Tag | Content |
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EnhancerAtlas ID | HS108-34682 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:41506010-41507260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUND(var.2) | MA0492.1 | chr6:41506578-41506593 | TGAAATGAGGTCATG | + | 6.07 | SCRT1 | MA0743.1 | chr6:41507075-41507090 | GCTCAACAGGTGGCA | + | 6.29 | SCRT2 | MA0744.1 | chr6:41507075-41507088 | GCTCAACAGGTGG | + | 6.11 | Zfx | MA0146.2 | chr6:41506841-41506855 | GGGGCCCAGGCCTG | + | 7.19 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27953 | chr6:41503923-41507175 | Fetal_Intestine | SE_28956 | chr6:41503802-41507213 | Fetal_Intestine_Large | SE_31492 | chr6:41506328-41506984 | Gastric |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 41506323 | 41507000 | chr6 | 41506487 | 41506686 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I041536 | chr6 | 41503971 | 41507010 |
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Enhancer Sequence | CTTACATAAT TGTGGAACCG TGTATGAATT TCAACCTTTC TGAGCTTTAG TCTTGTCATT 60 TATAGAATGA AGATAATAAT ACTATCAACC TGATTTAGGC TGGGTTCCCA CATAAGCAGC 120 CCCTGAGACA CTATTCCATT GCGAATGGTT GATTTAGGAG GTGAAGGAAA TACCAGTAGA 180 AAAGTGGGGA AGTAAGACAA GGAAAGGAGG CAACAAAGTA TATGTTACCA AGCCAGCTAC 240 AGGATGGGCT CAGTCCCACA GAGGAAACCC TGGGAGTATG CATGGCACAC ATGACTCGGA 300 GTTATCCCAC AAGGGGAGTA AGGGAGTAGG GGTATTTATA TACCAGTTCC CATCAGTTAT 360 GGGTGGAGGG CTCCCCCAGG AAGTGTTAGT TCCCTGGCAC TTCTGGTCTC CCACACAGTG 420 GAAAAGTGGG CTCTAATTCC CAAAGGAAAC CCTTAGGCTA GGAAAGTCAG GCACTAGTGA 480 TTGGAAGCCT TAGGGGTGAA AAGTCACAGT GCACCAGACA GGGCACCAAC AAGTATCTGT 540 TGCATCATCT TAGAGGACTG TTGGGAGGTG AAATGAGGTC ATGTGTGGAG CGTGCTTAGC 600 ACAGTGTCTG ATGCATGGGT GGTTCTTCTT TAAGCAAGAC CCAGCTTCAG TTTGCCTTCA 660 GCTGCCTGGC TCCAGGGACT TCCTGCTGCC TAACAACCTT GAGAGAGGTC CTGGGGGCTG 720 GAGAGCCATG GCTCAAGAGC AGAGGGGACT GGAGGAGAGA AGACCCTAGG GCACATGGTG 780 AAGACCAGAA AGAAGAGGGG GTGCAGGAGA ACCAGGAAGG AGCTGGGGCC TGGGGCCCAG 840 GCCTGGCATA GAATTACAAG GATGAGGAAG TGTGTGAGCC CCACTCCATG GACCCAGCCA 900 GATGCCACAC ACAATAAGGG ATGTATAAAG ACACTCTTAT CTTCACTTAT TTCTACTCTA 960 CATTCATTGC CTCTGACATT TGGAGCACTG CTTTCTCTCA AAAACAAAAT AGGACTGTTG 1020 TGGGAATCAG AGATACATAT TAAAAGTGCC TGGTGAACAG TTGATGCTCA ACAGGTGGCA 1080 GCTATTTTCA ATGTGAGTCT ACCTGGGCTT TAACTTCCCT CCTTCATATC CCACCTCACC 1140 CTCCAGTGCC AGCAGCTGAG ACTCCAAGCC CCAGGTCTTC CAGGTTCCAT GGGGAAGGAA 1200 TACATCCTCT GCTAAGCACA GAGTTCTGAA GACATCCTAA GTCAACAAGC 1250
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