Variant report

Variant	nsv525192
Chromosome Location	chr11:18722791-18793360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1849)
CpG islands
(count:1648)
Chromatin interactive
region (count:61)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1849 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18749193-18749311	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18785539-18786129	K562	blood:	n/a	n/a
3	ATF1	chr11:18727860-18728184	K562	blood:	n/a	n/a
4	ATF1	chr11:18785729-18786056	K562	blood:	n/a	n/a
5	ATF2	chr11:18785421-18785991	GM12878	blood:	n/a	n/a
6	ATF2	chr11:18785343-18786174	GM12878	blood:	n/a	n/a
7	ATF2	chr11:18791418-18791870	GM12878	blood:	n/a	n/a
8	ATF2	chr11:18743497-18743928	GM12878	blood:	n/a	n/a
9	ATF2	chr11:18789887-18790491	GM12878	blood:	n/a	n/a
10	ATF2	chr11:18791257-18791888	GM12878	blood:	n/a	n/a
11	ATF2	chr11:18789845-18790477	GM12878	blood:	n/a	n/a
12	ATF3	chr11:18785406-18786165	A549	lung:	n/a	n/a
13	BACH1	chr11:18743650-18743886	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr11:18789911-18790455	GM12878	blood:	n/a	chr11:18790186-18790197
15	BATF	chr11:18789973-18790308	GM12878	blood:	n/a	chr11:18790186-18790197
16	BATF	chr11:18733256-18733529	GM12878	blood:	n/a	n/a
17	BATF	chr11:18791507-18791780	GM12878	blood:	n/a	n/a
18	BATF	chr11:18785382-18785699	GM12878	blood:	n/a	chr11:18785591-18785601 chr11:18785570-18785581 chr11:18785590-18785601
19	BATF	chr11:18785355-18785795	GM12878	blood:	n/a	chr11:18785591-18785601 chr11:18785570-18785581 chr11:18785590-18785601
20	BATF	chr11:18791326-18791840	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:18789919-18790315	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:18791385-18791741	GM12878	blood:	n/a	chr11:18791484-18791493
23	BCL11A	chr11:18789985-18790390	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:18791384-18791771	GM12878	blood:	n/a	chr11:18791484-18791493
25	BCL11A	chr11:18785362-18785747	GM12878	blood:	n/a	chr11:18785589-18785598 chr11:18785590-18785599
26	BCL3	chr11:18789970-18790355	GM12878	blood:	n/a	n/a
27	BCLAF1	chr11:18789853-18790436	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:18743514-18743806	K562	blood:	n/a	n/a
29	BHLHE40	chr11:18745758-18745852	HepG2	liver:	n/a	n/a
30	BHLHE40	chr11:18792091-18792349	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:18785922-18786112	K562	blood:	n/a	n/a
32	BHLHE40	chr11:18742820-18742894	K562	blood:	n/a	n/a
33	BHLHE40	chr11:18753601-18753852	K562	blood:	n/a	n/a
34	BHLHE40	chr11:18791245-18791785	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:18732171-18732492	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:18745658-18745873	K562	blood:	n/a	n/a
37	BHLHE40	chr11:18789954-18790566	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:18749351-18749356	HepG2	liver:	n/a	n/a
39	BRCA1	chr11:18742812-18743003	H1-hESC	embryonic stem cell:	n/a	n/a
40	CCNT2	chr11:18727492-18727692	K562	blood:	n/a	n/a
41	CEBPB	chr11:18763236-18763460	K562	blood:	n/a	chr11:18763361-18763372
42	CEBPB	chr11:18787061-18787434	IMR90	lung:	n/a	n/a
43	CEBPB	chr11:18787058-18787433	A549	lung:	n/a	n/a
44	CEBPB	chr11:18785489-18786030	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:18787066-18787432	K562	blood:	n/a	n/a
46	CEBPB	chr11:18785531-18786042	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:18789899-18790460	GM12878	blood:	n/a	chr11:18790349-18790361
48	CEBPB	chr11:18787074-18787361	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:18743520-18743896	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr11:18787073-18787417	Hela-S3	cervix:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18747783-18747833	HEK293	kidney:	embryo
2	chr11:18747783-18747833	HEK293	kidney:	embryo
3	chr11:18730693-18730743	NB4	blood:	n/a
4	chr11:18727321-18727371	HNPCEpiC	eye:	n/a
5	chr11:18727628-18727678	NHBE	bronchial:	n/a
6	chr11:18740452-18740502	Caco-2	colon:	n/a
7	chr11:18727774-18727824	GM12892	blood:	n/a
8	chr11:18785792-18785842	Caco-2	colon:	n/a
9	chr11:18728598-18728648	CMK	blood:	n/a
10	chr11:18742694-18742744	PANC-1	pancreas:	n/a
11	chr11:18742662-18742712	HNPCEpiC	eye:	n/a
12	chr11:18740452-18740502	Hepatocyte	liver:	n/a
13	chr11:18727774-18727824	T-47D	breast:	n/a
14	chr11:18727949-18727999	GM06990	blood:	n/a
15	chr11:18723988-18724038	GM06990	blood:	n/a
16	chr11:18725481-18725531	Hela-S3	cervix:	n/a
17	chr11:18742662-18742712	HMEC	breast:	n/a
18	chr11:18743222-18743272	HUVEC	blood vessel:	n/a
19	chr11:18754846-18754896	GM19239	blood:	n/a
20	chr11:18725854-18725904	ovcar-3	ovarian:	n/a
21	chr11:18754796-18754846	MCF10A-Er-Src	breast:	n/a
22	chr11:18748167-18748217	NB4	blood:	n/a
23	chr11:18747783-18747833	NB4	blood:	n/a
24	chr11:18748167-18748217	HCF	heart:	n/a
25	chr11:18747315-18747365	HL-60	blood:	n/a
26	chr11:18747783-18747833	AG04449	skin:	fetal
27	chr11:18743222-18743272	HCPEpiC	choroid plexus:	n/a
28	chr11:18728598-18728648	U87	brain:	n/a
29	chr11:18728598-18728648	T-47D	breast:	n/a
30	chr11:18725481-18725531	PrEC	prostate:	n/a
31	chr11:18727628-18727678	HCF	heart:	n/a
32	chr11:18747783-18747833	HIPEpiC	eye:	n/a
33	chr11:18742662-18742712	ovcar-3	ovarian:	n/a
34	chr11:18727321-18727371	HMEC	breast:	n/a
35	chr11:18748134-18748184	A549	lung:	n/a
36	chr11:18742662-18742712	PrEC	prostate:	n/a
37	chr11:18754796-18754846	HRCEpiC	kidney:	n/a
38	chr11:18727321-18727371	AG10803	skin:	n/a
39	chr11:18754796-18754846	NT2-D1	testis:	n/a
40	chr11:18747651-18747701	NHBE	bronchial:	n/a
41	chr11:18754796-18754846	HCPEpiC	choroid plexus:	n/a
42	chr11:18743222-18743272	GM06990	blood:	n/a
43	chr11:18743376-18743426	MCF-7	breast:	n/a
44	chr11:18727774-18727824	CMK	blood:	n/a
45	chr11:18754846-18754896	HIPEpiC	eye:	n/a
46	chr11:18727949-18727999	PrEC	prostate:	n/a
47	chr11:18750217-18750267	NB4	blood:	n/a
48	chr11:18747919-18747969	HepG2	liver:	n/a
49	chr11:18754846-18754896	HCM	heart:	n/a
50	chr11:18742694-18742744	HPAEpiC	pulmonary alveolar:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:18767759..18770654-chr11:18771187..18773325,2	MCF-7	breast:
2	chr11:18767759..18770654-chr11:18771187..18773325,2	MCF-7	breast:
3	chr11:18758802..18760842-chr11:18762633..18764681,2	K562	blood:
4	chr11:18725792..18727506-chr11:18741119..18743990,2	MCF-7	breast:
5	chr11:18777614..18780552-chr11:18781772..18783935,2	K562	blood:
6	chr11:18784737..18787266-chr11:18788580..18790912,2	MCF-7	breast:
7	chr11:18747415..18747915-chr9:131084609..131085371,2	Hela-S3	cervix:
8	chr11:18721312..18723604-chr11:18725131..18727597,3	MCF-7	breast:
9	chr11:18739718..18740394-chr8:128823881..128824525,2	MCF-7	breast:
10	chr11:18742601..18744357-chr11:18744570..18746681,3	K562	blood:
11	chr11:18725792..18727506-chr11:18741119..18743990,2	MCF-7	breast:
12	chr11:18778455..18780307-chr11:18783518..18786208,2	K562	blood:
13	chr11:17752308..17753219-chr11:18785582..18786221,2	K562	blood:
14	chr11:18748906..18749558-chr11:18823928..18824847,2	K562	blood:
15	chr11:18716297..18718426-chr11:18735611..18738399,2	MCF-7	breast:
16	chr11:18737141..18739080-chr11:18744617..18746294,2	K562	blood:
17	chr11:18726664..18728604-chr11:18732867..18735616,2	MCF-7	breast:
18	chr11:18768182..18770334-chr11:18770348..18773584,3	K562	blood:
19	chr11:18787773..18789571-chr11:18794596..18797249,2	K562	blood:
20	chr11:18743551..18744248-chr11:18792745..18793490,2	K562	blood:
21	chr11:18721720..18723290-chr11:18778637..18780237,2	K562	blood:
22	chr11:18745653..18747287-chr11:18748846..18751758,2	K562	blood:
23	chr11:18137140..18137723-chr11:18752823..18753758,4	K562	blood:
24	chr11:18721026..18722984-chr11:18728211..18731423,3	MCF-7	breast:
25	chr11:18743551..18744248-chr11:18792745..18793490,2	K562	blood:
26	chr11:18720007..18721865-chr11:18724885..18727096,2	MCF-7	breast:
27	chr11:18742938..18746162-chr11:18746889..18750542,5	K562	blood:
28	chr11:18741015..18744617-chr11:18749870..18752348,3	K562	blood:
29	chr11:18742601..18744357-chr11:18744570..18746681,3	K562	blood:
30	chr11:18722257..18724313-chr11:18725395..18727849,2	K562	blood:
31	chr11:18728261..18730822-chr11:18735824..18737369,2	K562	blood:
32	chr11:18725063..18726661-chr11:18733495..18735180,2	MCF-7	breast:
33	chr11:18726495..18728843-chr11:18730635..18733881,3	MCF-7	breast:
34	chr11:18758802..18760842-chr11:18762633..18764681,2	K562	blood:
35	chr11:18720636..18723430-chr11:18730880..18733085,2	K562	blood:
36	chr11:18742483..18743153-chr17:61920211..61920994,2	HCT-116	colon:
37	chr11:18720165..18722334-chr11:18757984..18760833,2	K562	blood:
38	chr11:18765546..18768102-chr11:18770359..18772112,2	K562	blood:
39	chr11:18768182..18770334-chr11:18770348..18773584,3	K562	blood:
40	chr11:18737141..18739080-chr11:18744617..18746294,2	K562	blood:
41	chr11:18718875..18721131-chr11:18748920..18750996,2	K562	blood:
42	chr11:18720380..18722380-chr11:18736149..18738465,2	K562	blood:
43	chr11:18717490..18720693-chr11:18752029..18755616,3	MCF-7	breast:
44	chr11:18784737..18787266-chr11:18788580..18790912,2	MCF-7	breast:
45	chr11:18192847..18193418-chr11:18785532..18786067,2	MCF-7	breast:
46	chr11:18721064..18722963-chr11:18742444..18744897,2	MCF-7	breast:
47	chr11:18745653..18747287-chr11:18748846..18751758,2	K562	blood:
48	chr11:18728261..18730822-chr11:18735824..18737369,2	K562	blood:
49	chr11:18788071..18790307-chr11:18794596..18796717,2	K562	blood:
50	chr11:18778455..18780307-chr11:18783518..18786208,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPN5-1	chr11:18743349-18743588	NONHSAT018320
2	lnc-PTPN5-1	chr11:18745675-18745816	NONHSAT018320
3	lnc-PTPN5-1	chr11:18747621-18747721	NONHSAT018320

No data

Variant related genes	Relation type
IGSF22	TF binding region
PTPN5	TF binding region
ENSG00000254966	TF binding region
IGSF22	CpG island
PTPN5	CpG island
ENSG00000254966	CpG island
ENSG00000254966	chromatin interactions
ENSG00000110786	chromatin interactions
ENSG00000110768	chromatin interactions
ENSG00000151117	chromatin interactions
ENSG00000179057	chromatin interactions
ENSG00000108604	chromatin interactions
ENSG00000110756	chromatin interactions
ENSG00000167112	chromatin interactions
ENSG00000167113	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000166787	chromatin interactions

Extended variants
information (count: 2912 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2912 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs733460	chr11:18722791-18722792	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374527416	chr11:18722797-18722798	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370635793	chr11:18722824-18722825	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192174139	chr11:18722869-18722870	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs555033198	chr11:18722900-18722901	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs59226968	chr11:18722903-18722904	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs534168947	chr11:18722904-18722905	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs558694904	chr11:18722946-18722947	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576685491	chr11:18722966-18722967	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs184720297	chr11:18722985-18722986	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs150134414	chr11:18722987-18722988	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs556084814	chr11:18722996-18722997	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574281651	chr11:18723025-18723026	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541655715	chr11:18723031-18723032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139760572	chr11:18723054-18723055	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs527414310	chr11:18723068-18723069	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs367898132	chr11:18723092-18723093	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs545745130	chr11:18723104-18723105	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs371769220	chr11:18723109-18723110	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199688904	chr11:18723119-18723120	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs199661354	chr11:18723129-18723130	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148997299	chr11:18723154-18723155	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373427296	chr11:18723160-18723161	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200662128	chr11:18723173-18723174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs143821414	chr11:18723176-18723177	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375506271	chr11:18723184-18723185	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368896190	chr11:18723188-18723189	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs267602813	chr11:18723190-18723191	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144559255	chr11:18723210-18723211	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146633157	chr11:18723211-18723212	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs372971219	chr11:18723214-18723215	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376236030	chr11:18723217-18723218	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370577203	chr11:18723311-18723312	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372889645	chr11:18723329-18723330	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534042578	chr11:18723330-18723331	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs142350678	chr11:18723338-18723339	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201546830	chr11:18723351-18723352	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552495816	chr11:18723362-18723363	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146522347	chr11:18723388-18723389	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377641163	chr11:18723412-18723413	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376326393	chr11:18723418-18723419	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117231481	chr11:18723449-18723450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141369005	chr11:18723454-18723455	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs376043899	chr11:18723466-18723467	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150360512	chr11:18723474-18723475	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs7945285	chr11:18723477-18723478	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189439292	chr11:18723490-18723491	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs150240202	chr11:18723493-18723494	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368629045	chr11:18723502-18723503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371309512	chr11:18723516-18723517	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	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
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1515 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18720800-18727000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr11:18721000-18727400	Weak transcription	Aorta	Aorta
3	chr11:18721200-18726600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr11:18721400-18722800	Enhancers	Right Atrium	heart
5	chr11:18721400-18722800	Enhancers	HSMMtube	muscle
6	chr11:18721400-18723000	Enhancers	Right Ventricle	heart
7	chr11:18721400-18723200	Weak transcription	Thymus	Thymus
8	chr11:18721400-18726200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr11:18721400-18726400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr11:18721400-18726800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:18721400-18726800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr11:18721400-18726800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:18721600-18722800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr11:18721600-18722800	Enhancers	Fetal Muscle Trunk	muscle
15	chr11:18721600-18723000	Weak transcription	Primary T cells from cord blood	blood
16	chr11:18721600-18723000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:18721600-18724800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:18721600-18725800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:18721600-18725800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr11:18721600-18726600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:18721600-18726800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:18721600-18727000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr11:18721800-18722800	Weak transcription	Fetal Brain Female	brain
24	chr11:18721800-18723000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:18721800-18725400	Weak transcription	Colon Smooth Muscle	Colon
26	chr11:18721800-18726400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr11:18721800-18726400	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr11:18721800-18726800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr11:18721800-18727000	Weak transcription	Colonic Mucosa	Colon
30	chr11:18722000-18722800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:18722000-18723000	Weak transcription	Brain Substantia Nigra	brain
32	chr11:18722000-18723000	Weak transcription	Gastric	stomach
33	chr11:18722000-18723200	Enhancers	Adipose Nuclei	Adipose
34	chr11:18722000-18723200	Weak transcription	Fetal Kidney	kidney
35	chr11:18722000-18725400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:18722000-18725400	Weak transcription	Fetal Heart	heart
37	chr11:18722000-18725600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:18722000-18726600	Weak transcription	Brain Germinal Matrix	brain
39	chr11:18722000-18727400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:18722200-18722800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr11:18722200-18723000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:18722200-18723000	Weak transcription	Liver	Liver
43	chr11:18722200-18723000	Weak transcription	Brain Angular Gyrus	brain
44	chr11:18722200-18723200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:18722200-18726400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:18722200-18726400	Weak transcription	Esophagus	oesophagus
47	chr11:18722200-18726400	Weak transcription	Psoas Muscle	Psoas
48	chr11:18722200-18726600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:18722200-18726800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:18722400-18722800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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