| Tag | Content |
|---|
EnhancerAtlas ID | HS065-02231 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr17:44947610-44948220 |
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 |
|
| | 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 | CGGTGTGAGA AGGAGGACAT TTGAGGGCAA GGTAGCTGCA GCCCCCAAGC TGCCCTCCAC 60
ACTGGAAGCC AGTCAAGGCG TGGCCTCCTC AGCTGGAGTT GACATCCAGT TCTTCTCTGG 120
ACCTGCCAAG GGTCAAACTC TGAGGATTTC CTGCCAGGCT GCAGGGAGGG GTTTGGGTGT 180
AGACCTGGTG GACTGGAAAA TTACCCATTT GCCCCCAGAT TAATGATTAA CGGGTCCCTG 240
CCCTCACCCT GTCTGGGAGA GGAGCCCAGG GCCAGGCTAG GCCAACGGGA GCCCGATAGC 300
ATCTGTCTCT GCTCGGAGGT TTCGGAGATA TGCTCCATGA TGGGTTGACT GCACCTGATG 360
GGTGTGGAAT CTACAGGTGA TTTCTGAGGG CACCTGGGGC CTGGCCAGGC CGCATACCCT 420
CTGGTGAGGC TTCCAACTTC TGGGGCATAC AGAGAGGGCA TGGCCTCCAG CCAGATGTCC 480
TGGCTAAGGC AGGTGACTCC AAAGAGGAGA GCTGTGCCCT TGGCTCAGAG GAACATGGGC 540
TTCTCTGACC ACTCCTGGCT TGACCACAGG ACTTACCTTG GCCAGTGGCA CATGAGCAAC 600
AGTGGCAAGT 610
|
