Variant report

Variant rs16990830
Chromosome Location chr22:33001199-33001200
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:32993800-33001200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr22:32998800-33004000 Enhancers Placenta Placenta
3 chr22:32999200-33001400 Weak transcription NHEK skin
4 chr22:32999400-33001600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr22:32999400-33002200 Weak transcription Fetal Muscle Leg muscle
6 chr22:32999600-33004000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr22:32999800-33001200 Weak transcription HMEC breast
8 chr22:32999800-33001400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr22:33000000-33001200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr22:33000000-33002200 Weak transcription Fetal Stomach stomach
11 chr22:33000200-33001200 Weak transcription Placenta Amnion Placenta Amnion
12 chr22:33000200-33003400 Weak transcription Fetal Muscle Trunk muscle
13 chr22:33000400-33001600 Weak transcription Lung lung
14 chr22:33000600-33001800 Weak transcription Spleen Spleen
15 chr22:33000600-33002000 Weak transcription Fetal Adrenal Gland Adrenal Gland
16 chr22:33000600-33003000 Weak transcription Right Atrium heart
17 chr22:33000600-33003200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
18 chr22:33000600-33003200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
19 chr22:33000600-33003200 Weak transcription Left Ventricle heart

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