Tag | Content |
---|
EnhancerAtlas ID | HS133-27314 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:109833090-109835420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr6:109834162-109834172 | CTCAAGTGGT | - | 6.02 | RARA(var.2) | MA0730.1 | chr6:109833405-109833422 | TGACCTCTGGTTGTCCT | - | 6.62 | Sox3 | MA0514.1 | chr6:109835401-109835411 | AAAACAAAGG | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 109833903 | 109834031 | chr6 | 109834832 | 109835344 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I109513 | chr6 | 109834421 | 109835800 |
|
Enhancer Sequence | CCTTGTGCTC TGGATGTGGG ATCTTATTTT GCATGTCAAC GTTCTGCTGT CTTTGGAAAA 60 TATCATTATC TTTGTGAACA TTTAGGATAT GATTATGTCA GAGGCGTGCA AACAAGAGCA 120 ACTCCATCTT GAGTAGGGGC TGGGTAAATA AGGCTGAGAC ATACTGGGCT GCATTCCCAG 180 ACAGTTAAGG CATTCTAAGT CACAGGAAGA GACAGAAGGT CAGCACAAGA TACAGGTCAT 240 AAAGACCTTG CTGATAAAAC AGATTGCAGT AATGAAGCCT GCTAAAACCC ACCAAAACCA 300 AGATGGCAAT GAGAGTGACC TCTGGTTGTC CTCACTGCCA CACTCTCACC AGTGCCATGA 360 CAGTTTACAA ATGCCGTGGC AACATCAGGA AGTTACCCTA TGTGGTCTAA AATGGGGAGA 420 CATAAATAAT CCACCCCTTG TTTAGCATAT CATCAATAAA TAACCATAAA AATGGGCAAC 480 CAGAAACCCT GGGGGCTGCT GTGTCTATGG AGTAGCCATT CCTTCACTTT CCTAATAAAC 540 TTGCTTTCAC TGTACTCTAT GGACTCGCCT TGAATTCTTT CTTGCACGAG ATCCAAGAAC 600 CTTCTCTTGA GGTTTGGTTC TGGACCCCTT TCCTGTAACA ATTATAGACT CTTTTGTCAT 660 GTTAAGAACT TTATAAAGCC AAAATAAACT TTTCATCTGA AGAGCTGGAA CATAAAATTC 720 CCTTATCTCT CTTCTTTGTT CTCTATTCAG TCAGTCATTA AGACTTATTG TTTTCCTTGG 780 AAATGTATCC TATATCTGCC CTTTCCATTC TGTTCTCATT GTGACCACCC ACTGTTCTTG 840 TTGTTATCAT GTCATCTTGA AATACTACAA CCAACCAAGT TTTGGACTAT TTACCTTAAA 900 GTCCAAAGTT ACACAAAACA TTACAGGAAT ATAGTTTATC AAATGCCTTT CCAGAAATGA 960 TTAAGATAAT TGATTTACTA TTATTACTTG TTTTGAGACA GGCTCTCACT CTGTTGCCTA 1020 GGGTGGAGTA CAGTGGCACA ATCATGGCTC ACTGTAGCCT CAATTTCCTT GGCTCAAGTG 1080 GTCCTCCCAC CTCAGCCTCC TAAATAGTTG GGACTACAGG CATGTGCCAC CATTCCCAGC 1140 TAATGTTTTA ATTTTTTTAT GGATATGAGG TCTCACTATG TTACCCAGGC TGGTCCTGAA 1200 CTCCTGGGCT CAAGTAATCC TCCCACCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 1260 AGCCACTGTG CCTAGTATAG TAAATTATAT TTATAAAATA TTTTCATATA CTTTATATAC 1320 TTAACATATT TGACTATAAT TATGAATATT AGTTTGTAAT TTCTTGTATT GTCTTGGTTA 1380 GGTTTTGATA TTAGGGTCAT GTTAATTAAA AAATGGATTT GTATCCTATA TGCCTTTTTG 1440 ACTGTATGAA CCATATTCCT TAATAAAAAA GAAAATAAAA ATAACTTGGG AAACTTACTC 1500 TTTCCCCTTG CCTATGGGAG AGCTTATAAA AATACAGGCA TTATCTCTTG AGTTTTTAGT 1560 TCTTTGAAAA TTTCCTATAA TTTTTGTCTA AAACAATTTG ATTCTGGGCC ATTTCAGAGT 1620 TGGGTTATAT TTTCGAATGC CTTCTCTTCG ATGGTTATTG GTCTATTTAG GTTTTCTATC 1680 TCGTTTTGAG TCAGTCTTGA TAGTTGGTTT TCTGAAGAAG TGGCACTAGT TTTCAGTCAT 1740 TCTCACAGGA TTAACAAGAA TTCTAGACAG AAATACAGTT AAAATAAGCC TGAATCAGGC 1800 TGCACCTTTG ACCCACTTCC TTGTAACTGA AAGTCACATA GCAGTAGTTA CTGACCACTG 1860 GCATCCCCAT CATTCCTATA AATAGGATTT CTGATGTCAG ATGCACAAGG CTTTTGTTTA 1920 AGATAGATAG GATCTCTGAT GTTAGAATAA TAAGGCTATT GTTAAGGAAT TCCTTAAGCA 1980 GAACCTAAAT GCCAGCAGAA TAGCTGACAC CAACAGGAGG TTTAAAACCC CCACCGAATC 2040 AGCAGGAGAA GTCAGTTTCT TCATCTCCCT GTCCCATGAC TTCACCCTGC ATTCTTCAGC 2100 CAATCAATGA TTTTTGCACT TCAATTCAGC CCACTCCAAA ACTCTTAAAA ACCCTAGCCC 2160 CAGATTCCTC AGGGAGACGG ATTGGAGATT TCCTCCTGTC TCCTCACTCA GCCACCCTAC 2220 GATTAAATGT CTTTTTCTGC TGCAACCCAG TGTCTTGGTG AATTGACCTG CCATGTGCAT 2280 TGGGTACAAG CAGATTCTTT TATGCTTGAG GAAAACAAAG GCAAACATAC 2330
|