Variant report

Variant rs2048976
Chromosome Location chr2:181888798-181888799
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181856800-181897200 Weak transcription Primary B cells from cord blood blood
2 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:181860000-181894800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:181873600-181889600 Weak transcription Colon Smooth Muscle Colon
6 chr2:181885000-181890600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr2:181885800-181889600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr2:181886000-181901200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:181887800-181889200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr2:181887800-181889800 Weak transcription Fetal Heart heart
11 chr2:181887800-181890800 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr2:181888200-181891000 Weak transcription HUES64 Cell Line embryonic stem cell

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