Tag | Content |
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EnhancerAtlas ID | HS098-27127 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:11137320-11138450 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:11137393-11137408 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr19:11138429-11138450 | GCCTTCTCTCCTGCCTCCTCC | - | 6.73 |
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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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Enhancer Sequence | ACCTGCCACC ACCCAGCTAA TTTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG 60 ACCAGGCTGA TCTTGAACTC CTGACCTCAA GTGATCCACC CGCCTTGGCC TCCCAAAGTG 120 CTGGAATTAC AGGTGTGAGC CACCGCGCCC GGCCCCATTA TACAAATCTT TAGTGCTTGG 180 AGAGCTGACC ACTATTAACC CCAAGAGACA GGATTCCTGA GGCAGACCTG GCTTACAGAT 240 CCCACTCTGC CGCCTCCAAG CTCTGTGACT CTAGACAGCT TTCTTAACCT CTCTGAGCCT 300 AAACTCTGCT CACTAGTACA GAGGCACTCT TTACATCATG TGGGTGTTTT CTATAGCACC 360 CTTTGTAAGG GGCAGCCCAG ACTCCTTTAA GCCCCTAATG GATGTGGATG CTGTGTCTAG 420 ATTTTCACCA TTGCAAAGAA CCTTGCTAAA AGCATTCTTC CAGCTAAAGC CTCCATTCAA 480 TTCCCCTGGG GTAGTAAGCC ATTTGCAAGA AGAGAGGCGC CTAATGAAAA CATCACAAAT 540 TCTTTTTGAT GTGTTTTTTT ATACTGAGTT GTGGAACAGG GTCCTGTACA CCTGGCTTCA 600 AGGCTGGGAG GCCTGGCTTG GACATGTGGT CAGCCATATC ACGTCGTCCC CCTGCCAGCC 660 TCAGTGTCCA CATCTACAAC ACTTGGGGTT TGGCTGGAGA GAACATGAGA AGCCGAGGTG 720 GCCCTTCCTT CTGGGTCTAG CAGAGCATGG GTGTCTCCAG TGTGGCATTT GCTCCTGGGG 780 CTTCTTTATC GGGCAAGGGG ACAAGGTCTG GCTTCCCGGA GCATCCCTGT TCCAGCCCCG 840 TGTTGTGCCG GCCATGTGAC TCACAGCTCC TCTCATTTTC ATGAGTGTCT GGGTTTGACG 900 AGAAATACAT GTGCCACCCT GGTGATACGC CTCCCCAGCG AGGGTGGCCG GGCTTATTTC 960 AGTTGGGGGA AATGGCTTTG CTGAAGCTTT GGGTGGGTGA CGTCTGCTTA GGATGCATGT 1020 CTGTGCCCTT GAACCCGGCG CCTGGCCTGG AGGCGGGCGA TGCACCTCCT GCCTTACCTG 1080 CCTGCAGGGT TCCAGGTTTA ACATCCTGCG CCTTCTCTCC TGCCTCCTCC 1130
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