Variant report

Variant rs333436
Chromosome Location chr1:174708207-174708208
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174678200-174708600 Weak transcription Primary T cells from cord blood blood
2 chr1:174696600-174709400 Weak transcription GM12878-XiMat blood
3 chr1:174705800-174712200 Weak transcription Left Ventricle heart
4 chr1:174706000-174730400 Weak transcription Aorta Aorta
5 chr1:174706200-174708600 Weak transcription Fetal Intestine Large intestine
6 chr1:174706200-174709400 Weak transcription Primary B cells from cord blood blood
7 chr1:174706200-174734000 Weak transcription Primary B cells from peripheral blood blood
8 chr1:174707000-174709800 Weak transcription Fetal Intestine Small intestine
9 chr1:174707200-174715000 Weak transcription Fetal Heart heart
10 chr1:174707600-174712200 Weak transcription Liver Liver
11 chr1:174708000-174722000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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