Variant report

Variant rs473473
Chromosome Location chr6:74322512-74322513
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:119 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:74289600-74323800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:74290600-74338800 Weak transcription Ovary ovary
3 chr6:74291000-74323600 Weak transcription H1 Cell Line embryonic stem cell
4 chr6:74296200-74332000 Weak transcription Placenta Amnion Placenta Amnion
5 chr6:74296400-74325800 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr6:74296400-74354800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:74296400-74354800 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr6:74296400-74355000 Weak transcription Fetal Brain Male brain
9 chr6:74296600-74324000 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr6:74296600-74324200 Weak transcription Primary T killer memory cells from peripheral blood blood
11 chr6:74296600-74324400 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr6:74296600-74344000 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr6:74296800-74334000 Weak transcription Fetal Lung lung
14 chr6:74297000-74361800 Weak transcription GM12878-XiMat blood
15 chr6:74300800-74323600 Weak transcription Esophagus oesophagus
16 chr6:74303400-74355000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr6:74307200-74362400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
18 chr6:74307600-74356400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr6:74308000-74340200 Weak transcription Brain Substantia Nigra brain
20 chr6:74308400-74329000 Weak transcription NHEK skin
21 chr6:74311200-74355000 Weak transcription iPS-18 Cell Line embryonic stem cell
22 chr6:74311800-74324800 Weak transcription K562 blood
23 chr6:74312600-74332400 Strong transcription Primary neutrophils fromperipheralblood blood
24 chr6:74313200-74325000 Strong transcription Fetal Intestine Large intestine
25 chr6:74313200-74331800 Strong transcription Fetal Muscle Leg muscle
26 chr6:74313800-74331200 Strong transcription Fetal Muscle Trunk muscle
27 chr6:74314200-74362800 Weak transcription Stomach Mucosa stomach
28 chr6:74314400-74346400 Weak transcription Psoas Muscle Psoas
29 chr6:74314600-74323600 Weak transcription Pancreas Pancrea
30 chr6:74315000-74326000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
31 chr6:74315200-74348800 Weak transcription HMEC breast
32 chr6:74315400-74345200 Weak transcription ES-WA7 Cell Line embryonic stem cell
33 chr6:74315600-74362800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
34 chr6:74316000-74325400 Strong transcription Primary T cells from cord blood blood
35 chr6:74316200-74347000 Strong transcription Fetal Intestine Small intestine
36 chr6:74316400-74349200 Weak transcription HUVEC blood vessel
37 chr6:74316600-74355000 Weak transcription H9 Cell Line embryonic stem cell
38 chr6:74316800-74324200 Weak transcription NHLF lung
39 chr6:74318400-74350000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
40 chr6:74318400-74355000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
41 chr6:74318600-74323600 Weak transcription Cortex derived primary cultured neurospheres brain
42 chr6:74318600-74323800 Weak transcription Brain Cingulate Gyrus brain
43 chr6:74318800-74323600 Weak transcription Gastric stomach
44 chr6:74318800-74323800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
45 chr6:74318800-74324000 Weak transcription Fetal Brain Female brain
46 chr6:74318800-74324200 Weak transcription Spleen Spleen
47 chr6:74318800-74324600 Weak transcription Small Intestine intestine
48 chr6:74318800-74355200 Weak transcription Colonic Mucosa Colon
49 chr6:74319000-74341200 Weak transcription NH-A brain
50 chr6:74319400-74323400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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