Variant report

Variant rs61828235
Chromosome Location chr1:211879486-211879487
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211872800-211884000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:211876000-211880000 Enhancers Fetal Muscle Trunk muscle
3 chr1:211876800-211880400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:211877000-211880000 Enhancers Fetal Muscle Leg muscle
5 chr1:211877600-211880000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:211877800-211880200 Enhancers NHEK skin
7 chr1:211878000-211880200 Enhancers HMEC breast
8 chr1:211878200-211879600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr1:211878200-211880000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:211878400-211880000 Enhancers HSMMtube muscle
11 chr1:211878600-211880000 Enhancers Placenta Amnion Placenta Amnion
12 chr1:211878800-211879600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:211878800-211879600 Enhancers Left Ventricle heart
14 chr1:211879000-211879600 Enhancers Skeletal Muscle Female skeletal muscle
15 chr1:211879200-211884600 Weak transcription Esophagus oesophagus
16 chr1:211879200-211913600 Weak transcription Right Atrium heart
17 chr1:211879400-211880000 Enhancers Primary neutrophils fromperipheralblood blood
18 chr1:211879400-211884000 Weak transcription Spleen Spleen

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