Variant report

Variant	nsv829960
Chromosome Location	chr4:68649237-68809629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1026)
CpG islands
(count:368)
Chromatin interactive
region (count:58)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:68776107-68776264	HepG2	liver:	n/a	n/a
2	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
3	ATF1	chr4:68794343-68794570	K562	blood:	n/a	n/a
4	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:68727253-68727571	GM12878	blood:	n/a	n/a
6	BATF	chr4:68727274-68727575	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr4:68711997-68712017	K562	blood:	n/a	n/a
9	CEBPB	chr4:68658203-68658388	IMR90	lung:	n/a	chr4:68658271-68658282
10	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:68685507-68685646	A549	lung:	n/a	n/a
12	CEBPB	chr4:68670838-68670881	H1-hESC	embryonic stem cell:	n/a	chr4:68670851-68670862
13	CEBPB	chr4:68775691-68776000	A549	lung:	n/a	chr4:68775829-68775840
14	CEBPB	chr4:68739494-68739757	HepG2	liver:	n/a	chr4:68739607-68739620 chr4:68739608-68739619 chr4:68739634-68739645
15	CEBPB	chr4:68739532-68739750	A549	lung:	n/a	chr4:68739607-68739620 chr4:68739608-68739619 chr4:68739634-68739645
16	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:68682356-68682519	K562	blood:	n/a	n/a
18	CEBPB	chr4:68685527-68685727	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:68775653-68776022	IMR90	lung:	n/a	chr4:68775829-68775840
20	CEBPB	chr4:68794230-68794706	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:68775659-68776005	Hela-S3	cervix:	n/a	chr4:68775829-68775840
22	CEBPB	chr4:68687995-68688195	HepG2	liver:	n/a	chr4:68688067-68688078
23	CEBPB	chr4:68658253-68658299	K562	blood:	n/a	chr4:68658271-68658282
24	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
25	CEBPB	chr4:68775665-68776273	K562	blood:	n/a	chr4:68775829-68775840
26	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr4:68775720-68775923	H1-hESC	embryonic stem cell:	n/a	chr4:68775829-68775840
28	CEBPB	chr4:68670844-68670873	HepG2	liver:	n/a	chr4:68670851-68670862
29	CEBPB	chr4:68775674-68776023	HepG2	liver:	n/a	chr4:68775829-68775840
30	CEBPB	chr4:68658212-68658407	HepG2	liver:	n/a	chr4:68658271-68658282
31	CEBPB	chr4:68751495-68752334	IMR90	lung:	n/a	chr4:68752041-68752054
32	CHD1	chr4:68751078-68752771	IMR90	lung:	n/a	n/a
33	CTCF	chr4:68758780-68758930	AG09309	skin:	n/a	n/a
34	CTCF	chr4:68784320-68784470	GM12870	blood:	n/a	n/a
35	CTCF	chr4:68784240-68784390	GM12871	blood:	n/a	n/a
36	CTCF	chr4:68784220-68784370	HEK293	kidney:	n/a	n/a
37	CTCF	chr4:68758607-68759031	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:68737700-68737850	HMF	breast:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
39	CTCF	chr4:68776180-68776330	GM12870	blood:	n/a	n/a
40	CTCF	chr4:68758781-68758903	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:68737703-68737853	Pancreas_OC	pancreas:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
42	CTCF	chr4:68737720-68737870	NHDF-neo	bronchial:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
43	CTCF	chr4:68758880-68759030	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr4:68784300-68784450	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr4:68784580-68784730	HMEC	breast:	n/a	n/a
46	CTCF	chr4:68776160-68776310	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:68737720-68737870	HEK293	kidney:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
48	CTCF	chr4:68776120-68776270	GM12864	blood:	n/a	n/a
49	CTCF	chr4:68776014-68776322	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:68783999-68784733	SK-N-SH	brain:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68801145-68801195	NHBE	bronchial:	n/a
2	chr4:68776652-68776702	HRCEpiC	kidney:	n/a
3	chr4:68801145-68801195	NHBE	bronchial:	n/a
4	chr4:68776652-68776702	HRCEpiC	kidney:	n/a
5	chr4:68699819-68699869	GM12891	blood:	n/a
6	chr4:68801145-68801195	GM19239	blood:	n/a
7	chr4:68750080-68750130	CMK	blood:	n/a
8	chr4:68750080-68750130	K562	blood:	n/a
9	chr4:68776652-68776702	HAEpiC	amniotic membrane:	n/a
10	chr4:68751711-68751761	CMK	blood:	n/a
11	chr4:68751711-68751761	SK-N-SH	brain:	n/a
12	chr4:68801145-68801195	HEEpiC	esophagus:	n/a
13	chr4:68687131-68687181	AG10803	skin:	n/a
14	chr4:68687131-68687181	AG04449	skin:	fetal
15	chr4:68687131-68687181	SK-N-SH	brain:	n/a
16	chr4:68750080-68750130	NB4	blood:	n/a
17	chr4:68687131-68687181	H1-hESC	embryonic stem cell:	embryo
18	chr4:68750080-68750130	HCF	heart:	n/a
19	chr4:68750080-68750130	BJ	skin:	n/a
20	chr4:68751711-68751761	AG09309	skin:	n/a
21	chr4:68776652-68776702	GM12891	blood:	n/a
22	chr4:68687131-68687181	HCM	heart:	n/a
23	chr4:68776652-68776702	AG09319	gingival:	n/a
24	chr4:68687131-68687181	SKMC	muscle:	n/a
25	chr4:68751711-68751761	MCF-7	breast:	n/a
26	chr4:68699819-68699869	NHDF-neo	bronchial:	n/a
27	chr4:68751711-68751761	K562	blood:	n/a
28	chr4:68699819-68699869	PrEC	prostate:	n/a
29	chr4:68699819-68699869	SK-N-MC	brain:	n/a
30	chr4:68751711-68751761	PFSK-1	brain:	n/a
31	chr4:68776652-68776702	HIPEpiC	eye:	n/a
32	chr4:68750080-68750130	HRPEpiC	eye:	n/a
33	chr4:68750080-68750130	HNPCEpiC	eye:	n/a
34	chr4:68801145-68801195	GM12892	blood:	n/a
35	chr4:68687131-68687181	A549	lung:	n/a
36	chr4:68699819-68699869	BE2_C	brain:	n/a
37	chr4:68801145-68801195	HAEpiC	amniotic membrane:	n/a
38	chr4:68776652-68776702	RPTEC	kidney:	n/a
39	chr4:68699819-68699869	RPTEC	kidney:	n/a
40	chr4:68801145-68801195	K562	blood:	n/a
41	chr4:68687131-68687181	Hepatocyte	liver:	n/a
42	chr4:68776652-68776702	AG09309	skin:	n/a
43	chr4:68776652-68776702	HCM	heart:	n/a
44	chr4:68801145-68801195	GM06990	blood:	n/a
45	chr4:68801145-68801195	HepG2	liver:	n/a
46	chr4:68750080-68750130	AG09309	skin:	n/a
47	chr4:68751711-68751761	AG04450	lung:	fetal
48	chr4:68750080-68750130	Caco-2	colon:	n/a
49	chr4:68751711-68751761	HEEpiC	esophagus:	n/a
50	chr4:68750080-68750130	SKMC	muscle:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
2	chr4:68698521..68700206-chr4:68706739..68709118,2	MCF-7	breast:
3	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
4	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
5	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
6	chr4:68734136..68735963-chr4:68740619..68742852,2	K562	blood:
7	chr4:68713370..68716084-chr4:68718837..68721180,2	K562	blood:
8	chr4:68774616..68776298-chr4:68783211..68785677,2	K562	blood:
9	chr4:68737188..68737967-chr4:68783944..68784741,2	MCF-7	breast:
10	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
11	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
12	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
13	chr4:68698345..68700379-chr4:68701901..68703616,2	K562	blood:
14	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
15	chr4:68713370..68716084-chr4:68718837..68721180,2	K562	blood:
16	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
17	chr4:68577504..68578308-chr4:68794030..68794919,2	MCF-7	breast:
18	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
19	chr4:68689643..68691154-chr4:68704651..68706725,2	K562	blood:
20	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
21	chr4:68747971..68750609-chr4:68750969..68752547,2	MCF-7	breast:
22	chr4:68737188..68737967-chr4:68783944..68784741,2	MCF-7	breast:
23	chr4:68784466..68787667-chr4:69042128..69044915,3	MCF-7	breast:
24	chr4:68565327..68567735-chr4:68648210..68650966,2	K562	blood:
25	chr4:68689643..68691154-chr4:68704651..68706725,2	K562	blood:
26	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
27	chr4:68713463..68715636-chr4:68717898..68719818,2	MCF-7	breast:
28	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
29	chr4:68414627..68415373-chr4:68775821..68776638,2	MCF-7	breast:
30	chr4:68703226..68705108-chr4:68706609..68708217,2	K562	blood:
31	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
32	chr4:68737272..68738257-chr4:68775113..68776602,5	MCF-7	breast:
33	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
34	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
35	chr4:68645150..68645855-chr4:68653498..68654116,2	MCF-7	breast:
36	chr4:68637160..68639714-chr4:68656693..68658748,2	K562	blood:
37	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
38	chr4:68694216..68697743-chr4:68699161..68702893,3	K562	blood:
39	chr4:68737272..68738257-chr4:68775113..68776602,5	MCF-7	breast:
40	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
41	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
42	chr4:68784332..68784862-chr4:69040988..69041632,2	MCF-7	breast:
43	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
44	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
45	chr4:68713463..68715636-chr4:68717898..68719818,2	MCF-7	breast:
46	chr4:68738395..68739969-chr4:68740984..68743038,2	K562	blood:
47	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
48	chr4:68734136..68735963-chr4:68740619..68742852,2	K562	blood:
49	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
50	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNRHR-5	chr4:68699020-68699058	NONHSAT096713
2	lnc-GNRHR-5	chr4:68708276-68708343	NONHSAT096715
3	lnc-GNRHR-5	chr4:68708276-68708343	NONHSAT096714
4	lnc-GNRHR-5	chr4:68749644-68749719	NONHSAT096713
5	lnc-GNRHR-5	chr4:68703925-68704047	NONHSAT096715
6	lnc-GNRHR-5	chr4:68708276-68708343	NONHSAT096713
7	lnc-GNRHR-5	chr4:68703752-68704047	NONHSAT096714
8	lnc-GNRHR-5	chr4:68719786-68719904	NONHSAT096715
9	lnc-GNRHR-5	chr4:68725275-68725391	NONHSAT096715
10	lnc-GNRHR-5	chr4:68703890-68704047	NONHSAT096713
11	lnc-GNRHR-5	chr4:68704734-68704776	NONHSAT096713
12	lnc-GNRHR-5	chr4:68726105-68726154	NONHSAT096715
13	lnc-GNRHR-5	chr4:68725275-68725396	NONHSAT096714
14	lnc-GNRHR-5	chr4:68719786-68719904	NONHSAT096713
15	lnc-GNRHR-5	chr4:68749644-68749716	NONHSAT096714
16	lnc-GNRHR-5	chr4:68700801-68700839	NONHSAT096713
17	lnc-GNRHR-3	chr4:68651312-68651706	NONHSAT096710
18	lnc-GNRHR-5	chr4:68719786-68719904	NONHSAT096714
19	lnc-GNRHR-5	chr4:68749644-68749678	NONHSAT096715

No data

Variant related genes	Relation type
TMPRSS11D	TF binding region
TMPRSS11D	CpG island
ENSG00000153802	chromatin interactions
ENSG00000232398	chromatin interactions
ENSG00000248049	chromatin interactions
ENSG00000198092	chromatin interactions
ENSG00000033178	chromatin interactions

Extended variants
information (count: 4869 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4869 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372852599	chr4:68649276-68649277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs546605202	chr4:68649288-68649289	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192677813	chr4:68649302-68649303	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535444373	chr4:68649307-68649308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2582362	chr4:68649310-68649311	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182167863	chr4:68649319-68649320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369633475	chr4:68649371-68649372	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546189461	chr4:68649379-68649380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557692788	chr4:68649410-68649411	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564840409	chr4:68649549-68649550	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371441333	chr4:68649553-68649554	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79223945	chr4:68649561-68649562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs79411764	chr4:68649580-68649581	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201626043	chr4:68649581-68649582	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs572857000	chr4:68649591-68649592	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529699538	chr4:68649669-68649670	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs541834504	chr4:68649676-68649677	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs17088629	chr4:68649733-68649734	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs531157118	chr4:68649743-68649744	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs551132376	chr4:68649799-68649800	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371918380	chr4:68649825-68649826	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546871324	chr4:68649831-68649832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564560793	chr4:68649875-68649876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529424552	chr4:68649908-68649909	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533583468	chr4:68649924-68649925	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111237450	chr4:68649988-68649989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs566580672	chr4:68650019-68650020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs186767378	chr4:68650023-68650024	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs548749261	chr4:68650024-68650025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569109323	chr4:68650026-68650027	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537781685	chr4:68650040-68650041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150262509	chr4:68650066-68650067	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs191571677	chr4:68650086-68650087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533743527	chr4:68650161-68650162	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs9312187	chr4:68650165-68650166	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532331666	chr4:68650174-68650175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552368344	chr4:68650237-68650238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542207024	chr4:68650254-68650255	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs148969536	chr4:68650275-68650276	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs371867199	chr4:68650305-68650306	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114200759	chr4:68650347-68650348	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569094600	chr4:68650364-68650365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2711159	chr4:68650387-68650388	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs115374639	chr4:68650531-68650532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533524072	chr4:68650549-68650550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533401796	chr4:68650566-68650567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs377566142	chr4:68650580-68650581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540869424	chr4:68650583-68650584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184952957	chr4:68650622-68650623	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560286209	chr4:68650626-68650627	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Depressive disorder	21152026	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68643800-68650400	Weak transcription	Fetal Lung	lung
2	chr4:68645400-68650800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:68645800-68650400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:68646000-68650400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:68646000-68651400	Weak transcription	NHEK	skin
6	chr4:68646000-68651600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:68646400-68651400	Weak transcription	HMEC	breast
8	chr4:68648600-68654200	Weak transcription	Primary T cells from cord blood	blood
9	chr4:68650400-68651200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:68650400-68652000	Enhancers	Fetal Lung	lung
11	chr4:68650400-68652200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:68650800-68653000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:68651200-68651600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:68651200-68651800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:68651200-68652000	Enhancers	Ovary	ovary
16	chr4:68651400-68651800	Enhancers	NHEK	skin
17	chr4:68651400-68651800	Enhancers	Osteobl	bone
18	chr4:68651400-68652200	Enhancers	HMEC	breast
19	chr4:68651400-68668800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:68651600-68652000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:68651600-68652200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:68652200-68654000	Weak transcription	HMEC	breast
23	chr4:68652400-68652600	Weak transcription	Gastric	stomach
24	chr4:68652600-68652800	Enhancers	Gastric	stomach
25	chr4:68652800-68675000	Weak transcription	Gastric	stomach
26	chr4:68668600-68677200	Weak transcription	Right Ventricle	heart
27	chr4:68668800-68669400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:68669000-68678000	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr4:68669400-68674800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr4:68673800-68675000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:68674000-68676200	Weak transcription	Ovary	ovary
32	chr4:68674600-68675200	Weak transcription	Left Ventricle	heart
33	chr4:68674800-68675000	Enhancers	HepG2	liver
34	chr4:68674800-68675800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr4:68675000-68675400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:68675000-68675600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:68675000-68675600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:68675000-68675600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:68675000-68675600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:68675000-68675600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:68675000-68675600	ZNF genes & repeats	Gastric	stomach
42	chr4:68675000-68675600	ZNF genes & repeats	Lung	lung
43	chr4:68675000-68675600	Flanking Active TSS	HepG2	liver
44	chr4:68675000-68676000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:68675200-68675400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr4:68675200-68675400	ZNF genes & repeats	Left Ventricle	heart
47	chr4:68675600-68675800	Enhancers	HepG2	liver
48	chr4:68675600-68676800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:68699000-68719000	Weak transcription	Esophagus	oesophagus
50	chr4:68712600-68717600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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