Tag | Content |
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EnhancerAtlas ID | HS133-24077 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:79486500-79487720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr4:79487428-79487439 | CCACACCCTCC | + | 6.32 | RARA(var.2) | MA0730.1 | chr4:79487211-79487228 | AGGTCAGACAAAGGTGA | + | 6.42 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_34437 | chr4:79484978-79487832 | HCT-116 | SE_35890 | chr4:79485202-79491855 | HMEC | SE_57470 | chr4:79486500-79486947 | VACO_503 | SE_64594 | chr4:79485752-79487643 | NHEK |
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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 |
GH04I078563 | chr4 | 79484905 | 79491855 |
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Enhancer Sequence | AGTAGAGAGG AACATGACTC AGATGTTCAA GTACGGGAGA GCGATGATTG TGAGTTGGAC 60 AAGAGCAGGA GCAAAGAACC TGGGGAGGAG CGCCCATGCG ATTATCTTCT TAAAATAATC 120 TCAGCAGGCC TTGCTGATAG ATGGAATTCA GAGGGAAATG CAGGTGAAGG AATCAAAGGG 180 GACTCCCAGG TTTCTGGTGG CTGATGATTG CTCCTTTTAC AGGGATGGGG AAGGTTGAGG 240 AAACTGAGCA AATTGGCGAT GAGCACAGAA ACTGGAGCCA GATTGCCTAG GTTCAAATCC 300 TGGCTGTGCC ACAAACTACC TATGTGACCT TGGCGAGTGT CTTAACCGCT CTGGACCCTC 360 TTTTTTCTCC TCTATAAAAT CACGGTATTA ATTGTACCTA CCTCATAGGG TGGTTTTGAG 420 GATTAAATGA TCAGGTATAT GTAAAATACA AGTAAGTACT ATGTAAGTGT CAGAAGGGGG 480 AAGAAATAGC TTGGGAGGAA ACAATGAGTT GATATAGGAG ATAATCAAAA CAAATACATG 540 GAGGAGACAT TGAATATACA AGACCAGTGC TCAGAACTGA AGTCTGGGCT AGAGCTATAA 600 TGTGGGATTT TTCTGTATAC AGAAGAGGGA GTGGAAGAAA TAACCCACAG CAGGATTAGA 660 GGGAAAGAAA AGAGAGAGCC ACTTTCCACT TTAGAATTGC GTATTTTATA GAGGTCAGAC 720 AAAGGTGAGT GCATCCTGGA GAGGCGGGAA GAAACCTAGG AGGTGAGGCA CAGGAGCCAA 780 TGGAAGGCAG GCTAGCTGTG AGTGACACAT GCTCCAAGGG GTCAAGGCTT CTTATTATAA 840 CTCATGTGTC ATGGAAAATA CAACATCAAT GGCTTGTTTG TCCCTGTCTT CCCTGATTTC 900 TGAATCTCAT TCATCTTTCT ACTCCATCCC ACACCCTCCT CTGTTCTCAC ATTCCAGTCC 960 TCTTGCTCTG ACACTGCCCT GATGATGAAA TCACTCTATT TAAAAAAGAA AAGCTGAACT 1020 ATTCACAGTA GCAAAAATAT GGAATAAAAC TAAGGTTTAT CAACAGAGGA TTGAATTAAG 1080 AAAATGAATG TAGAATACTA TACTATACTA TACTATAGAA TACTACTCAG CCACTCAGCC 1140 ACAAAAAAAA AAAAAATGAA ATCATGTCTT TTGCAGGAAC ATGAATGGAA CTGGAGGCCA 1200 TTATCCTGAG TGAAATAACT 1220
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