Variant report

Variant	rs2761187
Chromosome Location	chr1:172099086-172099087
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10752861	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12090953	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2761184	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2761185	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2761186	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2761190	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2819531	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28378748	0.82[EUR][1000 genomes]
rs4244191	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4641331	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4916242	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6425637	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6425638	0.82[EUR][1000 genomes]
rs6665598	0.82[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532342	chr1:171922237-172133785	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172049400-172110800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:172062400-172109200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr1:172069200-172102000	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:172077200-172110600	Weak transcription	Brain Angular Gyrus	brain
5	chr1:172077400-172099400	Weak transcription	Fetal Brain Female	brain
6	chr1:172085800-172113400	Weak transcription	Pancreas	Pancrea
7	chr1:172090000-172109600	Weak transcription	Brain Germinal Matrix	brain
8	chr1:172090400-172108800	Weak transcription	Fetal Stomach	stomach
9	chr1:172090800-172102200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:172092000-172102800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:172094600-172110600	Weak transcription	Left Ventricle	heart
12	chr1:172095400-172102000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr1:172096000-172103200	Weak transcription	Gastric	stomach
14	chr1:172096400-172110600	Weak transcription	Brain Substantia Nigra	brain
15	chr1:172097600-172101600	Weak transcription	Brain Anterior Caudate	brain
16	chr1:172097600-172102000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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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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