Variant report

Variant	nsv830787
Chromosome Location	chr6:118631902-118805106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:708)
CpG islands
(count:368)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:118665112-118665442	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:118789925-118790949	HepG2	liver:	n/a	n/a
3	ATF1	chr6:118637071-118637263	K562	blood:	n/a	n/a
4	ATF2	chr6:118675749-118676232	GM12878	blood:	n/a	n/a
5	ATF2	chr6:118788378-118788709	GM12878	blood:	n/a	n/a
6	ATF2	chr6:118675693-118676264	GM12878	blood:	n/a	n/a
7	ATF3	chr6:118790642-118790921	K562	blood:	n/a	n/a
8	BACH1	chr6:118708219-118708390	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:118708234-118708493	K562	blood:	n/a	n/a
10	BACH1	chr6:118721836-118722106	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:118721799-118722067	K562	blood:	n/a	n/a
12	BATF	chr6:118675758-118676201	GM12878	blood:	n/a	chr6:118675990-118676001
13	BATF	chr6:118675774-118676194	GM12878	blood:	n/a	chr6:118675990-118676001
14	BCL11A	chr6:118675707-118676193	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:118675858-118676191	GM12878	blood:	n/a	n/a
16	BCL3	chr6:118675831-118676152	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:118675754-118676245	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:118790184-118790852	HepG2	liver:	n/a	n/a
19	CBX3	chr6:118674752-118674994	K562	blood:	n/a	n/a
20	CEBPB	chr6:118648432-118648761	H1-hESC	embryonic stem cell:	n/a	chr6:118648588-118648597 chr6:118648588-118648599 chr6:118648586-118648597 chr6:118648586-118648599 chr6:118648586-118648599
21	CEBPB	chr6:118645320-118645701	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:118641144-118641459	MCF-7	breast:	n/a	n/a
23	CEBPB	chr6:118790252-118791015	HepG2	liver:	n/a	chr6:118790816-118790827
24	CEBPB	chr6:118641101-118641353	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:118677887-118678213	IMR90	lung:	n/a	chr6:118678045-118678056
26	CEBPB	chr6:118665249-118665834	IMR90	lung:	n/a	chr6:118665377-118665388
27	CEBPB	chr6:118790231-118790626	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:118790202-118791017	IMR90	lung:	n/a	chr6:118790816-118790827
29	CEBPB	chr6:118648403-118648768	HepG2	liver:	n/a	chr6:118648588-118648597 chr6:118648588-118648599 chr6:118648586-118648597 chr6:118648586-118648599 chr6:118648586-118648599
30	CEBPB	chr6:118698914-118699234	A549	lung:	n/a	n/a
31	CEBPB	chr6:118665164-118665573	HepG2	liver:	n/a	chr6:118665377-118665388
32	CEBPB	chr6:118665136-118665541	HepG2	liver:	n/a	chr6:118665377-118665388
33	CEBPB	chr6:118758682-118758919	HepG2	liver:	n/a	chr6:118758789-118758800
34	CEBPB	chr6:118641106-118641395	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:118737613-118737852	HepG2	liver:	n/a	chr6:118737735-118737746 chr6:118737733-118737744
36	CEBPB	chr6:118698883-118699570	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr6:118803387-118803546	K562	blood:	n/a	chr6:118803450-118803461 chr6:118803479-118803490
38	CEBPB	chr6:118790635-118790939	K562	blood:	n/a	chr6:118790816-118790827
39	CEBPB	chr6:118790683-118790953	A549	lung:	n/a	chr6:118790816-118790827
40	CEBPB	chr6:118708864-118709963	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:118648420-118648711	A549	lung:	n/a	chr6:118648588-118648597 chr6:118648588-118648599 chr6:118648586-118648597 chr6:118648586-118648599 chr6:118648586-118648599
42	CEBPB	chr6:118790618-118791031	A549	lung:	n/a	chr6:118790816-118790827
43	CEBPB	chr6:118698887-118699258	K562	blood:	n/a	n/a
44	CEBPB	chr6:118637072-118637334	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:118698892-118699259	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:118648402-118648778	MCF-7	breast:	n/a	chr6:118648588-118648597 chr6:118648588-118648599 chr6:118648586-118648597 chr6:118648586-118648599 chr6:118648586-118648599
47	CEBPB	chr6:118741797-118741903	A549	lung:	n/a	n/a
48	CEBPB	chr6:118708962-118709944	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:118648408-118648773	IMR90	lung:	n/a	chr6:118648588-118648597 chr6:118648588-118648599 chr6:118648586-118648597 chr6:118648586-118648599 chr6:118648586-118648599
50	CEBPB	chr6:118655927-118656173	HepG2	liver:	n/a	chr6:118656039-118656050

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:118699056-118699106	GM19239	blood:	n/a
2	chr6:118672731-118672781	AG04449	skin:	fetal
3	chr6:118699056-118699106	GM19239	blood:	n/a
4	chr6:118672731-118672781	AG04449	skin:	fetal
5	chr6:118776527-118776577	NHDF-neo	bronchial:	n/a
6	chr6:118647446-118647496	MCF10A-Er-Src	breast:	n/a
7	chr6:118709682-118709732	SKMC	muscle:	n/a
8	chr6:118699056-118699106	HepG2	liver:	n/a
9	chr6:118776527-118776577	GM19239	blood:	n/a
10	chr6:118640897-118640947	SAEC	small airway:	n/a
11	chr6:118776527-118776577	NH-A	brain:	n/a
12	chr6:118647446-118647496	GM12891	blood:	n/a
13	chr6:118640897-118640947	T-47D	breast:	n/a
14	chr6:118647446-118647496	HCF	heart:	n/a
15	chr6:118776527-118776577	GM12878	blood:	n/a
16	chr6:118699056-118699106	SAEC	small airway:	n/a
17	chr6:118709682-118709732	HNPCEpiC	eye:	n/a
18	chr6:118709682-118709732	NHBE	bronchial:	n/a
19	chr6:118776527-118776577	ECC-1	luminal epithelium:	n/a
20	chr6:118699056-118699106	HCT-116	colon:	n/a
21	chr6:118776527-118776577	GM12892	blood:	n/a
22	chr6:118672731-118672781	SK-N-SH	brain:	n/a
23	chr6:118640897-118640947	MCF10A-Er-Src	breast:	n/a
24	chr6:118776527-118776577	HRE	kidney:	n/a
25	chr6:118672731-118672781	AG10803	skin:	n/a
26	chr6:118776527-118776577	Hela-S3	cervix:	n/a
27	chr6:118647446-118647496	Caco-2	colon:	n/a
28	chr6:118640897-118640947	A549	lung:	n/a
29	chr6:118699056-118699106	SKMC	muscle:	n/a
30	chr6:118776527-118776577	NT2-D1	testis:	n/a
31	chr6:118709682-118709732	HRE	kidney:	n/a
32	chr6:118709682-118709732	HEK293	kidney:	embryo
33	chr6:118640897-118640947	AG09309	skin:	n/a
34	chr6:118709682-118709732	AG09319	gingival:	n/a
35	chr6:118647446-118647496	HRCEpiC	kidney:	n/a
36	chr6:118647446-118647496	NB4	blood:	n/a
37	chr6:118672731-118672781	GM19239	blood:	n/a
38	chr6:118776527-118776577	HCPEpiC	choroid plexus:	n/a
39	chr6:118776527-118776577	SAEC	small airway:	n/a
40	chr6:118640897-118640947	HIPEpiC	eye:	n/a
41	chr6:118640897-118640947	GM19239	blood:	n/a
42	chr6:118699056-118699106	NT2-D1	testis:	n/a
43	chr6:118672731-118672781	NB4	blood:	n/a
44	chr6:118699056-118699106	HCM	heart:	n/a
45	chr6:118672731-118672781	GM12892	blood:	n/a
46	chr6:118647446-118647496	HepG2	liver:	n/a
47	chr6:118709682-118709732	GM12878	blood:	n/a
48	chr6:118709682-118709732	HUVEC	blood vessel:	n/a
49	chr6:118640897-118640947	IMR90	lung:	fetal
50	chr6:118699056-118699106	A549	lung:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:118666316..118669235-chr6:118671281..118673875,2	K562	blood:
2	chr6:118650721..118653631-chr6:118670431..118672117,2	K562	blood:
3	chr6:118631014..118632814-chr6:118644282..118647263,2	MCF-7	breast:
4	chr6:118720659..118723492-chr6:118725899..118729757,3	K562	blood:
5	chr6:118649795..118651737-chr6:118653045..118655743,2	K562	blood:
6	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
7	chr6:118630135..118632500-chr6:118803686..118805267,2	K562	blood:
8	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
9	chr6:118720659..118723492-chr6:118725899..118729757,3	K562	blood:
10	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
11	chr6:118648196..118651295-chr6:118653045..118655021,3	K562	blood:
12	chr6:118648196..118651295-chr6:118653045..118655021,3	K562	blood:
13	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
14	chr6:118652792..118655775-chr6:118673226..118674884,2	K562	blood:
15	chr6:118632785..118635288-chr6:118642370..118644781,2	K562	blood:
16	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
17	chr6:118649795..118651737-chr6:118653045..118655743,2	K562	blood:
18	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
19	chr6:118652792..118655775-chr6:118673226..118674884,2	K562	blood:
20	chr5:131992763..131993544-chr6:118675091..118675917,2	MCF-7	breast:
21	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
22	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
23	chr6:118650721..118653631-chr6:118670431..118672117,2	K562	blood:
24	chr6:118632785..118635288-chr6:118642370..118644781,2	K562	blood:
25	chr6:118766414..118769352-chr6:118774128..118777684,3	K562	blood:
26	chr6:118630135..118632500-chr6:118803686..118805267,2	K562	blood:
27	chr6:118640782..118642845-chr6:119024571..119027224,2	K562	blood:
28	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
29	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
30	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
31	chr6:118631014..118632814-chr6:118644282..118647263,2	MCF-7	breast:
32	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
33	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
34	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
35	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
36	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
37	chr6:118666316..118669235-chr6:118671281..118673875,2	K562	blood:
38	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLN-2	chr6:118772307-118773627	NONHSAT114692

No data

Variant related genes	Relation type
ENSG00000216809	TF binding region
ENSG00000216809	CpG island
ENSG00000216809	chromatin interactions

Extended variants
information (count: 5893 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:5893 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145627105	chr6:118631908-118631909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs283040	chr6:118631934-118631935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs76399856	chr6:118631978-118631979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62421496	chr6:118631993-118631994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368371131	chr6:118632013-118632014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561651109	chr6:118632056-118632057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547514212	chr6:118632084-118632085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575060823	chr6:118632140-118632141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544010019	chr6:118632274-118632275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141017782	chr6:118632285-118632286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4946336	chr6:118632335-118632336	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539481950	chr6:118632375-118632376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149906499	chr6:118632376-118632377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74339386	chr6:118632487-118632488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1690667	chr6:118632493-118632494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34654109	chr6:118632535-118632536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549431869	chr6:118632552-118632553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144941001	chr6:118632664-118632665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569644919	chr6:118632679-118632680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538403758	chr6:118632680-118632681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79819289	chr6:118632740-118632741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12524408	chr6:118632751-118632752	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538567331	chr6:118632812-118632813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554203846	chr6:118632826-118632827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112909203	chr6:118632827-118632828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs283051	chr6:118632836-118632837	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535120354	chr6:118632857-118632858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113681999	chr6:118632858-118632859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79391819	chr6:118632894-118632895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554775542	chr6:118632955-118632956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372884702	chr6:118632994-118632995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543948060	chr6:118633020-118633021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377135690	chr6:118633036-118633037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573491950	chr6:118633086-118633087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577447208	chr6:118633098-118633099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540496039	chr6:118633127-118633128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367555193	chr6:118633136-118633137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537695550	chr6:118633162-118633163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560212766	chr6:118633266-118633267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370856702	chr6:118633288-118633289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549120532	chr6:118633297-118633298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149045030	chr6:118633322-118633323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531840844	chr6:118633337-118633338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556018034	chr6:118633567-118633568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551945760	chr6:118633580-118633581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536053885	chr6:118633619-118633620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs283050	chr6:118633623-118633624	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs115085715	chr6:118633631-118633632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544991302	chr6:118633642-118633643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560067846	chr6:118633654-118633655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	22522925	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118627800-118638000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:118627800-118641000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:118629000-118640800	Weak transcription	Fetal Brain Female	brain
4	chr6:118629200-118635200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:118629200-118640600	Weak transcription	Ovary	ovary
6	chr6:118629200-118641000	Weak transcription	Brain Angular Gyrus	brain
7	chr6:118629400-118640600	Weak transcription	Brain Hippocampus Middle	brain
8	chr6:118629800-118632000	Enhancers	Fetal Heart	heart
9	chr6:118630600-118640800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:118631400-118632200	Weak transcription	Aorta	Aorta
11	chr6:118631400-118634000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr6:118631400-118634400	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:118631400-118635000	Weak transcription	Left Ventricle	heart
14	chr6:118631400-118638800	Weak transcription	Brain Germinal Matrix	brain
15	chr6:118631400-118640600	Weak transcription	Psoas Muscle	Psoas
16	chr6:118631600-118632000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:118631600-118634800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:118631600-118635200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:118631600-118637000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:118631600-118638800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:118632000-118633400	Weak transcription	Fetal Heart	heart
22	chr6:118632200-118633000	Enhancers	Aorta	Aorta
23	chr6:118633000-118635200	Weak transcription	Aorta	Aorta
24	chr6:118633400-118635600	Enhancers	Fetal Heart	heart
25	chr6:118633800-118634400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:118634000-118635600	Enhancers	Rectal Smooth Muscle	rectum
27	chr6:118634400-118634600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:118634400-118642600	Enhancers	Colon Smooth Muscle	Colon
29	chr6:118634600-118634800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:118634800-118635000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:118634800-118638000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:118635000-118635400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:118635000-118635400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:118635000-118635400	Enhancers	Right Ventricle	heart
35	chr6:118635000-118635600	Genic enhancers	Left Ventricle	heart
36	chr6:118635200-118635400	Enhancers	Aorta	Aorta
37	chr6:118635200-118635400	Enhancers	Pancreas	Pancrea
38	chr6:118635200-118637400	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr6:118635200-118638000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:118635400-118635600	Genic enhancers	Aorta	Aorta
41	chr6:118635400-118636800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:118635400-118642000	Weak transcription	Pancreas	Pancrea
43	chr6:118635400-118646400	Weak transcription	Right Ventricle	heart
44	chr6:118635600-118636000	Weak transcription	Fetal Heart	heart
45	chr6:118635600-118636800	Weak transcription	Left Ventricle	heart
46	chr6:118635600-118637000	Weak transcription	Rectal Smooth Muscle	rectum
47	chr6:118635600-118638200	Weak transcription	Aorta	Aorta
48	chr6:118636000-118641400	Enhancers	Fetal Heart	heart
49	chr6:118636400-118637200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:118636800-118637400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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