Variant report

Variant rs10798269
Chromosome Location chr1:173309713-173309714
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173299200-173310000 Weak transcription HSMMtube muscle
2 chr1:173299200-173311200 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr1:173299200-173316600 Weak transcription Brain Angular Gyrus brain
4 chr1:173299800-173316600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr1:173300600-173329200 Weak transcription Primary T cells from cord blood blood
6 chr1:173301000-173310600 Weak transcription Stomach Smooth Muscle stomach
7 chr1:173301400-173321200 Weak transcription Ovary ovary
8 chr1:173301600-173311000 Weak transcription Gastric stomach
9 chr1:173301800-173310200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr1:173303000-173310000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:173303000-173310000 Weak transcription NHDF-Ad bronchial
12 chr1:173309000-173310000 Weak transcription Muscle Satellite Cultured Cells --
13 chr1:173309000-173312400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:173309200-173324600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:173309600-173310000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr1:173309600-173311200 Enhancers NH-A brain
17 chr1:173309600-173312000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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