Variant report

Variant rs13376485
Chromosome Location chr1:161645877-161645878
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161633600-161646400 Weak transcription Primary B cells from cord blood blood
2 chr1:161641600-161647000 Weak transcription Pancreas Pancrea
3 chr1:161641600-161648200 Weak transcription K562 blood
4 chr1:161642600-161646000 Weak transcription GM12878-XiMat blood
5 chr1:161642600-161646200 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr1:161644800-161648400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:161644800-161648800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr1:161645000-161646800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:161645200-161647200 Weak transcription Spleen Spleen
10 chr1:161645400-161646800 Weak transcription Primary B cells from peripheral blood blood
11 chr1:161645600-161647400 Enhancers Brain Angular Gyrus brain
12 chr1:161645600-161648800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr1:161645800-161647600 Enhancers Brain Cingulate Gyrus brain

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