Variant report

Variant rs2187893
Chromosome Location chr1:172881927-172881928
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172879400-172884200 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:172880000-172883800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr1:172881200-172882400 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:172881400-172882200 ZNF genes & repeats NHLF lung
5 chr1:172881400-172883000 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:172881400-172883000 ZNF genes & repeats Dnd41 blood
7 chr1:172881400-172883000 ZNF genes & repeats NHEK skin
8 chr1:172881800-172882200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:172881800-172882200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr1:172881800-172882600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
11 chr1:172881800-172882600 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:172881800-172882800 ZNF genes & repeats HSMMtube muscle
13 chr1:172881800-172882800 ZNF genes & repeats HUVEC blood vessel
14 chr1:172881800-172883000 ZNF genes & repeats A549 lung

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