Variant report

Variant	nsv540911
Chromosome Location	chr11:4133055-4225100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1392)
CpG islands
(count:671)
Chromatin interactive
region (count:49)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
2	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
3	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:4205750-4205950	K562	blood:	n/a	n/a
5	ARID3A	chr11:4156148-4156493	HepG2	liver:	n/a	n/a
6	ATF1	chr11:4167279-4168246	K562	blood:	n/a	n/a
7	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
8	ATF1	chr11:4182582-4182803	K562	blood:	n/a	n/a
9	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
10	ATF3	chr11:4208748-4209028	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:4167574-4167591	K562	blood:	n/a	n/a
13	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
14	BACH1	chr11:4137391-4137635	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr11:4186428-4186725	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
18	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
19	BHLHE40	chr11:4167445-4168270	K562	blood:	n/a	n/a
20	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
21	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
22	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
23	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
24	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr11:4203292-4203924	K562	blood:	n/a	n/a
26	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
27	CBX3	chr11:4161476-4161946	HCT-116	colon:	n/a	n/a
28	CBX3	chr11:4167134-4168147	K562	blood:	n/a	n/a
29	CBX3	chr11:4161399-4161928	HCT-116	colon:	n/a	n/a
30	CBX3	chr11:4152290-4152720	K562	blood:	n/a	n/a
31	CBX3	chr11:4161301-4161848	K562	blood:	n/a	n/a
32	CBX3	chr11:4161255-4161917	K562	blood:	n/a	n/a
33	CBX3	chr11:4208019-4208474	K562	blood:	n/a	n/a
34	CBX3	chr11:4207969-4208291	K562	blood:	n/a	n/a
35	CCNT2	chr11:4167349-4168021	K562	blood:	n/a	n/a
36	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
37	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
38	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
39	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
40	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
41	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
42	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
43	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a
44	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
45	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
47	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
49	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
50	CEBPB	chr11:4139300-4139718	IMR90	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4209120-4209170	CMK	blood:	n/a
2	chr11:4208723-4208773	AG04449	skin:	fetal
3	chr11:4209120-4209170	AG10803	skin:	n/a
4	chr11:4208905-4208955	HEEpiC	esophagus:	n/a
5	chr11:4208723-4208773	GM12892	blood:	n/a
6	chr11:4208278-4208328	H1-hESC	embryonic stem cell:	embryo
7	chr11:4212446-4212496	SKMC	muscle:	n/a
8	chr11:4208723-4208773	HRCEpiC	kidney:	n/a
9	chr11:4208449-4208499	AoSMC	blood vessel:	n/a
10	chr11:4158576-4158626	GM12878	blood:	n/a
11	chr11:4158576-4158626	ECC-1	luminal epithelium:	n/a
12	chr11:4208449-4208499	HEK293	kidney:	embryo
13	chr11:4209397-4209447	HCM	heart:	n/a
14	chr11:4208905-4208955	U87	brain:	n/a
15	chr11:4208723-4208773	HIPEpiC	eye:	n/a
16	chr11:4158576-4158626	PFSK-1	brain:	n/a
17	chr11:4208905-4208955	HCT-116	colon:	n/a
18	chr11:4208278-4208328	ovcar-3	ovarian:	n/a
19	chr11:4212446-4212496	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:4212446-4212496	HNPCEpiC	eye:	n/a
21	chr11:4159839-4159889	U87	brain:	n/a
22	chr11:4206098-4206148	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:4158576-4158626	SAEC	small airway:	n/a
24	chr11:4158576-4158626	T-47D	breast:	n/a
25	chr11:4208905-4208955	BJ	skin:	n/a
26	chr11:4208449-4208499	IMR90	lung:	fetal
27	chr11:4209397-4209447	SKMC	muscle:	n/a
28	chr11:4206098-4206148	SK-N-SH_RA	brain:	n/a
29	chr11:4208278-4208328	HUVEC	blood vessel:	n/a
30	chr11:4209397-4209447	HUVEC	blood vessel:	n/a
31	chr11:4208723-4208773	AG10803	skin:	n/a
32	chr11:4208723-4208773	GM12878	blood:	n/a
33	chr11:4208723-4208773	BE2_C	brain:	n/a
34	chr11:4212471-4212521	HepG2	liver:	n/a
35	chr11:4212471-4212521	LNCaP	prostate:	n/a
36	chr11:4208905-4208955	MCF10A-Er-Src	breast:	n/a
37	chr11:4206098-4206148	GM19239	blood:	n/a
38	chr11:4208278-4208328	AG04450	lung:	fetal
39	chr11:4212471-4212521	PrEC	prostate:	n/a
40	chr11:4209120-4209170	NHDF-neo	bronchial:	n/a
41	chr11:4209397-4209447	LNCaP	prostate:	n/a
42	chr11:4208278-4208328	HRPEpiC	eye:	n/a
43	chr11:4158576-4158626	PANC-1	pancreas:	n/a
44	chr11:4208449-4208499	HRE	kidney:	n/a
45	chr11:4209397-4209447	NH-A	brain:	n/a
46	chr11:4208278-4208328	GM12878	blood:	n/a
47	chr11:4212446-4212496	NB4	blood:	n/a
48	chr11:4208905-4208955	HRE	kidney:	n/a
49	chr11:4208449-4208499	ECC-1	luminal epithelium:	n/a
50	chr11:4209120-4209170	HEEpiC	esophagus:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4149701..4154222-chr11:4154719..4157955,5	K562	blood:
2	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
3	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
4	chr11:4201110..4205265-chr11:4206798..4209054,5	K562	blood:
5	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
6	chr11:4131355..4133542-chr11:4137072..4140145,3	K562	blood:
7	chr11:4161568..4163586-chr11:4168274..4170312,2	K562	blood:
8	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
9	chr11:4149701..4154222-chr11:4154719..4157955,5	K562	blood:
10	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
11	chr11:4164447..4167115-chr11:4182459..4184235,3	K562	blood:
12	chr11:4162871..4165592-chr11:4176787..4178480,2	K562	blood:
13	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
14	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
15	chr11:4131355..4133542-chr11:4137072..4140145,3	K562	blood:
16	chr11:4146273..4149774-chr11:4150555..4152860,3	K562	blood:
17	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
18	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
19	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
20	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
21	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
22	chr11:4115681..4117881-chr11:4185154..4187618,2	K562	blood:
23	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
24	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
25	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
26	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
27	chr11:4164447..4167115-chr11:4182459..4184235,3	K562	blood:
28	chr11:4162871..4165592-chr11:4176787..4178480,2	K562	blood:
29	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
30	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
31	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
32	chr11:4143060..4145148-chr11:4146207..4148504,3	K562	blood:
33	chr11:4116269..4118457-chr11:4145281..4147453,2	MCF-7	breast:
34	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
35	chr11:4135275..4137434-chr11:4139419..4142096,2	K562	blood:
36	chr11:4139381..4140909-chr11:4144756..4147427,2	K562	blood:
37	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
38	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
39	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
40	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
41	chr11:4146273..4149774-chr11:4150555..4152860,3	K562	blood:
42	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
43	chr11:4141819..4145770-chr11:4146926..4149834,4	K562	blood:
44	chr11:4121718..4123279-chr11:4133044..4134599,2	K562	blood:
45	chr11:4147473..4149086-chr11:4158562..4161452,2	K562	blood:
46	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
47	chr11:4135275..4137434-chr11:4139419..4142096,2	K562	blood:
48	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
49	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRM1-2	chr11:4201859-4201941	NONHSAT017642
2	lnc-RRM1-2	chr11:4200829-4201124	NONHSAT017640
3	lnc-RRM1-2	chr11:4201862-4201941	NONHSAT017640
4	lnc-OR52B4-3	chr11:4223487-4223875	NONHSAT017641
5	lnc-OR52B4-3	chr11:4201787-4201939	NONHSAT017641
6	lnc-OR52B4-1	chr11:4159316-4159487	ENSG00000255276.1
7	lnc-OR52B4-1	chr11:4158346-4158519	ENSG00000255276.1
8	lnc-RRM1-2	chr11:4223489-4223881	NONHSAT017642
9	lnc-RRM1-2	chr11:4208382-4208434	NR_047550
10	lnc-RRM1-2	chr11:4223489-4223885	ENSG00000254480.1
11	lnc-RRM1-2	chr11:4223489-4223875	NONHSAT017640
12	lnc-RRM1-2	chr11:4223489-4223883	NR_047550
13	lnc-RRM1-2	chr11:4208370-4208434	ENSG00000254480.1

No data

Variant related genes	Relation type
OR55B1P	TF binding region
RRM1-AS1	TF binding region
ENSG00000254480	TF binding region
RRM1	TF binding region
OR55B1P	CpG island
RRM1-AS1	CpG island
ENSG00000254480	CpG island
RRM1	CpG island
ENSG00000254480	chromatin interactions
ENSG00000231548	chromatin interactions
ENSG00000255276	chromatin interactions
ENSG00000167325	chromatin interactions

Extended variants
information (count: 3709 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3709 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72555778	chr11:4133070-4133071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375890929	chr11:4133079-4133080	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562668206	chr11:4133094-4133095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578011277	chr11:4133095-4133096	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12807843	chr11:4133143-4133144	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12808005	chr11:4133178-4133179	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201413736	chr11:4133179-4133180	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142136268	chr11:4133212-4133213	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12789346	chr11:4133231-4133232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146368319	chr11:4133260-4133261	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545599553	chr11:4133269-4133270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs56336381	chr11:4133317-4133318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs182089546	chr11:4133422-4133423	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141454577	chr11:4133424-4133425	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537181055	chr11:4133462-4133463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185258041	chr11:4133474-4133475	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549775580	chr11:4133486-4133487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190131633	chr11:4133516-4133517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538317140	chr11:4133562-4133563	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2091905	chr11:4133586-4133587	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2091906	chr11:4133602-4133603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs11031000	chr11:4133603-4133604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567260180	chr11:4133617-4133618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377371904	chr11:4133618-4133619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2091907	chr11:4133626-4133627	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs59891969	chr11:4133656-4133657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570182010	chr11:4133657-4133658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2091908	chr11:4133730-4133731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566326801	chr11:4133742-4133743	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554476106	chr11:4133744-4133745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575906750	chr11:4133745-4133746	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs71466148	chr11:4133749-4133750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181223662	chr11:4133799-4133800	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539048159	chr11:4133862-4133863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2119986	chr11:4133868-4133869	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs578056541	chr11:4133876-4133877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545124856	chr11:4133879-4133880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554235547	chr11:4133889-4133890	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561947051	chr11:4133910-4133911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533913365	chr11:4133948-4133949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115265262	chr11:4134006-4134007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1735054	chr11:4134040-4134041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573520345	chr11:4134067-4134068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142548056	chr11:4134072-4134073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11031003	chr11:4134200-4134201	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs186397893	chr11:4134245-4134246	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189549073	chr11:4134249-4134250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558339217	chr11:4134272-4134273	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180836925	chr11:4134295-4134296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547217802	chr11:4134314-4134315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1684 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4117000-4137200	Weak transcription	Esophagus	oesophagus
2	chr11:4117000-4141000	Weak transcription	Ovary	ovary
3	chr11:4117200-4142200	Weak transcription	Colonic Mucosa	Colon
4	chr11:4117400-4141800	Weak transcription	Small Intestine	intestine
5	chr11:4117600-4137400	Weak transcription	Right Ventricle	heart
6	chr11:4117600-4144600	Weak transcription	HSMMtube	muscle
7	chr11:4117600-4145200	Weak transcription	Gastric	stomach
8	chr11:4117600-4153000	Weak transcription	Stomach Mucosa	stomach
9	chr11:4117800-4147800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:4117800-4160200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:4118000-4159200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr11:4118400-4146400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:4118400-4156200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:4118800-4141000	Weak transcription	Brain Germinal Matrix	brain
15	chr11:4119000-4137800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:4119400-4157600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:4121000-4159400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr11:4121600-4142800	Weak transcription	Fetal Brain Male	brain
19	chr11:4122000-4139800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:4122400-4158000	Strong transcription	Dnd41	blood
21	chr11:4122800-4135200	Strong transcription	Hela-S3	cervix
22	chr11:4122800-4136800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr11:4122800-4141800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:4122800-4158000	Strong transcription	Fetal Thymus	thymus
25	chr11:4123000-4135200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:4123000-4135600	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr11:4123000-4136000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:4123000-4138200	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr11:4123000-4152000	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:4123000-4157600	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr11:4123000-4157600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr11:4123000-4157800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:4123200-4135600	Strong transcription	Placenta	Placenta
34	chr11:4123200-4136600	Strong transcription	Osteobl	bone
35	chr11:4123200-4158000	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr11:4123800-4135000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:4123800-4135400	Strong transcription	Primary B cells from peripheral blood	blood
38	chr11:4124000-4157600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:4124000-4157800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:4124400-4138200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:4124600-4138000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr11:4124800-4138200	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr11:4125200-4138000	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr11:4125400-4137400	Weak transcription	Pancreas	Pancrea
45	chr11:4126000-4142000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:4126200-4137800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr11:4126400-4135000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:4126600-4166600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr11:4126800-4137000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr11:4127000-4135000	Strong transcription	HSMM	muscle

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