Variant report

Variant rs2456272
Chromosome Location chr16:12252055-12252056
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:70 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:12213800-12255400 Weak transcription Gastric stomach
2 chr16:12229800-12253600 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
3 chr16:12230200-12256200 Weak transcription Primary T regulatory cells fromperipheralblood blood
4 chr16:12231400-12268000 Weak transcription Pancreas Pancrea
5 chr16:12234600-12261600 Weak transcription Aorta Aorta
6 chr16:12234600-12265600 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr16:12242200-12252400 Weak transcription Brain Inferior Temporal Lobe brain
8 chr16:12242200-12252400 Weak transcription Left Ventricle heart
9 chr16:12242200-12252600 Weak transcription Brain Cingulate Gyrus brain
10 chr16:12242200-12252600 Weak transcription Skeletal Muscle Male skeletal muscle
11 chr16:12242200-12253800 Weak transcription Right Atrium heart
12 chr16:12242200-12255200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr16:12242200-12261600 Weak transcription Lung lung
14 chr16:12242200-12262800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
15 chr16:12242200-12299400 Weak transcription Primary T helper cells PMA-I stimulated --
16 chr16:12242400-12252400 Weak transcription Right Ventricle heart
17 chr16:12242400-12252600 Weak transcription Fetal Brain Female brain
18 chr16:12242400-12252800 Weak transcription Brain Anterior Caudate brain
19 chr16:12242400-12255800 Weak transcription Thymus Thymus
20 chr16:12242400-12256400 Weak transcription Fetal Kidney kidney
21 chr16:12242400-12264600 Weak transcription Primary T helper naive cells fromperipheralblood blood
22 chr16:12242400-12280600 Weak transcription Sigmoid Colon Sigmoid Colon
23 chr16:12243200-12255400 Weak transcription Psoas Muscle Psoas
24 chr16:12244000-12252800 Weak transcription Fetal Muscle Leg muscle
25 chr16:12244400-12255800 Weak transcription Duodenum Smooth Muscle Duodenum
26 chr16:12244800-12261200 Weak transcription Primary hematopoietic stem cells blood
27 chr16:12245600-12257200 Weak transcription Fetal Adrenal Gland Adrenal Gland
28 chr16:12245600-12261800 Weak transcription Fetal Thymus thymus
29 chr16:12246600-12252400 Weak transcription Brain Hippocampus Middle brain
30 chr16:12247000-12252400 Weak transcription Brain Substantia Nigra brain
31 chr16:12247400-12259400 Strong transcription Primary B cells from cord blood blood
32 chr16:12248000-12258400 Strong transcription Primary B cells from peripheral blood blood
33 chr16:12248200-12255200 Weak transcription Stomach Smooth Muscle stomach
34 chr16:12248800-12254000 Strong transcription Adipose Nuclei Adipose
35 chr16:12248800-12257800 Strong transcription Primary T cells from cord blood blood
36 chr16:12249600-12254000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
37 chr16:12249600-12256400 Weak transcription HepG2 liver
38 chr16:12249800-12252200 Weak transcription Monocytes-CD14+_RO01746 blood
39 chr16:12250000-12257000 Weak transcription Primary mononuclear cells fromperipheralblood Blood
40 chr16:12250000-12260800 Weak transcription Primary monocytes fromperipheralblood blood
41 chr16:12250600-12252800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
42 chr16:12250600-12253000 Genic enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
43 chr16:12250600-12254000 Enhancers HSMM muscle
44 chr16:12250800-12252800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
45 chr16:12251000-12252400 Weak transcription Fetal Muscle Trunk muscle
46 chr16:12251000-12252600 Enhancers Muscle Satellite Cultured Cells --
47 chr16:12251000-12253200 Enhancers NHDF-Ad bronchial
48 chr16:12251000-12253400 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
49 chr16:12251000-12253400 Weak transcription Fetal Stomach stomach
50 chr16:12251000-12255000 Enhancers NH-A brain

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