Variant report

Variant	nsv1050815
Chromosome Location	chr11:48126145-48342923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1924)
CpG islands
(count:1037)
Chromatin interactive
region (count:60)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1924 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48130883-48131832	K562	blood:	n/a	n/a
2	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48130891-48131217	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48131445-48131835	HepG2	liver:	n/a	n/a
5	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
6	ATF2	chr11:48131303-48131862	GM12878	blood:	n/a	n/a
7	ATF2	chr11:48128530-48129047	GM12878	blood:	n/a	n/a
8	ATF2	chr11:48125780-48126273	GM12878	blood:	n/a	n/a
9	ATF2	chr11:48128499-48129217	GM12878	blood:	n/a	n/a
10	ATF2	chr11:48131384-48131873	GM12878	blood:	n/a	n/a
11	ATF2	chr11:48125767-48126273	GM12878	blood:	n/a	n/a
12	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
13	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
14	BATF	chr11:48128657-48129110	GM12878	blood:	n/a	n/a
15	BATF	chr11:48131359-48131717	GM12878	blood:	n/a	n/a
16	BATF	chr11:48128651-48129130	GM12878	blood:	n/a	n/a
17	BATF	chr11:48131437-48131740	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:48128709-48129015	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
19	BCL11A	chr11:48131334-48131777	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:48128623-48129135	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
21	BCL3	chr11:48128638-48129194	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
22	BCL3	chr11:48128713-48129121	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
23	BCLAF1	chr11:48131240-48131877	GM12878	blood:	n/a	n/a
24	BCLAF1	chr11:48131284-48131807	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:48128565-48129092	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
26	BCLAF1	chr11:48128578-48129221	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
27	BHLHE40	chr11:48130984-48131970	K562	blood:	n/a	chr11:48131376-48131392
28	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:48128654-48129077	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:48131324-48131977	GM12878	blood:	n/a	chr11:48131376-48131392
31	BHLHE40	chr11:48131523-48131855	HepG2	liver:	n/a	n/a
32	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
33	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr11:48131531-48131726	HepG2	liver:	n/a	n/a
37	BRCA1	chr11:48130922-48131812	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr11:48136314-48136661	K562	blood:	n/a	n/a
39	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
40	CBX3	chr11:48175001-48175304	K562	blood:	n/a	n/a
41	CBX3	chr11:48136304-48136617	K562	blood:	n/a	n/a
42	CEBPB	chr11:48161546-48161713	K562	blood:	n/a	chr11:48161642-48161653
43	CEBPB	chr11:48151304-48151612	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr11:48186415-48186684	A549	lung:	n/a	n/a
45	CEBPB	chr11:48161560-48161749	HepG2	liver:	n/a	chr11:48161642-48161653
46	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
47	CEBPB	chr11:48161481-48161783	IMR90	lung:	n/a	chr11:48161642-48161653
48	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
49	CEBPB	chr11:48131210-48131931	GM12878	blood:	n/a	n/a
50	CEBPB	chr11:48151484-48151532	K562	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48129067-48129117	SK-N-SH	brain:	n/a
2	chr11:48326388-48326438	GM12892	blood:	n/a
3	chr11:48237358-48237408	HCM	heart:	n/a
4	chr11:48129067-48129117	HAEpiC	amniotic membrane:	n/a
5	chr11:48238724-48238774	HRE	kidney:	n/a
6	chr11:48129067-48129117	HRE	kidney:	n/a
7	chr11:48185069-48185119	PrEC	prostate:	n/a
8	chr11:48237353-48237403	GM06990	blood:	n/a
9	chr11:48238296-48238346	HCPEpiC	choroid plexus:	n/a
10	chr11:48191068-48191118	NT2-D1	testis:	n/a
11	chr11:48266856-48266906	HEEpiC	esophagus:	n/a
12	chr11:48161861-48161911	HL-60	blood:	n/a
13	chr11:48153832-48153882	Hela-S3	cervix:	n/a
14	chr11:48185069-48185119	HEEpiC	esophagus:	n/a
15	chr11:48185069-48185119	NH-A	brain:	n/a
16	chr11:48238296-48238346	HRPEpiC	eye:	n/a
17	chr11:48129067-48129117	U87	brain:	n/a
18	chr11:48185069-48185119	GM12891	blood:	n/a
19	chr11:48237353-48237403	ProgFib	skin:	n/a
20	chr11:48328132-48328182	HNPCEpiC	eye:	n/a
21	chr11:48327164-48327214	AG10803	skin:	n/a
22	chr11:48238724-48238774	HCF	heart:	n/a
23	chr11:48326388-48326438	NT2-D1	testis:	n/a
24	chr11:48327164-48327214	GM19239	blood:	n/a
25	chr11:48284249-48284299	PFSK-1	brain:	n/a
26	chr11:48185069-48185119	ProgFib	skin:	n/a
27	chr11:48161380-48161430	HCF	heart:	n/a
28	chr11:48327164-48327214	HCT-116	colon:	n/a
29	chr11:48284249-48284299	HRCEpiC	kidney:	n/a
30	chr11:48185069-48185119	NHDF-neo	bronchial:	n/a
31	chr11:48237353-48237403	AG10803	skin:	n/a
32	chr11:48284249-48284299	AG10803	skin:	n/a
33	chr11:48328132-48328182	A549	lung:	n/a
34	chr11:48185069-48185119	MCF-7	breast:	n/a
35	chr11:48237358-48237408	NT2-D1	testis:	n/a
36	chr11:48238296-48238346	GM12892	blood:	n/a
37	chr11:48327164-48327214	NHDF-neo	bronchial:	n/a
38	chr11:48327164-48327214	HCPEpiC	choroid plexus:	n/a
39	chr11:48185069-48185119	GM06990	blood:	n/a
40	chr11:48285200-48285250	HCM	heart:	n/a
41	chr11:48129067-48129117	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:48153832-48153882	A549	lung:	n/a
43	chr11:48161861-48161911	T-47D	breast:	n/a
44	chr11:48285200-48285250	SKMC	muscle:	n/a
45	chr11:48326388-48326438	HRCEpiC	kidney:	n/a
46	chr11:48237353-48237403	Jurkat	blood:	n/a
47	chr11:48285821-48285871	HUVEC	blood vessel:	n/a
48	chr11:48284249-48284299	HNPCEpiC	eye:	n/a
49	chr11:48285821-48285871	SK-N-MC	brain:	n/a
50	chr11:48153832-48153882	HMEC	breast:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:47956073..47956643-chr11:48155973..48156490,2	MCF-7	breast:
2	chr11:48000640..48001500-chr11:48131020..48132149,3	MCF-7	breast:
3	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
4	chr11:47968790..47969517-chr11:48130956..48131704,2	MCF-7	breast:
5	chr11:47999992..48004999-chr11:48128626..48133853,5	MCF-7	breast:
6	chr11:47955523..47956710-chr11:48130209..48132188,17	MCF-7	breast:
7	chr11:48125100..48126917-chr11:48129444..48131504,2	MCF-7	breast:
8	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
9	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
10	chr11:47985562..47986062-chr11:48130641..48131468,2	K562	blood:
11	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
12	chr11:48002635..48003533-chr11:48130431..48131591,3	MCF-7	breast:
13	chr11:47955553..47956701-chr11:48130593..48132313,16	K562	blood:
14	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
15	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
16	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
17	chr11:47985506..47986348-chr11:48130588..48131464,3	MCF-7	breast:
18	chr11:48001502..48002444-chr11:48131229..48132098,2	MCF-7	breast:
19	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
20	chr11:47985574..47986089-chr11:48131663..48132191,2	K562	blood:
21	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
22	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
23	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
24	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
25	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
26	chr11:48131666..48133452-chr11:48135727..48137956,2	MCF-7	breast:
27	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
28	chr11:48071477..48072173-chr11:48130347..48131089,2	MCF-7	breast:
29	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
30	chr11:47736486..47737053-chr11:48130967..48131472,2	K562	blood:
31	chr11:48125100..48126917-chr11:48129444..48131504,2	MCF-7	breast:
32	chr11:48036717..48039459-chr11:48129718..48132138,2	MCF-7	breast:
33	chr11:47955472..47956729-chr11:48130954..48132546,8	MCF-7	breast:
34	chr11:48068073..48069888-chr11:48129032..48131534,2	MCF-7	breast:
35	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
36	chr11:48162891..48165104-chr11:48166215..48167785,2	K562	blood:
37	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
38	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
39	chr11:47857319..47859657-chr11:48158646..48160993,2	K562	blood:
40	chr11:48046572..48047306-chr11:48130972..48131586,2	MCF-7	breast:
41	chr11:47879130..47879931-chr11:48131064..48131706,2	MCF-7	breast:
42	chr11:48120614..48123449-chr11:48129423..48131714,2	MCF-7	breast:
43	chr11:48129232..48130878-chr11:48134176..48136053,2	K562	blood:
44	chr11:47967425..47969925-chr11:48129768..48132712,2	MCF-7	breast:
45	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
46	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
47	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
48	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
49	chr11:48131666..48133452-chr11:48135727..48137956,2	MCF-7	breast:
50	chr11:48121014..48122957-chr11:48124539..48127155,2	K562	blood:

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
2	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
3	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
4	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256
5	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748
6	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
7	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
8	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
PTPRJ	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
PTPRJ	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island
ENSG00000254879	chromatin interactions
ENSG00000149177	chromatin interactions
ENSG00000165923	chromatin interactions
ENSG00000030066	chromatin interactions

Extended variants
information (count: 4020 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4020 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556813299	chr11:48126195-48126196	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558498618	chr11:48126242-48126243	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1503191	chr11:48126254-48126255	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192301216	chr11:48126284-48126285	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553108148	chr11:48126289-48126290	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572958631	chr11:48126438-48126439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12275069	chr11:48126472-48126473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184590695	chr11:48126544-48126545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577548185	chr11:48126659-48126660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575309440	chr11:48126661-48126662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201737906	chr11:48126675-48126676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561550207	chr11:48126760-48126761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146349425	chr11:48126872-48126873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530384457	chr11:48126890-48126891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540573528	chr11:48126922-48126923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189501970	chr11:48126950-48126951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532635390	chr11:48127070-48127071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73466894	chr11:48127153-48127154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs139414205	chr11:48127161-48127162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531580045	chr11:48127195-48127196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548142305	chr11:48127247-48127248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149630998	chr11:48127257-48127258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536503758	chr11:48127303-48127304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553004993	chr11:48127317-48127318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574972642	chr11:48127474-48127475	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11822306	chr11:48127475-48127476	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs558665099	chr11:48127484-48127485	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148710682	chr11:48127492-48127493	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544339884	chr11:48127560-48127561	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554577493	chr11:48127578-48127579	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574359183	chr11:48127597-48127598	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76226314	chr11:48127620-48127621	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560668483	chr11:48127653-48127654	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75472696	chr11:48127702-48127703	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144756235	chr11:48127748-48127749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147900701	chr11:48127779-48127780	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549320801	chr11:48127788-48127789	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61915879	chr11:48127795-48127796	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs115883057	chr11:48127805-48127806	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116501101	chr11:48127835-48127836	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374586922	chr11:48127850-48127851	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs191742631	chr11:48127898-48127899	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551643196	chr11:48127949-48127950	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571349497	chr11:48127973-48127974	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs367793530	chr11:48127974-48127975	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs139710567	chr11:48128079-48128080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11039517	chr11:48128097-48128098	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538821510	chr11:48128154-48128155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs558751041	chr11:48128164-48128165	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs10734562	chr11:48128189-48128190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:69)

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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:2704 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48114600-48131400	Weak transcription	Esophagus	oesophagus
2	chr11:48115800-48127400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr11:48116200-48127400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr11:48116400-48128600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr11:48116600-48131200	Weak transcription	Psoas Muscle	Psoas
6	chr11:48118800-48129800	Weak transcription	Lung	lung
7	chr11:48118800-48131200	Weak transcription	Ovary	ovary
8	chr11:48119600-48127800	Enhancers	Brain Substantia Nigra	brain
9	chr11:48119600-48131400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr11:48119800-48126800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:48119800-48127200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr11:48119800-48128800	Weak transcription	Hela-S3	cervix
13	chr11:48120600-48126200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr11:48121600-48127400	Enhancers	GM12878-XiMat	blood
15	chr11:48121600-48127600	Enhancers	Primary B cells from cord blood	blood
16	chr11:48121800-48128200	Enhancers	Fetal Intestine Small	intestine
17	chr11:48122000-48127000	Weak transcription	Primary T cells from cord blood	blood
18	chr11:48122200-48126200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr11:48122200-48128200	Enhancers	Fetal Intestine Large	intestine
20	chr11:48122600-48126400	Enhancers	NHDF-Ad	bronchial
21	chr11:48122600-48127600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr11:48122600-48127800	Enhancers	Brain Angular Gyrus	brain
23	chr11:48122600-48128200	Enhancers	Fetal Muscle Leg	muscle
24	chr11:48122600-48128400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr11:48122800-48128200	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr11:48122800-48130600	Enhancers	Spleen	Spleen
27	chr11:48123000-48126200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr11:48123200-48126800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr11:48123200-48131200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:48123400-48128200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr11:48123400-48129200	Weak transcription	Placenta	Placenta
32	chr11:48123400-48129200	Weak transcription	Fetal Thymus	thymus
33	chr11:48123400-48130400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr11:48123400-48131200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr11:48123600-48126800	Weak transcription	Gastric	stomach
36	chr11:48123600-48131200	Enhancers	Liver	Liver
37	chr11:48123800-48128600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:48123800-48129000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:48124000-48128600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:48124000-48128600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:48124000-48131200	Weak transcription	Fetal Lung	lung
42	chr11:48124200-48126600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr11:48124200-48131200	Enhancers	Primary B cells from peripheral blood	blood
44	chr11:48124600-48128000	Enhancers	Pancreas	Pancrea
45	chr11:48124800-48127000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr11:48124800-48127200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr11:48125200-48126400	Enhancers	Colon Smooth Muscle	Colon
48	chr11:48125200-48126400	Flanking Active TSS	A549	lung
49	chr11:48125200-48126600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:48125200-48126600	Enhancers	Fetal Heart	heart

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