Variant report

Variant rs72649977
Chromosome Location chr1:211708348-211708349
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211689400-211715000 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:211701600-211711000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:211701800-211712400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr1:211702600-211711600 Weak transcription Spleen Spleen
5 chr1:211703400-211711600 Weak transcription Esophagus oesophagus
6 chr1:211703800-211708800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:211704400-211710000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:211705200-211714600 Weak transcription Right Atrium heart
9 chr1:211705600-211711600 Weak transcription Fetal Heart heart
10 chr1:211705600-211714800 Weak transcription Brain Anterior Caudate brain
11 chr1:211705600-211714800 Weak transcription Right Ventricle heart
12 chr1:211705800-211710600 Weak transcription K562 blood
13 chr1:211707400-211709600 Enhancers Liver Liver
14 chr1:211707800-211708400 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr1:211708200-211714600 Weak transcription Pancreas Pancrea

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