| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04515 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:100203820-100205050 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr10:100204747-100204758 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr10:100204748-100204758 | TCAAGGTCAT | + | 6.02 | | Nr5a2 | MA0505.1 | chr10:100204744-100204759 | CAGGTCAAGGTCATG | + | 6.08 | | SCRT1 | MA0743.1 | chr10:100204567-100204582 | GTGCAACAGGTGTGA | + | 6.84 | | SCRT2 | MA0744.1 | chr10:100204567-100204580 | GTGCAACAGGTGT | + | 6.92 |
|
| | 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 |
| GH10I098445 | chr10 | 100204332 | 100204350 |
|
Enhancer Sequence | AAACAAAAAA CAGCTCCAGA AGATGAGCCT CAAAGCCCCT GAATTTACTT CAGCACCACA 60
GAAGTTTCAT TCAAATGCTG CTCTCCCTGT TCATGGTGAG AACAGAGGCT GCCTAAAGCC 120
CCTGTACCTA GTAGGCTGCA GCTTCTAGGG CCACAGCCAC CAGTGTCTTC AGCCCTCCCA 180
AATCTCCTTC CCCACCCCCC CGCCACACAC ACACACACCA CACACTCTGT GCTTGATTAT 240
GTAAGAAATG TCTTAACTAT TCACCCACTG GAAGATCTTT AATACAGCTT CCCACACTGT 300
GTGCCATGGC CCTCTGCGTG CGGCAAACCC TCGATCTTCT AAAACTTGGG GCAGCCTGAC 360
CAGGCTGGTG AGGACAGTGC TCCAGGCTGG CTGCTGCAGC TAAGAGGCCT CAGGCAGTGG 420
TTTCAAATCC TCTTATGTGC CTCAGGGTGT CACGCAGATA TAATCATGTG GTATGTGCGC 480
TAAGCCATGA CAATGATTAG GAAGCTCTGC TGTAACTCTC ACACAAGTGG ATTTCCAGTT 540
TTCTTGGGAG GATCACAGCA TCTCCAGGTC TTGTGTTCCG TCATCCCCAT GTCCAGCTTA 600
GTGGTCCTTA CTGAATTCCT CCCAAACTAA CTTGGTGCAA CTGGTCCCAA GGTATTTATG 660
GCAAATGCCA GGAGACATAA CAGCACAGTG AAGAAGGAAT GCAGCCTATT CCCACAGAAT 720
TACTCAATGC CAAGGCAGAC ACTGAGAGTG CAACAGGTGT GAAAAGGAGG TTGCTGGGAG 780
AGGCGGGTGG ACCTGAAGAG GCTGCTCTGG GACTCCCAGG TACATGTGAC AAAGCTGACC 840
AGAGTGTATG GGTTAGGGAG CAGTGGGCTA TGGAATGGAG GCTGTGGTTG TGAGCGGAGA 900
AGTGACCGGC TGGCTGGAGA TGGGCAGGTC AAGGTCATGA AGGCGGTCAT CTAGGTGCGG 960
GTGTCAGGTA ATGAGTGCTC ACCCCTTGGT GGGGGCTGGG AGGAGCTTTA AAGATGCAGC 1020
AGGCTGTGAT GACCTGCCTG GATTCGAGGG GTGAAGGAGA GATGAGGCAT CAGGATGGGG 1080
GTGGCCTCAG GATGCAGGGC TGGGGAGGGG ATGAGCAGGT GTGCAGAGCC CAGTAGCACT 1140
CAGTCCACTG CCTACCTCAT TCCATCTGCC TCCCAAAGCC CCAGGGTGGA TGCTGCCTGC 1200
CTCCCTGTCC TCCCCAGGTG GGGCAAGATC 1230
|
