| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11651 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:67940370-67942580 |
Target genes | | Number: 32 | 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) |
| Foxd3 | MA0041.1 | chr16:67942178-67942190 | GTTTGTTTGTTT | + | 6.32 | | Gata1 | MA0035.3 | chr16:67940590-67940601 | TCCTTATCTCT | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr16:67940486-67940501 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr16:67942390-67942405 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I067908 | chr16 | 67942438 | 67942893 |
|
Enhancer Sequence | CTCTTCTGCC TCAGCCTCCC AAGTAGCTGG GGTTACAGGT GTGCATCACC ATGCCCGGCT 60
AATGTTTTTG TATTTTTAGT AGAGATGGAG TTTCACCATG TTGGCCAGAC TGGTCTTGAA 120
CTCCTGACCT CAAGTGATCC GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG 180
AGCTACCGGG CCCAGCCTGT GTGTCATAAT TAATAGGAAA TCCTTATCTC TCTTCAACCC 240
TTGGGGTCCT CAGACATAGA GAAGAGCCCT CTCATTAGAA AGGTGGTGAC CTCTGGAAGC 300
AGTAACTTCA GCACTGCACC TTGTCCAGGG CCCCACCAGC CCCAGGGTAT TTAGTTCATG 360
GTTGGAACAT CTCTGTCTGG GAATCAAACT GGAAGGGACC CTGGATCCCC ATCATAAGGA 420
AGCAAGATAC CCTGATCTTC ATCCTGAGTT AAATCTGGGT GAAACTGCCA GTGTCCTCTC 480
TGAGCTCAAG CCCCTCTGAC TCTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTTGCCCA 540
GGCTGGAGTG CAGTGGCAGG ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCACGCC 600
ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG CGCCTGCCAC CACGCCCGGC 660
TAATTTTTTG TATTTTTAGT AGAGATGGGG TTTCACTGTG TTAGCCAGGA TAGTCTCGAT 720
CTCCTGACCT TGTGATCCGC CCGCCTCGGT CTCCCAAAGT GCTGAGGTTA CAGACCTGAG 780
CCACCGCGCC TGGCCAACTC TTTTTTTTTT TGACATGGAG TCTCACTCTT TTGTCCAGGC 840
TGGAGTGGGG TGGCGCAGTG TCAGCTCACA GCAACCTCTG CCTCCCGGGT TCAAGCAATT 900
CTTCTGCCTC AGCCCCCCAA GTGGCTGGGA TTACAGGCGC CCACCACCAC ACCCAGCTAA 960
TTTTTGTACT TGTAGTAGAA ATGGGGTTTC ACCATATTGG CCAGGCTGAT CTCAAACTCC 1020
TGACCTCAGG TGATCTGCCC GCCTCGGCCT TCCAAAGTGA TGGGATTACA GGCATGAGCC 1080
ACTGTGCCCG GCCCCGCCTC TGACTCTTGA ATGAAGACCA GGCGAGTTTT GCAGTCACTT 1140
GGTGGCAGTG TGCTGAGGCT TGTGGTCCCA AGTTCACTGG GGTTGATTCC AGCAGCTCTG 1200
GGCCTTGTGT GGGATTTCAG CCATCCATGT AGTGTGCTGG GGAAGTGAGA GACCCTGGAA 1260
TAGGGAGTTA AACTGCCAGG GTGGGGACAG TGCATTAGCA AAGGAGTGGA AGCCTTCCAG 1320
GAGAATGAGG GAGAGCCCCA GGGAAGTGGT TTGTTGCTTG TTACAGAGGG ACCAACCCCT 1380
GTAGGAAGCC TAAAGGGCTG GGAAAGATAT GCATGAAGGA GGCCTTGGAG AAGCAGCTTT 1440
CTGAGCCCTG GTGGGTGATG GTGTTAGAGA GCAGGCCTCC AACACTTCAC ACCCCCATTT 1500
CAGAAAAGAT GAGTCAAGAG TAATAAGAGG AATGATTTTA ACATTTTAGA AACATGGGCC 1560
TTCGGCTAGG ATAAGGGGCC CAGGCAGAGG AGTGAGGAGG GTGGGCGCCC TGACAGCTGA 1620
GGCTATGCGT GTTCCTGCCC CCTCTCAGGG TTGAAGAGCA GCATGAGACT GAGGCCCAGG 1680
GAGATGAGTC AAAGCCGTGA AGCTCGGGCC ATCTTTTCAG CTAGACCCTG TGTTGAGTCT 1740
GGGCTCTTGA ACAGCAAAGC CATACTCCCG ACCAGGGAAA TAAATGAGAG CCAGGACTTC 1800
AGTTTTTTGT TTGTTTGTTT GAGACAGAGT CTTACTCTGT CACCCAGGCT GGAGTGCAGT 1860
GGTGCAATCT CAGCTCACTG CAGCCTCCGC CTCCTGGGTT CAATCGATTC TTGTGCCTCA 1920
GCCTCCCGAG TAGGTGGGAT TACAGATGTG TGCCACCACG CCTGGCTAAT TTTTGTATTT 1980
TTAGTAGAGA TGGGTTTTCA CCATGTTGGC CAGCTGGTCT TGAACTCCTG ACCTCAGGTA 2040
ATCCACCTGC CTCAGCTTCC CAAGGTGTTG GGATTACAGG TGTGAGCCAT CACGCCTGGC 2100
CAGGAGTTTG GTTTTAATGA GACTGAGTTT CTGGAGAGGG AGGGCTGAGG AGGATGGCTG 2160
ATTTCCTTAG AGTTGGCCTG GCTGTGCTGA CTTGTTCTCT CTTTGTGTGT 2210
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