Variant report

Variant rs4451598
Chromosome Location chr1:174575714-174575715
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174566800-174586600 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr1:174568400-174588800 Weak transcription Esophagus oesophagus
3 chr1:174570400-174575800 Weak transcription Gastric stomach
4 chr1:174572600-174587800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
5 chr1:174572800-174606200 Weak transcription Primary T cells fromperipheralblood blood
6 chr1:174573000-174587200 Weak transcription Fetal Intestine Large intestine
7 chr1:174573200-174581800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr1:174573200-174589000 Weak transcription Ovary ovary
9 chr1:174573400-174577800 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr1:174573400-174584400 Weak transcription Fetal Stomach stomach
11 chr1:174573400-174586800 Weak transcription Pancreas Pancrea
12 chr1:174573400-174587000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr1:174573400-174587400 Weak transcription Primary T cells from cord blood blood
14 chr1:174573600-174584400 Weak transcription Fetal Intestine Small intestine
15 chr1:174574000-174587000 Weak transcription Primary B cells from cord blood blood
16 chr1:174574400-174588800 Weak transcription Primary B cells from peripheral blood blood

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