Variant report

Variant	nsv984581
Chromosome Location	chr6:163235106-163294421
allele	n/a
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	BACH1	chr6:163277893-163278240	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr6:163293683-163293879	K562	blood:	n/a	n/a
3	CEBPB	chr6:163289641-163289999	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:163289670-163289966	A549	lung:	n/a	n/a
5	CEBPB	chr6:163265469-163265817	HepG2	liver:	n/a	chr6:163265628-163265639
6	CEBPB	chr6:163254941-163255044	A549	lung:	n/a	chr6:163254971-163254982
7	CEBPB	chr6:163289803-163289880	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:163274043-163274199	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:163254840-163255091	HepG2	liver:	n/a	chr6:163254848-163254861 chr6:163254971-163254982
10	CEBPB	chr6:163265498-163265698	K562	blood:	n/a	chr6:163265628-163265639
11	CEBPB	chr6:163270461-163270490	HepG2	liver:	n/a	n/a
12	CHD2	chr6:163235253-163235303	HepG2	liver:	n/a	n/a
13	CHD2	chr6:163277838-163278273	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr6:163277830-163278317	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:163277960-163278110	SAEC	small airway:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
16	CTCF	chr6:163277958-163277990	GM10248	blood:	n/a	n/a
17	CTCF	chr6:163277892-163278123	Pancreas_OC	pancreas:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
18	CTCF	chr6:163277900-163278050	K562	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
19	CTCF	chr6:163277891-163278135	LNCaP	prostate:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
20	CTCF	chr6:163277260-163277410	BJ	skin:	n/a	n/a
21	CTCF	chr6:163277920-163278070	WI-38	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
22	CTCF	chr6:163277967-163278091	GM12892	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
23	CTCF	chr6:163267100-163267250	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr6:163277900-163278050	GM12867	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
25	CTCF	chr6:163277939-163278111	Lung_OC	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
26	CTCF	chr6:163267120-163267270	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr6:163277586-163278715	SK-N-SH	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
28	CTCF	chr6:163277940-163278090	HCFaa	heart:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
29	CTCF	chr6:163267140-163267290	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:163277920-163278070	HPAF	blood vessel:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
31	CTCF	chr6:163277912-163278120	SK-N-SH_RA	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
32	CTCF	chr6:163277960-163278110	GM12870	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
33	CTCF	chr6:163277860-163278010	WI-38	lung:	n/a	n/a
34	CTCF	chr6:163277845-163278141	A549	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
35	CTCF	chr6:163277920-163278070	WERI-Rb-1	eye:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
36	CTCF	chr6:163277960-163278110	HVMF	connective:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
37	CTCF	chr6:163276860-163277010	AG04449	skin:	n/a	n/a
38	CTCF	chr6:163277886-163278128	MCF-7	breast:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
39	CTCF	chr6:163277900-163278149	Fibrobl	skin:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
40	CTCF	chr6:163277907-163278102	K562	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
41	CTCF	chr6:163277980-163278130	GM12873	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
42	CTCF	chr6:163277940-163278090	SK-N-SH_RA	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
43	CTCF	chr6:163277920-163278070	BE2_C	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
44	CTCF	chr6:163277920-163278070	SK-N-SH_RA	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
45	CTCF	chr6:163277900-163278050	HFF	foreskin:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
46	CTCF	chr6:163277897-163278130	ProgFib	skin:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
47	CTCF	chr6:163278060-163278210	GM12868	blood:	n/a	n/a
48	CTCF	chr6:163277840-163277990	GM12866	blood:	n/a	n/a
49	CTCF	chr6:163277913-163278115	MCF-7	breast:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
50	CTCF	chr6:163277914-163278126	A549	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163273217-163273267	Hepatocyte	liver:	n/a
2	chr6:163276038-163276088	HAEpiC	amniotic membrane:	n/a
3	chr6:163278126-163278176	SAEC	small airway:	n/a
4	chr6:163275952-163276002	HRPEpiC	eye:	n/a
5	chr6:163289702-163289752	ECC-1	luminal epithelium:	n/a
6	chr6:163276038-163276088	GM06990	blood:	n/a
7	chr6:163289702-163289752	NT2-D1	testis:	n/a
8	chr6:163276038-163276088	T-47D	breast:	n/a
9	chr6:163289514-163289564	NHDF-neo	bronchial:	n/a
10	chr6:163278126-163278176	Hela-S3	cervix:	n/a
11	chr6:163278126-163278176	HL-60	blood:	n/a
12	chr6:163276038-163276088	NHBE	bronchial:	n/a
13	chr6:163289631-163289681	NHBE	bronchial:	n/a
14	chr6:163273217-163273267	PANC-1	pancreas:	n/a
15	chr6:163275952-163276002	NHBE	bronchial:	n/a
16	chr6:163276038-163276088	GM12892	blood:	n/a
17	chr6:163278126-163278176	CMK	blood:	n/a
18	chr6:163273217-163273267	SK-N-SH	brain:	n/a
19	chr6:163289514-163289564	LNCaP	prostate:	n/a
20	chr6:163275952-163276002	NH-A	brain:	n/a
21	chr6:163275952-163276002	BE2_C	brain:	n/a
22	chr6:163278126-163278176	SKMC	muscle:	n/a
23	chr6:163289702-163289752	AG09309	skin:	n/a
24	chr6:163276038-163276088	HCPEpiC	choroid plexus:	n/a
25	chr6:163275952-163276002	SK-N-SH	brain:	n/a
26	chr6:163278126-163278176	AoSMC	blood vessel:	n/a
27	chr6:163289514-163289564	Hela-S3	cervix:	n/a
28	chr6:163278126-163278176	HIPEpiC	eye:	n/a
29	chr6:163289631-163289681	PrEC	prostate:	n/a
30	chr6:163276038-163276088	AG09319	gingival:	n/a
31	chr6:163289514-163289564	NT2-D1	testis:	n/a
32	chr6:163275952-163276002	GM19239	blood:	n/a
33	chr6:163275980-163276030	HEK293	kidney:	embryo
34	chr6:163273217-163273267	BE2_C	brain:	n/a
35	chr6:163275980-163276030	BJ	skin:	n/a
36	chr6:163275980-163276030	SK-N-SH_RA	brain:	n/a
37	chr6:163289702-163289752	MCF-7	breast:	n/a
38	chr6:163276038-163276088	SKMC	muscle:	n/a
39	chr6:163275980-163276030	MCF-7	breast:	n/a
40	chr6:163278126-163278176	HCM	heart:	n/a
41	chr6:163275980-163276030	AG09319	gingival:	n/a
42	chr6:163273217-163273267	HEEpiC	esophagus:	n/a
43	chr6:163275952-163276002	BJ	skin:	n/a
44	chr6:163276038-163276088	PANC-1	pancreas:	n/a
45	chr6:163278126-163278176	ovcar-3	ovarian:	n/a
46	chr6:163275952-163276002	HepG2	liver:	n/a
47	chr6:163289631-163289681	ProgFib	skin:	n/a
48	chr6:163273217-163273267	MCF10A-Er-Src	breast:	n/a
49	chr6:163289631-163289681	Jurkat	blood:	n/a
50	chr6:163276038-163276088	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
2	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
3	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
4	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
5	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
6	chr4:72393798..72394589-chr6:163273105..163273631,2	MCF-7	breast:

Variant related genes	Relation type
PACRG	TF binding region
PACRG	CpG island

Extended variants
information (count: 1689 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566366340	chr6:163235114-163235115	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373472472	chr6:163235154-163235155	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs111431655	chr6:163235158-163235159	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201609837	chr6:163235167-163235168	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs375362455	chr6:163235168-163235169	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs62428960	chr6:163235169-163235170	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs78706312	chr6:163235171-163235172	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs544983734	chr6:163235174-163235175	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377178341	chr6:163235179-163235180	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs146271153	chr6:163235197-163235198	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs138091090	chr6:163235202-163235203	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs575481178	chr6:163235227-163235228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142680257	chr6:163235235-163235236	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376828813	chr6:163235239-163235240	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs111927177	chr6:163235259-163235260	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369315812	chr6:163235269-163235270	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs560873912	chr6:163235278-163235279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538821670	chr6:163235288-163235289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76289683	chr6:163235304-163235305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200691930	chr6:163235322-163235323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376896951	chr6:163235342-163235343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200987111	chr6:163235350-163235351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199913677	chr6:163235351-163235352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551735698	chr6:163235373-163235374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181622640	chr6:163235403-163235404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187593202	chr6:163235429-163235430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34399515	chr6:163235461-163235462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551248920	chr6:163235488-163235489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190330943	chr6:163235489-163235490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536829134	chr6:163235524-163235525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553648022	chr6:163235527-163235528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12664922	chr6:163235542-163235543	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs79014228	chr6:163235610-163235611	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181046889	chr6:163235639-163235640	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs575105569	chr6:163235653-163235654	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs543807853	chr6:163235687-163235688	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554402838	chr6:163235731-163235732	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs71567674	chr6:163235800-163235801	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185305227	chr6:163235801-163235802	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs537353464	chr6:163235824-163235825	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116334867	chr6:163235828-163235829	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532350401	chr6:163235832-163235833	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs545141418	chr6:163235838-163235839	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs189664081	chr6:163235839-163235840	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs527346112	chr6:163235840-163235841	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs374075830	chr6:163235865-163235866	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs551035533	chr6:163235876-163235877	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs567956811	chr6:163235906-163235907	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs530443618	chr6:163235956-163235957	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs182712841	chr6:163236025-163236026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Renal cell carcinoma	18592004	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
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163230800-163238400	Weak transcription	Gastric	stomach
2	chr6:163231200-163237800	Weak transcription	Pancreas	Pancrea
3	chr6:163232600-163240000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:163235200-163235600	Weak transcription	Brain Anterior Caudate	brain
5	chr6:163235200-163236000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:163235600-163236000	Active TSS	Brain Anterior Caudate	brain
7	chr6:163235600-163236200	Enhancers	Brain Hippocampus Middle	brain
8	chr6:163236000-163242000	Weak transcription	Brain Anterior Caudate	brain
9	chr6:163236200-163241000	Weak transcription	Brain Hippocampus Middle	brain
10	chr6:163237800-163238600	ZNF genes & repeats	Pancreas	Pancrea
11	chr6:163238000-163238200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:163238000-163238600	Enhancers	NHDF-Ad	bronchial
13	chr6:163238200-163238400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:163238400-163238600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:163238400-163238600	Enhancers	Gastric	stomach
16	chr6:163240600-163243000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:163241000-163241800	Enhancers	Brain Hippocampus Middle	brain
18	chr6:163241400-163242200	Enhancers	Fetal Brain Female	brain
19	chr6:163241400-163242400	Enhancers	Brain Angular Gyrus	brain
20	chr6:163241800-163242200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:163241800-163242200	Weak transcription	Brain Hippocampus Middle	brain
22	chr6:163241800-163242600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:163241800-163242800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:163241800-163242800	Enhancers	Fetal Brain Male	brain
25	chr6:163242000-163242400	Enhancers	Brain Anterior Caudate	brain
26	chr6:163242200-163242400	Enhancers	Brain Substantia Nigra	brain
27	chr6:163242200-163242800	Enhancers	Brain Germinal Matrix	brain
28	chr6:163242200-163243000	Active TSS	Brain Hippocampus Middle	brain
29	chr6:163242400-163242600	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr6:163242400-163242800	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr6:163242400-163243000	Active TSS	Brain Cingulate Gyrus	brain
32	chr6:163242400-163248400	Weak transcription	Brain Angular Gyrus	brain
33	chr6:163242600-163243000	Active TSS	Brain Anterior Caudate	brain
34	chr6:163242800-163243000	Active TSS	Brain Substantia Nigra	brain
35	chr6:163243000-163245000	Weak transcription	Brain Hippocampus Middle	brain
36	chr6:163243000-163245400	Weak transcription	Brain Anterior Caudate	brain
37	chr6:163243000-163245400	Weak transcription	Brain Substantia Nigra	brain
38	chr6:163243000-163245600	Weak transcription	Brain Cingulate Gyrus	brain
39	chr6:163243200-163243400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr6:163243400-163245600	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr6:163245000-163245600	Enhancers	Brain Hippocampus Middle	brain
42	chr6:163245200-163245400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:163245200-163245600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:163245400-163245600	Enhancers	Brain Anterior Caudate	brain
45	chr6:163245400-163245800	Enhancers	Brain Substantia Nigra	brain
46	chr6:163245400-163246200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:163245600-163245800	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr6:163245600-163245800	Flanking Active TSS	Brain Cingulate Gyrus	brain
49	chr6:163245600-163246000	Active TSS	Brain Hippocampus Middle	brain
50	chr6:163245600-163246000	Active TSS	Brain Inferior Temporal Lobe	brain

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