| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00241 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:12104260-12105680 |
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 | chr1:12105369-12105390 | TGAGGTGGAGTGGGGGGAAGG | + | 6.04 | | ZNF263 | MA0528.1 | chr1:12105372-12105393 | GGTGGAGTGGGGGGAAGGAAA | + | 6.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32538 | chr1:12104150-12109233 | GM12878 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 12105046 | 12105125 | | chr1 | 12105296 | 12105365 |
|
Enhancer Sequence | AAAAAAAAAA GCAAGCAGGG AACATGATGA CAGGGGCAGA GAGGACTGAT GAAGGATGGC 60
AGGCAGCTGC TAGAAGCCAG GGGAGAGGCA TAGGAGGGAC AGATTTTCTG TCAGAGCTTC 120
CAGAAGGAAG CAACCCTGCC AACACCTTGA TCTTGGACTT CCGGTCTCCA GAACTAGAGG 180
CTAGAAGTTT CAATTGTTTT AATCATACCG TTTGTGAGCA GTTACTACAG TGGCCCTAAG 240
AAATGAACAC AGACTGGGCG TGGTACCTCA TGCCTGTAAT CCTAGCACTC TGGGAGGCCG 300
AGGTGGGTGG ATCACTTGAG GTCAGGAGTT TGAGACCAGT CTGGCTAACA TGGTGAAACC 360
CCGTCTCTAC TGAAAATACA AAAATTAGCC GGTGTAATGG CATGCACCTG AAATCTCACT 420
TACTCGGGAG GCTGGGGCAC GAGAGTCGCT TGAACCTGGG AGGCAGAGGT TGCAGTGAGC 480
TGAGATCACG CCACTGCACT CCAACCTGGG TGACAGAGCG AGACTCTGAC TCAAAAAAAA 540
AAAAAAGAAA TGAATACAGT TCACAGTTGC CTGGATGAAT GATGAATGAG ATGCTGGGGT 600
GGCCACGTGA CGGCTGTTTG CTCACGGTCA AGTCCACAGT TTAGCTCTTA GCTTCAGTTG 660
GGAATTAATT TTCTGGGGCA AGCAGAAACC TCAGTGTCCT GGGCTGAACT GTGTCCCTCC 720
CCAAATTCAC ATTTGGAAGT CCTAACCTCC AGTACTTCAG AATGCAACAG TCCTTTGAGA 780
TAGTCTTTAA AGAGGCAATT AAGTTAAAAC AAGGCCTTTC AGGTGGACCC TAATCCAATA 840
CGACTGGTGT CCTTACAAAA AGGGGAAATT TGGCCACAGA CCTGTGCACG TACAGAGGAA 900
AGTCCAGGTG AGAACGCAGC GACAACATGG CCACCCGTGA GCCAAGGAGA GAGGTCTTGA 960
AAAAACCCAG CCCTGCTGAC GCCTCAACCT TCACCTCCAG AAGTGCGAGG AAGCTAATTT 1020
CTGTGGCTTA AGCCACCCCA TTTGCGGGAC TTTATGGCAG CCTGAGCAGA CTAACACGCT 1080
CATCATGCCA GAAAATTCCT TGTTGGGCTT GAGGTGGAGT GGGGGGAAGG AAACTCATCC 1140
CTGGCCCTCC ATCCTGAGAT TCCTGAACTC CAAAGCTCCC CGCTGCTTGA CCTCAGTGCT 1200
CCAAGCTGTA AATGCAGGTT TGTCTTACCG GCCAAAGCAG CCTCTCAAGA TGACACGTTG 1260
GGGAGATGAG GTCTCCCATA GATGGGAGGG GTGGACAGCA GGCAGTACCC CCAACCCTCT 1320
GCCCTGGTCA CCGACAAGCT GAGACAGCCT CATGGCCCTT GGTGTCTGGC CACTCCGGCA 1380
TCTGATGTAT CTTGGGGTTT TATAATCCTG GGGGTTCATC 1420
|
