| Tag | Content |
|---|
EnhancerAtlas ID | HS037-17382 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:7547300-7548520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr19:7547454-7547468 | ATTCCCAGGGGATT | + | 6.12 | | EBF1 | MA0154.3 | chr19:7547454-7547468 | ATTCCCAGGGGATT | - | 6.46 | | KLF16 | MA0741.1 | chr19:7548007-7548018 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr19:7548007-7548017 | GCCCCGCCCC | + | 6.02 | | PLAG1 | MA0163.1 | chr19:7547949-7547963 | CCCCCTTGGGACCC | - | 6.92 | | PLAG1 | MA0163.1 | chr19:7547966-7547980 | CCCCCTTGGGACCC | - | 6.92 | | SP4 | MA0685.1 | chr19:7548004-7548021 | GGAGCCCCGCCCCCTCT | + | 6.07 | | Stat6 | MA0520.1 | chr19:7548262-7548277 | GATTTCCTGAGAAGC | + | 6.69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 7547395 | 7547510 | | chr19 | 7547905 | 7548376 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I007482 | chr19 | 7547253 | 7549438 |
|
Enhancer Sequence | CAGTGCCCCT TGGAGGGAGG CTCTCAACGC AGCTGTGCAG TGCAGTCCTC TGCAGAGCTT 60
CAAAAACCCC ATGCCCAATG CCAGCCGTGA GGATTCTGCC TCACTCAGCC TGGGGCAGGC 120
CCCAGTACCG GGAATTTTCA CAGGGAATTT TCACATTCCC AGGGGATTCC CAGGCCAAGT 180
TGGGAGCCCT GTGTCAGAGC CTTCCTTCCC AAAGGCTTCC AGTTCCTGCA CAGGTGGGGA 240
CCTCTGTTGC CAGACTCTAT GCAGGGAGCA TGAGGTGGCC CGCAGCGAAC CCTGACCAGG 300
CTGAGATGGT GTGCCAACCC TTGGGCCACC GCACGCCCAC TGCTGACCAC GCGCCAGGCA 360
CAGTGCGGCA AGGCTCATGG CCTCCCTCAA CTCCGAGCAA GTTACAGACG GCCACGCTGA 420
GGCTCTCAGG GAAAGCCGCT GGCCCCCAGT TCCGGCAGGG ATGGGCCTCC AGGCCCTCGA 480
ATTGCAATGC ACACGCGGGC TCTCGGTCCT GCACAGTGCC CATACCCTCT GCCCCAAGTT 540
CTTAATCACA CGGCCTAGAG CCAGCGAGGC AGGACCAGTT GAGGCTGTAG AAACCAGCGC 600
TGAAGCCTGG TTTCTGGGAC TGGAGCCCCG CAGCCAACCG GGGGACCCGC CCCCTTGGGA 660
CCCCACCCCC CTTGGGACCC CGCCCACCGT GACCCCGCCC CATCGGAGCC CCGCCCCCTC 720
TACCTTTATC CTCCTTGTTA CCTGCCACAC CCTTCCCCTC CTCTCTGACT TCCCAGGAAG 780
CTCCTCCCCG CCCCCACCGC TGATTCCAGA TGCTGCTCTC CTTCTTTCTG GCCAGTCATG 840
ATCCTACCTC CCTCCGGGCT CTGAACCTCA CTCCAGCTTC CCTCATCTGC CTGGCGCGTC 900
CTGGCACATT GCCCACCTCC CTGAGGATGG CGGACCCCGC CCCAATGTGC TCATTCCGCC 960
CGGATTTCCT GAGAAGCGGC AGGGTCCAGG CTAGACTCTG GGGAGGGGCA GAGGCTCACC 1020
AGGGCAGGGA GGAACGCAGA CATATAAACC GGGAACCCAA CAAACAGGGC TCTTGTTCTG 1080
GCCAAGGGAC ACTCGAGGTG CAAGGGCCTC CACCCCTTGC CTGAGGGCTC TTCCACAGAG 1140
GGCATAGAGG AACGAGGGGT CTCAGGGATG CACCAGAGCG CTGTCCTAAT CAGACACGGA 1200
GGAGGAGGAT GCTATAGGTG 1220
|
