Tag | Content |
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EnhancerAtlas ID | HS127-27338 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr6:110734940-110736660 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| 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 | TGCATTTGGA GGAGTTTTCT ACTCATTCTT CACCCTTCCC TTTTTTTTCC CCCTGAAAGG 60 GGGTCTTGCT CTGTTGCCCA GCCTGGAGTA CAGCGACGAG ATCTCGGCTC ACTGCAACCT 120 CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC TGAGTAACTG GGATTACAGG 180 TGCCCACCAC CACGCCAGGT TAATTTTTGT ATTTTTAGTA GAGATAGGGT TTCAGCATGT 240 TGGCTAGGCT GGTCTCGAAC TCCTGACCTT GTGATCCGCC GGCCCCAGCC TCCCAAAGTG 300 CTGGGATTAC AGGCGTGAGC CACCATGCCC GGCTTCATCC CCCTTTCCTA AACCATTTTC 360 CCTATGGGCA CAACCTAGGG AAGGTTGACA GAAAACCACA GAGCTGTAGT CTTTGCTCCC 420 AGAACTACCT GAGGAGCAGT GGTGAGGGGC ATGACCCATG AGCAACTCAA AACTCAACTC 480 TGTCTACAAA GTTGTTTCTA ATAATAAGGA CATTACAGAA AGTTTCAGCA GCTGAACTCA 540 GTCTCCTCTG CCATCTGCCA CTGTCACCGG CCCCCTGTCT GTCCTGGACA GGTTCTGTAA 600 CCTGAGGAGC AGTCCGTGGT CTCCTAGCCT CCACTCCCTC ATCTGTAACA CAGAACAGAT 660 GGATTACTTG CTCCTTTGGG TGGTAAATAA GAGAGACCCA GTGAGGCGGT CTCATAAAGG 720 GGGCTCCTTG GGAGAGTCTG AATGGAAATG CAGGGGACAG ACATCCCGGA GCCCGGGCCA 780 GGTGTCCTGA GGCTGGCACC CTCTGTCCCA CCCCTCACCC ACGGAGCCTT GCTCCACTGT 840 CAGCATCCCC GCCTGCCTTT GCTTCCCTGT TTTTGGCTTT CCCCATCTGT TCCTGCTCTG 900 ACTCTTTCTG TATGGCTCAG GTTTAAACTC CAGAGAGAGA AAATGCAGTT GTACCAGTTG 960 GTCATTGCAT CCCCTGTTGG ACAAAATTCT AGCACCAGGC CAACTTGCTG GGCTAAACCA 1020 GCCTCTGAAT GTGCCCTTGG CATAGTTGCC CTTCTCTGTC CAAAGCACAG TAATCAGGGT 1080 ACTGGGCCAC ATGGTACAAA CCATGGCCAC CCACACACAG AGGTTCACCT TTCCTCTGGA 1140 AGGCTGGGCA GCTTCCTCAG CAAGGGCTGT TGGCAGGAAA AACGTGGGCT TGGTTGTTAG 1200 TGGCCTCTGC TTTCTCTTCC AGTTCTGAAG ATTCTCGCAC TATGAGACTT TAAAGCCCTC 1260 CAATGAAGTT TAGTGTGATA TTCCTATTCC TCGAGCAGTC TATGCATTTC TGTGCTAATT 1320 TGATACGTTA ATTTGATTGC TGTACAGTGG GCTGGTCAGC TGAGAGAGAG TGGGCCTGCC 1380 AGGGCTGAGG GAAGAGAAGG GAACGGGCCC AGGCCAGAGC AGTCTGGTGG GGGCCAGCTT 1440 GAGTAGAGCT GTCCTGCAGC CACCAGTGAC CTTATTGACT TCGCTGTTTC ACATCAGCCT 1500 CCCATGTCCA GCAACTCTCT CAAAACAGCT CTAATAAACT AAGTTGAAAG GGCAAGCAAT 1560 CTGTGGCTAA GAATAACCAG CTGCCAGGGA GGAGGAGTGA GCGAGCAATG TGGTGTGTCC 1620 TGGCACAGTG GCCTGTCCAT CACTGTCCCC TGACCCTATT CAGACACACT CCCAAACTCC 1680 CAGAGCATGG ACGGAACGAC CCCTCAGCTG AAAGCAAGAA 1720
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