Variant report

Variant	esv2757417
Chromosome Location	chr11:4162477-4325792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1350)
CpG islands
(count:732)
Chromatin interactive
region (count:37)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:4205750-4205950	K562	blood:	n/a	n/a
3	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
4	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
5	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
6	ATF1	chr11:4182582-4182803	K562	blood:	n/a	n/a
7	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
8	ATF1	chr11:4167279-4168246	K562	blood:	n/a	n/a
9	ATF3	chr11:4208748-4209028	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
11	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:4233294-4233648	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	chr11:4167574-4167591	K562	blood:	n/a	n/a
15	BATF	chr11:4186428-4186725	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
17	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
18	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
19	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
20	BHLHE40	chr11:4167445-4168270	K562	blood:	n/a	n/a
21	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
22	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
23	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr11:4167134-4168147	K562	blood:	n/a	n/a
25	CBX3	chr11:4208019-4208474	K562	blood:	n/a	n/a
26	CBX3	chr11:4207969-4208291	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	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
30	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
31	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
32	CCNT2	chr11:4167349-4168021	K562	blood:	n/a	n/a
33	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
34	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
35	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
36	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
37	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
38	CEBPB	chr11:4208020-4208479	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
41	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
42	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a
43	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr11:4205574-4206017	K562	blood:	n/a	chr11:4205745-4205756
45	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
46	CEBPB	chr11:4257961-4258189	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
47	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
48	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
49	CEBPB	chr11:4257958-4258231	HepG2	liver:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
50	CEBPB	chr11:4232611-4232857	HepG2	liver:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4233502-4233552	HCF	heart:	n/a
2	chr11:4208905-4208955	SKMC	muscle:	n/a
3	chr11:4208723-4208773	HNPCEpiC	eye:	n/a
4	chr11:4209397-4209447	GM19239	blood:	n/a
5	chr11:4258933-4258983	AoSMC	blood vessel:	n/a
6	chr11:4212471-4212521	Jurkat	blood:	n/a
7	chr11:4258933-4258983	GM12891	blood:	n/a
8	chr11:4233502-4233552	Hepatocyte	liver:	n/a
9	chr11:4208905-4208955	HMEC	breast:	n/a
10	chr11:4209397-4209447	GM12878	blood:	n/a
11	chr11:4209397-4209447	AG09309	skin:	n/a
12	chr11:4233502-4233552	RPTEC	kidney:	n/a
13	chr11:4208905-4208955	NH-A	brain:	n/a
14	chr11:4208449-4208499	ECC-1	luminal epithelium:	n/a
15	chr11:4208723-4208773	SAEC	small airway:	n/a
16	chr11:4212446-4212496	AG09309	skin:	n/a
17	chr11:4209397-4209447	GM06990	blood:	n/a
18	chr11:4208723-4208773	HepG2	liver:	n/a
19	chr11:4233502-4233552	SAEC	small airway:	n/a
20	chr11:4206098-4206148	HUVEC	blood vessel:	n/a
21	chr11:4209120-4209170	HepG2	liver:	n/a
22	chr11:4212446-4212496	Jurkat	blood:	n/a
23	chr11:4258933-4258983	U87	brain:	n/a
24	chr11:4208278-4208328	K562	blood:	n/a
25	chr11:4212471-4212521	NH-A	brain:	n/a
26	chr11:4233502-4233552	ovcar-3	ovarian:	n/a
27	chr11:4209397-4209447	Jurkat	blood:	n/a
28	chr11:4209397-4209447	PrEC	prostate:	n/a
29	chr11:4208723-4208773	HEK293	kidney:	embryo
30	chr11:4209120-4209170	PANC-1	pancreas:	n/a
31	chr11:4206098-4206148	Jurkat	blood:	n/a
32	chr11:4206098-4206148	AG04449	skin:	fetal
33	chr11:4209120-4209170	HCM	heart:	n/a
34	chr11:4212471-4212521	HAEpiC	amniotic membrane:	n/a
35	chr11:4209120-4209170	AG09309	skin:	n/a
36	chr11:4209120-4209170	AG09319	gingival:	n/a
37	chr11:4206098-4206148	AG10803	skin:	n/a
38	chr11:4209397-4209447	AG10803	skin:	n/a
39	chr11:4233502-4233552	GM12878	blood:	n/a
40	chr11:4212446-4212496	SAEC	small airway:	n/a
41	chr11:4259129-4259179	AG09319	gingival:	n/a
42	chr11:4208278-4208328	NH-A	brain:	n/a
43	chr11:4258933-4258983	HEEpiC	esophagus:	n/a
44	chr11:4208278-4208328	HRPEpiC	eye:	n/a
45	chr11:4259129-4259179	HCT-116	colon:	n/a
46	chr11:4208723-4208773	ovcar-3	ovarian:	n/a
47	chr11:4208449-4208499	GM06990	blood:	n/a
48	chr11:4212471-4212521	IMR90	lung:	fetal
49	chr11:4233502-4233552	AG09309	skin:	n/a
50	chr11:4208278-4208328	NHBE	bronchial:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
2	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
3	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
4	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
5	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
6	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
7	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
8	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
9	chr11:4170971..4173505-chr11:4175142..4177100,2	K562	blood:
10	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
11	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
12	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
13	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
14	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
15	chr11:4228086..4230506-chr11:4230807..4233604,2	K562	blood:
16	chr11:4164447..4167115-chr11:4182459..4184235,3	K562	blood:
17	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
18	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
19	chr11:4173240..4175304-chr11:4176412..4178994,2	K562	blood:
20	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
21	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
22	chr11:4201110..4205265-chr11:4206798..4209054,5	K562	blood:
23	chr11:4162871..4165592-chr11:4176787..4178480,2	K562	blood:
24	chr11:4115681..4117881-chr11:4185154..4187618,2	K562	blood:
25	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
26	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
27	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
28	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
29	chr11:4164447..4167814-chr11:4181176..4184235,3	K562	blood:
30	chr11:4164447..4167115-chr11:4182459..4184235,3	K562	blood:
31	chr11:4161568..4163586-chr11:4168274..4170312,2	K562	blood:
32	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
33	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
34	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
35	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
36	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
37	chr11:4162871..4165592-chr11:4176787..4178480,2	K562	blood:

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

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

No data

Variant related genes	Relation type
OR55B1P	TF binding region
ENSG00000255387	TF binding region
RRM1-AS1	TF binding region
SSU72P5	TF binding region
SSU72P4	TF binding region
ENSG00000254480	TF binding region
SSU72P2	TF binding region
SSU72P6	TF binding region
OR55B1P	CpG island
ENSG00000255387	CpG island
RRM1-AS1	CpG island
SSU72P5	CpG island
SSU72P4	CpG island
ENSG00000254480	CpG island
SSU72P2	CpG island
SSU72P6	CpG island
ENSG00000167325	chromatin interactions
ENSG00000255387	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000231548	chromatin interactions

Extended variants
information (count: 3231 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3231 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4910897	chr11:4162477-4162478	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7952234	chr11:4162499-4162500	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142614702	chr11:4162509-4162510	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536746447	chr11:4162638-4162639	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs11031110	chr11:4162652-4162653	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs532180965	chr11:4162692-4162693	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142375412	chr11:4162697-4162698	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540997074	chr11:4162783-4162784	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7945413	chr11:4162790-4162791	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs373598973	chr11:4162820-4162821	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs151012841	chr11:4162825-4162826	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543003035	chr11:4162832-4162833	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536201939	chr11:4162867-4162868	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs7945532	chr11:4162875-4162876	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs565406946	chr11:4162881-4162882	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs188569571	chr11:4162896-4162897	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543891449	chr11:4162897-4162898	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372575375	chr11:4162899-4162900	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565375772	chr11:4162964-4162965	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532709361	chr11:4162987-4162988	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547788906	chr11:4162997-4162998	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs139604879	chr11:4163010-4163011	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149672383	chr11:4163058-4163059	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs199981944	chr11:4163112-4163113	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547828558	chr11:4163163-4163164	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569299657	chr11:4163177-4163178	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575161828	chr11:4163184-4163185	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373857635	chr11:4163200-4163201	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558598407	chr11:4163230-4163231	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs73421256	chr11:4163253-4163254	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs115836231	chr11:4163255-4163256	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146673921	chr11:4163278-4163279	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10767853	chr11:4163292-4163293	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs563152314	chr11:4163342-4163343	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374334921	chr11:4163360-4163361	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564285706	chr11:4163365-4163366	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs377577283	chr11:4163366-4163367	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542144577	chr11:4163368-4163369	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35983593	chr11:4163382-4163383	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192803365	chr11:4163385-4163386	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34983792	chr11:4163397-4163398	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576492206	chr11:4163416-4163417	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569697696	chr11:4163454-4163455	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs10767854	chr11:4163495-4163496	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10742244	chr11:4163558-4163559	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs10742245	chr11:4163561-4163562	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs541564009	chr11:4163648-4163649	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs140228078	chr11:4163669-4163670	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145392793	chr11:4163699-4163700	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544051478	chr11:4163751-4163752	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	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:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4126600-4166600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:4148600-4164800	Weak transcription	HSMMtube	muscle
3	chr11:4148800-4165200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:4149200-4164600	Weak transcription	Gastric	stomach
5	chr11:4149600-4169400	Weak transcription	Pancreas	Pancrea
6	chr11:4153400-4165200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:4157000-4166000	Weak transcription	NH-A	brain
8	chr11:4159000-4163000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:4159000-4163400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:4159000-4164800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:4159200-4163800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
12	chr11:4159400-4162600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:4159400-4162600	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr11:4159400-4162600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr11:4159400-4162600	ZNF genes & repeats	Fetal Intestine Large	intestine
16	chr11:4159400-4162600	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr11:4159400-4163000	ZNF genes & repeats	Fetal Lung	lung
18	chr11:4159400-4163000	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr11:4159400-4163200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:4159400-4163200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
21	chr11:4159400-4163200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:4159400-4163400	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr11:4159400-4163400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:4159400-4163400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:4159400-4163400	ZNF genes & repeats	Fetal Brain Female	brain
26	chr11:4159400-4163400	Strong transcription	HSMM	muscle
27	chr11:4159400-4163800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
28	chr11:4159400-4163800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:4159400-4163800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr11:4159400-4164800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:4159400-4165000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:4159400-4165000	Strong transcription	Fetal Thymus	thymus
33	chr11:4159400-4165200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:4159400-4168000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:4159600-4162600	Strong transcription	HMEC	breast
36	chr11:4159600-4163600	Strong transcription	Osteobl	bone
37	chr11:4159800-4162800	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr11:4159800-4163000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:4160000-4162600	ZNF genes & repeats	A549	lung
40	chr11:4160000-4163800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:4160000-4169200	Weak transcription	NHLF	lung
42	chr11:4160000-4172200	Weak transcription	NHEK	skin
43	chr11:4160200-4162800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
44	chr11:4160400-4162800	ZNF genes & repeats	Primary B cells from cord blood	blood
45	chr11:4160400-4162800	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr11:4160400-4165000	Weak transcription	Brain Substantia Nigra	brain
47	chr11:4160400-4166000	Weak transcription	Placenta	Placenta
48	chr11:4160600-4162600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
49	chr11:4160600-4163000	ZNF genes & repeats	Ovary	ovary
50	chr11:4160600-4163200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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