| Tag | Content |
|---|
EnhancerAtlas ID | HS082-02946 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:206653880-206655100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr1:206654093-206654107 | GGGGCCCATGGGGG | + | 6.71 | | 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 | GTGTTCGCCT CAGGCCAGCT GGGACCTCTC AGCCCTGCCT TGTCTGCTCC TCACCCTAGA 60
TACTTCCAAC AATGCACCTC TTCTCCCCAA GCCAGGGCTA CTGCCTTCCC TGCCCTCCTA 120
GAATAGAGGG CACCCGCACC CTATCCCTTA TCCCCACCTC ACCAAATAAC TGCAATGGCT 180
CCCCCAAAAC CCAGTCCCTC ACCTGCAGGG GAAGGGGCCC ATGGGGGCAC AGACTCTCCA 240
GGTACCAAGG TGGCCTCCCT ATCCCAAGAA GGGGCTTGTG TCCTGCCAAG TCCTTCTCTG 300
AATGATTTAG AGTGCTCACC CTATGCCAAG TGCCAGCAGA ACTCTAGGGG GAGGACACAC 360
ACCCACGCAC AGTTCCTGGA TGTGACCAGG GATGGAGATC CAGGTGGTCT CGTTCTCCAT 420
GCCTCATCTC CTGCTTTCTC TGAGTCTTCA ACTTATCCTT GCCTTCCTTG GGTTCCCTGC 480
CCCAATCTTT GGAACCCCAC TCCCTCCACT CCCTTGTCTT GGGCTAATAA GGGGGGATGG 540
GTTGGAAAAA GAGAGAGACC GGGCAGGAGG AAGCCAAGTG GAAGGGTCTG GAGATGGGGA 600
ATGTGGGAAG ACTTCATTGG CCAGAGCACG ATTGAGAAGT AGGCACAGCA CCCCAAATCC 660
TGGAAGGCAC GAGGCCATGG TACGGGTGAG GGTGGGAGCT CTGCAGCCTA GGGATGCCAC 720
TGGTGACAGG AGTCTTTGGG AACAGAAGAT CAGAGACTGC CCATATGCCT GAAGGCCCCC 780
TCCTCCCGCC ACCCCCAGCC CTTGTCCTCA GGGAGCTCCA GGGAGTTTCC CAGCTGTGGG 840
CTGACTCATG CAGCCCCGCG TGCCTCCTGC TTCGCAGCAG CAACTCAGTT GATGGGGCAG 900
CTGGGAGGTG GAGGAGCAGG GAGGAGGAAG AGGAGCATCT CCAGATAACA GGGATGGAGT 960
CTCCATCCAG ACTGAGCCCC TCTCAAATGG TGACAGAGAG TAGGGTTCAG TCAGCAGAAC 1020
TGCAAGTGAA TCTCCTTTGA GCAGAGCTCT GTCCAGGGCA CAGAGGGGGC TCCAGGGGTA 1080
GATGTGGCAT CCTGTCATTC AGAGAGGCCC ATGCTTCCTC CGGAGCAGCT AGCCCTTCCT 1140
GGACATGTGA GGGCTGATGG GATTGTTGGG TAAGAGGAGA CCTGAGATGG GTAGAGGCAA 1200
CCACGGAGGC CTTCCTGAAG 1220
|
