| Tag | Content |
|---|
EnhancerAtlas ID | HS019-07121 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr17:44947240-44948550 |
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 | TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCG GGAAGTGGAG 60
GTTACAGTGA GCTGAGATCA CACCACTGCA CTCTAGCCTG GACCACATAG CAAGACTGTC 120
TCAAAAAAAA AAATGTTATA TATCATGTCA TATCATATGA CATATACTGT AGCTATAATG 180
ATATAATAAT CATAGCTATT ATTCTTAAAA TGGCATTTGA GGCAGGTCTT GAAGGATATG 240
CAGCTTCATT GGCCAAAATT TCCATCACTC CCTGCTTGCT CTCCCCTCTG TCAATCAGTT 300
GCTATCAGGG AGGTCCAGTT TCTGAAACAC AGGAATTGTG TGAGCAGAAG TCGCCACTCA 360
CACCAGCCCT CGGTGTGAGA AGGAGGACAT TTGAGGGCAA GGTAGCTGCA GCCCCCAAGC 420
TGCCCTCCAC ACTGGAAGCC AGTCAAGGCG TGGCCTCCTC AGCTGGAGTT GACATCCAGT 480
TCTTCTCTGG ACCTGCCAAG GGTCAAACTC TGAGGATTTC CTGCCAGGCT GCAGGGAGGG 540
GTTTGGGTGT AGACCTGGTG GACTGGAAAA TTACCCATTT GCCCCCAGAT TAATGATTAA 600
CGGGTCCCTG CCCTCACCCT GTCTGGGAGA GGAGCCCAGG GCCAGGCTAG GCCAACGGGA 660
GCCCGATAGC ATCTGTCTCT GCTCGGAGGT TTCGGAGATA TGCTCCATGA TGGGTTGACT 720
GCACCTGATG GGTGTGGAAT CTACAGGTGA TTTCTGAGGG CACCTGGGGC CTGGCCAGGC 780
CGCATACCCT CTGGTGAGGC TTCCAACTTC TGGGGCATAC AGAGAGGGCA TGGCCTCCAG 840
CCAGATGTCC TGGCTAAGGC AGGTGACTCC AAAGAGGAGA GCTGTGCCCT TGGCTCAGAG 900
GAACATGGGC TTCTCTGACC ACTCCTGGCT TGACCACAGG ACTTACCTTG GCCAGTGGCA 960
CATGAGCAAC AGTGGCAAGT GCCACATCCA AGCAGGAGCT CTAAGAGACA TTGCCTGCTT 1020
CCACCTTTGC TTTTTTTTTT TTTTTTTTTT TTTTGAGATA GGGTCTTGCT CTGTTTCCCA 1080
GGCTGGAGTG CAGTGATGCG ATCTCAGCTC ACTGCAGCCT CCACCTCCCG AGCTCAAGCT 1140
ATCCTTCCAC CTCAGCCTCC CAAGTAGCTG GGACTACAGG TGTGTGCCAC CATGCCCACA 1200
TAATTTTTCT ATTTTTAGTA GAGACAGGGT TTTGCTGTCA CACAGGCTGC TCTCAAACTC 1260
CTGGACTCAA GCGATCCACC TGCTCAGCCT CCCAAAGTGT GGAATTACAG 1310
|
