAG ACAGATAGGT AGATAGATAA TAGACATTTT TCTGTACAAT TTGAAAGTAA 180 GGTGCAGAGT TTTTGATATT TCCTCAAATA TCTCAGTTTG CACCTCCTGA AAAAACAAAG 240 TTTTTCTCCT TCATAGCCAT GGTACCATTA TCACACTAAG ACAATGGACT TAATTCTTAC 300 ATTAATTATT TAATAATTAA CTTACTAATC ACAAGGGCAA AACTGTTCTG TGGTTCAACA 360 CCTTAACCAA ATGATCCAAT TTAATATCAC CAGTAGTGGG ACAGTCTGTC ATTATGTGCC 420 TTCTGATGTG ATGCAGTAAG AAATACATAT CACCTACATA GTGTCTGTGC CAAGGTGTTT 480 AACCTGAATT TGATCATTTA AAAAAATCAG ATGAATTCAA TACACAGGAC ATGCTACAAG 540 CCAGCTGGCC TGAACTCTTC AAAAGAAGGC AGTCACATGA GAAAACAAAA ATGGAGAGGG 600 TGAGCTGTTT CTAATTATAA GAGGCAAAAA AGACAGAATA GCCAAATGCA ATGAGTAAAA 660 TTTATTCAAA CACAGATATA TAAGGGAAAA AGACATACTT GGGGGGGCAA TTGGGTACAT 720 TTTAATATAG ACTATAATGA CAATATTGAC TCCTTGTTAT TCTTATATAT AATAAATCCC 780 TGTTAGTAGT AGTTTTGGAT TCCAGTTCTA ACTTGGTTTT TTCTTTTGCT ATTGTTACTC 840 TTGTTTCACT GAGCACATGG AACTATATAT CTTATATTTT AATTTAAAAA GGAAGTATTT 900 TCTGTCTTAT TGCCTTGTGG AAGGTTTTGT AATGATTTGT TTCCAGAAGG CTGCCACCTT 960 GCTGCCTTTC AGGTGTTGAG TGGATCACTG AGGGAGCTCC ACTCTCTGGG ATCTTCAGGA 1020 CTTTTGCATT GCTGATCGTG GACTGGAGTT TTTAGGATAG GGGCCCAGCA AAAGAATGAG 1080 AGGAGTCAAG GCCAAGCGTG GGCAAGCCCC ATATGAAGAA ATAGATGACT CACCTCTGTG 1140 GAAGGTGGAG CCAAGCATCT CCAGGGCTGT AGATGTCCTA AAATACAGAT TTGTAAAAGT 1200 CTGTTGTAGT TCTGTGTAGA ATTTGGTCAT CCTTTCATTT GGAAAAGTGA GTGGTAGGAT 1260 TTTTGTTTCC TAAAGATGAC CTGTTTCCAG ATCCTGTTTT ATAGCATTTT TCGTTCATTC 1320 ATTAATTTCT CACTCAGCAA ATACATATTG AGTGTCTGCT GTGTGTCAGG TACTGTGCCA 1380 AGTGAAAGGG ATTATGGAAA AGACATTATG TGTCACCTCA 1420
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