Variant report

Variant	nsv1021857
Chromosome Location	chr6:183203-290558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2958)
CpG islands
(count:1098)
Chromatin interactive
region (count:73)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2958 , 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	chr6:220004-220874	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:221474-221994	HepG2	liver:	n/a	n/a
3	ATF1	chr6:272562-272614	K562	blood:	n/a	n/a
4	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
5	ATF1	chr6:232965-233203	K562	blood:	n/a	n/a
6	ATF1	chr6:269760-269795	K562	blood:	n/a	n/a
7	ATF2	chr6:216952-217397	GM12878	blood:	n/a	n/a
8	ATF2	chr6:290281-294331	GM12878	blood:	n/a	n/a
9	ATF2	chr6:217063-217455	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr6:193111-194543	GM12878	blood:	n/a	n/a
11	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
12	ATF2	chr6:231354-232300	GM12878	blood:	n/a	n/a
13	ATF2	chr6:224802-226028	GM12878	blood:	n/a	n/a
14	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
15	ATF2	chr6:188600-190870	GM12878	blood:	n/a	n/a
16	ATF2	chr6:230263-230821	GM12878	blood:	n/a	n/a
17	ATF2	chr6:286268-287911	GM12878	blood:	n/a	n/a
18	ATF2	chr6:235849-236489	GM12878	blood:	n/a	n/a
19	ATF2	chr6:226748-228552	GM12878	blood:	n/a	n/a
20	ATF2	chr6:221081-222611	GM12878	blood:	n/a	n/a
21	ATF2	chr6:209691-210220	GM12878	blood:	n/a	n/a
22	ATF2	chr6:216810-217515	GM12878	blood:	n/a	n/a
23	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
24	ATF2	chr6:209433-210258	GM12878	blood:	n/a	n/a
25	ATF2	chr6:270995-271517	GM12878	blood:	n/a	n/a
26	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
27	ATF2	chr6:226477-229964	GM12878	blood:	n/a	n/a
28	ATF2	chr6:228803-229965	GM12878	blood:	n/a	n/a
29	ATF2	chr6:235845-236520	GM12878	blood:	n/a	n/a
30	ATF2	chr6:224893-225951	GM12878	blood:	n/a	n/a
31	ATF2	chr6:188713-190294	GM12878	blood:	n/a	n/a
32	ATF2	chr6:271011-271641	GM12878	blood:	n/a	n/a
33	ATF2	chr6:286192-288235	GM12878	blood:	n/a	n/a
34	ATF2	chr6:220648-222383	GM12878	blood:	n/a	n/a
35	ATF2	chr6:217828-219955	GM12878	blood:	n/a	n/a
36	ATF2	chr6:290519-292253	GM12878	blood:	n/a	n/a
37	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
38	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
39	ATF2	chr6:231396-232311	GM12878	blood:	n/a	n/a
40	ATF2	chr6:217880-219360	GM12878	blood:	n/a	n/a
41	ATF2	chr6:230249-231059	GM12878	blood:	n/a	n/a
42	ATF2	chr6:193250-194551	GM12878	blood:	n/a	n/a
43	ATF3	chr6:219928-220235	K562	blood:	n/a	n/a
44	BACH1	chr6:219912-220319	H1-hESC	embryonic stem cell:	n/a	chr6:220124-220138
45	BACH1	chr6:219988-220177	K562	blood:	n/a	chr6:220124-220138
46	BACH1	chr6:220702-221015	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr6:209349-209668	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr6:231671-232067	GM12878	blood:	n/a	n/a
49	BATF	chr6:218763-219282	GM12878	blood:	n/a	n/a
50	BATF	chr6:193685-194335	GM12878	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:209809-209859	SAEC	small airway:	n/a
2	chr6:209763-209813	PFSK-1	brain:	n/a
3	chr6:225666-225716	HEEpiC	esophagus:	n/a
4	chr6:224733-224783	SK-N-MC	brain:	n/a
5	chr6:186671-186721	NT2-D1	testis:	n/a
6	chr6:230908-230958	AG04449	skin:	fetal
7	chr6:235035-235085	HUVEC	blood vessel:	n/a
8	chr6:209809-209859	T-47D	breast:	n/a
9	chr6:224339-224389	GM12891	blood:	n/a
10	chr6:186671-186721	GM12892	blood:	n/a
11	chr6:236559-236609	HRPEpiC	eye:	n/a
12	chr6:224713-224763	Jurkat	blood:	n/a
13	chr6:225824-225874	Caco-2	colon:	n/a
14	chr6:224733-224783	IMR90	lung:	fetal
15	chr6:230959-231009	GM12891	blood:	n/a
16	chr6:225824-225874	HUVEC	blood vessel:	n/a
17	chr6:202452-202502	GM19239	blood:	n/a
18	chr6:209763-209813	AG10803	skin:	n/a
19	chr6:220928-220978	HRPEpiC	eye:	n/a
20	chr6:209712-209762	K562	blood:	n/a
21	chr6:225666-225716	HIPEpiC	eye:	n/a
22	chr6:230959-231009	A549	lung:	n/a
23	chr6:236559-236609	BE2_C	brain:	n/a
24	chr6:220928-220978	K562	blood:	n/a
25	chr6:230908-230958	MCF-7	breast:	n/a
26	chr6:220928-220978	AG04449	skin:	fetal
27	chr6:230932-230982	HRPEpiC	eye:	n/a
28	chr6:225666-225716	MCF-7	breast:	n/a
29	chr6:230908-230958	HCT-116	colon:	n/a
30	chr6:209712-209762	SKMC	muscle:	n/a
31	chr6:224339-224389	K562	blood:	n/a
32	chr6:202452-202502	HEK293	kidney:	embryo
33	chr6:225824-225874	SKMC	muscle:	n/a
34	chr6:225824-225874	ECC-1	luminal epithelium:	n/a
35	chr6:186671-186721	Hepatocyte	liver:	n/a
36	chr6:230908-230958	A549	lung:	n/a
37	chr6:209712-209762	Hepatocyte	liver:	n/a
38	chr6:202452-202502	SKMC	muscle:	n/a
39	chr6:288505-288555	GM19239	blood:	n/a
40	chr6:224713-224763	GM12891	blood:	n/a
41	chr6:225666-225716	AG09309	skin:	n/a
42	chr6:209712-209762	HAEpiC	amniotic membrane:	n/a
43	chr6:202452-202502	IMR90	lung:	fetal
44	chr6:225824-225874	PrEC	prostate:	n/a
45	chr6:230908-230958	NH-A	brain:	n/a
46	chr6:186671-186721	HL-60	blood:	n/a
47	chr6:288505-288555	Hepatocyte	liver:	n/a
48	chr6:224339-224389	NH-A	brain:	n/a
49	chr6:224733-224783	RPTEC	kidney:	n/a
50	chr6:235035-235085	Caco-2	colon:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
2	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
3	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
4	chr6:201924..204091-chr6:207759..211489,3	K562	blood:
5	chr6:188512..189290-chr6:408309..409342,5	K562	blood:
6	chr6:215135..217089-chr6:292102..293904,2	MCF-7	breast:
7	chr6:181476..184276-chr6:186622..188907,2	MCF-7	breast:
8	chr6:193592..196624-chr6:199092..202281,3	K562	blood:
9	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
10	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
11	chr6:188540..189516-chr6:407870..409552,18	MCF-7	breast:
12	chr6:188538..189926-chr6:408487..409481,6	MCF-7	breast:
13	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
14	chr6:188655..189690-chr6:579041..579935,3	MCF-7	breast:
15	chr6:287235..289508-chr6:291225..294248,4	MCF-7	breast:
16	chr6:174671..177385-chr6:182024..184445,2	K562	blood:
17	chr6:188865..189410-chr6:351061..352002,2	MCF-7	breast:
18	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
19	chr6:217204..217743-chr6:408573..409085,2	K562	blood:
20	chr6:196917..201263-chr6:202620..206119,4	K562	blood:
21	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
22	chr6:277987..280477-chr6:1175656..1177980,2	K562	blood:
23	chr6:188184..189040-chr6:551172..552162,2	MCF-7	breast:
24	chr6:188398..189398-chr6:1436667..1437648,2	MCF-7	breast:
25	chr6:187321..190676-chr6:193869..196032,3	K562	blood:
26	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
27	chr6:216802..217456-chr6:1436640..1437220,2	K562	blood:
28	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
29	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
30	chr6:281531..285813-chr6:290498..294393,5	MCF-7	breast:
31	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
32	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
33	chr6:188851..189352-chr6:372580..373236,2	MCF-7	breast:
34	chr6:217782..221161-chr6:291544..295345,3	MCF-7	breast:
35	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
36	chr6:189816..192061-chr6:402339..404478,2	K562	blood:
37	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
38	chr6:188750..189642-chr6:786566..787558,2	MCF-7	breast:
39	chr6:284765..286882-chr6:287879..289536,2	MCF-7	breast:
40	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
41	chr6:257151..259180-chr6:290748..292745,2	MCF-7	breast:
42	chr6:190862..192633-chr6:194886..196390,2	MCF-7	breast:
43	chr6:188501..189288-chr6:558016..558846,2	MCF-7	breast:
44	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
45	chr6:228323..230023-chr6:368553..371061,2	K562	blood:
46	chr6:181397..184733-chr6:185247..188798,3	K562	blood:
47	chr6:181320..184707-chr6:184919..187235,3	K562	blood:
48	chr6:218667..220722-chr6:290754..293697,2	MCF-7	breast:
49	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
50	chr6:230872..233357-chr6:348225..349996,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL035696.1-3	chr6:224950-225088	XLOC_005118
2	lnc-EXOC2-6	chr6:187736-187906	ENSG00000263667.1
3	lnc-EXOC2-3	chr6:285321-285384	XLOC_005567
4	lnc-AL035696.1-2	chr6:184601-187741	XLOC_005117
5	lnc-EXOC2-3	chr6:277864-278155	XLOC_005567
6	lnc-EXOC2-6	chr6:198165-198509	ENSG00000263667.1
7	lnc-AL035696.1-2	chr6:183914-184371	XLOC_005117
8	lnc-EXOC2-6	chr6:186356-186561	ENSG00000263667.1
9	lnc-EXOC2-18	chr6:196682-196974	NONHSAT105977
10	lnc-EXOC2-6	chr6:184593-184809	ENSG00000263667.1
11	lnc-EXOC2-6	chr6:204887-205484	ENSG00000263667.1
12	lnc-AL035696.1-1	chr6:203313-204413	ENSG00000205653.1
13	lnc-AL035696.1-3	chr6:226079-226400	XLOC_005118
14	lnc-EXOC2-6	chr6:189476-189649	ENSG00000263667.1
15	lnc-AL035696.1-2	chr6:184161-184371	NONHSAT105976
16	lnc-AL035696.1-1	chr6:205487-206392	ENSG00000205653.1
17	lnc-AL035696.1-3	chr6:225686-226068	XLOC_005118
18	lnc-AL035696.1-2	chr6:186035-186494	NONHSAT105976
19	lnc-EXOC2-17	chr6:230321-230359	l_3086_chr6:222863-230359_lymphNode
20	lnc-EXOC2-3	chr6:285915-286279	XLOC_005567
21	lnc-EXOC2-17	chr6:222864-223155	l_3086_chr6:222863-230359_lymphNode

No data

Variant related genes	Relation type
ENSG00000263667	TF binding region
DUSP22	TF binding region
ENSG00000205653	TF binding region
ENSG00000263667	CpG island
DUSP22	CpG island
ENSG00000205653	CpG island
ENSG00000205653	chromatin interactions
ENSG00000112679	chromatin interactions
ENSG00000263667	chromatin interactions
TRRAP	miRNA target sites
TSC1	miRNA target sites

Extended variants
information (count: 4467 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4467 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372662534	chr6:183214-183215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547961137	chr6:183263-183264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570756918	chr6:183266-183267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs59890838	chr6:183285-183286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374855866	chr6:183302-183303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376669651	chr6:183349-183350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371236607	chr6:183421-183422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374431955	chr6:183638-183639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9378607	chr6:183776-183777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs17133620	chr6:183869-183870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114102991	chr6:183900-183901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76069513	chr6:183917-183918	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs114552411	chr6:183946-183947	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs1468342	chr6:184034-184035	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs202236184	chr6:184087-184088	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs116719947	chr6:184125-184126	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs377426897	chr6:184148-184149	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs371183651	chr6:184525-184526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539531150	chr6:184549-184550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6911810	chr6:184574-184575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116491333	chr6:184683-184684	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs115828162	chr6:184686-184687	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs115982461	chr6:184701-184702	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs116041850	chr6:184719-184720	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs73719549	chr6:184740-184741	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs193192047	chr6:184775-184776	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs201098941	chr6:184848-184849	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs116804351	chr6:184879-184880	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs116203822	chr6:184903-184904	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs386695891	chr6:184953-184954	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs114781730	chr6:184955-184956	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs372152746	chr6:184966-184967	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs145831965	chr6:185046-185047	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs371937589	chr6:185048-185049	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs373614344	chr6:185117-185118	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs367636043	chr6:185308-185309	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs371366927	chr6:185422-185423	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs116425320	chr6:185557-185558	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs556205458	chr6:185575-185576	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs115135565	chr6:185616-185617	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs576152030	chr6:185626-185627	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs73719550	chr6:185654-185655	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs535412553	chr6:185717-185718	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs73719551	chr6:185729-185730	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs115834324	chr6:185770-185771	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs369977294	chr6:185774-185775	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs544879196	chr6:185829-185830	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs371856103	chr6:185882-185883	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs116638017	chr6:185911-185912	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs376580551	chr6:185947-185948	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	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	15273396	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:178400-192200	Weak transcription	Right Atrium	heart
2	chr6:179600-191800	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:180200-186600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:180200-190800	Enhancers	Primary B cells from cord blood	blood
5	chr6:180800-186800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:181000-194800	Weak transcription	Spleen	Spleen
7	chr6:181200-183600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:181200-194400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:181400-188800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr6:181800-183600	Weak transcription	Thymus	Thymus
11	chr6:181800-184200	Weak transcription	Primary T cells from cord blood	blood
12	chr6:181800-188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr6:182000-184800	Enhancers	GM12878-XiMat	blood
14	chr6:183200-187800	Enhancers	Fetal Thymus	thymus
15	chr6:183600-184800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr6:183600-188000	Enhancers	Thymus	Thymus
17	chr6:184200-184600	Enhancers	Primary T cells from cord blood	blood
18	chr6:184200-184800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr6:184200-184800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:184600-188800	Weak transcription	Primary T cells from cord blood	blood
21	chr6:184800-186400	Weak transcription	GM12878-XiMat	blood
22	chr6:184800-188800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr6:184800-190600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr6:184800-193200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:185600-186000	Bivalent Enhancer	HepG2	liver
26	chr6:185800-188000	Enhancers	Fetal Intestine Large	intestine
27	chr6:186000-187400	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr6:186000-188000	Flanking Bivalent TSS/Enh	HepG2	liver
29	chr6:186000-188200	Enhancers	Fetal Lung	lung
30	chr6:186200-187000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:186200-187000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:186200-187000	Enhancers	Lung	lung
33	chr6:186200-187200	Enhancers	Fetal Heart	heart
34	chr6:186200-187200	Enhancers	Rectal Smooth Muscle	rectum
35	chr6:186200-187600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:186200-188000	Enhancers	Fetal Stomach	stomach
37	chr6:186400-186600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:186400-186600	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr6:186400-187400	Enhancers	Colon Smooth Muscle	Colon
40	chr6:186400-187600	Enhancers	GM12878-XiMat	blood
41	chr6:186400-188000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:186600-186800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:186600-186800	Enhancers	Liver	Liver
44	chr6:186600-188200	Enhancers	K562	blood
45	chr6:186800-187600	Enhancers	Primary hematopoietic stem cells	blood
46	chr6:186800-188000	Enhancers	Fetal Intestine Small	intestine
47	chr6:186800-188400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:187000-187200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr6:187000-188800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:187000-191600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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