Variant report

Variant	nsv604847
Chromosome Location	chr6:150338065-150358012
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	chr6:150338070-150338270	HepG2	liver:	n/a	n/a
2	BATF	chr6:150346621-150346888	GM12878	blood:	n/a	chr6:150346723-150346734 chr6:150346728-150346738 chr6:150346724-150346734
3	CEBPB	chr6:150338074-150338240	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr6:150339733-150339933	Hela-S3	cervix:	n/a	chr6:150339786-150339797
5	CEBPB	chr6:150338050-150338338	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:150339700-150339896	HepG2	liver:	n/a	chr6:150339786-150339797
7	CEBPB	chr6:150338134-150338334	K562	blood:	n/a	n/a
8	CEBPB	chr6:150353985-150354064	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:150349144-150349326	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:150338040-150338363	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:150346556-150346899	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:150338040-150338336	A549	lung:	n/a	n/a
13	CHD2	chr6:150346552-150346904	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr6:150338163-150338306	ProgFib	skin:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
15	CTCF	chr6:150338140-150338290	HepG2	liver:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
16	CTCF	chr6:150338400-150338550	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr6:150338160-150338310	NHDF-neo	bronchial:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
18	CTCF	chr6:150338120-150338270	Caco-2	colon:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
19	CTCF	chr6:150338140-150338290	AoAF	blood vessel:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
20	CTCF	chr6:150341440-150341590	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr6:150338140-150338290	HVMF	connective:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
22	CTCF	chr6:150338120-150338270	BJ	skin:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
23	CTCF	chr6:150338140-150338290	GM12864	blood:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
24	CTCF	chr6:150338120-150338270	GM12865	blood:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
25	CTCF	chr6:150338716-150338761	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr6:150337988-150338303	H1-hESC	embryonic stem cell:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
27	CTCF	chr6:150338140-150338290	HA-sp	spinal cord:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
28	CTCF	chr6:150338580-150338730	AG10803	skin:	n/a	n/a
29	CTCF	chr6:150338120-150338270	WI-38	lung:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
30	CTCF	chr6:150344108-150344152	GM20000	blood:	n/a	n/a
31	CTCF	chr6:150338140-150338290	HCT-116	colon:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
32	CTCF	chr6:150338120-150338270	HMF	breast:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
33	CTCF	chr6:150338109-150338287	GM19240	blood:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
34	CTCF	chr6:150341183-150341290	GM13976	blood:	n/a	n/a
35	CTCF	chr6:150338140-150338290	A549	lung:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
36	CTCF	chr6:150347680-150347830	HRE	kidney:	n/a	n/a
37	CTCF	chr6:150345677-150345737	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr6:150338120-150338270	SAEC	small airway:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
39	CTCF	chr6:150338100-150338250	NHEK	skin:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
40	CTCF	chr6:150338140-150338290	HL-60	blood:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
41	CTCF	chr6:150343122-150343123	GM13977	blood:	n/a	n/a
42	CTCF	chr6:150343050-150343120	GM13977	blood:	n/a	n/a
43	CTCF	chr6:150338140-150338290	HCPEpiC	choroid plexus:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
44	CTCF	chr6:150338120-150338270	GM06990	blood:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
45	CTCF	chr6:150337937-150338495	MCF-7	breast:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
46	CTCF	chr6:150338420-150338570	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:150338120-150338270	SK-N-SH_RA	brain:	n/a	chr6:150338228-150338241 chr6:150338221-150338242 chr6:150338226-150338244 chr6:150338227-150338243
48	CTCF	chr6:150338380-150338530	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:150338460-150338610	HVMF	connective:	n/a	n/a
50	CTCF	chr6:150338080-150338230	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150346721-150346771	T-47D	breast:	n/a
2	chr6:150338421-150338471	H1-hESC	embryonic stem cell:	embryo
3	chr6:150346721-150346771	HIPEpiC	eye:	n/a
4	chr6:150346721-150346771	T-47D	breast:	n/a
5	chr6:150338421-150338471	H1-hESC	embryonic stem cell:	embryo
6	chr6:150346721-150346771	HIPEpiC	eye:	n/a
7	chr6:150346787-150346837	AG09319	gingival:	n/a
8	chr6:150346787-150346837	IMR90	lung:	fetal
9	chr6:150346921-150346971	HEK293	kidney:	embryo
10	chr6:150346721-150346771	HMEC	breast:	n/a
11	chr6:150346816-150346866	RPTEC	kidney:	n/a
12	chr6:150346721-150346771	HNPCEpiC	eye:	n/a
13	chr6:150351274-150351324	CMK	blood:	n/a
14	chr6:150347012-150347062	AG04449	skin:	fetal
15	chr6:150346863-150346913	GM12891	blood:	n/a
16	chr6:150346721-150346771	GM12878	blood:	n/a
17	chr6:150346721-150346771	SK-N-SH	brain:	n/a
18	chr6:150346816-150346866	HNPCEpiC	eye:	n/a
19	chr6:150346800-150346850	T-47D	breast:	n/a
20	chr6:150347012-150347062	ECC-1	luminal epithelium:	n/a
21	chr6:150346787-150346837	NH-A	brain:	n/a
22	chr6:150346921-150346971	AG09309	skin:	n/a
23	chr6:150346800-150346850	PANC-1	pancreas:	n/a
24	chr6:150346858-150346908	CMK	blood:	n/a
25	chr6:150351274-150351324	NH-A	brain:	n/a
26	chr6:150347012-150347062	AG09319	gingival:	n/a
27	chr6:150346816-150346866	HRPEpiC	eye:	n/a
28	chr6:150338421-150338471	AG09319	gingival:	n/a
29	chr6:150346787-150346837	SAEC	small airway:	n/a
30	chr6:150338421-150338471	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:150346858-150346908	GM06990	blood:	n/a
32	chr6:150346858-150346908	GM12892	blood:	n/a
33	chr6:150346863-150346913	SK-N-SH_RA	brain:	n/a
34	chr6:150357289-150357339	AoSMC	blood vessel:	n/a
35	chr6:150357289-150357339	RPTEC	kidney:	n/a
36	chr6:150346858-150346908	HNPCEpiC	eye:	n/a
37	chr6:150346816-150346866	Caco-2	colon:	n/a
38	chr6:150347053-150347103	HCF	heart:	n/a
39	chr6:150346921-150346971	AoSMC	blood vessel:	n/a
40	chr6:150346886-150346936	Hela-S3	cervix:	n/a
41	chr6:150356698-150356748	SKMC	muscle:	n/a
42	chr6:150346816-150346866	BJ	skin:	n/a
43	chr6:150346800-150346850	HL-60	blood:	n/a
44	chr6:150346800-150346850	HCPEpiC	choroid plexus:	n/a
45	chr6:150356698-150356748	Hepatocyte	liver:	n/a
46	chr6:150347053-150347103	RPTEC	kidney:	n/a
47	chr6:150346858-150346908	PrEC	prostate:	n/a
48	chr6:150346787-150346837	HMEC	breast:	n/a
49	chr6:150356698-150356748	SAEC	small airway:	n/a
50	chr6:150346787-150346837	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:150255064..150255979-chr6:150337750..150338789,5	K562	blood:
2	chr6:150246157..150249113-chr6:150336737..150339289,2	K562	blood:
3	chr6:150354901..150357527-chr6:150362159..150364156,2	MCF-7	breast:
4	chr6:150323301..150326870-chr6:150337464..150339739,3	MCF-7	breast:
5	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
6	chr6:150155381..150157771-chr6:150346025..150347800,2	MCF-7	breast:
7	chr6:150350371..150352271-chr6:150387708..150390265,2	MCF-7	breast:
8	chr6:150250322..150251340-chr6:150337738..150338572,3	K562	blood:
9	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
10	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
11	chr6:150261749..150263311-chr6:150348518..150350047,2	MCF-7	breast:
12	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
13	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
14	chr6:150154861..150155845-chr6:150337730..150338274,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP1-2	chr6:150353905-150354172	NONHSAT115530
2	lnc-ULBP1-2	chr6:150354375-150354702	NONHSAT115530

Variant related genes	Relation type
RAET1L	TF binding region
RAET1M	TF binding region
RAET1L	CpG island
RAET1M	CpG island
ENSG00000213091	chromatin interactions
ENSG00000218358	chromatin interactions
ENSG00000235972	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000216621	chromatin interactions
ENSG00000131015	chromatin interactions
ENSG00000131019	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9479405	chr6:150338065-150338066	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531869183	chr6:150338067-150338068	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs545794996	chr6:150338097-150338098	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538011286	chr6:150338179-150338180	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557653593	chr6:150338188-150338189	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577797701	chr6:150338230-150338231	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545980269	chr6:150338231-150338232	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548903640	chr6:150338241-150338242	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192027258	chr6:150338244-150338245	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541826729	chr6:150338246-150338247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs562018916	chr6:150338287-150338288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs182071224	chr6:150338291-150338292	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551288739	chr6:150338295-150338296	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs562262699	chr6:150338359-150338360	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527914809	chr6:150338373-150338374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557441148	chr6:150338437-150338438	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564498570	chr6:150338445-150338446	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs187674871	chr6:150338447-150338448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527601112	chr6:150338511-150338512	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150692295	chr6:150338521-150338522	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs139938456	chr6:150338550-150338551	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs115289471	chr6:150338551-150338552	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149827820	chr6:150338566-150338567	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs191983011	chr6:150338590-150338591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376663816	chr6:150338610-150338611	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182123326	chr6:150338612-150338613	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547346829	chr6:150338616-150338617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs9479406	chr6:150338658-150338659	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs61152765	chr6:150338663-150338664	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs553000582	chr6:150338681-150338682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs145794759	chr6:150338688-150338689	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs34683659	chr6:150338727-150338728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186855193	chr6:150338758-150338759	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs555329518	chr6:150338761-150338762	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs60940053	chr6:150338824-150338825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190137168	chr6:150338829-150338830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575625872	chr6:150338839-150338840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544576479	chr6:150338847-150338848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs564840665	chr6:150338852-150338853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9479408	chr6:150338872-150338873	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534055165	chr6:150338881-150338882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145426695	chr6:150338902-150338903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528981214	chr6:150338909-150338910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs114727746	chr6:150338933-150338934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568866158	chr6:150338935-150338936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182781991	chr6:150338943-150338944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1324590	chr6:150338994-150338995	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs10155731	chr6:150339025-150339026	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188335803	chr6:150339029-150339030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs1324591	chr6:150339057-150339058	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

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
Autism	22495311	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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	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	chr6:150335200-150340400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:150336800-150339800	Weak transcription	HMEC	breast
3	chr6:150337000-150338200	Enhancers	K562	blood
4	chr6:150337600-150338200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
5	chr6:150337600-150338200	Bivalent Enhancer	Brain Hippocampus Middle	brain
6	chr6:150337600-150338200	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
7	chr6:150337600-150338200	Bivalent Enhancer	Brain Substantia Nigra	brain
8	chr6:150337600-150338200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
9	chr6:150337800-150338200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
10	chr6:150337800-150338200	Bivalent Enhancer	Brain Anterior Caudate	brain
11	chr6:150337800-150338200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr6:150337800-150338200	Bivalent Enhancer	GM12878-XiMat	blood
13	chr6:150338000-150338200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:150338000-150338200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr6:150338000-150338200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr6:150338000-150338200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
17	chr6:150338000-150338200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
18	chr6:150338000-150338200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:150338000-150338200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:150338000-150338200	Bivalent Enhancer	Brain Germinal Matrix	brain
21	chr6:150338000-150338200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr6:150338000-150338200	Bivalent Enhancer	Fetal Lung	lung
23	chr6:150338000-150338200	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr6:150338000-150338200	Bivalent Enhancer	Placenta	Placenta
25	chr6:150338000-150338200	Bivalent Enhancer	Fetal Stomach	stomach
26	chr6:150338000-150338200	Bivalent Enhancer	Stomach Mucosa	stomach
27	chr6:150338000-150338200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr6:150339800-150340000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:150339800-150340600	Enhancers	HMEC	breast
30	chr6:150340200-150340400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:150340200-150340600	Enhancers	Esophagus	oesophagus
32	chr6:150340400-150340600	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:150340400-150340600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:150340400-150340600	Bivalent Enhancer	Placenta	Placenta
35	chr6:150340400-150340600	Enhancers	NHEK	skin
36	chr6:150340400-150340800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:150340400-150340800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:150340600-150341600	Weak transcription	Esophagus	oesophagus
39	chr6:150340600-150345800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:150340600-150345800	Weak transcription	HMEC	breast
41	chr6:150340600-150346000	Weak transcription	NHEK	skin
42	chr6:150340800-150346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:150340800-150346000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:150341600-150342200	Enhancers	Esophagus	oesophagus
45	chr6:150342200-150345200	Weak transcription	Esophagus	oesophagus
46	chr6:150345200-150345800	Enhancers	Esophagus	oesophagus
47	chr6:150345800-150346000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:150345800-150346200	Enhancers	HMEC	breast
49	chr6:150345800-150346400	Enhancers	Hela-S3	cervix
50	chr6:150345800-150346600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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