Variant report

Variant rs6596835
Chromosome Location chr6:212006-212007
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:210400-213600 Enhancers GM12878-XiMat blood
2 chr6:210400-215200 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr6:210600-215400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
4 chr6:210600-215400 Weak transcription Primary T regulatory cells fromperipheralblood blood
5 chr6:210800-215400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr6:211400-212200 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
7 chr6:211600-212200 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr6:211800-212200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:211800-212200 Flanking Active TSS Brain Anterior Caudate brain
10 chr6:211800-212200 Flanking Active TSS Brain Cingulate Gyrus brain
11 chr6:211800-212200 Flanking Active TSS Brain Substantia Nigra brain
12 chr6:211800-212200 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr6:211800-212200 Enhancers Right Atrium heart
14 chr6:211800-212200 Enhancers NHEK skin
15 chr6:211800-212400 Enhancers Brain Inferior Temporal Lobe brain
16 chr6:212000-212200 Bivalent Enhancer Adipose Nuclei Adipose
17 chr6:212000-212200 Flanking Bivalent TSS/Enh Stomach Smooth Muscle stomach
18 chr6:212000-212400 Enhancers Brain Germinal Matrix brain
19 chr6:212000-212400 Flanking Active TSS Brain Hippocampus Middle brain

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