Variant report

Variant	nsv1047462
Chromosome Location	chr11:45898630-45953696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2629)
CpG islands
(count:4096)
Chromatin interactive
region (count:101)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2629 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45939422-45939874	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:45901718-45902111	K562	blood:	n/a	n/a
3	ARID3A	chr11:45921040-45921116	K562	blood:	n/a	n/a
4	ARID3A	chr11:45921441-45921541	K562	blood:	n/a	n/a
5	ARID3A	chr11:45907028-45907063	K562	blood:	n/a	n/a
6	ARID3A	chr11:45939775-45940079	K562	blood:	n/a	n/a
7	ATF1	chr11:45901614-45902133	K562	blood:	n/a	n/a
8	ATF1	chr11:45921213-45921587	K562	blood:	n/a	n/a
9	ATF2	chr11:45939137-45939942	GM12878	blood:	n/a	n/a
10	ATF2	chr11:45944870-45945146	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:45951481-45952091	GM12878	blood:	n/a	n/a
12	ATF2	chr11:45939175-45939642	GM12878	blood:	n/a	n/a
13	ATF2	chr11:45939276-45939783	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:45920751-45921633	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:45921305-45921598	GM12878	blood:	n/a	n/a
16	ATF2	chr11:45920836-45921630	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr11:45939644-45939943	GM12878	blood:	n/a	n/a
18	ATF2	chr11:45951365-45952105	GM12878	blood:	n/a	n/a
19	ATF3	chr11:45921190-45921495	H1-hESC	embryonic stem cell:	n/a	chr11:45921401-45921414
20	ATF3	chr11:45921233-45921578	H1-hESC	embryonic stem cell:	n/a	chr11:45921401-45921414
21	ATF3	chr11:45902017-45902286	K562	blood:	n/a	chr11:45902166-45902175
22	ATF3	chr11:45939259-45939963	A549	lung:	n/a	chr11:45939582-45939590
23	ATF3	chr11:45921125-45921680	K562	blood:	n/a	chr11:45921401-45921414
24	ATF3	chr11:45921288-45921589	A549	lung:	n/a	chr11:45921401-45921414
25	ATF3	chr11:45921230-45921547	K562	blood:	n/a	chr11:45921401-45921414
26	ATF3	chr11:45901671-45902155	K562	blood:	n/a	n/a
27	ATF3	chr11:45939190-45939620	A549	lung:	n/a	chr11:45939582-45939590
28	ATF3	chr11:45921322-45921627	A549	lung:	n/a	chr11:45921401-45921414
29	BACH1	chr11:45943360-45944159	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr11:45906869-45907095	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr11:45951645-45951976	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:45951636-45951961	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:45951571-45952016	GM12878	blood:	n/a	n/a
34	BCL3	chr11:45951548-45952081	GM12878	blood:	n/a	n/a
35	BCL3	chr11:45929347-45929593	GM12878	blood:	n/a	n/a
36	BCL3	chr11:45939029-45939668	A549	lung:	n/a	n/a
37	BCL3	chr11:45939139-45940098	A549	lung:	n/a	n/a
38	BCLAF1	chr11:45939160-45940001	GM12878	blood:	n/a	n/a
39	BCLAF1	chr11:45951510-45952152	GM12878	blood:	n/a	n/a
40	BCLAF1	chr11:45951503-45952071	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:45938839-45939950	GM12878	blood:	n/a	n/a
42	BHLHE40	chr11:45940352-45940398	K562	blood:	n/a	n/a
43	BHLHE40	chr11:45952186-45952270	K562	blood:	n/a	n/a
44	BHLHE40	chr11:45918145-45918150	K562	blood:	n/a	n/a
45	BHLHE40	chr11:45921277-45921714	HepG2	liver:	n/a	n/a
46	BHLHE40	chr11:45921011-45921713	K562	blood:	n/a	n/a
47	BHLHE40	chr11:45921317-45921651	A549	lung:	n/a	n/a
48	BHLHE40	chr11:45909686-45909741	K562	blood:	n/a	n/a
49	BHLHE40	chr11:45901694-45902579	K562	blood:	n/a	chr11:45902164-45902177 chr11:45902167-45902176 chr11:45902166-45902175 chr11:45902160-45902181
50	BHLHE40	chr11:45921330-45921680	GM12878	blood:	n/a	n/a

(count:4096 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45909813-45909863	PFSK-1	brain:	n/a
2	chr11:45951803-45951853	AG04449	skin:	fetal
3	chr11:45937020-45937070	Hepatocyte	liver:	n/a
4	chr11:45942176-45942226	AG04450	lung:	fetal
5	chr11:45940039-45940089	HCT-116	colon:	n/a
6	chr11:45939619-45939669	HCM	heart:	n/a
7	chr11:45942027-45942077	CMK	blood:	n/a
8	chr11:45931715-45931765	SK-N-MC	brain:	n/a
9	chr11:45924624-45924674	Jurkat	blood:	n/a
10	chr11:45909813-45909863	PFSK-1	brain:	n/a
11	chr11:45951803-45951853	AG04449	skin:	fetal
12	chr11:45937020-45937070	Hepatocyte	liver:	n/a
13	chr11:45942176-45942226	AG04450	lung:	fetal
14	chr11:45940039-45940089	HCT-116	colon:	n/a
15	chr11:45939619-45939669	HCM	heart:	n/a
16	chr11:45942027-45942077	CMK	blood:	n/a
17	chr11:45931715-45931765	SK-N-MC	brain:	n/a
18	chr11:45924624-45924674	Jurkat	blood:	n/a
19	chr11:45921388-45921438	RPTEC	kidney:	n/a
20	chr11:45944920-45944970	MCF10A-Er-Src	breast:	n/a
21	chr11:45906625-45906675	HL-60	blood:	n/a
22	chr11:45942176-45942226	T-47D	breast:	n/a
23	chr11:45937020-45937070	HRE	kidney:	n/a
24	chr11:45939458-45939508	HRE	kidney:	n/a
25	chr11:45952237-45952287	H1-hESC	embryonic stem cell:	embryo
26	chr11:45943572-45943622	ProgFib	skin:	n/a
27	chr11:45943979-45944029	HEK293	kidney:	embryo
28	chr11:45924434-45924484	MCF-7	breast:	n/a
29	chr11:45908036-45908086	AoSMC	blood vessel:	n/a
30	chr11:45908036-45908086	H1-hESC	embryonic stem cell:	embryo
31	chr11:45938923-45938973	Hepatocyte	liver:	n/a
32	chr11:45949793-45949843	AG10803	skin:	n/a
33	chr11:45922166-45922216	HUVEC	blood vessel:	n/a
34	chr11:45928370-45928420	CMK	blood:	n/a
35	chr11:45943572-45943622	ovcar-3	ovarian:	n/a
36	chr11:45928841-45928891	HAEpiC	amniotic membrane:	n/a
37	chr11:45924191-45924241	HUVEC	blood vessel:	n/a
38	chr11:45926170-45926220	SK-N-MC	brain:	n/a
39	chr11:45929369-45929419	T-47D	breast:	n/a
40	chr11:45950696-45950746	NH-A	brain:	n/a
41	chr11:45907078-45907128	AG09319	gingival:	n/a
42	chr11:45929369-45929419	K562	blood:	n/a
43	chr11:45944920-45944970	HAEpiC	amniotic membrane:	n/a
44	chr11:45950405-45950455	PrEC	prostate:	n/a
45	chr11:45950405-45950455	HMEC	breast:	n/a
46	chr11:45924434-45924484	HUVEC	blood vessel:	n/a
47	chr11:45943572-45943622	PrEC	prostate:	n/a
48	chr11:45929519-45929569	NHBE	bronchial:	n/a
49	chr11:45943572-45943622	A549	lung:	n/a
50	chr11:45922166-45922216	GM12878	blood:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:45896752..45899624-chr11:45938849..45941490,2	K562	blood:
2	chr11:45904421..45905932-chr11:45912544..45914291,2	MCF-7	breast:
3	chr11:45888702..45891057-chr11:45904911..45907023,2	MCF-7	breast:
4	chr11:45913514..45915838-chr11:45927907..45930385,2	MCF-7	breast:
5	chr11:45868680..45870553-chr11:45907106..45909020,2	K562	blood:
6	chr11:45896832..45899400-chr11:46142147..46144155,2	MCF-7	breast:
7	chr11:45872396..45874327-chr11:45903903..45905625,2	K562	blood:
8	chr11:45918756..45920830-chr11:46147616..46150404,2	K562	blood:
9	chr11:45921817..45923409-chr11:45925394..45927956,2	K562	blood:
10	chr11:45906496..45909660-chr11:45910667..45914809,5	K562	blood:
11	chr11:45899726..45902315-chr11:45996941..45999150,2	MCF-7	breast:
12	chr11:45915081..45916599-chr11:46391904..46393436,2	K562	blood:
13	chr11:45890873..45893526-chr11:45930539..45932384,2	K562	blood:
14	chr11:45869438..45872196-chr11:45903876..45906831,3	K562	blood:
15	chr11:45904421..45905932-chr11:45912544..45914291,2	MCF-7	breast:
16	chr11:45904585..45907305-chr11:45939491..45941669,2	K562	blood:
17	chr11:45868894..45870500-chr11:45937119..45938981,2	K562	blood:
18	chr11:45918493..45920124-chr11:45923045..45924721,2	MCF-7	breast:
19	chr11:45868765..45870683-chr11:45944601..45946304,2	MCF-7	breast:
20	chr11:45939300..45941780-chr11:46259462..46260979,2	K562	blood:
21	chr11:45925111..45927750-chr11:45943585..45946023,2	K562	blood:
22	chr11:45825139..45826817-chr11:45912487..45914933,2	MCF-7	breast:
23	chr11:45898608..45900937-chr11:45921279..45922958,2	MCF-7	breast:
24	chr11:45898608..45900937-chr11:45921279..45922958,2	MCF-7	breast:
25	chr11:45921817..45923409-chr11:45925394..45927956,2	K562	blood:
26	chr11:45915026..45916740-chr11:45938253..45939770,2	MCF-7	breast:
27	chr11:45937002..45939512-chr11:45985947..45988260,2	MCF-7	breast:
28	chr11:45950793..45953982-chr11:45956779..45958840,3	MCF-7	breast:
29	chr11:45901720..45903441-chr11:45911592..45913946,2	MCF-7	breast:
30	chr11:45825326..45828118-chr11:45934084..45936499,2	K562	blood:
31	chr11:45904999..45908778-chr11:45926674..45929138,4	MCF-7	breast:
32	chr11:45904574..45907083-chr11:45920026..45922634,2	MCF-7	breast:
33	chr11:45942684..45944705-chr11:46141351..46143147,2	K562	blood:
34	chr11:45952006..45954841-chr11:45955334..45958699,4	K562	blood:
35	chr11:45942020..45943576-chr11:46141975..46144467,2	MCF-7	breast:
36	chr11:45897697..45900039-chr11:45919922..45922515,2	K562	blood:
37	chr11:45896206..45898084-chr11:45902278..45904901,2	MCF-7	breast:
38	chr11:45919268..45921220-chr11:46000248..46001826,2	MCF-7	breast:
39	chr11:45868641..45870553-chr11:45905537..45909020,4	K562	blood:
40	chr11:45944749..45946540-chr11:45946715..45948340,2	K562	blood:
41	chr11:45897697..45900039-chr11:45919922..45922515,2	K562	blood:
42	chr11:45867884..45870625-chr11:45950267..45953158,3	MCF-7	breast:
43	chr11:45943430..45944211-chr5:39074478..39074986,2	HCT-116	colon:
44	chr11:45944787..45946706-chr11:45959461..45962306,2	K562	blood:
45	chr11:45883450..45885208-chr11:45897811..45899521,2	K562	blood:
46	chr11:45937934..45940310-chr17:56708373..56710113,2	MCF-7	breast:
47	chr11:45904326..45907019-chr11:45920750..45923690,3	MCF-7	breast:
48	chr11:45924750..45927395-chr11:45942360..45945085,3	K562	blood:
49	chr11:45949887..45952560-chr11:46020571..46022730,2	K562	blood:
50	chr11:45868921..45870450-chr11:45919310..45922192,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf94-2	chr11:45926604-45926823	expReg_chr11_3331_-
2	lnc-C11orf94-1	chr11:45927492-45927847	ENSG00000255498.1
3	lnc-C11orf94-1	chr11:45927960-45928012	ENSG00000255498.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CRY2	hsa-miR-93-5p	chr11:45904682-45904706
2	CRY2	hsa-miR-340-5p	chr11:45904686-45904709
3	CRY2	hsa-miR-130b-3p	chr11:45902623-45902646

Variant related genes	Relation type
MAPK8IP1	TF binding region
ENSG00000255498	TF binding region
GYLTL1B	TF binding region
PEX16	TF binding region
C11orf94	TF binding region
MAPK8IP1	CpG island
ENSG00000255498	CpG island
GYLTL1B	CpG island
PEX16	CpG island
C11orf94	CpG island
ENSG00000135365	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000234776	chromatin interactions
ENSG00000255498	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000121653	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000254639	chromatin interactions

Extended variants
information (count: 2349 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2349 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112670498	chr11:45898741-45898742	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs529070938	chr11:45898743-45898744	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs549213769	chr11:45898760-45898761	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs7479067	chr11:45898773-45898774	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs189754192	chr11:45898775-45898776	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs533942376	chr11:45898854-45898855	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182095308	chr11:45898856-45898857	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs12292973	chr11:45898884-45898885	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537081132	chr11:45898909-45898910	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs80217543	chr11:45898919-45898920	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs574012031	chr11:45898926-45898927	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs34936898	chr11:45898988-45898989	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs553707610	chr11:45899010-45899011	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs536411255	chr11:45899013-45899014	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs36056544	chr11:45899019-45899020	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs553155943	chr11:45899047-45899048	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs573406517	chr11:45899054-45899055	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs187861396	chr11:45899124-45899125	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576691803	chr11:45899229-45899230	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs541113024	chr11:45899243-45899244	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs564062636	chr11:45899431-45899432	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142008758	chr11:45899435-45899436	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs543465180	chr11:45899457-45899458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563540320	chr11:45899468-45899469	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529212734	chr11:45899579-45899580	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187848701	chr11:45899628-45899629	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs193282339	chr11:45899631-45899632	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559514732	chr11:45899742-45899743	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551835898	chr11:45899755-45899756	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555721439	chr11:45899767-45899768	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11038700	chr11:45899791-45899792	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs185516016	chr11:45899879-45899880	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145453356	chr11:45899882-45899883	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567574935	chr11:45899911-45899912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536547672	chr11:45899950-45899951	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12281674	chr11:45899962-45899963	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs137979720	chr11:45899967-45899968	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188839755	chr11:45899984-45899985	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561779799	chr11:45899987-45899988	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149508225	chr11:45900012-45900013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577679348	chr11:45900037-45900038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543401975	chr11:45900077-45900078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527395967	chr11:45900249-45900250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61882472	chr11:45900283-45900284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556997673	chr11:45900350-45900351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202211012	chr11:45900363-45900364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564682968	chr11:45900375-45900376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573725566	chr11:45900385-45900386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11038701	chr11:45900400-45900401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559421141	chr11:45900426-45900427	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3705 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45874200-45904200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr11:45875200-45905600	Strong transcription	Primary T cells from cord blood	blood
3	chr11:45875800-45904200	Strong transcription	Primary T cells fromperipheralblood	blood
4	chr11:45876400-45904200	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr11:45876800-45900200	Strong transcription	Primary B cells from cord blood	blood
6	chr11:45876800-45903600	Strong transcription	Primary B cells from peripheral blood	blood
7	chr11:45876800-45904600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:45877400-45899800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
9	chr11:45877400-45900200	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr11:45877400-45903800	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr11:45877400-45904200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr11:45879200-45901200	Weak transcription	A549	lung
13	chr11:45880000-45903400	Strong transcription	Placenta Amnion	Placenta Amnion
14	chr11:45880200-45904600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:45880400-45904200	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr11:45880600-45904600	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr11:45881200-45905200	Strong transcription	Fetal Intestine Large	intestine
18	chr11:45881800-45900200	Strong transcription	Brain Germinal Matrix	brain
19	chr11:45881800-45900400	Strong transcription	Fetal Intestine Small	intestine
20	chr11:45882000-45900000	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr11:45882000-45900200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr11:45882000-45902000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr11:45882000-45904800	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr11:45882200-45900000	Strong transcription	Ovary	ovary
25	chr11:45882200-45900200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:45882200-45900400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:45882400-45900200	Strong transcription	Spleen	Spleen
28	chr11:45882600-45900000	Strong transcription	Fetal Muscle Trunk	muscle
29	chr11:45882600-45900000	Strong transcription	Right Ventricle	heart
30	chr11:45882600-45902000	Strong transcription	Fetal Stomach	stomach
31	chr11:45882600-45902600	Strong transcription	Fetal Muscle Leg	muscle
32	chr11:45882600-45902800	Weak transcription	Right Atrium	heart
33	chr11:45882600-45905200	Strong transcription	Liver	Liver
34	chr11:45882800-45902600	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:45883000-45901600	Strong transcription	Colon Smooth Muscle	Colon
36	chr11:45883400-45902400	Strong transcription	Skeletal Muscle Female	skeletal muscle
37	chr11:45883800-45901400	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr11:45883800-45901600	Strong transcription	Rectal Smooth Muscle	rectum
39	chr11:45883800-45905000	Strong transcription	Placenta	Placenta
40	chr11:45885800-45902200	Strong transcription	Adipose Nuclei	Adipose
41	chr11:45885800-45906400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:45886800-45900000	Strong transcription	Brain Substantia Nigra	brain
43	chr11:45886800-45904000	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr11:45887800-45899800	Strong transcription	Lung	lung
45	chr11:45888800-45899600	Strong transcription	Aorta	Aorta
46	chr11:45893000-45906800	Weak transcription	HSMM	muscle
47	chr11:45893200-45902200	Weak transcription	Psoas Muscle	Psoas
48	chr11:45893200-45906600	Weak transcription	Small Intestine	intestine
49	chr11:45893400-45902600	Weak transcription	Stomach Mucosa	stomach
50	chr11:45893600-45899200	Weak transcription	Fetal Kidney	kidney

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