Tag | Content |
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EnhancerAtlas ID | HS133-00046 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:1614390-1616020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | ERG | MA0474.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | GLI2 | MA0734.2 | chr1:1615868-1615883 | GGACCACCCACAACC | + | 6.19 | Zfx | MA0146.2 | chr1:1615990-1616004 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24735 | chr1:1614536-1615205 | Colon_Crypt_3 | SE_32013 | chr1:1614622-1615903 | Gastric | SE_52422 | chr1:1614441-1616065 | Small_Intestine | SE_65325 | chr1:1613532-1616277 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 1615717 | 1615777 | chr1 | 1615180 | 1615915 | chr1 | 1614813 | 1615376 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001683 | chr1 | 1614749 | 1615855 |
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Enhancer Sequence | CTGTAATCCC ACCTACTCAA GAGGTTGAGG CAGGAGAATT GCTTGAACCC TGGAGGTGGA 60 AATCGCAGTG AGCCGACATC GAGACATTGC ACTCCAGCCT GGGGGACAGA GCGAGACTCT 120 GTCTCCAAAA ACAAACAAAT AAATAAACAA GCAAATAAAT AAAGTCCTGT GAGGAATGCA 180 CAGTTTCTCT GCACTCCCAC ACAACACTTC CCACAGGAGA TGCAGGTTAT TTCCACGTTG 240 AGCAATTCTC CACAGACACT AGCTGTGTGT CCTCTGGTTC AATTCCCTCC CGAAGCCGTC 300 CCCCTGGGGA GAGTGCCAGG TCCCCTGCGG CGAGGGCTGG ATCCCACAAG ACTGCCCCCT 360 CCTCAGATGC TGGTCAGCCT GTGGGCCGTG CTTCTGACCG GCAGCTATAC ATCGGGGTTC 420 CCACGACACC CTCCTGAGGA TCAATGAGTT TGACAGGACT GCCCTACAGA ACTGCAGAAA 480 GCACTTACGT TAAAAGAAAA CAGAGGAGCA GCCGGCCGCA GAGACGCGCA GGCAAGGCCT 540 GGGCAGGTGC TGGGTTTCAG GCCCTCTCTG GGCGCCACCC CCTGCCCCCA GCACCACAAT 600 CCGAAGACCA TCCCACTCTT TCATCTCTCA TTCACGGGTT TTTACAGCGT TTAATCTCCA 660 CCTTCGCTCG CTGCGTCCCT GAGGTTGGCG GGTGGGGCTC AAAGCTCCCA GCCTCCAATC 720 CTGGGGTCAC CTGGTGTTCT GGCGACCAGT CCCCCCTACC CCCGCTCTCC AGGGCCCCAC 780 CCCCTGCCTC ATCAGCATAA GCTCAGGTGT GATCAGCATA AGCTCCGGGG TGATCTGAAC 840 CACTCCTGTC ACTCAGGAAA TTCCAAGGCT TCGAGGAGCT TCTGTGCCAG GAACCAGGAA 900 CAAAGACCAA ACACATTTCA TATCAGAGCA CAAGTGCAAA ACATCATGGT TGGAAACAGG 960 GTCTCAGAGT CCTCCAGGTG CAGGTGCCTG TTCAGACCAG AGACCACAAA GTTGTAAGTC 1020 AAACCTTCAT GTTTGGCCAG CGGCGGTGGC CCACACCTAG AACCCCAGTA CTTTGGAAGG 1080 CCGAGGAGGG AGGATCGCTT GCTGTCCACT CACGTCTGGG GCACAGCCCA GGAGACCCGT 1140 GGGCCGCAGG GTAGACACTC AGCAGTCGTG AGACGCTTGC CCCAGTGCAC TGTCTTTTCA 1200 AGGCCACTGA CATCTCCACA GACAGCCCCC AGCCCGTCCT TTGGCTCTTA ATGTGCCTCA 1260 TCCACCTCCG CGTGCTGACA CCCACATCAG TGACATTTGG GCTAAGCCGC CTAATGCAGA 1320 GTGGCTATAA GCGCGCTGAG CCGCTCGTGA AATTCAGACA ACCCCACCGG AAGTGAGAGA 1380 GAGGACGGCT GTGAGCTCAG GGCAGCGTTT CTGCTGAAGG CGTTTGCTTT CCCACCATCA 1440 TAAAGTCAGA AAATCACAAC TCAGACCATG GTAAGTGGGG ACCACCCACA ACCCAAGTGG 1500 GCCTTGGAAA TTAAGAATAG GAGGCCGGGC GCGGGGGCTC ACGCCTGTCA TCCCAGGAGG 1560 CTGGGCACAG TGGCTCACGC CTGTCATCCC AGCACTGTGG GAGGCCGAGG CGGGTGGATC 1620 ACAAGGTCAG 1630
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