| Tag | Content |
|---|
EnhancerAtlas ID | HS105-27168 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr15:52580250-52581390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr15:52580658-52580669 | CCACACCCTGC | + | 6.62 | | ZNF143 | MA0088.2 | chr15:52580802-52580818 | TACCCACAAAGCAATG | + | 6.31 | | ZNF263 | MA0528.1 | chr15:52581320-52581341 | CTCTCTTCCTCCTCCTCTTCA | - | 6.3 | | ZNF263 | MA0528.1 | chr15:52581323-52581344 | TCTTCCTCCTCCTCTTCATTC | - | 7.01 | | ZNF263 | MA0528.1 | chr15:52581317-52581338 | CCCCTCTCTTCCTCCTCCTCT | - | 8.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 52580530 | 52580869 | | chr15 | 52581140 | 52581245 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I052286 | chr15 | 52579180 | 52582470 |
|
Enhancer Sequence | AGCTGAGAGC CCTGGGGGCC TTCCAAGGAA GCCTGGGCTC TGAGAAGTAA TGTGAAAGTC 60
ACTAGGCCAA TCAATCCTTT TGTTTAACAG AGCCCCTAAC TGAAGCCCAG AGAGAAATAA 120
CTCACCAAAC AGCAGACAGA GTCTCAAAGG ACCAGGACTC CAGCAGAGCT AGGGCCTGTG 180
ACTCCTAGTT TGAACTCCGT ATTAGTTAAG CGAATCTGGC CCTGAAAGTA ATCCTGAACT 240
CTGAACTGCA ACCATCTACT TGAGAGTCCA TGTGCTCTCC TAACTATAAT TTAGGATTGG 300
TTTCAGCTAA AAGTGGTATT AAATGGCAGG CAGTATTAGG ACATACGTAA CCACTGACGG 360
CTTCTCTTCT GAAGACCAGT GACTCCTCAG CCCAGTACCC CAGGCCGCCC ACACCCTGCG 420
ATCCTGGTGC TTCTGCTGGC ATTGAGTGCC CTGCAGCTGA AACCCAGCCT GGTAAGTAAA 480
CAACGGTGAG TTTACTCAGC TCCGGGTAAG TTCCACCCAT TCATTCCTGT CCCCTCCTCC 540
CTCACATTCC TCTACCCACA AAGCAATGCT TCAAACTGGA GGAAGAGTTA ACTTTACAGC 600
ATTCATCCAA ACAGATGCAG TCCGCAGTTC ATGCAAACAA TGTAACCAGC TGTCAACTGA 660
CCTCCAGAAT ATGGGGCCTT CCCATGAGGC AGGAGTCTGT GGACTGGGAT GGAACAGCTC 720
GCCAAGCCCT TCAGCGGAGC CAGGAAAGAG AGGGCCACCT CCCAACTTCC CTGAGTGCCC 780
TCCCCATGCC AAGGCGCCAA GCTGAGGCAG AGGCTCGGGA CCACTGAACC TTATGAGCTC 840
AAGACCATGC CAGCCACCCC CCCAAGGCAC ACAGGTGAGA TGAGAACAGC ATCTTCTCAC 900
GCCGCCTGCT TTTCTGAGGG ATCTTCTGGC ATGAGCCACA GAAATGACTT GAAGACTTAT 960
ATGGAAGATG GGACAAGATG GGACGACATG TGTTTCCCTC CTAGAACCGC TTTCTGGACT 1020
GGGAGTGTCC ACACTCCAGG TCAGCCAGGC CAGATTGTCA CACCATGCCC CTCTCTTCCT 1080
CCTCCTCTTC ATTCGCTCCT CATGGGCCCC TCCCCTGGCT CCCCTGCCCC TCCCACTGCC 1140
|
