Variant report

Variant	rs12375859
Chromosome Location	chr9:103143377-103143378
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10819758	1.00[ASN][1000 genomes]
rs10819760	1.00[ASN][1000 genomes]
rs10819765	1.00[ASN][1000 genomes]
rs10819766	1.00[ASN][1000 genomes]
rs10819768	1.00[ASN][1000 genomes]
rs10819771	0.81[EUR][1000 genomes]
rs10819772	0.82[EUR][1000 genomes]
rs10989047	1.00[ASN][1000 genomes]
rs10989050	1.00[ASN][1000 genomes]
rs10989051	1.00[ASN][1000 genomes]
rs10989062	1.00[ASN][1000 genomes]
rs10989063	1.00[ASN][1000 genomes]
rs10989068	1.00[ASN][1000 genomes]
rs10989069	1.00[ASN][1000 genomes]
rs10989072	1.00[ASN][1000 genomes]
rs10989073	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10989074	0.83[EUR][1000 genomes]
rs10989075	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10989077	1.00[ASN][1000 genomes]
rs11788648	1.00[ASN][1000 genomes]
rs11791943	1.00[ASN][1000 genomes]
rs11793726	1.00[ASN][1000 genomes]
rs11794753	1.00[ASN][1000 genomes]
rs11795004	1.00[ASN][1000 genomes]
rs12000794	0.83[EUR][1000 genomes]
rs12002124	0.87[EUR][1000 genomes]
rs12005177	1.00[ASN][1000 genomes]
rs12352336	1.00[ASN][1000 genomes]
rs12378432	0.89[AFR][1000 genomes]
rs12379480	1.00[ASN][1000 genomes]
rs13284601	0.81[EUR][1000 genomes]
rs3199998	1.00[ASN][1000 genomes]
rs41274951	1.00[ASN][1000 genomes]
rs41274961	1.00[ASN][1000 genomes]
rs62579387	1.00[ASN][1000 genomes]
rs7028101	1.00[ASN][1000 genomes]
rs7029342	1.00[ASN][1000 genomes]
rs7036972	1.00[ASN][1000 genomes]
rs7037122	1.00[ASN][1000 genomes]
rs7037419	1.00[ASN][1000 genomes]
rs7849019	1.00[ASN][1000 genomes]
rs7873560	1.00[ASN][1000 genomes]
rs7874036	1.00[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	nsv531599	chr9:102227922-103156864	Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv893623	chr9:102648036-103405197	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 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	chr9:103134400-103152600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:103140200-103145400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:103142800-103145400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:103142800-103145600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:103142800-103145600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:103142800-103145800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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