Variant report

Variant rs10496319
Chromosome Location chr2:86079214-86079215
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:101 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:86055000-86080000 Weak transcription Duodenum Mucosa Duodenum
2 chr2:86055200-86080400 Weak transcription Colonic Mucosa Colon
3 chr2:86063800-86080200 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr2:86065200-86080000 Strong transcription Monocytes-CD14+_RO01746 blood
5 chr2:86065400-86079400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr2:86066000-86080600 Weak transcription Small Intestine intestine
7 chr2:86066000-86106200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:86066200-86081400 Weak transcription Right Ventricle heart
9 chr2:86066400-86091400 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr2:86067000-86099000 Weak transcription Gastric stomach
11 chr2:86067200-86087000 Weak transcription Fetal Brain Male brain
12 chr2:86067400-86080400 Weak transcription Left Ventricle heart
13 chr2:86067400-86084800 Weak transcription Ovary ovary
14 chr2:86067600-86086200 Weak transcription Fetal Brain Female brain
15 chr2:86067800-86080000 Weak transcription K562 blood
16 chr2:86069400-86080400 Weak transcription Stomach Mucosa stomach
17 chr2:86070800-86080200 Weak transcription HUVEC blood vessel
18 chr2:86071000-86080600 Weak transcription Fetal Intestine Large intestine
19 chr2:86071200-86079400 Strong transcription Dnd41 blood
20 chr2:86071400-86080800 Weak transcription Fetal Intestine Small intestine
21 chr2:86071800-86080800 Weak transcription Sigmoid Colon Sigmoid Colon
22 chr2:86071800-86096200 Weak transcription Pancreatic Islets Pancreatic Islet
23 chr2:86072000-86090400 Strong transcription Cortex derived primary cultured neurospheres brain
24 chr2:86072000-86096800 Weak transcription Psoas Muscle Psoas
25 chr2:86072200-86080000 Strong transcription Primary monocytes fromperipheralblood blood
26 chr2:86072800-86079400 Weak transcription Primary hematopoietic stem cells blood
27 chr2:86073000-86083600 Weak transcription HUES6 Cell Line embryonic stem cell
28 chr2:86074000-86089800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
29 chr2:86074600-86080000 Weak transcription HSMMtube muscle
30 chr2:86074600-86080800 Weak transcription Duodenum Smooth Muscle Duodenum
31 chr2:86074600-86089600 Weak transcription NH-A brain
32 chr2:86074800-86086200 Weak transcription HSMM muscle
33 chr2:86075200-86082400 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
34 chr2:86075400-86080000 Weak transcription Pancreas Pancrea
35 chr2:86075400-86114000 Weak transcription Aorta Aorta
36 chr2:86076000-86090400 Strong transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
37 chr2:86076800-86081000 Strong transcription Liver Liver
38 chr2:86076800-86081400 Weak transcription Right Atrium heart
39 chr2:86077200-86079600 Genic enhancers Primary B cells from peripheral blood blood
40 chr2:86077200-86088600 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
41 chr2:86077400-86079600 Strong transcription Osteobl bone
42 chr2:86077400-86079800 Genic enhancers Primary mononuclear cells fromperipheralblood Blood
43 chr2:86077400-86080000 Strong transcription Fetal Adrenal Gland Adrenal Gland
44 chr2:86077600-86079600 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
45 chr2:86077600-86079600 Strong transcription Brain Germinal Matrix brain
46 chr2:86077600-86080200 Genic enhancers Fetal Thymus thymus
47 chr2:86077600-86082400 Strong transcription IMR90 fetal lung fibroblasts Cell Line lung
48 chr2:86077800-86079400 Strong transcription Primary hematopoietic stem cells short term culture blood
49 chr2:86078200-86080000 Genic enhancers Brain Hippocampus Middle brain
50 chr2:86078200-86080200 Genic enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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