Tag | Content |
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EnhancerAtlas ID | HS023-12466 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:12714010-12715430 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr19:12714439-12714451 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr19:12714439-12714451 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr19:12714437-12714452 | CTACTAAAAATAGAA | + | 6.57 | Nr2f6(var.2) | MA0728.1 | chr19:12715113-12715128 | GAGGTCAGGAGTTCA | + | 6.22 | SREBF2 | MA0596.1 | chr19:12714734-12714744 | ATGGGGTGAT | + | 6.02 |
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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 |
GH19I012603 | chr19 | 12714494 | 12715070 |
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Enhancer Sequence | GAGTATCTTT TGTTAAAATA TTTGGGCTGC CTGTAATCCC ACCATGTTGG GAGGCTGAGG 60 CAGGCAGGAT GCTTGAGCCC AGGAGTTCAA GACCAGCCTG GGCAACACAG TGAGATCCTA 120 TCTCTACAAA AAATACAAAA ATTGGCCAGG CATAGGGGTG TGTGCCTATA GTCTCAGCTA 180 CTTGAGAGGT TGAGGTGGGA GGGTCACCTG AGCTCAGGGA AGTCAAGGCT GCAGTGAGCT 240 GTGATGACAC CACTGCACTC CAGCCTAGGT GACAGAGTAA GACTCTGTCT CAAAAAACAA 300 ACAACAAAAA AAAGGCTGGG CGCTGGGGCT CACATCTGTA ATCCCAGTAC TTTGGGAGGC 360 CAAGGTAGGT GGATGCTTGA GCTCAGGTGT TTGAGACCAG TCTGGGCAAC ATGGCGAAAA 420 CCCATCTCTA CTAAAAATAG AAAAAAATAG CCAGATGTGG TGGCGTGCAC CTGTAGTCCC 480 AGCTACTCAG GAGGCTGTGG TGGGATCATT GCTTGAACCC GGGGGTGGAG GCTGCATTGA 540 GCCAAGATTG TGCCACTGTC ACTGGGTGAC AGAGTGAAGG AGACCCTATC TCAAAAAAAA 600 AAAAAAATGG CCTTTTGTAT TCAGTTCTTA AAATAGCTCT AGAAGAGTTC CAGAGTGACA 660 GGTGGAAGAA ATGTCTTTAG TTATTCATAA CCATCCCCTT TCCACCACAG CTAAGTTTAT 720 GTTAATGGGG TGATTTTTGG AAAGCTCCTA CAAACCACAG GATGTGAGGC TAGTTGCCAG 780 GGAACCAACC ATGTGACTGG AGCTTTGAAA CTTTCAGCTC TGTCCCCACC TCCAGGGAGG 840 GAAGAGAAAA CTGAAGGTTG AGTTGATCAC CCATAGTGAA TGATGTGATT AATCATGTCA 900 CCATAATAAA GCCACCATAA AAACCCAAAA ACACGGCTCA GAGAGCCTTC TGGTTGGTAA 960 ATAAGAACAT AACCATATGC CTGGAGGTAT CTCTTCATCT GGCTGTTCAT TCGTATCATT 1020 TAAAATATCC TTTGTAGGGC CAGGTGTGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG 1080 AGGCTGAGGC AGGTGGATCA CTTGAGGTCA GGAGTTCAAG ACCAGCTTGA CCAACATGAT 1140 GAAACCCCAT CTCTACTTAA AATACAAAAA TTAGGCCAGG TGCAGTGGCT CACACCTATA 1200 ATCCCAGCAC TTTGGGAGGA CAAGGTGGGC GGATCATGAG GTCAGGAGTT CGAGACCAGC 1260 CTGGCCAGCA TGGTGAAACC CTGCCTCTAC TAAAAACATA GACACACAGA AAAAAAATTA 1320 GCTGGGCATG GTGGCATGGG CCTGTAATCC AGCTACTTGA GAGACTGAGG TAGGAGAATC 1380 ACTTGACCCT GGTAGGCAGA GGCTGCAGTG AGCCAAGATT 1420
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