Variant report

Variant rs538811702
Chromosome Location chr14:105323357-105323358
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105311000-105330600 Weak transcription Right Atrium heart
2 chr14:105312600-105329000 Weak transcription HMEC breast
3 chr14:105313200-105327600 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr14:105318800-105326200 Weak transcription Pancreas Pancrea
5 chr14:105319000-105325800 Weak transcription H9 Cell Line embryonic stem cell
6 chr14:105320200-105330400 Weak transcription Placenta Amnion Placenta Amnion
7 chr14:105321600-105329400 Weak transcription Rectal Mucosa Donor 29 rectum
8 chr14:105322000-105323800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr14:105322400-105323800 Enhancers Brain Cingulate Gyrus brain
10 chr14:105322800-105323800 Enhancers H1 Cell Line embryonic stem cell
11 chr14:105322800-105323800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr14:105322800-105323800 Flanking Active TSS Foreskin Melanocyte Primary Cells skin03 Skin
13 chr14:105322800-105328600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr14:105322800-105329000 Weak transcription Fetal Intestine Small intestine
15 chr14:105323000-105324000 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr14:105323000-105324000 Enhancers Brain Angular Gyrus brain
17 chr14:105323000-105328800 Weak transcription HepG2 liver
18 chr14:105323200-105323600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
19 chr14:105323200-105323600 Flanking Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
20 chr14:105323200-105323600 Enhancers Brain Hippocampus Middle brain
21 chr14:105323200-105324200 Enhancers ES-WA7 Cell Line embryonic stem cell
22 chr14:105323200-105327200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
23 chr14:105323200-105328800 Weak transcription NHEK skin

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