Variant report

Variant rs227227
Chromosome Location chr1:210195000-210195001
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210183600-210198000 Weak transcription HMEC breast
2 chr1:210189400-210195200 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:210192800-210197800 Weak transcription Brain Inferior Temporal Lobe brain
4 chr1:210193400-210221000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:210194200-210195200 Strong transcription HUES48 Cell Line embryonic stem cell
6 chr1:210194200-210195200 Enhancers Fetal Brain Female brain
7 chr1:210194200-210195400 Enhancers Fetal Brain Male brain
8 chr1:210194400-210195000 Strong transcription HUES64 Cell Line embryonic stem cell
9 chr1:210194400-210195000 Strong transcription iPS-18 Cell Line embryonic stem cell
10 chr1:210194400-210195400 Strong transcription iPS-20b Cell Line embryonic stem cell
11 chr1:210194400-210196400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:210194800-210212400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr1:210195000-210201800 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr1:210195000-210221200 Weak transcription iPS-18 Cell Line embryonic stem cell

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