Variant report

Variant	nsv965139
Chromosome Location	chr3:195501325-195532219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:735)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195521828-195521896	K562	blood:	n/a	n/a
2	ARID3A	chr3:195530436-195530636	K562	blood:	n/a	n/a
3	ATF1	chr3:195527177-195527509	K562	blood:	n/a	n/a
4	ATF1	chr3:195517590-195517626	K562	blood:	n/a	n/a
5	ATF1	chr3:195531177-195532030	K562	blood:	n/a	n/a
6	ATF1	chr3:195517896-195518212	K562	blood:	n/a	n/a
7	BACH1	chr3:195512434-195512617	K562	blood:	n/a	n/a
8	BCL3	chr3:195527151-195527346	GM12878	blood:	n/a	n/a
9	BCL3	chr3:195527158-195527378	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:195512394-195512523	K562	blood:	n/a	n/a
11	BHLHE40	chr3:195521552-195521978	K562	blood:	n/a	chr3:195521722-195521743
12	BHLHE40	chr3:195530146-195530623	K562	blood:	n/a	n/a
13	BHLHE40	chr3:195501927-195502072	K562	blood:	n/a	n/a
14	BHLHE40	chr3:195529712-195529918	K562	blood:	n/a	n/a
15	BHLHE40	chr3:195531122-195531942	K562	blood:	n/a	n/a
16	CBX3	chr3:195507933-195508534	K562	blood:	n/a	n/a
17	CBX3	chr3:195501858-195502087	K562	blood:	n/a	n/a
18	CBX3	chr3:195531000-195532010	K562	blood:	n/a	n/a
19	CBX3	chr3:195512268-195513029	K562	blood:	n/a	n/a
20	CBX3	chr3:195501809-195502166	K562	blood:	n/a	n/a
21	CBX3	chr3:195530307-195530768	K562	blood:	n/a	n/a
22	CCNT2	chr3:195531224-195531783	K562	blood:	n/a	n/a
23	CEBPB	chr3:195527223-195527548	K562	blood:	n/a	n/a
24	CEBPB	chr3:195527231-195527517	K562	blood:	n/a	n/a
25	CEBPB	chr3:195527239-195527419	K562	blood:	n/a	n/a
26	CREB1	chr3:195517759-195518266	GM12878	blood:	n/a	n/a
27	CREB1	chr3:195517691-195518194	GM12878	blood:	n/a	n/a
28	CTCF	chr3:195501920-195502070	HCPEpiC	choroid plexus:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
29	CTCF	chr3:195501920-195502070	Caco-2	colon:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
30	CTCF	chr3:195501878-195502128	LNCaP	prostate:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
31	CTCF	chr3:195501900-195502050	AoAF	blood vessel:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
32	CTCF	chr3:195501960-195502110	HRE	kidney:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
33	CTCF	chr3:195501935-195502044	GM19239	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
34	CTCF	chr3:195525860-195526010	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:195501900-195502050	GM06990	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
36	CTCF	chr3:195501800-195502070	GM12872	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
37	CTCF	chr3:195501900-195502050	GM12871	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
38	CTCF	chr3:195501940-195502090	GM12869	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
39	CTCF	chr3:195501889-195502113	MCF-7	breast:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
40	CTCF	chr3:195501890-195502057	Lung_OC	lung:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
41	CTCF	chr3:195516160-195516310	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:195501940-195502090	HCM	heart:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
43	CTCF	chr3:195501940-195502090	NHDF-neo	bronchial:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
44	CTCF	chr3:195501815-195502161	IMR90	lung:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
45	CTCF	chr3:195501948-195502083	GM13976	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
46	CTCF	chr3:195501900-195502050	AG04449	skin:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
47	CTCF	chr3:195501910-195502085	MCF-7	breast:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
48	CTCF	chr3:195501960-195502110	AG09309	skin:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
49	CTCF	chr3:195501915-195502076	GM13977	blood:	n/a	chr3:195501982-195502000 chr3:195501984-195501997
50	CTCF	chr3:195501909-195502110	HepG2	liver:	n/a	chr3:195501982-195502000 chr3:195501984-195501997

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195530091-195530141	CMK	blood:	n/a
2	chr3:195531633-195531683	MCF-7	breast:	n/a
3	chr3:195531633-195531683	GM12892	blood:	n/a
4	chr3:195530091-195530141	CMK	blood:	n/a
5	chr3:195531633-195531683	MCF-7	breast:	n/a
6	chr3:195531633-195531683	GM12892	blood:	n/a
7	chr3:195530091-195530141	A549	lung:	n/a
8	chr3:195530133-195530183	GM12891	blood:	n/a
9	chr3:195530532-195530582	HMEC	breast:	n/a
10	chr3:195528619-195528669	HEEpiC	esophagus:	n/a
11	chr3:195530091-195530141	AoSMC	blood vessel:	n/a
12	chr3:195530133-195530183	SKMC	muscle:	n/a
13	chr3:195530654-195530704	PrEC	prostate:	n/a
14	chr3:195530091-195530141	BE2_C	brain:	n/a
15	chr3:195516738-195516788	HRCEpiC	kidney:	n/a
16	chr3:195530133-195530183	SK-N-SH	brain:	n/a
17	chr3:195530151-195530201	HAEpiC	amniotic membrane:	n/a
18	chr3:195530091-195530141	Caco-2	colon:	n/a
19	chr3:195530654-195530704	CMK	blood:	n/a
20	chr3:195516738-195516788	SK-N-MC	brain:	n/a
21	chr3:195530133-195530183	A549	lung:	n/a
22	chr3:195530133-195530183	HIPEpiC	eye:	n/a
23	chr3:195516738-195516788	ovcar-3	ovarian:	n/a
24	chr3:195516738-195516788	H1-hESC	embryonic stem cell:	embryo
25	chr3:195530151-195530201	A549	lung:	n/a
26	chr3:195530091-195530141	SK-N-SH_RA	brain:	n/a
27	chr3:195528619-195528669	NH-A	brain:	n/a
28	chr3:195530532-195530582	HEK293	kidney:	embryo
29	chr3:195516738-195516788	AG04450	lung:	fetal
30	chr3:195530133-195530183	HepG2	liver:	n/a
31	chr3:195528709-195528759	AG04450	lung:	fetal
32	chr3:195528619-195528669	PFSK-1	brain:	n/a
33	chr3:195531633-195531683	U87	brain:	n/a
34	chr3:195531298-195531348	HRPEpiC	eye:	n/a
35	chr3:195530654-195530704	HUVEC	blood vessel:	n/a
36	chr3:195530151-195530201	RPTEC	kidney:	n/a
37	chr3:195528460-195528510	HMEC	breast:	n/a
38	chr3:195529779-195529829	ECC-1	luminal epithelium:	n/a
39	chr3:195528460-195528510	SKMC	muscle:	n/a
40	chr3:195528619-195528669	CMK	blood:	n/a
41	chr3:195530532-195530582	HRE	kidney:	n/a
42	chr3:195530532-195530582	Jurkat	blood:	n/a
43	chr3:195531633-195531683	AG10803	skin:	n/a
44	chr3:195530151-195530201	IMR90	lung:	fetal
45	chr3:195516738-195516788	AG10803	skin:	n/a
46	chr3:195530091-195530141	SK-N-MC	brain:	n/a
47	chr3:195528460-195528510	SK-N-MC	brain:	n/a
48	chr3:195530532-195530582	ProgFib	skin:	n/a
49	chr3:195531298-195531348	HL-60	blood:	n/a
50	chr3:195530133-195530183	MCF-7	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195515076..195517287-chr3:195520045..195522414,2	MCF-7	breast:
2	chr3:195491017..195492648-chr3:195498441..195501399,2	MCF-7	breast:
3	chr3:195523794..195527143-chr3:195528140..195531252,3	MCF-7	breast:
4	chr3:195527832..195530110-chr3:195530818..195533509,2	K562	blood:
5	chr3:195515568..195518880-chr3:195520246..195523689,5	K562	blood:
6	chr3:64008802..64009744-chr3:195515964..195516596,2	MCF-7	breast:
7	chr3:195529866..195531889-chr3:195572578..195574552,2	MCF-7	breast:
8	chr3:195425420..195427950-chr3:195516747..195519415,2	K562	blood:
9	chr3:195520611..195522344-chr3:195574856..195577689,2	K562	blood:
10	chr3:195513116..195515414-chr3:195528175..195530294,2	K562	blood:
11	chr3:195513116..195515414-chr3:195528175..195530294,2	K562	blood:
12	chr3:195530953..195533764-chr3:195541586..195543592,2	MCF-7	breast:
13	chr3:195523728..195527160-chr3:195528335..195531835,4	MCF-7	breast:
14	chr3:195528182..195532092-chr3:195536465..195539276,3	MCF-7	breast:
15	chr3:195530055..195532719-chr3:195534968..195537902,2	MCF-7	breast:
16	chr3:195526679..195529067-chr3:195608126..195610477,2	K562	blood:
17	chr3:195523728..195527160-chr3:195528335..195531835,4	MCF-7	breast:
18	chr3:195515076..195517287-chr3:195520045..195522414,2	MCF-7	breast:
19	chr3:195495303..195497609-chr3:195498505..195502105,3	K562	blood:
20	chr3:195501485..195501996-chr3:195577440..195578360,2	K562	blood:
21	chr3:195523794..195527143-chr3:195528140..195531252,3	MCF-7	breast:
22	chr3:195515568..195518880-chr3:195520246..195523689,5	K562	blood:
23	chr3:195520506..195523672-chr3:195528245..195532035,4	K562	blood:
24	chr3:195529532..195531767-chr3:195548783..195551735,2	K562	blood:
25	chr3:195520257..195522111-chr3:195576189..195578344,2	K562	blood:
26	chr3:195527832..195530110-chr3:195530818..195533509,2	K562	blood:
27	chr3:195520506..195523672-chr3:195528245..195532035,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-11	chr3:195501684-195504220	l_2562_chr3:195497235-195506506_ovary
2	lnc-TNK2-10	chr3:195505666-195505928	NONHSAT094250
3	lnc-TNK2-11	chr3:195513084-195513287	l_2562_chr3:195497235-195506506_ovary
4	lnc-TNK2-11	chr3:195506240-195506583	l_2562_chr3:195497235-195506506_ovary

No data

Variant related genes	Relation type
MUC4	TF binding region
MUC4	CpG island
ENSG00000163636	chromatin interactions
ENSG00000207650	chromatin interactions
ENSG00000145113	chromatin interactions
ENSG00000242086	chromatin interactions

Extended variants
information (count: 3114 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3114 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545412586	chr3:195501351-195501352	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs116414129	chr3:195501389-195501390	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs55933155	chr3:195501414-195501415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs549493125	chr3:195501440-195501441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553343507	chr3:195501460-195501461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117432958	chr3:195501482-195501483	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7637496	chr3:195501500-195501501	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549036402	chr3:195501511-195501512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568924972	chr3:195501522-195501523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574988351	chr3:195501568-195501569	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs140857701	chr3:195501614-195501615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539386905	chr3:195501628-195501629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557325948	chr3:195501648-195501649	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182335415	chr3:195501655-195501656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373305175	chr3:195501657-195501658	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542508829	chr3:195501727-195501728	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs564383425	chr3:195501758-195501759	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs112114439	chr3:195501772-195501773	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs10666795	chr3:195501773-195501774	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs397950030	chr3:195501789-195501790	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs73205733	chr3:195501793-195501794	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541599946	chr3:195501825-195501826	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs186659805	chr3:195501882-195501883	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs578249473	chr3:195501906-195501907	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs190334224	chr3:195501908-195501909	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs2550251	chr3:195501938-195501939	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530903673	chr3:195501942-195501943	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs183115496	chr3:195501945-195501946	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs188200501	chr3:195501946-195501947	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs528585000	chr3:195501951-195501952	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs74510888	chr3:195501975-195501976	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs115474681	chr3:195501976-195501977	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs533032825	chr3:195501984-195501985	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs370708842	chr3:195502045-195502046	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs147768940	chr3:195502070-195502071	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs537021232	chr3:195502098-195502099	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs403544	chr3:195502106-195502107	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs548703195	chr3:195502116-195502117	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs567346555	chr3:195502120-195502121	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs534757461	chr3:195502132-195502133	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs112109766	chr3:195502148-195502149	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs114220016	chr3:195502169-195502170	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs114973310	chr3:195502170-195502171	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs539254132	chr3:195502184-195502185	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs192980792	chr3:195502189-195502190	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs72596503	chr3:195502203-195502204	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs11416201	chr3:195502204-195502205	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs112482238	chr3:195502205-195502206	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs72499646	chr3:195502209-195502210	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs72499647	chr3:195502221-195502222	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195484600-195507800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:195485000-195517200	Weak transcription	Right Atrium	heart
3	chr3:195490000-195502600	Strong transcription	Rectal Mucosa Donor 31	rectum
4	chr3:195493400-195502200	Strong transcription	Colonic Mucosa	Colon
5	chr3:195494400-195510800	Weak transcription	Gastric	stomach
6	chr3:195496600-195505000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr3:195496600-195510800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:195497400-195505000	Weak transcription	Spleen	Spleen
9	chr3:195497800-195505000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:195499000-195504800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:195499400-195505400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:195500200-195501400	Strong transcription	Placenta Amnion	Placenta Amnion
13	chr3:195500600-195502600	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr3:195501000-195502600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:195501400-195510800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr3:195501600-195502200	Enhancers	Fetal Muscle Trunk	muscle
17	chr3:195501800-195502200	Enhancers	Fetal Muscle Leg	muscle
18	chr3:195502200-195504800	Weak transcription	Colonic Mucosa	Colon
19	chr3:195502600-195502800	Enhancers	Pancreas	Pancrea
20	chr3:195502600-195503000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr3:195502600-195503000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:195502600-195503000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
23	chr3:195502600-195503000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
24	chr3:195502600-195503600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr3:195502800-195507600	Weak transcription	Pancreas	Pancrea
26	chr3:195503000-195504800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr3:195503000-195504800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr3:195503000-195505000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:195503000-195528800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr3:195503600-195511000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr3:195504800-195505000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:195504800-195505200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
33	chr3:195504800-195505200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
34	chr3:195504800-195505800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:195504800-195505800	ZNF genes & repeats	Colonic Mucosa	Colon
36	chr3:195505000-195505200	Bivalent Enhancer	Right Ventricle	heart
37	chr3:195505000-195505200	Flanking Active TSS	Spleen	Spleen
38	chr3:195505000-195505600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
39	chr3:195505000-195505800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:195505000-195506200	Strong transcription	Rectal Smooth Muscle	rectum
41	chr3:195505200-195505600	Active TSS	Spleen	Spleen
42	chr3:195505200-195505800	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr3:195505200-195513200	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr3:195505400-195505600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
45	chr3:195505600-195507200	Weak transcription	Spleen	Spleen
46	chr3:195505600-195513400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:195505600-195513400	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr3:195505600-195532200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr3:195505800-195507000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:195505800-195507200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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