Variant report

Variant	rs36095821
Chromosome Location	chr10:44844416-44844417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10508884	0.98[ASN][1000 genomes]
rs11238991	1.00[ASN][1000 genomes]
rs11815919	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12569869	0.91[ASN][1000 genomes]
rs12573553	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17156139	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028101	1.00[ASN][1000 genomes]
rs34050695	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34066403	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34386578	0.91[ASN][1000 genomes]
rs35698464	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4366439	1.00[ASN][1000 genomes]
rs56376391	0.91[ASN][1000 genomes]
rs58666734	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs66868726	0.83[EUR][1000 genomes]
rs7904065	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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1052337	chr10:44821390-44865015	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44830600-44845200	Weak transcription	Pancreas	Pancrea
2	chr10:44831400-44847200	Weak transcription	Right Atrium	heart
3	chr10:44833600-44847400	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:44835800-44847400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr10:44836800-44847400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr10:44838600-44867400	Weak transcription	Spleen	Spleen
7	chr10:44838800-44847400	Weak transcription	Left Ventricle	heart
8	chr10:44839600-44848000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:44843200-44845200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr10:44843800-44847200	Weak transcription	Fetal Stomach	stomach
11	chr10:44843800-44847400	Weak transcription	Ovary	ovary
12	chr10:44844400-44847400	Weak transcription	Adipose Nuclei	Adipose

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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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