| Tag | Content |
|---|
EnhancerAtlas ID | HS108-34436 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:33736190-33737340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:33736508-33736527 | TAGCCTGCAGGGGGCGGGG | + | 6.1 | | ZEB1 | MA0103.3 | chr6:33737263-33737274 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33549 | chr6:33736558-33740814 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 33736368 | 33736766 | | chr6 | 33736294 | 33736361 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I033767 | chr6 | 33735706 | 33741053 |
|
Enhancer Sequence | CTGCTTCAAG CTCTCACTCA CAGGGCTGGT GAGAAGTCAT GTTTTAGAGG GCCTTCCTGG 60
CCAGCGTCTT ATACAAATCC TGGAGTTTGT GTGGTTCTGT GCCCGGCCTC TAGACCATCT 120
TCACCACGGC TTCTTCTGTC ATGTGGTGCT GGGGGCTAGG CAGGTCCTCG GGGCTCCCCT 180
GGCTGTTCCA CTCAAGGAAA TGCAAGTAAA CACAGCTGCT CCTGGCCAAT TTGTCTGGCT 240
AGTCTGGGAG ACTTGTCCCA TCTCATACAG TCCAGCCTGG TCCCCTCTGT GGTCAGAACA 300
AGGCTGCCTT CCCAGAGATA GCCTGCAGGG GGCGGGGTGT GTGCTGCAAG GCAGTGGGAG 360
GGCTGGGGCT GTGGCAGATC AGAGTCACTC AGATTGGAAA AAGAAACACG AGTAAACAAA 420
ACCAGCCTGA AAGGAAACTG GAGGAATCCA GACGTTAGAA ACTCAGTGCC AGGTTGGGCA 480
CGGTGGCTCA TGCCTGCAAT TCCAGCACTT GGAGAGGCCA AGGCAGGAGG ATTGCTTGAG 540
CCCTGGAGTT TGAGACCAGC CTGGGCAACG TAGTAAAACC CTGTCTCTAC AAAAAGACAA 600
AATTAATCAA GCATGGTGGC ATGTGCCTGT GGTCCCAGCT ACCCGGGAGG CTGAGGTAGG 660
AGGATTGCTT GAGTGACGGA GGCTGCAGTG AGCTGTGATT GCACCATTGC ACTCCAGCCT 720
GGGCAACAGA GCGAGTCTGT CTCAAAAACA AAACAAAAAA ACCTCATTGC CAGGTTCTTC 780
TCCTTCTGGG ATCGAGGTTT CCATTAATCT ATTTCTTGAA TATTTATTGA GTGCCTCCTG 840
TGGGCCTGGC AGTGTTCTGA TTGCTGGGGA CACAGCAGTG AATGAGCCAG ACAGAGGCTT 900
GTGTAGTAAC TCACCTAGAT ACAGGGATAA AGTGATTTGC CCAAGATCCC AGCCACTGAA 960
GGCCAGAGCT GGTCCTGAGG ATGCTGAGCC CTAGGCCTCC ACCCCCACCC GTGTGCAGCG 1020
TCACTCCTGG GAAAACATGG GGGCGCCAGG TGGCATGGTG CCCACGGGGT CCTCCCACCT 1080
GCCCTCATCC CTTGCCTCTG TGTCCCTGCA CATCATGGGA CCCTCTGTTC AGACTCTCTG 1140
CTTGTGTCTA 1150
|
