Tag | Content |
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EnhancerAtlas ID | HS133-19266 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:47470030-47471470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr20:47470562-47470575 | CCCTTGACCTTTG | - | 7.82 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59612 | chr20:47363420-47493230 | Ly4 |
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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 |
GH20I048853 | chr20 | 47470097 | 47471250 |
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Enhancer Sequence | GATAGCATGG GGGGAACCAC CCCCATGATT CAATTACCTC CACCTGGTCC TGCCCTTGAC 60 ATGTGGGGAT TATGGAGATT ACAATTCAAG GTGGGATTTG GGTGGGGACA CAGAGCCAAA 120 CCATATCAGT AGGATACCTT CTGCCTTGGT ACACCATGCA CACACACACA TCCAACGCAC 180 ATGCACACAT ATGAACACAC ACACACTTGC ATACACCTTT AAGGACAGTC AATACAGTGT 240 GTTGAAAGCC TGCTGAGCTT AAACTCTGCA AACCTCAGTT GGATCCCAGC TCCACCAGCT 300 GAGTGACATC AAGCAAGACA CTTAGCCTCG ATGGGGATGA TCAAAATAGT CCTGGCTGCC 360 CTGCAGACCT TGGGTGGTGA GAAAACTCTT CATAAACTGT CAAGCATACA CATGAAAAGA 420 CTCATTATAA TATGAACCTG GATGGGTGAG CCAGATGGGG CAATCCACAG CCTTCTCTCC 480 ATGGGGTCCC GTGCACACCT CTCAGGACGT CACTGCAAGG TGGAAACCCA ATCCCTTGAC 540 CTTTGCAGTC AGGCAGCTGC TCCGAACAAC CCCTGGCAGT GCTAATCTCC AACTCTCCTC 600 TCACCATCGG GTCCAGCTGC TGGGCTGAGT CACACGCAGG CCGAGGGACA GGCACATGAC 660 TTGTGTGTGG AGCTGGTGTG AGTGTAGTGG TTGGGGGAGG GTAGTAAAGA CCACAAGAGG 720 TGATTACTCC CCACTTAGTA GGAAATTTCA CCTCCAGGGG AGGAGATCTA AGCCTGACTC 780 TAGGTCGGAA CTCAAGTGGC TGCCTGGCCT GTCTGGCAGA ATTCTTCCTC CGGGAAGCCC 840 ACTGGATGTG TATATGTGTG TGTGTGTCTG ACAGAGGGAG GGGCAGAGTG TGTACAAAAG 900 AATGATACTA AAAATAACTA GCCAGGCACC TGTGGCTCAT GCCTATAATC CCTGCTACTT 960 GGGAGGCTGA GGTGGGAGGA TCACTTGAGC CCAGGAGTTT GAGACTACAG TGAGCTATGA 1020 TTACACCACT GCACTCCAGC CTGGGCAACA GAGTGAGACA CCCTCTCTAA AAAATAAAAA 1080 CTAAAAAAAA CCACATGTAC TAAGCACTTA CCACATGCCA ACCTCTATCC TGAGCACCTC 1140 GAAGATTAAA CTCATTGAAT CTCCATTGAT ACTGGTATCA CCATCACCAT TACGATCATC 1200 CTCACTTTCC AGATGAAGAG GCCGAGGCCC AAAACAGGTA ATGAATTTTA CCAAGGTCAG 1260 TCATATAGCC CAGGTTCAGA GACAGTCTGA TTCTAGAGCC TCCGCTCTTA ACCTCTCAGC 1320 TACAGGGAAT TTCATTCCTT GAAGGGGGTT TCCAGAGGTC ATTTGGCCCA GTGCAGTGAG 1380 TGAGATGATG GAAACAGTCA ACCATGTTTG CACCTGGCTG TGTGACCCTG GGCAAATTGA 1440
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