| Tag | Content |
|---|
EnhancerAtlas ID | HS051-06298 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:57325140-57326500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr12:57326459-57326472 | TAATTAATTAGCT | + | 6.09 | | Lhx3 | MA0135.1 | chr12:57326456-57326469 | TATTAATTAATTA | - | 6.25 | | POU4F2 | MA0683.1 | chr12:57326450-57326466 | CTGAATTATTAATTAA | + | 6.37 | | POU6F1 | MA0628.1 | chr12:57326457-57326467 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr12:57326457-57326467 | ATTAATTAAT | - | 6.02 |
|
| | 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 |
| GH12I056930 | chr12 | 57324761 | 57327677 |
|
Enhancer Sequence | CTAGAAGGAA ATAATAATAT TTATAAATAA ATATATAAAA TATTTAAATA AAATAATTAT 60
GGAAAATGTG ATGAGGACTA TCCTTGAGAT ATTTCAATTA GGTTGGTACA AATGGAAAGA 120
AATAATGCTA AGTGTTGTCA TTCAACTCTG CAGGGGCCCA GGGTTGAAGA GCTTCAGGTC 180
CAGTCCTGGT TTTACCTCCA GCCTTGAACA AGTCACTTCC CTCTCTGGGC CTCAGGCTCT 240
TCATCAGATT AGACTAAAAC AGTTGTTTCC AGGCTGTATT TTGCAAGCCT TCTAGGGGGA 300
GGAAAATGCA GGAGAAGCTC TCCTTTCATT TGTTTTACAT ATTGGGGTTC TACTGTAAAC 360
CCCTCTAAAC ACTCCTCAAG GACCCCTTCC AGCTCCTTCA TGCAAGGATT CCCCAAGTCC 420
TACTGCCTGG TGATTCGCAC CACAGCCCCA GCCTCAGCAG CCCCAAGATA CTCTGCAGGC 480
GCATCCCACT GTCTCCTGAG GGCAGGTCTC AACACAAACA TAAATCCTAG TCCACCCCTC 540
CCTCTAGGGC TGGGGTCCCC ACCCAAGCCA TGCCCCTACC CAGTCTCCCT GCCTTTCTCC 600
ATTCAGGAGC AATGAGAAAG CATGAAAGAA CTTCCTCTCC CATCCCCCTA CCCACCCCAG 660
TTCCCAGTGT TTCTTAGACC AGGATATTGC CAAGTGGCTT AGGCAAAATA ATGGTCCCCC 720
AAAGATGTCC CCATCCTCAT TATCTCTGGA ACCTGTGAAT CTGCTGGATT ACATGGGAAA 780
GGGGAATTAA GGTTGCAGGT GGAATGGAGG TTGCTAATTA ATTGTCCTTA AAGTTAGGGA 840
GGAAGCTAAC ACGGGAAATT ATCCTGGATT AACCTGGTGA GCCCAATATA ATCACAAGTC 900
CTAAGTGGAA AGAGGCAGAA ACCGGAGAAT CAGAGAGCTT GAGAAAAGTG TGAAAAAGAC 960
TGGGCCCAAC CTTGCGGGCC TTGAAGATGG AGGTAGCAGG CCAGGAGCCA GGGGATGCCA 1020
GCTGCCTCTG GAAGCTGGAA AAGTCGATGA GACGGATTCT CCTCTACAGC CTCTAGAAGG 1080
AACACAGCTC TGCTGACTTT GATTTTAGAT CAGTGAGGCC TATTTTAGAC ATTACTCCTC 1140
CACAACTACA AGATAATATG TTTGTATTGT CTTCAGACCC CACAGTTGTG TTATTTGTTA 1200
CAATAGCAAC AGGAAACTCA CATGCTAAGT GAGGTATTAA GGCAAGTGGC TCAAGGCTGA 1260
ATGTAGGGAA CTGGCTGAGA CAGCCTGCTG AAGACAGAGG CTCACTCTTG CTGAATTATT 1320
AATTAATTAG CTCACTCAAA TCTATTTATT CAGTACCTTA 1360
|
