Variant report

Variant	rs7323422
Chromosome Location	chr13:50410180-50410181
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50396000-50414400	Weak transcription	Right Atrium	heart
2	chr13:50402200-50412800	Weak transcription	Fetal Intestine Small	intestine
3	chr13:50403000-50410200	Weak transcription	HepG2	liver
4	chr13:50404000-50410600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr13:50405800-50414200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr13:50406000-50410400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr13:50407800-50410600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr13:50407800-50410600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr13:50407800-50410800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr13:50407800-50410800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:50408000-50410200	Weak transcription	Esophagus	oesophagus
12	chr13:50408600-50410400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr13:50408800-50410200	Weak transcription	HMEC	breast
14	chr13:50408800-50410400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr13:50408800-50410400	Weak transcription	NHEK	skin
16	chr13:50409600-50410600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr13:50409800-50410600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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