Tag | Content |
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EnhancerAtlas ID | HS139-48051 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr6:110735120-110736660 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr6:110735332-110735343 | AAACCACAGAG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 110735934 | 110736023 | chr6 | 110736028 | 110736138 |
| Enhancer Sequence | TGCCCACCAC CACGCCAGGT TAATTTTTGT ATTTTTAGTA GAGATAGGGT TTCAGCATGT 60 TGGCTAGGCT GGTCTCGAAC TCCTGACCTT GTGATCCGCC GGCCCCAGCC TCCCAAAGTG 120 CTGGGATTAC AGGCGTGAGC CACCATGCCC GGCTTCATCC CCCTTTCCTA AACCATTTTC 180 CCTATGGGCA CAACCTAGGG AAGGTTGACA GAAAACCACA GAGCTGTAGT CTTTGCTCCC 240 AGAACTACCT GAGGAGCAGT GGTGAGGGGC ATGACCCATG AGCAACTCAA AACTCAACTC 300 TGTCTACAAA GTTGTTTCTA ATAATAAGGA CATTACAGAA AGTTTCAGCA GCTGAACTCA 360 GTCTCCTCTG CCATCTGCCA CTGTCACCGG CCCCCTGTCT GTCCTGGACA GGTTCTGTAA 420 CCTGAGGAGC AGTCCGTGGT CTCCTAGCCT CCACTCCCTC ATCTGTAACA CAGAACAGAT 480 GGATTACTTG CTCCTTTGGG TGGTAAATAA GAGAGACCCA GTGAGGCGGT CTCATAAAGG 540 GGGCTCCTTG GGAGAGTCTG AATGGAAATG CAGGGGACAG ACATCCCGGA GCCCGGGCCA 600 GGTGTCCTGA GGCTGGCACC CTCTGTCCCA CCCCTCACCC ACGGAGCCTT GCTCCACTGT 660 CAGCATCCCC GCCTGCCTTT GCTTCCCTGT TTTTGGCTTT CCCCATCTGT TCCTGCTCTG 720 ACTCTTTCTG TATGGCTCAG GTTTAAACTC CAGAGAGAGA AAATGCAGTT GTACCAGTTG 780 GTCATTGCAT CCCCTGTTGG ACAAAATTCT AGCACCAGGC CAACTTGCTG GGCTAAACCA 840 GCCTCTGAAT GTGCCCTTGG CATAGTTGCC CTTCTCTGTC CAAAGCACAG TAATCAGGGT 900 ACTGGGCCAC ATGGTACAAA CCATGGCCAC CCACACACAG AGGTTCACCT TTCCTCTGGA 960 AGGCTGGGCA GCTTCCTCAG CAAGGGCTGT TGGCAGGAAA AACGTGGGCT TGGTTGTTAG 1020 TGGCCTCTGC TTTCTCTTCC AGTTCTGAAG ATTCTCGCAC TATGAGACTT TAAAGCCCTC 1080 CAATGAAGTT TAGTGTGATA TTCCTATTCC TCGAGCAGTC TATGCATTTC TGTGCTAATT 1140 TGATACGTTA ATTTGATTGC TGTACAGTGG GCTGGTCAGC TGAGAGAGAG TGGGCCTGCC 1200 AGGGCTGAGG GAAGAGAAGG GAACGGGCCC AGGCCAGAGC AGTCTGGTGG GGGCCAGCTT 1260 GAGTAGAGCT GTCCTGCAGC CACCAGTGAC CTTATTGACT TCGCTGTTTC ACATCAGCCT 1320 CCCATGTCCA GCAACTCTCT CAAAACAGCT CTAATAAACT AAGTTGAAAG GGCAAGCAAT 1380 CTGTGGCTAA GAATAACCAG CTGCCAGGGA GGAGGAGTGA GCGAGCAATG TGGTGTGTCC 1440 TGGCACAGTG GCCTGTCCAT CACTGTCCCC TGACCCTATT CAGACACACT CCCAAACTCC 1500 CAGAGCATGG ACGGAACGAC CCCTCAGCTG AAAGCAAGAA 1540
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