| Tag | Content |
|---|
EnhancerAtlas ID | HS078-01852 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:206654340-206655080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:206654792-206654813 | GGAGCAGGGAGGAGGAAGAGG | + | 6.39 | | ZNF263 | MA0528.1 | chr1:206654786-206654807 | GGTGGAGGAGCAGGGAGGAGG | + | 6.59 | | ZNF263 | MA0528.1 | chr1:206654789-206654810 | GGAGGAGCAGGGAGGAGGAAG | + | 6.91 | | ZNF263 | MA0528.1 | chr1:206654783-206654804 | GGAGGTGGAGGAGCAGGGAGG | + | 7.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 206654677 | 206654826 | | chr1 | 206654444 | 206654508 | | chr1 | 206654628 | 206654823 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206480 | chr1 | 206654141 | 206655107 |
|
Enhancer Sequence | GCCTTCCTTG GGTTCCCTGC CCCAATCTTT GGAACCCCAC TCCCTCCACT CCCTTGTCTT 60
GGGCTAATAA GGGGGGATGG GTTGGAAAAA GAGAGAGACC GGGCAGGAGG AAGCCAAGTG 120
GAAGGGTCTG GAGATGGGGA ATGTGGGAAG ACTTCATTGG CCAGAGCACG ATTGAGAAGT 180
AGGCACAGCA CCCCAAATCC TGGAAGGCAC GAGGCCATGG TACGGGTGAG GGTGGGAGCT 240
CTGCAGCCTA GGGATGCCAC TGGTGACAGG AGTCTTTGGG AACAGAAGAT CAGAGACTGC 300
CCATATGCCT GAAGGCCCCC TCCTCCCGCC ACCCCCAGCC CTTGTCCTCA GGGAGCTCCA 360
GGGAGTTTCC CAGCTGTGGG CTGACTCATG CAGCCCCGCG TGCCTCCTGC TTCGCAGCAG 420
CAACTCAGTT GATGGGGCAG CTGGGAGGTG GAGGAGCAGG GAGGAGGAAG AGGAGCATCT 480
CCAGATAACA GGGATGGAGT CTCCATCCAG ACTGAGCCCC TCTCAAATGG TGACAGAGAG 540
TAGGGTTCAG TCAGCAGAAC TGCAAGTGAA TCTCCTTTGA GCAGAGCTCT GTCCAGGGCA 600
CAGAGGGGGC TCCAGGGGTA GATGTGGCAT CCTGTCATTC AGAGAGGCCC ATGCTTCCTC 660
CGGAGCAGCT AGCCCTTCCT GGACATGTGA GGGCTGATGG GATTGTTGGG TAAGAGGAGA 720
CCTGAGATGG GTAGAGGCAA 740
|
