Variant report

Variant	rs1786566
Chromosome Location	chr18:11824358-11824359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:11822024..11824929-chr18:11829878..11831566,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10048315	0.81[CHB][hapmap]
rs10048316	0.80[CHB][hapmap]
rs10468681	0.93[CEU][hapmap];0.90[CHD][hapmap]
rs11080534	0.85[CHD][hapmap]
rs1249630	0.81[CEU][hapmap]
rs12607811	0.82[JPT][hapmap]
rs12962767	0.93[CEU][hapmap];0.85[CHB][hapmap];0.86[AMR][1000 genomes]
rs12965108	0.89[ASW][hapmap];0.93[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.80[LWK][hapmap];0.91[MEX][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12965256	0.93[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.86[AMR][1000 genomes]
rs1364632	0.89[ASW][hapmap];0.93[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.80[LWK][hapmap];0.91[MEX][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1477481	0.87[CHD][hapmap]
rs1613471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1614379	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1617064	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1617792	0.85[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs1647553	0.81[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1647554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1647555	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1647557	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1647558	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1647559	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1647560	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16976671	0.93[CEU][hapmap];0.85[CHB][hapmap];0.87[AMR][1000 genomes]
rs16976714	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16976739	0.82[JPT][hapmap]
rs1786563	0.81[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1786564	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1786565	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1786567	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1786568	0.82[CHD][hapmap]
rs1786569	0.81[CEU][hapmap]
rs1786573	0.83[CEU][hapmap]
rs2161961	0.93[CEU][hapmap];0.82[CHD][hapmap]
rs2848452	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28510090	0.88[ASN][1000 genomes]
rs28690612	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58359702	0.81[AMR][1000 genomes]
rs61636989	0.87[AMR][1000 genomes]
rs62097372	0.99[ASN][1000 genomes]
rs7231090	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7240632	0.93[CEU][hapmap];0.89[CHB][hapmap];0.89[AMR][1000 genomes]
rs7240684	0.81[CHB][hapmap]
rs9303748	0.87[CHD][hapmap]
rs9303749	0.93[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.83[MEX][hapmap]
rs9952489	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9955115	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9959502	0.80[ASN][1000 genomes]
rs9959605	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9962277	0.87[CHD][hapmap]
rs9962861	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9962908	0.89[ASW][hapmap];0.88[CEU][hapmap];0.86[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9963000	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9963158	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9963378	0.80[AMR][1000 genomes]
rs9966733	0.87[CEU][hapmap];0.80[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9972997	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3362008	chr18:11647654-11959830	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833590	chr18:11757329-11924539	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1055453	chr18:11776790-12110135	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv543654	chr18:11776790-12110135	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11783400-11829200	Weak transcription	Right Atrium	heart
2	chr18:11808000-11830600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr18:11820400-11824800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr18:11821200-11826600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr18:11821800-11826600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr18:11821800-11828800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr18:11822800-11832200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr18:11822800-11836600	Weak transcription	Hela-S3	cervix
9	chr18:11823800-11826200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr18:11823800-11826200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:11823800-11828800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr18:11823800-11829000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr18:11824000-11826200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr18:11824000-11826200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr18:11824000-11826400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr18:11824000-11826400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr18:11824000-11826600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr18:11824000-11829000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:11824200-11826600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr18:11824200-11826600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr18:11824200-11828800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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