Variant report

Variant rs150597346
Chromosome Location chrX:31272649-31272650
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:31235000-31282000 Weak transcription Left Ventricle heart
2 chrX:31243200-31281800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chrX:31245200-31282000 Weak transcription Duodenum Smooth Muscle Duodenum
4 chrX:31245400-31284000 Weak transcription HSMMtube muscle
5 chrX:31245600-31279800 Weak transcription HepG2 liver
6 chrX:31247000-31280200 Weak transcription Pancreas Pancrea
7 chrX:31254000-31283200 Weak transcription Fetal Intestine Small intestine
8 chrX:31254200-31275200 Weak transcription Liver Liver
9 chrX:31257000-31282800 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chrX:31264000-31282200 Weak transcription Fetal Muscle Leg muscle
11 chrX:31264600-31279800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chrX:31264800-31282400 Weak transcription Cortex derived primary cultured neurospheres brain
13 chrX:31268800-31278400 Weak transcription HMEC breast
14 chrX:31270000-31273200 Weak transcription Hela-S3 cervix
15 chrX:31270000-31280800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
16 chrX:31271800-31279600 Weak transcription iPS-15b Cell Line embryonic stem cell
17 chrX:31271800-31280000 Weak transcription HUES48 Cell Line embryonic stem cell
18 chrX:31272200-31280800 Weak transcription Brain Angular Gyrus brain
19 chrX:31272600-31272800 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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