Tag | Content |
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EnhancerAtlas ID | HS133-00997 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:29309740-29310720 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBP | MA0108.2 | chr1:29310683-29310698 | CTGGGGTTTTTATAG | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I028983 | chr1 | 29309964 | 29310816 |
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Enhancer Sequence | AATGTGTTGC ATCATTTGTT TCATTCATTA ATTAACAAGG ATTTATTTGT TGAGCACTTA 60 TTGTGTCAAG TATTTCCTGC TCTTCATATT CCACTTGCTA AAAGCAGCTT TTTATAGTCT 120 TTGTTTCTAG GCATTTTGCA GTACGTTCTC AAAGTGATTG TAATGGTGGT TTTCTGTGCT 180 TCCTACTCAA AATGTGCTCA GTGGGCCAGC AGCATTGGCA ACATCTTATT AGAATTGTAG 240 AATCTCAGGC CCCTTTCCAG ACCTATTGAA TCAGACCCCT TATAGTGAAG CAGGATATTT 300 GCCTGACCTC TTCATGGGAA TTGTGACAGG CGTACCTTGT TTACTGAGCC TGCCACTCTC 360 AACTCCTTGT GGGAAGGAGC GTGCGAGTGA ACGAGGTGGG AACTGGAGTG CACAAGCGCT 420 GGAACGAGCT GACTGCCTTG GTGCTTGCAG TACTCAAGGC CACGCGGGCC TCACAGCAGT 480 ATCCAGGGGG CAGTATCTGC ATCCCTCCAA GCCCCAGAGG GCATGTTACA GTGCTCTTTT 540 AGCTTCGACA TGCCATCCAC GAACAGCTTA AGTGTTAGCA GCTCAGTGGG CCCTTTGCCT 600 TTTTGAGTGA GGTGCTGCCC TCTGCCAGTG AGGTCAGAGG GCCAGTGTGA CAGCCTTTTG 660 TATCTGCACA CATGGCTCCC GTGCTCTTGT CCGGTGTCCA GGAAAAATGA GGTCACAGGA 720 ATGAATTGAA GAATGGTAAA TACAGGGGAT TTTATTGCTG ATGAAAGTGG CTCTCAGCGG 780 GAAGGGGAGC TGAAAAGGGG CCGGGGGTGG GTAGATTATC TTCCTCTGAA GTACAGCCAT 840 CTCCAGCCGA ATTCTTCTCT GAAGTTACAC CATCAAGCTA TCCCTCTGAA GTCAAGCTGC 900 TTCTCTCCAA CATCCAGCTG TTTCTCCTCC CTCCCAGCTG AGTCTGGGGT TTTTATAGGC 960 ACAGGATGGG GTGAGGTGGG 980
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