Variant report

Variant rs12843613
Chromosome Location chrX:31256831-31256832
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:31235000-31282000 Weak transcription Left Ventricle heart
2 chrX:31243200-31281800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chrX:31245200-31282000 Weak transcription Duodenum Smooth Muscle Duodenum
4 chrX:31245400-31284000 Weak transcription HSMMtube muscle
5 chrX:31245600-31279800 Weak transcription HepG2 liver
6 chrX:31247000-31280200 Weak transcription Pancreas Pancrea
7 chrX:31253800-31259800 Strong transcription Hela-S3 cervix
8 chrX:31254000-31283200 Weak transcription Fetal Intestine Small intestine
9 chrX:31254200-31275200 Weak transcription Liver Liver
10 chrX:31255800-31258200 Weak transcription Primary B cells from cord blood blood
11 chrX:31255800-31259200 Weak transcription GM12878-XiMat blood
12 chrX:31256000-31257200 Enhancers HUES48 Cell Line embryonic stem cell
13 chrX:31256200-31257000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chrX:31256200-31257000 Enhancers H9 Cell Line embryonic stem cell
15 chrX:31256200-31257000 Enhancers HUES6 Cell Line embryonic stem cell
16 chrX:31256200-31257000 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chrX:31256200-31257200 Enhancers iPS-15b Cell Line embryonic stem cell
18 chrX:31256200-31257400 Enhancers ES-I3 Cell Line embryonic stem cell
19 chrX:31256200-31259200 Weak transcription Primary B cells from peripheral blood blood
20 chrX:31256400-31257400 Enhancers Fetal Heart heart
21 chrX:31256800-31257000 Enhancers Gastric stomach

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