| Tag | Content |
|---|
EnhancerAtlas ID | HS098-24229 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:44947170-44948520 |
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 | CCTGGCTAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAT GAAAATTAGC CAGGGATGGT 60
GGCGCACACC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCG 120
GGAAGTGGAG GTTACAGTGA GCTGAGATCA CACCACTGCA CTCTAGCCTG GACCACATAG 180
CAAGACTGTC TCAAAAAAAA AAATGTTATA TATCATGTCA TATCATATGA CATATACTGT 240
AGCTATAATG ATATAATAAT CATAGCTATT ATTCTTAAAA TGGCATTTGA GGCAGGTCTT 300
GAAGGATATG CAGCTTCATT GGCCAAAATT TCCATCACTC CCTGCTTGCT CTCCCCTCTG 360
TCAATCAGTT GCTATCAGGG AGGTCCAGTT TCTGAAACAC AGGAATTGTG TGAGCAGAAG 420
TCGCCACTCA CACCAGCCCT CGGTGTGAGA AGGAGGACAT TTGAGGGCAA GGTAGCTGCA 480
GCCCCCAAGC TGCCCTCCAC ACTGGAAGCC AGTCAAGGCG TGGCCTCCTC AGCTGGAGTT 540
GACATCCAGT TCTTCTCTGG ACCTGCCAAG GGTCAAACTC TGAGGATTTC CTGCCAGGCT 600
GCAGGGAGGG GTTTGGGTGT AGACCTGGTG GACTGGAAAA TTACCCATTT GCCCCCAGAT 660
TAATGATTAA CGGGTCCCTG CCCTCACCCT GTCTGGGAGA GGAGCCCAGG GCCAGGCTAG 720
GCCAACGGGA GCCCGATAGC ATCTGTCTCT GCTCGGAGGT TTCGGAGATA TGCTCCATGA 780
TGGGTTGACT GCACCTGATG GGTGTGGAAT CTACAGGTGA TTTCTGAGGG CACCTGGGGC 840
CTGGCCAGGC CGCATACCCT CTGGTGAGGC TTCCAACTTC TGGGGCATAC AGAGAGGGCA 900
TGGCCTCCAG CCAGATGTCC TGGCTAAGGC AGGTGACTCC AAAGAGGAGA GCTGTGCCCT 960
TGGCTCAGAG GAACATGGGC TTCTCTGACC ACTCCTGGCT TGACCACAGG ACTTACCTTG 1020
GCCAGTGGCA CATGAGCAAC AGTGGCAAGT GCCACATCCA AGCAGGAGCT CTAAGAGACA 1080
TTGCCTGCTT CCACCTTTGC TTTTTTTTTT TTTTTTTTTT TTTTGAGATA GGGTCTTGCT 1140
CTGTTTCCCA GGCTGGAGTG CAGTGATGCG ATCTCAGCTC ACTGCAGCCT CCACCTCCCG 1200
AGCTCAAGCT ATCCTTCCAC CTCAGCCTCC CAAGTAGCTG GGACTACAGG TGTGTGCCAC 1260
CATGCCCACA TAATTTTTCT ATTTTTAGTA GAGACAGGGT TTTGCTGTCA CACAGGCTGC 1320
TCTCAAACTC CTGGACTCAA GCGATCCACC 1350
|
