Variant report

Variant rs12410106
Chromosome Location chr1:94210964-94210965
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94199400-94217400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94206000-94212600 Weak transcription HMEC breast
3 chr1:94206200-94211600 Weak transcription Spleen Spleen
4 chr1:94206800-94212400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:94206800-94212400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:94207000-94211200 Weak transcription Adipose Nuclei Adipose
7 chr1:94208200-94215600 Weak transcription Aorta Aorta
8 chr1:94209000-94211000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:94209400-94211200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr1:94209400-94212400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:94209400-94212600 Enhancers NHEK skin
12 chr1:94209800-94211800 Enhancers GM12878-XiMat blood
13 chr1:94209800-94212600 Enhancers Fetal Thymus thymus
14 chr1:94210000-94211000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr1:94210200-94211800 Enhancers Primary B cells from peripheral blood blood
16 chr1:94210200-94212600 Enhancers Esophagus oesophagus
17 chr1:94210600-94211000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr1:94210800-94211000 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
19 chr1:94210800-94211000 Enhancers Primary B cells from cord blood blood
20 chr1:94210800-94211600 Weak transcription Sigmoid Colon Sigmoid Colon
21 chr1:94210800-94211800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
22 chr1:94210800-94215600 Weak transcription Thymus Thymus

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