Variant report

Variant	nsv1044266
Chromosome Location	chr11:47929586-48276132
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6583)
CpG islands
(count:2684)
Chromatin interactive
region (count:250)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:8)

(count:6583 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:47976936-47977170	K562	blood:	n/a	n/a
2	ARID3A	chr11:47969693-47969977	K562	blood:	n/a	n/a
3	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48123329-48123998	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:48130891-48131217	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:47937909-47938256	K562	blood:	n/a	n/a
7	ARID3A	chr11:48131445-48131835	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:48028182-48028572	K562	blood:	n/a	n/a
9	ARID3A	chr11:47965486-47966409	K562	blood:	n/a	n/a
10	ARID3A	chr11:47956016-47956300	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:47939311-47940092	K562	blood:	n/a	n/a
12	ARID3A	chr11:48012687-48013089	K562	blood:	n/a	n/a
13	ARID3A	chr11:47963827-47964024	HepG2	liver:	n/a	n/a
14	ARID3A	chr11:47945865-47946142	HepG2	liver:	n/a	n/a
15	ARID3A	chr11:48118839-48119112	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:48020351-48020690	HepG2	liver:	n/a	n/a
17	ARID3A	chr11:48034789-48035164	HepG2	liver:	n/a	n/a
18	ARID3A	chr11:48095041-48095124	K562	blood:	n/a	n/a
19	ARID3A	chr11:48114969-48116284	HepG2	liver:	n/a	n/a
20	ARID3A	chr11:47935457-47935526	K562	blood:	n/a	n/a
21	ARID3A	chr11:47956003-47956383	K562	blood:	n/a	n/a
22	ARID3A	chr11:47961091-47961319	K562	blood:	n/a	n/a
23	ARID3A	chr11:48130883-48131832	K562	blood:	n/a	n/a
24	ARID3A	chr11:48011206-48011933	K562	blood:	n/a	n/a
25	ARID3A	chr11:48007735-48008092	K562	blood:	n/a	n/a
26	ARID3A	chr11:47961582-47961753	K562	blood:	n/a	n/a
27	ARID3A	chr11:47936906-47936926	K562	blood:	n/a	n/a
28	ARID3A	chr11:48082899-48083240	K562	blood:	n/a	n/a
29	ARID3A	chr11:48014991-48015408	K562	blood:	n/a	n/a
30	ATF1	chr11:48028142-48028476	K562	blood:	n/a	n/a
31	ATF1	chr11:47939378-47940097	K562	blood:	n/a	n/a
32	ATF1	chr11:47969704-47970008	K562	blood:	n/a	n/a
33	ATF1	chr11:48082834-48083315	K562	blood:	n/a	n/a
34	ATF1	chr11:48007751-48008118	K562	blood:	n/a	n/a
35	ATF1	chr11:48005044-48005362	K562	blood:	n/a	n/a
36	ATF1	chr11:48014956-48015365	K562	blood:	n/a	n/a
37	ATF1	chr11:47957268-47957349	K562	blood:	n/a	n/a
38	ATF1	chr11:47956040-47956339	K562	blood:	n/a	n/a
39	ATF1	chr11:48077433-48077920	K562	blood:	n/a	n/a
40	ATF1	chr11:47965439-47966082	K562	blood:	n/a	n/a
41	ATF1	chr11:47968512-47968837	K562	blood:	n/a	n/a
42	ATF2	chr11:48128530-48129047	GM12878	blood:	n/a	n/a
43	ATF2	chr11:48041464-48042090	GM12878	blood:	n/a	n/a
44	ATF2	chr11:48028018-48028663	GM12878	blood:	n/a	n/a
45	ATF2	chr11:48041357-48042266	GM12878	blood:	n/a	n/a
46	ATF2	chr11:48125780-48126273	GM12878	blood:	n/a	n/a
47	ATF2	chr11:48128499-48129217	GM12878	blood:	n/a	n/a
48	ATF2	chr11:48131384-48131873	GM12878	blood:	n/a	n/a
49	ATF2	chr11:48027746-48028715	GM12878	blood:	n/a	n/a
50	ATF2	chr11:48085000-48085533	GM12878	blood:	n/a	n/a

(count:2684 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48153832-48153882	SK-N-SH	brain:	n/a
2	chr11:48036852-48036902	A549	lung:	n/a
3	chr11:48001669-48001719	NB4	blood:	n/a
4	chr11:48266856-48266906	HRPEpiC	eye:	n/a
5	chr11:48266856-48266906	HIPEpiC	eye:	n/a
6	chr11:48185069-48185119	HCPEpiC	choroid plexus:	n/a
7	chr11:48001835-48001885	NHBE	bronchial:	n/a
8	chr11:48118041-48118091	K562	blood:	n/a
9	chr11:47939769-47939819	ovcar-3	ovarian:	n/a
10	chr11:48237358-48237408	GM12891	blood:	n/a
11	chr11:48077221-48077271	AG10803	skin:	n/a
12	chr11:48085137-48085187	BE2_C	brain:	n/a
13	chr11:48153832-48153882	HIPEpiC	eye:	n/a
14	chr11:48038449-48038499	U87	brain:	n/a
15	chr11:48019467-48019517	Jurkat	blood:	n/a
16	chr11:48038449-48038499	SAEC	small airway:	n/a
17	chr11:48001669-48001719	K562	blood:	n/a
18	chr11:47939769-47939819	GM12878	blood:	n/a
19	chr11:47995865-47995915	MCF-7	breast:	n/a
20	chr11:48019467-48019517	HRE	kidney:	n/a
21	chr11:48161861-48161911	CMK	blood:	n/a
22	chr11:48185069-48185119	SK-N-SH_RA	brain:	n/a
23	chr11:48034953-48035003	NT2-D1	testis:	n/a
24	chr11:48038449-48038499	NHDF-neo	bronchial:	n/a
25	chr11:48238296-48238346	HCF	heart:	n/a
26	chr11:48034953-48035003	HRCEpiC	kidney:	n/a
27	chr11:47997690-47997740	GM19239	blood:	n/a
28	chr11:48052092-48052142	H1-hESC	embryonic stem cell:	embryo
29	chr11:48266856-48266906	HL-60	blood:	n/a
30	chr11:48052092-48052142	HCF	heart:	n/a
31	chr11:48001954-48002004	SK-N-SH_RA	brain:	n/a
32	chr11:48040772-48040822	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:48052092-48052142	HAEpiC	amniotic membrane:	n/a
34	chr11:48185069-48185119	AG09309	skin:	n/a
35	chr11:48129067-48129117	BE2_C	brain:	n/a
36	chr11:48019467-48019517	MCF-7	breast:	n/a
37	chr11:48191068-48191118	NB4	blood:	n/a
38	chr11:48112253-48112303	HEK293	kidney:	embryo
39	chr11:48112253-48112303	HNPCEpiC	eye:	n/a
40	chr11:48237353-48237403	AG04450	lung:	fetal
41	chr11:48026889-48026939	NHBE	bronchial:	n/a
42	chr11:48034953-48035003	AoSMC	blood vessel:	n/a
43	chr11:48026889-48026939	RPTEC	kidney:	n/a
44	chr11:48083100-48083150	HCT-116	colon:	n/a
45	chr11:48161861-48161911	HAEpiC	amniotic membrane:	n/a
46	chr11:48110045-48110095	HRCEpiC	kidney:	n/a
47	chr11:48001954-48002004	HAEpiC	amniotic membrane:	n/a
48	chr11:48001669-48001719	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:47995865-47995915	NB4	blood:	n/a
50	chr11:48026889-48026939	MCF10A-Er-Src	breast:	n/a

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr11:48061951..48065074-chr11:48065733..48069871,4	MCF-7	breast:
2	chr11:48162891..48165104-chr11:48166215..48167785,2	K562	blood:
3	chr11:48071477..48072173-chr11:48130347..48131089,2	MCF-7	breast:
4	chr11:48041770..48044575-chr11:48053476..48055088,2	MCF-7	breast:
5	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
6	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
7	chr11:48068334..48069860-chr11:48070016..48072544,2	MCF-7	breast:
8	chr11:48018299..48021070-chr11:48022717..48025055,2	MCF-7	breast:
9	chr11:48108133..48109846-chr11:48110400..48112858,3	MCF-7	breast:
10	chr11:48077645..48080175-chr11:48086953..48089270,2	MCF-7	breast:
11	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
12	chr11:48107721..48110377-chr11:48121800..48123863,2	MCF-7	breast:
13	chr11:47993972..47999221-chr11:48000961..48004940,8	MCF-7	breast:
14	chr11:47955523..47956710-chr11:48130209..48132188,17	MCF-7	breast:
15	chr11:48072810..48075370-chr11:48080373..48082997,2	K562	blood:
16	chr11:48081533..48083185-chr11:48091579..48093994,2	MCF-7	breast:
17	chr11:47933639..47935365-chr11:47935949..47938234,2	K562	blood:
18	chr11:48017573..48020205-chr11:48021877..48024706,2	K562	blood:
19	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
20	chr11:48069835..48071887-chr11:48083817..48085807,2	MCF-7	breast:
21	chr11:47968790..47969517-chr11:48130956..48131704,2	MCF-7	breast:
22	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
23	chr11:48121014..48122957-chr11:48124539..48127155,2	K562	blood:
24	chr11:48072169..48075662-chr11:48075736..48079290,4	MCF-7	breast:
25	chr11:48129232..48130878-chr11:48134176..48136053,2	K562	blood:
26	chr11:48049637..48052585-chr11:48057175..48059884,2	K562	blood:
27	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
28	chr11:48051913..48054330-chr11:48054555..48057402,3	MCF-7	breast:
29	chr11:48069835..48071887-chr11:48083817..48085807,2	MCF-7	breast:
30	chr11:48023169..48025909-chr11:48028991..48031119,2	K562	blood:
31	chr11:48011467..48013224-chr11:48076838..48078616,2	K562	blood:
32	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
33	chr11:48037574..48039959-chr11:48041081..48044491,3	K562	blood:
34	chr11:47985562..47986062-chr11:48130641..48131468,2	K562	blood:
35	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
36	chr11:48071477..48072173-chr11:48130347..48131089,2	MCF-7	breast:
37	chr11:48003107..48006285-chr11:48013442..48016525,3	MCF-7	breast:
38	chr11:47936350..47939236-chr11:47942544..47946300,3	MCF-7	breast:
39	chr11:48009714..48011875-chr11:48013703..48016314,2	K562	blood:
40	chr11:47994952..47996507-chr11:48001378..48004239,2	K562	blood:
41	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
42	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
43	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
44	chr11:47955684..47956212-chr11:48000981..48001494,2	MCF-7	breast:
45	chr11:48011771..48014595-chr11:48017994..48019667,2	K562	blood:
46	chr11:48026525..48028849-chr11:48051139..48053523,2	MCF-7	breast:
47	chr11:47975039..47977335-chr11:47978795..47981117,2	K562	blood:
48	chr11:48049637..48052585-chr11:48057175..48059884,2	K562	blood:
49	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
50	chr11:48068334..48069860-chr11:48070016..48072544,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRJ-1	chr11:47967903-47968054	NONHSAT021290
2	lnc-NUP160-1	chr11:48035958-48036229	ENSG00000254879.1
3	lnc-PTPRJ-1	chr11:47968934-47969181	NONHSAT021290
4	lnc-NUP160-1	chr11:48037379-48037407	ENSG00000254879.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3161	chr11:48118343-48118365	MIMAT0015035

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

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

Variant related genes	Relation type
MIR3161	TF binding region
OR4X2	TF binding region
OR4B2P	TF binding region
ENSG00000254780	TF binding region
PTPRJ	TF binding region
ENSG00000254879	TF binding region
OR4B1	TF binding region
MIR3161	CpG island
OR4X2	CpG island
OR4B2P	CpG island
ENSG00000254780	CpG island
PTPRJ	CpG island
ENSG00000254879	CpG island
OR4B1	CpG island
ENSG00000254780	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000254879	chromatin interactions
ENSG00000030066	chromatin interactions
ENSG00000149177	chromatin interactions
ENSG00000165923	chromatin interactions

Extended variants
information (count: 10092 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:10092 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530275183	chr11:47929586-47929587	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs7117644	chr11:47929604-47929605	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558225864	chr11:47929650-47929651	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs111424241	chr11:47929663-47929664	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs117983814	chr11:47929703-47929704	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs373342186	chr11:47929725-47929726	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79714998	chr11:47929729-47929730	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs79402483	chr11:47929730-47929731	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs77452531	chr11:47929731-47929732	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181998031	chr11:47929744-47929745	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs57069351	chr11:47929745-47929746	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs569309363	chr11:47929799-47929800	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs180920960	chr11:47929821-47929822	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs557342819	chr11:47929830-47929831	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs6485795	chr11:47929846-47929847	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs148651517	chr11:47929857-47929858	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs142230747	chr11:47929875-47929876	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376463837	chr11:47929897-47929898	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs572874430	chr11:47929901-47929902	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554418392	chr11:47929978-47929979	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs185314725	chr11:47929991-47929992	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377721408	chr11:47930027-47930028	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs544500178	chr11:47930206-47930207	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115369907	chr11:47930296-47930297	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs530189103	chr11:47930345-47930346	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs370312898	chr11:47930401-47930402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550746310	chr11:47930404-47930405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546879769	chr11:47930436-47930437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560604412	chr11:47930463-47930464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs28481961	chr11:47930464-47930465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76331606	chr11:47930466-47930467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75219614	chr11:47930468-47930469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532485194	chr11:47930491-47930492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552669168	chr11:47930520-47930521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576481296	chr11:47930524-47930525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569274746	chr11:47930574-47930575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374250547	chr11:47930578-47930579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567642571	chr11:47930591-47930592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386373786	chr11:47930603-47930604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386373787	chr11:47930621-47930622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs58348995	chr11:47930625-47930626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538285482	chr11:47930655-47930656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550853787	chr11:47930676-47930677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537454423	chr11:47930692-47930693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536419281	chr11:47930751-47930752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552909018	chr11:47930752-47930753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573026239	chr11:47930762-47930763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538333093	chr11:47930810-47930811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2930186	chr11:47930811-47930812	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs574882387	chr11:47930896-47930897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:10364 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47922200-47930000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr11:47923600-47929800	Weak transcription	GM12878-XiMat	blood
3	chr11:47925600-47943200	Enhancers	Placenta	Placenta
4	chr11:47927200-47942800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:47927800-47935000	Weak transcription	K562	blood
6	chr11:47927800-47936600	Weak transcription	Thymus	Thymus
7	chr11:47928000-47929600	Weak transcription	Fetal Intestine Large	intestine
8	chr11:47928000-47929600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr11:47928000-47929800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:47928200-47929600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:47928200-47929600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:47928200-47929600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:47928200-47929600	Weak transcription	Lung	lung
14	chr11:47928200-47936800	Weak transcription	Fetal Muscle Leg	muscle
15	chr11:47928400-47929800	Weak transcription	HUVEC	blood vessel
16	chr11:47928600-47929600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:47928600-47930200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr11:47928600-47930600	Enhancers	NHDF-Ad	bronchial
19	chr11:47928600-47930600	Enhancers	Osteobl	bone
20	chr11:47928800-47929600	Enhancers	HSMM	muscle
21	chr11:47929000-47930400	Enhancers	Primary B cells from peripheral blood	blood
22	chr11:47929000-47935600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr11:47929200-47929600	Enhancers	Pancreas	Pancrea
24	chr11:47929200-47929800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:47929200-47930200	Enhancers	Spleen	Spleen
26	chr11:47929200-47930400	Enhancers	Fetal Intestine Small	intestine
27	chr11:47929200-47930400	Enhancers	Hela-S3	cervix
28	chr11:47929200-47931600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:47929400-47930000	Weak transcription	HSMMtube	muscle
30	chr11:47929400-47930200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:47929400-47930800	Enhancers	Primary B cells from cord blood	blood
32	chr11:47929600-47929800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr11:47929600-47929800	Enhancers	Fetal Muscle Trunk	muscle
34	chr11:47929600-47929800	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr11:47929600-47930000	Weak transcription	Pancreas	Pancrea
36	chr11:47929600-47930000	Weak transcription	HSMM	muscle
37	chr11:47929600-47930200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:47929600-47930200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:47929600-47930200	Enhancers	Adipose Nuclei	Adipose
40	chr11:47929600-47930200	Enhancers	Lung	lung
41	chr11:47929600-47930400	Enhancers	Fetal Intestine Large	intestine
42	chr11:47929600-47931600	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr11:47929600-47932400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr11:47929800-47930000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:47929800-47930000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:47929800-47930200	Enhancers	A549	lung
47	chr11:47929800-47930200	Flanking Active TSS	GM12878-XiMat	blood
48	chr11:47929800-47930200	Enhancers	HUVEC	blood vessel
49	chr11:47929800-47930200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr11:47929800-47935200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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