Variant report

Variant	nsv823383
Chromosome Location	chr6:256659-382560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4134)
CpG islands
(count:3304)
Chromatin interactive
region (count:157)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4134 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:365843-365846	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:341288-341665	K562	blood:	n/a	n/a
3	ARID3A	chr6:324003-324078	K562	blood:	n/a	n/a
4	ARID3A	chr6:366574-366822	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:311696-312014	K562	blood:	n/a	n/a
6	ATF1	chr6:269760-269795	K562	blood:	n/a	n/a
7	ATF1	chr6:272562-272614	K562	blood:	n/a	n/a
8	ATF1	chr6:330062-330408	K562	blood:	n/a	n/a
9	ATF1	chr6:338835-339340	K562	blood:	n/a	n/a
10	ATF1	chr6:341171-341781	K562	blood:	n/a	n/a
11	ATF1	chr6:319279-319713	K562	blood:	n/a	n/a
12	ATF1	chr6:376562-376683	K562	blood:	n/a	n/a
13	ATF1	chr6:345837-346147	K562	blood:	n/a	n/a
14	ATF2	chr6:308768-309915	GM12878	blood:	n/a	n/a
15	ATF2	chr6:322925-323654	GM12878	blood:	n/a	n/a
16	ATF2	chr6:346309-348024	GM12878	blood:	n/a	n/a
17	ATF2	chr6:346731-347787	GM12878	blood:	n/a	n/a
18	ATF2	chr6:377970-378863	GM12878	blood:	n/a	n/a
19	ATF2	chr6:377462-379109	GM12878	blood:	n/a	n/a
20	ATF2	chr6:315344-321339	GM12878	blood:	n/a	n/a
21	ATF2	chr6:329750-331026	GM12878	blood:	n/a	chr6:330753-330764
22	ATF2	chr6:286268-287911	GM12878	blood:	n/a	n/a
23	ATF2	chr6:316068-318538	GM12878	blood:	n/a	n/a
24	ATF2	chr6:338764-339934	GM12878	blood:	n/a	n/a
25	ATF2	chr6:331102-332692	GM12878	blood:	n/a	n/a
26	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
27	ATF2	chr6:270995-271517	GM12878	blood:	n/a	n/a
28	ATF2	chr6:329574-332652	GM12878	blood:	n/a	chr6:330753-330764
29	ATF2	chr6:295599-298070	GM12878	blood:	n/a	n/a
30	ATF2	chr6:327633-329237	GM12878	blood:	n/a	n/a
31	ATF2	chr6:298148-299448	GM12878	blood:	n/a	n/a
32	ATF2	chr6:336665-337253	GM12878	blood:	n/a	n/a
33	ATF2	chr6:364377-365459	GM12878	blood:	n/a	n/a
34	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
35	ATF2	chr6:341792-342526	GM12878	blood:	n/a	n/a
36	ATF2	chr6:271011-271641	GM12878	blood:	n/a	n/a
37	ATF2	chr6:340419-342600	GM12878	blood:	n/a	n/a
38	ATF2	chr6:327184-329464	GM12878	blood:	n/a	n/a
39	ATF2	chr6:336374-338288	GM12878	blood:	n/a	n/a
40	ATF2	chr6:356596-357405	GM12878	blood:	n/a	n/a
41	ATF2	chr6:379225-379819	GM12878	blood:	n/a	n/a
42	ATF2	chr6:318549-321125	GM12878	blood:	n/a	n/a
43	ATF2	chr6:364566-365418	GM12878	blood:	n/a	n/a
44	ATF2	chr6:290519-292253	GM12878	blood:	n/a	n/a
45	ATF2	chr6:295807-297437	GM12878	blood:	n/a	n/a
46	ATF2	chr6:322358-324028	GM12878	blood:	n/a	n/a
47	ATF2	chr6:304636-306753	GM12878	blood:	n/a	n/a
48	ATF2	chr6:290281-294331	GM12878	blood:	n/a	n/a
49	ATF2	chr6:286192-288235	GM12878	blood:	n/a	n/a
50	ATF2	chr6:292427-294467	GM12878	blood:	n/a	n/a

(count:3304 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:291687-291737	HIPEpiC	eye:	n/a
2	chr6:362023-362073	T-47D	breast:	n/a
3	chr6:291909-291959	MCF-7	breast:	n/a
4	chr6:363972-364022	HCT-116	colon:	n/a
5	chr6:345972-346022	HUVEC	blood vessel:	n/a
6	chr6:348190-348240	AG10803	skin:	n/a
7	chr6:345932-345982	HAEpiC	amniotic membrane:	n/a
8	chr6:351116-351166	HRCEpiC	kidney:	n/a
9	chr6:364010-364060	HMEC	breast:	n/a
10	chr6:312026-312076	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:291687-291737	HIPEpiC	eye:	n/a
12	chr6:362023-362073	T-47D	breast:	n/a
13	chr6:291909-291959	MCF-7	breast:	n/a
14	chr6:363972-364022	HCT-116	colon:	n/a
15	chr6:345972-346022	HUVEC	blood vessel:	n/a
16	chr6:348190-348240	AG10803	skin:	n/a
17	chr6:345932-345982	HAEpiC	amniotic membrane:	n/a
18	chr6:351116-351166	HRCEpiC	kidney:	n/a
19	chr6:364010-364060	HMEC	breast:	n/a
20	chr6:312026-312076	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:341315-341365	BJ	skin:	n/a
22	chr6:351402-351452	SK-N-MC	brain:	n/a
23	chr6:373609-373659	SK-N-SH_RA	brain:	n/a
24	chr6:312058-312108	HAEpiC	amniotic membrane:	n/a
25	chr6:312105-312155	HL-60	blood:	n/a
26	chr6:362023-362073	AG09319	gingival:	n/a
27	chr6:290800-290850	HNPCEpiC	eye:	n/a
28	chr6:291687-291737	Hela-S3	cervix:	n/a
29	chr6:351361-351411	HCT-116	colon:	n/a
30	chr6:351361-351411	NB4	blood:	n/a
31	chr6:291903-291953	BE2_C	brain:	n/a
32	chr6:351609-351659	AG09309	skin:	n/a
33	chr6:312026-312076	NHDF-neo	bronchial:	n/a
34	chr6:291687-291737	HEK293	kidney:	embryo
35	chr6:345932-345982	SK-N-SH	brain:	n/a
36	chr6:317607-317657	HEEpiC	esophagus:	n/a
37	chr6:313464-313514	AG10803	skin:	n/a
38	chr6:291909-291959	SKMC	muscle:	n/a
39	chr6:348879-348929	HIPEpiC	eye:	n/a
40	chr6:291903-291953	HCT-116	colon:	n/a
41	chr6:345972-346022	MCF-7	breast:	n/a
42	chr6:293331-293381	Hela-S3	cervix:	n/a
43	chr6:373609-373659	AG04450	lung:	fetal
44	chr6:379514-379564	AG04449	skin:	fetal
45	chr6:364068-364118	K562	blood:	n/a
46	chr6:379489-379539	HRE	kidney:	n/a
47	chr6:348323-348373	SK-N-SH_RA	brain:	n/a
48	chr6:379489-379539	HIPEpiC	eye:	n/a
49	chr6:299762-299812	CMK	blood:	n/a
50	chr6:364068-364118	T-47D	breast:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:377372..380715-chr6:382037..384127,3	K562	blood:
2	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
3	chr6:272456..276094-chr6:277811..280765,3	K562	blood:
4	chr6:291243..293704-chr6:372402..375219,3	MCF-7	breast:
5	chr6:264177..266345-chr6:291888..293660,2	MCF-7	breast:
6	chr6:188615..189306-chr6:374006..374509,2	MCF-7	breast:
7	chr6:342821..344406-chr6:344671..346549,2	K562	blood:
8	chr6:285371..287917-chr6:411939..414727,2	MCF-7	breast:
9	chr6:281531..285813-chr6:290498..294393,5	MCF-7	breast:
10	chr6:345093..346655-chr6:349207..351597,2	K562	blood:
11	chr17:48943450..48944099-chr6:292243..292871,2	Hela-S3	cervix:
12	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
13	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
14	chr6:359508..363068-chr6:364315..366301,3	K562	blood:
15	chr6:296173..299152-chr6:320389..322030,2	K562	blood:
16	chr6:316885..319734-chr6:320903..323132,2	MCF-7	breast:
17	chr6:314578..316131-chr6:334736..337593,2	K562	blood:
18	chr11:62608627..62609393-chr6:291557..292282,3	HCT-116	colon:
19	chr6:295536..297795-chr6:305679..308154,2	K562	blood:
20	chr6:346792..349557-chr6:349608..351653,2	MCF-7	breast:
21	chr6:311325..314224-chr6:337384..339856,2	K562	blood:
22	chr6:291058..293680-chr6:321361..322968,2	MCF-7	breast:
23	chr12:6579777..6580703-chr6:291768..292740,2	Hela-S3	cervix:
24	chr6:293351..295006-chr6:303551..305599,2	MCF-7	breast:
25	chr6:290084..292565-chr6:342820..344839,2	MCF-7	breast:
26	chr6:303726..306245-chr6:306797..309200,2	K562	blood:
27	chr6:343029..344627-chr6:349915..351647,2	K562	blood:
28	chr19:30206179..30206679-chr6:291771..292378,2	HCT-116	colon:
29	chr6:296050..300472-chr6:301997..308154,8	K562	blood:
30	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
31	chr6:294663..298192-chr6:299302..301728,3	MCF-7	breast:
32	chr6:308595..310441-chr6:314037..315992,2	MCF-7	breast:
33	chr6:358684..360602-chr6:360702..362237,2	MCF-7	breast:
34	chr6:289307..292572-chr6:326823..329530,3	MCF-7	breast:
35	chr6:278056..279662-chr6:281316..283230,2	MCF-7	breast:
36	chr17:17719893..17722583-chr6:302740..304240,2	MCF-7	breast:
37	chr6:188851..189352-chr6:372580..373236,2	MCF-7	breast:
38	chr6:305778..307935-chr6:308138..311376,3	MCF-7	breast:
39	chr6:273516..275258-chr6:282028..283733,2	K562	blood:
40	chr16:30076765..30077507-chr6:291393..292212,2	Hela-S3	cervix:
41	chr6:290316..292856-chr6:349675..352106,2	MCF-7	breast:
42	chr16:31469537..31472221-chr6:320174..322214,2	MCF-7	breast:
43	chr6:291718..293642-chr6:314157..316984,3	K562	blood:
44	chr6:290910..293038-chr6:302160..304078,2	MCF-7	breast:
45	chr6:349537..354799-chr6:355768..361012,7	K562	blood:
46	chr6:352112..354409-chr6:363522..365435,2	K562	blood:
47	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
48	chr6:308595..310441-chr6:314037..315992,2	MCF-7	breast:
49	chr6:357098..359682-chr6:360381..362404,2	MCF-7	breast:
50	chr6:320813..322603-chr6:333485..335422,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-3	chr6:285915-286279	XLOC_005567
2	lnc-EXOC2-3	chr6:277864-278155	XLOC_005567
3	lnc-EXOC2-15	chr6:350248-352633	NONHSAT106021
4	lnc-EXOC2-3	chr6:285321-285384	XLOC_005567
5	lnc-EXOC2-15	chr6:353930-354323	NONHSAT106021

No data

Variant related genes	Relation type
DUSP22	TF binding region
DUSP22	CpG island
ENSG00000112679	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000198853	chromatin interactions
ENSG00000137265	chromatin interactions
ENSG00000260625	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000228629	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000131943	chromatin interactions
ENSG00000174365	chromatin interactions
ENSG00000140688	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000072310	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000101544	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000139190	chromatin interactions

Extended variants
information (count: 6509 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6509 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544857271	chr6:256696-256697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180936247	chr6:256714-256715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575796362	chr6:256724-256725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138395052	chr6:256728-256729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550573139	chr6:256729-256730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186012449	chr6:256740-256741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142975483	chr6:256744-256745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370952778	chr6:256758-256759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192092583	chr6:256762-256763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13340430	chr6:256765-256766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539242542	chr6:256768-256769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184044620	chr6:256829-256830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200433238	chr6:256850-256851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188598091	chr6:256898-256899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190685654	chr6:256914-256915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530396104	chr6:256919-256920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547285807	chr6:256927-256928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201152382	chr6:256931-256932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13340431	chr6:256944-256945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1033776	chr6:256959-256960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146141829	chr6:256967-256968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573721494	chr6:257024-257025	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs140183365	chr6:257026-257027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs542630617	chr6:257071-257072	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552646258	chr6:257112-257113	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs553261469	chr6:257134-257135	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201181189	chr6:257162-257163	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182915424	chr6:257166-257167	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs1011327	chr6:257186-257187	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs4959163	chr6:257201-257202	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545207171	chr6:257205-257206	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564892188	chr6:257211-257212	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs1011328	chr6:257216-257217	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4959628	chr6:257246-257247	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544338263	chr6:257326-257327	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561029199	chr6:257331-257332	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142482378	chr6:257348-257349	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546646804	chr6:257362-257363	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs112875964	chr6:257365-257366	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560855280	chr6:257375-257376	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532654904	chr6:257395-257396	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537289615	chr6:257409-257410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187253700	chr6:257435-257436	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569518014	chr6:257442-257443	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369292662	chr6:257448-257449	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538434272	chr6:257459-257460	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs117514427	chr6:257460-257461	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1011329	chr6:257461-257462	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567348825	chr6:257474-257475	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150822614	chr6:257484-257485	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Parkinson disease	20858604	CNVD
Neuroblastic tumor	20877625	CNVD
Pancreatic cancer	20877625	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3567 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:250600-258400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:251200-257200	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr6:251200-259400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr6:252600-257400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:252800-257400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:253400-256800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:253400-257000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:253400-257000	Weak transcription	NHEK	skin
9	chr6:253400-257200	Enhancers	GM12878-XiMat	blood
10	chr6:253600-257000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr6:253600-257200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:254600-257000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:254600-257200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:254600-257200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:254800-260000	Enhancers	Primary B cells from cord blood	blood
16	chr6:255600-256800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr6:256000-257200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:256200-256800	Enhancers	Placenta	Placenta
19	chr6:256200-257200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr6:256200-257800	Enhancers	Adipose Nuclei	Adipose
21	chr6:256200-259600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr6:256400-256800	Weak transcription	Primary B cells from peripheral blood	blood
23	chr6:256400-256800	Weak transcription	Primary T cells from cord blood	blood
24	chr6:256400-256800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:256400-257400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr6:256400-259600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr6:256600-257000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr6:256600-257400	Weak transcription	Fetal Thymus	thymus
29	chr6:256600-257800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:256600-258800	Enhancers	Primary hematopoietic stem cells	blood
31	chr6:256800-257200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr6:256800-258200	Enhancers	Primary T cells from cord blood	blood
33	chr6:256800-258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:256800-259800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:256800-261000	Enhancers	Primary B cells from peripheral blood	blood
36	chr6:257000-257600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:257000-257600	Enhancers	Osteobl	bone
38	chr6:257000-257800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:257000-257800	Enhancers	NHEK	skin
40	chr6:257000-258000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr6:257000-258000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr6:257000-258000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr6:257000-258200	Enhancers	Hela-S3	cervix
44	chr6:257200-257400	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr6:257200-257600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:257200-258000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr6:257200-258000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr6:257200-258000	Flanking Active TSS	GM12878-XiMat	blood
49	chr6:257200-258200	Enhancers	Primary T cells fromperipheralblood	blood
50	chr6:257200-258600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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