The 2.0 version of rSNPBase

Variant report

Variant rs74128393
Chromosome Location chr1:174377099-174377100
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174325800-174382800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr1:174353000-174382600 Weak transcription Primary T killer naive cells fromperipheralblood blood
3 chr1:174360000-174383000 Weak transcription Right Atrium heart
4 chr1:174361600-174382800 Weak transcription Primary T helper naive cells from peripheral blood blood
5 chr1:174363200-174382800 Weak transcription Left Ventricle heart
6 chr1:174367000-174382800 Weak transcription Primary T helper naive cells fromperipheralblood blood
7 chr1:174369400-174383000 Weak transcription GM12878-XiMat blood
8 chr1:174371200-174377200 Weak transcription Primary T cells from cord blood blood
9 chr1:174371200-174379000 Weak transcription Primary B cells from cord blood blood
10 chr1:174373000-174382800 Weak transcription Primary B cells from peripheral blood blood
11 chr1:174375800-174377800 Enhancers NHDF-Ad bronchial
12 chr1:174376000-174387200 Weak transcription Gastric stomach
13 chr1:174376200-174382800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:174377000-174383200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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Last update: Aug 31, 2015