Variant report

Variant	rs7837333
Chromosome Location	chr8:67840116-67840117
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000104218	Chromatin interaction
ENSG00000178125	Chromatin interaction
ENSG00000266491	Chromatin interaction
ENSG00000121022	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11780700	0.91[CHB][hapmap];0.85[CHD][hapmap]
rs11785782	0.84[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs68169458	0.81[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7837333	C8orf44///SGK3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67838000-67855000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:67838400-67840400	Weak transcription	GM12878-XiMat	blood
3	chr8:67838400-67840600	Weak transcription	Thymus	Thymus
4	chr8:67838400-67852800	Weak transcription	Psoas Muscle	Psoas
5	chr8:67838600-67841600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr8:67838600-67842800	Weak transcription	Right Atrium	heart
7	chr8:67839400-67840200	Flanking Active TSS	K562	blood

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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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