| Tag | Content |
|---|
EnhancerAtlas ID | HS019-08853 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr2:636390-637370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:637095-637106 | GGGCGGGAAGA | + | 6.14 |
|
| | 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 |
| GH02I000636 | chr2 | 636179 | 637357 |
|
Enhancer Sequence | CAGGCGCCCG GATTCACCGT CCAGCCGGGG CCCTGACCCC GGGTCCGTCC ACGCGGCTGC 60
GATGCTCGGT CATCCTGGCT CCGGCCCACC CCGGGGAGAC AGGCCCCTCA CCGGCCCCTC 120
TGAGGAGCAG GGCCAACACG CCGCGGGCTC TGCCGGCCCC GCAGGCCTCG GGTTCCATCG 180
CAGCAGCGTG GCCTGATGAC TCCATTTTGT CGCTGCGGAG GAGCCGCACC GAGTCCACAG 240
CGCCAGTGCG GGGGAGCCGC GCCGGGGAAG AGGGAGGAGG CGCGTCCACA GCAGCCTCGT 300
GTCTCCACAT GGGACGTTTC CTCGGCGGGG ACCCGGCGCG CCCAGGGGCT CAGGCTCGCT 360
CAGGCCTACG GAGGCGGGTG TATCCGCGTC CGGCCCGACT TGTGAGGAAA CAGCACACGT 420
GAAGCGAGCG GAGTCGGCGC AGCCTGGAAC AGGGTGAATC CGCAGAGTCC TCGGCCGCGC 480
ATGGCGGCTC TGTCAGCTCC AGGGACACAG GGACCGTCCC CGGGCCCATC AGCGCAATCG 540
GGAGGGCGTC CGTGTGCCCA CAGGCCCAGC TACACCTCCA CAAAGCTGGG AAAGACGAAC 600
ACGGGCCACC CTCAGCCACC TGCCCGGACC GCTGCGAGGC CCACGGGAGG GAAGACGCGC 660
CCTGGCACGC GGTGTGGTAA CCGCCCTTGG ACGCGGCGGC GCTTTGGGCG GGAAGAACCG 720
CGAATTCCAG AACATTTGGG ATCATTTGTT AAAAGAAAAA TCCTCGGGCG CCACCTAGCG 780
CTGACATGCT GCCTAACTCT TCTCAGCCCT CATTTTAGAG AACGGAAAAT GAAGCCCAAG 840
TTATTGACTA TAAAATGGGA AAAAACTAAA ACATTGCAAT ATGCAGATTG CATCACACAT 900
ATTATCTTAG CAGGTTTTCT TGCACTTGCC TTGCAGATAA ATAGGACATA TCTAGGTGGT 960
GCTGTGTCCA ATAAAATAAC 980
|
