Variant report

Variant	rs6822350
Chromosome Location	chr4:30801477-30801478
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1032176	0.91[AFR][1000 genomes]
rs10517219	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13104581	0.91[AFR][1000 genomes]
rs1447360	0.89[EUR][1000 genomes]
rs28716204	0.84[EUR][1000 genomes]
rs4235010	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4368569	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4466008	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4498103	0.90[EUR][1000 genomes]
rs4504214	0.89[EUR][1000 genomes]
rs4557224	0.85[EUR][1000 genomes]
rs4611883	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4615135	0.89[EUR][1000 genomes]
rs6812005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6827723	0.90[EUR][1000 genomes]
rs7654583	0.89[EUR][1000 genomes]
rs9291548	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9291553	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30791200-30804400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:30791400-30802400	Weak transcription	Aorta	Aorta
3	chr4:30791400-30802600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:30791600-30809800	Weak transcription	Fetal Lung	lung
5	chr4:30794600-30803800	Weak transcription	HSMMtube	muscle
6	chr4:30794600-30805000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:30795800-30824000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:30796000-30810400	Weak transcription	Fetal Heart	heart
9	chr4:30796200-30803400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:30796200-30804200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:30801200-30803200	Weak transcription	NHEK	skin
12	chr4:30801200-30809600	Weak transcription	Fetal Stomach	stomach

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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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