| Tag | Content |
|---|
EnhancerAtlas ID | HS098-37846 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:16907710-16908820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr3:16908736-16908747 | TTATGTAACCT | + | 6.14 |
|
| | 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 |
| GH03I016866 | chr3 | 16908261 | 16908430 |
|
Enhancer Sequence | CAGTTCTTTA TCCAAGAACA CTCCTAATAA ACCTCCTACA CATTAATCTC CATCTCAGAG 60
TCAGTTTCCT GGGGAATCAT TCTCAGAGAA TGACTGTGTG AATGAGAATT CGTTCAATTT 120
TTGACAGAAT TTCGTAAAAC ACAAAATGAG GGATCTTTGG CTATCAACAG CTTTGATACA 180
TATTTCTTCA TTCAACTTCT TCACAGTGGA CATTTCCATT TTATTCGAGT TTGATGTGAA 240
TAAAACCCTT TTCATGATGT GGTACTGACA ACCCCCCCAC CTCCCCACCT CCAGTGTTCT 300
TATGTTTTTC AAAATGCTGA ATACTGTTTG ATGTAAGATT CAAGGCTAAA CTTTCAGAGT 360
ATGTGATGAT TTGGGGCTTG ATTTACTGCT CTTTGGCCTT GGTTTGTTTC CGTTTGATTT 420
TGGAGGATCA TTAATCTTCC AGGGAAAGCC TCCAGGGGTG GATGGTGCCC TGGCCATTCA 480
TTGATGTAAG CAGAATTATT CAGATGCTCA TGTGTCTTCC CCTCTTCTGA CAATCTTTAT 540
CCTGTCTCCA AATGTGGCAA TATTTAGAAG GAGAAAAATA ACACTAGAGG GCAAAGGCAT 600
AATTGTTTGA GGTTTACCAC AAGGATGTAA CTGGGGCTAC CGCTGGTTTG TTAGTGAGAT 660
GACAAAGGGC ACTGAGCTCT GGCTCACTGG CAGCTGTTGA TCCAAGGCTG GAGAGAGTCA 720
CTTCACAGTG CACTGGAATT GCTTATCATC CAGGGAATCC CTTACAGCCC ATGGACCCAC 780
CAGTCTGCTG ATATGCCGGC TCTAGAAACT TATAGGTGCC TCTGCCCTCT CCAGGTTTCT 840
CCCCTGTGGA TGCTCTTACA CCTCGGCATG ACCTCAGATC TGGAGTCACA CTGGGAATCT 900
GAACCAGATT AGTGGGACCC TATACACTAA GTTGTGGGGA ACAGCATAGC ACGATGGTGA 960
AGTGGTCATG CACTAAAGCC TTGCTCCAGT CTTGGCTCTG CTCCTAATTG TGTGATCTTA 1020
GACAAGTTAT GTAACCTCTC TGTGCCTCAA TTTTCTCGTC TGCAAAATGA AGATGATAAC 1080
AGTGTCTAAT TTACAAGGTT GTTGTCAGGA 1110
|
