| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28793 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:75193420-75196100 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:75195544-75195559 | TGAACTCCTGACCTC | - | 6.22 | | RFX2 | MA0600.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | + | 6.18 | | RFX2 | MA0600.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | - | 6.19 | | RFX5 | MA0510.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | + | 6.44 | | RFX5 | MA0510.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | - | 6.52 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I075564 | chr7 | 75193814 | 75196122 |
|
Enhancer Sequence | CCTGGCTTCA AGCAATCCTA CTGCCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG 60
CCACCACATC TGGCAAAATC AACATCTTTT TCTCATTCTC AAATCTCTAT TTTGAATCTA 120
AACACTGAAG ACCAAGAAAC CTAAGAGAAT CCAGACTTAT ATATTCTTCA TTTTTATTTT 180
GTTTGTTTAT TTTTTGAGAT GGAGTGTCGC TCTTATTGCC CAGGCTGGAG TGCAATGGCG 240
CGATCTCGGC TCACTGCAAG CTCCACCTTC CAGGTTCAAG GGATTCTCCT GCCTCAGCCT 300
GCTGAGTTGC TGGGATTACA AGCATGTGCC ATCATGCCTG GGTAATTTTG TATCTTTAGT 360
AGAGATGGGG TTTCTCCATG TTGGTCAGGC TGGTTTCGAA CTCCCGACCT CAGGTGATCC 420
GCCCGTCTCG GCCTCCCAAA ATGTTGGGGT TATAGGCGTG AGCCAATGTG CCCTGCCTAT 480
TTGTAAATAT TTTTTTGAGA TTGGGTCTTA GTCTGTCGCC CAGGCTGGAG TATAGTGGCA 540
AAATCATAGC TCACTGCAGC CTTGACCTCC CTGGGCCCAA GGGATCCTCT CACCTCAGCC 600
TCCAAGTAGC TGGGAGTACA GGTGTGTGCC ACCACACCTG GCTAATTTTT TGTGTGTTTT 660
TGATAAAGAT GGGGTCTCTC TATGTTGTCC AGGCTGGTCT CAAACTCCTG GGCTCAAGCC 720
ATCTACCCAC CTTGGCCTTC CAAAGTGCTG GGATTATAGG TGAGAGCCAC CATGCTTGGC 780
CTGTTTTAAT TTTTTTAGAG ACAAGGTCTT GCTGTGTCAC CCAGGCTGAA GTGCAGTGGA 840
ACGATCAAGG CTTGCTGCAA TCTCAACCTC CTGGGCTCAA GCGATCCTCC CACCTCAGCC 900
TCCTGAGTAG CTGGAGTTAA CTACATCTAT TCTGAGATGA AAGGGGTACA TGGGCCTTAA 960
ATCCTTTGGC CTGCAACAAT GAACTTTCTC CAGCTTAGTC CAATAAACGA AACCCCCAGG 1020
GTCTCGTTAC AGCCTGTCAG ATCCCAAGAC TTAGGCCTGT CTCTGTCTCT GTGACATCAC 1080
TGCTGCTTCC CCTGAATTCA AGGACAGTGA GGTCTCAGAC AGCAGCCGTG TCTGTGTGGA 1140
ACAGCAAAGT GGCTACTCAG GGGAGATGTT TTTCTAAGCT AGAAGCAAAT GAAAGGAAAT 1200
GAAATCACCT GACCACACAT CCCCATCTTG CTGGTTTGGA GCCAACAGTA ACAGGCTCAA 1260
CTGCTTTCAC AAGCTACCGG AATTTGACAT TCCAGGAAAT CAGCCTCAGG GCCTGTCTCC 1320
TTGGACTAAA GAAGCCATTT ATCACAGAAT ATGTACTCGG CTTCTCAAAT GGAACAGGGG 1380
TACCAGGAGG TGGGTACAAC CACACACTTG TCCTTCGCTT GCTCCTGGGG AACCAGGCAG 1440
AGAAGCTGAA ACTTGGCATT TGGGAGTTAT GGTCAAGGGT GAGGAAATTA ACAGGAAAAA 1500
CAAGAGAGTG CACTTTTACA CAGCTAAGTC AGGAGGCCCT TCTCAGCCCC CTCTGTCCTC 1560
CCAACTCTCA CTCTATTATC CTTCCCTTTT GCCTGGTTTC GCCTCCCCTC CCCTCCTTTC 1620
CTTTTTTTTT TTTTGGATGG AGTCTTGCTC TGTTGCCCAA GCTGTAGTGC AGTGGCATGA 1680
TCTCAGCTCA TTGCAACCTC TGCCACCTGA GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT 1740
GAGTAGCTGG GATTACAGGG CTAATTTTTG TATTTACAGT AGAGACAGGG TTTCATCATG 1800
TTAGCCAGGC TGCTCTCAAA CTCCTGACCT CAAGCGATCC ACTTGCTTCG GCCTCCCAAA 1860
GTGCTGGGAT TACAGGTGTG AGCCACTGCA CCCAGCCTAA GTAAAGATCT TTTGTTTTTG 1920
TTTTTGTTTT GAGATGGAAT CTCATTCTGA CGCCCAGGCC TGAGTGCAGT GATGTGATCT 1980
TGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGCGATTC TTCTGCCTCA GCCTCCCGAG 2040
TAGCTGGGAT TACAGGTGTG CACCACCATG CCCTGCTAAT TTTTTAGTAG AGACGGGGTT 2100
TCACCATGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA AGTGATCTGC CCACCTCGGC 2160
CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTGCACC CGGCTGGTGT TAGCAACTTT 2220
TATTGAGGCG GCAGTGCACA GCCAGCAGCG GAGGTCCTGT TCCTTGCAGC GCAGGGCTAC 2280
TCCATACGCA GTGAGCCCAG AATAGCAGCT GTTACATTTA TACCCACTTT TAATTATATG 2340
TAAATTAAGG GGCAGATTAT GCAGAAATTT CTAGAAAAAA AGTGGTAAAT TCCAGATTGT 2400
CAGGTTATTG CCATGGAAAG GGGCGCTAAC TTCCGGATGT TGCCATAGCA ATGGTAAACT 2460
GTCACTGCAC ACTGGTAGGT GTGTCTTATG CAGAGGTGCT TCCGCCCTTT CCCTGTTTTA 2520
CTTGTCCTTA ATTTGGTCCG ATGCCCAAGC CCTGCCTCCA GAGTCCAGTC TCCCATCCCA 2580
CCTCAGAAGC AGGTCATATT TGTAGGGTAT CAACCAAACC TGCTAGTGGA TTGGACATGG 2640
GGGATGAGGA AAATGGTGAC TTCCAGATCT CTGGCCTAAA 2680
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