Variant report

Variant rs2855804
Chromosome Location chr6:31467365-31467366
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:90 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31464400-31467600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
2 chr6:31464600-31467400 Flanking Active TSS Dnd41 blood
3 chr6:31464800-31467400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr6:31465000-31467400 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
5 chr6:31465200-31467400 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
6 chr6:31465200-31467400 Active TSS H9 Cell Line embryonic stem cell
7 chr6:31465200-31467400 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
8 chr6:31465800-31467600 Active TSS HSMM muscle
9 chr6:31466200-31467400 Bivalent Enhancer Fetal Intestine Large intestine
10 chr6:31466200-31467400 Enhancers Lung lung
11 chr6:31466400-31467400 Enhancers Primary Natural Killer cells fromperipheralblood blood
12 chr6:31466400-31467400 Bivalent Enhancer Placenta Placenta
13 chr6:31466400-31473400 Weak transcription Aorta Aorta
14 chr6:31466600-31467400 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:31466600-31467400 Bivalent Enhancer Brain Angular Gyrus brain
16 chr6:31466600-31467400 Flanking Active TSS HMEC breast
17 chr6:31466600-31467400 Flanking Active TSS HUVEC blood vessel
18 chr6:31466600-31467600 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
19 chr6:31466600-31467600 Flanking Active TSS ES-UCSF4 Cell Line embryonic stem cell
20 chr6:31466600-31467600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
21 chr6:31466800-31467400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
22 chr6:31466800-31467400 Enhancers Primary monocytes fromperipheralblood blood
23 chr6:31466800-31467400 Enhancers Primary neutrophils fromperipheralblood blood
24 chr6:31466800-31467400 Enhancers Primary T helper naive cells fromperipheralblood blood
25 chr6:31466800-31467400 Enhancers Primary T helper memory cells from peripheral blood 1 blood
26 chr6:31466800-31467400 Enhancers Primary T helper 17 cells PMA-I stimulated --
27 chr6:31466800-31467400 Enhancers Primary T helper cells fromperipheralblood blood
28 chr6:31466800-31467400 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
29 chr6:31466800-31467400 Enhancers Primary T killer memory cells from peripheral blood blood
30 chr6:31466800-31467400 Bivalent Enhancer Brain Hippocampus Middle brain
31 chr6:31466800-31467400 Bivalent Enhancer Fetal Muscle Leg muscle
32 chr6:31466800-31467400 Enhancers Gastric stomach
33 chr6:31466800-31467400 Bivalent Enhancer Left Ventricle heart
34 chr6:31466800-31467400 Enhancers Right Atrium heart
35 chr6:31466800-31467600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
36 chr6:31466800-31467600 Enhancers Primary B cells from cord blood blood
37 chr6:31466800-31467600 Enhancers Primary B cells from peripheral blood blood
38 chr6:31466800-31467600 Enhancers Primary T cells fromperipheralblood blood
39 chr6:31466800-31467600 Enhancers Primary T helper cells PMA-I stimulated --
40 chr6:31466800-31467600 Enhancers Primary mononuclear cells fromperipheralblood Blood
41 chr6:31466800-31467600 Enhancers GM12878-XiMat blood
42 chr6:31466800-31473200 Weak transcription Primary hematopoietic stem cells blood
43 chr6:31466800-31473400 Weak transcription Primary T cells from cord blood blood
44 chr6:31466800-31473400 Weak transcription Thymus Thymus
45 chr6:31466800-31474200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
46 chr6:31466800-31477400 Weak transcription A549 lung
47 chr6:31466800-31481200 Weak transcription NHDF-Ad bronchial
48 chr6:31467000-31467400 Flanking Active TSS H1 Cell Line embryonic stem cell
49 chr6:31467000-31467400 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
50 chr6:31467000-31467400 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell

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