| Tag | Content |
|---|
EnhancerAtlas ID | HS106-01226 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr2:71921160-71922700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:71922525-71922536 | CCACACCCTGT | + | 6.14 | | ZNF263 | MA0528.1 | chr2:71922414-71922435 | GAGGGAGGAGGACAGGGAAGG | + | 6.55 | | ZNF263 | MA0528.1 | chr2:71922417-71922438 | GGAGGAGGACAGGGAAGGAGC | + | 6.75 |
|
| | 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 |
| GH02I071694 | chr2 | 71921461 | 71922603 |
|
Enhancer Sequence | CCAGTCAGAT CATGGGGCAG CAGCAAGGTG CCATCCAAGA TGTGGAGCTA ATGGAAGCAG 60
AGCTGCCTTC TGGGAGCTGA ACTAGGAAGG GACTGCGTGC GGGCTCAGAG CATAGACTGG 120
CAAAGGCTTG CCGAGGAGGC CACTGGTCCC AGGTCCTGGC AACTCTTAAT GGCCCATGCA 180
TTCACCCACC CAGGGAGAAA AACGTGAGTC TCAGACACCC ACCTTGACAA TGTCCAGGGA 240
AGAGAGGCTT GGCTTGTGAC TCCAGGGCAA GACTTTCTAT CCCCCATGGC TATTGGGGTG 300
TGGCCATGAT ATGTCCCTTG CCCTCCACAT TCCCAGGCAG CCTTCTGATG GTGCTGTGGC 360
TCCCGGTACA GGCCTGTTTG CAGGCGGTGC ATGTGTAAAT TATGCTGATG CAAGCTGTGT 420
TTCCCACTGT GCATTCACAT GGGGGCATTT TGGCTTCTAT GCCCCTCTCT GAGCTCTGCT 480
AAGGAGAGTC TGCCCCTTTG GGGACACACT CTGGACCCAC CTTCCTCAGA CCCACACAGT 540
CAGGGGTCTT AGCCTGCAAG CATGCCTAGG CTAGGAGCCC TCCTAGGTCG AGAATGTCCC 600
TGGAGAGGCC TGCCGGGGGA GACATGACCA GCCTCTCCTT GGAGACGCCC ATCTCATGGG 660
ATCGGGGAGG TTGGGCATTC ATGTCCACCC AGGCTAGGAA TGAGGTGCAT CTCCTGTCAG 720
ACCTAGGAGC AGTCCTCTGT GACATAGCTG CCTCCTCCTC TTCTTCCAGA GGGGAGGGCC 780
GCGATGGGGA GTCAGTTACT TTAAGGGAAT CCCTTACGGT CTTTGAATTG GGCTTGATTG 840
CATAAGAATG CCCAGAGGAG GCCAGGTGGA AGCCAGTTTT GAAAGAGGAG AGACGAATTG 900
GAGGAGATTC GATTTGCTGT TGTTTCTCAG GTGGTGGTGA GGTGGTGTGA GTGGTCAGTC 960
GGGGTGTCTG AGGCTGGGAG GAAGGAGAGT GATGGAGAAA TTTGGTCCTG GTAGGGGAGC 1020
CGAGGCCCCC AGGGGAAAGC CCCCACAGGA AGCGGTCCCT TGGAGAGAAG TCCAGGGCCT 1080
GGAGGAGCAG GCCTCAGACT GGAAGCGGGG GCTCTGCCGC TCCCTGGGGT CCTCTGGGGC 1140
CTCCTTAAGT AACCTAGGCC TGGCCAAGGA GAGCTGGGTT TTCACAGTAA GACTCAGGCT 1200
GCCAGAAGAA TGAAAAGAAT GGGCCTGAGG GAGCACCTCC GCCATGGATG GGAGGAGGGA 1260
GGAGGACAGG GAAGGAGCAG AGGCCCGTGT GTGTTGTGGG CAGCCGCACC AGCCCTGGGT 1320
CAGCATCCAG TCTGCCTTCC CTGGGGTCTC TGCATGGCAG AGGCTCCACA CCCTGTATAG 1380
TCAGGCTGCT TCAGGTGCCT GGGACTCACA TCCCACCAGG CCAGGCTCCC GGGCCCTCAC 1440
CCAGGACGAG CCCTCCTCTC CACCCCTTTC CTTTTCCCTC CTATCTGCAC CAGGTAAGGG 1500
AGCTTTGGAG AGGAGGGAGG AGCAGGAGCA GGGTGCTCCC 1540
|
