Variant report

Variant rs6696197
Chromosome Location chr1:174586998-174586999
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174568400-174588800 Weak transcription Esophagus oesophagus
2 chr1:174572600-174587800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr1:174572800-174606200 Weak transcription Primary T cells fromperipheralblood blood
4 chr1:174573000-174587200 Weak transcription Fetal Intestine Large intestine
5 chr1:174573200-174589000 Weak transcription Ovary ovary
6 chr1:174573400-174587000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr1:174573400-174587400 Weak transcription Primary T cells from cord blood blood
8 chr1:174574000-174587000 Weak transcription Primary B cells from cord blood blood
9 chr1:174574400-174588800 Weak transcription Primary B cells from peripheral blood blood
10 chr1:174582800-174606400 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr1:174583200-174589200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr1:174586800-174587200 ZNF genes & repeats Lung lung
13 chr1:174586800-174587600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
14 chr1:174586800-174587600 ZNF genes & repeats Pancreas Pancrea

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