Variant report

Variant	nsv601490
Chromosome Location	chr6:31079264-31084435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:298)
CpG islands
(count:1281)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr6:31082848-31083146	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr6:31082392-31082645	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr6:31082207-31083041	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr6:31082862-31083062	HepG2	liver:	n/a	n/a
5	CTCF	chr6:31082940-31083090	AG04449	skin:	n/a	n/a
6	CTCF	chr6:31082920-31083070	SAEC	small airway:	n/a	n/a
7	CTCF	chr6:31082960-31083110	K562	blood:	n/a	n/a
8	CTCF	chr6:31082776-31083143	K562	blood:	n/a	n/a
9	CTCF	chr6:31082920-31083070	HEK293	kidney:	n/a	n/a
10	CTCF	chr6:31082880-31083030	HCFaa	heart:	n/a	n/a
11	CTCF	chr6:31082900-31083050	K562	blood:	n/a	n/a
12	CTCF	chr6:31082870-31083089	MCF-7	breast:	n/a	n/a
13	CTCF	chr6:31082840-31082990	AG04450	lung:	n/a	n/a
14	CTCF	chr6:31081560-31081710	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr6:31082936-31083029	GM13976	blood:	n/a	n/a
16	CTCF	chr6:31082880-31083030	HCT-116	colon:	n/a	n/a
17	CTCF	chr6:31082858-31082978	GM20000	blood:	n/a	n/a
18	CTCF	chr6:31082920-31083070	GM12873	blood:	n/a	n/a
19	CTCF	chr6:31081620-31081770	AG04449	skin:	n/a	chr6:31081705-31081714
20	CTCF	chr6:31082900-31083050	AG10803	skin:	n/a	n/a
21	CTCF	chr6:31082920-31083070	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr6:31083040-31083190	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr6:31082722-31083245	K562	blood:	n/a	n/a
24	CTCF	chr6:31082900-31083050	HMEC	breast:	n/a	n/a
25	CTCF	chr6:31082940-31083090	GM12864	blood:	n/a	n/a
26	CTCF	chr6:31082925-31083088	LNCaP	prostate:	n/a	n/a
27	CTCF	chr6:31081660-31081810	AoAF	blood vessel:	n/a	chr6:31081705-31081714
28	CTCF	chr6:31082857-31083036	K562	blood:	n/a	n/a
29	CTCF	chr6:31082847-31083041	A549	lung:	n/a	n/a
30	CTCF	chr6:31082893-31083028	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr6:31082940-31083090	GM12871	blood:	n/a	n/a
32	CTCF	chr6:31082900-31083050	HepG2	liver:	n/a	n/a
33	CTCF	chr6:31081660-31081810	NHDF-neo	bronchial:	n/a	chr6:31081705-31081714
34	CTCF	chr6:31081760-31081910	HEK293	kidney:	n/a	n/a
35	CTCF	chr6:31081720-31081870	NHEK	skin:	n/a	n/a
36	CTCF	chr6:31082756-31083028	A549	lung:	n/a	n/a
37	CTCF	chr6:31082812-31083164	IMR90	lung:	n/a	n/a
38	CTCF	chr6:31082840-31082990	RPTEC	kidney:	n/a	n/a
39	CTCF	chr6:31082918-31083045	GM19240	blood:	n/a	n/a
40	CTCF	chr6:31082900-31083050	HCM	heart:	n/a	n/a
41	CTCF	chr6:31082880-31083030	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr6:31082898-31083142	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:31082800-31082950	GM06990	blood:	n/a	n/a
44	CTCF	chr6:31082900-31083050	AG04449	skin:	n/a	n/a
45	CTCF	chr6:31082880-31083030	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr6:31081620-31081770	AG10803	skin:	n/a	chr6:31081705-31081714
47	CTCF	chr6:31081620-31081770	HAc	cerebellar:	n/a	chr6:31081705-31081714
48	CTCF	chr6:31079120-31079270	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr6:31082864-31083141	NHEK	skin:	n/a	n/a
50	CTCF	chr6:31082805-31083137	K562	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31084146-31084196	LNCaP	prostate:	n/a
2	chr6:31080048-31080098	SKMC	muscle:	n/a
3	chr6:31082200-31082250	HRCEpiC	kidney:	n/a
4	chr6:31079698-31079748	SKMC	muscle:	n/a
5	chr6:31079617-31079667	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:31084146-31084196	NHBE	bronchial:	n/a
7	chr6:31082939-31082989	PFSK-1	brain:	n/a
8	chr6:31082835-31082885	H1-hESC	embryonic stem cell:	embryo
9	chr6:31079555-31079605	HIPEpiC	eye:	n/a
10	chr6:31082939-31082989	IMR90	lung:	fetal
11	chr6:31084146-31084196	BJ	skin:	n/a
12	chr6:31081323-31081373	AG09309	skin:	n/a
13	chr6:31082196-31082246	HNPCEpiC	eye:	n/a
14	chr6:31082631-31082681	HCF	heart:	n/a
15	chr6:31082534-31082584	Hepatocyte	liver:	n/a
16	chr6:31081617-31081667	HNPCEpiC	eye:	n/a
17	chr6:31082196-31082246	PrEC	prostate:	n/a
18	chr6:31082187-31082237	SK-N-MC	brain:	n/a
19	chr6:31080048-31080098	HMEC	breast:	n/a
20	chr6:31082187-31082237	GM12878	blood:	n/a
21	chr6:31081518-31081568	U87	brain:	n/a
22	chr6:31082835-31082885	HIPEpiC	eye:	n/a
23	chr6:31084146-31084196	BE2_C	brain:	n/a
24	chr6:31084146-31084196	ovcar-3	ovarian:	n/a
25	chr6:31080305-31080355	NH-A	brain:	n/a
26	chr6:31082534-31082584	RPTEC	kidney:	n/a
27	chr6:31080048-31080098	PANC-1	pancreas:	n/a
28	chr6:31081323-31081373	HCT-116	colon:	n/a
29	chr6:31079698-31079748	BE2_C	brain:	n/a
30	chr6:31081323-31081373	SK-N-MC	brain:	n/a
31	chr6:31081617-31081667	H1-hESC	embryonic stem cell:	embryo
32	chr6:31081518-31081568	HRPEpiC	eye:	n/a
33	chr6:31082196-31082246	Hepatocyte	liver:	n/a
34	chr6:31079617-31079667	MCF-7	breast:	n/a
35	chr6:31081905-31081955	SKMC	muscle:	n/a
36	chr6:31081905-31081955	ProgFib	skin:	n/a
37	chr6:31080305-31080355	Jurkat	blood:	n/a
38	chr6:31080529-31080579	IMR90	lung:	fetal
39	chr6:31080529-31080579	AG10803	skin:	n/a
40	chr6:31079306-31079356	HRPEpiC	eye:	n/a
41	chr6:31083322-31083372	GM12892	blood:	n/a
42	chr6:31079617-31079667	HCM	heart:	n/a
43	chr6:31082534-31082584	LNCaP	prostate:	n/a
44	chr6:31079306-31079356	HIPEpiC	eye:	n/a
45	chr6:31081617-31081667	HepG2	liver:	n/a
46	chr6:31081323-31081373	GM12891	blood:	n/a
47	chr6:31082196-31082246	U87	brain:	n/a
48	chr6:31082196-31082246	SAEC	small airway:	n/a
49	chr6:31079617-31079667	ovcar-3	ovarian:	n/a
50	chr6:31081617-31081667	T-47D	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31050562..31052756-chr6:31081245..31083912,2	MCF-7	breast:
2	chr6:30852881..30854431-chr6:31082824..31085360,2	MCF-7	breast:
3	chr6:30850897..30852602-chr6:31080609..31083224,2	MCF-7	breast:
4	chr6:30706968..30708550-chr6:31084295..31086669,2	MCF-7	breast:
5	chr6:31082945..31085753-chr6:31086345..31088520,3	MCF-7	breast:
6	chr6:30882036..30883658-chr6:31081525..31084682,3	MCF-7	breast:
7	chr6:31079457..31085209-chr6:31085850..31092700,13	MCF-7	breast:
8	chr6:31081417..31083958-chr6:31084326..31085918,2	K562	blood:
9	chr6:31080693..31083957-chr6:31087484..31089976,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSORS1C1-1	chr6:31082616-31082668	NONHSAT108723
2	lnc-PSORS1C1-1	chr6:31082602-31082668	NONHSAT108720
3	lnc-PSORS1C1-1	chr6:31082608-31082668	NONHSAT108721
4	lnc-PSORS1C1-1	chr6:31082550-31082668	NONHSAT108719
5	lnc-PSORS1C1-1	chr6:31082611-31082668	NONHSAT108722

No data

Variant related genes	Relation type
C6orf15	TF binding region
PSORS1C1	TF binding region
C6orf15	CpG island
PSORS1C1	CpG island
ENSG00000222895	chromatin interactions
ENSG00000204539	chromatin interactions
ENSG00000137411	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000204580	chromatin interactions

Extended variants
information (count: 270 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2233984	chr6:31079264-31079265	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548978054	chr6:31079284-31079285	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs138723075	chr6:31079306-31079307	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs142775868	chr6:31079307-31079308	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs560168888	chr6:31079310-31079311	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs112157845	chr6:31079317-31079318	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs113953136	chr6:31079338-31079339	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs146335336	chr6:31079350-31079351	Enhancers Weak transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs2233983	chr6:31079371-31079372	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567399515	chr6:31079416-31079417	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs150593466	chr6:31079417-31079418	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs2233982	chr6:31079440-31079441	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200262846	chr6:31079449-31079450	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs146256667	chr6:31079501-31079502	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375181771	chr6:31079503-31079504	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201890892	chr6:31079519-31079520	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369499605	chr6:31079529-31079530	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565921353	chr6:31079547-31079548	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536693439	chr6:31079548-31079549	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139294392	chr6:31079556-31079557	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144330935	chr6:31079570-31079571	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2233981	chr6:31079578-31079579	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs372406795	chr6:31079597-31079598	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111832758	chr6:31079606-31079607	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375696937	chr6:31079614-31079615	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142253539	chr6:31079618-31079619	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs1265054	chr6:31079643-31079644	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs2233980	chr6:31079644-31079645	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs79009277	chr6:31079645-31079646	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560033699	chr6:31079664-31079665	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs115247630	chr6:31079665-31079666	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142517080	chr6:31079675-31079676	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2233979	chr6:31079695-31079696	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs137965061	chr6:31079698-31079699	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2233978	chr6:31079703-31079704	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531449119	chr6:31079710-31079711	Enhancers Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200594594	chr6:31079754-31079755	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61733201	chr6:31079758-31079759	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148192966	chr6:31079760-31079761	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371008853	chr6:31079762-31079763	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571090574	chr6:31079771-31079772	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369158087	chr6:31079796-31079797	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551342144	chr6:31079813-31079814	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141894806	chr6:31079817-31079818	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373556899	chr6:31079831-31079832	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181252354	chr6:31079833-31079834	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547282944	chr6:31079834-31079835	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1265053	chr6:31079889-31079890	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs2233977	chr6:31079894-31079895	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs142530210	chr6:31079895-31079896	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31076800-31082200	Weak transcription	Spleen	Spleen
2	chr6:31077400-31081200	Weak transcription	Right Atrium	heart
3	chr6:31077600-31080400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:31077600-31082600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:31077800-31079600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
6	chr6:31077800-31080400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:31077800-31080600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:31078200-31079400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:31078200-31079600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr6:31078200-31082200	Weak transcription	Gastric	stomach
11	chr6:31078600-31081200	Weak transcription	Stomach Mucosa	stomach
12	chr6:31078800-31080000	Enhancers	HSMM	muscle
13	chr6:31078800-31081200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:31078800-31082200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:31078800-31082200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:31079000-31079600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr6:31079000-31081600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:31079000-31081600	Weak transcription	A549	lung
19	chr6:31079200-31081800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:31079400-31080200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:31079600-31079800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
22	chr6:31079600-31082800	Enhancers	Placenta Amnion	Placenta Amnion
23	chr6:31079800-31081800	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr6:31080000-31080400	Flanking Active TSS	HSMM	muscle
25	chr6:31080000-31082200	Enhancers	HSMMtube	muscle
26	chr6:31080200-31080400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:31080200-31080600	Enhancers	Fetal Muscle Trunk	muscle
28	chr6:31080200-31081000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:31080200-31082400	Enhancers	HMEC	breast
30	chr6:31080400-31080600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:31080400-31081000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
32	chr6:31080400-31081400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:31080400-31081600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr6:31080400-31081600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:31080400-31082000	Enhancers	HSMM	muscle
36	chr6:31080400-31082200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:31080600-31080800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:31080600-31081600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:31080600-31081600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:31080600-31082000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:31080600-31083800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:31080800-31082200	Enhancers	NHDF-Ad	bronchial
43	chr6:31081000-31081400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:31081000-31083200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:31081200-31081800	Enhancers	Hela-S3	cervix
46	chr6:31081200-31082000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr6:31081200-31082200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:31081200-31082200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:31081200-31082200	Enhancers	NH-A	brain
50	chr6:31081200-31082200	Enhancers	NHEK	skin

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