Variant report

Variant	nsv462592
Chromosome Location	chr6:165391-274847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2965)
CpG islands
(count:1161)
Chromatin interactive
region (count:66)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2965 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:221474-221994	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:220004-220874	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:168940-169157	HepG2	liver:	n/a	n/a
4	ATF1	chr6:232965-233203	K562	blood:	n/a	n/a
5	ATF1	chr6:272562-272614	K562	blood:	n/a	n/a
6	ATF1	chr6:269760-269795	K562	blood:	n/a	n/a
7	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
8	ATF2	chr6:188600-190870	GM12878	blood:	n/a	n/a
9	ATF2	chr6:216810-217515	GM12878	blood:	n/a	n/a
10	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
11	ATF2	chr6:230249-231059	GM12878	blood:	n/a	n/a
12	ATF2	chr6:216952-217397	GM12878	blood:	n/a	n/a
13	ATF2	chr6:271011-271641	GM12878	blood:	n/a	n/a
14	ATF2	chr6:224893-225951	GM12878	blood:	n/a	n/a
15	ATF2	chr6:220648-222383	GM12878	blood:	n/a	n/a
16	ATF2	chr6:188713-190294	GM12878	blood:	n/a	n/a
17	ATF2	chr6:181047-181898	GM12878	blood:	n/a	n/a
18	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
19	ATF2	chr6:193250-194551	GM12878	blood:	n/a	n/a
20	ATF2	chr6:231354-232300	GM12878	blood:	n/a	n/a
21	ATF2	chr6:235845-236520	GM12878	blood:	n/a	n/a
22	ATF2	chr6:226477-229964	GM12878	blood:	n/a	n/a
23	ATF2	chr6:217063-217455	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:221081-222611	GM12878	blood:	n/a	n/a
25	ATF2	chr6:181000-181701	GM12878	blood:	n/a	n/a
26	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
27	ATF2	chr6:193111-194543	GM12878	blood:	n/a	n/a
28	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
29	ATF2	chr6:209433-210258	GM12878	blood:	n/a	n/a
30	ATF2	chr6:209691-210220	GM12878	blood:	n/a	n/a
31	ATF2	chr6:230263-230821	GM12878	blood:	n/a	n/a
32	ATF2	chr6:235849-236489	GM12878	blood:	n/a	n/a
33	ATF2	chr6:231396-232311	GM12878	blood:	n/a	n/a
34	ATF2	chr6:217828-219955	GM12878	blood:	n/a	n/a
35	ATF2	chr6:270995-271517	GM12878	blood:	n/a	n/a
36	ATF2	chr6:226748-228552	GM12878	blood:	n/a	n/a
37	ATF2	chr6:228803-229965	GM12878	blood:	n/a	n/a
38	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
39	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
40	ATF2	chr6:224802-226028	GM12878	blood:	n/a	n/a
41	ATF2	chr6:217880-219360	GM12878	blood:	n/a	n/a
42	ATF3	chr6:219928-220235	K562	blood:	n/a	n/a
43	BACH1	chr6:209349-209668	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr6:220702-221015	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr6:219912-220319	H1-hESC	embryonic stem cell:	n/a	chr6:220124-220138
46	BACH1	chr6:219988-220177	K562	blood:	n/a	chr6:220124-220138
47	BATF	chr6:270957-271443	GM12878	blood:	n/a	n/a
48	BATF	chr6:253185-253459	GM12878	blood:	n/a	chr6:253319-253330
49	BATF	chr6:218090-218656	GM12878	blood:	n/a	n/a
50	BATF	chr6:188701-189864	GM12878	blood:	n/a	chr6:189809-189818

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:225824-225874	IMR90	lung:	fetal
2	chr6:230908-230958	BJ	skin:	n/a
3	chr6:225824-225874	IMR90	lung:	fetal
4	chr6:230908-230958	BJ	skin:	n/a
5	chr6:225666-225716	HEK293	kidney:	embryo
6	chr6:226092-226142	H1-hESC	embryonic stem cell:	embryo
7	chr6:220928-220978	SK-N-SH	brain:	n/a
8	chr6:236559-236609	AG09319	gingival:	n/a
9	chr6:224713-224763	AG04449	skin:	fetal
10	chr6:225824-225874	HUVEC	blood vessel:	n/a
11	chr6:179659-179709	U87	brain:	n/a
12	chr6:226092-226142	MCF-7	breast:	n/a
13	chr6:235035-235085	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:235035-235085	LNCaP	prostate:	n/a
15	chr6:230908-230958	AG09309	skin:	n/a
16	chr6:209763-209813	GM12878	blood:	n/a
17	chr6:236559-236609	PrEC	prostate:	n/a
18	chr6:202452-202502	BJ	skin:	n/a
19	chr6:220928-220978	ECC-1	luminal epithelium:	n/a
20	chr6:224339-224389	HMEC	breast:	n/a
21	chr6:179456-179506	GM19239	blood:	n/a
22	chr6:225666-225716	K562	blood:	n/a
23	chr6:220928-220978	U87	brain:	n/a
24	chr6:179659-179709	HRPEpiC	eye:	n/a
25	chr6:179659-179709	NT2-D1	testis:	n/a
26	chr6:236559-236609	AG04449	skin:	fetal
27	chr6:224339-224389	NHDF-neo	bronchial:	n/a
28	chr6:236559-236609	GM06990	blood:	n/a
29	chr6:209809-209859	PFSK-1	brain:	n/a
30	chr6:224733-224783	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:226092-226142	AG10803	skin:	n/a
32	chr6:224339-224389	AG04449	skin:	fetal
33	chr6:202452-202502	Jurkat	blood:	n/a
34	chr6:225666-225716	AG09309	skin:	n/a
35	chr6:225824-225874	AoSMC	blood vessel:	n/a
36	chr6:226092-226142	HUVEC	blood vessel:	n/a
37	chr6:230932-230982	RPTEC	kidney:	n/a
38	chr6:224733-224783	AoSMC	blood vessel:	n/a
39	chr6:230908-230958	SK-N-MC	brain:	n/a
40	chr6:179456-179506	AG09319	gingival:	n/a
41	chr6:179659-179709	AG04450	lung:	fetal
42	chr6:225824-225874	HRE	kidney:	n/a
43	chr6:186671-186721	Jurkat	blood:	n/a
44	chr6:225666-225716	Caco-2	colon:	n/a
45	chr6:209763-209813	HCF	heart:	n/a
46	chr6:209763-209813	ProgFib	skin:	n/a
47	chr6:235035-235085	HL-60	blood:	n/a
48	chr6:224713-224763	NH-A	brain:	n/a
49	chr6:230959-231009	HEEpiC	esophagus:	n/a
50	chr6:186671-186721	SK-N-SH_RA	brain:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:264177..266345-chr6:291888..293660,2	MCF-7	breast:
2	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
3	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
4	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
5	chr6:257151..259180-chr6:290748..292745,2	MCF-7	breast:
6	chr6:188501..189288-chr6:558016..558846,2	MCF-7	breast:
7	chr6:216802..217456-chr6:1436640..1437220,2	K562	blood:
8	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
9	chr6:215135..217089-chr6:292102..293904,2	MCF-7	breast:
10	chr6:196917..201263-chr6:202620..206119,4	K562	blood:
11	chr6:188865..189410-chr6:351061..352002,2	MCF-7	breast:
12	chr6:182386..184733-chr6:187298..189526,2	K562	blood:
13	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
14	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
15	chr6:178419..181938-chr6:182767..184759,3	K562	blood:
16	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
17	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
18	chr6:188398..189398-chr6:1436667..1437648,2	MCF-7	breast:
19	chr6:188615..189306-chr6:374006..374509,2	MCF-7	breast:
20	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
21	chr6:204380..207081-chr6:218001..219962,2	K562	blood:
22	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
23	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
24	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
25	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
26	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
27	chr6:162155..164910-chr6:167837..169506,2	K562	blood:
28	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
29	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
30	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
31	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
32	chr6:230872..233357-chr6:348225..349996,2	K562	blood:
33	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
34	chr6:201924..204091-chr6:207759..211489,3	K562	blood:
35	chr6:188184..189040-chr6:551172..552162,2	MCF-7	breast:
36	chr6:218667..220722-chr6:290754..293697,2	MCF-7	breast:
37	chr6:217204..217743-chr6:408573..409085,2	K562	blood:
38	chr6:188509..189446-chr6:686215..686918,2	MCF-7	breast:
39	chr6:226916..227829-chr6:408545..409059,2	K562	blood:
40	chr6:217782..221161-chr6:291544..295345,3	MCF-7	breast:
41	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
42	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
43	chr6:188817..189398-chr6:524504..525502,3	MCF-7	breast:
44	chr6:228323..230023-chr6:368553..371061,2	K562	blood:
45	chr6:188750..189642-chr6:786566..787558,2	MCF-7	breast:
46	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
47	chr6:184999..187022-chr6:291843..294537,2	MCF-7	breast:
48	chr6:190038..192340-chr6:196174..199027,2	K562	blood:
49	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
50	chr6:256291..258797-chr6:266153..268904,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-6	chr6:189476-189649	ENSG00000263667.1
2	lnc-EXOC2-17	chr6:222864-223155	l_3086_chr6:222863-230359_lymphNode
3	lnc-AL035696.1-6	chr6:171079-171400	NONHSAT105973
4	lnc-EXOC2-20	chr6:171827-172220	NONHSAT105972
5	lnc-AL035696.1-1	chr6:205487-206392	ENSG00000205653.1
6	lnc-AL035696.1-2	chr6:184161-184371	NONHSAT105976
7	lnc-AL035696.1-2	chr6:184601-187741	XLOC_005117
8	lnc-EXOC2-20	chr6:167607-167826	NONHSAT105971
9	lnc-AL035696.1-6	chr6:170686-171068	NONHSAT105973
10	lnc-EXOC2-20	chr6:169545-169753	NONHSAT105971
11	lnc-AL035696.1-1	chr6:203313-204413	ENSG00000205653.1
12	lnc-EXOC2-17	chr6:230321-230359	l_3086_chr6:222863-230359_lymphNode
13	lnc-EXOC2-6	chr6:186356-186561	ENSG00000263667.1
14	lnc-EXOC2-6	chr6:198165-198509	ENSG00000263667.1
15	lnc-AL035696.1-3	chr6:225686-226068	XLOC_005118
16	lnc-EXOC2-6	chr6:182366-182474	ENSG00000263667.1
17	lnc-AL035696.1-2	chr6:183914-184371	XLOC_005117
18	lnc-EXOC2-6	chr6:181466-181695	ENSG00000263667.1
19	lnc-EXOC2-20	chr6:168171-170561	NONHSAT105972
20	lnc-EXOC2-6	chr6:187736-187906	ENSG00000263667.1
21	lnc-AL035696.1-3	chr6:224950-225088	XLOC_005118
22	lnc-EXOC2-20	chr6:170352-170631	NONHSAT105971
23	lnc-AL035696.1-3	chr6:226079-226400	XLOC_005118
24	lnc-EXOC2-18	chr6:196682-196974	NONHSAT105977
25	lnc-EXOC2-6	chr6:184593-184809	ENSG00000263667.1
26	lnc-AL035696.1-2	chr6:186035-186494	NONHSAT105976
27	lnc-EXOC2-6	chr6:204887-205484	ENSG00000263667.1
28	lnc-AL035696.1-6	chr6:169950-170088	NONHSAT105973

No data

Variant related genes	Relation type
ENSG00000218577	TF binding region
ENSG00000263667	TF binding region
ENSG00000205653	TF binding region
ENSG00000218577	CpG island
ENSG00000263667	CpG island
ENSG00000205653	CpG island
ENSG00000205653	chromatin interactions
ENSG00000112679	chromatin interactions
ENSG00000263667	chromatin interactions
TSC1	miRNA target sites
TRRAP	miRNA target sites

Extended variants
information (count: 4050 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4050 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs719065	chr6:165632-165633	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535378867	chr6:165818-165819	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370612622	chr6:165899-165900	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551791705	chr6:165959-165960	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57803541	chr6:166095-166096	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75121857	chr6:166136-166137	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116753945	chr6:166189-166190	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111686581	chr6:166454-166455	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371259285	chr6:166483-166484	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11242666	chr6:166638-166639	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145595179	chr6:166646-166647	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs202156730	chr6:166732-166733	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578021823	chr6:166746-166747	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199991782	chr6:166750-166751	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373910961	chr6:166754-166755	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375930006	chr6:166904-166905	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368535590	chr6:167114-167115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371618889	chr6:167127-167128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374989245	chr6:167131-167132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368526980	chr6:167160-167161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9502835	chr6:167708-167709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs73719526	chr6:167749-167750	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532256716	chr6:167785-167786	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs9502836	chr6:168197-168198	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs369784219	chr6:168248-168249	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs113600288	chr6:168264-168265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs552195094	chr6:168315-168316	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs377187222	chr6:168410-168411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs142831339	chr6:168424-168425	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs201305470	chr6:168428-168429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs559071025	chr6:168466-168467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs60447526	chr6:168478-168479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs112541457	chr6:168571-168572	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs114344987	chr6:168801-168802	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs370707845	chr6:168843-168844	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs111246084	chr6:168991-168992	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs568921875	chr6:169054-169055	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs115357777	chr6:169141-169142	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs202175158	chr6:169152-169153	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs115431157	chr6:169257-169258	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs370462685	chr6:169494-169495	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs113086792	chr6:169533-169534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs200221467	chr6:169632-169633	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs538515352	chr6:169759-169760	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs563426150	chr6:169773-169774	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs139197019	chr6:169795-169796	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs529390246	chr6:169812-169813	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370950257	chr6:169822-169823	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs111916764	chr6:169958-169959	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs375242098	chr6:170038-170039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165600-167000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:165800-167000	Enhancers	Osteobl	bone
3	chr6:165800-167200	Enhancers	Fetal Muscle Trunk	muscle
4	chr6:166800-167000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:168600-169000	Enhancers	GM12878-XiMat	blood
6	chr6:174800-178200	Weak transcription	Right Atrium	heart
7	chr6:177200-179600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr6:178200-178400	ZNF genes & repeats	Right Atrium	heart
9	chr6:178200-178400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr6:178200-178600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
11	chr6:178200-179000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:178200-180200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:178400-192200	Weak transcription	Right Atrium	heart
14	chr6:179600-191800	Enhancers	Primary B cells from peripheral blood	blood
15	chr6:179800-180400	Enhancers	GM12878-XiMat	blood
16	chr6:180200-186600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:180200-190800	Enhancers	Primary B cells from cord blood	blood
18	chr6:180400-180600	Active TSS	Primary T cells from cord blood	blood
19	chr6:180400-180800	Enhancers	Fetal Thymus	thymus
20	chr6:180400-181200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr6:180400-181200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:180400-181400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr6:180400-181800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr6:180400-181800	Active TSS	Thymus	Thymus
25	chr6:180400-182000	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:180600-180800	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:180600-181000	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr6:180600-181000	Enhancers	Spleen	Spleen
29	chr6:180600-181200	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr6:180600-181400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr6:180600-181400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr6:180800-181000	Flanking Active TSS	Fetal Thymus	thymus
33	chr6:180800-181200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:180800-186800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr6:181000-181400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr6:181000-181400	Enhancers	Fetal Thymus	thymus
37	chr6:181000-181800	Enhancers	Primary T cells from cord blood	blood
38	chr6:181000-194800	Weak transcription	Spleen	Spleen
39	chr6:181200-183600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:181200-194400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:181400-183200	Weak transcription	Fetal Thymus	thymus
42	chr6:181400-188800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:181800-183600	Weak transcription	Thymus	Thymus
44	chr6:181800-184200	Weak transcription	Primary T cells from cord blood	blood
45	chr6:181800-188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr6:182000-184800	Enhancers	GM12878-XiMat	blood
47	chr6:183200-187800	Enhancers	Fetal Thymus	thymus
48	chr6:183600-184800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:183600-188000	Enhancers	Thymus	Thymus
50	chr6:184200-184600	Enhancers	Primary T cells from cord blood	blood

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