Variant report

Variant	rs1886980
Chromosome Location	chr6:34529374-34529375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
2	chr6:34520436..34525113-chr6:34525166..34530447,6	K562	blood:
3	chr6:34527055..34529917-chr6:34543453..34544974,2	MCF-7	breast:
4	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
5	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
6	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
7	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
8	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
9	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
10	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
11	chr6:34491195..34497458-chr6:34528901..34533837,5	K562	blood:
12	chr6:34216270..34217861-chr6:34527614..34529829,2	MCF-7	breast:
13	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:

No data

Variant related genes	Relation type
ENSG00000124664	Chromatin interaction
ENSG00000196114	Chromatin interaction
ENSG00000186577	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11754548	0.85[ASN][1000 genomes]
rs11756280	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs11756281	0.85[ASN][1000 genomes]
rs11758420	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs11758426	0.89[CHD][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs11758471	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs12660150	0.83[EUR][1000 genomes]
rs12660470	0.83[EUR][1000 genomes]
rs12661696	0.83[EUR][1000 genomes]
rs12663061	0.83[EUR][1000 genomes]
rs1409284	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2233637	0.92[ASN][1000 genomes]
rs2233639	0.84[CHD][hapmap];0.88[JPT][hapmap];0.92[ASN][1000 genomes]
rs2233647	1.00[CHB][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap]
rs2282249	0.90[ASN][1000 genomes]
rs2282251	0.92[ASN][1000 genomes]
rs2282252	0.92[ASN][1000 genomes]
rs2296575	0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs2395595	1.00[CHD][hapmap];0.88[JPT][hapmap];0.92[ASN][1000 genomes]
rs2395596	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34603400	0.83[EUR][1000 genomes]
rs3734362	1.00[CHB][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs3778069	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3778071	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3778075	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3798544	0.89[CHD][hapmap]
rs3798546	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3798549	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3798551	0.92[ASN][1000 genomes]
rs3798552	0.92[ASN][1000 genomes]
rs3800466	0.90[ASN][1000 genomes]
rs3800468	0.86[EUR][1000 genomes]
rs3822986	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3945698	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55660517	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56172934	1.00[AFR][1000 genomes]
rs56781192	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57705887	1.00[AFR][1000 genomes]
rs57769323	1.00[AFR][1000 genomes]
rs58067963	0.83[EUR][1000 genomes]
rs58218720	0.83[EUR][1000 genomes]
rs58264490	1.00[AFR][1000 genomes]
rs58302579	1.00[AFR][1000 genomes]
rs58741004	1.00[EUR][1000 genomes]
rs59316688	0.90[ASN][1000 genomes]
rs59428262	1.00[AFR][1000 genomes]
rs59719562	1.00[AFR][1000 genomes]
rs59736988	1.00[AFR][1000 genomes]
rs59738570	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59778290	0.90[ASN][1000 genomes]
rs60196871	0.93[AFR][1000 genomes]
rs60358080	0.90[ASN][1000 genomes]
rs60375159	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60793757	1.00[EUR][1000 genomes]
rs61453687	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6910822	0.88[AFR][1000 genomes]
rs6935147	1.00[AFR][1000 genomes]
rs73745005	1.00[AFR][1000 genomes]
rs73745006	0.95[AFR][1000 genomes]
rs73746683	0.95[AFR][1000 genomes]
rs73746688	1.00[AFR][1000 genomes]
rs7754038	0.85[ASN][1000 genomes]
rs7759185	0.92[YRI][hapmap];1.00[AFR][1000 genomes]
rs7763757	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];0.92[MKK][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]
rs913016	1.00[AFR][1000 genomes]
rs913017	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9791348	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers 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	49 gene(s)	inside rSNPs	diseases
6	nsv885786	chr6:34426884-34542662	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
7	esv1813536	chr6:34455242-34545123	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
8	nsv885787	chr6:34458533-34546560	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
9	nsv885788	chr6:34464010-34551912	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
10	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv885789	chr6:34474939-34546560	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
12	nsv885790	chr6:34483015-34542662	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
13	nsv885791	chr6:34483015-34546560	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
14	nsv516578	chr6:34483015-34561585	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases
15	esv1801907	chr6:34492567-34545860	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
16	nsv885792	chr6:34507311-34607958	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
17	nsv1023870	chr6:34509776-34544041	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
18	nsv1015306	chr6:34509776-34549107	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
19	nsv1032763	chr6:34509776-34552797	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
20	nsv1025472	chr6:34509776-34555969	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
21	nsv1021859	chr6:34515436-34535289	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
22	nsv1033534	chr6:34516588-34555969	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
23	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34527600-34529600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr6:34527600-34529800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr6:34527600-34530400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:34527600-34530400	Enhancers	Gastric	stomach
5	chr6:34527600-34532800	Enhancers	Stomach Mucosa	stomach
6	chr6:34527600-34533800	Enhancers	Placenta	Placenta
7	chr6:34528000-34529400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:34528200-34529400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:34528200-34529400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:34528200-34530200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:34528400-34529600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:34528600-34529400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr6:34528800-34529600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:34528800-34533800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:34528800-34542200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:34528800-34551400	Weak transcription	Right Atrium	heart
17	chr6:34529000-34530200	Enhancers	K562	blood
18	chr6:34529000-34530400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr6:34529000-34530800	Bivalent Enhancer	HepG2	liver
20	chr6:34529000-34533600	Weak transcription	Fetal Intestine Small	intestine
21	chr6:34529000-34534600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr6:34529000-34534600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:34529000-34535200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:34529200-34530800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:34529200-34533600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr6:34529200-34533600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:34529200-34534600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:34529200-34534600	Weak transcription	A549	lung

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