Variant report

Variant	nsv1017938
Chromosome Location	chr6:4729592-4774914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:366)
Chromatin interactive
region (count:38)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:4772867-4773525	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:4733133-4733552	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:4734664-4734771	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr6:4734461-4734854	A549	lung:	n/a	n/a
5	BHLHE40	chr6:4733098-4733508	K562	blood:	n/a	n/a
6	BHLHE40	chr6:4733176-4733463	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:4736046-4736261	K562	blood:	n/a	n/a
8	BRCA1	chr6:4734660-4734815	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr6:4740295-4740606	K562	blood:	n/a	n/a
10	CBX3	chr6:4733074-4733575	K562	blood:	n/a	n/a
11	CCNT2	chr6:4733175-4733488	K562	blood:	n/a	n/a
12	CEBPB	chr6:4761027-4761425	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:4761074-4761402	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:4752196-4752416	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:4740256-4740535	K562	blood:	n/a	n/a
16	CEBPB	chr6:4740266-4740583	K562	blood:	n/a	n/a
17	CEBPB	chr6:4761057-4761398	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:4761073-4761353	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:4761058-4761373	A549	lung:	n/a	n/a
20	CEBPB	chr6:4769769-4769823	K562	blood:	n/a	n/a
21	CEBPB	chr6:4761089-4761360	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:4733556-4733891	K562	blood:	n/a	n/a
23	CEBPB	chr6:4734518-4734798	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr6:4774262-4774450	A549	lung:	n/a	chr6:4774417-4774428 chr6:4774417-4774430
25	CEBPB	chr6:4774312-4774549	IMR90	lung:	n/a	chr6:4774417-4774428 chr6:4774417-4774430
26	CEBPB	chr6:4733258-4733806	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:4733226-4733909	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:4774261-4774533	HepG2	liver:	n/a	chr6:4774417-4774428 chr6:4774417-4774430
29	CEBPB	chr6:4761057-4761366	K562	blood:	n/a	n/a
30	CHD1	chr6:4773958-4774656	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr6:4774869-4775069	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:4772944-4773375	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr6:4734529-4735115	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr6:4733159-4733543	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr6:4733058-4733436	A549	lung:	n/a	n/a
36	CTCF	chr6:4734114-4734162	GM10248	blood:	n/a	n/a
37	CTCF	chr6:4758065-4758068	GM13976	blood:	n/a	n/a
38	CTCF	chr6:4733400-4733550	HEK293	kidney:	n/a	n/a
39	CTCF	chr6:4756380-4756530	GM12871	blood:	n/a	chr6:4756434-4756442
40	CTCF	chr6:4758001-4758062	GM13976	blood:	n/a	n/a
41	CTCF	chr6:4768440-4768590	GM12869	blood:	n/a	n/a
42	CTCF	chr6:4733280-4733430	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr6:4774600-4774750	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr6:4733226-4733508	K562	blood:	n/a	n/a
45	CUX1	chr6:4733099-4733371	K562	blood:	n/a	n/a
46	E2F4	chr6:4733230-4733476	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr6:4732963-4733641	A549	lung:	n/a	n/a
48	E2F6	chr6:4733107-4733514	K562	blood:	n/a	n/a
49	E2F6	chr6:4733090-4733582	A549	lung:	n/a	n/a
50	E2F6	chr6:4733177-4733423	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4774793-4774843	AG09309	skin:	n/a
2	chr6:4772890-4772940	PANC-1	pancreas:	n/a
3	chr6:4774793-4774843	SAEC	small airway:	n/a
4	chr6:4774309-4774359	HCPEpiC	choroid plexus:	n/a
5	chr6:4774309-4774359	SK-N-MC	brain:	n/a
6	chr6:4738782-4738832	HNPCEpiC	eye:	n/a
7	chr6:4734661-4734711	Caco-2	colon:	n/a
8	chr6:4774793-4774843	HL-60	blood:	n/a
9	chr6:4738782-4738832	MCF10A-Er-Src	breast:	n/a
10	chr6:4738782-4738832	Hepatocyte	liver:	n/a
11	chr6:4738782-4738832	HCT-116	colon:	n/a
12	chr6:4734661-4734711	RPTEC	kidney:	n/a
13	chr6:4774309-4774359	HRE	kidney:	n/a
14	chr6:4774309-4774359	HAEpiC	amniotic membrane:	n/a
15	chr6:4772890-4772940	AG04449	skin:	fetal
16	chr6:4734661-4734711	IMR90	lung:	fetal
17	chr6:4773278-4773328	AoSMC	blood vessel:	n/a
18	chr6:4773278-4773328	Hela-S3	cervix:	n/a
19	chr6:4734661-4734711	ECC-1	luminal epithelium:	n/a
20	chr6:4773278-4773328	HEEpiC	esophagus:	n/a
21	chr6:4774793-4774843	CMK	blood:	n/a
22	chr6:4772890-4772940	AG10803	skin:	n/a
23	chr6:4738782-4738832	PANC-1	pancreas:	n/a
24	chr6:4773278-4773328	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:4773278-4773328	MCF-7	breast:	n/a
26	chr6:4772890-4772940	U87	brain:	n/a
27	chr6:4774309-4774359	AoSMC	blood vessel:	n/a
28	chr6:4734661-4734711	SK-N-SH	brain:	n/a
29	chr6:4734661-4734711	NT2-D1	testis:	n/a
30	chr6:4738782-4738832	PFSK-1	brain:	n/a
31	chr6:4773278-4773328	Hepatocyte	liver:	n/a
32	chr6:4774309-4774359	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:4738782-4738832	NT2-D1	testis:	n/a
34	chr6:4773278-4773328	ProgFib	skin:	n/a
35	chr6:4738782-4738832	ProgFib	skin:	n/a
36	chr6:4734661-4734711	LNCaP	prostate:	n/a
37	chr6:4738782-4738832	HEEpiC	esophagus:	n/a
38	chr6:4774309-4774359	HepG2	liver:	n/a
39	chr6:4773278-4773328	H1-hESC	embryonic stem cell:	embryo
40	chr6:4773278-4773328	SAEC	small airway:	n/a
41	chr6:4774793-4774843	Hela-S3	cervix:	n/a
42	chr6:4773278-4773328	AG04450	lung:	fetal
43	chr6:4734661-4734711	ProgFib	skin:	n/a
44	chr6:4773278-4773328	U87	brain:	n/a
45	chr6:4774309-4774359	NT2-D1	testis:	n/a
46	chr6:4738782-4738832	SK-N-MC	brain:	n/a
47	chr6:4772890-4772940	ProgFib	skin:	n/a
48	chr6:4734661-4734711	HepG2	liver:	n/a
49	chr6:4738782-4738832	HL-60	blood:	n/a
50	chr6:4738782-4738832	NH-A	brain:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4733392..4734998-chr6:4742508..4744758,2	MCF-7	breast:
2	chr6:4754621..4757244-chr6:4826945..4828835,2	K562	blood:
3	chr6:4742875..4745464-chr6:4746219..4749155,2	K562	blood:
4	chr6:4728025..4731306-chr6:4774544..4778107,3	MCF-7	breast:
5	chr6:4730542..4732664-chr6:4733935..4736268,2	K562	blood:
6	chr6:4742191..4744161-chr6:4747870..4749647,2	MCF-7	breast:
7	chr6:4770328..4772807-chr6:4773025..4778379,5	MCF-7	breast:
8	chr6:4756162..4757939-chr6:4768050..4769568,2	K562	blood:
9	chr6:4742875..4745464-chr6:4746219..4749155,2	K562	blood:
10	chr6:4730542..4732664-chr6:4733935..4736268,2	K562	blood:
11	chr6:4747693..4749974-chr6:4813996..4815589,2	K562	blood:
12	chr6:4733801..4736473-chr6:4737548..4740491,3	K562	blood:
13	chr6:4762069..4764795-chr6:4775809..4777716,2	K562	blood:
14	chr6:4742191..4744161-chr6:4747870..4749647,2	MCF-7	breast:
15	chr6:4746486..4750179-chr6:4750849..4755110,4	K562	blood:
16	chr6:4758249..4760248-chr6:4797102..4799227,2	K562	blood:
17	chr6:4475486..4477630-chr6:4774016..4775629,2	MCF-7	breast:
18	chr6:4746486..4750179-chr6:4750849..4755110,4	K562	blood:
19	chr6:4746373..4750036-chr6:4750510..4753866,3	MCF-7	breast:
20	chr6:4734548..4736376-chr6:4775810..4777363,2	MCF-7	breast:
21	chr6:4757698..4760676-chr6:4762134..4764890,3	K562	blood:
22	chr6:4740877..4743157-chr6:4743622..4745166,2	MCF-7	breast:
23	chr6:4746373..4750036-chr6:4750510..4753866,3	MCF-7	breast:
24	chr6:4757698..4760676-chr6:4762134..4764890,3	K562	blood:
25	chr6:4756162..4757939-chr6:4768050..4769568,2	K562	blood:
26	chr6:4733801..4736473-chr6:4737548..4740491,3	K562	blood:
27	chr6:4732911..4734620-chr6:4774132..4776554,2	MCF-7	breast:
28	chr6:4755186..4757947-chr6:4774551..4778325,5	K562	blood:
29	chr6:4745475..4747986-chr6:4752486..4754197,2	K562	blood:
30	chr6:4768044..4769868-chr6:4774561..4776902,3	MCF-7	breast:
31	chr6:4733687..4736234-chr6:4773695..4776537,2	K562	blood:
32	chr6:4745475..4747986-chr6:4752486..4754197,2	K562	blood:
33	chr6:4740877..4743157-chr6:4743622..4745166,2	MCF-7	breast:
34	chr6:4731639..4734329-chr6:4773986..4778095,3	MCF-7	breast:
35	chr6:4755437..4757743-chr6:4775444..4778315,2	K562	blood:
36	chr6:4766091..4770015-chr6:4774591..4777896,5	K562	blood:
37	chr6:4758699..4760453-chr6:4775834..4777819,2	K562	blood:
38	chr6:4733392..4734998-chr6:4742508..4744758,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPP40-6	chr6:4764381-4764535	NONHSAT107487
2	lnc-RPP40-6	chr6:4762255-4763086	NONHSAT107487
3	lnc-RPP40-7	chr6:4734457-4734611	NONHSAT107486
4	lnc-RPP40-2	chr6:4774760-4774991	ENSG00000236336.1
5	lnc-RPP40-6	chr6:4760078-4760321	NONHSAT107487
6	lnc-RPP40-7	chr6:4730149-4730395	NONHSAT107486
7	lnc-RPP40-7	chr6:4730590-4730812	NONHSAT107486
8	lnc-RPP40-6	chr6:4760899-4761373	NONHSAT107487
9	lnc-RPP40-7	chr6:4731973-4732184	NONHSAT107486
10	lnc-RPP40-6	chr6:4761530-4761743	NONHSAT107487
11	lnc-RPP40-2	chr6:4774783-4775277	NONHSAT107489
12	lnc-RPP40-6	chr6:4761899-4762110	NONHSAT107487
13	lnc-RPP40-7	chr6:4730973-4731447	NONHSAT107486
14	lnc-RPP40-7	chr6:4732329-4733160	NONHSAT107486
15	lnc-RPP40-6	chr6:4760516-4760738	NONHSAT107487
16	lnc-RPP40-7	chr6:4731604-4731817	NONHSAT107486

No data

Variant related genes	Relation type
CDYL	TF binding region
CDYL	CpG island
ENSG00000236336	chromatin interactions
ENSG00000153046	chromatin interactions

Extended variants
information (count: 1640 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547859312	chr6:4729616-4729617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs149932800	chr6:4729640-4729641	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147624932	chr6:4729645-4729646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553604269	chr6:4729671-4729672	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35365138	chr6:4729694-4729695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs114179360	chr6:4729758-4729759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554030820	chr6:4729760-4729761	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377397978	chr6:4729790-4729791	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs62384813	chr6:4729832-4729833	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544629816	chr6:4729871-4729872	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142044287	chr6:4729884-4729885	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370198640	chr6:4729917-4729918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568216941	chr6:4729929-4729930	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546722961	chr6:4729972-4729973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551072790	chr6:4729973-4729974	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532218519	chr6:4730018-4730019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545592515	chr6:4730044-4730045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4959318	chr6:4730072-4730073	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113989543	chr6:4730099-4730100	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531271573	chr6:4730102-4730103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548188235	chr6:4730129-4730130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs567914975	chr6:4730161-4730162	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs530430053	chr6:4730177-4730178	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs547357987	chr6:4730219-4730220	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs567689147	chr6:4730290-4730291	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs147762963	chr6:4730336-4730337	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs17345926	chr6:4730429-4730430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs148830208	chr6:4730491-4730492	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185586216	chr6:4730503-4730504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554952135	chr6:4730504-4730505	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143793672	chr6:4730508-4730509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553698320	chr6:4730514-4730515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576706084	chr6:4730555-4730556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148169707	chr6:4730588-4730589	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562312167	chr6:4730589-4730590	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576088359	chr6:4730618-4730619	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs141120226	chr6:4730631-4730632	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs541517793	chr6:4730685-4730686	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs145107591	chr6:4730692-4730693	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs527341795	chr6:4730700-4730701	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs113936162	chr6:4730713-4730714	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs188485839	chr6:4730725-4730726	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs372079498	chr6:4730759-4730760	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs9392630	chr6:4730788-4730789	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9405770	chr6:4730795-4730796	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181093939	chr6:4730804-4730805	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs538347924	chr6:4730833-4730834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548437167	chr6:4730865-4730866	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371631984	chr6:4730868-4730869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533963535	chr6:4730877-4730878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4724200-4733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr6:4724600-4733000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:4725000-4732600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:4726800-4729800	Enhancers	Fetal Intestine Small	intestine
5	chr6:4728000-4734400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:4728200-4733000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:4728400-4729600	Enhancers	Fetal Intestine Large	intestine
8	chr6:4728400-4733200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:4728600-4732400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr6:4728600-4734400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:4728800-4732800	Weak transcription	Placenta	Placenta
12	chr6:4728800-4733000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:4728800-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:4728800-4733000	Weak transcription	Colonic Mucosa	Colon
15	chr6:4728800-4733200	Weak transcription	Stomach Mucosa	stomach
16	chr6:4729000-4730400	Enhancers	K562	blood
17	chr6:4729000-4733000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:4729000-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:4729400-4732800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:4729400-4733000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr6:4729400-4733000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:4729600-4733000	Weak transcription	Fetal Intestine Large	intestine
23	chr6:4729800-4733000	Weak transcription	Fetal Intestine Small	intestine
24	chr6:4730400-4730800	Weak transcription	K562	blood
25	chr6:4730800-4731400	Enhancers	K562	blood
26	chr6:4731400-4733000	Weak transcription	K562	blood
27	chr6:4732000-4733200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:4732400-4735400	Enhancers	Placenta Amnion	Placenta Amnion
29	chr6:4732600-4732800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:4732600-4732800	Enhancers	HMEC	breast
31	chr6:4732800-4733000	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr6:4732800-4733000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:4732800-4733000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:4732800-4733000	Enhancers	Brain Cingulate Gyrus	brain
35	chr6:4732800-4733000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:4732800-4733000	Enhancers	Fetal Lung	lung
37	chr6:4732800-4733000	Enhancers	Rectal Smooth Muscle	rectum
38	chr6:4732800-4733000	Enhancers	Hela-S3	cervix
39	chr6:4732800-4733000	Enhancers	NH-A	brain
40	chr6:4732800-4733000	Enhancers	NHEK	skin
41	chr6:4732800-4733000	Enhancers	Osteobl	bone
42	chr6:4732800-4733200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:4732800-4733200	Enhancers	Fetal Heart	heart
44	chr6:4732800-4733600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:4732800-4734000	Flanking Active TSS	HMEC	breast
46	chr6:4732800-4735200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:4732800-4735200	Enhancers	Placenta	Placenta
48	chr6:4733000-4733200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr6:4733000-4733200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:4733000-4733200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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