Variant report

Variant	nsv5201
Chromosome Location	chr6:11833966-11879236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:244)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:11834158-11835057	K562	blood:	n/a	n/a
2	ATF1	chr6:11866440-11866521	K562	blood:	n/a	n/a
3	ATF1	chr6:11834354-11834703	K562	blood:	n/a	n/a
4	ATF2	chr6:11876964-11878145	GM12878	blood:	n/a	n/a
5	ATF2	chr6:11833763-11835140	GM12878	blood:	n/a	n/a
6	ATF2	chr6:11851308-11853171	GM12878	blood:	n/a	n/a
7	ATF2	chr6:11854816-11855340	GM12878	blood:	n/a	n/a
8	ATF2	chr6:11876807-11877987	GM12878	blood:	n/a	n/a
9	ATF2	chr6:11834010-11835054	GM12878	blood:	n/a	n/a
10	ATF2	chr6:11851503-11853349	GM12878	blood:	n/a	n/a
11	ATF3	chr6:11834353-11834786	K562	blood:	n/a	chr6:11834684-11834695
12	BACH1	chr6:11834141-11834776	K562	blood:	n/a	n/a
13	BATF	chr6:11834320-11834900	GM12878	blood:	n/a	n/a
14	BATF	chr6:11855129-11855368	GM12878	blood:	n/a	n/a
15	BATF	chr6:11877138-11877648	GM12878	blood:	n/a	n/a
16	BATF	chr6:11851527-11852047	GM12878	blood:	n/a	n/a
17	BATF	chr6:11852193-11852897	GM12878	blood:	n/a	n/a
18	BATF	chr6:11834428-11834786	GM12878	blood:	n/a	n/a
19	BATF	chr6:11876925-11877701	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:11877146-11877674	GM12878	blood:	n/a	chr6:11877342-11877351
21	BCL11A	chr6:11852260-11852910	GM12878	blood:	n/a	chr6:11852717-11852726
22	BCL11A	chr6:11834423-11834828	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:11833936-11834955	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:11851550-11851974	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:11877046-11877661	GM12878	blood:	n/a	chr6:11877342-11877351
26	BCL3	chr6:11851515-11852111	GM12878	blood:	n/a	n/a
27	BCL3	chr6:11834493-11834880	GM12878	blood:	n/a	n/a
28	BCL3	chr6:11852136-11852967	GM12878	blood:	n/a	chr6:11852717-11852726
29	BCL3	chr6:11852365-11852875	GM12878	blood:	n/a	chr6:11852717-11852726
30	BCL3	chr6:11876975-11877692	GM12878	blood:	n/a	chr6:11877342-11877351
31	BCL3	chr6:11834164-11834952	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:11834289-11834946	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:11851525-11852184	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:11876856-11878149	GM12878	blood:	n/a	chr6:11877342-11877351
35	BCLAF1	chr6:11852251-11853031	GM12878	blood:	n/a	chr6:11852717-11852726
36	BCLAF1	chr6:11834219-11835064	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:11876790-11878443	GM12878	blood:	n/a	chr6:11877342-11877351
38	BCLAF1	chr6:11851587-11852960	GM12878	blood:	n/a	chr6:11852717-11852726
39	BHLHE40	chr6:11834157-11834760	K562	blood:	n/a	n/a
40	BHLHE40	chr6:11877027-11877787	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:11834115-11835104	GM12878	blood:	n/a	n/a
42	BRCA1	chr6:11835462-11835514	GM12878	blood:	n/a	n/a
43	CBX3	chr6:11847281-11847693	K562	blood:	n/a	n/a
44	CBX3	chr6:11855980-11856414	K562	blood:	n/a	chr6:11856390-11856401
45	CBX3	chr6:11833756-11834948	K562	blood:	n/a	n/a
46	CBX3	chr6:11847348-11847585	K562	blood:	n/a	n/a
47	CBX3	chr6:11834370-11834798	K562	blood:	n/a	n/a
48	CCNT2	chr6:11834170-11834801	K562	blood:	n/a	chr6:11834541-11834561
49	CEBPB	chr6:11869907-11870239	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:11864156-11864318	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:11855283-11855333	AG09309	skin:	n/a
2	chr6:11870215-11870265	HRPEpiC	eye:	n/a
3	chr6:11878092-11878142	PANC-1	pancreas:	n/a
4	chr6:11870215-11870265	U87	brain:	n/a
5	chr6:11855283-11855333	Hepatocyte	liver:	n/a
6	chr6:11855283-11855333	T-47D	breast:	n/a
7	chr6:11855283-11855333	ProgFib	skin:	n/a
8	chr6:11878092-11878142	BJ	skin:	n/a
9	chr6:11878092-11878142	Hela-S3	cervix:	n/a
10	chr6:11870215-11870265	HepG2	liver:	n/a
11	chr6:11855283-11855333	K562	blood:	n/a
12	chr6:11850038-11850088	HAEpiC	amniotic membrane:	n/a
13	chr6:11850038-11850088	GM06990	blood:	n/a
14	chr6:11870215-11870265	HCPEpiC	choroid plexus:	n/a
15	chr6:11870215-11870265	NH-A	brain:	n/a
16	chr6:11878092-11878142	GM12892	blood:	n/a
17	chr6:11855283-11855333	SK-N-SH	brain:	n/a
18	chr6:11870215-11870265	HCT-116	colon:	n/a
19	chr6:11855283-11855333	HCPEpiC	choroid plexus:	n/a
20	chr6:11855283-11855333	AoSMC	blood vessel:	n/a
21	chr6:11878092-11878142	HCPEpiC	choroid plexus:	n/a
22	chr6:11850038-11850088	HIPEpiC	eye:	n/a
23	chr6:11878092-11878142	LNCaP	prostate:	n/a
24	chr6:11878092-11878142	HRCEpiC	kidney:	n/a
25	chr6:11850038-11850088	HEK293	kidney:	embryo
26	chr6:11855283-11855333	SK-N-SH_RA	brain:	n/a
27	chr6:11870215-11870265	LNCaP	prostate:	n/a
28	chr6:11850038-11850088	GM19239	blood:	n/a
29	chr6:11855283-11855333	U87	brain:	n/a
30	chr6:11855283-11855333	GM19239	blood:	n/a
31	chr6:11850038-11850088	BJ	skin:	n/a
32	chr6:11870215-11870265	Caco-2	colon:	n/a
33	chr6:11870215-11870265	SK-N-SH	brain:	n/a
34	chr6:11870215-11870265	MCF-7	breast:	n/a
35	chr6:11850038-11850088	Hela-S3	cervix:	n/a
36	chr6:11850038-11850088	IMR90	lung:	fetal
37	chr6:11878092-11878142	AG04449	skin:	fetal
38	chr6:11850038-11850088	HCM	heart:	n/a
39	chr6:11878092-11878142	AG04450	lung:	fetal
40	chr6:11850038-11850088	SAEC	small airway:	n/a
41	chr6:11855283-11855333	GM12878	blood:	n/a
42	chr6:11878092-11878142	HL-60	blood:	n/a
43	chr6:11855283-11855333	IMR90	lung:	fetal
44	chr6:11850038-11850088	PFSK-1	brain:	n/a
45	chr6:11850038-11850088	CMK	blood:	n/a
46	chr6:11870215-11870265	GM12891	blood:	n/a
47	chr6:11855283-11855333	HCF	heart:	n/a
48	chr6:11855283-11855333	PFSK-1	brain:	n/a
49	chr6:11870215-11870265	GM12892	blood:	n/a
50	chr6:11878092-11878142	HUVEC	blood vessel:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:11848626..11851271-chr6:11851850..11855072,3	K562	blood:
2	chr6:11854081..11855921-chr6:11860130..11862778,2	MCF-7	breast:
3	chr6:11854715..11856234-chr6:11857664..11859320,2	K562	blood:
4	chr6:11878891..11880864-chr6:11887046..11889738,2	K562	blood:
5	chr6:11867335..11870900-chr6:11873220..11876785,3	K562	blood:
6	chr6:11845664..11847912-chr6:11959676..11961554,2	K562	blood:
7	chr6:11854081..11855921-chr6:11860130..11862778,2	MCF-7	breast:
8	chr6:11851522..11853386-chr6:11855084..11856597,2	K562	blood:
9	chr6:11843056..11848062-chr6:11852373..11856845,8	K562	blood:
10	chr6:11834747..11836299-chr6:11847370..11849609,2	K562	blood:
11	chr6:11865768..11869319-chr6:12009325..12011874,4	K562	blood:
12	chr6:11867335..11870900-chr6:11873220..11876785,3	K562	blood:
13	chr6:11834799..11837724-chr6:11847345..11849609,2	K562	blood:
14	chr6:11864063..11866982-chr6:11867941..11870630,2	K562	blood:
15	chr6:11827879..11830513-chr6:11831629..11834236,2	K562	blood:
16	chr6:11872455..11874003-chr6:11877314..11879438,2	K562	blood:
17	chr6:11827648..11830540-chr6:11831629..11835568,4	K562	blood:
18	chr6:11848626..11851271-chr6:11851850..11855072,3	K562	blood:
19	chr6:11778590..11780846-chr6:11834155..11835984,2	K562	blood:
20	chr6:11843056..11848062-chr6:11852373..11856845,8	K562	blood:
21	chr6:11851522..11853386-chr6:11855084..11856597,2	K562	blood:
22	chr6:11864063..11866982-chr6:11867941..11870630,2	K562	blood:
23	chr6:11870406..11872624-chr6:11873723..11875888,2	K562	blood:
24	chr6:11870281..11872395-chr6:11964255..11966450,2	K562	blood:
25	chr6:11853455..11855505-chr6:11871944..11874636,2	K562	blood:
26	chr6:11872455..11874003-chr6:11877314..11879438,2	K562	blood:
27	chr6:11868745..11870307-chr6:11874002..11876924,2	K562	blood:
28	chr6:11830706..11832561-chr6:11832566..11834578,2	K562	blood:
29	chr6:11834747..11836299-chr6:11847370..11849609,2	K562	blood:
30	chr6:11873602..11875677-chr6:12009027..12011838,2	K562	blood:
31	chr6:11844746..11849186-chr6:12011499..12014000,4	MCF-7	breast:
32	chr6:11868745..11870307-chr6:11874002..11876924,2	K562	blood:
33	chr6:11867657..11870618-chr6:11870825..11872427,2	K562	blood:
34	chr6:11864395..11867152-chr6:11883777..11885671,2	K562	blood:
35	chr6:11853455..11855505-chr6:11871944..11874636,2	K562	blood:
36	chr6:11876284..11878827-chr6:11879684..11881486,2	K562	blood:
37	chr6:11870406..11872624-chr6:11873723..11875888,2	K562	blood:
38	chr6:11865768..11868889-chr6:12009325..12011874,3	K562	blood:
39	chr6:11854715..11856234-chr6:11857664..11859320,2	K562	blood:
40	chr6:11867657..11870618-chr6:11870825..11872427,2	K562	blood:
41	chr6:11857117..11858868-chr6:11889391..11891505,2	K562	blood:
42	chr6:11834799..11837724-chr6:11847345..11849609,2	K562	blood:
43	chr6:11817460..11820356-chr6:11831613..11834346,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf105-1	chr6:11868339-11868724	XLOC_005607
2	lnc-C6orf105-3	chr6:11861859-11863203	NONHSAT107765
3	lnc-C6orf105-1	chr6:11865833-11865892	XLOC_005607

No data

Variant related genes	Relation type
ENSG00000215124	TF binding region
ENSG00000215124	CpG island
ENSG00000095951	chromatin interactions
ENSG00000111863	chromatin interactions
RBCK1	miRNA target sites
TNFRSF21	miRNA target sites

Extended variants
information (count: 1513 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550865416	chr6:11833973-11833974	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs543291448	chr6:11834004-11834005	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs571119705	chr6:11834093-11834094	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs115387558	chr6:11834153-11834154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552135242	chr6:11834156-11834157	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565511563	chr6:11834167-11834168	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534725122	chr6:11834173-11834174	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554665819	chr6:11834181-11834182	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111565175	chr6:11834194-11834195	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6902916	chr6:11834200-11834201	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs537242204	chr6:11834209-11834210	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557017123	chr6:11834224-11834225	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10223767	chr6:11834231-11834232	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552192803	chr6:11834263-11834264	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563493056	chr6:11834406-11834407	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180834510	chr6:11834421-11834422	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553351450	chr6:11834450-11834451	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13208185	chr6:11834477-11834478	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541926882	chr6:11834500-11834501	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561798477	chr6:11834506-11834507	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531055587	chr6:11834518-11834519	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78137886	chr6:11834533-11834534	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185488457	chr6:11834543-11834544	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10485419	chr6:11834552-11834553	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61704747	chr6:11834574-11834575	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145416914	chr6:11834583-11834584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559401463	chr6:11834609-11834610	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140996627	chr6:11834622-11834623	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144207804	chr6:11834623-11834624	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548354409	chr6:11834632-11834633	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147781393	chr6:11834682-11834683	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537281001	chr6:11834689-11834690	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs550731454	chr6:11834721-11834722	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570523822	chr6:11834722-11834723	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529377705	chr6:11834768-11834769	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs9296175	chr6:11834783-11834784	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374354106	chr6:11834866-11834867	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs9462160	chr6:11834883-11834884	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs555851628	chr6:11834906-11834907	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555479682	chr6:11834928-11834929	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575318061	chr6:11834994-11834995	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190983355	chr6:11835148-11835149	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2327487	chr6:11835155-11835156	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs9394332	chr6:11835174-11835175	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs113535509	chr6:11835175-11835176	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538255296	chr6:11835205-11835206	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545366807	chr6:11835212-11835213	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559163486	chr6:11835224-11835225	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs61127331	chr6:11835267-11835268	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs397968276	chr6:11835274-11835275	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11829600-11834200	Weak transcription	Fetal Lung	lung
2	chr6:11831000-11834400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:11831000-11835400	Weak transcription	Left Ventricle	heart
4	chr6:11831200-11834000	Weak transcription	Fetal Heart	heart
5	chr6:11833800-11834200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr6:11833800-11834200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:11833800-11834200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:11833800-11834200	Enhancers	Gastric	stomach
9	chr6:11833800-11834200	Enhancers	Pancreas	Pancrea
10	chr6:11833800-11834600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:11833800-11834600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:11833800-11834800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:11833800-11834800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:11833800-11835200	Flanking Active TSS	K562	blood
15	chr6:11833800-11835600	Flanking Active TSS	GM12878-XiMat	blood
16	chr6:11833800-11835800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr6:11833800-11835800	Enhancers	Liver	Liver
18	chr6:11833800-11836000	Enhancers	Fetal Muscle Leg	muscle
19	chr6:11834000-11834200	Enhancers	Esophagus	oesophagus
20	chr6:11834000-11834200	Enhancers	Stomach Mucosa	stomach
21	chr6:11834000-11834400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr6:11834000-11834600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr6:11834000-11836000	Enhancers	Fetal Heart	heart
24	chr6:11834200-11834600	Enhancers	HSMMtube	muscle
25	chr6:11834200-11834600	Enhancers	NHEK	skin
26	chr6:11834200-11834800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:11834200-11835200	Weak transcription	Pancreas	Pancrea
28	chr6:11834200-11835400	Weak transcription	Esophagus	oesophagus
29	chr6:11834200-11835400	Weak transcription	Gastric	stomach
30	chr6:11834200-11836400	Enhancers	Fetal Lung	lung
31	chr6:11834400-11834600	Enhancers	Spleen	Spleen
32	chr6:11834400-11835800	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr6:11835000-11835200	Enhancers	Stomach Mucosa	stomach
34	chr6:11835200-11835800	Enhancers	Pancreas	Pancrea
35	chr6:11835200-11836400	Enhancers	K562	blood
36	chr6:11835400-11835600	Enhancers	Placenta	Placenta
37	chr6:11835400-11835600	Enhancers	Gastric	stomach
38	chr6:11835400-11835600	Enhancers	Left Ventricle	heart
39	chr6:11835400-11835800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:11835400-11835800	Enhancers	Adipose Nuclei	Adipose
41	chr6:11835400-11835800	Enhancers	Esophagus	oesophagus
42	chr6:11835400-11835800	Enhancers	Right Ventricle	heart
43	chr6:11835600-11836200	Enhancers	GM12878-XiMat	blood
44	chr6:11835800-11838200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:11836200-11837800	ZNF genes & repeats	GM12878-XiMat	blood
46	chr6:11838200-11838400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
47	chr6:11839800-11840800	Weak transcription	Stomach Mucosa	stomach
48	chr6:11843600-11844400	Enhancers	K562	blood
49	chr6:11844000-11844200	Enhancers	Liver	Liver
50	chr6:11844400-11846200	Weak transcription	Liver	Liver

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