Tag | Content |
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EnhancerAtlas ID | HS133-01466 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:42083220-42084940 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:42083498-42083508 | TTTAATTAGA | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37004 | chr1:42081562-42085003 | HSMMtube |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I041618 | chr1 | 42083801 | 42083950 |
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Enhancer Sequence | ACCTCTTAAA GTGCGGCACC GCCTGGGGTG ATCTGGCTTA TGCCCCTTGC TCCCCATTCA 60 AAGACACACA GAGAGGGACA TTGACAGTGC ACAGGAGATA TCAACAGTGT TTCCTGACAT 120 CCATGATGCA CGGGAGAGAA CCAAGTAGGT AGGATTCAGA CTTCTCATCT TCACCTCTCC 180 CAAATCACAC ACATGCCTTC CTGAGAAAGA GACCCTTTGT GAGATATTAA AGACCAGCCA 240 AATTCTACTC CCACATCATA AGAAACTGGA GTTCACTCTT TAATTAGAGA AGATGCCAAT 300 GGCTTTGGAA CTGGACAGGC TTCTAAGCAT CTTTTAGTTC AGTGTCTTCT TTTACAAAAG 360 AGCCCTGGAG GGCAATGACC GCACCAGGCT CACATGTCAT TGGGTGTGTG GCAGCATTTC 420 CCTAAGCTGA GACCAGGGTC ACTGGTGGGT GCATTTCCCC AGCTCTCTCT GCCTGCTGGT 480 TCCTAGGAAC CATCTTACTA GAAAGGCGTA GTGTAAATAT TTTGCTAAGC AGCCAAGAGA 540 GGAAACTTAC CCAGGCTGAG CTGCCCTGTG CTGGGTGCTG GCCATGGACA CAATGCTCAA 600 TGAGGGCCAT TATCTGGGAA GGGAGGGCTG TTTGTTCCGC TGCGGGATGG TGCCAGAGCC 660 CGGAGCCACC AGGCTTGCCA CTCTGGCTGC CACACAGAAG AGTCTCCTTG CGCTCAGCAG 720 ACTCTGCGGT TATGCAATGC CGGGCCAGGA GGTTAACTCT CCCCAGGCCA GGAGCCAAGC 780 CTTGTTCCTT CCTGCCTAAG CATGTCCATC TGAAAATGCT GAAAATTGAG GGCCTCAGTG 840 TTTGCAAAAT GTGCTCGGGC CCTGAACCTG CTGGTTTATT CCAAAGGGCG TAGTGTTGAG 900 GAGCTGGTGT GCCCATCCTT GTGGCTCCTG GCAGCCTCCT ACCGAGGCCC AGTGCTCTGA 960 CAGCAGCGTC TGCCTGCCAT CCTCGGGCAC CACTCATAGG CCTTGCAACC CTTTGCCTGG 1020 GTGCCCCTGT CCCGTTCTTT CCCTTTCGGT GGTGTCTGGT CTAAGTCCTT TCTTAAGCCC 1080 GAGTTCTACT CACTTGTTCA AAGCCTTCCC TGACCACCCC AGGCCCCAGT GACCTGAGCT 1140 CAAGGATGAG TTTCCCAAGA CAAAAGGGAC CTTGGAAGTT ATCTATCCAC CTGGCCCATT 1200 TTCCAGATGA GGAAACTGAG GCTTGAAGAA GTTGACTAGT CTGAGAGAAG ACTGAACAGA 1260 TGTGTCAGCC TGGCTCCCCT CTCAGAACTC TTTCTCTTAT ACCTCACGTC CCATCTGTCA 1320 GCAAATCATG TTGGCTTGAC CTCAAAATGG AGCTGGAATC AGACCCCTTC CCATGGCCCC 1380 CGCAGTTGCC ACCCTGGTGT GTGACTCTAT CACCTCCTGA TCTGTCACAT CACTGCCTCC 1440 TAGCTGGCCT CGGGCTGCTG CCCCCGCCCC CTCCAGGGCA GCCTCCACAG CCTCCTTCGG 1500 CAGGACAGCC CACTCCTCTG CTCAGGCCTC CCAGGGCTTC TGGATGTTGT GCCTGCCTCT 1560 CCCTTCCAGC CTCCTCTGCT CCTGTGCCCC CACCCCCACT CCTCCAGCCA CACCAGCTTC 1620 CTTGCTGTTC CCAGCAGGCT GATCTTGCCT CCGCCTGGAA TACTCTTTTC TGATACCCCC 1680 AGCACTTGCT CCTCGCCTCC CTCAGGTCTT TACTCTCCAC 1720
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