Tag | Content |
---|
EnhancerAtlas ID | HS026-16698 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr2:1770290-1771680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:1771393-1771403 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:1771393-1771403 | GGCACGTGCC | - | 6.02 | Nr5a2 | MA0505.1 | chr2:1770515-1770530 | GTGTTCAAGGTCAGG | + | 6.83 | ZNF263 | MA0528.1 | chr2:1770875-1770896 | TGAGGAGGGACGGCAGGGAGA | + | 6.26 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 1770800 | 1771620 | chr2 | 1771092 | 1771558 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I001766 | chr2 | 1770361 | 1770550 |
|
Enhancer Sequence | GAGGCCTGGC CAGGGGTCTG TGGGATCCCC AGCCACAAGG CCGCTGAAGA GGTCCTGGAG 60 GAAGCATTCT CCCCAGCCTG CAGAGGGAGC AGGGCACGCC CAAGCCCTAC CTTGGACTGC 120 AGGCTTCTGA ACCCTGTAGT TGAAGGCTGT AGTTTGCAGC TCTTTGTTAC AGCAGCCACA 180 GGGAATGCGC CTCCAGCCTG TCTGGAAGTC AGCTCTTCCC ACAGGGTGTT CAAGGTCAGG 240 TGGGCTGCTC CCAGAGGAGC AGGTGCAGGC AGAGACCACA GGCTGCTGGA GGGAAGGGGA 300 TACCCAGCCT TTGCTGAGGC TCTGTCCCAC TTCTGTTTGT CGTATTTTAG CCATTTGGGG 360 TGCACCTAAC CACTGAGCTT ATTCCTTCTC TAGCTCCCTA CCTCCACCAC CCAGACCGTC 420 CCGCTGTGCA GCAGCCAGGC AGCGCCTCTC TTCGGGGCCT CTCCCCCAGT CCCCCTGCTG 480 AGCTCTGGAC ACTCTGGGAT GGACCCCCCG CTCAGATCAG GCAGGGTCTG GGTCAGGCAG 540 GGGCCAGGGG CTTAGCCCGC AGTGGCCTGA GCCCAGGCAG CTCGCTGAGG AGGGACGGCA 600 GGGAGAGACT TGGGTGTCCA CCCTGCCTCA TGGGCTGCTG ACCCTCCCCA CACTCCATCC 660 TGCCCTTCTG CCCTCCTGCC CTGGCTGCCA CCTTGTCCCC TGGACTGGCT CTCAGAACAG 720 CCGAGCACAT GGGGGATGGC CCAGAGGGGT CCCGGCCCCC GACCAGGTAG GCATCTCTGG 780 GTCAGCTGTG CCCCAGGGGG ATGGGTTGAG TCTCAGACCG GCCAGTGCCC CAGGGACCCC 840 TTTCCTTTCA CTTACAGGAG AGTTCCTCTG TCTCACTGCC TGGGGGAAAA ACCAGCTGAG 900 CCCGTCATGC AGATTTTCTA GGGAGCTGGG CCTGCAGGAG GCCTGGCTTT TGCCCTCTGC 960 TCCTGGGAGG TGACCTCTCG GCCGGCCCTC AGAATGTCTT GACTAATAAG AGCGTCTTTC 1020 TTTACCTGGG GCCGTGGGCC ACCCTGGAGA GCCGATGCTT ACAGTGTGAC TTGTGGTGGG 1080 GCCCAGCCTC AGGCGGACCT GCAGGCACGT GCCGCACCGG ATCCCCAGAG TCCGAGCCCG 1140 CCCCACCCCC CACGCCCTCC GTGGGGCTGG TGCGGCCTCC CAGGTGCTGG TCCCCCAGCA 1200 CTTACCACTA AGCCGCCGCA CCTGCTTCCT TCTTATTCAC CCTGGCCCTC CCTCTGCCTC 1260 TCCACACCAC CAGGCTTGAG TTAACTCACA CCTCCTTCCT CTGTATCGTC TCTGCAGTAT 1320 TTCTCAAATG TACTAAAAAA TCGTAAGAAT GACTTTCTGT GGATGTTTGT TAAAAGCATT 1380 TCCCAAGCCC 1390
|