| Tag | Content |
|---|
EnhancerAtlas ID | HS058-03752 |
Organism | Homo sapiens |
Tissue/cell | GM10847 |
Coordinate | chr19:4351250-4351870 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:4351537-4351554 | GAGGTCATTGTGCCCTT | - | 6.28 | | ESR2 | MA0258.2 | chr19:4351538-4351553 | AGGTCATTGTGCCCT | - | 6.07 | | GATA2 | MA0036.3 | chr19:4351556-4351567 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr19:4351556-4351567 | ACAGATAAGAA | - | 6.62 | | NKX2-5 | MA0063.2 | chr19:4351331-4351341 | CTCAAGTGGT | - | 6.02 | | PPARG | MA0066.1 | chr19:4351379-4351399 | GTGGGCCACTGTGCCCGACT | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCACCATGCC TGGCTAATTT TTGTATTTTT AGTAGAGATG GGGTTTCACC ATGTTGGCCA 60
GGCTGGTCTC GAACTCCTGA CCTCAAGTGG TCCACCGCCT CAGCCTCCCA AAGTGCTGGG 120
ATTGCAGGCG TGGGCCACTG TGCCCGACTG GGAGGAAAGG TTACTGAAAG ACGTGAAAGC 180
CACCTATGTA TGGTGCTGGC TCGCTCAATG AACGGAGCAT CTAGGTGTAT GCTAAATGCT 240
TTGTGCGTAT GATTTCATTT CACCCTGATG CCATCCCCGT GGAGTTGGAG GTCATTGTGC 300
CCTTTTACAG ATAAGAATAG ACTTGGCGGC CGGGCACGGT GGCTCACGCC TTTAATCCCA 360
GCACTTTGGG TGGCCGAGAT GGGCAAATCA CAAGGTCAGA CGATCGAGAC CATCCTGGCT 420
AACACGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAT TAGCTGGGCG TGGTGGCACA 480
TGCCTATAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAAA ATCACTTGAA CCCGGGAGGT 540
GGAGGTTGTA GTGAGCCGAG ATCATGCCAC TGCACTCCAG CCTCGGCGAC AGAGTGAGAC 600
TCTGTCTCAA AAAAAAAAAA 620
|
