| Tag | Content |
|---|
EnhancerAtlas ID | HS105-02177 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:38029080-38030620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:38029310-38029325 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr1:38029833-38029853 | CCCACCCCCACCCCCCAACA | + | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTTGGCATTT TTAAATTTTT TTTCTTTTGA GACGGAGTTT TGCTCTTGTT GCCCAGGCTG 60
GAGTGCAATG GCACCATCTC AACTCATTGC AACCTCTACC TCCCGGGTTG AAGTGATTCT 120
CTTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGCATGT GCCAGCACGC CCGGCAAATT 180
TCTGTATTTT GAATAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCA TGAACTCCTG 240
ACCTCACATG ATCTGCCCAC CTTGGCCTCC CAAAGTGCTG GAATTACAGG CTTGTAATAC 300
AGGAAGTGAG CTATTTTTAT TGGCTCAAAA CTGCATTGCA AATAAAGCAG CTTTGCTGTC 360
CCCAGGATAG ACCTACCTAA AGATCTGTCC AGTATTATTT TATTGGCTAC CAGAGGAACA 420
TAGTAAATAA CTCCCAAGTG TCTTAAGCTT TACATAAAGA GGGACAGCTC TCGGCTGGGT 480
GTGGTAGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCAGGTG GATCACATGA 540
GGTCAGGAGT TTGAGACCAG CCTGGCCAAC GTGGTGAAAC CCATTTCTAC TAAAAATACA 600
AAAAGTAGCT GGGCGTGGTG ATGTGCATCT GTAATCCAAG CTACTCAGGA GGCTGAGGCA 660
GGAGAATCAC TTGAACCCGG GAGGTAGAGG TTGCAGTGAA CCGATATCAC ACCATCACAC 720
TCCAGCCTGG GTGACAAGAG CAAAACTCCA TTCCCCACCC CCACCCCCCA ACAAAGAGGG 780
ACAGCTCTGT ATTCACTGGC AGCATTTCTC TAATTGTGTG CCAAGTTGTC TCAGTGGCTG 840
AAAATTCACT GTTTCCCAAA CCTCTGGTCC CAGCAGAACT CCCAGGATCC TAAACCAGAG 900
AGCCAATATT TTTTTTTTTT TGAGACGGAG TCTCCCTCTG TCACCCAGGC TGGAGTGCAG 960
TGGCACGATC TTGGCTCACT GCAAGCCCCG CCTCCCAGGT TCATGCTATT CTCCTGCCTC 1020
AGCCTCTGGA GTAGCTGGGA CTACAGACGC CTGCCACCAC GCCCAACTAA TTTTTGTATT 1080
TTTAGTAGAG ACGGGGTTTC ACCGTGTTAT CCAGGATGGT CTGGATCTCC TGACCTCACG 1140
ATCCGCCCGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG AATGAGCCAC TGCGCCCGGC 1200
CAGAGAGCCA AATGTTTAAC TTAGCAGACA TATTCTGGCC TGAAACCTGA GCCATGAAAA 1260
GCCCTTACAA CAATGCATTC AATATCCTTT TCAATGCTTT ATATCATACC CGGAGCCATT 1320
ATTGTGTTGA AACCAGGACA GCTCTGGCTT CTCCTCATAT ACTAAAGACT GTATGCCAAG 1380
CTAGAAACTA GCTAATCTAG AAAATATGGA TTTGGGGATC AAGGGGAAAA AGAACCCTTG 1440
GAGTGACAGC ATGTGGATTC TTCTTCCCAG AGATTTGATC ACCTCTCAGC TATTTGTATC 1500
AGGCTGCAAG TTTCAAGTAT TAATGGAGCT TGTTTTTGTT 1540
|
