Variant report

Variant rs111626631
Chromosome Location chr4:187826396-187826397
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187816400-187829400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:187821400-187826400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr4:187821600-187826400 Enhancers Muscle Satellite Cultured Cells --
4 chr4:187821600-187826400 Enhancers NHDF-Ad bronchial
5 chr4:187824200-187831600 Weak transcription Fetal Intestine Small intestine
6 chr4:187824800-187828800 Weak transcription Gastric stomach
7 chr4:187825000-187827200 Weak transcription Fetal Muscle Trunk muscle
8 chr4:187826000-187840200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:187826200-187826400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr4:187826200-187831600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:187826200-187837000 Weak transcription HMEC breast
12 chr4:187826200-187840800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:187826200-187841400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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