Variant report

Variant rs184076347
Chromosome Location chr16:74362832-74362833
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:123 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:74331800-74366400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr16:74332800-74401200 Weak transcription Stomach Mucosa stomach
3 chr16:74339600-74394000 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr16:74340600-74387000 Weak transcription Hela-S3 cervix
5 chr16:74340800-74400200 Weak transcription Primary T killer memory cells from peripheral blood blood
6 chr16:74341400-74366600 Weak transcription A549 lung
7 chr16:74341400-74371600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr16:74341400-74376200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr16:74341400-74400800 Weak transcription NH-A brain
10 chr16:74341600-74364200 Weak transcription Muscle Satellite Cultured Cells --
11 chr16:74341600-74364200 Weak transcription Esophagus oesophagus
12 chr16:74341600-74366400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr16:74341600-74371200 Weak transcription HUVEC blood vessel
14 chr16:74355200-74400800 Weak transcription Fetal Brain Male brain
15 chr16:74355600-74382200 Weak transcription GM12878-XiMat blood
16 chr16:74356600-74371400 Weak transcription ES-I3 Cell Line embryonic stem cell
17 chr16:74357600-74367600 Strong transcription Fetal Stomach stomach
18 chr16:74357800-74367600 Strong transcription Fetal Adrenal Gland Adrenal Gland
19 chr16:74358200-74367200 Strong transcription Fetal Intestine Small intestine
20 chr16:74359200-74363000 Strong transcription Stomach Smooth Muscle stomach
21 chr16:74359400-74367200 Strong transcription iPS-20b Cell Line embryonic stem cell
22 chr16:74359600-74364200 Weak transcription Colonic Mucosa Colon
23 chr16:74360000-74364800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
24 chr16:74360000-74378200 Weak transcription Primary B cells from cord blood blood
25 chr16:74360000-74401400 Weak transcription Small Intestine intestine
26 chr16:74360400-74364200 Weak transcription Rectal Smooth Muscle rectum
27 chr16:74360400-74364400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
28 chr16:74360600-74364200 Weak transcription Thymus Thymus
29 chr16:74360600-74364400 Weak transcription Lung lung
30 chr16:74360600-74364800 Weak transcription Brain Germinal Matrix brain
31 chr16:74360600-74364800 Weak transcription NHLF lung
32 chr16:74360600-74366600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
33 chr16:74360600-74371600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
34 chr16:74360600-74382600 Weak transcription HSMMtube muscle
35 chr16:74360800-74364400 Weak transcription Brain Substantia Nigra brain
36 chr16:74360800-74364400 Weak transcription Gastric stomach
37 chr16:74360800-74364600 Weak transcription Brain Cingulate Gyrus brain
38 chr16:74360800-74364800 Weak transcription Placenta Amnion Placenta Amnion
39 chr16:74360800-74364800 Weak transcription Right Ventricle heart
40 chr16:74360800-74366400 Weak transcription Brain Angular Gyrus brain
41 chr16:74360800-74383000 Weak transcription Primary T killer naive cells fromperipheralblood blood
42 chr16:74361000-74364200 Weak transcription Brain Hippocampus Middle brain
43 chr16:74361000-74364600 Weak transcription iPS-18 Cell Line embryonic stem cell
44 chr16:74361000-74364600 Weak transcription Primary T regulatory cells fromperipheralblood blood
45 chr16:74361000-74364800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
46 chr16:74361000-74366000 Weak transcription Fetal Lung lung
47 chr16:74361000-74366400 Weak transcription iPS-15b Cell Line embryonic stem cell
48 chr16:74361000-74366600 Weak transcription Colon Smooth Muscle Colon
49 chr16:74361000-74382000 Weak transcription Fetal Kidney kidney
50 chr16:74361000-74385000 Weak transcription K562 blood

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