Variant report

Variant rs16846717
Chromosome Location chr1:174121318-174121319
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174118800-174121600 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr1:174120000-174128000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:174120200-174122000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:174120400-174121800 Enhancers Hela-S3 cervix
5 chr1:174121000-174123400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
6 chr1:174121200-174123200 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
7 chr1:174121200-174123400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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