Variant report

Variant	esv1842719
Chromosome Location	chr8:85198548-85268951
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	CEBPB	chr8:85256179-85256451	H1-hESC	embryonic stem cell:	n/a	chr8:85256310-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256310-85256323 chr8:85256312-85256321
2	CEBPB	chr8:85207880-85208095	HepG2	liver:	n/a	chr8:85207954-85207965 chr8:85207952-85207965 chr8:85207952-85207963
3	CEBPB	chr8:85209341-85209469	HepG2	liver:	n/a	chr8:85209376-85209387
4	CEBPB	chr8:85260646-85260977	HepG2	liver:	n/a	chr8:85260800-85260813 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260800-85260811 chr8:85260802-85260813
5	CEBPB	chr8:85260632-85260936	IMR90	lung:	n/a	chr8:85260800-85260813 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260802-85260811 chr8:85260800-85260811 chr8:85260802-85260813
6	CEBPB	chr8:85244091-85244330	HepG2	liver:	n/a	chr8:85244182-85244193 chr8:85244183-85244192 chr8:85244181-85244192 chr8:85244183-85244192 chr8:85244183-85244192 chr8:85244183-85244192
7	CEBPB	chr8:85233047-85233056	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:85201230-85201766	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:85256193-85256443	HepG2	liver:	n/a	chr8:85256310-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256310-85256323 chr8:85256312-85256321
10	CEBPB	chr8:85256163-85256497	IMR90	lung:	n/a	chr8:85256310-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256310-85256323 chr8:85256312-85256321
11	CEBPB	chr8:85256243-85256464	K562	blood:	n/a	chr8:85256310-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256310-85256323 chr8:85256312-85256321
12	CEBPB	chr8:85256172-85256446	A549	lung:	n/a	chr8:85256310-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256312-85256321 chr8:85256310-85256323 chr8:85256312-85256321
13	CTCF	chr8:85209551-85209669	GM20000	blood:	n/a	n/a
14	CTCF	chr8:85268180-85268330	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr8:85209552-85209659	GM13976	blood:	n/a	n/a
16	CTCF	chr8:85211920-85212070	AG10803	skin:	n/a	n/a
17	CTCF	chr8:85252260-85252351	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr8:85257020-85257170	GM06990	blood:	n/a	n/a
19	CTCF	chr8:85265100-85265250	NHLF	lung:	n/a	chr8:85265217-85265233
20	E2F4	chr8:85213264-85213403	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr8:85232756-85232956	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr8:85263579-85263865	GM12878	blood:	n/a	n/a
23	EBF1	chr8:85265819-85265877	GM12878	blood:	n/a	n/a
24	EBF1	chr8:85209424-85209426	GM12878	blood:	n/a	n/a
25	EP300	chr8:85267186-85267195	GM12878	blood:	n/a	n/a
26	EP300	chr8:85265781-85265853	GM12878	blood:	n/a	chr8:85265831-85265840
27	FOS	chr8:85265707-85266366	MCF10A-Er-Src	breast:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85266226-85266237 chr8:85265831-85265841 chr8:85266225-85266234 chr8:85266225-85266232 chr8:85265831-85265841 chr8:85265832-85265841
28	FOS	chr8:85265691-85266005	MCF10A-Er-Src	breast:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265832-85265841
29	FOS	chr8:85265773-85265907	MCF10A-Er-Src	breast:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265832-85265841
30	FOS	chr8:85265678-85266390	MCF10A-Er-Src	breast:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85266226-85266237 chr8:85265831-85265841 chr8:85266225-85266234 chr8:85266225-85266232 chr8:85265831-85265841 chr8:85265832-85265841
31	FOXA1	chr8:85201296-85201520	T-47D	breast:	n/a	chr8:85201432-85201447
32	FOXA2	chr8:85201335-85201515	HepG2	liver:	n/a	n/a
33	FOXP2	chr8:85247968-85248174	SK-N-MC	brain:	n/a	n/a
34	JUND	chr8:85265742-85265974	HepG2	liver:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265848-85265859 chr8:85265831-85265841 chr8:85265830-85265841 chr8:85265832-85265841
35	JUND	chr8:85265740-85265869	H1-hESC	embryonic stem cell:	n/a	chr8:85265831-85265841 chr8:85265835-85265847 chr8:85265831-85265841 chr8:85265831-85265841 chr8:85265848-85265859 chr8:85265831-85265841 chr8:85265830-85265841 chr8:85265832-85265841
36	KAP1	chr8:85225172-85225790	HEK293	kidney:	n/a	n/a
37	MAFF	chr8:85200501-85200756	HepG2	liver:	n/a	n/a
38	MAFF	chr8:85262858-85263018	HepG2	liver:	n/a	chr8:85262932-85262950
39	MAFK	chr8:85200536-85200771	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAFK	chr8:85262808-85263099	HepG2	liver:	n/a	n/a
41	MAFK	chr8:85262802-85263002	HepG2	liver:	n/a	n/a
42	MAFK	chr8:85244341-85244553	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAFK	chr8:85203805-85203999	HepG2	liver:	n/a	chr8:85203887-85203901
44	MAFK	chr8:85200484-85200687	HepG2	liver:	n/a	n/a
45	MAFK	chr8:85260565-85260725	IMR90	lung:	n/a	n/a
46	MAFK	chr8:85200482-85200732	HepG2	liver:	n/a	n/a
47	MAX	chr8:85229734-85229795	NB4	blood:	n/a	n/a
48	MAX	chr8:85215685-85215768	NB4	blood:	n/a	chr8:85215710-85215721 chr8:85215711-85215721
49	MYC	chr8:85201349-85201542	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr8:85236004-85236062	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:85267094-85267144	SAEC	small airway:	n/a
2	chr8:85267094-85267144	HAEpiC	amniotic membrane:	n/a
3	chr8:85267094-85267144	HRE	kidney:	n/a
4	chr8:85267094-85267144	SK-N-SH_RA	brain:	n/a
5	chr8:85267094-85267144	HepG2	liver:	n/a
6	chr8:85267094-85267144	A549	lung:	n/a
7	chr8:85267094-85267144	HCT-116	colon:	n/a
8	chr8:85267094-85267144	AG10803	skin:	n/a
9	chr8:85267094-85267144	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:85267094-85267144	GM12878	blood:	n/a
11	chr8:85267094-85267144	H1-hESC	embryonic stem cell:	embryo
12	chr8:85267094-85267144	HUVEC	blood vessel:	n/a
13	chr8:85267094-85267144	Caco-2	colon:	n/a
14	chr8:85267094-85267144	NB4	blood:	n/a
15	chr8:85267094-85267144	LNCaP	prostate:	n/a
16	chr8:85267094-85267144	PrEC	prostate:	n/a
17	chr8:85267094-85267144	SKMC	muscle:	n/a
18	chr8:85267094-85267144	Hela-S3	cervix:	n/a
19	chr8:85267094-85267144	HCF	heart:	n/a
20	chr8:85267094-85267144	AG09319	gingival:	n/a
21	chr8:85267094-85267144	NH-A	brain:	n/a
22	chr8:85267094-85267144	GM12892	blood:	n/a
23	chr8:85267094-85267144	Hepatocyte	liver:	n/a
24	chr8:85267094-85267144	ECC-1	luminal epithelium:	n/a
25	chr8:85267094-85267144	MCF10A-Er-Src	breast:	n/a
26	chr8:85267094-85267144	HIPEpiC	eye:	n/a
27	chr8:85267094-85267144	U87	brain:	n/a
28	chr8:85267094-85267144	SK-N-MC	brain:	n/a
29	chr8:85267094-85267144	HEK293	kidney:	embryo
30	chr8:85267094-85267144	BE2_C	brain:	n/a
31	chr8:85267094-85267144	NHDF-neo	bronchial:	n/a
32	chr8:85267094-85267144	AG04449	skin:	fetal
33	chr8:85267094-85267144	Jurkat	blood:	n/a
34	chr8:85267094-85267144	T-47D	breast:	n/a
35	chr8:85267094-85267144	CMK	blood:	n/a
36	chr8:85267094-85267144	AG04450	lung:	fetal
37	chr8:85267094-85267144	BJ	skin:	n/a
38	chr8:85267094-85267144	GM12891	blood:	n/a
39	chr8:85267094-85267144	HCM	heart:	n/a
40	chr8:85267094-85267144	RPTEC	kidney:	n/a
41	chr8:85267094-85267144	GM06990	blood:	n/a
42	chr8:85267094-85267144	SK-N-SH	brain:	n/a
43	chr8:85267094-85267144	ProgFib	skin:	n/a
44	chr8:85267094-85267144	AoSMC	blood vessel:	n/a
45	chr8:85267094-85267144	HCPEpiC	choroid plexus:	n/a
46	chr8:85267094-85267144	HRCEpiC	kidney:	n/a
47	chr8:85267094-85267144	HRPEpiC	eye:	n/a
48	chr8:85267094-85267144	HNPCEpiC	eye:	n/a
49	chr8:85267094-85267144	ovcar-3	ovarian:	n/a
50	chr8:85267094-85267144	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:85254893..85257135-chr8:85258246..85262364,3	K562	blood:
2	chr8:85244937..85247622-chr8:85249588..85252468,2	MCF-7	breast:
3	chr8:85209287..85211713-chr8:85211805..85214280,2	MCF-7	breast:
4	chr8:85244937..85247622-chr8:85249588..85252468,2	MCF-7	breast:
5	chr8:85229678..85232410-chr8:85340813..85342661,2	K562	blood:
6	chr8:85209287..85211713-chr8:85211805..85214280,2	MCF-7	breast:
7	chr8:85254893..85257135-chr8:85258246..85262364,3	K562	blood:
8	chr8:85168225..85170591-chr8:85247775..85249276,2	K562	blood:

Variant related genes	Relation type
ENSG00000221185	TF binding region
ENSG00000221185	CpG island

Extended variants
information (count: 1544 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1544 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7831643	chr8:85198548-85198549	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114023744	chr8:85198574-85198575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545586853	chr8:85198599-85198600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565003524	chr8:85198644-85198645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530478935	chr8:85198683-85198684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145130986	chr8:85198698-85198699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185597705	chr8:85198701-85198702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370975412	chr8:85198727-85198728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35628160	chr8:85198731-85198732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546510793	chr8:85198766-85198767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188639514	chr8:85198790-85198791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34614520	chr8:85198799-85198800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538455464	chr8:85198840-85198841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148689421	chr8:85198841-85198842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192954379	chr8:85198880-85198881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35447512	chr8:85198894-85198895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571758591	chr8:85198920-85198921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569027498	chr8:85198939-85198940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375529459	chr8:85198951-85198952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77656997	chr8:85198977-85198978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557409475	chr8:85198989-85198990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547489254	chr8:85199006-85199007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373429526	chr8:85199048-85199049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538760140	chr8:85199106-85199107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184815092	chr8:85199187-85199188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575994120	chr8:85199216-85199217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543017090	chr8:85199230-85199231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553719777	chr8:85199261-85199262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377556429	chr8:85199275-85199276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545623826	chr8:85199277-85199278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565386152	chr8:85199321-85199322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74551943	chr8:85199332-85199333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142193231	chr8:85199394-85199395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80281272	chr8:85199408-85199409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146668052	chr8:85199420-85199421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546146268	chr8:85199555-85199556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116856323	chr8:85199560-85199561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532316042	chr8:85199572-85199573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200893813	chr8:85199600-85199601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201882914	chr8:85199601-85199602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60903377	chr8:85199603-85199604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188399800	chr8:85199616-85199617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568991199	chr8:85199628-85199629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554316521	chr8:85199677-85199678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117248357	chr8:85199686-85199687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554872933	chr8:85199718-85199719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140215459	chr8:85199719-85199720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528309682	chr8:85199725-85199726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181266747	chr8:85199748-85199749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573271412	chr8:85199788-85199789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85198000-85200600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:85198200-85200400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:85198400-85198600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:85198600-85200400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:85199000-85201000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:85199400-85201000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:85199400-85201600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:85199400-85205800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:85199600-85200400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:85199800-85201200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:85199800-85201200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:85199800-85204000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:85200000-85200400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr8:85200000-85200400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr8:85200200-85201000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr8:85200200-85201400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:85200400-85200600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr8:85200400-85201200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:85200400-85201200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:85200400-85201200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:85200400-85206400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:85200600-85201000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:85200600-85206800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:85200800-85201800	Enhancers	Liver	Liver
25	chr8:85201000-85201400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr8:85201000-85202600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr8:85201000-85203200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:85201000-85205600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr8:85201200-85201400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr8:85201200-85201400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:85201200-85201400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr8:85201200-85201400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:85201200-85202600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr8:85201200-85203600	Enhancers	Fetal Lung	lung
35	chr8:85201400-85201600	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr8:85201400-85201600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:85201400-85201800	Enhancers	Colon Smooth Muscle	Colon
38	chr8:85201400-85202200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr8:85201400-85202400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr8:85201400-85203400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:85201400-85203600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:85201600-85201800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:85201600-85201800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr8:85201600-85201800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr8:85201800-85202000	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr8:85201800-85203800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr8:85201800-85204000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr8:85201800-85206200	Weak transcription	Liver	Liver
49	chr8:85202000-85202600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr8:85202200-85203600	Enhancers	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links