Variant report

Variant rs11803350
Chromosome Location chr1:172684931-172684932
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172678400-172685800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr1:172679000-172685400 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
3 chr1:172679000-172685400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
4 chr1:172681000-172685400 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr1:172683400-172685000 Weak transcription HMEC breast
6 chr1:172683400-172689200 Weak transcription H1 Cell Line embryonic stem cell
7 chr1:172683600-172685000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr1:172684000-172688000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr1:172684000-172688400 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr1:172684000-172689000 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr1:172684000-172692400 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr1:172684600-172685000 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr1:172684600-172686200 Enhancers NHEK skin
14 chr1:172684800-172685600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:172684800-172685800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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