Variant report

Variant rs61819949
Chromosome Location chr1:209732150-209732151
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209726400-209735600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:209726600-209737800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:209726800-209738400 Weak transcription NHEK skin
4 chr1:209727000-209734000 Weak transcription HSMM muscle
5 chr1:209727000-209737600 Weak transcription HMEC breast
6 chr1:209728600-209738200 Weak transcription Esophagus oesophagus
7 chr1:209729400-209734200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr1:209729800-209733800 Weak transcription Fetal Kidney kidney
9 chr1:209730000-209732200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:209730200-209734200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr1:209730400-209735000 Weak transcription ES-WA7 Cell Line embryonic stem cell
12 chr1:209730600-209733800 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr1:209730800-209733800 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr1:209731400-209734000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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