Variant report

Variant	nsv818795
Chromosome Location	chr11:4167416-4238930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1241)
CpG islands
(count:610)
Chromatin interactive
region (count:34)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
2	ARID3A	chr11:4205750-4205950	K562	blood:	n/a	n/a
3	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
5	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
6	ATF1	chr11:4167279-4168246	K562	blood:	n/a	n/a
7	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
8	ATF1	chr11:4182582-4182803	K562	blood:	n/a	n/a
9	ATF3	chr11:4208748-4209028	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:4233294-4233648	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:4167574-4167591	K562	blood:	n/a	n/a
12	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
15	BATF	chr11:4186428-4186725	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
17	BHLHE40	chr11:4167445-4168270	K562	blood:	n/a	n/a
18	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
19	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
20	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
21	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
22	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
24	CBX3	chr11:4207969-4208291	K562	blood:	n/a	n/a
25	CBX3	chr11:4208019-4208474	K562	blood:	n/a	n/a
26	CBX3	chr11:4167134-4168147	K562	blood:	n/a	n/a
27	CBX3	chr11:4203292-4203924	K562	blood:	n/a	n/a
28	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
29	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
30	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
31	CCNT2	chr11:4167349-4168021	K562	blood:	n/a	n/a
32	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
33	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
34	CEBPB	chr11:4233297-4233351	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
36	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
37	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
38	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
39	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:4208020-4208479	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
42	CEBPB	chr11:4205574-4206017	K562	blood:	n/a	chr11:4205745-4205756
43	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
45	CEBPB	chr11:4228834-4228864	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr11:4216252-4216447	K562	blood:	n/a	n/a
47	CEBPB	chr11:4232611-4232857	HepG2	liver:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
48	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
49	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
50	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4212471-4212521	GM12878	blood:	n/a
2	chr11:4208723-4208773	HCPEpiC	choroid plexus:	n/a
3	chr11:4208278-4208328	SK-N-SH_RA	brain:	n/a
4	chr11:4206098-4206148	AG10803	skin:	n/a
5	chr11:4208905-4208955	SK-N-SH	brain:	n/a
6	chr11:4212471-4212521	HRCEpiC	kidney:	n/a
7	chr11:4208449-4208499	NB4	blood:	n/a
8	chr11:4209120-4209170	HL-60	blood:	n/a
9	chr11:4208723-4208773	LNCaP	prostate:	n/a
10	chr11:4208723-4208773	Hela-S3	cervix:	n/a
11	chr11:4209397-4209447	U87	brain:	n/a
12	chr11:4208905-4208955	HCPEpiC	choroid plexus:	n/a
13	chr11:4233502-4233552	U87	brain:	n/a
14	chr11:4212446-4212496	HMEC	breast:	n/a
15	chr11:4209397-4209447	HCPEpiC	choroid plexus:	n/a
16	chr11:4212471-4212521	HIPEpiC	eye:	n/a
17	chr11:4209120-4209170	HCT-116	colon:	n/a
18	chr11:4208723-4208773	CMK	blood:	n/a
19	chr11:4206098-4206148	PrEC	prostate:	n/a
20	chr11:4206098-4206148	Hepatocyte	liver:	n/a
21	chr11:4212471-4212521	HCF	heart:	n/a
22	chr11:4208278-4208328	MCF-7	breast:	n/a
23	chr11:4209397-4209447	HAEpiC	amniotic membrane:	n/a
24	chr11:4212471-4212521	HAEpiC	amniotic membrane:	n/a
25	chr11:4208723-4208773	ProgFib	skin:	n/a
26	chr11:4208449-4208499	BE2_C	brain:	n/a
27	chr11:4209120-4209170	HUVEC	blood vessel:	n/a
28	chr11:4209120-4209170	U87	brain:	n/a
29	chr11:4206098-4206148	AG04450	lung:	fetal
30	chr11:4209397-4209447	HNPCEpiC	eye:	n/a
31	chr11:4208723-4208773	HNPCEpiC	eye:	n/a
32	chr11:4206098-4206148	A549	lung:	n/a
33	chr11:4212471-4212521	H1-hESC	embryonic stem cell:	embryo
34	chr11:4208449-4208499	ProgFib	skin:	n/a
35	chr11:4208278-4208328	Jurkat	blood:	n/a
36	chr11:4208278-4208328	HMEC	breast:	n/a
37	chr11:4208723-4208773	HRCEpiC	kidney:	n/a
38	chr11:4212446-4212496	MCF10A-Er-Src	breast:	n/a
39	chr11:4209120-4209170	NHBE	bronchial:	n/a
40	chr11:4208723-4208773	HEEpiC	esophagus:	n/a
41	chr11:4233502-4233552	HEK293	kidney:	embryo
42	chr11:4206098-4206148	ProgFib	skin:	n/a
43	chr11:4206098-4206148	AG09309	skin:	n/a
44	chr11:4209120-4209170	T-47D	breast:	n/a
45	chr11:4212471-4212521	NHBE	bronchial:	n/a
46	chr11:4209397-4209447	HMEC	breast:	n/a
47	chr11:4206098-4206148	HNPCEpiC	eye:	n/a
48	chr11:4212446-4212496	Hela-S3	cervix:	n/a
49	chr11:4208905-4208955	NHBE	bronchial:	n/a
50	chr11:4209120-4209170	CMK	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
2	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
3	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
4	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
5	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
6	chr11:4115681..4117881-chr11:4185154..4187618,2	K562	blood:
7	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
8	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
9	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
10	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
11	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
12	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
13	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
14	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
15	chr11:4162871..4165592-chr11:4176787..4178480,2	K562	blood:
16	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
17	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
18	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
19	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
20	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
21	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
22	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
23	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
24	chr11:4228086..4230506-chr11:4230807..4233604,2	K562	blood:
25	chr11:4201110..4205265-chr11:4206798..4209054,5	K562	blood:
26	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
27	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
28	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
29	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
30	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
31	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
32	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
33	chr11:4164447..4167115-chr11:4182459..4184235,3	K562	blood:
34	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
OR55B1P	TF binding region
ENSG00000255387	TF binding region
ENSG00000254480	TF binding region
OR55B1P	CpG island
ENSG00000255387	CpG island
ENSG00000254480	CpG island
ENSG00000254480	chromatin interactions
ENSG00000167325	chromatin interactions
ENSG00000255387	chromatin interactions

Extended variants
information (count: 2657 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2657 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10835678	chr11:4167416-4167417	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10835679	chr11:4167432-4167433	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150461227	chr11:4167434-4167435	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114292004	chr11:4167446-4167447	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571549345	chr11:4167489-4167490	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11031123	chr11:4167493-4167494	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs549645853	chr11:4167495-4167496	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115838743	chr11:4167513-4167514	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116251958	chr11:4167577-4167578	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550429046	chr11:4167600-4167601	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs10742246	chr11:4167604-4167605	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs184731280	chr11:4167674-4167675	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs12290431	chr11:4167726-4167727	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527255615	chr11:4167739-4167740	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553462622	chr11:4167792-4167793	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs565392796	chr11:4167793-4167794	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535930684	chr11:4167814-4167815	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs56167232	chr11:4167846-4167847	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs10767857	chr11:4167889-4167890	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs10742247	chr11:4167903-4167904	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs189452347	chr11:4167976-4167977	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs535218790	chr11:4167989-4167990	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs7126014	chr11:4167997-4167998	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs10767858	chr11:4168029-4168030	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs7115496	chr11:4168046-4168047	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs527827843	chr11:4168090-4168091	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182052026	chr11:4168101-4168102	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561352060	chr11:4168128-4168129	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs7115615	chr11:4168140-4168141	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184472398	chr11:4168143-4168144	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540115942	chr11:4168159-4168160	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs532017796	chr11:4168179-4168180	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs190102255	chr11:4168208-4168209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74500060	chr11:4168211-4168212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374556160	chr11:4168215-4168216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565317465	chr11:4168233-4168234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145366651	chr11:4168237-4168238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116063023	chr11:4168287-4168288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149187277	chr11:4168303-4168304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10835684	chr11:4168308-4168309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs71472160	chr11:4168318-4168319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4593997	chr11:4168319-4168320	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs4399324	chr11:4168332-4168333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370398000	chr11:4168334-4168335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4480537	chr11:4168335-4168336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4593998	chr11:4168343-4168344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs543167295	chr11:4168357-4168358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561401723	chr11:4168492-4168493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531823443	chr11:4168543-4168544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372502827	chr11:4168584-4168585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4149600-4169400	Weak transcription	Pancreas	Pancrea
2	chr11:4159400-4168000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:4160000-4169200	Weak transcription	NHLF	lung
4	chr11:4160000-4172200	Weak transcription	NHEK	skin
5	chr11:4161400-4169400	Weak transcription	Brain Anterior Caudate	brain
6	chr11:4161600-4179600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:4162400-4167600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:4162400-4168200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:4162400-4168200	Weak transcription	Fetal Kidney	kidney
10	chr11:4162400-4169400	Weak transcription	Brain Germinal Matrix	brain
11	chr11:4162400-4172200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:4162600-4167800	Weak transcription	Spleen	Spleen
13	chr11:4163000-4173000	Weak transcription	Psoas Muscle	Psoas
14	chr11:4163200-4168600	Weak transcription	Fetal Brain Male	brain
15	chr11:4163200-4170800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:4163400-4169200	Weak transcription	Aorta	Aorta
17	chr11:4163400-4169200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:4163400-4173000	Weak transcription	HSMM	muscle
19	chr11:4163600-4168600	Weak transcription	Brain Angular Gyrus	brain
20	chr11:4163600-4168600	Weak transcription	Fetal Muscle Leg	muscle
21	chr11:4163800-4167600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:4163800-4169200	Weak transcription	Left Ventricle	heart
23	chr11:4164800-4169600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:4165000-4168800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:4165000-4168800	Weak transcription	GM12878-XiMat	blood
26	chr11:4165000-4169000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:4165200-4168000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr11:4165200-4172200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:4165400-4169200	Weak transcription	Dnd41	blood
30	chr11:4165600-4169600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:4165800-4169400	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr11:4166000-4167600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:4166000-4168400	Weak transcription	A549	lung
34	chr11:4166000-4168600	Weak transcription	Primary T cells from cord blood	blood
35	chr11:4166200-4167800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr11:4166200-4167800	Weak transcription	Fetal Brain Female	brain
37	chr11:4166800-4167800	Enhancers	Primary hematopoietic stem cells	blood
38	chr11:4167000-4167800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:4167000-4168200	Strong transcription	Thymus	Thymus
40	chr11:4167000-4168200	Flanking Active TSS	K562	blood
41	chr11:4167400-4168000	Strong transcription	Fetal Stomach	stomach
42	chr11:4167400-4169200	Weak transcription	Right Atrium	heart
43	chr11:4167600-4168200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:4167800-4168600	Enhancers	Spleen	Spleen
45	chr11:4167800-4169600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:4168000-4169400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:4168000-4169600	Weak transcription	Fetal Stomach	stomach
48	chr11:4168200-4169400	Enhancers	K562	blood
49	chr11:4168200-4170000	Weak transcription	Thymus	Thymus
50	chr11:4168200-4172200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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