| Tag | Content |
|---|
EnhancerAtlas ID | HS133-30473 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr8:41539630-41542060 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr8:41541434-41541449 | CATGCTGAGTCACAT | - | 6.03 | | NR2C2 | MA0504.1 | chr8:41541368-41541383 | TGGGGGCAGAGGTCA | + | 6.77 | | RARA(var.2) | MA0730.1 | chr8:41540792-41540809 | AGGTCAAGATGAGGTCA | + | 7.28 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I041683 | chr8 | 41540642 | 41543786 |
|
Enhancer Sequence | TCATGACAGT CTATGGGTGG GCTCCGTGTC ACCCCTCCAG CCCCCACACC TGCCCTCTCT 60
CCCACTGTCC CTTTGCCCCC GCCTCCAGCC CCGTCCTGTG AACGCATCAG GAAAGCCCCC 120
TTCACACTCC CTGCTCTGAA ATCTTCCACC TCAGTGCCGA CGCATGGCTC CCACCTCATC 180
TCTGGCAAGT CCTCGAGTGC CACCCGCTTC CCTTGCACCA TGAGTCCCCC TGGCCCCGAC 240
TCCGGTCTGT TTCTCCTGCA CCATGCACGT TAACTGCTGG TGTGTGATAC AATTCCCCGC 300
GTGGCTCTCC TCACAGGAGG GAAAAGCTCC ACAAAGGCAG AGTTTTGTTT TGTTTTGTCT 360
GGTTGAGAAC AGGTATCTCT CTCCTGCCTA GCACAGTGCC TGGCATGTGG TTGATACTTG 420
AAAAATATTT GCCAAATGGG CTGACCCCCT GAAGCAGAGC CCTTTCAGCA GACATGGAGT 480
GCACAGGCCC AGTCCCACAC AGGAATTGAG AACCACTCGG GCAAGAATGC CTCAAGGCCT 540
GGTGGGAGCT AGGGGTCTGT GGCCCGGGGA GATGCTCACA GATGCCCAGG TCTGTAACTG 600
TGAATATTCA CACTCATGTG GCTCTGGTGG CCCATTGTCC TGTAGGTGCT TAATCAGGGC 660
ACAGGAAATC AAAAGCGTGC CCCTCTGACT TGACCAAAAG TATGCGCTGG GTGTCAAAGA 720
AGTCTCGACA CATGGGAAGG GAGAGGAGCT TTGTCACTAG AATTTCCCCA GGTTTGTGGC 780
TTCCCTCAAC CGCCCTCAGC CCACTGAGCT CCTGTAAAGC TCTGGCCAGG TCCCCTGAGG 840
GGAGGCTGGA ATCCCCAAGG GGGTGGACCT GGGGAGTGGG CCGGGCACAC GCAGCAGGCA 900
GCACCACACA GCAACACCCA CGGACACACA CACACATGTA TGCACACGCA CACACATGAA 960
CACGTGCACA CACACACACA TGCACGCACA CATGCACACA CATACGCACA CACACAAGTA 1020
CACCCAGGAC ATGGCCATGA GATGCGTGGG GAGACAGGGC TGGGGGCCAT GACATGCATG 1080
TGGACGTGGC CGGCTCTGCG CCTGCCGAAA TGGGGACAGT GGAGACAGTG GAGACAGGCA 1140
GCACGATAGC GTGAGTGCAC AGAGGTCAAG ATGAGGTCAG AGGCAGAAGA GAGGCAATGG 1200
GACGTGATCA GCAGATGGGC CCTGCTCCCA GGATGCAAGA TGGCACACTT CAGGAGACAC 1260
AGGATGCAGA GCAGGGGACA GGGAGGGCTC AGCGAGCAGG GTCCCCTGGT AGGGGCTCCG 1320
TGCCCAGGCC CACCTGGGAC TCGCCCTCAG CCGCGCCCCC AAACTGTGTA CCCAGTCACA 1380
GGTGCCCACC CTCAGCCTGG GCGTGGCGGG GATGGCCCCT AAGACAAGGA GCTTGAGGAG 1440
CATACACATC ACCATGCAGG CATCCAGGGT GACGCGTCAG CCACCTGAGG AAGCCACGTC 1500
ACAGACATGG AAATTTTGTT TCAAGGTCTG TAAGGAATTT TAGGGATCCA ATCCAACTTG 1560
CTGATTTTAC AGAAGGGGAG AGGGCTCAGT CATGCAGGGA GTTGGCAGGA AGGAAGGGCC 1620
TAGAACCCAG ACCTCCTGGC CGGAGAGTGG GGCCTCGCTG TTTATGTGCC CGCTGGCCAG 1680
AGAGGGGGCG GGCGAGGAAG GTGTTGCGAG GGGGCCTGGC CCAGGAGTGG CAGGGGCTTG 1740
GGGGCAGAGG TCACAGCCTC CTGTACATCC TCTCCTTGGG CTGGATCTCA CGGGGGATCC 1800
CTGCCATGCT GAGTCACATC AACAAAGAAT GAGGGGAAGG AGATGAGATG ATAGAAAAGG 1860
GGGAGAGGAA AAAGCAGAGA GACCCGGCTC CAGGAAGAGC AAACTGCTCA GTCCCTAGAA 1920
GTGGCCACAG CAGGATTTGT AAAACACCGT CCAGTTAAAC TGCACTAGAC CTTGGGCCAG 1980
GAATCTCCAT GCCCTCTGCT TCCCAACCAC TGACTGTTTT ACAGATGGGG ACACTGACAC 2040
CCCAAAGAGG GCCCACGCCT TGCAAAGAGC TACCGGAAAG TCTGCAGCTG TGTAGGGGCA 2100
GTCTCTAGCT AGAGGCCTCT GACTCAGCTT TTTCTCATAC ACCACGCCCT GTGGGGACGC 2160
AGTTGCTGAT GGCAAGGGCC TGGGGGCCAT TCTGCAGGGC TGCAAAGGCT AAGGCGGAGG 2220
CGATGCCCAC CTGCACAGGA GCAGCCATCT CTCTCTCCTT CGCCTCTGCT TCCCCGGAAA 2280
GGAGGAACTT GTTGCTGACA AACCAGACCT CCCACCAATG GGAGGCAGAG CGGGCTTTGA 2340
GGGATGACGT ATTGTGGGAA GGGGTTATTG GTGCTGATGC CTGTAGGGCA GGGCTCCGGC 2400
TCAGTCCCCA TCTGGTCCAG GTGACACTCA 2430
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