Variant report

Variant rs227200
Chromosome Location chr1:210249486-210249487
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210224400-210250000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:210244400-210250000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:210246200-210250000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr1:210247600-210249800 Weak transcription Right Atrium heart
5 chr1:210247600-210253800 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr1:210248400-210250600 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr1:210248600-210250000 Weak transcription H1 Cell Line embryonic stem cell
8 chr1:210248600-210250200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr1:210248600-210250600 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr1:210248600-210250600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr1:210248600-210251600 Weak transcription Brain Angular Gyrus brain
12 chr1:210248600-210261000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr1:210248600-210273200 Weak transcription Fetal Brain Female brain

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