Variant report

Variant	rs61938965
Chromosome Location	chr12:118021383-118021384
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10774936	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10774937	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850846	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850847	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850848	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850851	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850854	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10850855	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11068563	0.92[EUR][1000 genomes]
rs11068565	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12308267	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12369419	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400590	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6490129	0.91[EUR][1000 genomes]
rs7132400	0.91[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	nsv832527	chr12:117974007-118110244	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118018000-118021400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr12:118019000-118025000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:118019200-118021400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr12:118019200-118021400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:118019200-118021400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr12:118019200-118021600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr12:118019600-118021400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:118020000-118021800	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr12:118020400-118021400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:118021200-118021400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:118021200-118021400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:118021200-118021600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:118021200-118022800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr12:118021200-118023000	Enhancers	ES-UCSF4 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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