Variant report

Variant rs6835957
Chromosome Location chr4:101855237-101855238
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:101853400-101855800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
2 chr4:101854400-101855400 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:101854600-101855400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr4:101854800-101855400 Enhancers Primary neutrophils fromperipheralblood blood
5 chr4:101854800-101855400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:101854800-101857800 Weak transcription Fetal Brain Female brain
7 chr4:101855000-101855400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr4:101855000-101855400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr4:101855000-101855400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr4:101855000-101855400 Enhancers Adipose Nuclei Adipose
11 chr4:101855000-101855400 Enhancers Placenta Placenta
12 chr4:101855200-101855400 Enhancers Spleen Spleen
13 chr4:101855200-101855400 Enhancers NHDF-Ad bronchial
14 chr4:101855200-101859600 Weak transcription Ovary ovary

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