Variant report

Variant rs555376426
Chromosome Location chr1:174794598-174794599
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174772200-174796600 Weak transcription Primary T helper cells PMA-I stimulated --
2 chr1:174777600-174799800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:174782000-174800800 Weak transcription Duodenum Mucosa Duodenum
4 chr1:174782200-174794800 Weak transcription Fetal Intestine Small intestine
5 chr1:174782200-174813000 Weak transcription Primary T regulatory cells fromperipheralblood blood
6 chr1:174782600-174799200 Weak transcription Liver Liver
7 chr1:174784400-174797200 Weak transcription Esophagus oesophagus
8 chr1:174784800-174806600 Weak transcription HSMMtube muscle
9 chr1:174785600-174796000 Weak transcription Primary B cells from cord blood blood
10 chr1:174785600-174796800 Weak transcription Primary B cells from peripheral blood blood
11 chr1:174786800-174798200 Weak transcription Left Ventricle heart
12 chr1:174789000-174797400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr1:174792600-174801600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
14 chr1:174794000-174795800 Enhancers Thymus Thymus
15 chr1:174794200-174796400 Enhancers Fetal Thymus thymus
16 chr1:174794400-174797400 Weak transcription NHEK skin

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