Variant report

Variant rs942126
Chromosome Location chr1:59211628-59211629
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59206200-59214200 Weak transcription Fetal Kidney kidney
2 chr1:59206200-59221000 Weak transcription Fetal Intestine Small intestine
3 chr1:59207600-59220000 Weak transcription Placenta Amnion Placenta Amnion
4 chr1:59207800-59220000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:59207800-59220000 Weak transcription Psoas Muscle Psoas
6 chr1:59208000-59215000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:59210600-59212600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:59210800-59211800 Enhancers Cortex derived primary cultured neurospheres brain
9 chr1:59210800-59212200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr1:59210800-59212600 Enhancers NHEK skin
11 chr1:59210800-59212800 Enhancers HMEC breast
12 chr1:59211000-59212600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:59211200-59212600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr1:59211200-59212600 Enhancers NH-A brain
15 chr1:59211200-59212800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:59211200-59212800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr1:59211200-59213000 Enhancers Muscle Satellite Cultured Cells --
18 chr1:59211400-59213200 Enhancers HepG2 liver
19 chr1:59211600-59212800 Enhancers HSMM muscle
20 chr1:59211600-59218200 Weak transcription NHDF-Ad bronchial
21 chr1:59211600-59221000 Weak transcription Stomach Mucosa stomach

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