Variant report

Variant	nsv1045527
Chromosome Location	chr11:4162019-4225100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1253)
CpG islands
(count:550)
Chromatin interactive
region (count:35)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr11:4208203-4208403	K562	blood:	n/a	n/a
3	ARID3A	chr11:4205750-4205950	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	chr11:4218126-4218315	K562	blood:	n/a	n/a
7	ATF1	chr11:4167279-4168246	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	chr11:4167574-4167591	K562	blood:	n/a	n/a
11	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
13	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr11:4186428-4186725	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:4167445-4168270	K562	blood:	n/a	n/a
16	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
17	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
18	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
19	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
20	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
21	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
22	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
24	CBX3	chr11:4203292-4203924	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	chr11:4207969-4208291	K562	blood:	n/a	n/a
28	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
29	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
30	CCNT2	chr11:4167349-4168021	K562	blood:	n/a	n/a
31	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
32	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
33	CEBPB	chr11:4205574-4206017	K562	blood:	n/a	chr11:4205745-4205756
34	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
35	CEBPB	chr11:4216252-4216447	K562	blood:	n/a	n/a
36	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
37	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
38	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
39	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
41	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a
43	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
44	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
45	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
46	CEBPB	chr11:4208020-4208479	Hela-S3	cervix:	n/a	n/a
47	CEBPD	chr11:4216035-4216623	K562	blood:	n/a	n/a
48	CEBPD	chr11:4216067-4216617	K562	blood:	n/a	n/a
49	CHD1	chr11:4208309-4208509	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr11:4203332-4203663	Hela-S3	cervix:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4209397-4209447	HCT-116	colon:	n/a
2	chr11:4209397-4209447	HCT-116	colon:	n/a
3	chr11:4212446-4212496	SK-N-SH_RA	brain:	n/a
4	chr11:4209397-4209447	HCF	heart:	n/a
5	chr11:4212471-4212521	NB4	blood:	n/a
6	chr11:4209397-4209447	RPTEC	kidney:	n/a
7	chr11:4208449-4208499	HUVEC	blood vessel:	n/a
8	chr11:4209397-4209447	IMR90	lung:	fetal
9	chr11:4208449-4208499	T-47D	breast:	n/a
10	chr11:4208449-4208499	Jurkat	blood:	n/a
11	chr11:4208905-4208955	HUVEC	blood vessel:	n/a
12	chr11:4206098-4206148	SK-N-MC	brain:	n/a
13	chr11:4208449-4208499	BJ	skin:	n/a
14	chr11:4208449-4208499	GM06990	blood:	n/a
15	chr11:4208723-4208773	NHBE	bronchial:	n/a
16	chr11:4209120-4209170	GM12878	blood:	n/a
17	chr11:4208449-4208499	NB4	blood:	n/a
18	chr11:4209120-4209170	AG09309	skin:	n/a
19	chr11:4208449-4208499	AG09309	skin:	n/a
20	chr11:4206098-4206148	GM19239	blood:	n/a
21	chr11:4208449-4208499	SK-N-SH	brain:	n/a
22	chr11:4208723-4208773	SK-N-SH	brain:	n/a
23	chr11:4212446-4212496	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:4208278-4208328	ECC-1	luminal epithelium:	n/a
25	chr11:4209397-4209447	H1-hESC	embryonic stem cell:	embryo
26	chr11:4208449-4208499	HRCEpiC	kidney:	n/a
27	chr11:4209397-4209447	HNPCEpiC	eye:	n/a
28	chr11:4208905-4208955	Hepatocyte	liver:	n/a
29	chr11:4208449-4208499	SK-N-MC	brain:	n/a
30	chr11:4212471-4212521	AG10803	skin:	n/a
31	chr11:4212446-4212496	ECC-1	luminal epithelium:	n/a
32	chr11:4208723-4208773	T-47D	breast:	n/a
33	chr11:4208449-4208499	GM12891	blood:	n/a
34	chr11:4206098-4206148	HRPEpiC	eye:	n/a
35	chr11:4208905-4208955	ovcar-3	ovarian:	n/a
36	chr11:4208449-4208499	NHDF-neo	bronchial:	n/a
37	chr11:4209120-4209170	HRE	kidney:	n/a
38	chr11:4209120-4209170	NH-A	brain:	n/a
39	chr11:4209397-4209447	CMK	blood:	n/a
40	chr11:4212471-4212521	HCF	heart:	n/a
41	chr11:4206098-4206148	HRCEpiC	kidney:	n/a
42	chr11:4208905-4208955	Jurkat	blood:	n/a
43	chr11:4209120-4209170	H1-hESC	embryonic stem cell:	embryo
44	chr11:4209397-4209447	Hepatocyte	liver:	n/a
45	chr11:4209397-4209447	MCF10A-Er-Src	breast:	n/a
46	chr11:4208278-4208328	RPTEC	kidney:	n/a
47	chr11:4212446-4212496	HRCEpiC	kidney:	n/a
48	chr11:4208278-4208328	NHDF-neo	bronchial:	n/a
49	chr11:4206098-4206148	HAEpiC	amniotic membrane:	n/a
50	chr11:4208449-4208499	U87	brain:	n/a

(count:35 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 2508 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2508 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144211034	chr11:4162023-4162024	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373504130	chr11:4162127-4162128	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs35509908	chr11:4162144-4162145	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142485294	chr11:4162145-4162146	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201964325	chr11:4162155-4162156	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200084469	chr11:4162156-4162157	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs140836942	chr11:4162161-4162162	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560317748	chr11:4162165-4162166	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192167558	chr11:4162170-4162171	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549521212	chr11:4162210-4162211	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561332382	chr11:4162216-4162217	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531954489	chr11:4162217-4162218	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs550352798	chr11:4162286-4162287	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143139151	chr11:4162304-4162305	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183842159	chr11:4162338-4162339	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs147479364	chr11:4162397-4162398	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565558983	chr11:4162423-4162424	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377398951	chr11:4162446-4162447	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	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
20	rs7952234	chr11:4162499-4162500	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142614702	chr11:4162509-4162510	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536746447	chr11:4162638-4162639	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	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
24	rs532180965	chr11:4162692-4162693	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142375412	chr11:4162697-4162698	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540997074	chr11:4162783-4162784	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	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
28	rs373598973	chr11:4162820-4162821	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs151012841	chr11:4162825-4162826	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543003035	chr11:4162832-4162833	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536201939	chr11:4162867-4162868	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	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
33	rs565406946	chr11:4162881-4162882	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188569571	chr11:4162896-4162897	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543891449	chr11:4162897-4162898	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372575375	chr11:4162899-4162900	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565375772	chr11:4162964-4162965	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532709361	chr11:4162987-4162988	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547788906	chr11:4162997-4162998	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139604879	chr11:4163010-4163011	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149672383	chr11:4163058-4163059	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199981944	chr11:4163112-4163113	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547828558	chr11:4163163-4163164	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569299657	chr11:4163177-4163178	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575161828	chr11:4163184-4163185	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs373857635	chr11:4163200-4163201	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558598407	chr11:4163230-4163231	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	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
49	rs115836231	chr11:4163255-4163256	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146673921	chr11:4163278-4163279	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 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:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr11:4149400-4162200	Weak transcription	Psoas Muscle	Psoas
6	chr11:4149600-4169400	Weak transcription	Pancreas	Pancrea
7	chr11:4153400-4165200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr11:4157000-4162200	Weak transcription	Colon Smooth Muscle	Colon
9	chr11:4157000-4166000	Weak transcription	NH-A	brain
10	chr11:4157400-4162200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr11:4159000-4163000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:4159000-4163400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:4159000-4164800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:4159200-4163800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
15	chr11:4159400-4162200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:4159400-4162400	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr11:4159400-4162400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
18	chr11:4159400-4162400	ZNF genes & repeats	GM12878-XiMat	blood
19	chr11:4159400-4162600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:4159400-4162600	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:4159400-4162600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr11:4159400-4162600	ZNF genes & repeats	Fetal Intestine Large	intestine
23	chr11:4159400-4162600	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr11:4159400-4163000	ZNF genes & repeats	Fetal Lung	lung
25	chr11:4159400-4163000	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr11:4159400-4163200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:4159400-4163200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
28	chr11:4159400-4163200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr11:4159400-4163400	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr11:4159400-4163400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr11:4159400-4163400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:4159400-4163400	ZNF genes & repeats	Fetal Brain Female	brain
33	chr11:4159400-4163400	Strong transcription	HSMM	muscle
34	chr11:4159400-4163800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr11:4159400-4163800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:4159400-4163800	Strong transcription	Duodenum Mucosa	Duodenum
37	chr11:4159400-4164800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:4159400-4165000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:4159400-4165000	Strong transcription	Fetal Thymus	thymus
40	chr11:4159400-4165200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:4159400-4168000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:4159600-4162600	Strong transcription	HMEC	breast
43	chr11:4159600-4163600	Strong transcription	Osteobl	bone
44	chr11:4159800-4162400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
45	chr11:4159800-4162800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr11:4159800-4163000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:4160000-4162600	ZNF genes & repeats	A549	lung
48	chr11:4160000-4163800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:4160000-4169200	Weak transcription	NHLF	lung
50	chr11:4160000-4172200	Weak transcription	NHEK	skin

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