Variant report

Variant	rs9947074
Chromosome Location	chr18:30278974-30278975
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12104007	1.00[AMR][1000 genomes]
rs16963999	1.00[AMR][1000 genomes]
rs16964005	1.00[AMR][1000 genomes]
rs16964017	1.00[AMR][1000 genomes]
rs16964035	1.00[AMR][1000 genomes]
rs16964036	1.00[AMR][1000 genomes]
rs16964062	1.00[AMR][1000 genomes]
rs16964082	1.00[AMR][1000 genomes]
rs16964115	1.00[AMR][1000 genomes]
rs16964116	1.00[AMR][1000 genomes]
rs16964117	1.00[AMR][1000 genomes]
rs28458243	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28496433	1.00[AMR][1000 genomes]
rs28771668	1.00[AMR][1000 genomes]
rs55742357	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56017479	1.00[AMR][1000 genomes]
rs61164044	1.00[AMR][1000 genomes]
rs9783891	1.00[AMR][1000 genomes]
rs9783904	1.00[AMR][1000 genomes]
rs9944992	1.00[AMR][1000 genomes]
rs9945125	1.00[AMR][1000 genomes]
rs9949048	1.00[AMR][1000 genomes]
rs9949112	1.00[AMR][1000 genomes]
rs9949158	1.00[AMR][1000 genomes]
rs9951977	1.00[AMR][1000 genomes]
rs9956243	1.00[AMR][1000 genomes]
rs9956679	1.00[AMR][1000 genomes]
rs9958205	1.00[AMR][1000 genomes]
rs9963068	1.00[AMR][1000 genomes]
rs9965451	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060732	chr18:30267156-30304435	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1062187	chr18:30267156-30306081	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1056335	chr18:30267904-30305840	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1059928	chr18:30267904-30306081	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1062522	chr18:30268383-30306081	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30260400-30282200	Weak transcription	Fetal Kidney	kidney
2	chr18:30275400-30284000	Weak transcription	Primary B cells from cord blood	blood
3	chr18:30276000-30284200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr18:30277200-30286000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:30278000-30280200	Enhancers	HepG2	liver
6	chr18:30278200-30279200	Enhancers	Stomach Mucosa	stomach
7	chr18:30278200-30279200	Enhancers	HUVEC	blood vessel
8	chr18:30278200-30279600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr18:30278800-30287400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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