Variant report

Variant	nsv981911
Chromosome Location	chr8:11829748-11842047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
2	CHD2	chr8:11832848-11832898	K562	blood:	n/a	n/a
3	CTCF	chr8:11839760-11839910	HAc	cerebellar:	n/a	n/a
4	CTCF	chr8:11839720-11839870	HMEC	breast:	n/a	n/a
5	CTCF	chr8:11839720-11839870	HEK293	kidney:	n/a	n/a
6	CTCF	chr8:11839740-11839890	HMF	breast:	n/a	n/a
7	CTCF	chr8:11839680-11839830	HCT-116	colon:	n/a	n/a
8	CTCF	chr8:11839880-11840030	HCT-116	colon:	n/a	n/a
9	CTCF	chr8:11839720-11839870	NHEK	skin:	n/a	n/a
10	CTCF	chr8:11839700-11839850	HMF	breast:	n/a	n/a
11	CTCF	chr8:11839680-11839830	HCFaa	heart:	n/a	n/a
12	CTCF	chr8:11839700-11839850	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr8:11839660-11839810	HCM	heart:	n/a	n/a
14	CTCF	chr8:11830382-11830448	Fibrobl	skin:	n/a	n/a
15	EGR1	chr8:11835901-11836136	K562	blood:	n/a	n/a
16	EP300	chr8:11831065-11832276	SK-N-SH	brain:	n/a	n/a
17	EP300	chr8:11831651-11831974	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr8:11831667-11831947	SK-N-SH_RA	brain:	n/a	n/a
19	FOS	chr8:11839269-11839318	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr8:11839614-11839964	MCF10A-Er-Src	breast:	n/a	chr8:11839795-11839806 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
21	FOS	chr8:11839614-11839974	MCF10A-Er-Src	breast:	n/a	chr8:11839795-11839806 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
22	FOS	chr8:11839617-11839987	MCF10A-Er-Src	breast:	n/a	chr8:11839795-11839806 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
23	FOSL1	chr8:11839663-11839916	K562	blood:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
24	FOSL1	chr8:11839483-11840130	HCT-116	colon:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
25	FOSL1	chr8:11839667-11839878	K562	blood:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
26	FOSL1	chr8:11839387-11840182	HCT-116	colon:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
27	FOSL2	chr8:11839636-11839894	HepG2	liver:	n/a	chr8:11839795-11839806 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
28	GATA2	chr8:11831138-11832186	SH-SY5Y	brain:	n/a	chr8:11831735-11831756 chr8:11831743-11831760
29	GATA3	chr8:11831205-11832071	SH-SY5Y	brain:	n/a	chr8:11831735-11831756 chr8:11831743-11831760
30	GATA3	chr8:11831473-11832019	SK-N-SH	brain:	n/a	chr8:11831735-11831756 chr8:11831743-11831760
31	GATA3	chr8:11836301-11836350	SH-SY5Y	brain:	n/a	n/a
32	JUND	chr8:11839435-11840197	HCT-116	colon:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
33	JUND	chr8:11839655-11839947	HepG2	liver:	n/a	chr8:11839795-11839806 chr8:11839797-11839808 chr8:11839798-11839807 chr8:11839820-11839829 chr8:11839799-11839808
34	MAFK	chr8:11837109-11837133	HepG2	liver:	n/a	n/a
35	MAX	chr8:11839426-11840169	HCT-116	colon:	n/a	chr8:11839798-11839807
36	MAX	chr8:11839640-11839906	K562	blood:	n/a	chr8:11839798-11839807
37	MAZ	chr8:11837159-11837243	HepG2	liver:	n/a	n/a
38	MXI1	chr8:11836671-11836683	K562	blood:	n/a	n/a
39	MYC	chr8:11839624-11839939	MCF10A-Er-Src	breast:	n/a	chr8:11839798-11839807
40	MYC	chr8:11840430-11840466	NB4	blood:	n/a	n/a
41	MYC	chr8:11839656-11839939	MCF10A-Er-Src	breast:	n/a	chr8:11839798-11839807
42	MYC	chr8:11835048-11835095	GM12878	blood:	n/a	n/a
43	MYC	chr8:11831455-11831468	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr8:11840750-11840878	H1-hESC	embryonic stem cell:	n/a	n/a
45	REST	chr8:11831627-11831935	SK-N-SH	brain:	n/a	chr8:11831877-11831895 chr8:11831850-11831863
46	SPI1	chr8:11836858-11837086	GM12891	blood:	n/a	n/a
47	STAT3	chr8:11836058-11836237	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr8:11841689-11841851	MCF10A-Er-Src	breast:	n/a	n/a
49	TCF7L2	chr8:11839565-11839966	HCT-116	colon:	n/a	chr8:11839798-11839807
50	YY1	chr8:11839631-11839899	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11839780-11839830	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:11832261-11832311	ProgFib	skin:	n/a
3	chr8:11839844-11839894	BJ	skin:	n/a
4	chr8:11839780-11839830	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:11832261-11832311	ProgFib	skin:	n/a
6	chr8:11839844-11839894	BJ	skin:	n/a
7	chr8:11839138-11839188	NB4	blood:	n/a
8	chr8:11839138-11839188	GM06990	blood:	n/a
9	chr8:11839764-11839814	BJ	skin:	n/a
10	chr8:11838843-11838893	K562	blood:	n/a
11	chr8:11835607-11835657	LNCaP	prostate:	n/a
12	chr8:11839138-11839188	HAEpiC	amniotic membrane:	n/a
13	chr8:11833039-11833089	AG09309	skin:	n/a
14	chr8:11841980-11842030	ovcar-3	ovarian:	n/a
15	chr8:11832261-11832311	HMEC	breast:	n/a
16	chr8:11838532-11838582	HCT-116	colon:	n/a
17	chr8:11833039-11833089	K562	blood:	n/a
18	chr8:11832039-11832089	HRE	kidney:	n/a
19	chr8:11833039-11833089	IMR90	lung:	fetal
20	chr8:11833039-11833089	MCF-7	breast:	n/a
21	chr8:11835607-11835657	AG10803	skin:	n/a
22	chr8:11839844-11839894	AG10803	skin:	n/a
23	chr8:11839138-11839188	AG04449	skin:	fetal
24	chr8:11839844-11839894	HL-60	blood:	n/a
25	chr8:11839780-11839830	HEEpiC	esophagus:	n/a
26	chr8:11831823-11831873	PrEC	prostate:	n/a
27	chr8:11835607-11835657	ovcar-3	ovarian:	n/a
28	chr8:11833191-11833241	GM06990	blood:	n/a
29	chr8:11831823-11831873	RPTEC	kidney:	n/a
30	chr8:11832261-11832311	H1-hESC	embryonic stem cell:	embryo
31	chr8:11841980-11842030	NT2-D1	testis:	n/a
32	chr8:11832565-11832615	T-47D	breast:	n/a
33	chr8:11839844-11839894	HNPCEpiC	eye:	n/a
34	chr8:11838532-11838582	HCPEpiC	choroid plexus:	n/a
35	chr8:11833039-11833089	HEK293	kidney:	embryo
36	chr8:11838532-11838582	SAEC	small airway:	n/a
37	chr8:11832565-11832615	AG09319	gingival:	n/a
38	chr8:11839844-11839894	U87	brain:	n/a
39	chr8:11838843-11838893	NH-A	brain:	n/a
40	chr8:11841980-11842030	LNCaP	prostate:	n/a
41	chr8:11838532-11838582	SK-N-MC	brain:	n/a
42	chr8:11832039-11832089	AG09319	gingival:	n/a
43	chr8:11839764-11839814	HAEpiC	amniotic membrane:	n/a
44	chr8:11839764-11839814	GM19239	blood:	n/a
45	chr8:11835607-11835657	Hepatocyte	liver:	n/a
46	chr8:11832261-11832311	HRE	kidney:	n/a
47	chr8:11841980-11842030	HCF	heart:	n/a
48	chr8:11838843-11838893	NHDF-neo	bronchial:	n/a
49	chr8:11838843-11838893	Hela-S3	cervix:	n/a
50	chr8:11841980-11842030	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
2	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
3	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
4	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
5	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
6	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
7	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
8	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:

Variant related genes	Relation type
DEFB136	TF binding region
DEFB135	TF binding region
DEFB136	CpG island
DEFB135	CpG island
ENSG00000205884	chromatin interactions

Extended variants
information (count: 704 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190157592	chr8:11829781-11829782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569927606	chr8:11829804-11829805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12550755	chr8:11829874-11829875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs59216436	chr8:11829877-11829878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6422372	chr8:11829933-11829934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541500923	chr8:11829948-11829949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374603532	chr8:11829963-11829964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35571550	chr8:11829964-11829965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73663069	chr8:11829973-11829974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80221300	chr8:11829979-11829980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199891897	chr8:11829981-11829982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138674297	chr8:11829993-11829994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574777992	chr8:11830005-11830006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181461359	chr8:11830013-11830014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139748534	chr8:11830020-11830021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368242018	chr8:11830054-11830055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184143750	chr8:11830057-11830058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371307486	chr8:11830061-11830062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542802473	chr8:11830081-11830082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11998678	chr8:11830150-11830151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs532145886	chr8:11830151-11830152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148900915	chr8:11830164-11830165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs386722353	chr8:11830208-11830209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114524103	chr8:11830209-11830210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544367748	chr8:11830238-11830239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539098791	chr8:11830245-11830246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112034254	chr8:11830259-11830260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569988711	chr8:11830268-11830269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564536055	chr8:11830269-11830270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537321833	chr8:11830291-11830292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552438227	chr8:11830334-11830335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570618100	chr8:11830359-11830360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77966721	chr8:11830412-11830413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553439732	chr8:11830451-11830452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574805206	chr8:11830453-11830454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188525236	chr8:11830457-11830458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143661418	chr8:11830468-11830469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138247743	chr8:11830477-11830478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75612098	chr8:11830489-11830490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368100342	chr8:11830499-11830500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9657521	chr8:11830502-11830503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs540434933	chr8:11830509-11830510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559416390	chr8:11830514-11830515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529726961	chr8:11830535-11830536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529457673	chr8:11830567-11830568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549509468	chr8:11830579-11830580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548236078	chr8:11830590-11830591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77038506	chr8:11830596-11830597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557855847	chr8:11830598-11830599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530868940	chr8:11830606-11830607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	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
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11821800-11833000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11821800-11834400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:11826600-11832000	Weak transcription	Pancreas	Pancrea
4	chr8:11828600-11835200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:11831400-11831800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:11831400-11832600	Enhancers	Duodenum Mucosa	Duodenum
7	chr8:11831400-11832600	Enhancers	Fetal Intestine Large	intestine
8	chr8:11831600-11832600	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr8:11832000-11832600	Enhancers	Pancreas	Pancrea
10	chr8:11832400-11833000	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr8:11833000-11836600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:11834400-11836000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:11835000-11835600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:11835000-11835600	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr8:11835000-11836000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:11835000-11836000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:11835000-11836200	Bivalent Enhancer	Fetal Stomach	stomach
18	chr8:11835000-11836400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:11835200-11835600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr8:11835200-11836000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr8:11835200-11836200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:11835200-11836200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:11835400-11835800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:11835400-11836200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr8:11835400-11836200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:11835600-11836000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr8:11835600-11836000	Enhancers	NH-A	brain
28	chr8:11835600-11836400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:11835600-11836600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:11835800-11836000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
31	chr8:11836000-11836400	Flanking Active TSS	NH-A	brain
32	chr8:11836000-11836600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr8:11836000-11836600	Enhancers	HMEC	breast
34	chr8:11836000-11837400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr8:11836600-11837600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:11836600-11839400	Weak transcription	HMEC	breast
37	chr8:11836800-11837400	Enhancers	Primary B cells from peripheral blood	blood
38	chr8:11837400-11838600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:11837600-11838600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:11838600-11843600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:11838600-11843600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:11839400-11839800	Enhancers	HMEC	breast
43	chr8:11839400-11840000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:11839400-11840200	Enhancers	NH-A	brain
45	chr8:11839600-11839800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:11839600-11839800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:11839600-11839800	Bivalent Enhancer	NHEK	skin
48	chr8:11839600-11840000	Bivalent Enhancer	A549	lung

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