| Tag | Content |
|---|
EnhancerAtlas ID | HS108-28225 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:58456430-58457650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:58456472-58456483 | GCAGGGTGTGG | - | 6.62 | | STAT3 | MA0144.2 | chr3:58457157-58457168 | CTTCTGGGAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09926 | chr3:58455183-58462116 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 58457172 | 58457525 | | chr3 | 58456668 | 58457496 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I058469 | chr3 | 58455661 | 58459042 |
|
Enhancer Sequence | ATTCTGATCT CCCACAGACG TTGCAGGTGG AGTGTCCTGA TGGCAGGGTG TGGATCACAT 60
CTCTGCTCTC AGGAGGTGGG GAGAGGGGAT CTGGGGCCTC CTCGACTTCC ATAGGGGAGG 120
TTGGGCCTGC ACTGTCCACC ATGACCCATA CAACCACAGA CAGAAGTTCC TTGGTAGTAA 180
CCAGCATGTG TTCATTACAG TGAATGAAAA GACCAGAGCA GGTAGCATGG ATCTCAGCCG 240
CAGCTCATGG ACCACCCAGC GCTGGGAATT GCAGAGGTTC CCTAACCTTT CCTAAGCCTG 300
AGTTTACTCA TGCAGAAAAT GCCAGGGTGG ACTTGGAGGG TAGCTACAGG CCCTGTGAGC 360
ACTAAGATTT CCTGAGACTT CGCTGCTGTC CATGCCCCTC CCCTGTTTTG ACCTTTCCAA 420
CAGACTGGAG GCTAGAATGA AGATAAGGAG TACCATTTTT TTGTTAGGCA CTGGGAGACG 480
GCCCAGACTT TGATATAGCA AAGGTTAATG TTCTGTCATC TCAAAGATCC ATTTCCCCAG 540
GCTGTCGGAA TGTAAATGTT AAGGTGATGA AAATAGTGAA GCCTAGGTTC CGGCTCATTT 600
GAGTCAGAGC CCCTCACCCC TCACAGTGCA ACCCTGGTGC ACAGGGCCTC CTCTGTGGCC 660
TGAACCTTCA TAAACTTGGG TTTAGGTTGT CAGCACTGAT TTAAAGAGAT TTGCTTTGTT 720
CAGTTTGCTT CTGGGAAAGA ACTGACATTC ACAGCAGGGT TTGGGGGTTA AGAATGAAAC 780
CTGAGCTGGC TTCTTCCCCA CTGGGTGTGT GCAGAGTGAG TCAGATGTTT GCACAGAAGG 840
CTGTGGTGTC AAATCAAATC CACAAATTTG CAGGCCTTAT GCCTTTACCA CTTCAAACCG 900
GAAAGGTGTT GCAACATAAC AGTTTTAATT GCTAAACCCT AGCTGCAAAC CCAAATCTCT 960
GGATTTAATA AGAATTGGGT GTGAAAGACT GTGAACAGTG GCAGTTTTCT GCCAGGTGAG 1020
TTTATTTGTT CCTTCATTCC CTCATTTGCT TCCTCGTTGG TGCCCAAGCC CACACCAAAG 1080
GCCTCTGGCC AGTCACTGCC TGCGCGCCCT CCTCCTGATG ATGGACCTGT GGTCTCGCCT 1140
GTAGGTTTAC CTTCTTTCCT GCTCTTGGTT GAGATTTGCG GACCTTTGTA TCCACTGTGG 1200
TCTCCTTGGA ACAAGCAACT 1220
|
