Variant report

Variant rs7574282
Chromosome Location chr2:181881590-181881591
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181856800-181897200 Weak transcription Primary B cells from cord blood blood
2 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:181860000-181894800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:181871000-181886600 Weak transcription Brain Hippocampus Middle brain
5 chr2:181873200-181885000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:181873600-181882000 Weak transcription Pancreas Pancrea
8 chr2:181873600-181887800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr2:181873600-181889600 Weak transcription Colon Smooth Muscle Colon
10 chr2:181876200-181881600 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr2:181876200-181882000 Weak transcription Duodenum Smooth Muscle Duodenum
12 chr2:181876200-181885000 Weak transcription Brain Angular Gyrus brain
13 chr2:181877600-181882200 Weak transcription Primary T helper naive cells from peripheral blood blood
14 chr2:181877600-181882800 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr2:181878400-181881800 Weak transcription Left Ventricle heart
16 chr2:181878600-181881600 Weak transcription Psoas Muscle Psoas
17 chr2:181878800-181881800 Weak transcription Skeletal Muscle Female skeletal muscle
18 chr2:181878800-181883800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr2:181880000-181881800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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