Variant report

Variant rs6002074
Chromosome Location chr22:22734628-22734629
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22725800-22735600 Weak transcription Pancreas Pancrea
2 chr22:22726600-22734800 Weak transcription Thymus Thymus
3 chr22:22728200-22737400 Enhancers Primary B cells from cord blood blood
4 chr22:22728400-22737000 Enhancers Primary B cells from peripheral blood blood
5 chr22:22730800-22736000 Weak transcription Primary hematopoietic stem cells blood
6 chr22:22734400-22734800 Enhancers HSMM muscle
7 chr22:22734400-22735200 Enhancers HSMMtube muscle
8 chr22:22734400-22736000 Enhancers Fetal Muscle Leg muscle
9 chr22:22734600-22734800 Bivalent Enhancer H1 Cell Line embryonic stem cell
10 chr22:22734600-22734800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
11 chr22:22734600-22734800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr22:22734600-22734800 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
13 chr22:22734600-22734800 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
14 chr22:22734600-22734800 Enhancers Fetal Intestine Small intestine
15 chr22:22734600-22734800 Bivalent Enhancer Left Ventricle heart
16 chr22:22734600-22735000 Enhancers Fetal Muscle Trunk muscle
17 chr22:22734600-22735200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
18 chr22:22734600-22735200 Enhancers Fetal Thymus thymus
19 chr22:22734600-22736000 Enhancers GM12878-XiMat blood
20 chr22:22734600-22736200 Strong transcription Right Atrium heart

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