Variant report

Variant rs16918354
Chromosome Location chr9:101942256-101942257
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:101931600-101947000 Weak transcription Right Atrium heart
2 chr9:101935200-101947200 Weak transcription Gastric stomach
3 chr9:101936400-101943800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr9:101936600-101949600 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr9:101939200-101946400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr9:101939400-101943600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr9:101939400-101945400 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr9:101939800-101942600 Weak transcription HepG2 liver
9 chr9:101940200-101942800 Weak transcription Fetal Intestine Small intestine
10 chr9:101940200-101943000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:101941000-101942800 Enhancers GM12878-XiMat blood
12 chr9:101941000-101943400 Enhancers Fetal Muscle Leg muscle
13 chr9:101941200-101942400 Enhancers Fetal Muscle Trunk muscle
14 chr9:101941400-101943000 Weak transcription Fetal Lung lung
15 chr9:101941800-101942800 Weak transcription Primary B cells from peripheral blood blood
16 chr9:101941800-101943600 Weak transcription Primary B cells from cord blood blood
17 chr9:101941800-101946800 Weak transcription Breast Myoepithelial Primary Cells Breast
18 chr9:101942000-101943800 Enhancers Fetal Intestine Large intestine
19 chr9:101942200-101946800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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