Variant report

Variant	nsv517610
Chromosome Location	chr13:95931992-96035883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2083)
CpG islands
(count:857)
Chromatin interactive
region (count:34)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2083 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95937866-95938402	K562	blood:	n/a	n/a
3	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
4	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
5	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
7	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
8	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:96033005-96033202	K562	blood:	n/a	n/a
10	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
11	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
13	ATF1	chr13:95938012-95938442	K562	blood:	n/a	n/a
14	ATF2	chr13:96032895-96033280	GM12878	blood:	n/a	n/a
15	ATF2	chr13:95932888-95933441	GM12878	blood:	n/a	n/a
16	ATF2	chr13:95933714-95934499	GM12878	blood:	n/a	n/a
17	ATF2	chr13:95932871-95933559	GM12878	blood:	n/a	n/a
18	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
19	ATF3	chr13:95938112-95938426	K562	blood:	n/a	n/a
20	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
21	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr13:95933185-95933517	GM12878	blood:	n/a	chr13:95933299-95933308
25	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
26	BCLAF1	chr13:96032838-96033332	GM12878	blood:	n/a	n/a
27	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
28	BCLAF1	chr13:95933136-95933564	GM12878	blood:	n/a	chr13:95933299-95933308
29	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
30	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
31	BCLAF1	chr13:95937861-95938393	K562	blood:	n/a	n/a
32	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
33	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
34	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
35	BHLHE40	chr13:96032939-96033253	K562	blood:	n/a	n/a
36	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
37	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:96035160-96035373	GM12878	blood:	n/a	n/a
39	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
40	BHLHE40	chr13:95934235-95934425	GM12878	blood:	n/a	n/a
41	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
42	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
43	BHLHE40	chr13:95937918-95938449	K562	blood:	n/a	n/a
44	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
45	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
46	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95958190-95958240	HCPEpiC	choroid plexus:	n/a
2	chr13:95953482-95953532	Hela-S3	cervix:	n/a
3	chr13:95954382-95954432	CMK	blood:	n/a
4	chr13:95958190-95958240	HCPEpiC	choroid plexus:	n/a
5	chr13:95953482-95953532	Hela-S3	cervix:	n/a
6	chr13:95954382-95954432	CMK	blood:	n/a
7	chr13:95953574-95953624	HRPEpiC	eye:	n/a
8	chr13:95953505-95953555	GM06990	blood:	n/a
9	chr13:95958190-95958240	SKMC	muscle:	n/a
10	chr13:96008021-96008071	HIPEpiC	eye:	n/a
11	chr13:95954534-95954584	BE2_C	brain:	n/a
12	chr13:95953229-95953279	SAEC	small airway:	n/a
13	chr13:95952937-95952987	AG04449	skin:	fetal
14	chr13:95953505-95953555	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:95954534-95954584	HRE	kidney:	n/a
16	chr13:95954382-95954432	HMEC	breast:	n/a
17	chr13:95953941-95953991	GM12878	blood:	n/a
18	chr13:95954534-95954584	AG04449	skin:	fetal
19	chr13:95952902-95952952	IMR90	lung:	fetal
20	chr13:95953941-95953991	SK-N-SH_RA	brain:	n/a
21	chr13:95952937-95952987	SKMC	muscle:	n/a
22	chr13:95952937-95952987	HL-60	blood:	n/a
23	chr13:95954534-95954584	Hepatocyte	liver:	n/a
24	chr13:95933097-95933147	GM06990	blood:	n/a
25	chr13:95933097-95933147	HNPCEpiC	eye:	n/a
26	chr13:95953229-95953279	SK-N-SH	brain:	n/a
27	chr13:95953505-95953555	H1-hESC	embryonic stem cell:	embryo
28	chr13:95933097-95933147	PANC-1	pancreas:	n/a
29	chr13:96008021-96008071	HNPCEpiC	eye:	n/a
30	chr13:95953229-95953279	U87	brain:	n/a
31	chr13:95954080-95954130	Caco-2	colon:	n/a
32	chr13:95953574-95953624	AG04449	skin:	fetal
33	chr13:95953229-95953279	ovcar-3	ovarian:	n/a
34	chr13:95932467-95932517	NB4	blood:	n/a
35	chr13:95953941-95953991	NB4	blood:	n/a
36	chr13:95954534-95954584	Jurkat	blood:	n/a
37	chr13:95932467-95932517	GM19239	blood:	n/a
38	chr13:95954534-95954584	CMK	blood:	n/a
39	chr13:95954382-95954432	PFSK-1	brain:	n/a
40	chr13:95953505-95953555	HEK293	kidney:	embryo
41	chr13:95953505-95953555	AG09309	skin:	n/a
42	chr13:95954534-95954584	GM12892	blood:	n/a
43	chr13:95954534-95954584	GM19239	blood:	n/a
44	chr13:95933097-95933147	CMK	blood:	n/a
45	chr13:95954080-95954130	AG09309	skin:	n/a
46	chr13:95954080-95954130	SK-N-SH	brain:	n/a
47	chr13:95954382-95954432	HAEpiC	amniotic membrane:	n/a
48	chr13:95952902-95952952	HepG2	liver:	n/a
49	chr13:95958190-95958240	HUVEC	blood vessel:	n/a
50	chr13:95954534-95954584	SK-N-MC	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95843696..95844640-chr13:96032651..96033707,6	K562	blood:
2	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
3	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
4	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
5	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
6	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
7	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
8	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
9	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
10	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
11	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
12	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
13	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
14	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
15	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
16	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
17	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
18	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
19	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
20	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
21	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
22	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:
23	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
24	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
25	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
26	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
27	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
28	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
29	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
30	chr13:95922109..95924473-chr13:95936856..95939759,2	K562	blood:
31	chr13:95841276..95841834-chr13:96032679..96033583,3	K562	blood:
32	chr13:95843719..95844609-chr13:96033049..96033649,3	MCF-7	breast:
33	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
34	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-1	chr13:95956351-95956401	XLOC_010696
2	lnc-CLDN10-6	chr13:95957471-95958654	NONHSAT034755
3	lnc-ABCC4-1	chr13:95954705-95955669	XLOC_010696
4	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758

No data

Variant related genes	Relation type
RNY3P8	TF binding region
RNY4P27	TF binding region
ABCC4	TF binding region
RNY3P8	CpG island
RNY4P27	CpG island
ABCC4	CpG island
ENSG00000125257	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000083544	chromatin interactions
SMAD4	miRNA target sites

Extended variants
information (count: 3951 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3951 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148422	chr13:95931992-95931993	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564316735	chr13:95931994-95931995	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9524879	chr13:95932010-95932011	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9524880	chr13:95932017-95932018	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs146538737	chr13:95932029-95932030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79828993	chr13:95932055-95932056	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529414712	chr13:95932071-95932072	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549175415	chr13:95932095-95932096	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76376614	chr13:95932100-95932101	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59517595	chr13:95932107-95932108	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs557874563	chr13:95932110-95932111	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58751681	chr13:95932140-95932141	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs58423375	chr13:95932141-95932142	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528663647	chr13:95932164-95932165	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545589093	chr13:95932179-95932180	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4148421	chr13:95932240-95932241	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs542800638	chr13:95932309-95932310	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553204167	chr13:95932343-95932344	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573118290	chr13:95932386-95932387	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140675601	chr13:95932409-95932410	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372578787	chr13:95932425-95932426	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73548861	chr13:95932468-95932469	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533148549	chr13:95932498-95932499	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543816915	chr13:95932512-95932513	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370513324	chr13:95932656-95932657	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs60098321	chr13:95932668-95932669	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10708482	chr13:95932671-95932672	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs398024029	chr13:95932688-95932689	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57732108	chr13:95932689-95932690	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs58999862	chr13:95932713-95932714	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139812501	chr13:95932724-95932725	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368576235	chr13:95932726-95932727	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138955523	chr13:95932739-95932740	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565925792	chr13:95932775-95932776	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528694808	chr13:95932783-95932784	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61654581	chr13:95932827-95932828	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551166972	chr13:95932879-95932880	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571340666	chr13:95932906-95932907	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs60577821	chr13:95932915-95932916	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556923966	chr13:95932929-95932930	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs9590233	chr13:95932961-95932962	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377274918	chr13:95933192-95933193	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113275392	chr13:95933221-95933222	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536545204	chr13:95933229-95933230	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553340986	chr13:95933237-95933238	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9516554	chr13:95933243-95933244	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573055752	chr13:95933261-95933262	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4773868	chr13:95933268-95933269	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs551336574	chr13:95933276-95933277	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116582882	chr13:95933320-95933321	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95913600-95932800	Weak transcription	Primary B cells from peripheral blood	blood
2	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
3	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr13:95924200-95932800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr13:95924800-95932200	Weak transcription	HUVEC	blood vessel
7	chr13:95925800-95932200	Weak transcription	Psoas Muscle	Psoas
8	chr13:95926600-95952400	Weak transcription	Brain Hippocampus Middle	brain
9	chr13:95926800-95932800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr13:95926800-95948600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:95927000-95932000	Weak transcription	Right Ventricle	heart
12	chr13:95927000-95932800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr13:95927000-95937800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr13:95927000-95938000	Weak transcription	Colonic Mucosa	Colon
15	chr13:95927200-95932000	Weak transcription	Lung	lung
16	chr13:95927200-95941600	Weak transcription	Gastric	stomach
17	chr13:95927800-95932000	Weak transcription	Brain Anterior Caudate	brain
18	chr13:95928400-95932000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr13:95928400-95932600	Weak transcription	HSMMtube	muscle
20	chr13:95928400-95932600	Weak transcription	NH-A	brain
21	chr13:95928400-95933800	Weak transcription	Fetal Kidney	kidney
22	chr13:95928400-95934000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:95928400-95937600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr13:95928400-95937800	Weak transcription	Fetal Intestine Small	intestine
25	chr13:95928600-95932000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:95928600-95932200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr13:95928600-95932200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr13:95928600-95932200	Weak transcription	HSMM	muscle
29	chr13:95928600-95932800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr13:95928600-95932800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr13:95928600-95932800	Weak transcription	Osteobl	bone
32	chr13:95928600-95933000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr13:95928600-95933200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr13:95928800-95932200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr13:95928800-95932600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr13:95928800-95932800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:95928800-95932800	Weak transcription	Fetal Stomach	stomach
38	chr13:95928800-95932800	Weak transcription	NHEK	skin
39	chr13:95929000-95932200	Weak transcription	Colon Smooth Muscle	Colon
40	chr13:95929000-95932800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr13:95929000-95932800	Weak transcription	Fetal Lung	lung
42	chr13:95929000-95933800	Weak transcription	Small Intestine	intestine
43	chr13:95929200-95932000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr13:95929200-95932000	Weak transcription	NHDF-Ad	bronchial
45	chr13:95929200-95932800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr13:95930600-95933200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:95930800-95932400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr13:95931000-95932000	Weak transcription	Left Ventricle	heart
49	chr13:95931000-95932000	Weak transcription	Right Atrium	heart
50	chr13:95931200-95932400	Enhancers	Spleen	Spleen

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