Variant report

Variant	esv3380413
Chromosome Location	chr11:4159374-4323846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1374)
CpG islands
(count:794)
Chromatin interactive
region (count:37)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1374 , 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	chr11:4205750-4205950	K562	blood:	n/a	n/a
2	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
4	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
5	ATF1	chr11:4167279-4168246	K562	blood:	n/a	n/a
6	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
7	ATF1	chr11:4182582-4182803	K562	blood:	n/a	n/a
8	ATF1	chr11:4218126-4218315	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	chr11:4167574-4167591	K562	blood:	n/a	n/a
13	BACH1	chr11:4233294-4233648	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr11:4186428-4186725	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
17	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
18	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
19	BHLHE40	chr11:4167445-4168270	K562	blood:	n/a	n/a
20	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
21	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
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	chr11:4208019-4208474	K562	blood:	n/a	n/a
25	CBX3	chr11:4161476-4161946	HCT-116	colon:	n/a	n/a
26	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
27	CBX3	chr11:4161301-4161848	K562	blood:	n/a	n/a
28	CBX3	chr11:4203292-4203924	K562	blood:	n/a	n/a
29	CBX3	chr11:4167134-4168147	K562	blood:	n/a	n/a
30	CBX3	chr11:4161399-4161928	HCT-116	colon:	n/a	n/a
31	CBX3	chr11:4161255-4161917	K562	blood:	n/a	n/a
32	CBX3	chr11:4207969-4208291	K562	blood:	n/a	n/a
33	CCNT2	chr11:4167349-4168021	K562	blood:	n/a	n/a
34	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
35	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
36	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
37	CEBPB	chr11:4257958-4258231	HepG2	liver:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
38	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
39	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
40	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
41	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
42	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
43	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
44	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
45	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
46	CEBPB	chr11:4208893-4208908	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	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr11:4257961-4258189	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
50	CEBPB	chr11:4257965-4258134	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4208723-4208773	Hepatocyte	liver:	n/a
2	chr11:4208723-4208773	Hepatocyte	liver:	n/a
3	chr11:4212471-4212521	HRE	kidney:	n/a
4	chr11:4209397-4209447	HRCEpiC	kidney:	n/a
5	chr11:4208905-4208955	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:4206098-4206148	HCT-116	colon:	n/a
7	chr11:4208723-4208773	NHBE	bronchial:	n/a
8	chr11:4212446-4212496	HCM	heart:	n/a
9	chr11:4258933-4258983	HMEC	breast:	n/a
10	chr11:4208278-4208328	GM12891	blood:	n/a
11	chr11:4159839-4159889	HCM	heart:	n/a
12	chr11:4209397-4209447	HCF	heart:	n/a
13	chr11:4258933-4258983	MCF10A-Er-Src	breast:	n/a
14	chr11:4206098-4206148	HMEC	breast:	n/a
15	chr11:4233502-4233552	AG09319	gingival:	n/a
16	chr11:4233502-4233552	HCM	heart:	n/a
17	chr11:4212446-4212496	MCF10A-Er-Src	breast:	n/a
18	chr11:4212471-4212521	CMK	blood:	n/a
19	chr11:4159839-4159889	PFSK-1	brain:	n/a
20	chr11:4233502-4233552	HL-60	blood:	n/a
21	chr11:4208905-4208955	K562	blood:	n/a
22	chr11:4259129-4259179	AoSMC	blood vessel:	n/a
23	chr11:4212471-4212521	PrEC	prostate:	n/a
24	chr11:4159839-4159889	ProgFib	skin:	n/a
25	chr11:4159839-4159889	AoSMC	blood vessel:	n/a
26	chr11:4212471-4212521	RPTEC	kidney:	n/a
27	chr11:4209120-4209170	HCPEpiC	choroid plexus:	n/a
28	chr11:4209397-4209447	GM06990	blood:	n/a
29	chr11:4209397-4209447	AG04449	skin:	fetal
30	chr11:4259129-4259179	ProgFib	skin:	n/a
31	chr11:4233502-4233552	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:4258933-4258983	HEK293	kidney:	embryo
33	chr11:4206098-4206148	A549	lung:	n/a
34	chr11:4208723-4208773	K562	blood:	n/a
35	chr11:4233502-4233552	MCF-7	breast:	n/a
36	chr11:4208905-4208955	SK-N-SH_RA	brain:	n/a
37	chr11:4258933-4258983	PrEC	prostate:	n/a
38	chr11:4208278-4208328	HCT-116	colon:	n/a
39	chr11:4209120-4209170	ECC-1	luminal epithelium:	n/a
40	chr11:4208723-4208773	AG04450	lung:	fetal
41	chr11:4212471-4212521	HMEC	breast:	n/a
42	chr11:4208905-4208955	SK-N-MC	brain:	n/a
43	chr11:4208278-4208328	HCPEpiC	choroid plexus:	n/a
44	chr11:4208449-4208499	NHBE	bronchial:	n/a
45	chr11:4208723-4208773	Hela-S3	cervix:	n/a
46	chr11:4209397-4209447	HCM	heart:	n/a
47	chr11:4209120-4209170	NH-A	brain:	n/a
48	chr11:4212471-4212521	ECC-1	luminal epithelium:	n/a
49	chr11:4208723-4208773	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:4206098-4206148	H1-hESC	embryonic stem cell:	embryo

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

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

(count:12 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3372 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3372 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573526379	chr11:4159384-4159385	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
2	rs535688696	chr11:4159388-4159389	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
3	rs9937	chr11:4159457-4159458	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs1042858	chr11:4159466-4159467	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs112706528	chr11:4159521-4159522	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2229196	chr11:4159567-4159568	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147460045	chr11:4159577-4159578	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139927481	chr11:4159587-4159588	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376890449	chr11:4159618-4159619	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200593091	chr11:4159657-4159658	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562532769	chr11:4159690-4159691	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1042919	chr11:4159764-4159765	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs866902	chr11:4159771-4159772	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56199078	chr11:4159781-4159782	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56134721	chr11:4159829-4159830	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551505351	chr11:4159838-4159839	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566548109	chr11:4159860-4159861	ZNF genes & repeats Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs534138602	chr11:4159869-4159870	ZNF genes & repeats Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs548994216	chr11:4159926-4159927	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1042927	chr11:4159929-4159930	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs143006593	chr11:4159970-4159971	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557053148	chr11:4160003-4160004	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1042929	chr11:4160007-4160008	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371659538	chr11:4160053-4160054	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3177020	chr11:4160099-4160100	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148224418	chr11:4160105-4160106	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs578075840	chr11:4160140-4160141	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4910892	chr11:4160172-4160173	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs188021120	chr11:4160275-4160276	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369753545	chr11:4160309-4160310	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs180954658	chr11:4160332-4160333	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs376673300	chr11:4160466-4160467	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs562337618	chr11:4160468-4160469	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369066312	chr11:4160570-4160571	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs386372951	chr11:4160571-4160572	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs71047198	chr11:4160588-4160589	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs111420501	chr11:4160592-4160593	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544186383	chr11:4160622-4160623	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560788846	chr11:4160638-4160639	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs10767849	chr11:4160641-4160642	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs528351272	chr11:4160646-4160647	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs533108461	chr11:4160647-4160648	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs10767850	chr11:4160657-4160658	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs11031096	chr11:4160681-4160682	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs111888095	chr11:4160718-4160719	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs145326062	chr11:4160720-4160721	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs549284498	chr11:4160721-4160722	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530561999	chr11:4160725-4160726	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs73421230	chr11:4160726-4160727	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs529261495	chr11:4160730-4160731	ZNF genes & repeats Weak transcription Strong transcription	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:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4117800-4160200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:4121000-4159400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:4126600-4166600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:4138200-4160600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:4138800-4160400	Strong transcription	Placenta	Placenta
6	chr11:4143200-4159400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:4144000-4159400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr11:4144800-4160800	Weak transcription	Colonic Mucosa	Colon
9	chr11:4145600-4159400	Weak transcription	Fetal Heart	heart
10	chr11:4148600-4164800	Weak transcription	HSMMtube	muscle
11	chr11:4148800-4165200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:4149200-4159400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr11:4149200-4159400	Weak transcription	Brain Anterior Caudate	brain
14	chr11:4149200-4159600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:4149200-4160600	Weak transcription	Spleen	Spleen
16	chr11:4149200-4164600	Weak transcription	Gastric	stomach
17	chr11:4149400-4162200	Weak transcription	Psoas Muscle	Psoas
18	chr11:4149600-4169400	Weak transcription	Pancreas	Pancrea
19	chr11:4149800-4159400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:4149800-4160600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:4153400-4159400	Weak transcription	NHEK	skin
22	chr11:4153400-4165200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:4153600-4159400	Weak transcription	Brain Angular Gyrus	brain
24	chr11:4155600-4159600	Weak transcription	Aorta	Aorta
25	chr11:4156600-4159400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr11:4156600-4159800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr11:4156800-4159400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr11:4157000-4159400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:4157000-4159400	Weak transcription	Brain Hippocampus Middle	brain
30	chr11:4157000-4159400	Weak transcription	Brain Substantia Nigra	brain
31	chr11:4157000-4159400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr11:4157000-4159400	Weak transcription	Ovary	ovary
33	chr11:4157000-4159400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr11:4157000-4159400	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr11:4157000-4159400	Weak transcription	Right Ventricle	heart
36	chr11:4157000-4159400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr11:4157000-4159400	Weak transcription	HepG2	liver
38	chr11:4157000-4159400	Weak transcription	NHLF	lung
39	chr11:4157000-4159600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr11:4157000-4162200	Weak transcription	Colon Smooth Muscle	Colon
41	chr11:4157000-4166000	Weak transcription	NH-A	brain
42	chr11:4157200-4159400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr11:4157200-4159400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr11:4157200-4159400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr11:4157400-4159400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr11:4157400-4159400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:4157400-4159400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:4157400-4159400	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr11:4157400-4159400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:4157400-4159400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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