Tag | Content |
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EnhancerAtlas ID | HS108-34736 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:42515050-42516250 |
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) |
CTCF | MA0139.1 | chr6:42515493-42515512 | GGGCGCCCCCTGCAGGCTC | - | 6 | MITF | MA0620.2 | chr6:42515918-42515936 | AGTGGTCACATGACCAGA | + | 6.38 | MITF | MA0620.2 | chr6:42515918-42515936 | AGTGGTCACATGACCAGA | - | 6.38 |
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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 |
GH06I042547 | chr6 | 42514739 | 42516325 |
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Enhancer Sequence | GCATCTTGGA TCCACATCTG GGTATTAGAT TATTAGAAGG GCATCAGAAT TTGCATGCGG 60 TCCGAACCAG CCACTGCCTC CGAAGCCTTG CAGACCACAG TGCCTGCTGC CCTTCCTCTG 120 GGTCCATATC ACCAATCAGA ATATGAAGTG TGTCTCCTTA ACTGCTGATG ACCGGAGCCT 180 TCTGGGAATT CCTGAGGGAG GGGAAGGACT TAGCCTGTGG CTTCTAGTCC TGAGGATGCT 240 CCCTTTGAAT GTCAGTTACC AGCTGCTTAT GGAAGCTAAG ACAAGGGACA TCAAGTACTT 300 CGGGGTCCCA AGCTGTATAA CAGGAATCGG TCACGTTCAA ACAAAAGCTA GCTCCAGTGC 360 TGAAGAGGAA CTCCAGAGAT CGAAAAGCTC AGCCCCACGG AGGTTGGTCC CTCCTCCGGC 420 ACTGCGGAGG CCAGCCTGGG CAAGGGCGCC CCCTGCAGGC TCCCGGCATC GGTGCCGGAG 480 AAGCACGGTG GACTCTGAGC TGCCGCCGGT TTTGTGGGTG GCTTTGCCTC CCTCACTTCT 540 AAAACCTCCA GCGGTGGCGG TCCCCTTATA CCCTGCCTGG GGGGGATACT TGGAGAGGAG 600 AATGAGGGGC TTCTTCCCAG TGGGCAGAAC CAAAGGCAGT ACCGATGACT TGAAGCTGGG 660 CTCTAGAGAG CAAACAAGAC TTTCCTGTAT TCAAATTCGC AGGCAGTGAT TTATGTTTAG 720 GCCACTGGCT TGGCTGCCGG CTGTGGATTC CATTGACTGG CGGACAAAAT TAAGCTCCTG 780 GTTCCTCACG TGGATGCCAT CAGATCCCTA GTGAAGAATC CCGTGGAACA AAGCTGTAGA 840 TGTTCTGATA AGATGAGAGA GGCAGACAAG TGGTCACATG ACCAGAGAGA CCGTGGAGGA 900 GTGGATGCTG CCTTGGCCTG GGGGAGGACC CAACGTATTT AGCAGTCCAC GCACGTGCTA 960 CTCACAGCAG CCCTGTGAGC TTATCCTTTC CCTACCCTTT TCTGTGCCTG GAGGCACCGG 1020 CCTAAAGGTA GGTTATATTT CACTGCTGCC CTCTCATCAG AGCCAAAACT ATGTTGTCAC 1080 AATTAATGCT GAATTCGGTA AAAGCCACCA CTAAGGAGAT GTACAGAAAA ACAGCATTCC 1140 TGATTTCTTA GCATCTGATT TGTCAAGAAT GGGTTTATAA TCTGAATATA AAATGGCCCT 1200
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