Variant report

Variant	nsv538445
Chromosome Location	chr6:134512542-134638259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1613)
CpG islands
(count:549)
Chromatin interactive
region (count:57)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:134570760-134571744	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:134520773-134521670	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:134518771-134520368	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:134636384-134636729	K562	blood:	n/a	n/a
5	ARID3A	chr6:134571291-134571608	K562	blood:	n/a	n/a
6	ARID3A	chr6:134580051-134580515	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:134516545-134517293	K562	blood:	n/a	n/a
8	ARID3A	chr6:134614633-134615266	K562	blood:	n/a	n/a
9	ARID3A	chr6:134516161-134516887	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:134518232-134518429	K562	blood:	n/a	n/a
11	ARID3A	chr6:134519199-134519568	K562	blood:	n/a	n/a
12	ARID3A	chr6:134517706-134517976	K562	blood:	n/a	n/a
13	ARID3A	chr6:134617113-134617582	K562	blood:	n/a	n/a
14	ATF1	chr6:134517610-134518335	K562	blood:	n/a	n/a
15	ATF1	chr6:134557149-134557476	K562	blood:	n/a	n/a
16	ATF1	chr6:134617059-134617490	K562	blood:	n/a	n/a
17	ATF1	chr6:134548729-134548820	K562	blood:	n/a	n/a
18	ATF1	chr6:134609872-134610100	K562	blood:	n/a	n/a
19	ATF1	chr6:134571365-134571587	K562	blood:	n/a	n/a
20	ATF2	chr6:134556974-134557702	GM12878	blood:	n/a	n/a
21	ATF2	chr6:134517596-134518143	GM12878	blood:	n/a	n/a
22	ATF2	chr6:134556934-134557658	GM12878	blood:	n/a	n/a
23	ATF2	chr6:134589104-134589440	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:134520856-134521463	GM12878	blood:	n/a	n/a
25	ATF2	chr6:134567885-134569110	GM12878	blood:	n/a	n/a
26	ATF2	chr6:134567949-134569078	GM12878	blood:	n/a	n/a
27	ATF3	chr6:134519080-134519616	A549	lung:	n/a	n/a
28	ATF3	chr6:134519066-134519510	A549	lung:	n/a	n/a
29	ATF3	chr6:134617009-134617559	K562	blood:	n/a	chr6:134617205-134617214
30	ATF3	chr6:134557100-134557443	K562	blood:	n/a	n/a
31	BACH1	chr6:134571391-134571570	K562	blood:	n/a	n/a
32	BACH1	chr6:134598360-134598512	K562	blood:	n/a	n/a
33	BACH1	chr6:134589127-134589482	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:134574896-134575202	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:134575044-134575118	K562	blood:	n/a	n/a
36	BATF	chr6:134609542-134609874	GM12878	blood:	n/a	n/a
37	BATF	chr6:134557102-134557605	GM12878	blood:	n/a	chr6:134557370-134557380 chr6:134557369-134557380
38	BATF	chr6:134568081-134569003	GM12878	blood:	n/a	n/a
39	BATF	chr6:134629963-134630214	GM12878	blood:	n/a	chr6:134630116-134630125
40	BATF	chr6:134567923-134568982	GM12878	blood:	n/a	n/a
41	BATF	chr6:134517728-134518061	GM12878	blood:	n/a	n/a
42	BATF	chr6:134609610-134609951	GM12878	blood:	n/a	n/a
43	BATF	chr6:134557227-134557510	GM12878	blood:	n/a	chr6:134557370-134557380 chr6:134557369-134557380
44	BCL11A	chr6:134568051-134568978	GM12878	blood:	n/a	chr6:134568454-134568463 chr6:134568834-134568843 chr6:134568404-134568413 chr6:134568835-134568844
45	BCL11A	chr6:134568303-134568915	GM12878	blood:	n/a	chr6:134568454-134568463 chr6:134568834-134568843 chr6:134568404-134568413 chr6:134568835-134568844
46	BCL11A	chr6:134557052-134557618	GM12878	blood:	n/a	chr6:134557408-134557417 chr6:134557119-134557128 chr6:134557369-134557378
47	BCL3	chr6:134568216-134568897	GM12878	blood:	n/a	chr6:134568454-134568463 chr6:134568834-134568843 chr6:134568404-134568413 chr6:134568835-134568844
48	BCL3	chr6:134568171-134568941	GM12878	blood:	n/a	chr6:134568454-134568463 chr6:134568834-134568843 chr6:134568404-134568413 chr6:134568835-134568844
49	BCL3	chr6:134519071-134519710	A549	lung:	n/a	n/a
50	BCL3	chr6:134557088-134557576	GM12878	blood:	n/a	chr6:134557408-134557417 chr6:134557119-134557128 chr6:134557369-134557378

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:134617250-134617300	CMK	blood:	n/a
2	chr6:134588828-134588878	HRCEpiC	kidney:	n/a
3	chr6:134570471-134570521	RPTEC	kidney:	n/a
4	chr6:134617250-134617300	GM12892	blood:	n/a
5	chr6:134617250-134617300	HepG2	liver:	n/a
6	chr6:134609828-134609878	ProgFib	skin:	n/a
7	chr6:134617250-134617300	HCT-116	colon:	n/a
8	chr6:134617250-134617300	GM19239	blood:	n/a
9	chr6:134632095-134632145	K562	blood:	n/a
10	chr6:134632095-134632145	GM19239	blood:	n/a
11	chr6:134570471-134570521	HepG2	liver:	n/a
12	chr6:134637428-134637478	SAEC	small airway:	n/a
13	chr6:134632095-134632145	GM12878	blood:	n/a
14	chr6:134617250-134617300	NB4	blood:	n/a
15	chr6:134513473-134513523	HRPEpiC	eye:	n/a
16	chr6:134513473-134513523	U87	brain:	n/a
17	chr6:134637428-134637478	HCT-116	colon:	n/a
18	chr6:134538515-134538565	HRE	kidney:	n/a
19	chr6:134513473-134513523	CMK	blood:	n/a
20	chr6:134513473-134513523	SKMC	muscle:	n/a
21	chr6:134538515-134538565	NT2-D1	testis:	n/a
22	chr6:134570471-134570521	SAEC	small airway:	n/a
23	chr6:134513473-134513523	MCF-7	breast:	n/a
24	chr6:134617250-134617300	PrEC	prostate:	n/a
25	chr6:134637428-134637478	BE2_C	brain:	n/a
26	chr6:134538515-134538565	HAEpiC	amniotic membrane:	n/a
27	chr6:134637428-134637478	NHBE	bronchial:	n/a
28	chr6:134637428-134637478	AoSMC	blood vessel:	n/a
29	chr6:134538515-134538565	HCT-116	colon:	n/a
30	chr6:134538515-134538565	MCF-7	breast:	n/a
31	chr6:134632095-134632145	HAEpiC	amniotic membrane:	n/a
32	chr6:134617250-134617300	GM12891	blood:	n/a
33	chr6:134570471-134570521	HCF	heart:	n/a
34	chr6:134637428-134637478	NB4	blood:	n/a
35	chr6:134538515-134538565	HNPCEpiC	eye:	n/a
36	chr6:134637428-134637478	Hepatocyte	liver:	n/a
37	chr6:134636441-134636491	H1-hESC	embryonic stem cell:	embryo
38	chr6:134637428-134637478	HMEC	breast:	n/a
39	chr6:134636441-134636491	NT2-D1	testis:	n/a
40	chr6:134538515-134538565	HCPEpiC	choroid plexus:	n/a
41	chr6:134617250-134617300	NT2-D1	testis:	n/a
42	chr6:134538515-134538565	HL-60	blood:	n/a
43	chr6:134637428-134637478	AG09309	skin:	n/a
44	chr6:134637428-134637478	GM19239	blood:	n/a
45	chr6:134617250-134617300	SK-N-SH	brain:	n/a
46	chr6:134513473-134513523	AG04449	skin:	fetal
47	chr6:134617250-134617300	MCF10A-Er-Src	breast:	n/a
48	chr6:134617250-134617300	AG04449	skin:	fetal
49	chr6:134570471-134570521	HRCEpiC	kidney:	n/a
50	chr6:134588828-134588878	ProgFib	skin:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:134553108..134554693-chr6:134556354..134559341,2	MCF-7	breast:
2	chr6:134589884..134592427-chr6:134597728..134599330,2	K562	blood:
3	chr6:134623713..134625251-chr6:134626637..134628598,2	K562	blood:
4	chr6:134514437..134516552-chr6:134517731..134520415,2	K562	blood:
5	chr6:134494524..134497370-chr6:134518785..134521243,2	K562	blood:
6	chr6:134495995..134497860-chr6:134516059..134518356,3	K562	blood:
7	chr6:134495224..134497350-chr6:134568529..134571029,2	K562	blood:
8	chr6:134607134..134608802-chr6:134611969..134614571,2	MCF-7	breast:
9	chr6:134495841..134499603-chr6:134615728..134618642,4	K562	blood:
10	chr6:134493854..134498756-chr6:134634030..134638028,6	K562	blood:
11	chr6:134589884..134592427-chr6:134597728..134599330,2	K562	blood:
12	chr6:134609063..134612103-chr6:134614431..134617312,3	K562	blood:
13	chr6:134588941..134593504-chr6:134594019..134597387,4	K562	blood:
14	chr6:134495315..134497270-chr6:134514850..134516385,2	MCF-7	breast:
15	chr6:134607134..134608802-chr6:134611969..134614571,2	MCF-7	breast:
16	chr6:134573601..134575857-chr6:134580838..134582440,2	K562	blood:
17	chr6:134494576..134496856-chr6:134537015..134539253,2	K562	blood:
18	chr6:134564852..134567842-chr6:134570433..134573007,2	K562	blood:
19	chr6:134607821..134612304-chr6:134613330..134616343,3	K562	blood:
20	chr6:134577103..134579223-chr6:134579601..134582557,3	K562	blood:
21	chr6:134616658..134618437-chr6:134628981..134631732,2	K562	blood:
22	chr6:134609063..134612103-chr6:134614431..134617312,3	K562	blood:
23	chr6:134633192..134634769-chr6:134638936..134640565,2	K562	blood:
24	chr12:120636787..120639653-chr6:134510766..134512846,2	MCF-7	breast:
25	chr6:134564852..134569014-chr6:134570433..134573870,3	K562	blood:
26	chr6:134494401..134497908-chr6:134517206..134521243,5	K562	blood:
27	chr6:134494670..134496213-chr6:134512364..134514214,2	K562	blood:
28	chr6:134496079..134499053-chr6:134513924..134516840,3	K562	blood:
29	chr6:134495934..134501020-chr6:134516975..134520712,4	MCF-7	breast:
30	chr6:134490789..134492865-chr6:134561939..134563668,2	MCF-7	breast:
31	chr6:134493854..134499218-chr6:134633035..134638028,6	K562	blood:
32	chr2:6765990..6766785-chr6:134526832..134527545,2	MCF-7	breast:
33	chr6:134607821..134612304-chr6:134613330..134616343,3	K562	blood:
34	chr6:134568760..134570457-chr6:134573885..134575458,2	K562	blood:
35	chr6:134623713..134625251-chr6:134626637..134628598,2	K562	blood:
36	chr6:134497565..134500024-chr6:134569368..134571128,2	MCF-7	breast:
37	chr6:134553108..134554693-chr6:134556354..134559341,2	MCF-7	breast:
38	chr6:134627553..134630473-chr6:134631444..134633247,2	K562	blood:
39	chr6:134506367..134509100-chr6:134517089..134519394,2	MCF-7	breast:
40	chr6:134495471..134497320-chr6:134511912..134514651,2	MCF-7	breast:
41	chr6:134612590..134614352-chr6:134622724..134625635,2	MCF-7	breast:
42	chr6:134490949..134493620-chr6:134519330..134521030,2	MCF-7	breast:
43	chr6:134495708..134497480-chr6:134580300..134582156,3	MCF-7	breast:
44	chr6:134494410..134495941-chr6:134608709..134610509,2	K562	blood:
45	chr6:134494102..134496580-chr6:134615581..134618361,2	MCF-7	breast:
46	chr6:134616658..134618437-chr6:134628981..134631732,2	K562	blood:
47	chr6:134612590..134614352-chr6:134622724..134625635,2	MCF-7	breast:
48	chr6:134588941..134593504-chr6:134594019..134597387,4	K562	blood:
49	chr6:134573601..134575857-chr6:134580838..134582440,2	K562	blood:
50	chr6:134514437..134516552-chr6:134517731..134520415,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A12-8	chr6:134551538-134551619	NONHSAT115023
2	lnc-SLC2A12-8	chr6:134536083-134536231	NONHSAT115023
3	lnc-SLC2A12-8	chr6:134539819-134539910	NONHSAT115023

No data

Variant related genes	Relation type
SGK1	TF binding region
KRT8P42	TF binding region
RNA5SP218	TF binding region
ENSG00000201309	TF binding region
ENSG00000238631	TF binding region
SGK1	CpG island
KRT8P42	CpG island
RNA5SP218	CpG island
ENSG00000201309	CpG island
ENSG00000238631	CpG island
ENSG00000200058	chromatin interactions
ENSG00000118515	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000255857	chromatin interactions
ENSG00000201309	chromatin interactions

Extended variants
information (count: 4790 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4790 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79219218	chr6:134512552-134512553	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs549921789	chr6:134512554-134512555	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs570024131	chr6:134512566-134512567	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs559217658	chr6:134512570-134512571	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs192746972	chr6:134512580-134512581	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs145270539	chr6:134512653-134512654	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569421465	chr6:134512658-134512659	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs368939724	chr6:134512678-134512679	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs111323503	chr6:134512683-134512684	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs566166905	chr6:134512713-134512714	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376115796	chr6:134512753-134512754	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs374477634	chr6:134512767-134512768	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs9493851	chr6:134512816-134512817	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs79847647	chr6:134512824-134512825	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs78676423	chr6:134512825-134512826	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs183741247	chr6:134512843-134512844	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs189172357	chr6:134512844-134512845	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs540920635	chr6:134512868-134512869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575586773	chr6:134512898-134512899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs192100420	chr6:134512914-134512915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113567420	chr6:134512963-134512964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374779894	chr6:134512964-134512965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551732508	chr6:134512973-134512974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71003671	chr6:134512991-134512992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561488040	chr6:134512998-134512999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572085419	chr6:134513004-134513005	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs562403842	chr6:134513005-134513006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541286898	chr6:134513118-134513119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564667186	chr6:134513227-134513228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367711220	chr6:134513247-134513248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533465124	chr6:134513258-134513259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145983553	chr6:134513312-134513313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs1743959	chr6:134513333-134513334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184698033	chr6:134513349-134513350	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549379783	chr6:134513350-134513351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188672201	chr6:134513351-134513352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9376015	chr6:134513356-134513357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142183913	chr6:134513383-134513384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547292516	chr6:134513396-134513397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1743958	chr6:134513398-134513399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs79494119	chr6:134513421-134513422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556086828	chr6:134513504-134513505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565112916	chr6:134513515-134513516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575922881	chr6:134513535-134513536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs77956852	chr6:134513552-134513553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1628660	chr6:134513617-134513618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191632406	chr6:134513642-134513643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs71003672	chr6:134513720-134513721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549853407	chr6:134513743-134513744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533423355	chr6:134513745-134513746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	20164919	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Intracranial tumor	22048656	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2011 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134499800-134523200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:134505200-134516400	Weak transcription	Fetal Intestine Small	intestine
3	chr6:134506600-134522800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:134508000-134518000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:134508800-134515000	Weak transcription	Brain Anterior Caudate	brain
6	chr6:134509000-134514400	Weak transcription	Brain Hippocampus Middle	brain
7	chr6:134509000-134537800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:134509200-134513800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:134509200-134516400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:134509200-134516400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:134509200-134520000	Weak transcription	Pancreas	Pancrea
12	chr6:134509400-134518000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:134509600-134516400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:134511600-134515400	Weak transcription	Fetal Intestine Large	intestine
15	chr6:134511600-134522800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:134511800-134513000	Enhancers	HepG2	liver
17	chr6:134512000-134512600	Enhancers	Brain Substantia Nigra	brain
18	chr6:134512000-134512600	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr6:134512000-134512600	Enhancers	K562	blood
20	chr6:134512000-134514600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:134512200-134512600	Enhancers	Primary T cells from cord blood	blood
22	chr6:134512200-134512600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr6:134512200-134512600	Enhancers	Brain Angular Gyrus	brain
24	chr6:134512200-134512600	Flanking Active TSS	Fetal Heart	heart
25	chr6:134512400-134512600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:134512600-134512800	Enhancers	Fetal Heart	heart
27	chr6:134512600-134513800	Weak transcription	K562	blood
28	chr6:134512600-134514400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:134512600-134514600	Weak transcription	Brain Angular Gyrus	brain
30	chr6:134512600-134515000	Weak transcription	Brain Substantia Nigra	brain
31	chr6:134512600-134517600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:134512600-134521000	Weak transcription	Primary T cells from cord blood	blood
33	chr6:134512800-134516200	Weak transcription	Fetal Heart	heart
34	chr6:134513000-134513400	Weak transcription	HepG2	liver
35	chr6:134513200-134514600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:134513400-134513600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr6:134513400-134514000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:134513400-134514800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr6:134513400-134514800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:134513400-134514800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:134513400-134520200	Enhancers	HepG2	liver
42	chr6:134513600-134514000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr6:134513600-134514400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:134513600-134514400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:134513600-134514400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:134513800-134514000	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr6:134513800-134514000	Enhancers	Fetal Brain Male	brain
48	chr6:134513800-134514000	Enhancers	Right Ventricle	heart
49	chr6:134513800-134516200	Enhancers	K562	blood
50	chr6:134514000-134514600	Weak transcription	Brain Inferior Temporal Lobe	brain

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