Tag | Content |
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EnhancerAtlas ID | HS133-15726 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:42973400-42974890 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA | MA0729.1 | chr19:42974191-42974209 | CCATGACCTTTTGGGCTT | - | 6.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33863 | chr19:42973682-42974380 | HCC1954 |
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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 |
GH19I042470 | chr19 | 42974152 | 42974353 |
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Enhancer Sequence | ATCACTTGAA CCCAGCAGGT GGAGGTTGCA GTGAGCTGAG ATCATACCAC TGCACTCCAG 60 CCTGGGTAAT AGAGTGAGAC TCCATCTCAA AAAAAGGGAG GGAGGGGCAT TTGTGGAGAA 120 AGATGCACAA GAAATGCTCA GGCCAGGCAT GGTGGCACAT GCCTGTAATC CCAATCCTTT 180 GGGAGGCCGA GGTGGGAGGA CTCCTTGAGC CCAGGAATTC AAGACCAGTC TGGGCAACAT 240 AGCGAGACCT TATCTCTAAA AAAAAAAAAA AAAAAAAATT TAAAAATTTA GCTGAGTATG 300 GTGACACATG CCTGTAGTCC CAGCTACTTG AGAGGCTGAG GCAAGATGAT CACTAGAGCC 360 TTGGTGGTCG AGGCTGCAGT GAGTCATGAT TGCCCCACAG CACTCCAGCC TGAGTGACAG 420 AGGGCAGAGT CTGTCTCAAA ATAAAAAAAT AAAAAAGACA TACTCAGACC AACTGGTGCC 480 ACATTTTTGT CGGAGGCTCA TACATTAAGC TGCTGTCCCC TCCACCACAC AGAGGCACAA 540 AGGCAGTGGC AGCTGGGACT TCCTTCCCTG TTTTCTCCCA TTCTTCTAAT TCTTCATGAT 600 GCCCTTTTGT GACTTCTTTC CCCCTTTAAT ACTGCTTTTG ATATCATTTC AGCCTGATGT 660 CACTTGTGCA AAATCACTGG GGGTAGGCTG GGTGAAAATT TTCCAAACCA CACATTCTTT 720 TTTTTTTTGG GACAGAGTCT CACTCTGTTG CACAGGCTGG AGTACCATGT CACAATCACG 780 ACTCACTGCA GCCATGACCT TTTGGGCTTA AGTGATTTTC CTGCCTCAGC TTCCGGAGCA 840 GCTGGCGCAT GCGACCACAC TTGGCTAATT TTTTGTAGAG ACAGGGTCTC ACTTTGTTGC 900 CTACACTGGT CTCAAACTCC TGGGCTCATG TGATCCTCCT GCATCAGCCT CCCAAAGTGC 960 TAGGATTATA TATCAGCTTG AGCTGCTGTA CTCAGCCCAA ACCCCACATT CTTTTTTTAT 1020 TTTTGTTTTT TATTTTTTGA GACAGGGTCT TGCTGTATCA CCCAGGCTGA AGTGCAGTGG 1080 TGTGAACATA CCTCACTGCA GTCTCAACCT CCTGGGCTCA AGCGATCCTC CCACCTCAGC 1140 CTCCTGGGTA GCTGAGACCA CAGGTGTGAG GTGTGTGCCA CCACATGTGG CTAACTTTTT 1200 AACTTATTTT TGTAGGGACG GGGTCTTGCT ATATTGTTCA GGTTAGTCTC TAGCTCCTGG 1260 GCTCAAGTGA TCCTCCTGCC TCAGCCTCCC ATAGTGCTGG GATTATAGGC ATGAGCCACT 1320 GCGTCTGGCC CAAACCCCAT GTTTTTTTTT TTTTTTTTGA GACGGATTCT CTGTCGCCTA 1380 GGCTGCAGTG CGATGGTGTG ATCTTGGCTC ACTGCAATCT CTGCCTCTTG GGTTCAAGTG 1440 ATTCTCCTGC CTCAGCCTCC CTAGTAGCCA GGATTACAGG TGCCCACCAC 1490
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