Variant report

Variant	nsv831261
Chromosome Location	chr8:20996095-21193619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:183)
Chromatin interactive
region (count:25)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:21032011-21032389	GM12878	blood:	n/a	n/a
2	ATF2	chr8:21039702-21040202	GM12878	blood:	n/a	n/a
3	ATF2	chr8:21039736-21040167	GM12878	blood:	n/a	n/a
4	BACH1	chr8:21178801-21179140	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:21035178-21035180	K562	blood:	n/a	n/a
6	BACH1	chr8:21180019-21180360	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:21110712-21110723	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:21039838-21040187	GM12878	blood:	n/a	n/a
9	BATF	chr8:21039791-21040093	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:21039822-21040106	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:21039777-21040139	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:21032090-21032306	GM12878	blood:	n/a	n/a
13	BCL3	chr8:21017339-21018243	GM12878	blood:	n/a	n/a
14	BCL3	chr8:21000353-21000601	GM12878	blood:	n/a	chr8:21000463-21000472 chr8:21000464-21000473
15	BCL3	chr8:21017363-21018430	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:21039870-21040070	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:21147859-21148117	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:21032073-21032327	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:21096295-21096298	K562	blood:	n/a	n/a
20	BRCA1	chr8:21121799-21121925	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr8:21176791-21176811	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:21066713-21066847	A549	lung:	n/a	n/a
23	CEBPB	chr8:21121465-21121795	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:21105229-21105433	A549	lung:	n/a	chr8:21105317-21105328
25	CEBPB	chr8:21105206-21105406	HepG2	liver:	n/a	chr8:21105317-21105328
26	CEBPB	chr8:21071950-21072152	IMR90	lung:	n/a	chr8:21072084-21072095
27	CEBPB	chr8:21157647-21157831	HepG2	liver:	n/a	chr8:21157782-21157793 chr8:21157781-21157794
28	CEBPB	chr8:21005690-21005742	HepG2	liver:	n/a	chr8:21005710-21005721
29	CEBPB	chr8:21105360-21105454	K562	blood:	n/a	n/a
30	CEBPB	chr8:21162597-21162745	K562	blood:	n/a	n/a
31	CEBPB	chr8:21073119-21073178	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:21121538-21121797	MCF-7	breast:	n/a	n/a
33	CEBPB	chr8:21154459-21154773	K562	blood:	n/a	chr8:21154624-21154635
34	CEBPB	chr8:21154472-21154769	HepG2	liver:	n/a	chr8:21154624-21154635
35	CEBPB	chr8:21157759-21157846	K562	blood:	n/a	chr8:21157782-21157793 chr8:21157781-21157794
36	CEBPB	chr8:21165823-21166012	HepG2	liver:	n/a	chr8:21165873-21165884
37	CEBPB	chr8:21084807-21085012	MCF-7	breast:	n/a	n/a
38	CEBPB	chr8:21071954-21072206	HepG2	liver:	n/a	chr8:21072084-21072095
39	CEBPB	chr8:21096322-21096357	K562	blood:	n/a	n/a
40	CHD1	chr8:21032115-21032389	GM12878	blood:	n/a	n/a
41	CREB1	chr8:21039817-21040281	GM12878	blood:	n/a	n/a
42	CREB1	chr8:21039816-21040284	GM12878	blood:	n/a	n/a
43	CTCF	chr8:21104480-21104630	K562	blood:	n/a	n/a
44	CTCF	chr8:21104384-21104544	ProgFib	skin:	n/a	chr8:21104455-21104476 chr8:21104460-21104478
45	CTCF	chr8:21104344-21104608	Pancreas_OC	pancreas:	n/a	chr8:21104455-21104476 chr8:21104460-21104478
46	CTCF	chr8:21104360-21104510	GM12873	blood:	n/a	chr8:21104455-21104476 chr8:21104460-21104478
47	CTCF	chr8:21033660-21033810	K562	blood:	n/a	chr8:21033724-21033742
48	CTCF	chr8:21078840-21078990	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr8:21104361-21104516	T-47D	breast:	n/a	chr8:21104455-21104476 chr8:21104460-21104478
50	CTCF	chr8:21104380-21104530	HEK293	kidney:	n/a	chr8:21104455-21104476 chr8:21104460-21104478

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:21155107-21155157	HepG2	liver:	n/a
2	chr8:21179380-21179430	K562	blood:	n/a
3	chr8:21155107-21155157	AG04450	lung:	fetal
4	chr8:21179380-21179430	NHDF-neo	bronchial:	n/a
5	chr8:21155258-21155308	A549	lung:	n/a
6	chr8:21179380-21179430	MCF-7	breast:	n/a
7	chr8:21179380-21179430	NH-A	brain:	n/a
8	chr8:21155107-21155157	NH-A	brain:	n/a
9	chr8:21155107-21155157	GM12878	blood:	n/a
10	chr8:21179380-21179430	Caco-2	colon:	n/a
11	chr8:21155258-21155308	HepG2	liver:	n/a
12	chr8:21155107-21155157	SKMC	muscle:	n/a
13	chr8:21179380-21179430	HEK293	kidney:	embryo
14	chr8:21155107-21155157	SAEC	small airway:	n/a
15	chr8:21155258-21155308	CMK	blood:	n/a
16	chr8:21179380-21179430	HL-60	blood:	n/a
17	chr8:21179380-21179430	IMR90	lung:	fetal
18	chr8:21155107-21155157	K562	blood:	n/a
19	chr8:21179380-21179430	HRCEpiC	kidney:	n/a
20	chr8:21179380-21179430	HCM	heart:	n/a
21	chr8:21179380-21179430	ECC-1	luminal epithelium:	n/a
22	chr8:21179380-21179430	T-47D	breast:	n/a
23	chr8:21155258-21155308	HCPEpiC	choroid plexus:	n/a
24	chr8:21155258-21155308	HUVEC	blood vessel:	n/a
25	chr8:21155107-21155157	HIPEpiC	eye:	n/a
26	chr8:21155107-21155157	SK-N-SH	brain:	n/a
27	chr8:21179380-21179430	Hepatocyte	liver:	n/a
28	chr8:21179380-21179430	SK-N-SH	brain:	n/a
29	chr8:21179380-21179430	CMK	blood:	n/a
30	chr8:21179380-21179430	HUVEC	blood vessel:	n/a
31	chr8:21179380-21179430	HRPEpiC	eye:	n/a
32	chr8:21155258-21155308	AG09309	skin:	n/a
33	chr8:21155107-21155157	Jurkat	blood:	n/a
34	chr8:21155107-21155157	NT2-D1	testis:	n/a
35	chr8:21155258-21155308	HCM	heart:	n/a
36	chr8:21155107-21155157	HAEpiC	amniotic membrane:	n/a
37	chr8:21155258-21155308	Hela-S3	cervix:	n/a
38	chr8:21155258-21155308	HL-60	blood:	n/a
39	chr8:21155107-21155157	Hepatocyte	liver:	n/a
40	chr8:21155258-21155308	ECC-1	luminal epithelium:	n/a
41	chr8:21155107-21155157	HUVEC	blood vessel:	n/a
42	chr8:21155258-21155308	NT2-D1	testis:	n/a
43	chr8:21155258-21155308	NB4	blood:	n/a
44	chr8:21155258-21155308	HEEpiC	esophagus:	n/a
45	chr8:21179380-21179430	GM12891	blood:	n/a
46	chr8:21179380-21179430	HCF	heart:	n/a
47	chr8:21155258-21155308	GM12878	blood:	n/a
48	chr8:21155107-21155157	HMEC	breast:	n/a
49	chr8:21179380-21179430	HCT-116	colon:	n/a
50	chr8:21155107-21155157	CMK	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:21000566..21002926-chr8:21006520..21008330,2	K562	blood:
2	chr8:20940533..20944455-chr8:21040696..21044387,3	K562	blood:
3	chr8:21121981..21124701-chr8:21143370..21145716,2	MCF-7	breast:
4	chr8:21046396..21048432-chr8:21052883..21055018,2	K562	blood:
5	chr8:21104851..21107287-chr8:21162749..21165665,2	K562	blood:
6	chr8:21046396..21048432-chr8:21052883..21055018,2	K562	blood:
7	chr8:21000646..21002417-chr8:21003581..21006297,2	K562	blood:
8	chr8:21085653..21087927-chr8:21091745..21093754,2	K562	blood:
9	chr8:21182356..21184212-chr8:21190773..21192966,2	K562	blood:
10	chr8:21182356..21184212-chr8:21190773..21192966,2	K562	blood:
11	chr8:21085653..21087927-chr8:21091745..21093754,2	K562	blood:
12	chr8:21113902..21115824-chr8:21182173..21184691,2	MCF-7	breast:
13	chr8:21000566..21002926-chr8:21006520..21008330,2	K562	blood:
14	chr8:21015073..21016879-chr8:21019625..21021848,2	K562	blood:
15	chr8:21000646..21002417-chr8:21003581..21006297,2	K562	blood:
16	chr8:21113902..21115824-chr8:21182173..21184691,2	MCF-7	breast:
17	chr8:20292913..20293496-chr8:21104301..21104905,3	MCF-7	breast:
18	chr8:21039519..21041986-chr8:21043567..21045082,2	K562	blood:
19	chr8:20898532..20899166-chr8:21104084..21105006,2	MCF-7	breast:
20	chr8:21015073..21016879-chr8:21019625..21021848,2	K562	blood:
21	chr8:21121981..21124701-chr8:21143370..21145716,2	MCF-7	breast:
22	chr8:21182410..21184426-chr8:21186846..21188480,2	MCF-7	breast:
23	chr8:21182410..21184426-chr8:21186846..21188480,2	MCF-7	breast:
24	chr8:21039519..21041986-chr8:21043567..21045082,2	K562	blood:
25	chr8:21104851..21107287-chr8:21162749..21165665,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XPO7-3	chr8:21165280-21166986	NONHSAT125426
2	lnc-XPO7-3	chr8:21165621-21166925	XLOC_006735
3	lnc-XPO7-3	chr8:21155709-21155918	NONHSAT125426
4	lnc-GFRA2-6	chr8:21030675-21030922	l_3557_chr8:20853997-20856467_brain
5	lnc-XPO7-3	chr8:21165281-21165685	ENSG00000254334
6	lnc-XPO7-3	chr8:21165281-21165404	XLOC_006735
7	lnc-XPO7-3	chr8:21155750-21155918	XLOC_006735
8	lnc-XPO7-3	chr8:21155717-21155918	ENSG00000254334
9	lnc-XPO7-3	chr8:21155710-21155918	XLOC_006735
10	lnc-XPO7-3	chr8:21165621-21166960	XLOC_006735

No data

Variant related genes	Relation type
ENSG00000215945	TF binding region
ENSG00000254334	TF binding region
ENSG00000215945	CpG island
ENSG00000254334	CpG island

Extended variants
information (count: 6075 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:6075 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576633983	chr8:20996116-20996117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143313791	chr8:20996123-20996124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562101316	chr8:20996160-20996161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529266390	chr8:20996182-20996183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185952714	chr8:20996183-20996184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370118504	chr8:20996199-20996200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559986823	chr8:20996216-20996217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116074941	chr8:20996268-20996269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201910922	chr8:20996271-20996272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549787557	chr8:20996273-20996274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374240814	chr8:20996275-20996276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111291823	chr8:20996279-20996280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1563920	chr8:20996414-20996415	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537562779	chr8:20996424-20996425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35255962	chr8:20996436-20996437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139040760	chr8:20996539-20996540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547060802	chr8:20996568-20996569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150051232	chr8:20996569-20996570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561355624	chr8:20996603-20996604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528813253	chr8:20996609-20996610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1563919	chr8:20996617-20996618	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs553819979	chr8:20996627-20996628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572312042	chr8:20996632-20996633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539328388	chr8:20996691-20996692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145415868	chr8:20996704-20996705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576290921	chr8:20996766-20996767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17495898	chr8:20996768-20996769	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs533015824	chr8:20996797-20996798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562160970	chr8:20996817-20996818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573992230	chr8:20996819-20996820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541425326	chr8:20996855-20996856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559441525	chr8:20996892-20996893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373728699	chr8:20996914-20996915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533699334	chr8:20996938-20996939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188718920	chr8:20996953-20996954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143563411	chr8:20996967-20996968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556558188	chr8:20996981-20996982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76693456	chr8:20996989-20996990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549509989	chr8:20997007-20997008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142508671	chr8:20997011-20997012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73625111	chr8:20997018-20997019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs76685469	chr8:20997028-20997029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185691291	chr8:20997029-20997030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147938958	chr8:20997044-20997045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558064095	chr8:20997046-20997047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569913384	chr8:20997052-20997053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537234210	chr8:20997064-20997065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141636753	chr8:20997077-20997078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190808676	chr8:20997093-20997094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541138052	chr8:20997116-20997117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Depressive disorder	21152026	CNVD

Chromatin state (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20988200-20996800	Weak transcription	Right Atrium	heart
2	chr8:20989000-20996600	Weak transcription	Placenta	Placenta
3	chr8:20995200-20996400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:20995400-20996600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:20995800-20996200	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:20995800-20996400	Enhancers	Fetal Brain Male	brain
7	chr8:20996000-20996200	Enhancers	Gastric	stomach
8	chr8:20996600-20997400	Enhancers	Placenta	Placenta
9	chr8:20996800-20997000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:20996800-20997000	Enhancers	Gastric	stomach
11	chr8:20996800-20997000	Enhancers	Right Atrium	heart
12	chr8:20996800-20997800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:20996800-21001400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:20997000-20998600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:20997400-20998600	Weak transcription	Placenta	Placenta
16	chr8:20998600-20999200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:20998600-21001200	Enhancers	Placenta	Placenta
18	chr8:20999200-21000400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:21000200-21000800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:21000200-21001200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr8:21000400-21001600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:21000400-21002000	Enhancers	Fetal Muscle Leg	muscle
23	chr8:21000800-21001200	Enhancers	HSMMtube	muscle
24	chr8:21000800-21001600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr8:21006800-21007000	Enhancers	Left Ventricle	heart
26	chr8:21007000-21011800	Weak transcription	Left Ventricle	heart
27	chr8:21016200-21017600	Enhancers	Fetal Brain Male	brain
28	chr8:21016400-21016800	Enhancers	Fetal Brain Female	brain
29	chr8:21017600-21021600	Weak transcription	Fetal Brain Male	brain
30	chr8:21019600-21020200	Active TSS	Spleen	Spleen
31	chr8:21020000-21027200	Enhancers	Fetal Intestine Small	intestine
32	chr8:21020200-21024000	Enhancers	Fetal Intestine Large	intestine
33	chr8:21020200-21026000	Weak transcription	Spleen	Spleen
34	chr8:21020600-21021800	Enhancers	Duodenum Mucosa	Duodenum
35	chr8:21020800-21024600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr8:21020800-21024800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr8:21020800-21025000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr8:21021000-21023600	Enhancers	Colonic Mucosa	Colon
39	chr8:21021400-21021800	Enhancers	Fetal Thymus	thymus
40	chr8:21021600-21023600	Enhancers	Fetal Brain Male	brain
41	chr8:21021600-21024000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:21021800-21022000	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr8:21021800-21022200	Weak transcription	Fetal Thymus	thymus
44	chr8:21021800-21024000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:21022000-21022400	Enhancers	Duodenum Mucosa	Duodenum
46	chr8:21022000-21024000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr8:21022200-21023600	Enhancers	Fetal Thymus	thymus
48	chr8:21022200-21024000	Enhancers	Primary hematopoietic stem cells	blood
49	chr8:21022400-21022600	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr8:21022400-21022600	Enhancers	Skeletal Muscle Male	skeletal muscle

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