The 2.0 version of rSNPBase

Variant report

Variant rs6734495
Chromosome Location chr2:171734582-171734583
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171730000-171734600 Weak transcription NH-A brain
2 chr2:171730200-171734600 Weak transcription Primary B cells from peripheral blood blood
3 chr2:171730200-171734600 Weak transcription Hela-S3 cervix
4 chr2:171730200-171735000 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr2:171730400-171734600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr2:171730400-171734600 Weak transcription Primary T helper naive cells from peripheral blood blood
7 chr2:171730400-171734600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr2:171730400-171734600 Weak transcription Dnd41 blood
9 chr2:171730400-171734800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr2:171730600-171734600 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr2:171731200-171740400 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr2:171734000-171735200 Enhancers HMEC breast
13 chr2:171734200-171735200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:171734200-171735400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:171734400-171734600 Enhancers Pancreas Pancrea
16 chr2:171734400-171735400 Enhancers NHEK skin

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Last update: Aug 31, 2015