| Tag | Content |
|---|
EnhancerAtlas ID | HS108-40289 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:144918420-144919210 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:144918778-144918797 | TGGCCAGGAGGGGGTGCTG | + | 6.39 | | RREB1 | MA0073.1 | chr8:144918868-144918888 | GGGGGGGGGGTGGGAGGGGT | - | 6.75 | | ZNF263 | MA0528.1 | chr8:144918852-144918873 | GGGGGATGGGAGGGGTGGGGG | + | 6.21 | | ZNF740 | MA0753.2 | chr8:144918866-144918879 | GTGGGGGGGGGGT | - | 6.32 | | ZNF740 | MA0753.2 | chr8:144918868-144918881 | GGGGGGGGGGTGG | - | 6.44 |
|
| | 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 |
| GH08I143836 | chr8 | 144918307 | 144919330 |
|
Enhancer Sequence | GGAAGGGACA GCAAAGACTG GAAAGGGGGG AATCTCTAAG AGGAGCCCAT CTCACTGCTA 60
GTGGCTTGGC AAGCTAAGGA AAGCTTCGAG AAGAGTCGAC ATTAGGGGCT GGGTACTGAA 120
GGCTGAATAG GAGCTTTCAC CGCGGAGAGA ACAACTTGAA CAAAGAGGGA ACTGTGGGCG 180
TGGGGAAAGG GAGGTTGGGC GGGACAGGAC CGCGCCGAAG TGCACGGTGC CTGCGGGATC 240
AGGCCTCCCA GAGCCTGGGC GTCAGCTGAG GACTCCCATG ATCTCTGCTG GCAGCCAGGA 300
GCAGGCAGTT TGCCTGTTAG GACATGAATT CTGGCTGCAC TGCACCGAGA GAGGCCCCTG 360
GCCAGGAGGG GGTGCTGCAG GAAAAGTCTG GGGAGACACC AGGACATAGA TGTCCGGGAA 420
TCAGCACCAG GTGGGGGATG GGAGGGGTGG GGGGGGGGTG GGAGGGGTGC GGGGGTGGGG 480
GAAGATTGCT GGCAGGGTGG AAGAGCCCGG GTGAGTTCTG GAGGAAGGAT GCTTGGAGTA 540
GGTTCAGGGC AGGCAGCAGG ATGCAGGGGA AGGATCTGAG GGGACAGGGA GCCTCCCGGA 600
AAAGGAGAGT GCCCAGCCTG TCCTATAACC CCCATGACCC CCACAAGGGG GTCAGCCTGG 660
ATCTGGTCTC TGGCAGCCAG GAGGAGAGCT GGGCTGTGGG GATGCAGGCC CTAAGAGAAG 720
GAGGGGCACC TCTTATCTGG CTGTTAGAAG GTCTGAGGGA TGGCACTGAG CAGCAGGAGA 780
GGGGACTCAC 790
|
