Tag | Content |
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EnhancerAtlas ID | HS133-23603 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:196392480-196393930 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX3 | MA0684.1 | chr3:196393123-196393133 | TTTGCGGTTT | - | 6.02 | Zfx | MA0146.2 | chr3:196392607-196392621 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09200 | chr3:196391083-196393673 | CD14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I196666 | chr3 | 196392594 | 196393770 |
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Enhancer Sequence | TCAGCCTCCT GAGTAGCTGG GATGACAGGT GCCTGCCACC ACGCCCAGCT AATTTTTGTA 60 TTTTTAGTAG AGATGGGGTT TCACCATGTT GGCCAGGCCG GCCTCGAACT CCTGACCTTG 120 TGATCCGCCC GCCTCGGCCT CCCACAGTGC TGGGATGACA GGCTGAGCCA CGGCGCCTGC 180 TGATTTCTTT TTTTAAACGA CCCCAGTTGC AAGCAATTGG ACAAACTCTA ATCCTTGGTT 240 TGTATCACTG GTCATATCAC TTTTTATTTA TTTAATGTGC CAGATAACTT CCATTTGCCC 300 CTCCAGATCT ACTTCCCACT CTTTTCCACC CTGCCCCAGG AGGCTGGCCT CAATGGGCTC 360 CCTTGCCCTT TGGCTTCCAG TGGTATTTGG CTAAGAAGGA GGTTTGGCAA ATCACAGGGG 420 AGGAAGAAAG TGAGGTCAGA GTATTTATTC TCCTGACTCC TCCCTGTAGA TTTGTCTCAA 480 ACTGGCTGCA CCTATCAACC AAACTCACAC TCGTCTCAAG GCGGCTCTTT GCACACGAAT 540 CTCTGCCTTA GGTATCTAGG AACCACTCAC TCCCCTGGCT CTCTTCTCTG GGCCTAGCAT 600 GGGTAACAGC TCTGCCTCAC CAGCTCGTGT AATTGCATTA TCCTTTGCGG TTTGCCCTCC 660 CCTCTCCACC GCTTTGTGAA TCGTCCCTTT GTAAATCCTC CTGACTTGTC CTTGTTTGAA 720 CGTGCCATCT GGTTCCTGCT GGGTCCCTGC ATGACGCAGC TGGCTACTCA TTTAGTAATC 780 CTGAGCCCGA GAGATTCCAG CACTTGTGTC AGGGAGCCAC AGAGTGCTAA GGATGCGCGG 840 CCAGCGCTAG GAAAGCAAAT CTCCCGAAGA TGGAGTCCCC TGATTTCCAT GGAGTCCATG 900 CGTGGACATG AGGAAGAAGG TGGACATGAG GAAGATGGCA CGCCTCAGTG TGTTACAAAC 960 ATATTCATAT TTTACCCAAA TTAGAGTGGG AGAAGTTTCC AGCCTTGGAG ACCTTCTTTA 1020 AAAGAGTGTG GGTGTTGCAA TGACCAAAGC AAACAGATGA TGGAGCTGGG GAAAAAAAAA 1080 GTGTTATTTA AAAAAATCCT TCTCGGCCGG GTGCAGTGGC TCATGCCTAT AATCCCAGCA 1140 CTCTGGAAGG CTGAAGCAGG CGGATCACCT GAGGTCAGGA GTTTGAGACC AGCCTGCCCA 1200 ACATGGCGAA ACCCCGTCTC CACTAAAAAT ACAAAAAATT ACCCGGCGTG GTGGCACATG 1260 CCTGTAATCC CAGCTACTGC GGGGGCTGAG GCAGGAGGAT CTCTTGAACC CGGGAGGCGG 1320 AGGTTGCATT GAGCCAAGAT CGTGCCACTG CACTCCAGCC TGGGTGACAA GAGCGAAACT 1380 GTGTCTCAAA AAAACAAAAA CGAAAAACAA AAAAAAACAC TTCTCACCAA CTAGTCATCT 1440 TCTATTTCAT 1450
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