Variant report

Variant rs6958837
Chromosome Location chr7:27252246-27252247
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27245800-27253000 Weak transcription Gastric stomach
2 chr7:27250400-27252600 Bivalent Enhancer Fetal Intestine Large intestine
3 chr7:27250800-27252400 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
4 chr7:27251000-27252600 Enhancers Rectal Mucosa Donor 31 rectum
5 chr7:27251000-27253000 Weak transcription Pancreas Pancrea
6 chr7:27252000-27252400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
7 chr7:27252000-27253400 Bivalent Enhancer Primary B cells from peripheral blood blood
8 chr7:27252200-27252400 Bivalent Enhancer Fetal Heart heart
9 chr7:27252200-27252600 Bivalent Enhancer HUVEC blood vessel
10 chr7:27252200-27252600 Bivalent Enhancer NHDF-Ad bronchial
11 chr7:27252200-27252800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr7:27252200-27252800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr7:27252200-27252800 Bivalent Enhancer Brain Hippocampus Middle brain
14 chr7:27252200-27253000 Bivalent Enhancer Colonic Mucosa Colon
15 chr7:27252200-27253000 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr7:27252200-27253200 Bivalent Enhancer Primary hematopoietic stem cells blood
17 chr7:27252200-27253200 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
18 chr7:27252200-27253200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
19 chr7:27252200-27253400 Bivalent Enhancer H1 Cell Line embryonic stem cell
20 chr7:27252200-27253600 Bivalent Enhancer Primary T cells fromperipheralblood blood
21 chr7:27252200-27253800 Bivalent Enhancer Fetal Muscle Trunk muscle
22 chr7:27252200-27254200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
23 chr7:27252200-27254200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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