Variant report

Variant rs35768943
Chromosome Location chr1:211873666-211873667
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211872200-211878800 Weak transcription Right Atrium heart
2 chr1:211872400-211874400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:211872400-211874800 Weak transcription K562 blood
4 chr1:211872600-211877000 Weak transcription Pancreas Pancrea
5 chr1:211872600-211877200 Weak transcription Spleen Spleen
6 chr1:211872600-211878000 Weak transcription HMEC breast
7 chr1:211872800-211876800 Weak transcription Brain Anterior Caudate brain
8 chr1:211872800-211877000 Weak transcription Fetal Thymus thymus
9 chr1:211872800-211884000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:211873000-211874600 Weak transcription GM12878-XiMat blood
11 chr1:211873000-211874600 Weak transcription NHEK skin
12 chr1:211873000-211875200 Weak transcription Brain Cingulate Gyrus brain
13 chr1:211873000-211875800 Weak transcription Brain Hippocampus Middle brain
14 chr1:211873000-211876000 Weak transcription Fetal Muscle Trunk muscle
15 chr1:211873000-211876400 Weak transcription Brain Inferior Temporal Lobe brain
16 chr1:211873000-211876400 Weak transcription Brain Substantia Nigra brain
17 chr1:211873000-211876600 Weak transcription Brain Angular Gyrus brain
18 chr1:211873000-211877600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr1:211873200-211874400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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