Variant report

Variant	rs4944144
Chromosome Location	chr11:76869774-76869775
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10793238	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11607721	0.81[CEU][hapmap]
rs2156568	0.96[CEU][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3737454	0.90[JPT][hapmap]
rs4944145	0.84[YRI][hapmap]
rs4944146	0.96[CEU][hapmap];0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4944147	0.81[CEU][hapmap]
rs4945151	1.00[CEU][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4945152	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4945153	0.96[CEU][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6592710	0.87[EUR][1000 genomes]
rs7104528	0.92[CEU][hapmap];0.80[CHB][hapmap];0.90[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs762667	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7924655	0.93[CEU][hapmap];0.91[JPT][hapmap];0.86[EUR][1000 genomes]
rs7937262	0.96[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7943982	0.96[CEU][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][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	esv1816632	chr11:76751285-76927014	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76852800-76873000	Weak transcription	Ovary	ovary
2	chr11:76862400-76872000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:76864800-76882200	Weak transcription	HepG2	liver
4	chr11:76865000-76882800	Strong transcription	Fetal Intestine Large	intestine
5	chr11:76865600-76882000	Strong transcription	Fetal Intestine Small	intestine
6	chr11:76866000-76872400	Weak transcription	Spleen	Spleen
7	chr11:76866800-76870600	Strong transcription	Liver	Liver
8	chr11:76868400-76870200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:76868800-76870000	Enhancers	Placenta	Placenta
10	chr11:76869000-76870800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr11:76869200-76870000	Bivalent Enhancer	NHEK	skin
12	chr11:76869400-76889200	Weak transcription	Pancreas	Pancrea
13	chr11:76869600-76870000	Weak transcription	Gastric	stomach

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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