Variant report

Variant	rs1836996
Chromosome Location	chr15:62368895-62368896
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:62368123..62372059-chr15:62380802..62384502,3	K562	blood:
2	chr15:62367214..62369987-chr15:62379884..62381677,2	MCF-7	breast:
3	chr15:62358113..62359712-chr15:62366749..62369204,2	MCF-7	breast:
4	chr15:62358486..62361832-chr15:62367406..62369384,3	MCF-7	breast:
5	chr15:62364286..62366641-chr15:62368283..62370031,2	MCF-7	breast:
6	chr15:62367794..62369962-chr15:62404995..62406833,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198535	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10047986	0.93[ASN][1000 genomes]
rs1030859	0.97[ASN][1000 genomes]
rs1030860	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1030861	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10468026	0.85[ASN][1000 genomes]
rs10468027	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10519153	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10851707	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11071650	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11629596	0.96[ASN][1000 genomes]
rs11630347	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11632441	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11633500	0.84[ASN][1000 genomes]
rs11635977	0.97[ASN][1000 genomes]
rs11639147	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12438690	0.86[ASN][1000 genomes]
rs12438803	0.93[ASN][1000 genomes]
rs12439356	0.86[ASN][1000 genomes]
rs12442212	0.87[ASN][1000 genomes]
rs12442589	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12442675	0.85[ASN][1000 genomes]
rs12592402	0.85[ASN][1000 genomes]
rs12592464	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12898209	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12900703	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12901575	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12913951	0.93[ASN][1000 genomes]
rs1370177	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1436958	0.81[ASN][1000 genomes]
rs1436959	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1436961	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1436963	0.93[ASN][1000 genomes]
rs1436964	0.93[ASN][1000 genomes]
rs1436965	0.83[AFR][1000 genomes]
rs1534542	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1561197	0.88[AFR][1000 genomes]
rs17205407	0.93[ASN][1000 genomes]
rs17205463	0.86[ASN][1000 genomes]
rs17271403	0.93[ASN][1000 genomes]
rs17271438	0.88[ASN][1000 genomes]
rs2414754	0.80[EUR][1000 genomes]
rs2414759	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28542204	0.97[ASN][1000 genomes]
rs2899677	0.81[ASN][1000 genomes]
rs34096515	0.88[ASN][1000 genomes]
rs34138933	0.81[ASN][1000 genomes]
rs3784445	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4143841	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4143842	0.93[ASN][1000 genomes]
rs4143843	0.83[ASN][1000 genomes]
rs4372632	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4564516	0.97[ASN][1000 genomes]
rs4638519	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4775455	0.85[ASN][1000 genomes]
rs4775457	0.93[ASN][1000 genomes]
rs4775458	0.93[ASN][1000 genomes]
rs7161883	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7162536	0.93[ASN][1000 genomes]
rs7167876	0.84[AFR][1000 genomes]
rs7168164	0.86[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7177276	0.88[ASN][1000 genomes]
rs7177711	0.87[ASN][1000 genomes]
rs7178424	0.87[ASN][1000 genomes]
rs7178540	0.87[ASN][1000 genomes]
rs7178945	0.88[ASN][1000 genomes]
rs7182842	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs731820	0.88[ASN][1000 genomes]
rs8025404	0.81[EUR][1000 genomes]
rs8025877	0.88[ASN][1000 genomes]
rs8026008	0.88[ASN][1000 genomes]
rs8038932	0.96[ASN][1000 genomes]
rs8039651	0.97[ASN][1000 genomes]
rs893158	0.88[ASN][1000 genomes]
rs9635310	0.89[EUR][1000 genomes]
rs9920758	0.86[EUR][1000 genomes]
rs9989353	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9989354	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv457176	chr15:62178695-62519658	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv569643	chr15:62178695-62519658	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv471247	chr15:62202481-62519658	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv569646	chr15:62202482-62519658	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv1044748	chr15:62276183-62521856	Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv542405	chr15:62276183-62521856	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv457178	chr15:62340126-62394324	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv569652	chr15:62340126-62394324	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	nsv1560	chr15:62354264-62399304	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv948606	chr15:62364932-63088916	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62367800-62379800	Weak transcription	Pancreas	Pancrea
2	chr15:62368400-62369400	Enhancers	Hela-S3	cervix

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