| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11969 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:87615420-87618180 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr16:87617473-87617483 | AAACCGCAAA | + | 6.02 | | ZNF740 | MA0753.2 | chr16:87617785-87617798 | GTGGGGGGGGGGA | - | 6.3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I087580 | chr16 | 87614501 | 87618115 |
|
Enhancer Sequence | AGTAAACATT TTATTTGCCC ATACATACGG AAAAGTGCAC AAATTGCGAA CGTCCAGCTT 60
GATGAATTTT CACAATTCCC ATGTATAATC AGCACCCGAT TAAGGCATAG AACATTCTAG 120
ACCTCCTTCC AGGCCCTCCC TCCTCTCCCA AGGGTGGCCA GCCCAGCTCC AAATGCCCCA 180
GGCTAGTTTC CAAGGTTGTG GCCTCTGAGT CATCATAAAC AGAGCCTCCC AGGGTCTGGC 240
CTCTTGCACA CAGACTTGTG CTGTGAGAGT CATCCTTGCT GTGTGTGCGC GAAGCTGTTC 300
ATTTCCTTGC TGTATAGTGG AGCAGAGGCG ATCTCAGCTT TCCGGTATGA TGATTTATAT 360
TTCTCATTAA TCTTCAAAAT TTTCAAAAAT CAAATGGAGG AAAAAAACAA GTTGATTTTC 420
CAACAACAAA AACCCAGCGC TGTCCTGGGA CCTCTGGTCC AGGAAAAGCT GCAAAACATA 480
CCATTTCTGG CCTCGGCCAG CCTGTCTGTC TGTCAGCAGC GTCACCGCAG GCGGCTCCTC 540
TTGGGTCCCA TGATCCAACT CCAGCAGGCA GATGAGGCCT GGAGCCAGGC GGGCGGCAGC 600
CCAGCTCCAG CTAAATATAC GTGTGGGAGG CTCCTCCCGG CCTGTGGGTC CCTCCTGGCC 660
CTTTTCTTTC CCACTAAAGC TGGAGGTTCG GGAGAACAAA GGCAGCTCCC CTGAAAGAGC 720
CAAGGCCAGG CGGGAGGTGC CCTGGAGAGC GGCCGAGCCC GAGAGCCGGG GCAGGGCTGC 780
CTCAGACCAG AGAGCCGGCC CTGCCAGCCA TCGGCCGTCG AAGAAGGCGT GCAGCTTACG 840
CAGACCTCGG GTGATTTTGG AGCAAAGCTC CCAGCACTTA GCTGAAACGG AAAGGCCTCT 900
GCAGCCTGGA GGACATATGG GGTTCCCCCT CCCCTCCGAG GCCAGGCTGC GGGCAGGCGT 960
TCTGGAGCCT CCAGGTCTCC CACACCACCC ACGCCCCGTG AGCTTGCAGG AGCTGCCTGT 1020
CTCCTGGAGT GCTTCCTCCT GACTGTGCCA TGAGCACACG CGCTAGATAC ACGCTGGCCT 1080
TCTTGCCTTC CTAGCATGGG AAGGAGCTAG AACCAAGGGA AAGATGGGCC AGAGCGTCCC 1140
TCTGCCGTGT GGCTCAGGGG AAACAGCTCT GCTCACATCT CCAGGATCTG CCTTGGAGGC 1200
TCAGGAGGAG GTGGGTGCAG AGCCAGCCAG AGGGCTTTGC ATCCCAGCCC CACTGGCCAC 1260
CACCTGTGTG GTCATAGGAA AACCATTTTG CCTCTAGAGT CTCAGTTCCC TCATCTGTAA 1320
AATGGGGATG ACTGTAGGAC CCGAATTATA GTGTTGTGAG AATTAAGTGG GTTAAAAAAA 1380
TAAAACTCTT AGAACAATAT TGGGCTCATG ATAAGCACTT GATATTATTA GGTGTGCAAA 1440
CTCACACATG CACACATACA CTAATACATA CACACACACA CATTCATGCA TGTACACACG 1500
TACCAGTACA CACATACACA TACATACACA GCCATGCACA CAGGGACAAT TCACATATAT 1560
ATACGTATAT ACACATGCAA GCATACATAT ATCTATACAT ATGTACATTA CACATGTATA 1620
CACACACATG CATACAGAGA CACACTATGA CACACACACA CACACACGCA CATGTGAGTC 1680
ACCTAAAATC TGGACCAGGG CCACGTGCAG CCCTAGAGAA GGAGAAATCT CGCCGTGCCT 1740
GGCGCAGTGG CCTTGGGAAG GTCTCCTACT TGTTATTCAT TCTCCTTCTA AATTATTATT 1800
CATTCTTACT AATGACAAAG CGGTTCCTCT CTTGGGTCAG AGGCTGGCCC TGCTGTCTTA 1860
GATTGGATTC CCTGGGGAGC CAGTTCCCTG GGAGCTGGGA TCTGAGTAGA AAGAGTCTGT 1920
CGGGAGGGGA TCCAAGAAGC ACAGTGGGAG AGTGGGGGCG CAGTGGGGAA GGGAAGGAGC 1980
CAGCCGAGAT GTGGCAGTAA GCAGCTGGGG CTCTGTCCTG CTGCAGTGTG GGGGCAGGGG 2040
GCAGTCGCAG GACAAACCGC AAACCTTGAC TCCCGTTTGT TGTTGGACGA GGGCTGCTCC 2100
TGGGGCGAAA AATCCCAGCA CTTCCAGCCT ACCGTGTGCC CCGGACTCTG GCGTGACCCT 2160
CGCTCCTAGA TTCATGGGCT CTCTGGCGAC ATCTCTGCAC ACCTGTTGGC CACACGTGGT 2220
CCTCTATTCA CACATGAGCA GATACTCAGT GCAGGCGTTC ACGTGCCAGG CCAGGGTTCA 2280
GGGGAGCGAG GCACACATCC CTGCCTGCAG GAGGCTTACC CCCTTCATCC AGAAGGTTCC 2340
ACAAAGCCAA GTAGAATGGG AAAGTGTGGG GGGGGGGATG TGAAGGAGGT GGACAAAGGC 2400
CAGACAGCAG TGAGCTCTGA GGGATGGGTA AGAATTGGGT GTGGGGGGTG GTTCCTCAAA 2460
AGTATATGGA GAATCATCCT ATGACCTAGC AATTCTGCTT CTAGGTGTCT ACTCAAGAGA 2520
ATTCAAACAG GCGCTCAGAC AGATACCTGC GCACCCGCGT TCACAGCAGC ATTACCCACA 2580
ACAGCCAGAG GCTGGACACT ACCAAGGGTC TGTTATGGTT GAAGAGATAA ACACAGTGTG 2640
TATACAGTGG GGTGTTATTC AGCCACGGAA AGGAAAGAAG CTCTGAGTCA CACCGCAACA 2700
TGCCCTGGAA ACTGTGATCC AATCATAAAA TATGATAACA TATTGTGATT CCATTTATGT 2760
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