| Tag | Content |
|---|
EnhancerAtlas ID | HS042-11352 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:114297370-114298640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr12:114297570-114297586 | ATAAATATTTAATGTG | + | 6 | | ZEB1 | MA0103.3 | chr12:114298061-114298072 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr12:114297413-114297434 | TTCCCTTCTCTCCTCTCCTCC | - | 6.8 |
|
| | 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 |
| GH12I113860 | chr12 | 114297812 | 114301901 |
|
Enhancer Sequence | AGGGATCAAA CTGGTAACCA CGGCCTTGGA CCATCCCCCC CGGTTCCCTT CTCTCCTCTC 60
CTCCAGGTTA AACCTTTGAG AAATTGTAGG ACAAAGGGAT AGGGCTTTCT CAGGCCTCCC 120
TTGCCTCCCT GTCTCACTTC CCACCTCCCA ATCCCTTTCT AATGTCCATT TATCAAATAT 180
ATATGCACAA ATTGCTACCG ATAAATATTT AATGTGCACG GCATCTGAAG AGAGGTATTA 240
TTTTATTTGA AAATCTACAC ACACTTGCGG CTGCCTGGGC ACACACACAT ATGCACGATG 300
GTCTAGGATG CTTCGGGGCC AAAGACTGAT TGGGTAAAAA ACACAGTAAA GGCCGTAAGC 360
TCTCGTGAAA TGATATAAGC TAAATCCGAA GTGTTAACCC ACAGCCCTGC CAGCATGACC 420
AGGCATCTGC CAGCCCAATT TCTGAAGGCA GGACAGTGTG TAAATGCGGC ATTATGAATC 480
CTCAAAATGA ATCTGCACGT CTCCTCGGAG CTCTCCCCAG CAGCTCTGCT CCCCCCTCCT 540
GGTGCCTCCT CTGTGCAGGC AACGAGAAAC GGCAGAGAGG CACTGGTGAC AAGGCCAGCC 600
TCCCGGGGAG GGGAAGGAGC CAGGAACGTG GGGAGTGGAG CCCGGTCAGG TTTCCCTGCT 660
GGAGGGGGGC CAGGGCTGGG GACCAGAGGC TGGGCAGGTG GGGACAAGGT GAGGTTGGAG 720
AGCTGAGGAG TCAAGCCCAC AAACCCTACT TCATTCTGCC ACCTAAAGGC GGATGCATCC 780
CATGACAGAC ACAGTCTCTC TTCCCTCCAC CAAAGCCCCT CTGCCATGCT GGCTTTGAAC 840
AGGGAGGGAA GGGCGTGGAC AAATTTTCTT GTAAGCTCGT TCAGATGAAT GGTTCTTTGG 900
GTCCAAGTCT TCAGAAGCCC ACTGGGACTA CAGGGATGGC ACATCCGGCA GCTAAGGGGC 960
TGGAGCCTGA GAGCGTTCAG AGCTGGTATG AGGCAACTGA GAGGCACATG GAAGACCAGG 1020
CTGGGTGCTT TCTCAACACG GCCATAGACA GCCACTGGGT GAGCTGGTTC CTCTGTCCGT 1080
GCCTTGGCCT CACCTAACTG CACTAGCCCC GAGATGTCTT TCCTGACCCC TGGAGGCTGG 1140
GGTGACTGCC CCCATCCACA GTGTCACCGC TCACTGTGCC CCCTGACCAG GGCTCTGTGG 1200
GGTGCATGCC TTCCCTGGCC AGGGCTAGGG CTCAGCTCCG CAAGAGTCCA GGCCCCATCT 1260
ATCTTGCTCA 1270
|
