| Tag | Content |
|---|
EnhancerAtlas ID | HS105-34485 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:44947200-44948390 |
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 | CTAAAAATAT GAAAATTAGC CAGGGATGGT GGCGCACACC TGTAGTCCCA GCTACTCGGG 60
AGGCTGAGGC AGGAGAATTG CTTGAACCCG GGAAGTGGAG GTTACAGTGA GCTGAGATCA 120
CACCACTGCA CTCTAGCCTG GACCACATAG CAAGACTGTC TCAAAAAAAA AAATGTTATA 180
TATCATGTCA TATCATATGA CATATACTGT AGCTATAATG ATATAATAAT CATAGCTATT 240
ATTCTTAAAA TGGCATTTGA GGCAGGTCTT GAAGGATATG CAGCTTCATT GGCCAAAATT 300
TCCATCACTC CCTGCTTGCT CTCCCCTCTG TCAATCAGTT GCTATCAGGG AGGTCCAGTT 360
TCTGAAACAC AGGAATTGTG TGAGCAGAAG TCGCCACTCA CACCAGCCCT CGGTGTGAGA 420
AGGAGGACAT TTGAGGGCAA GGTAGCTGCA GCCCCCAAGC TGCCCTCCAC ACTGGAAGCC 480
AGTCAAGGCG TGGCCTCCTC AGCTGGAGTT GACATCCAGT TCTTCTCTGG ACCTGCCAAG 540
GGTCAAACTC TGAGGATTTC CTGCCAGGCT GCAGGGAGGG GTTTGGGTGT AGACCTGGTG 600
GACTGGAAAA TTACCCATTT GCCCCCAGAT TAATGATTAA CGGGTCCCTG CCCTCACCCT 660
GTCTGGGAGA GGAGCCCAGG GCCAGGCTAG GCCAACGGGA GCCCGATAGC ATCTGTCTCT 720
GCTCGGAGGT TTCGGAGATA TGCTCCATGA TGGGTTGACT GCACCTGATG GGTGTGGAAT 780
CTACAGGTGA TTTCTGAGGG CACCTGGGGC CTGGCCAGGC CGCATACCCT CTGGTGAGGC 840
TTCCAACTTC TGGGGCATAC AGAGAGGGCA TGGCCTCCAG CCAGATGTCC TGGCTAAGGC 900
AGGTGACTCC AAAGAGGAGA GCTGTGCCCT TGGCTCAGAG GAACATGGGC TTCTCTGACC 960
ACTCCTGGCT TGACCACAGG ACTTACCTTG GCCAGTGGCA CATGAGCAAC AGTGGCAAGT 1020
GCCACATCCA AGCAGGAGCT CTAAGAGACA TTGCCTGCTT CCACCTTTGC TTTTTTTTTT 1080
TTTTTTTTTT TTTTGAGATA GGGTCTTGCT CTGTTTCCCA GGCTGGAGTG CAGTGATGCG 1140
ATCTCAGCTC ACTGCAGCCT CCACCTCCCG AGCTCAAGCT ATCCTTCCAC 1190
|
