Tag | Content |
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EnhancerAtlas ID | HS133-00879 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:27627950-27629120 |
Target genes | Number: 33 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr1:27628632-27628645 | GATAAATTAATTT | - | 6.17 |
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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 |
GH01I027298 | chr1 | 27624550 | 27628566 |
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Enhancer Sequence | TGGTGAGTGG GCACTGAGGA GGGGGTGCTG TTACTCTTTC TCTTTGAGAT GCTGCATGAC 60 ATTCTGGAGA GGTCATGGTT CTGGGATTGG AGAGGCCTGG GTTCAGATGT TGATTCAGAA 120 ACCATGCAAC TTTGGGGCAG TTACTTGGTG TCTCTCTCAG AGTGTTTCCT GGTCTGAAAA 180 GGAGGCATGC CAGCACCTCC CACTGAGCGT TTCTATTGAG GATCAGCATG TTTAAATGGC 240 ATGTTTAAAG CACCTGGGGG AGTGCCTGGT GCCCAGGATA GGAGGAAGCT GAGCTCAGTC 300 AGGCTCCCGC TAGGCATTCA CACCTGCTTA GACAGGGCCC TGGTGGTTCC ACTTGGGCAT 360 CTGAGAGGCA GAAGCTGGTC ATTGTGTTTG TTCCGAGTGT ACAAGTGCAG CAGAGACAAT 420 AGCGCAGAGC AGTAGAAATG CCTCAGGCTT GGAATGTGGG GCCTCGGTTC CAAATGCAGC 480 TCCACCACCT GACTGTGTGG CCTTGAAGAA AGCACAGCCT CTCTACCTAC CTGCACAAAG 540 AGCACGAAGC CCTGCCCAGC TCCCCTCAGT GTGCTGGAGA ATGAACTGGG CCATCGGAGT 600 GTGGTCTGTA AACGTGAACG GTGAGCTCAT AGGAGGCAGA CATGGATCTT CACCTCTCTC 660 CTTTGCAGTT TACCAACCAC GTGATAAATT AATTTGTTTA ATGAATAGTT ATCAGACACC 720 TGCCATGTGC CAGGCACTGT GCTGGGTCCT GGGAATAGAG CTGTGACTAA GTCACGTGGA 780 ATTTCTGTGT TTATGGCATT TACAGTCTAG TGAAGGAACC AAGTGATAAA GGAGAAACAA 840 AAAAGTATGA CAAGTGCCAT GGGGACCTGA ATGGTGTGCA TGCTGGGAGG GGGTGGGCTT 900 GATGGCATTC TGGGGTTCTT CAGGAAGAAA CATTTAAACT AAGATCTAAA GGATCCAAAG 960 GAAGCATTAA CTAGATACAA AATATAGCTG TGTGGCCTAG CGCGGTGGCT CACGCTTATA 1020 ATCCCAGCAC TTTGGGAGGC TGATGTGGGA AAATAGCTTG AGCCCAGGAG TTCAATATCA 1080 GCTAGGACAA CATAGCAAGA TCCCATCTCA ACAAAAGAAA AATTAAAAAA AATTAGCCAG 1140 GGGTGGTGGC ACACACCTGT AGTCCCAGCT 1170
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