Variant report

Variant rs534379240
Chromosome Location chr2:86965637-86965638
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:86948800-86972600 Weak transcription Primary T helper naive cells from peripheral blood blood
2 chr2:86949000-86970200 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr2:86949000-86970200 Weak transcription Primary T regulatory cells fromperipheralblood blood
4 chr2:86949000-86970200 Weak transcription Fetal Intestine Small intestine
5 chr2:86949000-86979600 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr2:86951400-86970200 Weak transcription Primary T helper cells fromperipheralblood blood
7 chr2:86956400-86970400 Weak transcription Primary T cells fromperipheralblood blood
8 chr2:86956800-86971200 Weak transcription Skeletal Muscle Female skeletal muscle
9 chr2:86959600-86969800 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr2:86961600-86971200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
11 chr2:86962200-86975400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:86962200-86977000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr2:86963600-86969200 Weak transcription Fetal Thymus thymus
14 chr2:86963600-86972400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
15 chr2:86965200-86978800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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