Variant report

Variant rs10853731
Chromosome Location chr19:40405162-40405163
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:40399200-40411800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr19:40400200-40410600 Weak transcription Fetal Stomach stomach
3 chr19:40402000-40419600 Weak transcription Rectal Smooth Muscle rectum
4 chr19:40402800-40406000 Strong transcription Sigmoid Colon Sigmoid Colon
5 chr19:40403800-40405400 Enhancers Primary T helper naive cells fromperipheralblood blood
6 chr19:40403800-40405400 Enhancers Primary T helper 17 cells PMA-I stimulated --
7 chr19:40404000-40406000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr19:40404200-40405200 Weak transcription Spleen Spleen
9 chr19:40404200-40410600 Weak transcription Rectal Mucosa Donor 29 rectum
10 chr19:40404400-40412000 Weak transcription Colonic Mucosa Colon
11 chr19:40404600-40405200 Weak transcription Rectal Mucosa Donor 31 rectum
12 chr19:40404600-40405600 Weak transcription Fetal Thymus thymus
13 chr19:40404600-40407600 Weak transcription Primary T cells from cord blood blood
14 chr19:40404600-40408000 Weak transcription Duodenum Mucosa Duodenum
15 chr19:40404600-40409000 Weak transcription HepG2 liver
16 chr19:40404600-40412800 Weak transcription A549 lung
17 chr19:40404600-40414800 Weak transcription Stomach Mucosa stomach
18 chr19:40404600-40421000 Weak transcription Fetal Intestine Small intestine
19 chr19:40404800-40419600 Weak transcription Fetal Intestine Large intestine
20 chr19:40404800-40429600 Weak transcription Primary B cells from cord blood blood

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