Tag | Content |
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EnhancerAtlas ID | HS108-36069 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:160991910-160993580 |
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) |
PAX6 | MA0069.1 | chr6:160992125-160992139 | TTCACGCTTTACTT | + | 6.16 | YY1 | MA0095.2 | chr6:160993349-160993361 | TCAGCCATCTTG | - | 6.04 |
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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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Enhancer Sequence | TGGTATTCTC TGTATTTCCT TAATTTGAAT GTTGGCCTGT CTTGCTAGGT TGGGGAAGTT 60 CTCCTGGATA ATATCCTGAA GAGTGTTTTC CAACTTGGTT CCATTCTCCC ATCACTTTCA 120 GGTACACCAA TCAAACGTAG GTTCAATCTT TTCACATAGT CCCATACTTG GAGGATTTGT 180 TCATTCCTTT TCATTCTTTA TTCCTTAATC TTGTTTTCAC GCTTTACTTC ATTAAGTTGA 240 TTTTCAATCT CTGATATCCT TTCTTCCACT TGATCGATTT TGCTATTGAT ACTTGTGTAT 300 GTGTCATGAA GTTCTCGTGC TGTGTTTTTC AGCTCCCTAA GGTCATTTAT GTTCTTCTCT 360 AAACTGCTTA CTGTAGTTAG CAATTCCTCT GACCTTTTTC AAGGTTCTTA GCTTCCTTGC 420 ATTGTGTTAG AACATGCTCC TTTAGCTCAG AGGAGTTTCT TATTATCTTC TGAAACCAGG 480 ACCCACTTGA GGAGGCAGTC TGTCCCTTAT CAGAGCTCTA GTGCTGTGTT GGGGGATCTG 540 GTGCTCTTTT CAGAGCTGGC AGGCAGGAAA CTAAGTCTGC TGGAGCTGCA CTCACAGCCA 600 CCCCTTCCTC CAGTTGCTCT GTCCCAGGGA GATGGGAGTT TTATCTATAA GCTTCTGACT 660 GGGGCTGCTG CCTTTCTTTC AGAGATGCCC TGCCCAGAGA GGAGGAATCT AGAGAGGCAC 720 TCTTGCTACA ATGGCTTTGC CAAGCTGCAG TGCACCCTGC CCAGTTCAAA CTTCCTAGCG 780 GTTTTGCTTA CACTGTGAGG GGAAAACCTC CTACTCAAGC CCCAGTATTT GTGGATACCC 840 CTCCTCCCAC CAAGCTTGAG CGTCCCAGGT CAACTTCAGA CTGCTGTGCT GGCAGCAAGA 900 ATTTCAAGCC AGTGGAGCTT AGCTTGCTGG GCTCCATGGG GGTGGGATCC ACTGAGAAAG 960 ACCACTTAGC TCCCTGGCTT CAGCCCTTTC TTCACGGGGG TGAATGGTTC TGTCTTGCTG 1020 GCATTCCAGG GACCACTGGG GTATGAAAAA AAACTCCTGC AGCTAGCTTA GTGTCTGCCC 1080 AAATGCCAGC CCAGTTTTGG GCTTGAAATC CAGGGCCCTG GTGGTGTAGG CACCCAAGGG 1140 AATCTCCTGG TCTTCAGGTT GCAAAGACCG TGGGAAAAGC ATAGTATTTG TGCCAGAATG 1200 CACTGGTCTT CACGGCACAG TCCCTCACGG CTTCCTTTGG CTAGGGGAGG GAGTTCCCTG 1260 ACCCCTTCCA CTTCCCAGGT GAGGTGACAC CCCACCCTGC TTCAGGTCAC CCTCTGTGGG 1320 CTGCACCCAC TGTCTAACCA GTCCCAATGA GATGAGCCGG GTACCTTGGT TGGAAATGCA 1380 GAAATGACCC ACCCTATGTG TTGATCTCAC GGGGAGCGGC AGACTGGAGC TGTTCCTATT 1440 CAGCCATCTT GCCAGCCACC AACTCTTTTT GTATCCTTTA AGTGGAGCAT TTAGGCCATT 1500 TAGATTCAAT TTTAGCATTG AAATGTGAGG TGCCACTGCA TTCATCATAT TCTTTATTGC 1560 CTCCGTACTT TGGTTTTGTT TTTTGTTTTT GTTTTTTAAC TTGTACTTTT GTTTTATAGG 1620 TCCTGTGTGA TTTATGCTTT AAAGAGATTC TGTTTTCATG TGTTTCTAGG 1670
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