Variant report

Variant rs4768119
Chromosome Location chr12:46807902-46807903
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46795000-46809200 Weak transcription Esophagus oesophagus
2 chr12:46797000-46819800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr12:46799000-46809200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr12:46801000-46808200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:46802000-46812200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr12:46803200-46809400 Weak transcription Left Ventricle heart
7 chr12:46804800-46808600 Weak transcription Osteobl bone
8 chr12:46804800-46809400 Weak transcription Adipose Nuclei Adipose
9 chr12:46805400-46809000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr12:46806400-46812000 Weak transcription Primary B cells from cord blood blood
11 chr12:46807400-46808400 Enhancers HUVEC blood vessel
12 chr12:46807400-46808600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr12:46807600-46808000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr12:46807600-46809000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr12:46807800-46808800 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr12:46807800-46809200 Enhancers NHEK skin
17 chr12:46807800-46809600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr12:46807800-46815600 Weak transcription HepG2 liver

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