Variant report

Variant	nsv1044162
Chromosome Location	chr13:95936858-96032829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1712)
CpG islands
(count:732)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95937866-95938402	K562	blood:	n/a	n/a
3	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
6	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
7	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
9	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
10	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
11	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
12	ATF1	chr13:95938012-95938442	K562	blood:	n/a	n/a
13	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
14	ATF3	chr13:95938112-95938426	K562	blood:	n/a	n/a
15	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
18	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
20	BCLAF1	chr13:95937861-95938393	K562	blood:	n/a	n/a
21	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
22	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
23	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
25	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
26	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
27	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
28	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
29	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
30	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
31	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
32	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
33	BHLHE40	chr13:95937918-95938449	K562	blood:	n/a	n/a
34	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
35	BRCA1	chr13:95953565-95953620	HepG2	liver:	n/a	n/a
36	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr13:95938077-95938390	K562	blood:	n/a	n/a
43	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
44	CBX3	chr13:95937978-95938484	K562	blood:	n/a	n/a
45	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
46	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a
47	CCNT2	chr13:95949924-95950191	K562	blood:	n/a	n/a
48	CCNT2	chr13:95938000-95938463	K562	blood:	n/a	n/a
49	CCNT2	chr13:95952980-95954262	K562	blood:	n/a	n/a
50	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95954534-95954584	HNPCEpiC	eye:	n/a
2	chr13:95952902-95952952	SKMC	muscle:	n/a
3	chr13:95953941-95953991	HCM	heart:	n/a
4	chr13:95954534-95954584	AG10803	skin:	n/a
5	chr13:95958190-95958240	NH-A	brain:	n/a
6	chr13:95953941-95953991	IMR90	lung:	fetal
7	chr13:95952902-95952952	A549	lung:	n/a
8	chr13:95958190-95958240	HCPEpiC	choroid plexus:	n/a
9	chr13:96008021-96008071	HCT-116	colon:	n/a
10	chr13:95954382-95954432	AG10803	skin:	n/a
11	chr13:95953574-95953624	ovcar-3	ovarian:	n/a
12	chr13:95953229-95953279	H1-hESC	embryonic stem cell:	embryo
13	chr13:95954080-95954130	HMEC	breast:	n/a
14	chr13:95953505-95953555	GM19239	blood:	n/a
15	chr13:95954534-95954584	MCF-7	breast:	n/a
16	chr13:95953229-95953279	BE2_C	brain:	n/a
17	chr13:95953229-95953279	ovcar-3	ovarian:	n/a
18	chr13:95958190-95958240	AG09319	gingival:	n/a
19	chr13:95952902-95952952	AG09319	gingival:	n/a
20	chr13:95953229-95953279	HNPCEpiC	eye:	n/a
21	chr13:95953941-95953991	NH-A	brain:	n/a
22	chr13:95953229-95953279	SAEC	small airway:	n/a
23	chr13:95953941-95953991	ProgFib	skin:	n/a
24	chr13:95952937-95952987	NHDF-neo	bronchial:	n/a
25	chr13:95954080-95954130	T-47D	breast:	n/a
26	chr13:95953482-95953532	HUVEC	blood vessel:	n/a
27	chr13:95953229-95953279	NHDF-neo	bronchial:	n/a
28	chr13:95954382-95954432	GM12891	blood:	n/a
29	chr13:95953482-95953532	HRPEpiC	eye:	n/a
30	chr13:95954080-95954130	GM12878	blood:	n/a
31	chr13:95958190-95958240	AG04449	skin:	fetal
32	chr13:95954534-95954584	HCT-116	colon:	n/a
33	chr13:95952902-95952952	GM06990	blood:	n/a
34	chr13:95958190-95958240	AoSMC	blood vessel:	n/a
35	chr13:95958190-95958240	AG09309	skin:	n/a
36	chr13:95952937-95952987	HepG2	liver:	n/a
37	chr13:95954080-95954130	H1-hESC	embryonic stem cell:	embryo
38	chr13:95954080-95954130	SKMC	muscle:	n/a
39	chr13:95952937-95952987	GM06990	blood:	n/a
40	chr13:95953574-95953624	PANC-1	pancreas:	n/a
41	chr13:95953941-95953991	AoSMC	blood vessel:	n/a
42	chr13:95953229-95953279	HL-60	blood:	n/a
43	chr13:95952937-95952987	BJ	skin:	n/a
44	chr13:95958190-95958240	HPAEpiC	pulmonary alveolar:	n/a
45	chr13:95954534-95954584	PANC-1	pancreas:	n/a
46	chr13:95953482-95953532	AG04449	skin:	fetal
47	chr13:95952902-95952952	K562	blood:	n/a
48	chr13:95953505-95953555	HCF	heart:	n/a
49	chr13:95954534-95954584	AG04450	lung:	fetal
50	chr13:95953505-95953555	MCF-7	breast:	n/a

(count:29 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 3612 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3612 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7983813	chr13:95936858-95936859	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151103479	chr13:95936922-95936923	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544754814	chr13:95936982-95936983	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76896328	chr13:95937000-95937001	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540049675	chr13:95937004-95937005	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182067248	chr13:95937035-95937036	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575033143	chr13:95937122-95937123	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7986283	chr13:95937149-95937150	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs113039840	chr13:95937159-95937160	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201029179	chr13:95937160-95937161	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575744941	chr13:95937241-95937242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28627636	chr13:95937245-95937246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111614862	chr13:95937372-95937373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112675015	chr13:95937451-95937452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542919017	chr13:95937487-95937488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545871249	chr13:95937496-95937497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562678175	chr13:95937502-95937503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531708855	chr13:95937530-95937531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28702918	chr13:95937543-95937544	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546134534	chr13:95937576-95937577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543618798	chr13:95937587-95937588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567356353	chr13:95937590-95937591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562750138	chr13:95937624-95937625	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562928877	chr13:95937672-95937673	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531845679	chr13:95937673-95937674	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542387342	chr13:95937705-95937706	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7996539	chr13:95937763-95937764	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527716895	chr13:95937791-95937792	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547749613	chr13:95937825-95937826	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186653027	chr13:95937838-95937839	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144957378	chr13:95937895-95937896	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375113200	chr13:95937959-95937960	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142104582	chr13:95937961-95937962	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377595107	chr13:95937967-95937968	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535170575	chr13:95938003-95938004	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs555079783	chr13:95938008-95938009	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372836147	chr13:95938009-95938010	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs145864210	chr13:95938013-95938014	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs377209197	chr13:95938037-95938038	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs566450707	chr13:95938048-95938049	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs192436756	chr13:95938077-95938078	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11619105	chr13:95938082-95938083	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114752229	chr13:95938113-95938114	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs577879545	chr13:95938169-95938170	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs72645817	chr13:95938172-95938173	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs183832948	chr13:95938190-95938191	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs370919246	chr13:95938191-95938192	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138695171	chr13:95938222-95938223	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs375880052	chr13:95938223-95938224	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7328426	chr13:95938256-95938257	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
2	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr13:95926600-95952400	Weak transcription	Brain Hippocampus Middle	brain
5	chr13:95926800-95948600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:95927000-95937800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr13:95927000-95938000	Weak transcription	Colonic Mucosa	Colon
8	chr13:95927200-95941600	Weak transcription	Gastric	stomach
9	chr13:95928400-95937600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr13:95928400-95937800	Weak transcription	Fetal Intestine Small	intestine
11	chr13:95932200-95937600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr13:95932400-95939200	Weak transcription	Left Ventricle	heart
13	chr13:95932600-95938000	Weak transcription	Right Atrium	heart
14	chr13:95932600-95939200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:95933000-95952600	Weak transcription	Primary T cells from cord blood	blood
16	chr13:95933200-95937800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr13:95933400-95937600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr13:95933400-95952600	Weak transcription	Fetal Stomach	stomach
19	chr13:95933600-95937800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr13:95933600-95951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:95933800-95938000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:95933800-95938000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr13:95933800-95938200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr13:95933800-95941800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr13:95933800-95952400	Weak transcription	HSMM	muscle
26	chr13:95933800-95952400	Weak transcription	NHDF-Ad	bronchial
27	chr13:95934000-95937800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:95934000-95937800	Weak transcription	Colon Smooth Muscle	Colon
29	chr13:95934000-95941000	Weak transcription	HUVEC	blood vessel
30	chr13:95934000-95941400	Weak transcription	Fetal Kidney	kidney
31	chr13:95934000-95941600	Weak transcription	A549	lung
32	chr13:95934000-95949600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr13:95934000-95951600	Weak transcription	Osteobl	bone
34	chr13:95934200-95937800	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr13:95934200-95938000	Weak transcription	Psoas Muscle	Psoas
36	chr13:95934200-95941600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr13:95934600-95943600	Weak transcription	NHLF	lung
38	chr13:95934800-95937200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr13:95935200-95937600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr13:95935400-95949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:95936400-95938000	Enhancers	GM12878-XiMat	blood
42	chr13:95936600-95937000	Genic enhancers	K562	blood
43	chr13:95936600-95937600	Enhancers	Lung	lung
44	chr13:95937000-95938000	Enhancers	K562	blood
45	chr13:95937200-95937600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr13:95937400-95938400	Enhancers	Stomach Smooth Muscle	stomach
47	chr13:95937600-95938200	Enhancers	Brain Substantia Nigra	brain
48	chr13:95937600-95938400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr13:95937600-95939000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr13:95937600-95939000	Enhancers	Primary B cells from peripheral blood	blood

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