Tag | Content |
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EnhancerAtlas ID | HS175-27483 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr6:137024250-137025680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX21 | MA0690.1 | chr6:137024740-137024750 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr6:137024739-137024750 | TTTCACACCTT | - | 6.62 |
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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 |
GH06I136703 | chr6 | 137024328 | 137024741 |
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Enhancer Sequence | GAGCTTCTGG AAGGAAAAGC TCTCAGCATT CAAATGTATT GATAGAGATG CTCGAAATAT 60 TCAACTTTTT ATAAGGACAT TCAGCACCTG AAACGCAACA CCTCTCTCTC AAGTCAGCGG 120 GCAACTTCTT CAAAATGTAC AATATTTGGT TCTTTTATCA GCCTGCTTCT CCACAAGTCC 180 AAGCTGGGCT AGGCAGGATG GACTTCTTTC TGCCATTCCG GTCTCAGGGA GTGCTACCTT 240 CTCTGAAGGA CACTGACATA ATGGCTACCC TCTTTTTAGC ACATCACCTT ACGTTCATTT 300 TCTAATTTGT CTGCTTCTTT GTTCGCTGAT TTTCTACCAA TTAGACTGTC TACACAACAG 360 TTACACATGT GCTTGTTTCC ACTTCCAGCC TCCCCTGTGA GAACCCTGAG GTACCAAGCC 420 CAAAGCCTGG CGTGCAGCGC ATGTCCAATC AGTATTTGTT TAAAAAAACG TGTGAGATAA 480 ATTAAACAGT TTCACACCTT TAACAAATTA AACAGTATTT TAAAACAGTG CATTGAAGCA 540 TGAAGCAATA ATTGCTCATT TCCTGTTGAG ATAGGAAGGA TAAGAGTTTA TAATGGCAAC 600 ATTATTTATG CTGAAATATG CCTCTGCCCT GGTTAAATCT TAAGCATAAG TTTCAAAATT 660 ACTTCAGAGT TGTATAATCA CTACTATAAA AAAAGGCTTA AAATTTCTGA TTTAAGGAGA 720 AATTAGCAAT TGTATTGTTA ATTTTGTCGT CTTAAATCAA ATCTTGTGCA GGCTTTTATA 780 ATATATTGTA TATTATCTTC ACTCCGAGTT GCAGAGGTAC ATTCTTTAAG GTTTTTAAAT 840 ACTGGCTTAC TTTCTGAAAT AAATGTACAA CCATTGGCCA CAACCATTGG CCTAACAAGG 900 CTGTTTCCAC TTTATATTAT AATTCTTCTT CACGCAGCAT TTTTAAAGTT TAAAATTTAC 960 TTTTCTCATG TTTTCACATT TGTTTAATTC TGTGTGGAGG GTAGGAATTC TGTAGTGTGG 1020 TCTCAGAGGC AGAATACAAT ACTTAGGAAC TTACATCAAT CTCTTCAAGT AGAAAATAGA 1080 TAAAGATATC TATATATCAG TGTATATGTA ATTATACTAT ATTGAGCTAG CTAGCTCTCA 1140 ATATAAGCTA GCTATCAGTA TTGTTATTCC TATACCTTAT CATGATTACA GACACTGGAG 1200 AGACGATCTA GAAAACCCTG TCATATCAAG GCTTCACTGA GGTTGGGGAA TCACGATTTA 1260 GAAAAGGGAA AAGGGAACAG CATATTGGAA AGGATGGCAT GAATGCTGCC ATGGAAACAT 1320 ACTATAGACA CATATACATA CACACATATG TGTGTGTATC TGTGTGTGGA TATAGGCTGC 1380 TTTAGTGCCA CTCATAATTC CACAACATTG AATACACTAT AAAAGATTTT 1430
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