Tag | Content |
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EnhancerAtlas ID | HS133-07429 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:48278850-48279810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:48279016-48279034 | CCTGGCTTCCATCCCTCC | - | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_52529 | chr12:48275452-48280304 | Small_Intestine |
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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 |
GH12I047885 | chr12 | 48279021 | 48279170 |
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Enhancer Sequence | GCCCACCCCA CCAGCAATTC ATGTTCTGAG TACACAGAAC ATCCCACTGC TTTTGCTGGG 60 ACCGTCCCCA GAGCAACCCT CTCCTGACCC TGCTTTAGAA ATACCAAACC CCCAGCACTA 120 AGCTTCAGAG AAGCAGAGGG GGAGGAGCTC AACTCTGTAG AAAGCCCCTG GCTTCCATCC 180 CTCCAGGGCC TGCATCCCAC ATCAAAAACC CTGCCTGACC CTGACCCCAG TGCTGACCTT 240 GCCTTAGCAA GAAATGAGAA GATAACACGT TTCCTTCCAG TCACTGAAGC CACAACCATT 300 GCCTCTCCTA CACGTCTGCC TGTCAGCCCA CACCACAGGC GGCCCCATCT TGCGGCAGCT 360 TCTGTTAAAT GGGCATCCCC GGGGCCATCT CGCCTACGGC AGTCTTGCAG GGTGGCAATT 420 GCCAGGTGTC CTGGGCAGAG CCCTGGGAGG ACAAAAATCA AAGTCCCTCA TGGCTCAGTT 480 TAACTCCACA TTGACTGGAC CCTCCTAAGG GTGGTAAAGC TGTGACTCTG AGAAGGACCA 540 TGGAGTGGAC AAGAAGTCTG ACCGCTAATG TCTTTTCTAG CTCTGAGAGC ATGCAACTCC 600 AAGACTGGAA TTCCCATCAT GAGAAGCACT ATTTTTTTTT CTTTTTAAGA GACAAGGTCT 660 CCTCTGTTAC CCAGGCTAGA GTGCAGTTGC ACAATCACAG CTCACTGCAG CCTCTAATTC 720 CTGGGCTCAA GCAATCTTCC ACCTCAGCTT CTCAAGTAGC TGGGGTTACA GGTGTGAGCC 780 ACGCCAGGAA AGAAGACCTT AAATGAGATG AAGCTTTCTC CCTGATCCCT CATTAGCCAG 840 ATGAACCACA ACATTCATGC CTCAGTGAGT GAGACTCACT CATCCTCAGA TGCCAATGAG 900 CAGGAAGGGC ACAAAAGATG TGGCCCCTAA TCGACCCCAG GAGAGGGGTC CTCTCTCTGC 960
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