Tag | Content |
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EnhancerAtlas ID | HS094-36302 | Organism | Homo sapiens | Tissue/cell | hMADS-3 | Coordinate | chr6:110735190-110736660 | 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 | GGTCTCGAAC TCCTGACCTT GTGATCCGCC GGCCCCAGCC TCCCAAAGTG CTGGGATTAC 60 AGGCGTGAGC CACCATGCCC GGCTTCATCC CCCTTTCCTA AACCATTTTC CCTATGGGCA 120 CAACCTAGGG AAGGTTGACA GAAAACCACA GAGCTGTAGT CTTTGCTCCC AGAACTACCT 180 GAGGAGCAGT GGTGAGGGGC ATGACCCATG AGCAACTCAA AACTCAACTC TGTCTACAAA 240 GTTGTTTCTA ATAATAAGGA CATTACAGAA AGTTTCAGCA GCTGAACTCA GTCTCCTCTG 300 CCATCTGCCA CTGTCACCGG CCCCCTGTCT GTCCTGGACA GGTTCTGTAA CCTGAGGAGC 360 AGTCCGTGGT CTCCTAGCCT CCACTCCCTC ATCTGTAACA CAGAACAGAT GGATTACTTG 420 CTCCTTTGGG TGGTAAATAA GAGAGACCCA GTGAGGCGGT CTCATAAAGG GGGCTCCTTG 480 GGAGAGTCTG AATGGAAATG CAGGGGACAG ACATCCCGGA GCCCGGGCCA GGTGTCCTGA 540 GGCTGGCACC CTCTGTCCCA CCCCTCACCC ACGGAGCCTT GCTCCACTGT CAGCATCCCC 600 GCCTGCCTTT GCTTCCCTGT TTTTGGCTTT CCCCATCTGT TCCTGCTCTG ACTCTTTCTG 660 TATGGCTCAG GTTTAAACTC CAGAGAGAGA AAATGCAGTT GTACCAGTTG GTCATTGCAT 720 CCCCTGTTGG ACAAAATTCT AGCACCAGGC CAACTTGCTG GGCTAAACCA GCCTCTGAAT 780 GTGCCCTTGG CATAGTTGCC CTTCTCTGTC CAAAGCACAG TAATCAGGGT ACTGGGCCAC 840 ATGGTACAAA CCATGGCCAC CCACACACAG AGGTTCACCT TTCCTCTGGA AGGCTGGGCA 900 GCTTCCTCAG CAAGGGCTGT TGGCAGGAAA AACGTGGGCT TGGTTGTTAG TGGCCTCTGC 960 TTTCTCTTCC AGTTCTGAAG ATTCTCGCAC TATGAGACTT TAAAGCCCTC CAATGAAGTT 1020 TAGTGTGATA TTCCTATTCC TCGAGCAGTC TATGCATTTC TGTGCTAATT TGATACGTTA 1080 ATTTGATTGC TGTACAGTGG GCTGGTCAGC TGAGAGAGAG TGGGCCTGCC AGGGCTGAGG 1140 GAAGAGAAGG GAACGGGCCC AGGCCAGAGC AGTCTGGTGG GGGCCAGCTT GAGTAGAGCT 1200 GTCCTGCAGC CACCAGTGAC CTTATTGACT TCGCTGTTTC ACATCAGCCT CCCATGTCCA 1260 GCAACTCTCT CAAAACAGCT CTAATAAACT AAGTTGAAAG GGCAAGCAAT CTGTGGCTAA 1320 GAATAACCAG CTGCCAGGGA GGAGGAGTGA GCGAGCAATG TGGTGTGTCC TGGCACAGTG 1380 GCCTGTCCAT CACTGTCCCC TGACCCTATT CAGACACACT CCCAAACTCC CAGAGCATGG 1440 ACGGAACGAC CCCTCAGCTG AAAGCAAGAA 1470
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