| Tag | Content |
|---|
EnhancerAtlas ID | HS043-11280 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr12:122310340-122311360 |
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 | TGGCCAGTCT AGTCTTGAAC TACTGACCTC AAGTGATCCA CCTGCCTCAG CCTCCCAAAG 60
CATTGGGATT GCAGGCATGA GCCACCGTGC CTGGCCTAAA ATTTCTTGTC TCTCCAGCAT 120
CCACTCCTGT TCTCATAACA GCGTCTCCCT TCTCCATCCT TTCCCTGCTC CGTTCATGTC 180
GTTTGGGTGG GGCATGTGAG CCAGGACTGG GCAGTGAGAA TCCCTGTGAT TGGTTCAGGG 240
CTGGGCACCT GGCCAGAACT GGCCATATGG ATTTGCTCTG GATCTTCTGC TTGAGAAAAG 300
AGGCTCACTC TGAGCTCTGA GTATGCTGCA CTGATCCAGT GGTGCTGCGG GGGCCAACCC 360
TGAGTCAGCT GAAGGAAAAC ATGCTTGTAT ATAAAGCCAG AACAGAGAAA CCAGAGCTGA 420
GAGAAGATAG GCTGATTCCT GATGTCTGAG CAACTTGTTC CAGGCAGAAA CAAGCTCCTG 480
GATGAGTCAA ACCTTTTTCC CTTTTGCTTA AGCTAGTTTG AGTTGGGTTT CTGGCATTTA 540
CAACCACTGG TGCTGACAAA CACAAAGAAA GAAACAATAA CACCACCACC ATCTGTGAGC 600
ATGTATTCAC TGTCAAGCAC CGAGGTAGGG ATCATGGGGA TTGTCTGTTC CACAGGGAGG 660
TAGTACTTGA TCATTTTGTT TGCATTTGCT GGCACACATA AAATAAAGTT GACTGATTTT 720
AGCAGTTTTT ATTATTATTT TAAAACTCTC TGCAGACATT GCATCCCTGT GGTAGATTCT 780
ACTGTCCATA ACCCTTCAAG GAAGGCCTCA ATGCCCAGCT GTAGGGAGAC TGGTTGGCTG 840
TCACCTCCTA TCGGATCTGC CTCAGCTGTA GAGACTTGGC CACAGCTTTC CCAGAGCAGC 900
CCACTTTTTG TGATTGAGCA AGGGAGTAGA GAGGCTGGTC CCTTTCAGCC CAATGGGGGT 960
GACTCTGACC AGTGAGTCTG TCTCCAGGGC CCCGGTAGGG CTGGCCAAGG CCTTGTGGAG 1020
|
