Tag | Content |
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EnhancerAtlas ID | HS133-10073 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:55580970-55581910 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr15:55581595-55581613 | CTTTCCTCCTTTCCCTCC | - | 6.26 | IRF1 | MA0050.2 | chr15:55581540-55581561 | AAACTGAAAGCAAAAGAGGGA | - | 6.04 | IRF1 | MA0050.2 | chr15:55581534-55581555 | ACAGTTAAACTGAAAGCAAAA | - | 6.05 | MSC | MA0665.1 | chr15:55581185-55581195 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr15:55581185-55581195 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr15:55581185-55581195 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr15:55581185-55581195 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09264 | chr15:55568622-55583321 | CD14 | SE_14785 | chr15:55579727-55583273 | CD4_Memory_Primary_7pool | SE_18099 | chr15:55579872-55583433 | CD4p_CD25-_CD45ROp_Memory | SE_18557 | chr15:55579573-55583428 | CD4p_CD25-_Il17-_PMAstim_Th | SE_22366 | chr15:55573126-55583471 | CD8_primiary |
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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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Enhancer Sequence | ACTGTTTTCC AGATTGTATT TTCCCTCTAA AGCAAGTTTT TAAGGCCGAA AAAAAAAAAA 60 GAACAAGAAC AGTGAGTGGA GAATCAACAA ATTTAATTAG CAATGATTAC AGAAAACTTA 120 AATAGCACAC ACAACTCTAT AATCCCTCTA CCCCCAATTC CAACATCTGA CTGATCAACC 180 AACCATAAAA TGTGAGAATC CATCCAGAAG GAAAGAACAG CTGTTAAGCT GTAGGGGTAA 240 GGACCCTGTG GCAGAAGACC CTGAGGCCAT GTGGGCCCAG GTGGCCAGCA GGAGCGGAAA 300 GGCTGGGAAG GCTCCTCAGT CCAGGGCTCA CAAGACTCCC TTCGCTTCAG GCCTGACTTT 360 GCTGAACTGG TGATCTATTG GGACAGAGAC AGGCTTTGGC AATAGTTACC AAAGCCTGTC 420 ATCATATCTG CACCACCACC AGTCCCGACC GGAGGGCCTG GCTGCCAGGT AGTTTTCAGT 480 CTAACTGACA GGAGAAGAGA GAGCCCCTCC CTCGCAGCTA GTCTGCAGTC CAGACCCTCA 540 CCAACCGGAG GGCAACCAGG TTAAACAGTT AAACTGAAAG CAAAAGAGGG AGGAATGAAC 600 CGGGGGGCGT GCGGGAGGTC GGGGACTTTC CTCCTTTCCC TCCTGGAAAG TTTCCTACCC 660 CTGATGGGCA TCCTCCCACC TGGATGCAAC CCGGAGGCGA TCTGAGACCC TGGCCGGACC 720 TGGGACCGCA CCTGGCCAGC ACCAGGCAGT TGTCATCACT GGGGTCTGCG CTGAGGGCCT 780 GGGAGAGAAG CCACTCTTCA GGCGGGCTCG GGCGCCTGGA GGCGGGGAGG AAGGGCGGCG 840 CACTCGGACC CCAGCCCTAG GACGGCCCCA GGGGGACGCC TCGCTCGGCC CTCCCGGAGG 900 GACCGGACCC GCCGCGCGCC TCCCGCTCCT CAGGCCCCCT 940
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