Variant report

Variant	nsv823929
Chromosome Location	chr6:167312238-167317985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:732)
Chromatin interactive
region (count:0)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:167317880-167318113	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr6:167312119-167313330	GM12878	blood:	n/a	chr6:167312871-167312884 chr6:167312873-167312882 chr6:167312876-167312885
3	BCL3	chr6:167313715-167314695	GM12878	blood:	n/a	n/a
4	BCL3	chr6:167313871-167314706	GM12878	blood:	n/a	n/a
5	BCL3	chr6:167314979-167315950	GM12878	blood:	n/a	n/a
6	BCL3	chr6:167313342-167313588	GM12878	blood:	n/a	n/a
7	BCL3	chr6:167312133-167313195	GM12878	blood:	n/a	chr6:167312871-167312884 chr6:167312873-167312882 chr6:167312876-167312885
8	BCL3	chr6:167315018-167316313	GM12878	blood:	n/a	n/a
9	CHD2	chr6:167317260-167317288	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr6:167317980-167318130	BE2_C	brain:	n/a	n/a
11	CTCF	chr6:167317700-167317850	GM12865	blood:	n/a	n/a
12	CTCF	chr6:167317940-167318090	Caco-2	colon:	n/a	n/a
13	CTCF	chr6:167317960-167318110	BE2_C	brain:	n/a	n/a
14	E2F6	chr6:167317564-167318538	H1-hESC	embryonic stem cell:	n/a	n/a
15	E2F6	chr6:167316952-167317301	H1-hESC	embryonic stem cell:	n/a	chr6:167317167-167317179
16	E2F6	chr6:167317896-167318261	H1-hESC	embryonic stem cell:	n/a	n/a
17	EBF1	chr6:167317600-167317990	GM12878	blood:	n/a	chr6:167317788-167317799
18	EBF1	chr6:167317648-167318017	GM12878	blood:	n/a	chr6:167317788-167317799
19	EBF1	chr6:167317559-167317976	GM12878	blood:	n/a	chr6:167317788-167317799
20	KAP1	chr6:167317950-167318244	U2OS	brain:	n/a	n/a
21	MAX	chr6:167317959-167318225	K562	blood:	n/a	n/a
22	MAX	chr6:167317936-167318263	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr6:167317855-167318346	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr6:167317848-167318332	H1-hESC	embryonic stem cell:	n/a	n/a
25	MXI1	chr6:167317942-167318169	H1-hESC	embryonic stem cell:	n/a	n/a
26	MYC	chr6:167315656-167315706	H1-hESC	embryonic stem cell:	n/a	n/a
27	NFATC1	chr6:167314220-167314593	GM12878	blood:	n/a	n/a
28	NFATC1	chr6:167315572-167315916	GM12878	blood:	n/a	n/a
29	NFATC1	chr6:167312372-167312855	GM12878	blood:	n/a	n/a
30	NFATC1	chr6:167314959-167316027	GM12878	blood:	n/a	n/a
31	NFATC1	chr6:167313812-167314127	GM12878	blood:	n/a	n/a
32	NFATC1	chr6:167312476-167312848	GM12878	blood:	n/a	n/a
33	NFATC1	chr6:167312858-167313171	GM12878	blood:	n/a	n/a
34	PBX3	chr6:167312390-167312826	GM12878	blood:	n/a	n/a
35	PBX3	chr6:167315085-167315233	GM12878	blood:	n/a	n/a
36	PBX3	chr6:167313870-167314164	GM12878	blood:	n/a	n/a
37	PBX3	chr6:167314328-167314573	GM12878	blood:	n/a	n/a
38	PBX3	chr6:167312892-167313144	GM12878	blood:	n/a	n/a
39	PBX3	chr6:167315345-167315828	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:167314618-167315173	K562	blood:	n/a	n/a
41	POLR2A	chr6:167317757-167318399	H1-neurons	neurons:	n/a	n/a
42	POLR2A	chr6:167317308-167317313	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:167317764-167318448	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr6:167315782-167315803	H1-hESC	embryonic stem cell:	n/a	n/a
45	POU2F2	chr6:167315316-167315742	GM12891	blood:	n/a	n/a
46	POU2F2	chr6:167317508-167318012	GM12878	blood:	n/a	n/a
47	POU2F2	chr6:167317587-167317928	GM12878	blood:	n/a	n/a
48	RAD21	chr6:167317953-167318176	H1-hESC	embryonic stem cell:	n/a	n/a
49	REST	chr6:167317696-167318551	H1-neurons	neurons:	n/a	n/a
50	REST	chr6:167317599-167318686	H1-neurons	neurons:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167317799-167317849	NB4	blood:	n/a
2	chr6:167313693-167313743	H1-hESC	embryonic stem cell:	embryo
3	chr6:167314433-167314483	HCF	heart:	n/a
4	chr6:167313144-167313194	SK-N-MC	brain:	n/a
5	chr6:167317799-167317849	SKMC	muscle:	n/a
6	chr6:167315653-167315703	SK-N-SH	brain:	n/a
7	chr6:167314745-167314795	HEK293	kidney:	embryo
8	chr6:167314233-167314283	HCPEpiC	choroid plexus:	n/a
9	chr6:167314745-167314795	NB4	blood:	n/a
10	chr6:167312934-167312984	RPTEC	kidney:	n/a
11	chr6:167313693-167313743	SAEC	small airway:	n/a
12	chr6:167312423-167312473	SK-N-MC	brain:	n/a
13	chr6:167313144-167313194	GM12878	blood:	n/a
14	chr6:167315975-167316025	HCPEpiC	choroid plexus:	n/a
15	chr6:167313693-167313743	BJ	skin:	n/a
16	chr6:167315975-167316025	CMK	blood:	n/a
17	chr6:167317799-167317849	HRPEpiC	eye:	n/a
18	chr6:167317799-167317849	AoSMC	blood vessel:	n/a
19	chr6:167314233-167314283	Jurkat	blood:	n/a
20	chr6:167312934-167312984	AG09319	gingival:	n/a
21	chr6:167312423-167312473	HUVEC	blood vessel:	n/a
22	chr6:167313693-167313743	GM06990	blood:	n/a
23	chr6:167315653-167315703	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:167315653-167315703	H1-hESC	embryonic stem cell:	embryo
25	chr6:167314745-167314795	PFSK-1	brain:	n/a
26	chr6:167315975-167316025	LNCaP	prostate:	n/a
27	chr6:167314962-167315012	Hepatocyte	liver:	n/a
28	chr6:167313267-167313317	AoSMC	blood vessel:	n/a
29	chr6:167315653-167315703	HepG2	liver:	n/a
30	chr6:167312423-167312473	AG09309	skin:	n/a
31	chr6:167312934-167312984	HNPCEpiC	eye:	n/a
32	chr6:167312423-167312473	BJ	skin:	n/a
33	chr6:167313144-167313194	CMK	blood:	n/a
34	chr6:167312423-167312473	PrEC	prostate:	n/a
35	chr6:167315975-167316025	NHBE	bronchial:	n/a
36	chr6:167312934-167312984	BJ	skin:	n/a
37	chr6:167313144-167313194	T-47D	breast:	n/a
38	chr6:167312423-167312473	HCF	heart:	n/a
39	chr6:167312934-167312984	AG10803	skin:	n/a
40	chr6:167314233-167314283	A549	lung:	n/a
41	chr6:167313267-167313317	MCF10A-Er-Src	breast:	n/a
42	chr6:167317799-167317849	HRCEpiC	kidney:	n/a
43	chr6:167317799-167317849	MCF10A-Er-Src	breast:	n/a
44	chr6:167313144-167313194	SK-N-SH_RA	brain:	n/a
45	chr6:167314962-167315012	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:167312934-167312984	HRPEpiC	eye:	n/a
47	chr6:167313144-167313194	AG10803	skin:	n/a
48	chr6:167312423-167312473	LNCaP	prostate:	n/a
49	chr6:167315653-167315703	SAEC	small airway:	n/a
50	chr6:167317799-167317849	Jurkat	blood:	n/a

No data

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASET2-3	chr6:167317848-167318299	NONHSAT116059
2	lnc-FGFR1OP-1	chr6:167317788-167318323	XLOC_005539
3	lnc-FGFR1OP-1	chr6:167317788-167318557	NR_046644
4	lnc-FGFR1OP-1	chr6:167317186-167317276	XLOC_005539
5	lnc-FGFR1OP-1	chr6:167317186-167317276	NR_046644
6	lnc-FGFR1OP-1	chr6:167314134-167317318	l_3322_chr6:167314133-167321259_testes
7	lnc-RNASET2-3	chr6:167315613-167316152	NONHSAT116059

No data

Variant related genes	Relation type
RPS6KA2-AS1	TF binding region
RPS6KA2-AS1	CpG island

Extended variants
information (count: 353 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533030896	chr6:167312242-167312243	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs75635151	chr6:167312304-167312305	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536330777	chr6:167312306-167312307	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554314336	chr6:167312311-167312312	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566169526	chr6:167312326-167312327	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs185383960	chr6:167312334-167312335	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572786468	chr6:167312337-167312338	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533513217	chr6:167312344-167312345	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538447932	chr6:167312353-167312354	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs556451474	chr6:167312362-167312363	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571789084	chr6:167312363-167312364	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539377088	chr6:167312367-167312368	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs554497659	chr6:167312369-167312370	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs572520595	chr6:167312370-167312371	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs558893835	chr6:167312373-167312374	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs190677863	chr6:167312391-167312392	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs555058232	chr6:167312402-167312403	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs576427371	chr6:167312413-167312414	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs35625055	chr6:167312417-167312418	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs544419902	chr6:167312420-167312421	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373044505	chr6:167312424-167312425	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs9348205	chr6:167312441-167312442	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs182758572	chr6:167312474-167312475	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544947122	chr6:167312481-167312482	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs559966124	chr6:167312482-167312483	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544432383	chr6:167312491-167312492	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs73788181	chr6:167312498-167312499	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs548668163	chr6:167312508-167312509	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs6915656	chr6:167312511-167312512	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574865958	chr6:167312518-167312519	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531333677	chr6:167312520-167312521	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149042061	chr6:167312525-167312526	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs529479234	chr6:167312527-167312528	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs34296209	chr6:167312531-167312532	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs371010419	chr6:167312539-167312540	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs149118244	chr6:167312540-167312541	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571912038	chr6:167312554-167312555	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539233661	chr6:167312560-167312561	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs548113008	chr6:167312563-167312564	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs566336272	chr6:167312565-167312566	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536669297	chr6:167312578-167312579	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs554640938	chr6:167312595-167312596	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs576365462	chr6:167312600-167312601	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs73254672	chr6:167312605-167312606	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs146706901	chr6:167312607-167312608	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs559003474	chr6:167312624-167312625	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs146983044	chr6:167312625-167312626	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs578107647	chr6:167312627-167312628	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373681221	chr6:167312633-167312634	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs560031808	chr6:167312636-167312637	Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	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
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167297800-167320400	Weak transcription	Primary B cells from cord blood	blood
2	chr6:167298200-167320800	Weak transcription	Primary T cells from cord blood	blood
3	chr6:167302000-167314800	Weak transcription	Gastric	stomach
4	chr6:167307600-167317200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr6:167312000-167314800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:167312200-167312600	Enhancers	Pancreas	Pancrea
7	chr6:167312200-167312800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:167312200-167315800	ZNF genes & repeats	Placenta	Placenta
9	chr6:167312200-167316800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr6:167312400-167312600	Enhancers	Spleen	Spleen
11	chr6:167312600-167313200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:167312600-167313800	Weak transcription	Spleen	Spleen
13	chr6:167312600-167314000	Weak transcription	Pancreas	Pancrea
14	chr6:167312800-167313400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167313000-167314200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr6:167313200-167317200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:167313400-167313600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167313600-167315600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:167313800-167316000	ZNF genes & repeats	Spleen	Spleen
20	chr6:167314000-167315800	ZNF genes & repeats	Pancreas	Pancrea
21	chr6:167314000-167316400	Weak transcription	Brain Hippocampus Middle	brain
22	chr6:167314800-167315400	Enhancers	Gastric	stomach
23	chr6:167315400-167320000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr6:167315400-167321200	Weak transcription	Gastric	stomach
25	chr6:167315600-167317000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:167315800-167320400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:167315800-167341600	Weak transcription	Pancreas	Pancrea
28	chr6:167316000-167317600	Weak transcription	Spleen	Spleen
29	chr6:167316400-167316600	Enhancers	Brain Hippocampus Middle	brain
30	chr6:167316400-167320400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr6:167316600-167317000	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:167316600-167317400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr6:167316600-167318800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:167316600-167318800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:167316800-167317600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:167316800-167317600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:167316800-167318600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr6:167316800-167318800	Enhancers	Fetal Brain Male	brain
39	chr6:167317000-167317200	Enhancers	Brain Cingulate Gyrus	brain
40	chr6:167317000-167317600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:167317000-167317600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:167317000-167317600	Enhancers	Brain Germinal Matrix	brain
43	chr6:167317000-167317600	Enhancers	Brain Hippocampus Middle	brain
44	chr6:167317000-167317600	Enhancers	Fetal Brain Female	brain
45	chr6:167317000-167317800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:167317000-167317800	Enhancers	Brain Substantia Nigra	brain
47	chr6:167317200-167317400	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr6:167317200-167317600	Enhancers	Brain Angular Gyrus	brain
49	chr6:167317200-167318200	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:167317200-167318200	Bivalent Enhancer	Fetal Muscle Leg	muscle

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