Tag | Content |
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EnhancerAtlas ID | HS145-11779 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr19:41180030-41180960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr19:41180389-41180400 | AAACCACAAAC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGTCCTACT GCTAGGAAGG GGCAGGCTGA CTCTGGACCC CATGCTCCAA ATGACTGCCC 60 GCCCTGTCTC CCTCTGACCT GTCTCTCCAT ATCATGTTGT CTTTCTCTGT CACTGTCTGT 120 TCCCCTCTGT CTCCCACCTC CCAGCCTTCT TCCCACCTCA AGTAGCTCCT CCCTTCCTCC 180 AGTCATTCTA GACATGGCTT GGATGCTTCA TCCTCTGAGA AGCTTTCCAG ATTGTTCCAG 240 GCTCTCAGCC TGGCTCCCTC CACTCTGAGA CTGTTCTCTG TACTCTGGGA GGAAACCTGA 300 CCTCCCCACT CAGCAGGAGA GGCAGGCTCT TCAAGGGCAG GGCTGCCCTC ACCCCTGCCA 360 AACCACAAAC ACACATCTAC CCTCCTACCA GGGCCTCCCC GAGCTGCAGC CTGAATGCCA 420 TGGAGATTAA ACTCAGGCCC AGAGAGACCC TCCCATAAGG ATGTCGCCCA GTGCTGCTTC 480 TCCCATCGTG ACACAATGGG GCACCCATGC AGGCCTGGCC CAAGGCAGTG GAAACAGCCC 540 AGGACAGGTT GGAACCAGGA AACCTCCTCT GCCTCCACTC ACTGTGTGAC CTCAGGAAGT 600 CCCCTCCCCT CTCTGGGCTC CAGTTTGCCA ACTAGAAACC TGGGATAAAC ATCTCAGTGC 660 TACCTCCCAA GCCTCTGAGA GGGTCAGTTT AGGTAGTGAA TGTTAAATGT TTTGGAATCC 720 AACAAAAGCA TGCCTGGACA CAGTGGTTCA CGCCTGTAAT CCCAGCACTT TGAGAGGCCA 780 AGGTGGGGGG ATCAGTTGAA GCCAGGAGTT CAAGACCAGC CTTGCCAACA TGGTGAAACA 840 CCATCTCTAC TAAAAATACA AAAAAAGATT AGCTGGGTGT GGTGGCACAC GCCTGGGATT 900 CCAGCTACTC TGGAGGCTGA GGCAGGAGAA 930
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