Variant report

Variant	rs6910473
Chromosome Location	chr6:31140808-31140809
allele	A/G
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	CTBP2	chr6:31139596-31141574	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr6:31139393-31141556	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:31140471-31141189	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr6:31139607-31141000	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr6:31140680-31141051	A549	lung:	n/a	n/a
6	SP1	chr6:31139460-31141202	H1-hESC	embryonic stem cell:	n/a	chr6:31140936-31140945 chr6:31140935-31140944 chr6:31139694-31139704 chr6:31139693-31139705 chr6:31140934-31140946 chr6:31139694-31139703 chr6:31139759-31139773 chr6:31139693-31139705 chr6:31140837-31140846 chr6:31139640-31139654 chr6:31140934-31140946 chr6:31139701-31139711 chr6:31139634-31139648 chr6:31140935-31140945 chr6:31140931-31140945
7	SP1	chr6:31139383-31141260	H1-hESC	embryonic stem cell:	n/a	chr6:31140936-31140945 chr6:31140935-31140944 chr6:31139694-31139704 chr6:31139693-31139705 chr6:31140934-31140946 chr6:31139694-31139703 chr6:31139759-31139773 chr6:31139693-31139705 chr6:31140837-31140846 chr6:31139640-31139654 chr6:31140934-31140946 chr6:31139701-31139711 chr6:31139634-31139648 chr6:31140935-31140945 chr6:31140931-31140945
8	TAF1	chr6:31140631-31141111	H1-hESC	embryonic stem cell:	n/a	n/a
9	GTF2F1	chr6:31140622-31141110	H1-hESC	embryonic stem cell:	n/a	n/a
10	SIN3A	chr6:31139655-31141151	H1-hESC	embryonic stem cell:	n/a	n/a
11	TBP	chr6:31139535-31141093	H1-hESC	embryonic stem cell:	n/a	n/a
12	JUN	chr6:31140769-31141709	K562	blood:	n/a	chr6:31141454-31141464 chr6:31141455-31141463 chr6:31141456-31141463 chr6:31141453-31141465 chr6:31141455-31141463
13	MXI1	chr6:31140544-31141028	H1-hESC	embryonic stem cell:	n/a	n/a
14	RAD21	chr6:31140356-31141311	H1-hESC	embryonic stem cell:	n/a	chr6:31141105-31141114
15	NANOG	chr6:31140580-31141102	H1-hESC	embryonic stem cell:	n/a	chr6:31140686-31140695 chr6:31140882-31140896 chr6:31140886-31140895
16	TAF7	chr6:31139392-31141219	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr6:31139513-31141397	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAX	chr6:31140256-31141008	H1-hESC	embryonic stem cell:	n/a	n/a
19	SIN3AK20	chr6:31140645-31141109	H1-hESC	embryonic stem cell:	n/a	n/a
20	POU5F1	chr6:31140574-31141112	H1-hESC	embryonic stem cell:	n/a	chr6:31140884-31140898 chr6:31140884-31140898
21	TCF12	chr6:31140650-31141090	H1-hESC	embryonic stem cell:	n/a	chr6:31141044-31141054
22	POLR2A	chr6:31140680-31140932	HepG2	liver:	n/a	n/a
23	BACH1	chr6:31140544-31141096	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr6:31138461-31141328	A549	lung:	n/a	n/a
25	YY1	chr6:31140686-31141136	H1-hESC	embryonic stem cell:	n/a	chr6:31140941-31140952
26	MYC	chr6:31139720-31140953	H1-hESC	embryonic stem cell:	n/a	n/a
27	HDAC2	chr6:31140623-31141101	H1-hESC	embryonic stem cell:	n/a	n/a
28	TAF1	chr6:31139517-31141186	H1-hESC	embryonic stem cell:	n/a	n/a
29	EP300	chr6:31140569-31141119	H1-hESC	embryonic stem cell:	n/a	n/a
30	YY1	chr6:31140561-31141161	H1-hESC	embryonic stem cell:	n/a	chr6:31140941-31140952
31	MAX	chr6:31140468-31141109	H1-hESC	embryonic stem cell:	n/a	n/a
32	HDAC2	chr6:31140746-31141027	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr6:31139558-31141134	H1-hESC	embryonic stem cell:	n/a	n/a
34	TCF12	chr6:31140674-31141056	H1-hESC	embryonic stem cell:	n/a	chr6:31141044-31141054
35	CHD2	chr6:31140594-31141102	H1-hESC	embryonic stem cell:	n/a	n/a
36	SP4	chr6:31140575-31141084	H1-hESC	embryonic stem cell:	n/a	chr6:31140930-31140946
37	POLR2A	chr6:31140585-31141072	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr6:31139588-31141161	H1-hESC	embryonic stem cell:	n/a	n/a
39	POU5F1	chr6:31140672-31141009	H1-hESC	embryonic stem cell:	n/a	chr6:31140884-31140898 chr6:31140884-31140898
40	TEAD4	chr6:31140606-31141195	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr6:31140642-31141005	H1-hESC	embryonic stem cell:	n/a	n/a
42	TEAD4	chr6:31140636-31141216	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr6:31139540-31141118	H1-hESC	embryonic stem cell:	n/a	n/a
44	NANOG	chr6:31140724-31141062	H1-hESC	embryonic stem cell:	n/a	chr6:31140882-31140896 chr6:31140886-31140895
45	POLR2A	chr6:31139365-31141730	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31140282..31142540-chr6:31144471..31147209,2	MCF-7	breast:
2	chr6:31139031..31142217-chr6:31144167..31146313,5	MCF-7	breast:
3	chr6:31139871..31141451-chr6:31144407..31146818,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCHCR1-1	chr6:31139386-31141810	XLOC_005677

Variant related genes	Relation type
POU5F1	TF binding region
ENSG00000204528	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1044870	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs130077	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2233945	0.93[ASN][1000 genomes]
rs2233946	0.93[ASN][1000 genomes]
rs2233947	0.86[ASN][1000 genomes]
rs28742577	0.93[ASN][1000 genomes]
rs4321863	0.86[ASN][1000 genomes]
rs6909939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6913074	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7739334	0.80[ASN][1000 genomes]
rs7769586	0.80[ASN][1000 genomes]
rs9263733	0.86[ASN][1000 genomes]
rs9263745	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263766	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263768	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263769	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9263774	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263775	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263776	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263777	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263778	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263781	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263782	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263783	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263785	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263786	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263790	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263792	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263794	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9263796	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9263800	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263802	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263809	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263810	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263811	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263816	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs9263817	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263818	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263822	0.93[ASN][1000 genomes]
rs9263825	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263827	0.93[ASN][1000 genomes]
rs9263832	0.93[ASN][1000 genomes]
rs9263833	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263838	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263843	0.93[ASN][1000 genomes]
rs9263855	0.93[ASN][1000 genomes]
rs9263903	0.86[ASN][1000 genomes]
rs9263989	0.86[ASN][1000 genomes]
rs9263994	0.86[ASN][1000 genomes]
rs9264039	0.86[ASN][1000 genomes]
rs9264041	0.80[ASN][1000 genomes]
rs9264069	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv1029442	chr6:31006647-31449207	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
7	nsv427750	chr6:31028290-31234581	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription 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	47 gene(s)	inside rSNPs	diseases
8	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
9	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
10	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
11	nsv525933	chr6:31081205-31142245	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription 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	25 gene(s)	inside rSNPs	diseases
12	nsv1019637	chr6:31104401-31354706	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv1029569	chr6:31104401-31412740	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
14	nsv538174	chr6:31104401-31412740	Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
15	nsv1034391	chr6:31131121-31279595	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
16	nsv1025909	chr6:31131121-31354706	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
17	nsv538175	chr6:31131121-31354706	Active TSS Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS 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 miRNA	51 gene(s)	inside rSNPs	diseases
18	nsv1015890	chr6:31131121-31449207	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
19	nsv538176	chr6:31131121-31449207	Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31127200-31146800	Weak transcription	Small Intestine	intestine
2	chr6:31127600-31143000	Weak transcription	Right Ventricle	heart
3	chr6:31127600-31147800	Weak transcription	Primary B cells from cord blood	blood
4	chr6:31127600-31148000	Weak transcription	Right Atrium	heart
5	chr6:31127800-31142800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:31127800-31142800	Weak transcription	HSMM	muscle
7	chr6:31127800-31146200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:31127800-31147800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr6:31127800-31147800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr6:31127800-31153200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr6:31128000-31143200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:31128200-31143600	Weak transcription	NHDF-Ad	bronchial
13	chr6:31130200-31146200	Weak transcription	Lung	lung
14	chr6:31130400-31147800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr6:31130600-31146800	Weak transcription	Colonic Mucosa	Colon
16	chr6:31130800-31141800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:31131000-31141000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr6:31131000-31143200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr6:31131000-31143400	Weak transcription	Esophagus	oesophagus
20	chr6:31131000-31147800	Weak transcription	Adipose Nuclei	Adipose
21	chr6:31131000-31148000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:31131000-31148000	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr6:31131200-31143600	Weak transcription	Osteobl	bone
24	chr6:31131400-31142800	Weak transcription	HepG2	liver
25	chr6:31131600-31143400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:31131600-31143400	Weak transcription	Fetal Lung	lung
27	chr6:31131600-31143600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr6:31131800-31141200	Weak transcription	A549	lung
29	chr6:31132000-31148000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:31133000-31143800	Weak transcription	Dnd41	blood
31	chr6:31133000-31148000	Weak transcription	Thymus	Thymus
32	chr6:31133000-31148200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr6:31133600-31143000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr6:31133600-31143200	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr6:31134200-31145800	Weak transcription	GM12878-XiMat	blood
36	chr6:31135000-31143400	Weak transcription	Fetal Thymus	thymus
37	chr6:31137600-31143200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:31138000-31141400	Weak transcription	HMEC	breast
39	chr6:31138000-31143400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:31138000-31146600	Weak transcription	Spleen	Spleen
41	chr6:31138000-31146800	Weak transcription	Hela-S3	cervix
42	chr6:31138000-31157400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr6:31138200-31142800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr6:31139200-31141000	Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr6:31139200-31141200	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr6:31139400-31141000	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr6:31139400-31141200	Active TSS	H9 Cell Line	embryonic stem cell
48	chr6:31139400-31148000	Weak transcription	Fetal Intestine Small	intestine
49	chr6:31139600-31141000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:31139600-31141400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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