Variant report

Variant rs60060452
Chromosome Location chr18:9421060-9421061
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:9414800-9422200 Enhancers Fetal Muscle Leg muscle
2 chr18:9417200-9428400 Weak transcription Gastric stomach
3 chr18:9417600-9429200 Weak transcription Stomach Smooth Muscle stomach
4 chr18:9417800-9425000 Weak transcription Right Atrium heart
5 chr18:9418200-9428400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr18:9418400-9422600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr18:9418800-9422800 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr18:9419000-9422400 Weak transcription NHEK skin
9 chr18:9419000-9423200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr18:9419000-9426400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr18:9419600-9427200 Weak transcription Fetal Kidney kidney
12 chr18:9420000-9422200 Enhancers K562 blood
13 chr18:9420200-9421200 Weak transcription Fetal Stomach stomach
14 chr18:9420200-9421400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr18:9420200-9421400 Enhancers Esophagus oesophagus
16 chr18:9420400-9421200 Weak transcription Fetal Muscle Trunk muscle
17 chr18:9420400-9423200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr18:9420400-9423200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr18:9420600-9423200 Weak transcription HMEC breast

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