Variant report

Variant rs11799704
Chromosome Location chr1:174382778-174382779
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174325800-174382800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr1:174360000-174383000 Weak transcription Right Atrium heart
3 chr1:174361600-174382800 Weak transcription Primary T helper naive cells from peripheral blood blood
4 chr1:174363200-174382800 Weak transcription Left Ventricle heart
5 chr1:174367000-174382800 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr1:174369400-174383000 Weak transcription GM12878-XiMat blood
7 chr1:174373000-174382800 Weak transcription Primary B cells from peripheral blood blood
8 chr1:174376000-174387200 Weak transcription Gastric stomach
9 chr1:174376200-174382800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:174377000-174383200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:174380400-174382800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
12 chr1:174381200-174438800 Weak transcription Primary B cells from cord blood blood
13 chr1:174382000-174383600 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr1:174382200-174383400 Enhancers NHLF lung
15 chr1:174382400-174383600 Enhancers Primary T helper cells PMA-I stimulated --
16 chr1:174382600-174383400 Enhancers Primary T killer naive cells fromperipheralblood blood

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