Variant report

Variant	rs12915175
Chromosome Location	chr15:74049061-74049062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1129484	0.98[ASN][1000 genomes]
rs11638072	0.81[ASN][1000 genomes]
rs12910404	0.85[ASN][1000 genomes]
rs12917099	0.86[ASN][1000 genomes]
rs1351159	0.81[ASN][1000 genomes]
rs1351161	0.81[ASN][1000 genomes]
rs1542544	0.81[ASN][1000 genomes]
rs2127019	0.82[ASN][1000 genomes]
rs2279154	0.82[ASN][1000 genomes]
rs2279155	0.82[ASN][1000 genomes]
rs28627084	0.81[ASN][1000 genomes]
rs28649098	0.82[ASN][1000 genomes]
rs4886892	0.81[ASN][1000 genomes]
rs4886896	0.81[ASN][1000 genomes]
rs4887036	0.82[ASN][1000 genomes]
rs4887039	0.82[ASN][1000 genomes]
rs4887114	0.86[ASN][1000 genomes]
rs8042653	0.81[ASN][1000 genomes]
rs896599	0.93[ASN][1000 genomes]
rs922457	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471252	chr15:74006691-74089793	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv569970	chr15:74016622-74059081	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74046000-74056200	Weak transcription	Right Atrium	heart
2	chr15:74046400-74050200	Weak transcription	Right Ventricle	heart
3	chr15:74046600-74052200	Weak transcription	Fetal Brain Male	brain
4	chr15:74046800-74050800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr15:74047400-74056200	Weak transcription	Esophagus	oesophagus
6	chr15:74047600-74051800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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