Tag | Content |
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EnhancerAtlas ID | HS133-32000 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:102118200-102119600 |
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) |
ZNF263 | MA0528.1 | chr9:102119187-102119208 | AGAGGAGAGGGAGGTGGGAGG | + | 6.69 | ZNF263 | MA0528.1 | chr9:102119196-102119217 | GGAGGTGGGAGGGAAGAGGGA | + | 6.97 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_51391 | chr9:102117539-102123394 | Skeletal_Muscle |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I099356 | chr9 | 102118606 | 102119483 |
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Enhancer Sequence | AGGGCTTGAT CATGGAAGGA AGTCTTAGTG TGTGTGCCGA AGGGTATGGG CTCAAATTTG 60 AGGGCACTAA ACAGGCACGG AAGGTTCCAA GCCTGGAACT CACAGCTGCA GCTCACTCTG 120 GTGGGTTTAT TCATGGGGCC CTGCTCAAAT CTTCCCTAGC AAAGCTGCTT TCTCTCTAGA 180 TCGGGGTTTC TCAACAGCAA CACTATCATT TGAGGCTGGA TTATTCTTTG TTGGGGGTGG 240 GGGCTGTTCT GTGCATCAGA GGCTGTTCAG CAACAGCATC CTTAGCCTCT ATTCACTAGA 300 TTCTGGTAGC ACTTCCCCAG TTTCCACAAC CAACAACGTC TTCAAACATT ACCAGAAGTC 360 CCCTGGGTGG CAAAATAGCT CCTGATTGAG AATCCCTGAT TTGTTTTTCT TTTTTGTGAA 420 TATGTACACA GATGACTCCT CCTGTATTTG TCCTCTTCCC TCTCCCCAAG GCCTGGCAAT 480 GTCCTGCTTC CAGCCTTTCC ATGAGGGACA CTGGATGCTG CCATTGGCTC CCTGCATTGC 540 CTTATTTCAG CACCTGTGGC TCATGCTCGT GGAGCTGGGG CTGGTTGTGG GGAAGCAGCT 600 GCCAATAGCT CTGTCTACCT CTGGATCGGG TCAGTAAGGC ACCTCATCTC CTGCAGGGCA 660 CACCATGTAG TGTCCAGGAG CTTCCCGGTT GGATTCCCAC CCCAAGGTCA GCTGGGAACA 720 GAACTGTCCA AGCCTGTTGG CCCTGTACCC TCTGTCCGTC AGTCTCACTG TCTGCTACGC 780 TGCAGTCTGG AGGGAAGCAT CAGCTCAGGA AGCCTGCCAG GGAGAGGGCA GCAGGCCGGG 840 GACAGAGGGC AGGTGGTGGT AGCTGGAGAC CATGTGACTC CTGGAGGCTG TGTGTGTCAC 900 AGGGCAGAGC TGGCCACTGG CTCTTCCCTT GGCTCAGCCT GAGAAGCCTT CACATGACAT 960 CTCTGTGGGA GCCTTCATGT TGTGGGCAGA GGAGAGGGAG GTGGGAGGGA AGAGGGAAGT 1020 GTTTTTAGGA TCCAAGCTAG AAATACAAAA TACATTTGTG AATCACAAGC TGATCCTCAT 1080 CACATGACCA CAATAGCTTT GCCAATGCAG AAATCAGGCT TCGGACACAC ATACGAAAAA 1140 ATCTATCCTG CCCCTGCTAT GTCTGGGCTG TGGTGGCCAA GAGAGTAAGA GAGTAAGAAA 1200 GTGGGGCACT GGAATTGGAG CAGGAGGCCA GGGAGCCAGC TATGCAGCCG GTCTCCATGT 1260 CCCAAAGCGT CACCAAAACC AGAACACAAA ACCAGCCCCC ATTCCAGCAT TTTCTACATG 1320 CTTATTCATA TGGTAATCTC ATAACAGCCA CATTTCCCAG TGGAAAACCG AGGCCCAGAG 1380 TGATTCCTCC ATGTTCCATT 1400
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