Variant report

Variant	rs4798714
Chromosome Location	chr18:8893907-8893908
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12956773	1.00[ASW][hapmap]
rs17408774	0.86[EUR][1000 genomes]
rs4133048	1.00[EUR][1000 genomes]
rs4420597	0.95[EUR][1000 genomes]
rs4797335	0.86[EUR][1000 genomes]
rs4797336	0.86[EUR][1000 genomes]
rs4797337	0.86[EUR][1000 genomes]
rs4797338	1.00[EUR][1000 genomes]
rs4798698	0.89[CEU][hapmap]
rs4798699	0.90[EUR][1000 genomes]
rs4798702	1.00[EUR][1000 genomes]
rs4798711	1.00[EUR][1000 genomes]
rs4798712	1.00[EUR][1000 genomes]
rs4798713	1.00[EUR][1000 genomes]
rs4798715	1.00[EUR][1000 genomes]
rs58257250	1.00[ASN][1000 genomes]
rs73939583	0.94[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	nsv1064883	chr18:8709670-9133224	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv833584	chr18:8728616-8904213	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8891600-8894000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr18:8891600-8894600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr18:8891600-8895000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr18:8891600-8895200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr18:8891600-8895400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr18:8891800-8894600	Weak transcription	HSMMtube	muscle
7	chr18:8891800-8895000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr18:8891800-8896000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:8891800-8896000	Weak transcription	HMEC	breast
10	chr18:8891800-8903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr18:8892200-8894400	Weak transcription	Osteobl	bone
12	chr18:8892400-8894000	Weak transcription	A549	lung
13	chr18:8892400-8894400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr18:8892600-8894000	Weak transcription	NHDF-Ad	bronchial
15	chr18:8892600-8894400	Weak transcription	NHLF	lung
16	chr18:8893200-8894000	Flanking Active TSS	K562	blood
17	chr18:8893400-8894200	Enhancers	Colon Smooth Muscle	Colon

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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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