Tag | Content |
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EnhancerAtlas ID | HS133-27078 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:45420930-45423070 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr6:45420931-45420942 | AAGGGGATTAG | + | 6.32 | JUN(var.2) | MA0489.1 | chr6:45422235-45422249 | ATGAGTCATCTCTT | - | 7.95 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_39619 | chr6:45420652-45421547 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I045453 | chr6 | 45421190 | 45422964 |
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Enhancer Sequence | AAAGGGGATT AGTGGCCCTC CTTTTTTGCT GTGAGGCCAC AGGATTGATA GTGGGAAGGA 60 AAATCAGCTG GAGAGAGGTT TGGTTTCCTC CTGTTGTTTA TCTTTATAAA AAAGAACGCT 120 CTTCTCAAAC ACGTTGCTAT AGGAAAGGTC TCTTCATTAC CTATGTGGGG ACAGTGGAGG 180 GCCAGTTCCA TATTTTCTGC AGTAACTGAG GCTGGCTCTG TTTTCCTGAG GAATAAGCTG 240 TGAAACTGAG GATATACTAG GTTATCTGAA GCAACAGAAC ACCCACTGGT ATACCCACAA 300 AAAGTGTTTG ATTATCTGTT CTCCCCTGAG GACTTTACTT AAGACTTATA AACCAGTCTC 360 CCTTTCCTTA AGAGGTACTG TGATAGAGAC AGAGTGAGAG CTTTCAGTGG TCAGGGCTTT 420 CTAGAAGGCT GGACACATGG CCATGATAAT GCCTAAAGCA CAATCAAGAA GGATGGAGGC 480 TTTTATGAAG GTCTTGAGAT TCAAAGGGAA CAAAAGTGGA TGGTTTGGAG AGTGTGTCAG 540 TGAAGGTCCT GTGCTTTGAT CATGTCTCAG GAGATTCCCC ACATTGACTC TCTTTGGGTA 600 TTTATGAAAG TCTACATTGT TGGCACAGAT CTGATATAGC AAGGAAATTT GCTGGGGCCA 660 GGGATCCAAG AGTTTTTGGA TTGTATAATT AGGAAAGCAC TGATGGTCCA AAACGCAGGA 720 TGAACATTCA TTTTATTTTT TACAGAACAT ATTTTTGTCC CCTTTCTGTA TATTATATAT 780 TGGTTCTATA TTTTGTGAGA CCTGGTGCAG CAGTTCCTTG GTAGAGCCAA ATAGCCTGAA 840 TGAAGAGAAG GAGAGATGCC TCTTCCTTTG CTTTCATTCT AGATTGTGTT GGAGCTATGC 900 TGAGGATGGT GAATAGAGAA ACTGATTGTA GTTAATTTGT CACCTCGTAG CCCAGTGGTA 960 GCATTTGAAT GGAAGTAAGT TAATGGAAAA GGACTTTGCA AGACATACCA GCCCCAACCA 1020 CTCATTCTTG CTGAGGGTCA ACCCACTGTC AGATATAGGT GGAGAAGCCC TTCTGTGGTA 1080 TGGAGGCACC ATTTCTTTAT TCTCTTGTTA GGAAAACTGA AATATAAATA AATAAAAATT 1140 TGCAACTGAA TTGGAAAAAA TCTGACACTG AAGGATGAAA TGTAGCTTTC GTAGCATGAG 1200 ATTTGTGGCA CAAACTGACC AGAGGAAGGA AATCTGATGA TCTAGATAGA TGCCTTTGGT 1260 TATTACCACT TTTGCTAAAT GCCTCTCTGC TAAGAACTCA ACAGGATGAG TCATCTCTTA 1320 GCTGTAAACA AAAACTTTTA TGGGGAAGGG AGAAATCCTT GTGTTTGAAG GAATAGGTGG 1380 CATTTCCGGC TAATTTATAA ATGTCTCCTT TCATTCCTTT CTAAATTGGG ACAAATTGCT 1440 CCAAAAAGTC TATCAGAAGA TTATGTATGT ATGTAGGTAT TTATCTATGT ATGTGTGTGT 1500 GTATGTACTT TTGTTACAGC AATGAGGTCC TCCAGCTGAA CCATAGCTGA GTTCTATTCC 1560 TACTTCTATT CCTGGTGCTA TTTGGTCAGT TCTTAGAATG GATTTTGATA GTTTTCACTT 1620 CAGGAAAACA CAGTCTCAGG CCGGGCATGC TGGCTCATGC CTGTAATCCC AGTACTTTGG 1680 GAGGCTGAGG CAGGTGGATC ACTTGAGGTC AGGAGTTCGA GACCAGCCTT GCCAACATAG 1740 TGAAACCCCG TCTCTACTAA AAATATAAAA ATTTGCTGGG CATGGTGGCA GGCGACTGTA 1800 GTCCCAACTA CTTAGGAGGT TGAGGCAGGA GAATCGCTTG AACCTGGGAG GTGGAGGCTG 1860 CAGTGAGCCG AGATCGTGCC ATTGCACTCC AGCCTGGGCG ACAGTGAGAC TTTGGGAAGA 1920 AAAAAAAGAA AAGAAAACAT AGTCTCACCG TTCTCCTCCA CATAAATGTG GCCAGGCTGT 1980 TGGAAAGCTC GTGGTTTAGA AATTATTTAA AACAACTGCG TTAGAAAATA TTATTTGTAC 2040 AATAGCATCT TAAATCCCAA GACCTCTATA CAACTTACAA AGTAACTGTA GAAATTCAGG 2100 GAAATTCTTC TTTTTTAAGT TTTATTTCAT TTTTAATTGA 2140
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