Variant report

Variant	nsv528627
Chromosome Location	chr6:4614058-4731340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1320)
CpG islands
(count:977)
Chromatin interactive
region (count:73)
LncRNA
region (count:55)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4650189-4650193	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:4647875-4648330	K562	blood:	n/a	n/a
3	ARID3A	chr6:4620543-4620713	K562	blood:	n/a	n/a
4	ARID3A	chr6:4688038-4689055	K562	blood:	n/a	n/a
5	ARID3A	chr6:4727891-4728610	K562	blood:	n/a	n/a
6	ARID3A	chr6:4620926-4621110	K562	blood:	n/a	n/a
7	ATF1	chr6:4637948-4638292	K562	blood:	n/a	n/a
8	ATF1	chr6:4727873-4728686	K562	blood:	n/a	n/a
9	ATF1	chr6:4650013-4650245	K562	blood:	n/a	n/a
10	ATF1	chr6:4703497-4703955	K562	blood:	n/a	n/a
11	ATF1	chr6:4688278-4688845	K562	blood:	n/a	n/a
12	ATF1	chr6:4664352-4664687	K562	blood:	n/a	n/a
13	ATF1	chr6:4620690-4621206	K562	blood:	n/a	n/a
14	ATF2	chr6:4638038-4638379	GM12878	blood:	n/a	n/a
15	ATF2	chr6:4647829-4648277	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr6:4688192-4688813	K562	blood:	n/a	n/a
17	ATF3	chr6:4637956-4638325	K562	blood:	n/a	n/a
18	BACH1	chr6:4688454-4688891	K562	blood:	n/a	n/a
19	BACH1	chr6:4727908-4728397	K562	blood:	n/a	n/a
20	BACH1	chr6:4687552-4687554	K562	blood:	n/a	n/a
21	BACH1	chr6:4621276-4621439	K562	blood:	n/a	n/a
22	BACH1	chr6:4648012-4648220	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:4663252-4663269	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:4702214-4702221	K562	blood:	n/a	n/a
25	BACH1	chr6:4684779-4684781	K562	blood:	n/a	n/a
26	BATF	chr6:4638043-4638406	GM12878	blood:	n/a	chr6:4638160-4638171
27	BATF	chr6:4637945-4638444	GM12878	blood:	n/a	chr6:4638160-4638171
28	BCL3	chr6:4620863-4621242	K562	blood:	n/a	n/a
29	BHLHE40	chr6:4640512-4640781	K562	blood:	n/a	n/a
30	BHLHE40	chr6:4728943-4729262	K562	blood:	n/a	n/a
31	BHLHE40	chr6:4664284-4664656	K562	blood:	n/a	n/a
32	BHLHE40	chr6:4645225-4645479	K562	blood:	n/a	n/a
33	BHLHE40	chr6:4678878-4678985	K562	blood:	n/a	n/a
34	BHLHE40	chr6:4647883-4648125	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:4620882-4621389	K562	blood:	n/a	n/a
36	BHLHE40	chr6:4647720-4648244	K562	blood:	n/a	n/a
37	BHLHE40	chr6:4688206-4688863	K562	blood:	n/a	n/a
38	BHLHE40	chr6:4619670-4619703	K562	blood:	n/a	n/a
39	BHLHE40	chr6:4669255-4669418	K562	blood:	n/a	n/a
40	BHLHE40	chr6:4712904-4713058	K562	blood:	n/a	n/a
41	BHLHE40	chr6:4646453-4646651	K562	blood:	n/a	chr6:4646584-4646593 chr6:4646584-4646593
42	BHLHE40	chr6:4727878-4728673	K562	blood:	n/a	n/a
43	BHLHE40	chr6:4705056-4705069	K562	blood:	n/a	n/a
44	BHLHE40	chr6:4688309-4688571	A549	lung:	n/a	n/a
45	BHLHE40	chr6:4647807-4648197	A549	lung:	n/a	n/a
46	BHLHE40	chr6:4647818-4648225	HepG2	liver:	n/a	n/a
47	BRCA1	chr6:4686513-4686621	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr6:4647896-4648052	HepG2	liver:	n/a	n/a
49	BRCA1	chr6:4647878-4648141	H1-hESC	embryonic stem cell:	n/a	n/a
50	CBX3	chr6:4647692-4648265	K562	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4705358-4705408	LNCaP	prostate:	n/a
2	chr6:4705358-4705408	LNCaP	prostate:	n/a
3	chr6:4647922-4647972	K562	blood:	n/a
4	chr6:4705358-4705408	AG09319	gingival:	n/a
5	chr6:4668978-4669028	HUVEC	blood vessel:	n/a
6	chr6:4655948-4655998	BJ	skin:	n/a
7	chr6:4647922-4647972	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:4655948-4655998	GM19239	blood:	n/a
9	chr6:4655948-4655998	ovcar-3	ovarian:	n/a
10	chr6:4724799-4724849	AoSMC	blood vessel:	n/a
11	chr6:4706244-4706294	K562	blood:	n/a
12	chr6:4655948-4655998	HL-60	blood:	n/a
13	chr6:4706336-4706386	GM19239	blood:	n/a
14	chr6:4706336-4706386	HCF	heart:	n/a
15	chr6:4663795-4663845	AG09319	gingival:	n/a
16	chr6:4725682-4725732	ECC-1	luminal epithelium:	n/a
17	chr6:4724799-4724849	GM06990	blood:	n/a
18	chr6:4724799-4724849	T-47D	breast:	n/a
19	chr6:4724822-4724872	GM12892	blood:	n/a
20	chr6:4725682-4725732	PFSK-1	brain:	n/a
21	chr6:4724822-4724872	HL-60	blood:	n/a
22	chr6:4705358-4705408	HNPCEpiC	eye:	n/a
23	chr6:4665238-4665288	SK-N-SH	brain:	n/a
24	chr6:4665238-4665288	MCF10A-Er-Src	breast:	n/a
25	chr6:4726088-4726138	NT2-D1	testis:	n/a
26	chr6:4724822-4724872	HEEpiC	esophagus:	n/a
27	chr6:4655948-4655998	HAEpiC	amniotic membrane:	n/a
28	chr6:4706427-4706477	U87	brain:	n/a
29	chr6:4706427-4706477	ProgFib	skin:	n/a
30	chr6:4672226-4672276	HAEpiC	amniotic membrane:	n/a
31	chr6:4724822-4724872	GM12878	blood:	n/a
32	chr6:4706170-4706220	HRPEpiC	eye:	n/a
33	chr6:4672226-4672276	MCF10A-Er-Src	breast:	n/a
34	chr6:4661470-4661520	MCF10A-Er-Src	breast:	n/a
35	chr6:4706427-4706477	SAEC	small airway:	n/a
36	chr6:4672226-4672276	AG10803	skin:	n/a
37	chr6:4705358-4705408	HUVEC	blood vessel:	n/a
38	chr6:4665238-4665288	HRCEpiC	kidney:	n/a
39	chr6:4706427-4706477	Hela-S3	cervix:	n/a
40	chr6:4663795-4663845	H1-hESC	embryonic stem cell:	embryo
41	chr6:4724822-4724872	SK-N-SH_RA	brain:	n/a
42	chr6:4706427-4706477	NH-A	brain:	n/a
43	chr6:4661470-4661520	HCM	heart:	n/a
44	chr6:4706427-4706477	BE2_C	brain:	n/a
45	chr6:4706427-4706477	HRCEpiC	kidney:	n/a
46	chr6:4706336-4706386	MCF10A-Er-Src	breast:	n/a
47	chr6:4706336-4706386	ProgFib	skin:	n/a
48	chr6:4706244-4706294	NH-A	brain:	n/a
49	chr6:4726088-4726138	PANC-1	pancreas:	n/a
50	chr6:4647922-4647972	HCT-116	colon:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:66728501..66730272-chr6:4624652..4627057,2	MCF-7	breast:
2	chr6:4644884..4647079-chr6:4776179..4778195,2	MCF-7	breast:
3	chr6:4728025..4731306-chr6:4774544..4778107,3	MCF-7	breast:
4	chr6:4675333..4676875-chr6:4782888..4785440,2	MCF-7	breast:
5	chr6:4638267..4640875-chr6:4647205..4649117,2	K562	blood:
6	chr6:4615595..4617785-chr6:4618078..4620387,2	MCF-7	breast:
7	chr6:4620258..4622044-chr6:4624001..4626369,2	K562	blood:
8	chr6:4685147..4686807-chr6:4775069..4777618,2	K562	blood:
9	chr6:4646287..4650411-chr6:4774854..4780233,12	K562	blood:
10	chr6:4645018..4646864-chr6:4803237..4804893,2	MCF-7	breast:
11	chr6:4646287..4650373-chr6:4775181..4778438,7	K562	blood:
12	chr6:4612784..4615620-chr6:4617174..4619845,3	MCF-7	breast:
13	chr6:4718988..4722844-chr6:4724027..4728055,6	K562	blood:
14	chr6:4721409..4723079-chr6:4724678..4726244,2	K562	blood:
15	chr6:4690130..4692411-chr6:4780659..4782960,2	K562	blood:
16	chr6:4647964..4649572-chr6:4651556..4653127,2	MCF-7	breast:
17	chr6:4709760..4712712-chr6:4714559..4717359,2	K562	blood:
18	chr6:4612784..4615620-chr6:4617174..4619845,3	MCF-7	breast:
19	chr6:4621801..4624729-chr6:4774076..4776880,2	MCF-7	breast:
20	chr6:4624057..4625751-chr6:4629629..4631647,2	MCF-7	breast:
21	chr6:4632734..4636747-chr6:4678109..4681305,3	K562	blood:
22	chr6:4687463..4689972-chr6:4776640..4778169,2	MCF-7	breast:
23	chr6:4646609..4648240-chr6:4675199..4677622,2	MCF-7	breast:
24	chr6:4617288..4619775-chr6:4621638..4623955,2	MCF-7	breast:
25	chr6:4682974..4686881-chr6:4686986..4689567,5	K562	blood:
26	chr6:4719796..4721427-chr6:4726780..4729427,2	K562	blood:
27	chr6:4669229..4672483-chr6:4677301..4680282,4	K562	blood:
28	chr6:4682974..4686881-chr6:4686986..4689567,5	K562	blood:
29	chr6:4635793..4639188-chr6:4775538..4778985,3	K562	blood:
30	chr6:4695384..4697674-chr6:4700163..4703758,3	K562	blood:
31	chr6:4620258..4622044-chr6:4624001..4626369,2	K562	blood:
32	chr6:4687332..4689780-chr6:4704649..4707466,2	MCF-7	breast:
33	chr6:4632734..4636747-chr6:4678109..4681305,3	K562	blood:
34	chr6:4669614..4671479-chr6:4675062..4677327,2	MCF-7	breast:
35	chr6:4702083..4703624-chr6:4704730..4707412,2	MCF-7	breast:
36	chr6:4690917..4693298-chr6:4715950..4718588,2	K562	blood:
37	chr6:4609256..4612508-chr6:4614034..4616803,3	MCF-7	breast:
38	chr6:4680994..4683726-chr6:4685254..4687018,2	K562	blood:
39	chr6:4718988..4722844-chr6:4724027..4728055,6	K562	blood:
40	chr6:4713443..4715108-chr6:4726463..4728712,2	MCF-7	breast:
41	chr6:4691449..4692204-chr6:142470501..142471255,2	MCF-7	breast:
42	chr6:4686580..4688742-chr6:4786418..4788333,2	K562	blood:
43	chr6:4629550..4631893-chr6:4635065..4638489,3	MCF-7	breast:
44	chr6:4646609..4648240-chr6:4675199..4677622,2	MCF-7	breast:
45	chr6:4647784..4649778-chr6:4649867..4652480,2	K562	blood:
46	chr6:4639154..4641926-chr6:4642797..4645246,2	MCF-7	breast:
47	chr6:4687974..4688722-chr6:4699245..4700235,2	MCF-7	breast:
48	chr6:4713443..4715108-chr6:4726463..4728712,2	MCF-7	breast:
49	chr6:4680994..4683726-chr6:4685254..4687018,2	K562	blood:
50	chr6:4671964..4676370-chr6:4676405..4678296,5	K562	blood:

(count:55 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDYL-4	chr6:4702697-4702888	NONHSAT107479
2	lnc-RPP40-8	chr6:4706718-4706802	NONHSAT107480
3	lnc-RPP40-7	chr6:4730973-4731447	NONHSAT107486
4	lnc-RPP40-8	chr6:4704607-4704897	NONHSAT107480
5	lnc-CDYL-8	chr6:4661139-4661258	NONHSAT107471
6	lnc-RPP40-7	chr6:4730590-4730812	NONHSAT107486
7	lnc-RPP40-8	chr6:4708189-4708367	NONHSAT107480
8	lnc-RPP40-8	chr6:4705386-4705507	NONHSAT107480
9	lnc-CDYL-10	chr6:4633462-4633496	FPKM1_group_27000_transcript_2
10	lnc-PPP1R3G-5	chr6:4714176-4714273	NONHSAT107481
11	lnc-RPP40-8	chr6:4705625-4705657	NONHSAT107480
12	lnc-CDYL-6	chr6:4687553-4687606	NONHSAT107475
13	lnc-CDYL-10	chr6:4633715-4637305	FPKM1_group_27000_transcript_2
14	lnc-CDYL-7	chr6:4674871-4674970	NONHSAT107472
15	lnc-CDYL-5	chr6:4693080-4693273	NONHSAT107478
16	lnc-CDYL-7	chr6:4675697-4675792	NONHSAT107472
17	lnc-PPP1R3G-5	chr6:4717517-4717570	NONHSAT107481
18	lnc-RPP40-8	chr6:4706279-4706353	NONHSAT107480
19	lnc-PPP1R3G-5	chr6:4717349-4717434	NONHSAT107481
20	lnc-CDYL-4	chr6:4697792-4697891	NONHSAT107479
21	lnc-CDYL-4	chr6:4699515-4699708	NONHSAT107479
22	lnc-CDYL-10	chr6:4633462-4633496	NONHSAT107466
23	lnc-CDYL-5	chr6:4691357-4691456	NONHSAT107478
24	lnc-RPP40-8	chr6:4706910-4707013	NONHSAT107480
25	lnc-RPP40-8	chr6:4703245-4703904	NONHSAT107480
26	lnc-PPP1R3G-5	chr6:4713624-4713669	NONHSAT107481
27	lnc-CDYL-4	chr6:4697538-4697657	NONHSAT107479
28	lnc-CDYL-6	chr6:4684216-4684313	NONHSAT107475
29	lnc-CDYL-4	chr6:4698618-4698713	NONHSAT107479
30	lnc-CDYL-6	chr6:4683664-4683709	NONHSAT107475
31	lnc-CDYL-5	chr6:4692183-4692278	NONHSAT107478
32	lnc-RPP40-8	chr6:4708623-4708706	NONHSAT107480
33	lnc-CDYL-6	chr6:4687385-4687470	NONHSAT107475
34	lnc-RPP40-8	chr6:4708005-4708055	NONHSAT107480
35	lnc-CDYL-8	chr6:4666301-4666493	NONHSAT107471
36	lnc-RPP40-8	chr6:4705004-4705115	NONHSAT107480
37	lnc-CDYL-7	chr6:4676594-4676787	NONHSAT107472
38	lnc-RPP40-8	chr6:4710461-4710990	NONHSAT107480
39	lnc-CDYL-7	chr6:4679779-4679971	NONHSAT107472
40	lnc-RPP40-8	chr6:4706568-4706636	NONHSAT107480
41	lnc-RPP40-8	chr6:4707099-4707350	NONHSAT107480
42	lnc-RPP40-8	chr6:4704021-4704135	NONHSAT107480
43	lnc-CDYL-7	chr6:4674617-4674736	NONHSAT107472
44	lnc-RPP40-7	chr6:4730149-4730395	NONHSAT107486
45	lnc-CDYL-8	chr6:4662219-4662314	NONHSAT107471
46	lnc-RPP40-9	chr6:4675353-4676068	NONHSAT107473
47	lnc-RPP40-8	chr6:4707619-4707916	NONHSAT107480
48	lnc-RPP40-9	chr6:4676599-4676717	NONHSAT107473
49	lnc-RPP40-8	chr6:4705195-4705290	NONHSAT107480
50	lnc-CDYL-8	chr6:4661393-4661492	NONHSAT107471

No data

Variant related genes	Relation type
CDYL	TF binding region
PSMC1P11	TF binding region
ENSG00000238801	TF binding region
CDYL	CpG island
PSMC1P11	CpG island
ENSG00000238801	CpG island
ENSG00000217385	chromatin interactions
ENSG00000238801	chromatin interactions
ENSG00000205444	chromatin interactions
ENSG00000153046	chromatin interactions
ENSG00000236336	chromatin interactions

Extended variants
information (count: 5056 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5056 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11756102	chr6:4614058-4614059	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149023830	chr6:4614115-4614116	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560471665	chr6:4614169-4614170	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115429108	chr6:4614300-4614301	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552383268	chr6:4614343-4614344	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568851300	chr6:4614349-4614350	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182879986	chr6:4614357-4614358	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531481415	chr6:4614360-4614361	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547982123	chr6:4614379-4614380	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570055465	chr6:4614412-4614413	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113903846	chr6:4614450-4614451	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553223205	chr6:4614494-4614495	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201895661	chr6:4614654-4614655	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143031932	chr6:4614657-4614658	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543951052	chr6:4614714-4614715	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559145354	chr6:4614718-4614719	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114123913	chr6:4614736-4614737	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544654655	chr6:4614747-4614748	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2143456	chr6:4614858-4614859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs148364155	chr6:4614866-4614867	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs9504170	chr6:4614867-4614868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560461968	chr6:4614869-4614870	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556301462	chr6:4614892-4614893	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113835891	chr6:4614893-4614894	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188883877	chr6:4614894-4614895	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368165252	chr6:4614899-4614900	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs193236916	chr6:4614903-4614904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558903881	chr6:4614908-4614909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547846380	chr6:4614929-4614930	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199767422	chr6:4614933-4614934	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6597083	chr6:4614934-4614935	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185420993	chr6:4614935-4614936	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146404580	chr6:4614949-4614950	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138401263	chr6:4614961-4614962	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556674095	chr6:4614981-4614982	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547418377	chr6:4614985-4614986	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142987827	chr6:4615044-4615045	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569400265	chr6:4615126-4615127	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538080882	chr6:4615147-4615148	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571272712	chr6:4615198-4615199	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs62384945	chr6:4615219-4615220	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575021987	chr6:4615247-4615248	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191231985	chr6:4615261-4615262	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368643377	chr6:4615263-4615264	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554256555	chr6:4615264-4615265	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577172543	chr6:4615271-4615272	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184199317	chr6:4615279-4615280	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562654600	chr6:4615281-4615282	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576157607	chr6:4615341-4615342	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs116488023	chr6:4615342-4615343	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4606000-4616800	Enhancers	Fetal Muscle Leg	muscle
2	chr6:4607600-4615200	Weak transcription	Lung	lung
3	chr6:4610800-4614200	Enhancers	Fetal Stomach	stomach
4	chr6:4612200-4614200	Enhancers	Rectal Smooth Muscle	rectum
5	chr6:4613000-4614200	Enhancers	HSMMtube	muscle
6	chr6:4613000-4614400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:4613200-4614400	Enhancers	Fetal Muscle Trunk	muscle
8	chr6:4613200-4614800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:4613400-4614800	Enhancers	Stomach Smooth Muscle	stomach
10	chr6:4613600-4614200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:4613600-4616200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:4613600-4619200	Weak transcription	Fetal Heart	heart
13	chr6:4613800-4614200	Bivalent Enhancer	HSMM	muscle
14	chr6:4613800-4616000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:4613800-4617600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:4613800-4621600	Weak transcription	Right Atrium	heart
17	chr6:4614200-4614400	Bivalent Enhancer	Fetal Stomach	stomach
18	chr6:4614200-4617000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:4614400-4614600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:4614400-4615800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr6:4614600-4629000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:4615200-4615600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:4615200-4615800	Enhancers	Lung	lung
24	chr6:4615400-4619800	Weak transcription	Placenta	Placenta
25	chr6:4615600-4617000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:4615800-4616400	Enhancers	Fetal Muscle Trunk	muscle
27	chr6:4615800-4616600	Weak transcription	Lung	lung
28	chr6:4616000-4616800	Enhancers	Adipose Nuclei	Adipose
29	chr6:4616000-4616800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr6:4616200-4617200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:4616400-4616600	Bivalent Enhancer	Osteobl	bone
32	chr6:4616400-4616800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:4616600-4616800	Enhancers	Lung	lung
34	chr6:4617000-4625800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:4617600-4617800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr6:4617600-4617800	Bivalent Enhancer	K562	blood
37	chr6:4619200-4619400	Active TSS	Fetal Heart	heart
38	chr6:4619200-4620400	Enhancers	K562	blood
39	chr6:4619800-4622400	Enhancers	Placenta	Placenta
40	chr6:4620000-4620600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:4620400-4621400	Flanking Active TSS	K562	blood
42	chr6:4620600-4621000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr6:4621400-4623000	Enhancers	K562	blood
44	chr6:4622200-4623000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:4622400-4624800	Weak transcription	Placenta	Placenta
46	chr6:4624600-4625200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr6:4624800-4625800	Enhancers	Placenta	Placenta
48	chr6:4625400-4626200	Bivalent Enhancer	K562	blood
49	chr6:4625800-4626000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:4626000-4626400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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