Variant report

Variant rs1223234
Chromosome Location chr1:226123389-226123390
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:226112600-226125200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:226112600-226126800 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr1:226112600-226126800 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr1:226112800-226126800 Weak transcription Right Atrium heart
5 chr1:226113000-226124000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:226113000-226124400 Weak transcription H9 Cell Line embryonic stem cell
7 chr1:226114800-226127000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:226116400-226124600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr1:226116600-226126800 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr1:226121000-226123800 Weak transcription NHEK skin
11 chr1:226121000-226124400 Weak transcription NHDF-Ad bronchial
12 chr1:226121400-226124000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:226121400-226124000 Weak transcription HMEC breast
14 chr1:226121400-226124400 Weak transcription Osteobl bone
15 chr1:226122600-226124000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr1:226123000-226124400 Weak transcription K562 blood

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