Variant report

Variant rs17152950
Chromosome Location chr7:26004912-26004913
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:26002800-26007200 Weak transcription Spleen Spleen
2 chr7:26002800-26009000 Weak transcription Right Atrium heart
3 chr7:26003400-26005200 Bivalent Enhancer Primary B cells from peripheral blood blood
4 chr7:26003400-26005600 Flanking Active TSS GM12878-XiMat blood
5 chr7:26003800-26005000 Enhancers Rectal Mucosa Donor 29 rectum
6 chr7:26003800-26005600 Enhancers Fetal Lung lung
7 chr7:26004000-26005000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr7:26004000-26005000 Enhancers Fetal Thymus thymus
9 chr7:26004000-26005200 Enhancers Pancreas Pancrea
10 chr7:26004000-26005200 Enhancers Rectal Mucosa Donor 31 rectum
11 chr7:26004400-26005000 Bivalent Enhancer Hela-S3 cervix
12 chr7:26004400-26005200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr7:26004400-26005200 Enhancers Fetal Muscle Leg muscle
14 chr7:26004600-26005000 Enhancers Stomach Mucosa stomach
15 chr7:26004600-26005000 Enhancers NHEK skin
16 chr7:26004600-26005200 Bivalent Enhancer Duodenum Mucosa Duodenum
17 chr7:26004800-26005000 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr7:26004800-26005000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr7:26004800-26005200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr7:26004800-26005400 Enhancers Liver Liver
21 chr7:26004800-26007200 Weak transcription Gastric stomach

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