Variant report

Variant rs10150704
Chromosome Location chr14:37690402-37690403
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37675800-37693600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr14:37676000-37695600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr14:37676600-37699400 Weak transcription A549 lung
4 chr14:37680000-37693600 Weak transcription K562 blood
5 chr14:37681000-37694200 Weak transcription Pancreas Pancrea
6 chr14:37681400-37693400 Weak transcription Brain Anterior Caudate brain
7 chr14:37682000-37693200 Weak transcription HepG2 liver
8 chr14:37682000-37695800 Weak transcription Gastric stomach
9 chr14:37684200-37694200 Weak transcription Aorta Aorta
10 chr14:37687800-37693200 Weak transcription Duodenum Smooth Muscle Duodenum
11 chr14:37690200-37693800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr14:37690400-37691000 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr14:37690400-37691000 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
14 chr14:37690400-37691000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr14:37690400-37691000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr14:37690400-37691000 ZNF genes & repeats Ovary ovary
17 chr14:37690400-37691600 Strong transcription HUVEC blood vessel

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