Variant report

Variant rs11164816
Chromosome Location chr1:93261498-93261499
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93258000-93268400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:93258000-93270200 Weak transcription Right Atrium heart
3 chr1:93258200-93263000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:93258200-93263600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr1:93258800-93269800 Weak transcription Fetal Heart heart
6 chr1:93260400-93261600 Enhancers Osteobl bone
7 chr1:93260800-93261600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:93261000-93261600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:93261000-93262600 Weak transcription NH-A brain
10 chr1:93261200-93263200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:93261200-93270200 Weak transcription Muscle Satellite Cultured Cells --
12 chr1:93261400-93262400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:93261400-93268600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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