Variant report

Variant	rs12149390
Chromosome Location	chr16:77135152-77135153
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:77129914..77131450-chr16:77133881..77136315,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11149959	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11149960	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11639600	0.95[AMR][1000 genomes]
rs11640047	0.92[AMR][1000 genomes]
rs11640246	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11645600	0.92[AMR][1000 genomes]
rs11647843	0.92[AMR][1000 genomes]
rs12149026	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12597268	0.92[AMR][1000 genomes]
rs12597818	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12597829	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12600205	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1393427	0.92[AMR][1000 genomes]
rs1393428	0.92[AMR][1000 genomes]
rs1393429	0.89[AMR][1000 genomes]
rs1393430	0.95[AMR][1000 genomes]
rs16945226	0.92[AMR][1000 genomes]
rs16945231	0.95[AMR][1000 genomes]
rs4888596	1.00[AMR][1000 genomes]
rs55658540	0.92[AMR][1000 genomes]
rs56293134	0.92[AMR][1000 genomes]
rs56346470	0.90[AMR][1000 genomes]
rs56763145	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs57539404	0.92[AMR][1000 genomes]
rs57588410	0.92[AMR][1000 genomes]
rs57816702	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58216456	0.92[AMR][1000 genomes]
rs58759340	0.82[EUR][1000 genomes]
rs58815676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60444907	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60508128	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61701158	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794594	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72794597	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794598	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794599	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794600	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794601	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72794602	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72796505	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72796511	0.92[AMR][1000 genomes]
rs7500211	0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063069	chr16:76462850-77214064	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv542963	chr16:76462850-77214064	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv906947	chr16:76682263-77160626	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
4	nsv869201	chr16:76714549-77233646	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
5	nsv1057677	chr16:76861946-77230013	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
6	nsv1065343	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv542965	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv906952	chr16:76944357-77155717	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1055234	chr16:77003426-77467286	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	nsv1065048	chr16:77003426-77675163	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
11	esv2830376	chr16:77014551-77658185	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
12	nsv1065149	chr16:77032082-77671890	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
13	nsv1062349	chr16:77039764-77458731	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
14	nsv542967	chr16:77039764-77458731	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
15	nsv906953	chr16:77125102-77152334	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv573122	chr16:77130339-77152334	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv573123	chr16:77130339-77160626	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77134800-77135800	Weak transcription	Fetal Lung	lung

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