| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16428 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:110734760-110736660 | 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 | TCAGCCACTC AGAATAAGAC TTAGCCTATT GGTGTTTCTT GTGAGATAAA GAGGATAACC 60
CCATAAGCTC ACTTTCCATT AAATATTGGT GTATAAGCAA CAAGATCTCC ATGGGCTTTT 120
AGAGAGTAAC ACAAAACTGG CTTGGATTTG CCTTTAGAAC ACCTAGCCAG TAAGTAGGTC 180
TGCATTTGGA GGAGTTTTCT ACTCATTCTT CACCCTTCCC TTTTTTTTCC CCCTGAAAGG 240
GGGTCTTGCT CTGTTGCCCA GCCTGGAGTA CAGCGACGAG ATCTCGGCTC ACTGCAACCT 300
CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC TGAGTAACTG GGATTACAGG 360
TGCCCACCAC CACGCCAGGT TAATTTTTGT ATTTTTAGTA GAGATAGGGT TTCAGCATGT 420
TGGCTAGGCT GGTCTCGAAC TCCTGACCTT GTGATCCGCC GGCCCCAGCC TCCCAAAGTG 480
CTGGGATTAC AGGCGTGAGC CACCATGCCC GGCTTCATCC CCCTTTCCTA AACCATTTTC 540
CCTATGGGCA CAACCTAGGG AAGGTTGACA GAAAACCACA GAGCTGTAGT CTTTGCTCCC 600
AGAACTACCT GAGGAGCAGT GGTGAGGGGC ATGACCCATG AGCAACTCAA AACTCAACTC 660
TGTCTACAAA GTTGTTTCTA ATAATAAGGA CATTACAGAA AGTTTCAGCA GCTGAACTCA 720
GTCTCCTCTG CCATCTGCCA CTGTCACCGG CCCCCTGTCT GTCCTGGACA GGTTCTGTAA 780
CCTGAGGAGC AGTCCGTGGT CTCCTAGCCT CCACTCCCTC ATCTGTAACA CAGAACAGAT 840
GGATTACTTG CTCCTTTGGG TGGTAAATAA GAGAGACCCA GTGAGGCGGT CTCATAAAGG 900
GGGCTCCTTG GGAGAGTCTG AATGGAAATG CAGGGGACAG ACATCCCGGA GCCCGGGCCA 960
GGTGTCCTGA GGCTGGCACC CTCTGTCCCA CCCCTCACCC ACGGAGCCTT GCTCCACTGT 1020
CAGCATCCCC GCCTGCCTTT GCTTCCCTGT TTTTGGCTTT CCCCATCTGT TCCTGCTCTG 1080
ACTCTTTCTG TATGGCTCAG GTTTAAACTC CAGAGAGAGA AAATGCAGTT GTACCAGTTG 1140
GTCATTGCAT CCCCTGTTGG ACAAAATTCT AGCACCAGGC CAACTTGCTG GGCTAAACCA 1200
GCCTCTGAAT GTGCCCTTGG CATAGTTGCC CTTCTCTGTC CAAAGCACAG TAATCAGGGT 1260
ACTGGGCCAC ATGGTACAAA CCATGGCCAC CCACACACAG AGGTTCACCT TTCCTCTGGA 1320
AGGCTGGGCA GCTTCCTCAG CAAGGGCTGT TGGCAGGAAA AACGTGGGCT TGGTTGTTAG 1380
TGGCCTCTGC TTTCTCTTCC AGTTCTGAAG ATTCTCGCAC TATGAGACTT TAAAGCCCTC 1440
CAATGAAGTT TAGTGTGATA TTCCTATTCC TCGAGCAGTC TATGCATTTC TGTGCTAATT 1500
TGATACGTTA ATTTGATTGC TGTACAGTGG GCTGGTCAGC TGAGAGAGAG TGGGCCTGCC 1560
AGGGCTGAGG GAAGAGAAGG GAACGGGCCC AGGCCAGAGC AGTCTGGTGG GGGCCAGCTT 1620
GAGTAGAGCT GTCCTGCAGC CACCAGTGAC CTTATTGACT TCGCTGTTTC ACATCAGCCT 1680
CCCATGTCCA GCAACTCTCT CAAAACAGCT CTAATAAACT AAGTTGAAAG GGCAAGCAAT 1740
CTGTGGCTAA GAATAACCAG CTGCCAGGGA GGAGGAGTGA GCGAGCAATG TGGTGTGTCC 1800
TGGCACAGTG GCCTGTCCAT CACTGTCCCC TGACCCTATT CAGACACACT CCCAAACTCC 1860
CAGAGCATGG ACGGAACGAC CCCTCAGCTG AAAGCAAGAA 1900
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