Tag | Content |
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EnhancerAtlas ID | HS116-29977 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:110735000-110736660 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr6:110735332-110735343 | AAACCACAGAG | - | 6.14 |
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| 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 |
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Enhancer Sequence | GGGTCTTGCT CTGTTGCCCA GCCTGGAGTA CAGCGACGAG ATCTCGGCTC ACTGCAACCT 60 CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC TGAGTAACTG GGATTACAGG 120 TGCCCACCAC CACGCCAGGT TAATTTTTGT ATTTTTAGTA GAGATAGGGT TTCAGCATGT 180 TGGCTAGGCT GGTCTCGAAC TCCTGACCTT GTGATCCGCC GGCCCCAGCC TCCCAAAGTG 240 CTGGGATTAC AGGCGTGAGC CACCATGCCC GGCTTCATCC CCCTTTCCTA AACCATTTTC 300 CCTATGGGCA CAACCTAGGG AAGGTTGACA GAAAACCACA GAGCTGTAGT CTTTGCTCCC 360 AGAACTACCT GAGGAGCAGT GGTGAGGGGC ATGACCCATG AGCAACTCAA AACTCAACTC 420 TGTCTACAAA GTTGTTTCTA ATAATAAGGA CATTACAGAA AGTTTCAGCA GCTGAACTCA 480 GTCTCCTCTG CCATCTGCCA CTGTCACCGG CCCCCTGTCT GTCCTGGACA GGTTCTGTAA 540 CCTGAGGAGC AGTCCGTGGT CTCCTAGCCT CCACTCCCTC ATCTGTAACA CAGAACAGAT 600 GGATTACTTG CTCCTTTGGG TGGTAAATAA GAGAGACCCA GTGAGGCGGT CTCATAAAGG 660 GGGCTCCTTG GGAGAGTCTG AATGGAAATG CAGGGGACAG ACATCCCGGA GCCCGGGCCA 720 GGTGTCCTGA GGCTGGCACC CTCTGTCCCA CCCCTCACCC ACGGAGCCTT GCTCCACTGT 780 CAGCATCCCC GCCTGCCTTT GCTTCCCTGT TTTTGGCTTT CCCCATCTGT TCCTGCTCTG 840 ACTCTTTCTG TATGGCTCAG GTTTAAACTC CAGAGAGAGA AAATGCAGTT GTACCAGTTG 900 GTCATTGCAT CCCCTGTTGG ACAAAATTCT AGCACCAGGC CAACTTGCTG GGCTAAACCA 960 GCCTCTGAAT GTGCCCTTGG CATAGTTGCC CTTCTCTGTC CAAAGCACAG TAATCAGGGT 1020 ACTGGGCCAC ATGGTACAAA CCATGGCCAC CCACACACAG AGGTTCACCT TTCCTCTGGA 1080 AGGCTGGGCA GCTTCCTCAG CAAGGGCTGT TGGCAGGAAA AACGTGGGCT TGGTTGTTAG 1140 TGGCCTCTGC TTTCTCTTCC AGTTCTGAAG ATTCTCGCAC TATGAGACTT TAAAGCCCTC 1200 CAATGAAGTT TAGTGTGATA TTCCTATTCC TCGAGCAGTC TATGCATTTC TGTGCTAATT 1260 TGATACGTTA ATTTGATTGC TGTACAGTGG GCTGGTCAGC TGAGAGAGAG TGGGCCTGCC 1320 AGGGCTGAGG GAAGAGAAGG GAACGGGCCC AGGCCAGAGC AGTCTGGTGG GGGCCAGCTT 1380 GAGTAGAGCT GTCCTGCAGC CACCAGTGAC CTTATTGACT TCGCTGTTTC ACATCAGCCT 1440 CCCATGTCCA GCAACTCTCT CAAAACAGCT CTAATAAACT AAGTTGAAAG GGCAAGCAAT 1500 CTGTGGCTAA GAATAACCAG CTGCCAGGGA GGAGGAGTGA GCGAGCAATG TGGTGTGTCC 1560 TGGCACAGTG GCCTGTCCAT CACTGTCCCC TGACCCTATT CAGACACACT CCCAAACTCC 1620 CAGAGCATGG ACGGAACGAC CCCTCAGCTG AAAGCAAGAA 1660
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