Variant report

Variant	nsv896932
Chromosome Location	chr11:5392484-5424170
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	BACH1	chr11:5401821-5401831	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:5401412-5401568	K562	blood:	n/a	n/a
3	CEBPB	chr11:5410351-5410419	K562	blood:	n/a	n/a
4	CTCF	chr11:5411560-5411710	HPF	lung:	n/a	n/a
5	CTCF	chr11:5411600-5411750	BJ	skin:	n/a	n/a
6	CTCF	chr11:5411580-5411730	GM12868	blood:	n/a	n/a
7	CTCF	chr11:5402043-5402306	Kidney_OC	kidney:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
8	CTCF	chr11:5402024-5402294	GM19239	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
9	CTCF	chr11:5402120-5402270	GM12870	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
10	CTCF	chr11:5402048-5402299	Spleen_OC	spleen:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
11	CTCF	chr11:5402080-5402230	HFF	foreskin:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
12	CTCF	chr11:5402100-5402250	HA-sp	spinal cord:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
13	CTCF	chr11:5411329-5411402	GM12891	blood:	n/a	n/a
14	CTCF	chr11:5401912-5402327	HepG2	liver:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
15	CTCF	chr11:5411540-5411690	HMF	breast:	n/a	n/a
16	CTCF	chr11:5411500-5411650	AG04450	lung:	n/a	n/a
17	CTCF	chr11:5411340-5411490	GM12866	blood:	n/a	n/a
18	CTCF	chr11:5401976-5402271	K562	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
19	CTCF	chr11:5411500-5411650	GM12864	blood:	n/a	n/a
20	CTCF	chr11:5402100-5402250	HMEC	breast:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
21	CTCF	chr11:5402120-5402270	K562	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
22	CTCF	chr11:5402050-5402292	Medullo	brain:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
23	CTCF	chr11:5402100-5402250	GM12871	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
24	CTCF	chr11:5402005-5402331	Gliobla	brain:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
25	CTCF	chr11:5411520-5411670	GM12872	blood:	n/a	n/a
26	CTCF	chr11:5402080-5402230	A549	lung:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
27	CTCF	chr11:5406671-5406739	Lung_OC	lung:	n/a	n/a
28	CTCF	chr11:5402080-5402230	HBMEC	blood vessel:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
29	CTCF	chr11:5411560-5411707	K562	blood:	n/a	n/a
30	CTCF	chr11:5402100-5402250	HEEpiC	esophagus:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
31	CTCF	chr11:5401772-5402492	SK-N-SH	brain:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
32	CTCF	chr11:5411540-5411690	GM12872	blood:	n/a	n/a
33	CTCF	chr11:5411620-5411770	HCT-116	colon:	n/a	n/a
34	CTCF	chr11:5402080-5402230	SAEC	small airway:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
35	CTCF	chr11:5402660-5402810	GM12866	blood:	n/a	n/a
36	CTCF	chr11:5402015-5402318	A549	lung:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
37	CTCF	chr11:5402120-5402270	GM12872	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
38	CTCF	chr11:5411560-5411710	GM12873	blood:	n/a	n/a
39	CTCF	chr11:5411576-5411704	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr11:5402060-5402210	GM12865	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
41	CTCF	chr11:5411517-5411750	GM12878	blood:	n/a	n/a
42	CTCF	chr11:5402026-5402305	LNCaP	prostate:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
43	CTCF	chr11:5411580-5411730	HCT-116	colon:	n/a	n/a
44	CTCF	chr11:5402120-5402270	GM12878	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
45	CTCF	chr11:5402026-5402302	ECC-1	luminal epithelium:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
46	CTCF	chr11:5402080-5402230	HFF-Myc	foreskin:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
47	CTCF	chr11:5411580-5411730	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr11:5402100-5402250	HAc	cerebellar:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
49	CTCF	chr11:5402080-5402230	HPAF	blood vessel:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
50	CTCF	chr11:5411420-5411570	NHLF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5410452-5410502	Jurkat	blood:	n/a
2	chr11:5410452-5410502	Jurkat	blood:	n/a
3	chr11:5410053-5410103	NB4	blood:	n/a
4	chr11:5408788-5408838	HMEC	breast:	n/a
5	chr11:5410053-5410103	HNPCEpiC	eye:	n/a
6	chr11:5410053-5410103	ECC-1	luminal epithelium:	n/a
7	chr11:5410053-5410103	HCPEpiC	choroid plexus:	n/a
8	chr11:5410053-5410103	AG09309	skin:	n/a
9	chr11:5408788-5408838	HCM	heart:	n/a
10	chr11:5410053-5410103	HepG2	liver:	n/a
11	chr11:5410452-5410502	HEK293	kidney:	embryo
12	chr11:5410053-5410103	AG10803	skin:	n/a
13	chr11:5410452-5410502	Hepatocyte	liver:	n/a
14	chr11:5410452-5410502	AG04449	skin:	fetal
15	chr11:5408788-5408838	AG04450	lung:	fetal
16	chr11:5410452-5410502	HCF	heart:	n/a
17	chr11:5410452-5410502	GM19239	blood:	n/a
18	chr11:5408788-5408838	AG09309	skin:	n/a
19	chr11:5410053-5410103	PFSK-1	brain:	n/a
20	chr11:5410452-5410502	NT2-D1	testis:	n/a
21	chr11:5410452-5410502	PANC-1	pancreas:	n/a
22	chr11:5410053-5410103	SK-N-SH	brain:	n/a
23	chr11:5410053-5410103	AG04449	skin:	fetal
24	chr11:5408788-5408838	SKMC	muscle:	n/a
25	chr11:5408788-5408838	AoSMC	blood vessel:	n/a
26	chr11:5410053-5410103	HCT-116	colon:	n/a
27	chr11:5410452-5410502	HRE	kidney:	n/a
28	chr11:5410452-5410502	NHDF-neo	bronchial:	n/a
29	chr11:5410452-5410502	IMR90	lung:	fetal
30	chr11:5408788-5408838	H1-hESC	embryonic stem cell:	embryo
31	chr11:5408788-5408838	PANC-1	pancreas:	n/a
32	chr11:5408788-5408838	T-47D	breast:	n/a
33	chr11:5410053-5410103	NH-A	brain:	n/a
34	chr11:5410452-5410502	CMK	blood:	n/a
35	chr11:5408788-5408838	HIPEpiC	eye:	n/a
36	chr11:5408788-5408838	AG09319	gingival:	n/a
37	chr11:5410452-5410502	SAEC	small airway:	n/a
38	chr11:5408788-5408838	Caco-2	colon:	n/a
39	chr11:5410053-5410103	NHDF-neo	bronchial:	n/a
40	chr11:5408788-5408838	HUVEC	blood vessel:	n/a
41	chr11:5410452-5410502	SKMC	muscle:	n/a
42	chr11:5410452-5410502	HAEpiC	amniotic membrane:	n/a
43	chr11:5408788-5408838	HRE	kidney:	n/a
44	chr11:5410053-5410103	BJ	skin:	n/a
45	chr11:5410053-5410103	HEK293	kidney:	embryo
46	chr11:5410452-5410502	ProgFib	skin:	n/a
47	chr11:5408788-5408838	BJ	skin:	n/a
48	chr11:5410053-5410103	Jurkat	blood:	n/a
49	chr11:5408788-5408838	SK-N-SH_RA	brain:	n/a
50	chr11:5410452-5410502	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:5398331-5406514..11:5707362-5712027	K562	blood:
2	chr11:5404523..5406570-chr11:5525377..5527235,2	K562	blood:
3	chr11:5415584..5416428-chr20:41864268..41865032,2	MCF-7	breast:
4	chr11:5145386..5146091-chr11:5401599..5402243,2	K562	blood:
5	chr11:5403316..5405023-chr11:5406492..5408561,2	K562	blood:
6	chr11:5402164..5402741-chr11:5497230..5497968,2	MCF-7	breast:
7	chr11:5145037..5145858-chr11:5401710..5402214,2	MCF-7	breast:
8	chr11:5403316..5405023-chr11:5406492..5408561,2	K562	blood:
9	11:5218976-5222789..11:5398331-5406514	GM12878	blood:
10	11:4778081-4789138..11:5398331-5406514	Hela-S3	cervix:
11	chr11:5403286..5405023-chr11:5406097..5408561,2	K562	blood:
12	chr11:5385575..5387754-chr11:5392449..5394884,2	K562	blood:
13	11:5146608-5154908..11:5398331-5406514	GM12878	blood:
14	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
15	11:5250847-5268367..11:5406514-5407716	Hela-S3	cervix:
16	11:5243048-5250847..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
17	11:5018576-5020673..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
18	chr11:5225752..5226648-chr11:5401460..5402799,4	MCF-7	breast:
19	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
20	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
21	chr11:5145230..5145917-chr11:5402049..5402594,2	MCF-7	breast:
22	11:5250847-5268367..11:5398331-5406514	Hela-S3	cervix:
23	11:5398331-5406514..11:5700314-5707362	GM12878	blood:
24	chr11:5405070..5407795-chr11:5524807..5526877,2	K562	blood:
25	11:5398331-5406514..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
26	chr11:5403286..5405023-chr11:5406097..5408561,2	K562	blood:

Variant related genes	Relation type
OR51M1	TF binding region
OR51J1	TF binding region
OR51M1	CpG island
OR51J1	CpG island
ENSG00000175520	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000205494	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000221031	chromatin interactions

Extended variants
information (count: 1907 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1907 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs728925	chr11:5392484-5392485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547019044	chr11:5392490-5392491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562415789	chr11:5392509-5392510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572979995	chr11:5392523-5392524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4910774	chr11:5392544-5392545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551019233	chr11:5392553-5392554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569341758	chr11:5392595-5392596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141305266	chr11:5392605-5392606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551534120	chr11:5392627-5392628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188152823	chr11:5392645-5392646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533998471	chr11:5392663-5392664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192714273	chr11:5392707-5392708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116306770	chr11:5392730-5392731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184291096	chr11:5392735-5392736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11037061	chr11:5392740-5392741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs59397650	chr11:5392741-5392742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs61891984	chr11:5392761-5392762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57666779	chr11:5392772-5392773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs573316924	chr11:5392773-5392774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4910775	chr11:5392805-5392806	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs189347720	chr11:5392814-5392815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375383948	chr11:5392834-5392835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550980592	chr11:5392841-5392842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562900384	chr11:5392877-5392878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4910776	chr11:5392884-5392885	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs551541637	chr11:5392966-5392967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs884222	chr11:5392972-5392973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs527465353	chr11:5393029-5393030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143215153	chr11:5393033-5393034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568579067	chr11:5393044-5393045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372010066	chr11:5393069-5393070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1546216	chr11:5393094-5393095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs111859363	chr11:5393113-5393114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181869592	chr11:5393140-5393141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148300569	chr11:5393161-5393162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4306312	chr11:5393165-5393166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538639207	chr11:5393172-5393173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553541265	chr11:5393176-5393177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184808358	chr11:5393195-5393196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189376415	chr11:5393197-5393198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556032820	chr11:5393201-5393202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574368527	chr11:5393217-5393218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141441584	chr11:5393225-5393226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540292894	chr11:5393232-5393233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181435776	chr11:5393259-5393260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2647611	chr11:5393269-5393270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545405048	chr11:5393271-5393272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373724834	chr11:5393272-5393273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560348244	chr11:5393277-5393278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4296065	chr11:5393280-5393281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5392400-5393600	Weak transcription	K562	blood
2	chr11:5393000-5393200	Enhancers	Osteobl	bone
3	chr11:5393000-5393600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5393600-5393800	Genic enhancers	K562	blood
5	chr11:5393600-5394800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:5393800-5394400	Strong transcription	K562	blood
7	chr11:5394400-5401000	Weak transcription	K562	blood
8	chr11:5401000-5404400	Strong transcription	K562	blood
9	chr11:5402400-5405000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:5404400-5407400	Weak transcription	K562	blood
11	chr11:5404600-5405400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr11:5404600-5405600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr11:5404600-5406000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr11:5404600-5406400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:5404800-5405400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr11:5405000-5405400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr11:5405000-5405400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr11:5405000-5405400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:5405000-5405400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:5405000-5405800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr11:5405000-5405800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:5405000-5405800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:5405000-5406000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr11:5405400-5406800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:5405400-5408400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr11:5405400-5408600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr11:5405600-5408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr11:5405800-5408400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr11:5405800-5408800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr11:5406000-5408400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr11:5406000-5410200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr11:5406800-5408600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:5407400-5409200	Strong transcription	K562	blood
34	chr11:5408400-5410200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr11:5408400-5410200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr11:5408400-5410400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:5408600-5409600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:5408600-5410000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr11:5408600-5410200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr11:5408800-5410600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr11:5409200-5410600	Weak transcription	K562	blood
42	chr11:5409600-5412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:5410200-5410400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr11:5410600-5412600	Strong transcription	K562	blood
45	chr11:5411200-5411400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:5412200-5412400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:5412600-5415000	Weak transcription	K562	blood
48	chr11:5415000-5417000	Strong transcription	K562	blood
49	chr11:5415800-5417000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:5417000-5417400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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