Variant report

Variant rs117782184
Chromosome Location chr22:23244964-23244965
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:23237800-23245600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr22:23243800-23245000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
3 chr22:23243800-23245000 Bivalent Enhancer Rectal Mucosa Donor 31 rectum
4 chr22:23243800-23245800 Bivalent Enhancer Fetal Muscle Trunk muscle
5 chr22:23243800-23245800 Bivalent Enhancer Fetal Muscle Leg muscle
6 chr22:23243800-23246000 Enhancers HSMMtube muscle
7 chr22:23243800-23247400 Strong transcription Right Atrium heart
8 chr22:23243800-23247600 Enhancers Dnd41 blood
9 chr22:23244000-23245000 Bivalent Enhancer Small Intestine intestine
10 chr22:23244000-23245000 Enhancers Stomach Smooth Muscle stomach
11 chr22:23244200-23245200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
12 chr22:23244400-23246000 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr22:23244400-23246000 Enhancers Fetal Lung lung
14 chr22:23244600-23246000 Enhancers Fetal Stomach stomach
15 chr22:23244600-23246000 Enhancers HSMM muscle
16 chr22:23244600-23247000 Enhancers GM12878-XiMat blood
17 chr22:23244800-23245200 Enhancers Sigmoid Colon Sigmoid Colon
18 chr22:23244800-23245400 Genic enhancers Primary B cells from cord blood blood
19 chr22:23244800-23245400 Genic enhancers Primary B cells from peripheral blood blood

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