Variant report

Variant	nsv1028698
Chromosome Location	chr6:167698769-167770661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1300)
CpG islands
(count:2504)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
8	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
9	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
10	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
16	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
17	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
18	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
19	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
20	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
21	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
23	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
29	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
33	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
34	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
42	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
43	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
44	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
45	CEBPB	chr6:167722105-167722600	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:167723191-167723562	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:167705118-167705446	H1-hESC	embryonic stem cell:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
48	CEBPB	chr6:167699860-167700082	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167705618-167706114	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr6:167698937-167699146	HepG2	liver:	n/a	n/a

(count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167708827-167708877	BJ	skin:	n/a
2	chr6:167704188-167704238	SK-N-SH_RA	brain:	n/a
3	chr6:167705253-167705303	AG04450	lung:	fetal
4	chr6:167708827-167708877	BJ	skin:	n/a
5	chr6:167704188-167704238	SK-N-SH_RA	brain:	n/a
6	chr6:167705253-167705303	AG04450	lung:	fetal
7	chr6:167704769-167704819	HRPEpiC	eye:	n/a
8	chr6:167704808-167704858	Caco-2	colon:	n/a
9	chr6:167737937-167737987	HCT-116	colon:	n/a
10	chr6:167764620-167764670	BE2_C	brain:	n/a
11	chr6:167727700-167727750	PrEC	prostate:	n/a
12	chr6:167709720-167709770	Caco-2	colon:	n/a
13	chr6:167768382-167768432	HNPCEpiC	eye:	n/a
14	chr6:167727700-167727750	HNPCEpiC	eye:	n/a
15	chr6:167756099-167756149	NHDF-neo	bronchial:	n/a
16	chr6:167738594-167738644	GM12878	blood:	n/a
17	chr6:167739618-167739668	ECC-1	luminal epithelium:	n/a
18	chr6:167765110-167765160	MCF10A-Er-Src	breast:	n/a
19	chr6:167704769-167704819	GM06990	blood:	n/a
20	chr6:167705253-167705303	AG04449	skin:	fetal
21	chr6:167737937-167737987	CMK	blood:	n/a
22	chr6:167765215-167765265	GM06990	blood:	n/a
23	chr6:167709237-167709287	AG04450	lung:	fetal
24	chr6:167764523-167764573	NT2-D1	testis:	n/a
25	chr6:167763320-167763370	GM19239	blood:	n/a
26	chr6:167763975-167764025	BE2_C	brain:	n/a
27	chr6:167761204-167761254	T-47D	breast:	n/a
28	chr6:167763758-167763808	HRE	kidney:	n/a
29	chr6:167739618-167739668	HMEC	breast:	n/a
30	chr6:167738342-167738392	HRE	kidney:	n/a
31	chr6:167727700-167727750	NB4	blood:	n/a
32	chr6:167717313-167717363	Hepatocyte	liver:	n/a
33	chr6:167709720-167709770	BE2_C	brain:	n/a
34	chr6:167738592-167738642	HMEC	breast:	n/a
35	chr6:167703894-167703944	SK-N-SH_RA	brain:	n/a
36	chr6:167764523-167764573	HL-60	blood:	n/a
37	chr6:167710360-167710410	NHBE	bronchial:	n/a
38	chr6:167738592-167738642	PrEC	prostate:	n/a
39	chr6:167763975-167764025	AG09319	gingival:	n/a
40	chr6:167768382-167768432	HEEpiC	esophagus:	n/a
41	chr6:167765215-167765265	SK-N-MC	brain:	n/a
42	chr6:167762783-167762833	SK-N-SH	brain:	n/a
43	chr6:167753807-167753857	ECC-1	luminal epithelium:	n/a
44	chr6:167704769-167704819	SK-N-SH_RA	brain:	n/a
45	chr6:167765110-167765160	NB4	blood:	n/a
46	chr6:167705750-167705800	MCF-7	breast:	n/a
47	chr6:167704808-167704858	MCF-7	breast:	n/a
48	chr6:167704673-167704723	SK-N-MC	brain:	n/a
49	chr6:167703894-167703944	HEK293	kidney:	embryo
50	chr6:167761204-167761254	HRCEpiC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
2	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
3	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
4	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
5	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
6	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
7	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
8	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
9	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
10	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
11	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
12	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
13	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
14	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
15	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
16	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
17	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
18	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
2	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
3	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095

No data

Variant related genes	Relation type
UNC93A	TF binding region
TTLL2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TTLL2	CpG island
ENSG00000217447	CpG island
ENSG00000112494	chromatin interactions

Extended variants
information (count: 3477 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3477 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs206990	chr6:167698769-167698770	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575144483	chr6:167698796-167698797	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs546045308	chr6:167698851-167698852	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs73260911	chr6:167698878-167698879	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73260912	chr6:167698893-167698894	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs146102446	chr6:167698929-167698930	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs571880200	chr6:167698963-167698964	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs77251635	chr6:167698965-167698966	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs148741608	chr6:167698981-167698982	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs562862632	chr6:167698988-167698989	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs550987634	chr6:167699014-167699015	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs552498032	chr6:167699034-167699035	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs9459961	chr6:167699049-167699050	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370814854	chr6:167699064-167699065	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs73262989	chr6:167699068-167699069	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568181593	chr6:167699069-167699070	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs535497025	chr6:167699083-167699084	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs556786274	chr6:167699087-167699088	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs73262990	chr6:167699103-167699104	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185440979	chr6:167699113-167699114	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs558019715	chr6:167699164-167699165	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs73790181	chr6:167699168-167699169	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73790183	chr6:167699176-167699177	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs112464964	chr6:167699181-167699182	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562275390	chr6:167699200-167699201	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574163065	chr6:167699224-167699225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs73262994	chr6:167699226-167699227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs189857299	chr6:167699250-167699251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533358614	chr6:167699286-167699287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551836972	chr6:167699287-167699288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180918800	chr6:167699317-167699318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs206991	chr6:167699378-167699379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs73790185	chr6:167699387-167699388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534838048	chr6:167699399-167699400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73262999	chr6:167699408-167699409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs138265267	chr6:167699426-167699427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs72179325	chr6:167699427-167699428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535291089	chr6:167699446-167699447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534979428	chr6:167699448-167699449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56194869	chr6:167699449-167699450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs206992	chr6:167699450-167699451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139628590	chr6:167699452-167699453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs202029209	chr6:167699454-167699455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144483801	chr6:167699465-167699466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7767375	chr6:167699467-167699468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112132877	chr6:167699469-167699470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534183034	chr6:167699471-167699472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149482948	chr6:167699472-167699473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs76456224	chr6:167699486-167699487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs206993	chr6:167699569-167699570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167689200-167702400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:167692400-167702400	Weak transcription	Thymus	Thymus
3	chr6:167693400-167698800	Weak transcription	Fetal Brain Female	brain
4	chr6:167696000-167699600	Weak transcription	Fetal Intestine Small	intestine
5	chr6:167696800-167705800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr6:167697000-167702400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:167697200-167702000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:167697200-167702400	Weak transcription	Fetal Thymus	thymus
9	chr6:167697200-167705200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:167697400-167702000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:167697400-167702400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:167697600-167699600	Enhancers	HepG2	liver
13	chr6:167697600-167700800	Weak transcription	Fetal Brain Male	brain
14	chr6:167697600-167702400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:167697600-167706200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:167698600-167699000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:167698600-167699000	Enhancers	Gastric	stomach
18	chr6:167698600-167699000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr6:167698600-167699200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:167698600-167699200	Enhancers	Fetal Muscle Leg	muscle
21	chr6:167698600-167699200	Enhancers	Pancreas	Pancrea
22	chr6:167698800-167699000	Flanking Active TSS	Liver	Liver
23	chr6:167698800-167699200	Enhancers	Fetal Brain Female	brain
24	chr6:167698800-167699200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr6:167699000-167699200	Active TSS	Liver	Liver
26	chr6:167699000-167702400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr6:167699200-167701200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:167699200-167701600	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:167699200-167702400	Weak transcription	Liver	Liver
30	chr6:167699600-167700000	Enhancers	Fetal Intestine Small	intestine
31	chr6:167699600-167700200	Flanking Active TSS	HepG2	liver
32	chr6:167700000-167701800	Weak transcription	Fetal Intestine Small	intestine
33	chr6:167700200-167704400	Enhancers	HepG2	liver
34	chr6:167700800-167702800	Enhancers	Fetal Brain Male	brain
35	chr6:167701200-167701600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:167701200-167701800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:167701200-167702800	Enhancers	Fetal Lung	lung
38	chr6:167701600-167701800	Enhancers	Fetal Muscle Leg	muscle
39	chr6:167701600-167702600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:167701800-167702200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:167701800-167704800	Enhancers	Fetal Intestine Small	intestine
42	chr6:167702000-167702600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr6:167702000-167703000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr6:167702200-167702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:167702400-167702800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr6:167702400-167702800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr6:167702400-167702800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
48	chr6:167702400-167702800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:167702400-167702800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:167702400-167702800	Enhancers	Thymus	Thymus

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