| Tag | Content |
|---|
EnhancerAtlas ID | HS118-08110 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:44947090-44948620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr17:44947827-44947842 | GATTAATGATTAACG | + | 7.12 | | HNF1B | MA0153.2 | chr17:44947828-44947841 | ATTAATGATTAAC | + | 6.05 | | HNF1B | MA0153.2 | chr17:44947828-44947841 | ATTAATGATTAAC | - | 7.22 | | MEF2A | MA0052.3 | chr17:44948447-44948459 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr17:44948447-44948459 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr17:44948446-44948461 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I046870 | chr17 | 44947721 | 44947890 |
|
Enhancer Sequence | GCAGTGGCTC ACGTCTGTAA TTCCAGCACT CTGGGAGGCT GAGGCGGGCA GGTCACTTGA 60
AGTCAGGAGT TCGAAACCAG CCTGGCTAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAT 120
GAAAATTAGC CAGGGATGGT GGCGCACACC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC 180
AGGAGAATTG CTTGAACCCG GGAAGTGGAG GTTACAGTGA GCTGAGATCA CACCACTGCA 240
CTCTAGCCTG GACCACATAG CAAGACTGTC TCAAAAAAAA AAATGTTATA TATCATGTCA 300
TATCATATGA CATATACTGT AGCTATAATG ATATAATAAT CATAGCTATT ATTCTTAAAA 360
TGGCATTTGA GGCAGGTCTT GAAGGATATG CAGCTTCATT GGCCAAAATT TCCATCACTC 420
CCTGCTTGCT CTCCCCTCTG TCAATCAGTT GCTATCAGGG AGGTCCAGTT TCTGAAACAC 480
AGGAATTGTG TGAGCAGAAG TCGCCACTCA CACCAGCCCT CGGTGTGAGA AGGAGGACAT 540
TTGAGGGCAA GGTAGCTGCA GCCCCCAAGC TGCCCTCCAC ACTGGAAGCC AGTCAAGGCG 600
TGGCCTCCTC AGCTGGAGTT GACATCCAGT TCTTCTCTGG ACCTGCCAAG GGTCAAACTC 660
TGAGGATTTC CTGCCAGGCT GCAGGGAGGG GTTTGGGTGT AGACCTGGTG GACTGGAAAA 720
TTACCCATTT GCCCCCAGAT TAATGATTAA CGGGTCCCTG CCCTCACCCT GTCTGGGAGA 780
GGAGCCCAGG GCCAGGCTAG GCCAACGGGA GCCCGATAGC ATCTGTCTCT GCTCGGAGGT 840
TTCGGAGATA TGCTCCATGA TGGGTTGACT GCACCTGATG GGTGTGGAAT CTACAGGTGA 900
TTTCTGAGGG CACCTGGGGC CTGGCCAGGC CGCATACCCT CTGGTGAGGC TTCCAACTTC 960
TGGGGCATAC AGAGAGGGCA TGGCCTCCAG CCAGATGTCC TGGCTAAGGC AGGTGACTCC 1020
AAAGAGGAGA GCTGTGCCCT TGGCTCAGAG GAACATGGGC TTCTCTGACC ACTCCTGGCT 1080
TGACCACAGG ACTTACCTTG GCCAGTGGCA CATGAGCAAC AGTGGCAAGT GCCACATCCA 1140
AGCAGGAGCT CTAAGAGACA TTGCCTGCTT CCACCTTTGC TTTTTTTTTT TTTTTTTTTT 1200
TTTTGAGATA GGGTCTTGCT CTGTTTCCCA GGCTGGAGTG CAGTGATGCG ATCTCAGCTC 1260
ACTGCAGCCT CCACCTCCCG AGCTCAAGCT ATCCTTCCAC CTCAGCCTCC CAAGTAGCTG 1320
GGACTACAGG TGTGTGCCAC CATGCCCACA TAATTTTTCT ATTTTTAGTA GAGACAGGGT 1380
TTTGCTGTCA CACAGGCTGC TCTCAAACTC CTGGACTCAA GCGATCCACC TGCTCAGCCT 1440
CCCAAAGTGT GGAATTACAG GTGTGAGCCA CTGTGCCCAG CCCACCTTTG ATCTTTTACC 1500
CTGGCTATGA GGCCAGGATA TCCCAGAACA 1530
|
