Variant report

Variant rs1674759
Chromosome Location chr1:161645259-161645260
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr1:161644600-161645400 Strong transcription Primary B cells from peripheral blood blood
7 chr1:161644800-161648400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:161644800-161648800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:161645000-161646800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr1:161645200-161645600 Genic enhancers Fetal Adrenal Gland Adrenal Gland
11 chr1:161645200-161647200 Weak transcription Spleen Spleen

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