| Tag | Content |
|---|
EnhancerAtlas ID | HS108-28158 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:53032620-53033720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr3:53033574-53033585 | AGCCACACCCT | + | 6.02 | | NR2F1 | MA0017.2 | chr3:53033660-53033673 | CAAAGGTCATGAG | + | 6.3 |
|
| | 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 |
| GH03I052998 | chr3 | 53032572 | 53033970 |
|
Enhancer Sequence | AGCCATGGCT AAGAAAGCGC CAGCGCCCAC CCACCTGGGC CAATGGACTG GTTCTGCTCG 60
TGCCACGCTG GTTCTGCTCC TCGCCATCTC GGCAGTTCAG AAAGAACCCC AACGAGCTTG 120
TGATCTCCCG GGTCCTGTGG GCGTATCAAC AGGGGGCCAG CCCTGTCCCT CAACCCTGGG 180
GAGCTGGTGC TGCCGATCGA CCTGACTGGC CCACAACGTC TTCAGCTACC ACTGCAAGGG 240
CCTGCGGGGT GACGGCTGTG CAGCGCTGCT CGCCTAGCTG TTGATCGCCT GGCTGTTGAT 300
GGGCTGGCAC CCGCAGAGCT GCCCTGCCGG CCACCGACCA CCATGGAGGG AGCATTCAGC 360
TGGTGCGCGA GCTGGGTACT AAACTGGCTC TACTGTGAGC CGCCCTCGGC CCCTCCATCT 420
CCTCTTACCC CTTGTCATCC ATGCGTAAGC CGGGGACGCC CGAGGACATG CTCTTCACCC 480
AAGGCCTGCG CCGGCGTCTG CTGATCAAGG GCCCAGTACA AAGGCCGTCA TGGAGATCCA 540
GGCCTTCGCC AACAGCGGCC TGTTCTGGTG CAAGGGCCAG CCGGGCAGCC CAAGGACCTC 600
ACGACTGGCT GCTGGGTCAA GGCGTTCCCG GGGTGAAGGT GGATAAGCAG ACCACCAAGG 660
GCTCCTGGAA CCCTACGTGA AGGAGGCCAA GCACAGCCGT GGACACCGGC CTGAAGGCTG 720
GGAAAGGAGC CGACGCCCCA CCTCCTCTGA CCAGGCCTGC GGGGAGGAGC CACCCACGCG 780
CCACAGCAAG TCCTGGACCT GGCCCTGCAT TCCAGGGTGG GGCAGGGAGG CTGGATTCTG 840
AGAGAGCTGC TTCCGGATTG CGTTGGGGTA GTCAAGGAGC TCGGGACATC GCAGGGGAGG 900
CAAAAAGCCT TGGCCAGTGC TCTTTTGGTG TATCCCTTCA GCTTCCAGAG GGGAAGCCAC 960
ACCCTGATGC TATGTTCAAA CGCTCCAGAA GACAGGAGTT CGTGTCCTTG CCCCTAACCA 1020
CTGCTGTGGA TGTCACTGGC CAAAGGTCAT GAGGGGAGTG GGCCACATGA GTGGCCACTT 1080
GCCATGACTC CCTGAGCAGG 1100
|
