| Tag | Content |
|---|
EnhancerAtlas ID | HS076-06975 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr10:43605500-43606650 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr10:43605618-43605629 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr10:43605619-43605629 | GGGGCGGGGC | - | 6.02 | | SP3 | MA0746.2 | chr10:43605617-43605630 | GGGGGGCGGGGCA | - | 6.01 | | ZEB1 | MA0103.3 | chr10:43606475-43606486 | GGGCAGGTGGG | - | 6.14 |
|
| | 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 |
| GH10I043109 | chr10 | 43605361 | 43607108 |
|
Enhancer Sequence | CCACGAGGGA GCCCACCCTT GGACATATCT AAGCTCCCCG ACCACCTCCT TGGCCTTTAA 60
TGGGAGTGGG ATCAGAGACA GAGGGGCGAC AAGACAGAGG GCCCCGGGGG GTCTCATGGG 120
GGGCGGGGCA AGAGCAGGCA TTGCTGAAGT TGGGTCACCT GCCCTCTGTC AGGAGCAACG 180
GGGGCCTGAA TCCCAGTCCA GCCTCAGCCT CACTGTGGTC TCACCTTTCT CCCCAGTTTG 240
TAAAGCTGTG AATTAGGGAC AGGAACCCTG AACAATTTTG AGAGTCACAT GAGCATTTGG 300
AAGTGGGCTT TGTAGGGGAA AGTGAGGAGG CCCAGGAGGC TGGTTTTTGC TGTGGTCACT 360
TGTGGGCCTG GGAGAGCCCA GCCCTGCTCT GGCCCGCCCC CATCTCGCCA TCTGTGGAAC 420
TTTTGGTTTC AAGCAGCTGC AAGAGTTGCC AAGAGGTTGA AAGAATTCAG CTGCCTGACT 480
CCAGGTCCTG GCATCCCCAG GAGAGGCCCC TCTTTCCCAG GGGCTCTGGT CAAAGTCCCA 540
GAGCCTGGCA TCCCCAGGAG AAGAGGCTCC TCTTTCCCAG AGGCTCTGCT CAAAGTCCCA 600
GGGAGGCCCC CTGGTCCTGC ATGGGCTGGG GCAACCATGC TCCCGAGTCT TGTGGCTGGG 660
GTTCAGTGCT CTGACCAGGG GACACCAGGG CAGGGTGGAC CTCTAAACCC TGTGCACTGA 720
GGGAGGAGTG AGGGGTCCCC AGAGCACTGC TGGGGCAGCT GGGAGCAGCC AGGGAGGAGC 780
CTGGGAGACA TTCCGGCGGC TTTGTTGTCT GAGTGAGGGA GGAAAGGGGA GTAAAGGGTT 840
GAGTCAGGGC CTGCCTGGGG CTTTTCCTGC CACCAAACTG AACCTCGAGG CCCTGGGTTG 900
CCTTGACCTC CAGCTCCCAG GAACAGGGGC AGCTGGTAAC ATGTGGCCTG AGTGGAACGG 960
GGCAGGGCAG GGCTGGGGCA GGTGGGTGGG TATGAAGGCT CTGAGGGGTG GAGGACAGGG 1020
TGCTCGGGGG GGCTGCTGTC TCCAGGCCCA GTTGGGGGCT GTTCCAGGAC TTAGGCTGTG 1080
TGGGAATCTC TACCCTCAGG CCATTACAGG CCGGTCCAGC TGCCTGGCTA AGGTGTTCCC 1140
CTGTGCCCCC 1150
|
