| Tag | Content |
|---|
EnhancerAtlas ID | HS091-35183 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:135969400-135971980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr3:135969976-135969986 | GGCACGTGTC | - | 6.02 | | Npas2 | MA0626.1 | chr3:135969976-135969986 | GGCACGTGTC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr3:135971307-135971322 | TGAACTCCTGACCTC | - | 6.22 | | STAT3 | MA0144.2 | chr3:135971064-135971075 | TTTCCCAGAAG | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGTCCTG AGGGGCCTAA GTGAGTCCCG CCCCTGGCGT CCGCGACCTA TCACTGCGTG 60
CCCGGCTTGC GGCGTCCGAG GCCTCCCTGC CAATCCGCAC GGTGCCTGGA GGGGCCGGAG 120
CAAGGGTGTT CACCTTGAAA ACCTGTAGCG TTTCTCGTGG AGGCGGGTAT AACCAGCAGA 180
AGCACCTGTG TGCTTTTTCA TACTGTTTAA CCCTTGGGAT TTAGACGGAT CTGGCTCGTC 240
TCTAGCCAGC TCAACACTTA ACATAAGCTT TTGGGCAACT TATTAAATCT CTGTGGGTCA 300
TTTTAATAAT AATTCTTCCT TCACAAGTGT ATCGTTAGAC CATAGATAGC AAAATGATAG 360
GCGCTCAGTA AAAACCATGT GCTTATTCTC GTGCCCCATG AAAGAGTGAT GGTAGGTTCT 420
TTCTCCTTTG TGGAAGCAGG AAAACTGAAC TTGGGCATAC TCCACTAACA TGAAATGGGG 480
GATGTGCGCG TGCAGGAACT TGTGGAACTT CTGCCCGCAG AATGCCTGGT CGAGCTCTTT 540
AGGGCCTTAG CATGCCTCGC CTTGATGGGT AGCAAAGGCA CGTGTCGGAA GCAGGTGGCC 600
TTTCTGGGAG TGCGCAGGCT ACTCTCGATG TTTGGCTGGA CTGAGCAGTT GAAACACTGC 660
CACCCACCGC CTGGGTTTTG AGGCGAGAAT CCAGCTGGCC TTCAGAGATA AGCTGGGCGG 720
CCCATTTTGG AGAGGTGATC CCTGACTTGA AACCAGGCTT GCCCAGTGTG TCCGTGACTG 780
GTGGGTGAGT CTGGACCGTT GTGCTGAACG AATTAACCAA CGGGAAGGTG CAGAAGTGAA 840
ACTCTTACAG ATGAAGAGTA TTCAGGCACA ACTCACAACC ATGAGGGAGG CACTGGGGGA 900
GGGATGGGGT CTTAAAGTGA GGAGATTTGA ACAGCTCTAT ATTTGTCTAA TATTGATTCA 960
GATGTCATAA ATTCGCATTT GACAAGGGTC CAAAGGTAAC AGTTCCTTTT GACACTTGAG 1020
AGTGAAATGT AAATTTAGTG ATGGTTTGTG GTGCTAGGAG TGCTTTCTCT CCCCTGGGGC 1080
TACTTCTAAC CTACTCTGTT AGGGCTGAGG GAGATGTTAG ATCATCCTCT GGAAAGGCCT 1140
GTCAGTGCTC CTGTACACTC TTTCTGTTGG GGCCTATTGC TCAATTCTTC CCTGGAACAT 1200
CGCCTAGCCC TTTCCCAGGT AGATCCTACT AGGTTTAGAT GAAGCCTCCA GAAGCTGTTT 1260
TTCTTTTGCC AAAGTTAACT TAGGAGGCTG ATTTAATATG AACCCCCTCC TGCACCCCTT 1320
TTTATTTTTA TGTTTTGATA CGGAGTTTTG CTCTTGTTGC CCAGGCTGGA GTGCCATGGT 1380
GCGATCTTGG CTCATTGCAA CCTCTGCCTC CCAGGTTCAA GCTATTCTCC TGCCTCAGCC 1440
TCCCAAGTAG CTGGGATTAC AGGTGCCCAC GACCATGCCT GGCAACTTTT TTTTTGTATT 1500
TTTAGCAGAG ACAGGGTTTC ACCATGTTGG CCAGGCCGGT CTTGTACGCC TGACCTCAAG 1560
TGATTCACCC ACCTTGGCGT CCCAAAGTGT TGGGATTATG GGTGTGAGCC ACTGCACCCG 1620
GCCCTGCACC CCTTTTAAAA CAATTTTTGA CCATTTCCGT AGATTTTCCC AGAAGAGGAA 1680
TTAGTGGGTC AAAGGGTGTA AGTTTATTTA TTTTTTTTGA GACAGAGTTC ACTCTGTTGC 1740
CCAGGCTAGA GTGCAGCAGC TCACTGCAAC TTCTGCTTCC CAGCTTCAAG CAATTCTCCT 1800
GCCTCAGCCT CCAGAGTACC TGGGGTTACA GGTATGTGTC ACCACATCTG GCTAATTTTT 1860
GTATTTTTAG TAGAGATGGA GTTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC 1920
TCAGGTGATC CACCCGCGTC TGCCTCCCAA AGTGCTGGGA TGACAGAATT TTTTTTTTTT 1980
TTTCCTTGAG ACAGGGTCTT ACTCTGTCAC CCAGGCTGGA GGGCAGTGGT GTAATCATGG 2040
CTCACTGCAT CCTTGACCTT CTGGGCTCCA GTGATCCTTC CACTTCAGCC TCCTACCCAG 2100
CTAATTTTTT TTTTTTTTTT TTTTTGGTAG AGACAGGGTC TCGCTTTGTT GCCCAGGCTG 2160
GTCTCAACTC CTGGGCTCAA GCAGTCCTCC CACCTTGGCC TTCCAAAGTG CTGGGATTAC 2220
AGGTGTGAGC CGCAGTGCCT GGTCAGTATA AATATATTTT AAAAATCTGT ATATATGTTG 2280
CCAAATTGGT TTCCTGAAAA CTTACTCTAC TTTACATGAC AGTGTATAGG ATTGCCTGTT 2340
TTTTGTTTTG TTTTTTTTTT TTTAAATGCA ACCTCACCAG CTTTGGCTAC TTTCCTAAGG 2400
GGAAAATAAT AGCCAATTTG AGGTATTTTT TGTTTGTTTT TGTTTTTTTC GGGGAGGGGG 2460
GGATAGGACA GTAGGCTAGG GTATTTGCCT CGGGTTGAGA GCTTGGGAGT CCAAGCAATG 2520
GAGGTTTTTT TTTTTTTTTT TTTTTTTTTA AGATAGAGTC TTGCTCTGTC ACCCAGGCTG 2580
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