Variant report

Variant	rs73396583
Chromosome Location	chr6:28068048-28068049
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10484404	0.87[EUR][1000 genomes]
rs1150685	0.84[EUR][1000 genomes]
rs1890809	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2622315	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56355079	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6929559	0.84[EUR][1000 genomes]
rs73396550	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7739332	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs73396583	AL022393.7	cis	Thyroid	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28058200-28072200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:28058800-28072000	Weak transcription	HMEC	breast
3	chr6:28059400-28072000	Weak transcription	Brain Substantia Nigra	brain
4	chr6:28061400-28072000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:28064600-28072200	Weak transcription	Placenta	Placenta
6	chr6:28067200-28072200	Weak transcription	Esophagus	oesophagus

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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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