Variant report

Variant	rs11915113
Chromosome Location	chr3:196066869-196066870
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	IRF1	chr3:196066608-196066963	K562	blood:	n/a	n/a
2	MAFK	chr3:196066668-196066984	IMR90	lung:	n/a	n/a
3	TRIM28	chr3:196066452-196067137	K562	blood:	n/a	n/a
4	POLR2A	chr3:196066501-196067735	U87	brain:	n/a	n/a
5	JUND	chr3:196066566-196067065	A549	lung:	n/a	chr3:196066836-196066847
6	MAFK	chr3:196066640-196066992	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:196066681-196066995	Hela-S3	cervix:	n/a	n/a
8	FOSL2	chr3:196066517-196067097	A549	lung:	n/a	n/a
9	EP300	chr3:196066578-196067618	K562	blood:	n/a	n/a
10	MAZ	chr3:196066749-196067001	K562	blood:	n/a	n/a
11	TEAD4	chr3:196066442-196067076	K562	blood:	n/a	n/a
12	NFE2	chr3:196066683-196067000	K562	blood:	n/a	chr3:196066796-196066811
13	IRF1	chr3:196066637-196067059	K562	blood:	n/a	n/a
14	CEBPB	chr3:196066727-196066928	K562	blood:	n/a	n/a
15	JUND	chr3:196066724-196066991	HepG2	liver:	n/a	chr3:196066836-196066847
16	POLR2A	chr3:196066753-196066973	Hela-S3	cervix:	n/a	n/a
17	MAFK	chr3:196066529-196067046	K562	blood:	n/a	n/a
18	CHD2	chr3:196066781-196066988	Hela-S3	cervix:	n/a	n/a
19	FOSL1	chr3:196066445-196067262	HCT-116	colon:	n/a	chr3:196066836-196066847
20	HEY1	chr3:196066786-196067058	K562	blood:	n/a	n/a
21	EP300	chr3:196066544-196067110	A549	lung:	n/a	n/a
22	RCOR1	chr3:196066629-196067150	K562	blood:	n/a	n/a
23	JUN	chr3:196066645-196067016	K562	blood:	n/a	n/a
24	MYC	chr3:196066507-196067108	K562	blood:	n/a	n/a
25	ATF1	chr3:196066740-196066989	K562	blood:	n/a	n/a
26	STAT3	chr3:196066789-196066956	MCF10A-Er-Src	breast:	n/a	n/a
27	MAX	chr3:196066717-196067129	K562	blood:	n/a	n/a
28	POLR2A	chr3:196066711-196067108	K562	blood:	n/a	n/a
29	E2F6	chr3:196066580-196067129	A549	lung:	n/a	n/a
30	MAFF	chr3:196066550-196067118	K562	blood:	n/a	chr3:196066794-196066812
31	POLR2A	chr3:196066674-196067688	U87	brain:	n/a	n/a
32	CBX3	chr3:196066465-196067185	K562	blood:	n/a	n/a
33	JUND	chr3:196066734-196066915	HepG2	liver:	n/a	chr3:196066836-196066847
34	MYC	chr3:196066656-196066987	MCF10A-Er-Src	breast:	n/a	n/a
35	CEBPB	chr3:196066567-196067057	K562	blood:	n/a	n/a
36	MAFK	chr3:196066684-196066938	H1-hESC	embryonic stem cell:	n/a	n/a
37	FOSL1	chr3:196066721-196067025	K562	blood:	n/a	chr3:196066836-196066847
38	ARID3A	chr3:196066607-196067672	K562	blood:	n/a	n/a
39	FOS	chr3:196066590-196067034	MCF10A-Er-Src	breast:	n/a	chr3:196066836-196066847
40	EP300	chr3:196066708-196066933	GM12878	blood:	n/a	n/a
41	POLR2A	chr3:196066771-196066966	HCT-116	colon:	n/a	n/a
42	ZNF384	chr3:196063585-196067637	K562	blood:	n/a	n/a
43	POLR2A	chr3:196066739-196067135	K562	blood:	n/a	n/a
44	FOS	chr3:196066718-196066957	HUVEC	blood vessel:	n/a	chr3:196066836-196066847
45	BCLAF1	chr3:196066716-196067272	K562	blood:	n/a	n/a
46	BHLHE40	chr3:196066468-196067076	K562	blood:	n/a	n/a
47	NR2F2	chr3:196066411-196067179	K562	blood:	n/a	n/a
48	MYC	chr3:196066799-196066941	NB4	blood:	n/a	n/a
49	CUX1	chr3:196066540-196066979	K562	blood:	n/a	n/a
50	MAFK	chr3:196066686-196066983	HepG2	liver:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:196065700..196067576-chr3:196094863..196096889,2	K562	blood:
2	chr3:196065505..196067615-chr3:196082041..196085251,3	K562	blood:
3	chr3:196043015..196047197-chr3:196061951..196068288,11	K562	blood:
4	chr3:196050279..196052047-chr3:196065186..196067594,2	MCF-7	breast:
5	chr3:196048792..196050575-chr3:196065911..196067478,2	MCF-7	breast:
6	chr3:196064683..196067033-chr3:196229952..196232006,2	K562	blood:
7	chr3:196062778..196068235-chr3:196157235..196160927,9	K562	blood:
8	chr3:196043730..196046568-chr3:196064807..196067685,4	MCF-7	breast:
9	chr3:196012576..196016636-chr3:196061383..196069148,11	K562	blood:
10	chr3:196012352..196016755-chr3:196062622..196069148,9	K562	blood:

No data

Variant related genes	Relation type
ENSG00000273331	TF binding region
TM4SF19	TF binding region
ENSG00000213123	Chromatin interaction
ENSG00000163961	Chromatin interaction
ENSG00000163960	Chromatin interaction
ENSG00000161217	Chromatin interaction
ENSG00000145107	Chromatin interaction
ENSG00000272741	Chromatin interaction
ENSG00000235897	Chromatin interaction
ENSG00000225822	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11185523	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13083065	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34242111	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35270876	0.83[AMR][1000 genomes]
rs58677048	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	esv2757913	chr3:195379484-196071593	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
3	nsv997797	chr3:195658360-196212958	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv1009811	chr3:195851796-196138071	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	nsv461131	chr3:195858887-196072442	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
6	nsv593071	chr3:195858887-196072442	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
7	nsv1009178	chr3:195864466-196081670	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
8	nsv536892	chr3:195864466-196081670	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
9	nsv1003550	chr3:195885340-196159824	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
10	nsv536893	chr3:195885340-196159824	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
11	nsv1014563	chr3:195934010-196085951	Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
12	nsv878181	chr3:195946535-196072442	Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking 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	36 gene(s)	inside rSNPs	diseases
13	nsv1003194	chr3:195960270-196342423	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
14	nsv536894	chr3:195960270-196342423	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
15	nsv878182	chr3:195974181-196228360	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
16	nsv1003764	chr3:196028141-196190687	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
17	nsv536895	chr3:196028141-196190687	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
18	nsv4183	chr3:196034067-196079109	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
19	esv1836491	chr3:196051403-196078427	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
20	esv1844755	chr3:196057616-196190350	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
21	esv1827330	chr3:196061833-196069055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
22	esv1835563	chr3:196061833-196069055	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11915113	RNF168	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:196054600-196091000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:196062800-196075000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:196064600-196070200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr3:196064800-196068400	Enhancers	NH-A	brain
5	chr3:196065400-196067200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:196065400-196067400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:196065400-196067600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:196065400-196068000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:196065400-196068400	Enhancers	HMEC	breast
10	chr3:196065400-196069800	Weak transcription	Esophagus	oesophagus
11	chr3:196065400-196071800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:196065600-196067000	Enhancers	A549	lung
13	chr3:196065600-196067800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:196065600-196068600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr3:196065600-196070000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:196065600-196074200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:196065600-196074200	Weak transcription	HSMM	muscle
18	chr3:196065600-196075200	Weak transcription	Fetal Muscle Leg	muscle
19	chr3:196065600-196080800	Weak transcription	HSMMtube	muscle
20	chr3:196065600-196082400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr3:196065600-196082600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr3:196065600-196084200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:196065800-196067200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr3:196065800-196067600	Flanking Active TSS	K562	blood
25	chr3:196065800-196068600	Enhancers	NHEK	skin
26	chr3:196066000-196068400	Enhancers	Hela-S3	cervix
27	chr3:196066200-196067000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr3:196066200-196081200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr3:196066400-196067000	Enhancers	Placenta	Placenta
30	chr3:196066400-196068600	Enhancers	Osteobl	bone
31	chr3:196066600-196068600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:196066600-196068600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:196066600-196068600	Enhancers	NHDF-Ad	bronchial
34	chr3:196066800-196067400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:196066800-196067400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:196066800-196068000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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