| Tag | Content |
|---|
EnhancerAtlas ID | HS024-03960 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr12:122310090-122311480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:122310355-122310370 | TGAACTACTGACCTC | - | 6.07 | | RARA | MA0729.1 | chr12:122310352-122310370 | TCTTGAACTACTGACCTC | - | 6.1 | | ZNF263 | MA0528.1 | chr12:122310490-122310511 | TCTCCATCCTTTCCCTGCTCC | - | 6.81 |
|
| | 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 |
| GH12I121871 | chr12 | 122309456 | 122312164 |
|
Enhancer Sequence | GCCAAGATCA CGCCACTACA CTCCAGCCTG GGCGACAGAG CGAGACTCCT CTCAAAAAAA 60
AAAAAGAGAT GGAGTCTTGC TCTGTCGCCC AGGCTGGAGT GCAATGGTGC ACTCCCACTG 120
CAACCTCCGC CTCCCAGCTT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC 180
TAACAGGAGC CCGCCACCAG GACCAGTTAG TTTCTTTTGT ATTTTTAGTA GAGACGGGGT 240
TTCACCATGT TGGCCAGTCT AGTCTTGAAC TACTGACCTC AAGTGATCCA CCTGCCTCAG 300
CCTCCCAAAG CATTGGGATT GCAGGCATGA GCCACCGTGC CTGGCCTAAA ATTTCTTGTC 360
TCTCCAGCAT CCACTCCTGT TCTCATAACA GCGTCTCCCT TCTCCATCCT TTCCCTGCTC 420
CGTTCATGTC GTTTGGGTGG GGCATGTGAG CCAGGACTGG GCAGTGAGAA TCCCTGTGAT 480
TGGTTCAGGG CTGGGCACCT GGCCAGAACT GGCCATATGG ATTTGCTCTG GATCTTCTGC 540
TTGAGAAAAG AGGCTCACTC TGAGCTCTGA GTATGCTGCA CTGATCCAGT GGTGCTGCGG 600
GGGCCAACCC TGAGTCAGCT GAAGGAAAAC ATGCTTGTAT ATAAAGCCAG AACAGAGAAA 660
CCAGAGCTGA GAGAAGATAG GCTGATTCCT GATGTCTGAG CAACTTGTTC CAGGCAGAAA 720
CAAGCTCCTG GATGAGTCAA ACCTTTTTCC CTTTTGCTTA AGCTAGTTTG AGTTGGGTTT 780
CTGGCATTTA CAACCACTGG TGCTGACAAA CACAAAGAAA GAAACAATAA CACCACCACC 840
ATCTGTGAGC ATGTATTCAC TGTCAAGCAC CGAGGTAGGG ATCATGGGGA TTGTCTGTTC 900
CACAGGGAGG TAGTACTTGA TCATTTTGTT TGCATTTGCT GGCACACATA AAATAAAGTT 960
GACTGATTTT AGCAGTTTTT ATTATTATTT TAAAACTCTC TGCAGACATT GCATCCCTGT 1020
GGTAGATTCT ACTGTCCATA ACCCTTCAAG GAAGGCCTCA ATGCCCAGCT GTAGGGAGAC 1080
TGGTTGGCTG TCACCTCCTA TCGGATCTGC CTCAGCTGTA GAGACTTGGC CACAGCTTTC 1140
CCAGAGCAGC CCACTTTTTG TGATTGAGCA AGGGAGTAGA GAGGCTGGTC CCTTTCAGCC 1200
CAATGGGGGT GACTCTGACC AGTGAGTCTG TCTCCAGGGC CCCGGTAGGG CTGGCCAAGG 1260
CCTTGTGGAG TCTCCACCAC TGAGTTCTCC TTCTCCCCAG TCCAGCCTCC TCTGCTTCCT 1320
TTCACTGATG TGGATCCTTA AAATCATTTT ATGGCCGGGC GCGGTGGCTC ACGCCTGTAA 1380
TCCCAGCACT 1390
|
