Variant report

Variant	nsv6042
Chromosome Location	chr8:1050096-1086523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:1711)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:1067672-1067993	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr8:1083078-1083309	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:1060509-1060574	K562	blood:	n/a	n/a
4	BHLHE40	chr8:1081205-1081343	K562	blood:	n/a	chr8:1081230-1081239 chr8:1081229-1081238 chr8:1081224-1081245 chr8:1081230-1081239 chr8:1081231-1081240
5	BHLHE40	chr8:1058357-1058815	HepG2	liver:	n/a	n/a
6	BHLHE40	chr8:1058414-1058822	K562	blood:	n/a	n/a
7	BHLHE40	chr8:1060374-1060612	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:1079259-1079453	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr8:1067504-1067974	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr8:1076460-1076610	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr8:1086377-1086545	Gliobla	brain:	n/a	n/a
12	CTCF	chr8:1086376-1086542	MCF-7	breast:	n/a	n/a
13	CTCF	chr8:1076284-1076397	Lung_OC	lung:	n/a	n/a
14	CTCF	chr8:1067705-1067709	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr8:1086343-1086569	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr8:1086340-1086490	HEK293	kidney:	n/a	n/a
17	CTCF	chr8:1086340-1086490	HepG2	liver:	n/a	n/a
18	CTCF	chr8:1086350-1086555	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:1055977-1056033	GM10248	blood:	n/a	n/a
20	CTCF	chr8:1086362-1086507	HepG2	liver:	n/a	n/a
21	CTCF	chr8:1060008-1060039	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr8:1057833-1057976	LNCaP	prostate:	n/a	n/a
23	CTCF	chr8:1086380-1086530	K562	blood:	n/a	n/a
24	CTCF	chr8:1086360-1086510	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr8:1058932-1059061	LNCaP	prostate:	n/a	n/a
26	CTCF	chr8:1086403-1086523	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:1057832-1057905	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:1086384-1086523	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:1086390-1086535	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:1086378-1086535	K562	blood:	n/a	n/a
31	CTCF	chr8:1086369-1086538	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:1086245-1086590	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:1086380-1086530	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:1086267-1086590	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:1059618-1059698	Lung_OC	lung:	n/a	n/a
36	CTCF	chr8:1086404-1086509	HepG2	liver:	n/a	n/a
37	CTCF	chr8:1086253-1086553	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:1086380-1086530	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr8:1059578-1059721	LNCaP	prostate:	n/a	n/a
40	CTCF	chr8:1086410-1086512	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr8:1086340-1086490	Hela-S3	cervix:	n/a	n/a
42	E2F4	chr8:1073353-1073841	MCF10A-Er-Src	breast:	n/a	n/a
43	EP300	chr8:1082988-1083333	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr8:1082908-1083315	H1-hESC	embryonic stem cell:	n/a	n/a
45	FOSL1	chr8:1080408-1080586	K562	blood:	n/a	chr8:1080522-1080529 chr8:1080517-1080528 chr8:1080518-1080527 chr8:1080517-1080529 chr8:1080518-1080528
46	GABPA	chr8:1059101-1059478	GM12878	blood:	n/a	n/a
47	GATA2	chr8:1074569-1074858	SH-SY5Y	brain:	n/a	n/a
48	GATA2	chr8:1080135-1080989	SH-SY5Y	brain:	n/a	chr8:1080520-1080529 chr8:1080461-1080478
49	GATA3	chr8:1074522-1074772	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr8:1081606-1082057	SH-SY5Y	brain:	n/a	chr8:1081870-1081879

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1078200-1078250	Caco-2	colon:	n/a
2	chr8:1053508-1053558	HCT-116	colon:	n/a
3	chr8:1082686-1082736	Caco-2	colon:	n/a
4	chr8:1078200-1078250	Caco-2	colon:	n/a
5	chr8:1053508-1053558	HCT-116	colon:	n/a
6	chr8:1082686-1082736	Caco-2	colon:	n/a
7	chr8:1054487-1054537	ovcar-3	ovarian:	n/a
8	chr8:1080133-1080183	HEK293	kidney:	embryo
9	chr8:1054048-1054098	ECC-1	luminal epithelium:	n/a
10	chr8:1076811-1076861	Caco-2	colon:	n/a
11	chr8:1078200-1078250	ProgFib	skin:	n/a
12	chr8:1053480-1053530	ovcar-3	ovarian:	n/a
13	chr8:1085741-1085791	PrEC	prostate:	n/a
14	chr8:1076811-1076861	HCT-116	colon:	n/a
15	chr8:1053157-1053207	HCT-116	colon:	n/a
16	chr8:1054487-1054537	HNPCEpiC	eye:	n/a
17	chr8:1054487-1054537	RPTEC	kidney:	n/a
18	chr8:1051510-1051560	ovcar-3	ovarian:	n/a
19	chr8:1054786-1054836	HRPEpiC	eye:	n/a
20	chr8:1054487-1054537	IMR90	lung:	fetal
21	chr8:1054065-1054115	H1-hESC	embryonic stem cell:	embryo
22	chr8:1053480-1053530	GM12878	blood:	n/a
23	chr8:1080669-1080719	HepG2	liver:	n/a
24	chr8:1080133-1080183	MCF10A-Er-Src	breast:	n/a
25	chr8:1082686-1082736	HMEC	breast:	n/a
26	chr8:1054048-1054098	Hepatocyte	liver:	n/a
27	chr8:1053439-1053489	HRPEpiC	eye:	n/a
28	chr8:1076811-1076861	CMK	blood:	n/a
29	chr8:1080555-1080605	PANC-1	pancreas:	n/a
30	chr8:1068250-1068300	Hepatocyte	liver:	n/a
31	chr8:1085741-1085791	Hela-S3	cervix:	n/a
32	chr8:1053508-1053558	AG09319	gingival:	n/a
33	chr8:1078200-1078250	PrEC	prostate:	n/a
34	chr8:1078142-1078192	HCT-116	colon:	n/a
35	chr8:1078142-1078192	ECC-1	luminal epithelium:	n/a
36	chr8:1054065-1054115	HL-60	blood:	n/a
37	chr8:1076811-1076861	HCF	heart:	n/a
38	chr8:1051585-1051635	AoSMC	blood vessel:	n/a
39	chr8:1080916-1080966	AG09309	skin:	n/a
40	chr8:1082686-1082736	HRE	kidney:	n/a
41	chr8:1068250-1068300	GM12878	blood:	n/a
42	chr8:1051703-1051753	RPTEC	kidney:	n/a
43	chr8:1078142-1078192	K562	blood:	n/a
44	chr8:1080555-1080605	HAEpiC	amniotic membrane:	n/a
45	chr8:1085741-1085791	NHDF-neo	bronchial:	n/a
46	chr8:1076811-1076861	NH-A	brain:	n/a
47	chr8:1053157-1053207	HUVEC	blood vessel:	n/a
48	chr8:1082686-1082736	SK-N-MC	brain:	n/a
49	chr8:1054065-1054115	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:1050972-1051022	HCT-116	colon:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1055778..1058022-chr8:1059688..1062614,2	K562	blood:
2	chr8:1055778..1058022-chr8:1059688..1062614,2	K562	blood:
3	chr8:1012791..1015412-chr8:1066556..1068717,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO25-5	chr8:1054882-1055066	ENSG00000254269
2	lnc-FBXO25-5	chr8:1054883-1055066	ENSG00000237647.4

No data

Variant related genes	Relation type
ENSG00000254269	TF binding region
ENSG00000254269	CpG island

Extended variants
information (count: 2087 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368979193	chr8:1050111-1050112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148169418	chr8:1050119-1050120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117566952	chr8:1050122-1050123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575963862	chr8:1050124-1050125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117891488	chr8:1050137-1050138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555224890	chr8:1050149-1050150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542179690	chr8:1050166-1050167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572110312	chr8:1050167-1050168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541129574	chr8:1050205-1050206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560774127	chr8:1050210-1050211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185545107	chr8:1050235-1050236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370009739	chr8:1050249-1050250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57169878	chr8:1050285-1050286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374527619	chr8:1050293-1050294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543482738	chr8:1050302-1050303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563258940	chr8:1050321-1050322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532885164	chr8:1050322-1050323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552566378	chr8:1050324-1050325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377635727	chr8:1050327-1050328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190259562	chr8:1050343-1050344	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs182909845	chr8:1050350-1050351	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548669625	chr8:1050368-1050369	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568263995	chr8:1050379-1050380	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373701000	chr8:1050383-1050384	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2701955	chr8:1050412-1050413	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550587582	chr8:1050413-1050414	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs141980292	chr8:1050446-1050447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150093329	chr8:1050467-1050468	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs558531095	chr8:1050472-1050473	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs138368545	chr8:1050493-1050494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112136851	chr8:1050507-1050508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375132993	chr8:1050508-1050509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199547550	chr8:1050524-1050525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11988219	chr8:1050525-1050526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141673075	chr8:1050532-1050533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574620026	chr8:1050538-1050539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375386980	chr8:1050545-1050546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543522288	chr8:1050559-1050560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563140817	chr8:1050580-1050581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533348504	chr8:1050587-1050588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187627714	chr8:1050602-1050603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80110250	chr8:1050615-1050616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113419023	chr8:1050634-1050635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559751547	chr8:1050653-1050654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193230391	chr8:1050688-1050689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548541723	chr8:1050714-1050715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139352211	chr8:1050721-1050722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142567997	chr8:1050753-1050754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577629228	chr8:1050794-1050795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184082642	chr8:1050799-1050800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Schizophrenia	23813976	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1045800-1050400	Weak transcription	Fetal Brain Male	brain
2	chr8:1046400-1051600	Weak transcription	Brain Germinal Matrix	brain
3	chr8:1046800-1050800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:1050400-1051600	Enhancers	Fetal Brain Male	brain
5	chr8:1054200-1054800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:1054800-1055200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:1055200-1057200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:1057000-1057600	Enhancers	Fetal Muscle Leg	muscle
9	chr8:1057200-1057400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr8:1057200-1058000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:1057200-1058000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:1057400-1057600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:1057400-1058600	Enhancers	Fetal Muscle Trunk	muscle
14	chr8:1057600-1057800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:1057600-1067200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:1058400-1058600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:1058600-1060200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:1060200-1060600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:1060400-1060600	Enhancers	Esophagus	oesophagus
20	chr8:1060400-1060600	ZNF genes & repeats	Pancreas	Pancrea
21	chr8:1060400-1060800	ZNF genes & repeats	Gastric	stomach
22	chr8:1060400-1061200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr8:1060800-1061000	Weak transcription	Gastric	stomach
24	chr8:1061000-1061200	Enhancers	Gastric	stomach
25	chr8:1065800-1066400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr8:1066000-1068400	Enhancers	Fetal Brain Male	brain
27	chr8:1066200-1069400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:1066400-1067400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:1066600-1067800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:1066600-1068400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr8:1067000-1067600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:1067000-1068000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:1067000-1069000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:1067000-1069800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr8:1067200-1067400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:1067200-1067400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
37	chr8:1067200-1067600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr8:1067200-1067800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:1067200-1068000	Enhancers	Fetal Brain Female	brain
40	chr8:1067200-1068200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr8:1067200-1068600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:1067200-1069000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:1067200-1069600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr8:1067400-1067600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:1067400-1067600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr8:1067400-1068600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:1067400-1068600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr8:1067400-1068800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr8:1067600-1068600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:1067600-1068800	Enhancers	HUES6 Cell Line	embryonic stem cell

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