| Tag | Content |
|---|
EnhancerAtlas ID | HS176-03385 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:206654320-206655160 |
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 | TGAGTCTTCA ACTTATCCTT GCCTTCCTTG GGTTCCCTGC CCCAATCTTT GGAACCCCAC 60
TCCCTCCACT CCCTTGTCTT GGGCTAATAA GGGGGGATGG GTTGGAAAAA GAGAGAGACC 120
GGGCAGGAGG AAGCCAAGTG GAAGGGTCTG GAGATGGGGA ATGTGGGAAG ACTTCATTGG 180
CCAGAGCACG ATTGAGAAGT AGGCACAGCA CCCCAAATCC TGGAAGGCAC GAGGCCATGG 240
TACGGGTGAG GGTGGGAGCT CTGCAGCCTA GGGATGCCAC TGGTGACAGG AGTCTTTGGG 300
AACAGAAGAT CAGAGACTGC CCATATGCCT GAAGGCCCCC TCCTCCCGCC ACCCCCAGCC 360
CTTGTCCTCA GGGAGCTCCA GGGAGTTTCC CAGCTGTGGG CTGACTCATG CAGCCCCGCG 420
TGCCTCCTGC TTCGCAGCAG CAACTCAGTT GATGGGGCAG CTGGGAGGTG GAGGAGCAGG 480
GAGGAGGAAG AGGAGCATCT CCAGATAACA GGGATGGAGT CTCCATCCAG ACTGAGCCCC 540
TCTCAAATGG TGACAGAGAG TAGGGTTCAG TCAGCAGAAC TGCAAGTGAA TCTCCTTTGA 600
GCAGAGCTCT GTCCAGGGCA CAGAGGGGGC TCCAGGGGTA GATGTGGCAT CCTGTCATTC 660
AGAGAGGCCC ATGCTTCCTC CGGAGCAGCT AGCCCTTCCT GGACATGTGA GGGCTGATGG 720
GATTGTTGGG TAAGAGGAGA CCTGAGATGG GTAGAGGCAA CCACGGAGGC CTTCCTGAAG 780
GATGAGGCTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTG AGACGGAGCC TCGCTCTGTC 840
|
