Variant report

Variant	rs6702269
Chromosome Location	chr1:113393497-113393498
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:113391987-113393555	MCF10A-Er-Src	breast:	n/a	n/a
2	STAT3	chr1:113393349-113393653	MCF10A-Er-Src	breast:	n/a	chr1:113393590-113393598
3	FOS	chr1:113393407-113393535	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr1:113392052-113393544	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000215866	TF binding region

Extended variants
information (count: 103 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs11102546	0.84[ASN][1000 genomes]
rs11102549	1.00[ASN][1000 genomes]
rs11102550	1.00[ASN][1000 genomes]
rs11102552	1.00[ASN][1000 genomes]
rs11102554	1.00[ASN][1000 genomes]
rs11102555	1.00[ASN][1000 genomes]
rs11102556	1.00[ASN][1000 genomes]
rs11578123	0.84[ASN][1000 genomes]
rs11578535	0.84[ASN][1000 genomes]
rs12066438	0.86[ASN][1000 genomes]
rs12066478	1.00[ASN][1000 genomes]
rs12079364	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12081613	0.92[ASN][1000 genomes]
rs12082068	0.92[ASN][1000 genomes]
rs12082284	0.92[ASN][1000 genomes]
rs12083391	0.92[ASN][1000 genomes]
rs12083699	0.92[ASN][1000 genomes]
rs12084078	0.92[ASN][1000 genomes]
rs12085206	0.92[ASN][1000 genomes]
rs12085380	0.92[ASN][1000 genomes]
rs12086719	0.92[ASN][1000 genomes]
rs12087350	0.92[ASN][1000 genomes]
rs12088632	0.92[ASN][1000 genomes]
rs12090523	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12092282	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12093508	1.00[ASN][1000 genomes]
rs12094711	1.00[ASN][1000 genomes]
rs12094750	1.00[ASN][1000 genomes]
rs12097209	0.92[ASN][1000 genomes]
rs12097373	0.92[ASN][1000 genomes]
rs12741871	0.92[ASN][1000 genomes]
rs12742016	0.92[ASN][1000 genomes]
rs12754894	1.00[ASN][1000 genomes]
rs12756538	0.92[ASN][1000 genomes]
rs34186834	0.92[ASN][1000 genomes]
rs34517984	0.92[ASN][1000 genomes]
rs34789338	1.00[ASN][1000 genomes]
rs34839402	0.92[ASN][1000 genomes]
rs34889921	0.92[ASN][1000 genomes]
rs34903691	1.00[ASN][1000 genomes]
rs34915129	0.92[ASN][1000 genomes]
rs34986359	0.92[ASN][1000 genomes]
rs35086049	0.92[ASN][1000 genomes]
rs35386139	1.00[ASN][1000 genomes]
rs35603180	0.92[ASN][1000 genomes]
rs35744129	0.86[ASN][1000 genomes]
rs6537759	1.00[ASN][1000 genomes]
rs6537760	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6662943	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6667358	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6667856	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6670288	1.00[JPT][hapmap]
rs6674386	0.92[ASN][1000 genomes]
rs6677225	0.92[ASN][1000 genomes]
rs6677237	0.92[ASN][1000 genomes]
rs6687010	0.92[ASN][1000 genomes]
rs6687045	1.00[ASN][1000 genomes]
rs6687054	0.92[ASN][1000 genomes]
rs6692406	0.92[ASN][1000 genomes]
rs6698018	0.92[ASN][1000 genomes]
rs71513997	0.92[ASN][1000 genomes]
rs71514000	0.92[ASN][1000 genomes]
rs71659377	0.92[ASN][1000 genomes]
rs71659378	1.00[ASN][1000 genomes]
rs7513783	0.92[ASN][1000 genomes]
rs7516867	1.00[ASN][1000 genomes]
rs7517501	1.00[ASN][1000 genomes]
rs7520778	1.00[ASN][1000 genomes]
rs7526841	0.86[ASN][1000 genomes]
rs7527193	1.00[ASN][1000 genomes]
rs7527283	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7528133	0.92[ASN][1000 genomes]
rs7537461	1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7539492	0.92[ASN][1000 genomes]
rs7539588	0.92[ASN][1000 genomes]
rs7539948	1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7541584	0.92[ASN][1000 genomes]
rs7543983	0.92[ASN][1000 genomes]
rs7554350	0.92[ASN][1000 genomes]
rs9429493	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9429494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9970307	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	158 gene(s)	inside rSNPs	diseases
4	nsv533295	chr1:113167645-113589588	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
8	nsv818378	chr1:113263711-113434818	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv1008434	chr1:113288282-113447426	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
10	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer 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	68 gene(s)	inside rSNPs	diseases
11	nsv1004102	chr1:113295805-113551210	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
12	nsv872160	chr1:113301657-113409751	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1000352	chr1:113350929-113405903	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1011519	chr1:113351374-113402040	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	esv3399982	chr1:113358580-113542255	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
16	esv3374684	chr1:113359959-113414316	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
18	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
19	esv3360645	chr1:113375959-113414652	Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	esv3362439	chr1:113376621-113450321	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
21	nsv522967	chr1:113384015-113400990	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6702269	WDR77	cis	parietal	SCAN

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113388600-113394600	Weak transcription	Hela-S3	cervix
2	chr1:113391800-113393600	Flanking Active TSS	HUVEC	blood vessel
3	chr1:113391800-113393800	Enhancers	Fetal Brain Male	brain
4	chr1:113391800-113394200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:113391800-113394800	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr1:113392000-113393600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:113392000-113394400	Flanking Active TSS	Placenta	Placenta
8	chr1:113392200-113393600	Active TSS	Osteobl	bone
9	chr1:113392400-113393800	Active TSS	Brain Anterior Caudate	brain
10	chr1:113392400-113394800	Active TSS	Duodenum Mucosa	Duodenum
11	chr1:113392400-113397800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:113392600-113393600	Active TSS	Brain Cingulate Gyrus	brain
13	chr1:113392600-113394800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:113392800-113393600	Active TSS	Fetal Brain Female	brain
15	chr1:113392800-113393800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:113392800-113394400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:113392800-113394600	Weak transcription	HMEC	breast
18	chr1:113392800-113395000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:113392800-113397200	Weak transcription	Pancreas	Pancrea
20	chr1:113393000-113393600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:113393000-113393800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr1:113393000-113393800	Active TSS	Brain Hippocampus Middle	brain
23	chr1:113393000-113394200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:113393000-113394200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:113393000-113394800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr1:113393000-113395200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:113393000-113397200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:113393000-113397200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:113393000-113397600	Weak transcription	A549	lung
30	chr1:113393000-113397800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:113393200-113393600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr1:113393200-113393600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr1:113393200-113393600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:113393200-113393600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
35	chr1:113393200-113393600	Bivalent/Poised TSS	NHLF	lung
36	chr1:113393200-113393800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:113393200-113393800	Flanking Active TSS	NHEK	skin
38	chr1:113393200-113394800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:113393200-113397200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:113393400-113393600	Enhancers	Fetal Heart	heart
41	chr1:113393400-113393800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:113393400-113395600	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr1:113393400-113397600	Weak transcription	NH-A	brain

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