Tag | Content |
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EnhancerAtlas ID | HS133-01469 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:42136690-42138580 |
Target genes | |
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) |
Nfe2l2 | MA0150.2 | chr1:42138119-42138134 | AAGAATGACTCTGCA | + | 6.34 | TFAP2C | MA0524.2 | chr1:42138089-42138101 | TGCCCTGGGGCT | - | 6.11 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_25389 | chr1:42128062-42151877 | DND41 | SE_37004 | chr1:42135687-42138210 | HSMMtube | SE_37004 | chr1:42138338-42140596 | HSMMtube | SE_39755 | chr1:42136970-42140463 | Jurkat | SE_58724 | chr1:42087777-42140608 | Ly1 | SE_59507 | chr1:42123200-42165829 | Ly3 | SE_61251 | chr1:42088347-42140325 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I041670 | chr1 | 42135706 | 42140484 |
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Enhancer Sequence | AAATTTTCCC TGATTATCAT CCCTTTCTGC TTCAACCAGA CACCCCCAAG CAAAGGCAGC 60 TCCTGCGGGT GGGGGACAGG CCCCTCCCCA CCCTGCCTCT CCTAAGCCTC CCTCTCAGGG 120 GACTTGTGAG GAGTTAATGA AGTTGAGCCC AGGAAAGCAC CACAGGTAGA CTGTAGAACG 180 CTGGGCCCCC AGCTGGCTAT CACCATCACT GCCCAGCCTC GACAGGGAGG CAGGGGCTTC 240 GCCTTTCCTC TGCTACACAC TGGCAGATGC AAGAAGCAGA TCCGCTCCGA AGCCTAGATG 300 AAGTCGCAGT TAGCAGCCTA ATTTTAGACT GAGCATCTGC TCTTCCGTCC CAGAGATGCA 360 GCTCTGTCTG GGATTTGCTC CTTCTGGAAT TGCCGGAGAA ACGAATCCTG CTCTCGGGGG 420 CAGGCACTGG TGGTGTCCAG ATCAGAGCTG ACCAATAGGC CCTGCCATGG GGAAGGCCTC 480 AGGAGCTGTG CCACCCTGGC CATCCTGTGT CCTCCTAGCT GAGCTCCCAT CTCACACTGA 540 CATCTACAGA GTCCTATAGC TTCCATCTTG GAGTCCCACT CTGCCTTCTC AGAAAGCCAC 600 AGGTCAAATG AGGCTCCGCC TCACGCAGAA CAGGGGACCT CCTGGACAGG AGTGGCTTTT 660 ATCCATCCCC ACACCCACAG CTCCCAGCGC AGACCCCGAA GAATTCATCC CAGGTGAGTA 720 CGGCCCAGTC AGACTAAGAC TAGGAGAGCA CAAAGGAAGG ACCAGTTGTT TGCAAATCTT 780 CCCAGGAAAG CTTGTCAGAG GAGATGAGTT TTGAGTTGGA TTTTGAAGAG TGGGTAGGTA 840 TTTATCAGTG GAAAAGCCAG GAAAAGCTAT GGAGGCAGGG GAAACAGCTG AAAAGAATAT 900 GAAAGTTGGA GAATGGCCTG AAGGGAGGGA GAAGAAAGTG GGGAGACCCT GGTGGGGATT 960 GGGCAGGGGC TGGGTGCAGT TGAGTTGGGC CACAACTCCA GGCTAAGCAG TTGGGGTTGT 1020 ATCTGCAGGT GGGAGAGTCT ATGGGGGCCC TTAGCGCATG AGTGTGCTCT GACAGATGGC 1080 TGTGGAAGAC TTCCAGGTGG GAAGCCCATG CCCCTCTCAC CTGGGAGAGC CACTTTCCCT 1140 GTTGACTTCC TCCATGGTTT GCCAGGTCCT TTGGGGCCCT CCCCACCTCC CTGGCACATG 1200 TGGGGCAGGC CCCATGTGCA GAGTACACTG TGGATACTCA CTCCCCTCCC AGACCCCCAC 1260 CTGAGCTCTG CCCACACATC TCCTGGCATC AGGCCCATCA CCTCCCACCC TTCTGACCGC 1320 TGCAGCCACT GCTTGGTCCT TGTCTGAATC CCCAGTTCCC ATGGGCAGTG TTCTTTTGCT 1380 TCTCCGGCCT CAGCTTCTCT GCCCTGGGGC TGTTATCTCA AGATTCCTCA AGAATGACTC 1440 TGCAGTCCCA CGTGCCTCTC CCTACCTTTC TGTTTGTGGG CGGCAAGCCC TGTTCTCTGA 1500 GCTAAGGACT TTCTACACAT CACCTTGCTT TATCCCCCAA CAATCCTGGA AGATGTTTAT 1560 TATTTATCCC TTTTTACAGG TGAAGAAAAG GGTTTGATGA GCTTAATTTG TGATTGATCA 1620 CACAGCCAGG AAGTGGTAGA GTGGAGGCCG TCTGCCTCTC AGTCCTCTCC CACCAGGTTC 1680 CCCCAGCCTT GAGGGCAGGG CTTGAGCAGT GATGCCCAGG CCAGAGGCAG TCAAGACATC 1740 TGGCCAGTTC AGGTGGGGAG TGAGGAGAGT GAAAGAGGAG GAAGACTCAG CCAGGGACCA 1800 TGCCTGGATT CCCTTGAGAA AGAATGAGTT AAACACTTAC GTAAAGAGAT TTGCAAATAG 1860 ATTCTACAAA ACAACATTTG GATGATTTAA 1890
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