Variant report

Variant	rs5945140
Chromosome Location	chrX:154355630-154355631
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154307800-154357400	Weak transcription	Brain Hippocampus Middle	brain
2	chrX:154314600-154355800	Weak transcription	Brain Angular Gyrus	brain
3	chrX:154343000-154356600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chrX:154344000-154356600	Weak transcription	Pancreas	Pancrea
5	chrX:154345400-154356600	Weak transcription	Primary T cells from cord blood	blood
6	chrX:154350000-154356600	Weak transcription	A549	lung
7	chrX:154350200-154356800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chrX:154350400-154356000	Weak transcription	Adipose Nuclei	Adipose
9	chrX:154350600-154356200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chrX:154352000-154355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chrX:154352400-154356400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chrX:154352400-154356600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chrX:154355200-154356600	Enhancers	HepG2	liver

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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