| Tag | Content |
|---|
EnhancerAtlas ID | HS133-27657 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:168134310-168136540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr6:168135072-168135082 | ATGGAATGTG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 168134351 | 168135412 | | chr6 | 168135695 | 168135858 | | chr6 | 168135864 | 168136350 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I167733 | chr6 | 168134254 | 168135592 |
|
Enhancer Sequence | CTCTCACCTG AATTCCTGTC TCTCCATCAT CTCTCACCTG AGTTCCTGTC TCTCCACCTC 60
TCACCTGAGT TCCTGTCTCT CCACACCCTC ACCTGAGTTT CCTGTGTCAC CTGTTGTAAC 120
AGCCCTCTCT TAAGAGGTCA GCTGGTTAGG AAGCTCCAGT GTGAAAACCG TCCATAGGCA 180
TTGGTGGTTC ACGGGACATT TTCCTTGGCA GAAACTTCAG TTTTACTGAG AACTGAGCTG 240
GAAATGTACG TGTAAGCACA AGAGGCCTCC CAGAGCATTT GACCCAAATC CAGCACCAGT 300
GTTGCATCCT CTTGCTGTAA AATAGGACAT TTTTTCAAAA GGAGTGTGAA GTAAGTATTG 360
ATTCACAAAG TGCCCTGAAG TCCTTGGATA CTCCTGTCCC TGAATTCCCT CCGTGGATTC 420
CCCACCCCGT CTCTCAGTGT TTGGACAAGC GTGGGTTTTC TGACCAAACA TTCTAAACAA 480
TGGCCTAAAT TCATCCCTGA GAGGCTGGCA TTCAGCCTTC TGTTTTCAAT CTTTTTGAAC 540
TCAACTGTGT ACTTGGACTG AGATTTTACA TTGTGCAACT TCCTGACAGT AACGTGCCAT 600
TACCCTGGGG GGTAAAGGGC TATTTAAGTC CAGACTCAGC CATTCCCACC AGCCACAACA 660
GAGCCAGACC TCTCCGTGCC CCGGGAGGGT GCCCTGAACT CAAAATGTCC CTTGGCGATT 720
GGGTTTAATA ACAGCATTTT CAAAGGCACT CCCCAGTCCA CCATGGAATG TGGAGGCTGC 780
CTCCTCTCCT GCCTCCGCTT TGCGGCACAG CTGTGGCTCT GGGTCCCACA TGACTGCACA 840
AAGTCAATGC CAAGGGCGTG ACCAGGGTGC CCGAGACCTC ACTGTGGTCT GGGTGGAGCC 900
CCAGCACTCA GGGTGCAGCT GCGCAAAGAT TGCAGGCGCC TCTCCTGGGG CCTGAGCTTG 960
TAAGTGTCCT TTGGATGTTG GGATGGGACA CCTGACTCCT CAGTAGGGCA CAAGGGGCCA 1020
CTGTAGGAAT AAAACTCAGA AAATCCCCCT GTTCACACTC AGCAACAGCC AAGCCCCCTT 1080
CAGTGTGATG CTGTGGGTGC TGACCTACAA ATCCTCACCC AGACACCTGC CACCCCGGAC 1140
CCCACAGAAT GGGCAGGACG AAGATCCTCC TGGTTTGGGG CGAGGAAGTG ACACCCTGGT 1200
CCCAGGACAT CTCCAGGGTC CTCTGTCAGA TACACACCCT CACCAAGCTG GCAAATAGGA 1260
TGTGTCCCCA TTTCACAGAT GAGGAAAGTG GAGCCCAGAG AGCTTCCACG ACTTTCCCAG 1320
GGTTGCAACA GAGCGAGGAG GGTCAAAAGG AGGATGGAAT GGGCATGGCC CCCAGCCCGT 1380
CCTTGACCAC CAGTTCCTTC CTCTGTCTCC AGTTCCAAAG GGGTCATCAC AGAGCACTTT 1440
GAAACCCCAG GGCTTCCCCC ACCGACCTCC CCCACTGACC TCCGCCGCTG ACTTCCCCTG 1500
CTGACCTCTG CCACTGACCT CCCCCTCTGA CCTCTGCCGC TGACCTCCAC CGCTGACCTC 1560
CCCCGCTGAC CTTCCGCCGA CCTCTGCCGC TGACCTCCCC CTCTGACCTC CGCCATTGAC 1620
CTTCCCTGCT GACCTCCACC GCAGACCTCC CCCGCTGACC TCTGCCGCTG ACGTCCCCCA 1680
CTGACCTCCC CCTCTGACCT CCGCCACTGA CCTCCGCAGC TGACATCCCC CGCTGACCTC 1740
CCCCGCTGAC CTCCGCCACT GACCTCTGCC ACTGAACTCC ACTGCTGACC TCCCCCACTG 1800
GCCTCTGCCG CTGACCTCTG CCGCTGCCCT CCCCCGCTGA CCTCCCCCGC TGACCTCCCC 1860
CACTGACCTC TGCTGCTGAC CTCTGCTGCT GCCCTCCCCC GCTGACCTTC CCCACTGACC 1920
TCCCCCACTG ACCTCTGCCA CTGACCTCTG CTGCTGACCT CCCCTGCTGA CCTCTGCTGC 1980
TGACTTCTGC CACTGACCTC TGCCGCTGAC CTCTGCTGCT GACCTCCCCC GCTGACCTCC 2040
CCCACTGACC TCTGCCATTG ATCTCCCCCG CTGGCCTCTA CCACTGACCT CTGCCACTGA 2100
CCTCCCCTGC TGAACTCTGC TCCCTCTATT TGTCCAGCTC CAGCTGCTCA AGAGACCCTG 2160
CAACCCTGAG GCCACCCCCT CTCCGTCAAC CCCATGGACA AAGTGAGCTC CTTCCCCAGC 2220
TAGAGAGGCC 2230
|
