Variant report

Variant rs13376262
Chromosome Location chr1:211711013-211711014
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211689400-211715000 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:211701800-211712400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr1:211702600-211711600 Weak transcription Spleen Spleen
4 chr1:211703400-211711600 Weak transcription Esophagus oesophagus
5 chr1:211705200-211714600 Weak transcription Right Atrium heart
6 chr1:211705600-211711600 Weak transcription Fetal Heart heart
7 chr1:211705600-211714800 Weak transcription Brain Anterior Caudate brain
8 chr1:211705600-211714800 Weak transcription Right Ventricle heart
9 chr1:211708200-211714600 Weak transcription Pancreas Pancrea
10 chr1:211710000-211712600 Enhancers Stomach Mucosa stomach
11 chr1:211710200-211714600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr1:211710400-211711600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr1:211710600-211711200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:211710600-211711200 Enhancers K562 blood
15 chr1:211710600-211713000 Enhancers Fetal Muscle Trunk muscle
16 chr1:211710800-211711200 Enhancers Osteobl bone
17 chr1:211711000-211711200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr1:211711000-211712800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
19 chr1:211711000-211713000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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