| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41649 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:131964640-131966150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr9:131965441-131965451 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr9:131965438-131965455 | TAAGGGGCGGGGCTGGG | - | 6.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53874 | chr9:131964865-131965891 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 131964929 | 131965182 | | chr9 | 131965304 | 131965800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129202 | chr9 | 131964601 | 131966079 |
|
Enhancer Sequence | TCTGGGCCAA TTTCCTCATC GGTATAATGA AGGGGTTGGC AGGGCTAGTT CTGAATTTTC 60
CCAACCCACC CATAAAATTC ACCCTTCAAA TTCTAAAGAT TCCATTCCGT GGTCTAACTC 120
TGTGTGTCTG TCCTTGGTTC CAAAAGTCCC CGTCCTTGTG GCCCCTGTTG TTTTGGACCC 180
ATCACAGGTA ATTATGTATT TGTGTGATTA AACATCCCTG GCCTGTCTCC CTGCCTGGGC 240
TGTGTGCTCA GCAAAGAACC ATGCCTGTCT CTGTCTTTGT CCTTTAAGAG ATCAGCACAG 300
GGCCTAGCGC ATAGTAGGTG CTCACTAAAT ACTGTAGCAG CTGGTATTGT TGGGAAATGA 360
TGCTGGGAGA GGCTGCTGCT GGAGAGAAGG GAGCCACCGA CCGCCCTGCA GGCAGTCAGC 420
GCCCTCAGTC CCTTCCTCCT CGCGGGCCGC AGAGGCTCCC CTTTCCCCGA GACGATAAGA 480
ATGCCCAGAC GCCCCAAAAC CCAGGCCGCG CCCCTCCGGG TAGAACTACA GTCCCCAGAA 540
GGCCGCGAGG GGCGGAGCCA CCAGCGCCCG CCCCGCCCGG GCCCGCCATG CCGCACAGCA 600
TCATGGGAGT TGTAGTTCAG GCCCTGTCCC CCGGGCAGCC GCTGGCGCGG ACGTTCGCGG 660
AGCAGCCCGG CGCCCGCGCG GCTCACGGGG CCCTAGGACC CCTCCCCTGG GGGACCTCCA 720
CCCTCCGCAG GCCTTTTGAA TTAATCCTAC TGCGCCGGGG ACCCCAGGAC AGTTCTGTCG 780
CGTACTCCCG GGACCCTTTA AGGGGCGGGG CTGGGATCCT GCCCCACCCT TGACTCCCCC 840
ACCCTCCTCT CTCAAACATC ACCCCGGGCG CTTTAAAACG CTTGATCTCG CTGGAACCTT 900
TTCGGTCTCC GTTAGCCACA CCTTGATTGT CGAGTGTGTG TCTGGCCCTT TGGGGACAGC 960
GCTTAAAGTC GGGGTGGGCG GGGGAGGGGA TCACCGACAT TCAGTCTTGA GTGACACACC 1020
AGATGACCCC ACCGGAGAGG AGGAGGGTGG CACAGGGGCC TGACGGACCT GGGGTATGGG 1080
CAAGGCTTCC AGGGGCCGGT GACATTCAGA CTAGGCCTGG GTTGGCCAGG GCAGGAGCAG 1140
GGAAGGGTGT TCCAGTCAGA GGGAACAGCA TGAAGGAGGG CTTCGAGGCT TTAGGGGAAG 1200
CAAAAGAAGG CCTGGGAGGC TGGCAGGCAG AGAACGGCTG GGGAGGGGCC GCTGGGAGGG 1260
GTGGAGAGGT GAGTAGGGCC CGTGGGAAGC ACCTGGCGAA GAGTGTTTCT GATCCCCAAA 1320
TCCAGTATGC GTGCCGGGTT CTCGGGCAGA GTGGCCAGGC GGAACGTGAC CAGGGTTCAG 1380
TGGCAGAGCC TGGAACCAGC CTGGGGGTCC TGCTTCTCAG GCCCCGGCGT GTCCTTAGGG 1440
GAAGGGGAAG GAGACTTCCC AGGGCAGGGC TGCAGCAAGA GCTGGCACAA TGCCATCCTC 1500
AGGGGGCACA 1510
|
