Tag | Content |
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EnhancerAtlas ID | HS041-17091 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr6:6855900-6858070 |
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) |
HES2 | MA0616.2 | chr6:6856355-6856365 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr6:6856355-6856365 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr6:6856091-6856106 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09639 | chr6:6856206-6860523 | CD14 | SE_34636 | chr6:6854073-6860691 | HeLa |
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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 |
GH06I006854 | chr6 | 6855045 | 6859895 |
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Enhancer Sequence | TCATGGTGGT TCACACATGT AATCCCAGCA CTTTGGCAGA TCACTTGGCC CAGAAGTTCA 60 AGACCAGCCT GGGCAACATA GTGAAACTCC GTCTCTACAA AAAAAATACA AAAATTAGCA 120 AGTCTGGCTG GGTGCAGTGG CTCATGCCTG TAATCCTAGC ACTTTGGGAG GCTGAGGTGG 180 GTGGATCACC TGAGGTCAGG AGTTCAAGAC CAGCCTGGCC AACATGGCAA AACCCCATCT 240 CTACTAAAAA TACAAAAATT AGCCGGGCAT AGTGGCATGC GCCTGTAATC CCAGCTACTT 300 GGGAGACTGA GGCAGGAGAA TCGCTTGAAC CCAGGAGGTG GAGGTTGCGG TGAGTGGAGA 360 TTGCACCACT ACACTCCAGC CTGGGCAACA GAGTGAGACT CAGTCTCAAA CAAAAACAAA 420 AGCAAAAACA AAAACAAAAA TTAGCCGGGC GTAGTGGCAC GTGCCTATAG TCCCAGATAC 480 TCGGGAGGCT CAGATGGGAG AATCACTTGA ACCCAGGGAG CAACAGAGTG AGACCCTTTC 540 TCAAAAACGC AAACAACAAC AACAAAAATT AGCCAGGTTT GGTGGCTTAC ACCTGTGGTC 600 CCAGCTACCT GGGAGGCTGA GATGGGAGGA TCAAGGATCA AGGAGGTTGA GGCTGCAGTG 660 AGCCATGATT GCACTATTGA ACTCCAGCCT GGGCAACAGA GCAAGACCTT GTCAAAAAGA 720 AAAGGAAGAA CGAAGGAAGA AACTAAGGCA GAATGGGAGA TAGTGATGAT GGGTGGGTGG 780 GGTTGCATTC CACAGAGCTG TCAGATAATG GGAGGAAGGA GCTAGACATG GAGGGTCTGG 840 GAAAAGCATC CCAGGATGAG GAACCAACAG AGATCCTGTG TCGCAGGACC AGGTTTGGAG 900 GCTGCTGGCA CCATGAGGAC GTGAGGGCTG TAAGCTGGCA GAGCTCTTAG AGTGAGCATG 960 CTGAGAGCTG TAGGTCATGG GTCGGAGCGT GGGTTCTATT CTACTGTGAC AGGAAGTCAT 1020 GCCGTGAGAG GATTTCCCCG CAGTGAAGTC AGGTGATTCG TGTCCTTAAA TGCTGCCCGA 1080 GGACTTCTGA GTAGGTGGAG CCTAGGGAGG GAGAGCAGAG GCAAGGGGAT CAGTCGAGCC 1140 CCGCTGGTGG GATGAGTCTG CCGGGACAAG GGGTGCTAGC TGTGGTCCTC GTCTGCCTTG 1200 TTCTCAGCTG TATCCTGGCC CCCAGATGAA GCCTGGCCAC AGTGTACTTG GTAAATAGTG 1260 GTTGCAGGAA TGACTGAAAT CCTGGCCTGA GTGAGCTCAC AACTTTCCAT ATGAGGCAAA 1320 TAAGCAGATC TGTTGGTTAT GACCCAGATA CGTGGTGACC AGGGCAAACG TTTGTCAGAG 1380 GAGTGACGGG TGGGGGCTGG ACTGTCTTCC CGGTACAGCT GTGGAGGAAA GCAGGCAGTG 1440 CAGCTGGGAC ATGCAGCCGC TGTCCCCTGG GGCTGGCGGA AGGGTGTGGA GTGACGGAGA 1500 GGGAGAGCTG CTGATCAGGG AGCTGGGCAT CCCGTTGCAG CCTTACTGGG AAGCTTGCAT 1560 CCCAGAGCCG ACTTGCCTCA CCTTTATTCA GGGATTCAGG CCCTTCCCCT CCCCCAAGGG 1620 CTTGCTTAAT TCCCCTGGCT TCCTTGAGGC ATACTCAGAA ATTCCTTTCA GTTCCCCTTT 1680 CTGCTGGCTG TGCTTGAGGC AGGGATGGGC CAAATACCCT CCACGCCCTT GGTCCATCCA 1740 GAAGTACTGA GTCAACAGCC CTTTCCCAGA ATCTACCTCC ATCTCTTTCC ACACCTGCAG 1800 CCGGACTGTT CCCAGGAATG AGGTGGGGCA GGACCTGAGA GCAAAGTGTG AGCTGGTGTG 1860 CAGAACCACC CGGAGGTGGA AGGAAGCTAG AATCTAGTGT AGGGTGCCTC TGACACTTGT 1920 CCCACACATA GATCTCCCAG GGATGACTGT GTGGGTCCGA GGTGGGATGG AAAACTTGCA 1980 TTTCTTACAG GCTGCTGGGG ATGCTGGTGC TGAGGCTTCC GATCACCCTG GAGGCACGGC 2040 TCTGTATGAA GGCAGGGTGA GGTTGGCAGA GGAGAGATAA ATACAGTCAC AATTTACTGA 2100 GTGCCAGACA CCGGGCTAAG GGCATTATGT GAATAATCTC TTTTAATCCT CACCAGCCCT 2160 GTGAGTTGGC 2170
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