Variant report

Variant	nsv482881
Chromosome Location	chr8:20239114-20445136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1357)
CpG islands
(count:488)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:20271094-20271250	K562	blood:	n/a	n/a
2	ATF1	chr8:20309615-20309972	K562	blood:	n/a	n/a
3	ATF1	chr8:20367463-20367735	K562	blood:	n/a	n/a
4	ATF2	chr8:20315613-20316114	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:20292815-20293268	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr8:20367426-20367805	K562	blood:	n/a	n/a
7	ATF3	chr8:20400419-20400769	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:20315539-20316098	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:20292808-20293548	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:20400618-20400678	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:20365701-20366181	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:20293822-20293940	K562	blood:	n/a	n/a
13	BACH1	chr8:20407009-20407053	K562	blood:	n/a	n/a
14	BCL11A	chr8:20365827-20366138	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr8:20315722-20316039	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr8:20339842-20340593	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:20292863-20293219	K562	blood:	n/a	chr8:20293148-20293161
18	BHLHE40	chr8:20292812-20293407	GM12878	blood:	n/a	chr8:20293148-20293161
19	BHLHE40	chr8:20367345-20367789	K562	blood:	n/a	n/a
20	BHLHE40	chr8:20292859-20293117	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:20262423-20262701	HepG2	liver:	n/a	chr8:20262552-20262563
22	CEBPB	chr8:20317339-20317637	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:20366815-20367256	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:20311774-20311954	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:20270121-20270401	K562	blood:	n/a	chr8:20270244-20270255
26	CEBPB	chr8:20301425-20301715	Hela-S3	cervix:	n/a	chr8:20301566-20301579 chr8:20301567-20301578
27	CEBPB	chr8:20265870-20266037	HepG2	liver:	n/a	chr8:20265959-20265970
28	CEBPB	chr8:20285477-20285977	IMR90	lung:	n/a	chr8:20285559-20285570
29	CEBPB	chr8:20411692-20411981	HepG2	liver:	n/a	chr8:20411840-20411851
30	CEBPB	chr8:20266593-20267623	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr8:20301445-20301695	A549	lung:	n/a	chr8:20301566-20301579 chr8:20301567-20301578
32	CEBPB	chr8:20267248-20267513	K562	blood:	n/a	n/a
33	CEBPB	chr8:20319996-20320130	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:20292789-20293712	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr8:20262430-20262708	A549	lung:	n/a	chr8:20262552-20262563
36	CEBPB	chr8:20301564-20301743	K562	blood:	n/a	chr8:20301566-20301579 chr8:20301567-20301578
37	CEBPB	chr8:20266637-20267118	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr8:20400501-20400817	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:20317308-20317631	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:20269619-20270494	ECC-1	luminal epithelium:	n/a	chr8:20270244-20270255
41	CEBPB	chr8:20267290-20267516	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:20411676-20411954	IMR90	lung:	n/a	chr8:20411840-20411851
43	CEBPB	chr8:20317365-20317569	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:20288811-20288879	A549	lung:	n/a	n/a
45	CEBPB	chr8:20269865-20270462	ECC-1	luminal epithelium:	n/a	chr8:20270244-20270255
46	CEBPB	chr8:20270081-20270417	HepG2	liver:	n/a	chr8:20270244-20270255
47	CEBPB	chr8:20253328-20253540	HepG2	liver:	n/a	chr8:20253459-20253470
48	CEBPB	chr8:20292801-20293532	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr8:20301438-20301722	HepG2	liver:	n/a	chr8:20301566-20301579 chr8:20301567-20301578
50	CEBPB	chr8:20403973-20404127	HepG2	liver:	n/a	chr8:20404069-20404080 chr8:20404068-20404079

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20325457-20325507	HNPCEpiC	eye:	n/a
2	chr8:20316262-20316312	HRPEpiC	eye:	n/a
3	chr8:20316262-20316312	T-47D	breast:	n/a
4	chr8:20325457-20325507	PrEC	prostate:	n/a
5	chr8:20375578-20375628	HCF	heart:	n/a
6	chr8:20375300-20375350	HNPCEpiC	eye:	n/a
7	chr8:20350779-20350829	PANC-1	pancreas:	n/a
8	chr8:20299360-20299410	NH-A	brain:	n/a
9	chr8:20375300-20375350	HIPEpiC	eye:	n/a
10	chr8:20350779-20350829	ovcar-3	ovarian:	n/a
11	chr8:20299360-20299410	HEK293	kidney:	embryo
12	chr8:20314553-20314603	AG09319	gingival:	n/a
13	chr8:20375300-20375350	AG04450	lung:	fetal
14	chr8:20375300-20375350	NHBE	bronchial:	n/a
15	chr8:20350779-20350829	SK-N-SH	brain:	n/a
16	chr8:20316262-20316312	MCF10A-Er-Src	breast:	n/a
17	chr8:20293200-20293250	SKMC	muscle:	n/a
18	chr8:20314553-20314603	PANC-1	pancreas:	n/a
19	chr8:20316262-20316312	RPTEC	kidney:	n/a
20	chr8:20299360-20299410	GM12878	blood:	n/a
21	chr8:20325457-20325507	PFSK-1	brain:	n/a
22	chr8:20293200-20293250	AG04449	skin:	fetal
23	chr8:20314553-20314603	IMR90	lung:	fetal
24	chr8:20375300-20375350	AG04449	skin:	fetal
25	chr8:20316262-20316312	HAEpiC	amniotic membrane:	n/a
26	chr8:20350779-20350829	HCM	heart:	n/a
27	chr8:20375578-20375628	PFSK-1	brain:	n/a
28	chr8:20325457-20325507	GM19239	blood:	n/a
29	chr8:20375578-20375628	Caco-2	colon:	n/a
30	chr8:20293200-20293250	PANC-1	pancreas:	n/a
31	chr8:20375578-20375628	HMEC	breast:	n/a
32	chr8:20316262-20316312	Caco-2	colon:	n/a
33	chr8:20375300-20375350	PFSK-1	brain:	n/a
34	chr8:20325457-20325507	NHDF-neo	bronchial:	n/a
35	chr8:20375300-20375350	HRPEpiC	eye:	n/a
36	chr8:20375300-20375350	HRE	kidney:	n/a
37	chr8:20350779-20350829	HRPEpiC	eye:	n/a
38	chr8:20293200-20293250	BE2_C	brain:	n/a
39	chr8:20375578-20375628	PrEC	prostate:	n/a
40	chr8:20375300-20375350	SK-N-SH_RA	brain:	n/a
41	chr8:20375578-20375628	SK-N-SH	brain:	n/a
42	chr8:20325457-20325507	HEEpiC	esophagus:	n/a
43	chr8:20325457-20325507	AG10803	skin:	n/a
44	chr8:20299360-20299410	HepG2	liver:	n/a
45	chr8:20314553-20314603	HUVEC	blood vessel:	n/a
46	chr8:20375300-20375350	AG10803	skin:	n/a
47	chr8:20375578-20375628	HIPEpiC	eye:	n/a
48	chr8:20316262-20316312	U87	brain:	n/a
49	chr8:20325457-20325507	Caco-2	colon:	n/a
50	chr8:20316262-20316312	PANC-1	pancreas:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:20326837..20329294-chr8:20351798..20353854,2	K562	blood:
2	chr8:20400181..20400690-chr8:20854628..20855500,2	MCF-7	breast:
3	chr8:20407943..20410567-chr8:20412938..20415018,2	K562	blood:
4	chr8:20315158..20318143-chr8:20322413..20324006,2	K562	blood:
5	chr8:20441277..20443722-chr8:20449364..20451237,2	K562	blood:
6	chr8:20237063..20238741-chr8:20241384..20243460,2	MCF-7	breast:
7	chr8:20292679..20293278-chr8:20647078..20647630,2	MCF-7	breast:
8	chr8:20406914..20408549-chr8:20413495..20415864,2	K562	blood:
9	chr8:20315158..20318143-chr8:20322413..20324006,2	K562	blood:
10	chr8:20359613..20362385-chr8:20365022..20367728,2	K562	blood:
11	chr8:20359613..20362385-chr8:20365022..20367728,2	K562	blood:
12	chr8:20406914..20408549-chr8:20413495..20415864,2	K562	blood:
13	chr8:20292816..20293400-chr8:21763210..21764065,2	MCF-7	breast:
14	chr8:20326837..20329294-chr8:20351798..20353854,2	K562	blood:
15	chr3:64008815..64009393-chr8:20366564..20367344,2	MCF-7	breast:
16	chr8:20292913..20293496-chr8:21104301..21104905,3	MCF-7	breast:
17	chr8:20400252..20401136-chr8:20408626..20409143,2	MCF-7	breast:
18	chr8:20292611..20293286-chr8:21266630..21267414,2	MCF-7	breast:
19	chr8:20238473..20239020-chr8:20292504..20293024,2	MCF-7	breast:
20	chr8:20297170..20297886-chr8:20854968..20855533,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253178	TF binding region
ENSG00000253178	CpG island
ENSG00000163636	chromatin interactions
ENSG00000253178	chromatin interactions

Extended variants
information (count: 7733 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:7733 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145447477	chr8:20239152-20239153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530478903	chr8:20239158-20239159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189888307	chr8:20239170-20239171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576599872	chr8:20239261-20239262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111783210	chr8:20239277-20239278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146065454	chr8:20239282-20239283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528389563	chr8:20239289-20239290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181567112	chr8:20239291-20239292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555580755	chr8:20239324-20239325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186105250	chr8:20239349-20239350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191041924	chr8:20239374-20239375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550695746	chr8:20239375-20239376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369488842	chr8:20239408-20239409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56171374	chr8:20239430-20239431	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534126414	chr8:20239450-20239451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs118089905	chr8:20239457-20239458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567099205	chr8:20239458-20239459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534378059	chr8:20239478-20239479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570510473	chr8:20239509-20239510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538057141	chr8:20239527-20239528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180819501	chr8:20239585-20239586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186054376	chr8:20239592-20239593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556645282	chr8:20239608-20239609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556356512	chr8:20239631-20239632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553136332	chr8:20239654-20239655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574907687	chr8:20239657-20239658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191360289	chr8:20239664-20239665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370037700	chr8:20239694-20239695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560626269	chr8:20239713-20239714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4922178	chr8:20239760-20239761	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs79131538	chr8:20239776-20239777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4921708	chr8:20239811-20239812	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532259259	chr8:20239836-20239837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4922179	chr8:20239896-20239897	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569130126	chr8:20239910-20239911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530095419	chr8:20239918-20239919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548735391	chr8:20239928-20239929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182826961	chr8:20239956-20239957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372212705	chr8:20239993-20239994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188345065	chr8:20240003-20240004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190449051	chr8:20240006-20240007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538125209	chr8:20240038-20240039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183181833	chr8:20240057-20240058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574919304	chr8:20240106-20240107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535827560	chr8:20240110-20240111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554282373	chr8:20240113-20240114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114972832	chr8:20240151-20240152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116634828	chr8:20240158-20240159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142955374	chr8:20240216-20240217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377035897	chr8:20240235-20240236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20232400-20242600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:20234200-20239400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:20234800-20239400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr8:20236600-20245600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:20236800-20239200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:20236800-20239400	Weak transcription	NH-A	brain
7	chr8:20236800-20239800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr8:20237000-20239400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:20237000-20240600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:20238000-20239600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:20238400-20239400	Weak transcription	HSMM	muscle
12	chr8:20238400-20239400	Weak transcription	NHDF-Ad	bronchial
13	chr8:20238600-20239800	Weak transcription	HSMMtube	muscle
14	chr8:20238800-20239200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:20238800-20239600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:20239000-20239600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:20239000-20239800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:20239000-20240000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:20239000-20240200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:20239000-20240200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:20239000-20241000	Enhancers	HMEC	breast
22	chr8:20239000-20241400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:20239000-20241600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:20239200-20239800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr8:20239200-20241400	Enhancers	NHEK	skin
26	chr8:20239400-20239600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:20239400-20239800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:20239400-20240000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr8:20239400-20240200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr8:20239400-20240200	Enhancers	HSMM	muscle
31	chr8:20239400-20240200	Enhancers	NH-A	brain
32	chr8:20239400-20240200	Enhancers	NHDF-Ad	bronchial
33	chr8:20239600-20240400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:20239600-20241400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:20239800-20240200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:20239800-20240200	Enhancers	HSMMtube	muscle
37	chr8:20239800-20241200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr8:20240200-20241200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:20240400-20240600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:20240600-20241400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:20240600-20242200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:20241200-20241400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:20241200-20241600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr8:20241400-20241600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:20241400-20243400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:20242600-20242800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:20242600-20243000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:20242600-20243400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:20243400-20244800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:20244800-20245400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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