Variant report

Variant	rs6604062
Chromosome Location	chr1:92356781-92356782
allele	C/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	FOSL2	chr1:92356552-92356947	A549	lung:	n/a	n/a
2	MYC	chr1:92356692-92356964	MCF10A-Er-Src	breast:	n/a	n/a
3	STAT3	chr1:92356691-92356890	MCF10A-Er-Src	breast:	n/a	n/a
4	NR3C1	chr1:92356681-92357357	A549	lung:	n/a	n/a
5	FOS	chr1:92356550-92357636	MCF10A-Er-Src	breast:	n/a	n/a
6	RPC155	chr1:92356591-92357425	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:92356658-92357542	Hela-S3	cervix:	n/a	chr1:92357209-92357220 chr1:92357209-92357218 chr1:92357207-92357218
8	FOS	chr1:92356636-92356943	MCF10A-Er-Src	breast:	n/a	n/a
9	FOSL2	chr1:92356552-92356907	HepG2	liver:	n/a	n/a
10	SMC3	chr1:92356762-92356938	Hela-S3	cervix:	n/a	n/a
11	FOS	chr1:92356573-92357387	MCF10A-Er-Src	breast:	n/a	n/a
12	TCF7L2	chr1:92356383-92357872	Hela-S3	cervix:	n/a	n/a
13	RAD21	chr1:92356734-92356836	Hela-S3	cervix:	n/a	n/a
14	MAX	chr1:92356683-92356876	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:92356690-92357499	IMR90	lung:	n/a	chr1:92357209-92357220 chr1:92357209-92357218 chr1:92357207-92357218
16	FOS	chr1:92356564-92357386	MCF10A-Er-Src	breast:	n/a	n/a
17	STAT3	chr1:92356769-92356866	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:92348748..92351822-chr1:92353645..92358232,4	K562	blood:
2	chr1:92354436..92357349-chr1:92361835..92364580,4	K562	blood:

Variant related genes	Relation type
TGFBR3	TF binding region
ENSG00000069702	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10875041	0.90[ASN][1000 genomes]
rs1192525	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1192526	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1192527	0.90[ASN][1000 genomes]
rs1488692	0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1805109	0.82[ASW][hapmap];0.87[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs1805110	0.82[ASW][hapmap];0.83[YRI][hapmap]
rs2245653	0.96[ASN][1000 genomes]
rs2245663	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2306888	1.00[TSI][hapmap]
rs2391092	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2479872	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.88[MEX][hapmap];0.93[ASN][1000 genomes]
rs2489175	0.95[ASN][1000 genomes]
rs2489186	0.80[MKK][hapmap]
rs2489187	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2489189	0.82[ASW][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2634018	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2634028	0.84[LWK][hapmap];1.00[YRI][hapmap]
rs2634030	0.84[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap]
rs2770189	0.85[ASN][1000 genomes]
rs2799510	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2799523	1.00[YRI][hapmap]
rs2799526	0.80[JPT][hapmap];1.00[YRI][hapmap]
rs2799527	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2799541	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.88[MEX][hapmap];0.95[ASN][1000 genomes]
rs2799542	1.00[ASN][1000 genomes]
rs2996478	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4261158	1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs4658117	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6604063	1.00[ASN][1000 genomes]
rs6676301	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6702560	0.93[ASN][1000 genomes]
rs721052	1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7527634	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS 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	4 gene(s)	inside rSNPs	diseases
7	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription 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	15 gene(s)	inside rSNPs	diseases
11	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription 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	15 gene(s)	inside rSNPs	diseases
18	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv830581	chr1:92317207-92511175	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	nsv871415	chr1:92340684-92641607	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
26	esv2750842	chr1:92356781-92579675	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92352400-92356800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr1:92352400-92356800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:92352400-92357200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:92352400-92357400	Weak transcription	HSMMtube	muscle
5	chr1:92352400-92357400	Weak transcription	NH-A	brain
6	chr1:92352400-92357600	Weak transcription	Right Atrium	heart
7	chr1:92352400-92362600	Weak transcription	Psoas Muscle	Psoas
8	chr1:92352400-92366600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr1:92352600-92356800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:92352600-92356800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr1:92352600-92356800	Weak transcription	Fetal Stomach	stomach
12	chr1:92352600-92357000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr1:92352600-92357000	Weak transcription	HUVEC	blood vessel
14	chr1:92352600-92357200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr1:92352600-92357200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:92352600-92357200	Weak transcription	Fetal Kidney	kidney
17	chr1:92352600-92357400	Weak transcription	Liver	Liver
18	chr1:92352600-92357600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:92352600-92357600	Weak transcription	Fetal Muscle Leg	muscle
20	chr1:92352600-92357600	Weak transcription	Spleen	Spleen
21	chr1:92352600-92362800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr1:92352600-92370600	Weak transcription	K562	blood
23	chr1:92352800-92356800	Weak transcription	Adipose Nuclei	Adipose
24	chr1:92352800-92357600	Weak transcription	Ovary	ovary
25	chr1:92353000-92357800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:92354000-92357200	Enhancers	Placenta	Placenta
27	chr1:92354400-92357400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:92355000-92357000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:92355200-92356800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:92355200-92357200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:92355200-92357200	Enhancers	GM12878-XiMat	blood
32	chr1:92355200-92357600	Enhancers	HepG2	liver
33	chr1:92355200-92358200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:92355200-92358200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:92355400-92358200	Enhancers	NHDF-Ad	bronchial
36	chr1:92355600-92356800	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr1:92355600-92356800	Weak transcription	Fetal Lung	lung
38	chr1:92355600-92357400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr1:92355800-92356800	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr1:92355800-92357200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr1:92355800-92357200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:92355800-92357200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:92355800-92357200	Enhancers	A549	lung
44	chr1:92355800-92357400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr1:92355800-92357600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr1:92355800-92357600	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:92355800-92357600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:92356000-92357000	Enhancers	Esophagus	oesophagus
49	chr1:92356000-92357200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr1:92356200-92357200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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