Variant report

Variant rs16827656
Chromosome Location chr1:161640824-161640825
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 chr1:161640800-161641000 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr1:161640800-161641200 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr1:161640800-161641200 Strong transcription GM12878-XiMat blood
5 chr1:161640800-161641600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:161640800-161641600 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:161640800-161641600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:161640800-161641600 Enhancers K562 blood
9 chr1:161640800-161641800 Enhancers H1 Cell Line embryonic stem cell
10 chr1:161640800-161641800 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr1:161640800-161642000 Enhancers Cortex derived primary cultured neurospheres brain
12 chr1:161640800-161642400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr1:161640800-161643800 Strong transcription Primary B cells from peripheral blood blood

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