| Tag | Content |
|---|
EnhancerAtlas ID | HS105-20918 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:122310250-122311560 |
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 | GCCTCCTGAG TAGCTGGGAC TAACAGGAGC CCGCCACCAG GACCAGTTAG TTTCTTTTGT 60
ATTTTTAGTA GAGACGGGGT TTCACCATGT TGGCCAGTCT AGTCTTGAAC TACTGACCTC 120
AAGTGATCCA CCTGCCTCAG CCTCCCAAAG CATTGGGATT GCAGGCATGA GCCACCGTGC 180
CTGGCCTAAA ATTTCTTGTC TCTCCAGCAT CCACTCCTGT TCTCATAACA GCGTCTCCCT 240
TCTCCATCCT TTCCCTGCTC CGTTCATGTC GTTTGGGTGG GGCATGTGAG CCAGGACTGG 300
GCAGTGAGAA TCCCTGTGAT TGGTTCAGGG CTGGGCACCT GGCCAGAACT GGCCATATGG 360
ATTTGCTCTG GATCTTCTGC TTGAGAAAAG AGGCTCACTC TGAGCTCTGA GTATGCTGCA 420
CTGATCCAGT GGTGCTGCGG GGGCCAACCC TGAGTCAGCT GAAGGAAAAC ATGCTTGTAT 480
ATAAAGCCAG AACAGAGAAA CCAGAGCTGA GAGAAGATAG GCTGATTCCT GATGTCTGAG 540
CAACTTGTTC CAGGCAGAAA CAAGCTCCTG GATGAGTCAA ACCTTTTTCC CTTTTGCTTA 600
AGCTAGTTTG AGTTGGGTTT CTGGCATTTA CAACCACTGG TGCTGACAAA CACAAAGAAA 660
GAAACAATAA CACCACCACC ATCTGTGAGC ATGTATTCAC TGTCAAGCAC CGAGGTAGGG 720
ATCATGGGGA TTGTCTGTTC CACAGGGAGG TAGTACTTGA TCATTTTGTT TGCATTTGCT 780
GGCACACATA AAATAAAGTT GACTGATTTT AGCAGTTTTT ATTATTATTT TAAAACTCTC 840
TGCAGACATT GCATCCCTGT GGTAGATTCT ACTGTCCATA ACCCTTCAAG GAAGGCCTCA 900
ATGCCCAGCT GTAGGGAGAC TGGTTGGCTG TCACCTCCTA TCGGATCTGC CTCAGCTGTA 960
GAGACTTGGC CACAGCTTTC CCAGAGCAGC CCACTTTTTG TGATTGAGCA AGGGAGTAGA 1020
GAGGCTGGTC CCTTTCAGCC CAATGGGGGT GACTCTGACC AGTGAGTCTG TCTCCAGGGC 1080
CCCGGTAGGG CTGGCCAAGG CCTTGTGGAG TCTCCACCAC TGAGTTCTCC TTCTCCCCAG 1140
TCCAGCCTCC TCTGCTTCCT TTCACTGATG TGGATCCTTA AAATCATTTT ATGGCCGGGC 1200
GCGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAAGCT GAGGCGGGCG GATCACAAGG 1260
TCAGGAGATC GAGACCATCC TGGATAACAC CATGAAACCC CATCTCTACT 1310
|
