| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12973 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:1848860-1849850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr17:1849619-1849629 | GGCACGTGTC | - | 6.02 | | Npas2 | MA0626.1 | chr17:1849619-1849629 | GGCACGTGTC | + | 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 |
| GH17I001945 | chr17 | 1849250 | 1849470 |
|
Enhancer Sequence | TTTCAAACTC CTGGCCTCAA GCAATCCTCC CACCTGGGCC TCCCAAAGTG CTGGGATAAC 60
CGTTGTGAGC CACCACGCCC GGCCGCCCTG CTTCACTTTA CCCCACAGCA TTCCCCCTCT 120
TCTAATACAC TACGTGATTT CCTTATTTTT CTTATTGACT TTCCATCTCT CCGCACTGAG 180
TGTATGTTGA CTCCGTGAGG ACGGTGGTTT TGCCTGCTGT GTTCTCCGCA GTACCCTCAG 240
GGCCCAGAAC ACTGGCATCC AGCAGGTGAC CTGTCACAAT GGCTGGATGA AGGAAGAATC 300
TTTCTGAGTC AGCAGGGGGA CTGAGAGATG CTGCTCAGGA AGCCCTAGGC CCAGGGCCTG 360
GCTCCTAGCA GGCGCTCCAT AAACAGAGGG GCGCTTACCC AAAGCGAGGA GACTCAGAGC 420
CTCCAGGGTG AGAGCAGAGA CTAGGCCCTG GCTCTATCTG GAGGCTTCCT GGTCAATCAC 480
GGGGTGACCA CACGGTGAGG AGAGCTCTGG GAAGGAGGAT CCAGCCCCAG GCCAGCCAGA 540
GGCCCAGGGC AGGGTGACCA GGGCAGGTTT GCCTGGGACA GAGGGGTTTT CCAGGATGTG 600
TGGGACTTTC AGTGCTAAAA CCAGGACAGT CCCAAACAAA CCAACCAACC AGGACAGGTC 660
AGTCATCCAG GTCATTCAGG TCAGGCAAAT CCAAGCCTGT GCCTCCCTCA ACAAAAACCT 720
CTGAATGCAG GAAGGGGAGG GGCACACAGG CAGGCACAAG GCACGTGTCT TCTCAAACAC 780
CATGCGTCCC GCTCAGTCCC TGCAGCCAGG AGGCCGGCCT GGGCCCAGAC TGAGCCTGTG 840
CGTGGTGTGT GTACCTGTGT GTCATGGGCA TGTGTACGTG TGTGCACAGG GTCTGTGTCC 900
ATCTATGTTG AATGTGTGTC TGTGGGTGCA CGGGGTCTGC GTGGATCTAT GTGTGATTGT 960
GTGTCTGTGT GTGCATGGCA AATGTGTGTG 990
|
