Variant report

Variant	nsv523914
Chromosome Location	chr11:5207389-5231565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5220105-5220182	K562	blood:	n/a	n/a
2	ARID3A	chr11:5226025-5226451	K562	blood:	n/a	n/a
3	ARID3A	chr11:5217315-5217701	K562	blood:	n/a	n/a
4	ARID3A	chr11:5222439-5222656	K562	blood:	n/a	n/a
5	ARID3A	chr11:5220569-5220574	K562	blood:	n/a	n/a
6	ARID3A	chr11:5218875-5219075	K562	blood:	n/a	n/a
7	ATF1	chr11:5226066-5226378	K562	blood:	n/a	n/a
8	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr11:5226014-5226422	K562	blood:	n/a	n/a
10	BACH1	chr11:5217475-5217660	K562	blood:	n/a	n/a
11	BHLHE40	chr11:5226138-5226199	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:5217386-5217656	K562	blood:	n/a	n/a
13	BRCA1	chr11:5226084-5226312	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:5218668-5219156	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:5218644-5219064	K562	blood:	n/a	n/a
16	CEBPB	chr11:5228170-5228443	K562	blood:	n/a	n/a
17	CEBPB	chr11:5228798-5228866	K562	blood:	n/a	n/a
18	CEBPB	chr11:5218052-5218310	H1-hESC	embryonic stem cell:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
19	CEBPB	chr11:5217466-5217539	K562	blood:	n/a	n/a
20	CEBPB	chr11:5218017-5218228	K562	blood:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
21	CHD2	chr11:5226266-5226379	GM12878	blood:	n/a	n/a
22	CTCF	chr11:5217340-5217580	K562	blood:	n/a	n/a
23	CTCF	chr11:5226140-5226290	AG04450	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
24	CTCF	chr11:5226160-5226310	GM12867	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
25	CTCF	chr11:5226100-5226250	GM12875	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
26	CTCF	chr11:5226140-5226290	GM12868	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
27	CTCF	chr11:5226140-5226290	WERI-Rb-1	eye:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
28	CTCF	chr11:5226120-5226270	GM12870	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
29	CTCF	chr11:5226140-5226290	SAEC	small airway:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
30	CTCF	chr11:5226180-5226330	HEEpiC	esophagus:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
31	CTCF	chr11:5226081-5226290	A549	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
32	CTCF	chr11:5218237-5218251	K562	blood:	n/a	n/a
33	CTCF	chr11:5226120-5226270	GM12871	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
34	CTCF	chr11:5226144-5226301	Fibrobl	skin:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
35	CTCF	chr11:5226180-5226330	GM12865	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
36	CTCF	chr11:5225819-5226511	HCT-116	colon:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
37	CTCF	chr11:5226100-5226250	SAEC	small airway:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
38	CTCF	chr11:5225780-5225930	K562	blood:	n/a	n/a
39	CTCF	chr11:5226116-5226287	SK-N-SH_RA	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
40	CTCF	chr11:5226067-5226342	Hela-S3	cervix:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
41	CTCF	chr11:5226140-5226290	HPF	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
42	CTCF	chr11:5226150-5226280	GM19240	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
43	CTCF	chr11:5226140-5226290	HRE	kidney:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
44	CTCF	chr11:5225766-5226490	SK-N-SH	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
45	CTCF	chr11:5226160-5226310	HAc	cerebellar:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
46	CTCF	chr11:5226130-5226272	Spleen_OC	spleen:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
47	CTCF	chr11:5226140-5226290	HCFaa	heart:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
48	CTCF	chr11:5226070-5226345	Gliobla	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
49	CTCF	chr11:5226120-5226270	AG10803	skin:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
50	CTCF	chr11:5226180-5226330	BE2_C	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5221539-5221589	SK-N-SH_RA	brain:	n/a
2	chr11:5221539-5221589	ProgFib	skin:	n/a
3	chr11:5223080-5223130	SK-N-SH	brain:	n/a
4	chr11:5223080-5223130	HIPEpiC	eye:	n/a
5	chr11:5223080-5223130	GM06990	blood:	n/a
6	chr11:5223080-5223130	HNPCEpiC	eye:	n/a
7	chr11:5221539-5221589	Hepatocyte	liver:	n/a
8	chr11:5221539-5221589	GM19239	blood:	n/a
9	chr11:5221539-5221589	AG04449	skin:	fetal
10	chr11:5221539-5221589	BE2_C	brain:	n/a
11	chr11:5223080-5223130	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:5223080-5223130	K562	blood:	n/a
13	chr11:5221539-5221589	T-47D	breast:	n/a
14	chr11:5223080-5223130	SAEC	small airway:	n/a
15	chr11:5221539-5221589	HCF	heart:	n/a
16	chr11:5223080-5223130	U87	brain:	n/a
17	chr11:5221539-5221589	ovcar-3	ovarian:	n/a
18	chr11:5221539-5221589	AG09309	skin:	n/a
19	chr11:5223080-5223130	CMK	blood:	n/a
20	chr11:5223080-5223130	Hepatocyte	liver:	n/a
21	chr11:5221539-5221589	MCF-7	breast:	n/a
22	chr11:5223080-5223130	HCT-116	colon:	n/a
23	chr11:5223080-5223130	NHBE	bronchial:	n/a
24	chr11:5221539-5221589	GM12878	blood:	n/a
25	chr11:5223080-5223130	Jurkat	blood:	n/a
26	chr11:5221539-5221589	NB4	blood:	n/a
27	chr11:5221539-5221589	HRCEpiC	kidney:	n/a
28	chr11:5221539-5221589	NHBE	bronchial:	n/a
29	chr11:5221539-5221589	HAEpiC	amniotic membrane:	n/a
30	chr11:5223080-5223130	HepG2	liver:	n/a
31	chr11:5223080-5223130	HEK293	kidney:	embryo
32	chr11:5223080-5223130	ovcar-3	ovarian:	n/a
33	chr11:5221539-5221589	RPTEC	kidney:	n/a
34	chr11:5221539-5221589	AG09319	gingival:	n/a
35	chr11:5221539-5221589	SK-N-MC	brain:	n/a
36	chr11:5223080-5223130	PFSK-1	brain:	n/a
37	chr11:5223080-5223130	MCF10A-Er-Src	breast:	n/a
38	chr11:5223080-5223130	A549	lung:	n/a
39	chr11:5221539-5221589	HNPCEpiC	eye:	n/a
40	chr11:5223080-5223130	AG09319	gingival:	n/a
41	chr11:5223080-5223130	GM12891	blood:	n/a
42	chr11:5221539-5221589	GM12891	blood:	n/a
43	chr11:5221539-5221589	GM12892	blood:	n/a
44	chr11:5221539-5221589	SK-N-SH	brain:	n/a
45	chr11:5221539-5221589	HRE	kidney:	n/a
46	chr11:5221539-5221589	AG04450	lung:	fetal
47	chr11:5223080-5223130	HAEpiC	amniotic membrane:	n/a
48	chr11:5223080-5223130	ECC-1	luminal epithelium:	n/a
49	chr11:5221539-5221589	HCT-116	colon:	n/a
50	chr11:5221539-5221589	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5152006..5154660-chr11:5213226..5215210,2	K562	blood:
2	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
3	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
4	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
5	11:5222789-5225325..11:5469844-5475173	K562	blood:
6	11:5222789-5225325..11:5527719-5533869	K562	blood:
7	chr11:5149697..5151826-chr11:5212442..5214718,2	K562	blood:
8	11:5146608-5154908..11:5222789-5225325	K562	blood:
9	chr11:5150860..5154299-chr11:5221551..5224711,3	K562	blood:
10	11:5222789-5225325..11:5250847-5268367	K562	blood:
11	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
12	chr11:5222818..5224901-chr11:5309713..5311258,2	K562	blood:
13	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
14	11:5222789-5225325..11:5533869-5541626	K562	blood:
15	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
16	chr11:5224853..5227509-chr11:5231125..5233882,2	K562	blood:
17	11:5217159-5218976..11:5700314-5707362	K562	blood:
18	chr11:5191979..5193506-chr11:5217289..5219722,2	K562	blood:
19	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
20	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
21	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
22	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
23	11:5217159-5218976..11:5321718-5325668	K562	blood:
24	chr11:5216220..5220735-chr11:5221265..5224295,5	K562	blood:
25	chr11:5217946..5220374-chr11:5295563..5297750,2	K562	blood:
26	11:5222789-5225325..11:5616559-5618985	H1-hESC	embryonic stem cell:	embryo
27	11:5222789-5225325..11:5700314-5707362	K562	blood:
28	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:
29	chr11:5229274..5231190-chr11:5233196..5235582,2	K562	blood:
30	11:5146608-5154908..11:5217159-5218976	K562	blood:
31	chr11:5225340..5227662-chr11:5228751..5230686,2	K562	blood:
32	chr11:5218893..5221432-chr11:5224834..5227380,3	K562	blood:
33	chr11:5145799..5146631-chr11:5217510..5218294,2	K562	blood:
34	11:5222789-5225325..11:5714465-5718134	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51B6-1	chr11:5228064-5228538	XLOC_009040
2	lnc-OR51B6-1	chr11:5226271-5226317	XLOC_009040

Variant related genes	Relation type
OR51V1	TF binding region
OR52A1	TF binding region
ENSG00000224091	TF binding region
OR51V1	CpG island
OR52A1	CpG island
ENSG00000224091	CpG island
ENSG00000260629	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000176752	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000175518	chromatin interactions
HSPA13	miRNA target sites

Extended variants
information (count: 962 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569170572	chr11:5207739-5207740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs188475714	chr11:5207757-5207758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs181066571	chr11:5207775-5207776	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs79822791	chr11:5207824-5207825	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs533621596	chr11:5207864-5207865	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs74575214	chr11:5207873-5207874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs549048936	chr11:5207874-5207875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552752540	chr11:5207888-5207889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs6421045	chr11:5207915-5207916	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148406785	chr11:5207919-5207920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552760283	chr11:5207935-5207936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs557175136	chr11:5207964-5207965	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs575493135	chr11:5207968-5207969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs142494711	chr11:5208249-5208250	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs570339035	chr11:5208262-5208263	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs146462523	chr11:5208264-5208265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556365942	chr11:5208278-5208279	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs34198979	chr11:5208279-5208280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10654717	chr11:5208286-5208287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs34648722	chr11:5208287-5208288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs71050472	chr11:5208290-5208291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200092009	chr11:5208291-5208292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs527259938	chr11:5208386-5208387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs185549018	chr11:5208388-5208389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs7939459	chr11:5208393-5208394	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs367733343	chr11:5208396-5208397	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188000544	chr11:5208426-5208427	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs181063445	chr11:5208437-5208438	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs74370727	chr11:5208438-5208439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539711897	chr11:5208448-5208449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs140889105	chr11:5208468-5208469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs145840425	chr11:5208490-5208491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371822933	chr11:5208519-5208520	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551732274	chr11:5209001-5209002	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs183368438	chr11:5209004-5209005	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7479443	chr11:5209013-5209014	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7482952	chr11:5209038-5209039	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574769860	chr11:5209040-5209041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201451334	chr11:5209064-5209065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs138481906	chr11:5209067-5209068	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs67484300	chr11:5209068-5209069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs71050473	chr11:5209069-5209070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs199837802	chr11:5209070-5209071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200695037	chr11:5209071-5209072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs567685478	chr11:5209098-5209099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185965718	chr11:5209101-5209102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs7479475	chr11:5209105-5209106	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575623075	chr11:5211494-5211495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs74765645	chr11:5211496-5211497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs114742645	chr11:5211522-5211523	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Lung cancer	18438408	CNVD
Autism	22495311	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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5217000-5217200	Enhancers	K562	blood
2	chr11:5217200-5217800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:5217200-5217800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr11:5217200-5217800	Flanking Active TSS	K562	blood
5	chr11:5217400-5217600	Enhancers	NHLF	lung
6	chr11:5217400-5217800	Enhancers	H9 Cell Line	embryonic stem cell
7	chr11:5217600-5220200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:5217600-5226000	Weak transcription	NHLF	lung
9	chr11:5217800-5219200	Enhancers	K562	blood
10	chr11:5218200-5219400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:5218600-5219800	Enhancers	Osteobl	bone
12	chr11:5219200-5220400	Weak transcription	K562	blood
13	chr11:5219400-5222800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:5220200-5224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:5220400-5223200	Enhancers	K562	blood
16	chr11:5221000-5221800	Enhancers	Brain Germinal Matrix	brain
17	chr11:5221600-5221800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:5221800-5222600	Weak transcription	Brain Germinal Matrix	brain
19	chr11:5222600-5222800	Enhancers	Brain Germinal Matrix	brain
20	chr11:5222600-5223000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:5222800-5223200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:5223000-5229600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:5223200-5224800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:5223200-5224800	Weak transcription	K562	blood
25	chr11:5224200-5226200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:5224800-5225000	Enhancers	K562	blood
27	chr11:5224800-5225200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:5225000-5225400	Weak transcription	K562	blood
29	chr11:5225200-5231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:5225400-5226400	Enhancers	K562	blood
31	chr11:5226000-5226200	Enhancers	NHLF	lung
32	chr11:5226000-5226400	Enhancers	Osteobl	bone
33	chr11:5226400-5227600	Weak transcription	K562	blood
34	chr11:5227600-5228400	Enhancers	K562	blood
35	chr11:5228400-5231600	Weak transcription	K562	blood
36	chr11:5229600-5231600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:5231400-5231800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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