Variant report

Variant	nsv981133
Chromosome Location	chr6:34385156-34393521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:305)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:34386164-34386655	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:34392079-34392437	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:34391889-34391968	K562	blood:	n/a	n/a
4	BHLHE40	chr6:34393211-34393288	GM12878	blood:	n/a	n/a
5	CBX3	chr6:34393403-34394246	K562	blood:	n/a	n/a
6	CEBPB	chr6:34387333-34387533	HepG2	liver:	n/a	chr6:34387410-34387421
7	CEBPB	chr6:34387295-34387572	K562	blood:	n/a	chr6:34387410-34387421
8	CEBPB	chr6:34387365-34387572	IMR90	lung:	n/a	chr6:34387410-34387421
9	CEBPB	chr6:34387343-34387512	Hela-S3	cervix:	n/a	chr6:34387410-34387421
10	CHD1	chr6:34393019-34393549	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr6:34393086-34394169	GM12878	blood:	n/a	n/a
12	CHD2	chr6:34386312-34386477	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr6:34393209-34393475	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr6:34391940-34391955	K562	blood:	n/a	n/a
15	CHD2	chr6:34393310-34393505	HepG2	liver:	n/a	n/a
16	CHD2	chr6:34393115-34393352	GM12878	blood:	n/a	n/a
17	CHD2	chr6:34393092-34394002	K562	blood:	n/a	n/a
18	CTCF	chr6:34385305-34385370	GM10266	blood:	n/a	n/a
19	CTCF	chr6:34391000-34391150	NHEK	skin:	n/a	n/a
20	CTCF	chr6:34392300-34392450	HepG2	liver:	n/a	n/a
21	CTCF	chr6:34389360-34389510	HepG2	liver:	n/a	n/a
22	CTCF	chr6:34392506-34392579	Lung_OC	lung:	n/a	n/a
23	E2F4	chr6:34392133-34392293	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr6:34393121-34393259	MCF10A-Er-Src	breast:	n/a	chr6:34393228-34393239 chr6:34393231-34393239 chr6:34393228-34393239 chr6:34393228-34393239 chr6:34393229-34393240 chr6:34393231-34393239 chr6:34393223-34393238 chr6:34393228-34393239 chr6:34393232-34393239 chr6:34393230-34393240 chr6:34393228-34393239
25	EGR1	chr6:34392553-34392840	K562	blood:	n/a	chr6:34392711-34392724
26	EGR1	chr6:34392590-34392882	K562	blood:	n/a	chr6:34392711-34392724
27	ELF1	chr6:34393478-34394326	HCT-116	colon:	n/a	chr6:34394007-34394016 chr6:34393869-34393882
28	ELF1	chr6:34393177-34394106	GM12878	blood:	n/a	chr6:34394007-34394016 chr6:34393869-34393882
29	ELK1	chr6:34385593-34385652	K562	blood:	n/a	n/a
30	EP300	chr6:34393194-34393320	HepG2	liver:	n/a	n/a
31	EP300	chr6:34391095-34391334	SK-N-SH_RA	brain:	n/a	n/a
32	ETS1	chr6:34384555-34385200	K562	blood:	n/a	chr6:34385134-34385141
33	FAM48A	chr6:34385809-34385906	GM12878	blood:	n/a	n/a
34	FOS	chr6:34391045-34391306	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:34391043-34391318	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr6:34391025-34391308	HUVEC	blood vessel:	n/a	n/a
37	FOS	chr6:34391052-34391307	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:34391016-34391340	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr6:34393415-34394162	HepG2	liver:	n/a	chr6:34393890-34393899
40	FOSL2	chr6:34390970-34391370	SK-N-SH	brain:	n/a	n/a
41	FOXA2	chr6:34385279-34385518	HepG2	liver:	n/a	n/a
42	FOXM1	chr6:34393482-34394196	GM12878	blood:	n/a	n/a
43	FOXM1	chr6:34393075-34394286	GM12878	blood:	n/a	n/a
44	GABPA	chr6:34393284-34394247	MCF-7	breast:	n/a	chr6:34393849-34393863 chr6:34393849-34393860
45	GABPA	chr6:34393496-34394136	K562	blood:	n/a	chr6:34393849-34393863 chr6:34393849-34393860
46	HEY1	chr6:34387563-34388411	K562	blood:	n/a	n/a
47	HEY1	chr6:34389209-34389788	K562	blood:	n/a	n/a
48	HEY1	chr6:34391422-34394196	K562	blood:	n/a	chr6:34393924-34393939
49	HEY1	chr6:34389326-34389753	K562	blood:	n/a	n/a
50	HEY1	chr6:34389293-34389714	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34393330-34393380	SK-N-SH	brain:	n/a
2	chr6:34390021-34390071	K562	blood:	n/a
3	chr6:34393398-34393448	SKMC	muscle:	n/a
4	chr6:34393330-34393380	RPTEC	kidney:	n/a
5	chr6:34393398-34393448	HAEpiC	amniotic membrane:	n/a
6	chr6:34393330-34393380	BE2_C	brain:	n/a
7	chr6:34391778-34391828	HCT-116	colon:	n/a
8	chr6:34393330-34393380	ECC-1	luminal epithelium:	n/a
9	chr6:34393398-34393448	NB4	blood:	n/a
10	chr6:34393330-34393380	AG04449	skin:	fetal
11	chr6:34392105-34392155	HMEC	breast:	n/a
12	chr6:34390021-34390071	SAEC	small airway:	n/a
13	chr6:34390021-34390071	ovcar-3	ovarian:	n/a
14	chr6:34393398-34393448	HIPEpiC	eye:	n/a
15	chr6:34393330-34393380	PrEC	prostate:	n/a
16	chr6:34390021-34390071	HRPEpiC	eye:	n/a
17	chr6:34393330-34393380	H1-hESC	embryonic stem cell:	embryo
18	chr6:34392105-34392155	Caco-2	colon:	n/a
19	chr6:34391778-34391828	SKMC	muscle:	n/a
20	chr6:34391778-34391828	NHBE	bronchial:	n/a
21	chr6:34391778-34391828	MCF-7	breast:	n/a
22	chr6:34392105-34392155	AG09319	gingival:	n/a
23	chr6:34390021-34390071	HCM	heart:	n/a
24	chr6:34393398-34393448	AG04449	skin:	fetal
25	chr6:34392105-34392155	BJ	skin:	n/a
26	chr6:34390021-34390071	NH-A	brain:	n/a
27	chr6:34393398-34393448	HRPEpiC	eye:	n/a
28	chr6:34391778-34391828	AG04450	lung:	fetal
29	chr6:34393330-34393380	HMEC	breast:	n/a
30	chr6:34391778-34391828	HEK293	kidney:	embryo
31	chr6:34392105-34392155	AG09309	skin:	n/a
32	chr6:34391778-34391828	GM06990	blood:	n/a
33	chr6:34390021-34390071	BJ	skin:	n/a
34	chr6:34393330-34393380	GM06990	blood:	n/a
35	chr6:34392105-34392155	SKMC	muscle:	n/a
36	chr6:34392105-34392155	HEK293	kidney:	embryo
37	chr6:34391778-34391828	SK-N-MC	brain:	n/a
38	chr6:34392105-34392155	SAEC	small airway:	n/a
39	chr6:34393398-34393448	HRCEpiC	kidney:	n/a
40	chr6:34390021-34390071	BE2_C	brain:	n/a
41	chr6:34393398-34393448	Jurkat	blood:	n/a
42	chr6:34392105-34392155	SK-N-SH	brain:	n/a
43	chr6:34391778-34391828	IMR90	lung:	fetal
44	chr6:34393398-34393448	A549	lung:	n/a
45	chr6:34393398-34393448	PFSK-1	brain:	n/a
46	chr6:34390021-34390071	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:34390021-34390071	Hela-S3	cervix:	n/a
48	chr6:34392105-34392155	AG04449	skin:	fetal
49	chr6:34390021-34390071	PrEC	prostate:	n/a
50	chr6:34393398-34393448	ProgFib	skin:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:34379707..34381540-chr6:34384149..34385889,2	MCF-7	breast:
2	chr6:34202622..34206817-chr6:34391790..34393979,3	MCF-7	breast:
3	chr6:34176766..34178294-chr6:34387966..34390024,2	K562	blood:
4	chr6:34379437..34382145-chr6:34384252..34386142,2	MCF-7	breast:
5	chr6:34210941..34212491-chr6:34389886..34392402,2	K562	blood:
6	chr6:34162021..34165758-chr6:34380623..34387316,6	K562	blood:
7	chr6:34391617..34394715-chr6:34431838..34435722,3	MCF-7	breast:
8	chr6:34211137..34213160-chr6:34384345..34386352,2	MCF-7	breast:
9	chr11:46449218..46452238-chr6:34392341..34394490,5	MCF-7	breast:
10	chr6:34203866..34208750-chr6:34388488..34394053,10	MCF-7	breast:
11	chr6:34212124..34218246-chr6:34379945..34387655,19	K562	blood:
12	chr6:34203686..34207490-chr6:34388234..34395019,9	K562	blood:
13	chr6:34111438..34113496-chr6:34384142..34385841,2	MCF-7	breast:
14	chr6:34357967..34362826-chr6:34390808..34395314,8	K562	blood:
15	chr6:32936292..32939162-chr6:34392465..34394663,2	MCF-7	breast:
16	chr11:46449233..46452238-chr6:34392226..34393967,6	K562	blood:
17	chr11:46450213..46450713-chr6:34392822..34393736,2	Hela-S3	cervix:
18	chr6:34212618..34219497-chr6:34387813..34394246,15	K562	blood:
19	chr6:34358195..34361774-chr6:34391620..34393850,4	K562	blood:
20	chr6:34203584..34206226-chr6:34392090..34394590,2	K562	blood:
21	chr6:34358853..34362255-chr6:34392162..34395391,9	MCF-7	breast:
22	chr6:34215435..34217871-chr6:34390764..34394019,4	MCF-7	breast:
23	chr6:34384595..34386120-chr6:35175075..35178043,2	K562	blood:
24	chr6:34209798..34218235-chr6:34387971..34396103,20	K562	blood:
25	chr6:34206861..34220421-chr6:34379359..34386848,24	K562	blood:
26	chr13:28023643..28024354-chr6:34393046..34393849,2	Hela-S3	cervix:
27	chr6:34358377..34360251-chr6:34384641..34386602,2	MCF-7	breast:
28	chr6:34389543..34392332-chr6:34575346..34578264,2	K562	blood:
29	chr6:34393013..34393817-chr9:130212883..130213745,2	Hela-S3	cervix:
30	chr6:34391519..34392061-chr7:12443222..12443860,2	Hela-S3	cervix:
31	chr11:46450238..46451231-chr6:34393265..34393905,3	MCF-7	breast:
32	chr6:34204321..34205956-chr6:34384818..34387597,2	K562	blood:
33	chr6:34358383..34362134-chr6:34382278..34385330,4	K562	blood:
34	chr6:34190763..34192270-chr6:34389997..34392195,2	K562	blood:
35	chr6:34202249..34205186-chr6:34388234..34391222,2	K562	blood:
36	chr6:34369067..34370833-chr6:34388211..34390911,2	K562	blood:
37	chr6:34385629..34388479-chr6:34571535..34574090,2	K562	blood:
38	chr17:60554747..60557192-chr6:34392556..34394064,2	MCF-7	breast:
39	chr6:34392408..34394621-chr6:34663502..34666102,2	K562	blood:
40	chr6:34161815..34164629-chr6:34383451..34385385,2	MCF-7	breast:
41	chr6:34194332..34197149-chr6:34382426..34385429,3	K562	blood:
42	chr6:34356693..34361584-chr6:34376924..34385699,12	K562	blood:
43	chr15:101834947..101835608-chr6:34393258..34393900,2	Hela-S3	cervix:
44	chr6:34392363..34394175-chr6:34723427..34725918,3	MCF-7	breast:
45	chr1:202857686..202858599-chr6:34391693..34392391,2	Hela-S3	cervix:
46	chr6:34392492..34394082-chr6:34758851..34761190,2	MCF-7	breast:
47	chr6:34218726..34220421-chr6:34383770..34386594,2	K562	blood:
48	chr6:34392840..34394590-chr6:34855825..34858514,2	K562	blood:
49	chr11:46449211..46452238-chr6:34390894..34393967,4	K562	blood:
50	chr6:34306948..34308563-chr6:34383951..34386778,2	K562	blood:

No data

Variant related genes	Relation type
RPS10	TF binding region
RPS10	CpG island
ENSG00000196821	chromatin interactions
ENSG00000131876	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000146872	chromatin interactions
ENSG00000146530	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000197958	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000122033	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000183155	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000272288	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000244313	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000272325	chromatin interactions

Extended variants
information (count: 420 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572453740	chr6:34385187-34385188	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs552819919	chr6:34385209-34385210	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs564129427	chr6:34385220-34385221	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535030777	chr6:34385229-34385230	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200231286	chr6:34385240-34385241	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs112078820	chr6:34385241-34385242	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs370136285	chr6:34385247-34385248	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs200869507	chr6:34385260-34385261	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs139095177	chr6:34385302-34385303	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368815453	chr6:34385347-34385348	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs374706146	chr6:34385358-34385359	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs144732838	chr6:34385392-34385393	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs376286138	chr6:34385395-34385396	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs138867571	chr6:34385423-34385424	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs75259239	chr6:34385434-34385435	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs76012133	chr6:34385440-34385441	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs539210378	chr6:34385488-34385489	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs116500841	chr6:34385498-34385499	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs16889714	chr6:34385517-34385518	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574882985	chr6:34385543-34385544	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs535111167	chr6:34385586-34385587	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs553228067	chr6:34385618-34385619	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs574755288	chr6:34385635-34385636	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183984949	chr6:34385660-34385661	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190411459	chr6:34385676-34385677	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368687904	chr6:34385706-34385707	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181685259	chr6:34385717-34385718	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576018222	chr6:34385757-34385758	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546370583	chr6:34385766-34385767	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564666478	chr6:34385798-34385799	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142089082	chr6:34385818-34385819	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375937481	chr6:34385830-34385831	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540307714	chr6:34385836-34385837	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs150425872	chr6:34385841-34385842	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs187596278	chr6:34385849-34385850	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550174277	chr6:34385860-34385861	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577070969	chr6:34385865-34385866	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568769799	chr6:34385908-34385909	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201724991	chr6:34385919-34385920	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533055900	chr6:34385922-34385923	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551305430	chr6:34385929-34385930	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566645904	chr6:34385937-34385938	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs546067827	chr6:34385966-34385967	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553404722	chr6:34385971-34385972	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568477883	chr6:34386055-34386056	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370540329	chr6:34386070-34386071	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191872288	chr6:34386085-34386086	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559654960	chr6:34386106-34386107	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557394189	chr6:34386128-34386129	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149897629	chr6:34386158-34386159	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34372400-34389400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:34379200-34385400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr6:34379200-34391800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:34381800-34391000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:34382000-34388000	Strong transcription	Dnd41	blood
6	chr6:34382000-34390000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:34382000-34391600	Strong transcription	NHEK	skin
8	chr6:34382000-34392000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:34382000-34392000	Strong transcription	Primary T cells from cord blood	blood
10	chr6:34382400-34389400	Strong transcription	K562	blood
11	chr6:34382400-34389600	Weak transcription	Fetal Brain Male	brain
12	chr6:34382400-34391800	Strong transcription	NHDF-Ad	bronchial
13	chr6:34382400-34392000	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr6:34382400-34392000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:34382400-34392000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:34382600-34387600	Weak transcription	Fetal Kidney	kidney
17	chr6:34382600-34387800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:34382600-34392000	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr6:34382800-34386000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:34383000-34391000	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:34383000-34392200	Weak transcription	Right Atrium	heart
22	chr6:34383200-34385600	Genic enhancers	HepG2	liver
23	chr6:34383200-34389200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr6:34383200-34389400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:34383200-34391600	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:34383200-34391600	Strong transcription	Fetal Thymus	thymus
27	chr6:34383400-34389400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:34383400-34390000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr6:34383400-34390000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:34383400-34390000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:34383400-34392000	Strong transcription	H9 Cell Line	embryonic stem cell
32	chr6:34383400-34392000	Strong transcription	Fetal Lung	lung
33	chr6:34383400-34392600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:34383400-34392600	Strong transcription	Lung	lung
35	chr6:34383600-34385200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr6:34383600-34386800	Strong transcription	Brain Germinal Matrix	brain
37	chr6:34383600-34389000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr6:34383600-34389400	Strong transcription	GM12878-XiMat	blood
39	chr6:34383600-34390200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr6:34383600-34391200	Strong transcription	Osteobl	bone
41	chr6:34383600-34391400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:34383600-34391400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:34383600-34391400	Strong transcription	Fetal Muscle Trunk	muscle
44	chr6:34383600-34391600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr6:34383600-34391600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr6:34383600-34392000	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr6:34383600-34392000	Strong transcription	Fetal Brain Female	brain
48	chr6:34383600-34392000	Strong transcription	Fetal Intestine Small	intestine
49	chr6:34383600-34392000	Strong transcription	Thymus	Thymus
50	chr6:34383600-34392200	Strong transcription	Fetal Muscle Leg	muscle

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