Variant report

Variant	esv1816797
Chromosome Location	chr8:6816723-6882130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:672)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:6829807-6830004	K562	blood:	n/a	n/a
2	BACH1	chr8:6829927-6829940	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:6825706-6825903	K562	blood:	n/a	chr8:6825850-6825859 chr8:6825848-6825857 chr8:6825847-6825860 chr8:6825849-6825858 chr8:6825843-6825864 chr8:6825849-6825858
4	CEBPB	chr8:6872820-6873018	HepG2	liver:	n/a	chr8:6872838-6872849 chr8:6872837-6872848
5	CEBPB	chr8:6882109-6882181	A549	lung:	n/a	n/a
6	CTCF	chr8:6827880-6828030	HEK293	kidney:	n/a	chr8:6827881-6827890 chr8:6827923-6827930
7	CTCF	chr8:6829829-6829883	LNCaP	prostate:	n/a	n/a
8	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
9	CTCF	chr8:6827996-6828116	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
11	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
15	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
16	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
17	CTCF	chr8:6828040-6828190	HepG2	liver:	n/a	n/a
18	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
20	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
21	CTCF	chr8:6827960-6828110	K562	blood:	n/a	n/a
22	CTCF	chr8:6827997-6828044	Gliobla	brain:	n/a	n/a
23	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
24	CTCF	chr8:6828045-6828050	Gliobla	brain:	n/a	n/a
25	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
26	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
27	E2F4	chr8:6823871-6824074	MCF10A-Er-Src	breast:	n/a	n/a
28	ELF1	chr8:6826345-6826676	GM12878	blood:	n/a	n/a
29	FOS	chr8:6829914-6829972	MCF10A-Er-Src	breast:	n/a	n/a
30	GABPA	chr8:6878604-6878734	Hela-S3	cervix:	n/a	n/a
31	JUN	chr8:6829481-6830053	K562	blood:	n/a	n/a
32	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
33	JUND	chr8:6829930-6830012	HepG2	liver:	n/a	n/a
34	JUND	chr8:6829868-6829984	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
36	JUND	chr8:6829764-6829956	H1-hESC	embryonic stem cell:	n/a	n/a
37	KAP1	chr8:6829739-6830136	U2OS	brain:	n/a	n/a
38	KAP1	chr8:6829741-6830106	HEK293	kidney:	n/a	n/a
39	MAFF	chr8:6825659-6825678	K562	blood:	n/a	n/a
40	MAFF	chr8:6825520-6825751	HepG2	liver:	n/a	chr8:6825656-6825674
41	MAFF	chr8:6818690-6818696	HepG2	liver:	n/a	n/a
42	MAFF	chr8:6829846-6829893	HepG2	liver:	n/a	n/a
43	MAFK	chr8:6829787-6829987	HepG2	liver:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
44	MAFK	chr8:6829763-6829959	H1-hESC	embryonic stem cell:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
45	MAFK	chr8:6825552-6825788	IMR90	lung:	n/a	n/a
46	MAFK	chr8:6829943-6829957	Hela-S3	cervix:	n/a	n/a
47	MAFK	chr8:6821864-6821951	HepG2	liver:	n/a	chr8:6821896-6821907 chr8:6821891-6821906 chr8:6821891-6821907 chr8:6821896-6821907 chr8:6821895-6821906 chr8:6821894-6821908
48	MAFK	chr8:6825499-6825829	HepG2	liver:	n/a	n/a
49	MAFK	chr8:6825571-6825794	HepG2	liver:	n/a	n/a
50	MAFK	chr8:6825667-6825713	H1-hESC	embryonic stem cell:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6827800-6827850	HUVEC	blood vessel:	n/a
2	chr8:6827800-6827850	HUVEC	blood vessel:	n/a
3	chr8:6827814-6827864	Hela-S3	cervix:	n/a
4	chr8:6827814-6827864	RPTEC	kidney:	n/a
5	chr8:6826392-6826442	NH-A	brain:	n/a
6	chr8:6838024-6838074	HRCEpiC	kidney:	n/a
7	chr8:6875661-6875711	NH-A	brain:	n/a
8	chr8:6876695-6876745	HCF	heart:	n/a
9	chr8:6838024-6838074	HL-60	blood:	n/a
10	chr8:6876695-6876745	GM06990	blood:	n/a
11	chr8:6827800-6827850	HRPEpiC	eye:	n/a
12	chr8:6838024-6838074	AG09319	gingival:	n/a
13	chr8:6875661-6875711	HRPEpiC	eye:	n/a
14	chr8:6876781-6876831	K562	blood:	n/a
15	chr8:6875661-6875711	GM12892	blood:	n/a
16	chr8:6838024-6838074	MCF10A-Er-Src	breast:	n/a
17	chr8:6827814-6827864	AG09309	skin:	n/a
18	chr8:6875661-6875711	MCF-7	breast:	n/a
19	chr8:6827814-6827864	Hepatocyte	liver:	n/a
20	chr8:6826392-6826442	SAEC	small airway:	n/a
21	chr8:6827814-6827864	HepG2	liver:	n/a
22	chr8:6827814-6827864	HEK293	kidney:	embryo
23	chr8:6827800-6827850	NHBE	bronchial:	n/a
24	chr8:6828103-6828153	GM19239	blood:	n/a
25	chr8:6876781-6876831	HCM	heart:	n/a
26	chr8:6838024-6838074	AoSMC	blood vessel:	n/a
27	chr8:6838024-6838074	AG04450	lung:	fetal
28	chr8:6837932-6837982	ovcar-3	ovarian:	n/a
29	chr8:6876781-6876831	AG09309	skin:	n/a
30	chr8:6873754-6873804	A549	lung:	n/a
31	chr8:6828103-6828153	HMEC	breast:	n/a
32	chr8:6828103-6828153	AoSMC	blood vessel:	n/a
33	chr8:6873754-6873804	GM19239	blood:	n/a
34	chr8:6826392-6826442	BJ	skin:	n/a
35	chr8:6876695-6876745	ECC-1	luminal epithelium:	n/a
36	chr8:6876155-6876205	HRCEpiC	kidney:	n/a
37	chr8:6875661-6875711	Hepatocyte	liver:	n/a
38	chr8:6837932-6837982	HL-60	blood:	n/a
39	chr8:6827800-6827850	HEEpiC	esophagus:	n/a
40	chr8:6876781-6876831	SK-N-SH	brain:	n/a
41	chr8:6876155-6876205	SKMC	muscle:	n/a
42	chr8:6873754-6873804	AoSMC	blood vessel:	n/a
43	chr8:6827814-6827864	NHDF-neo	bronchial:	n/a
44	chr8:6875661-6875711	AG09319	gingival:	n/a
45	chr8:6873754-6873804	ProgFib	skin:	n/a
46	chr8:6875661-6875711	AG04449	skin:	fetal
47	chr8:6827814-6827864	SK-N-SH	brain:	n/a
48	chr8:6876695-6876745	AG09309	skin:	n/a
49	chr8:6838024-6838074	PrEC	prostate:	n/a
50	chr8:6827800-6827850	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:6876740..6878297-chr8:6880024..6881649,2	K562	blood:
2	chr8:6876740..6878297-chr8:6880024..6881649,2	K562	blood:
3	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFA1-1	chr8:6825663-6825775	NONHSAT124803
2	lnc-DEFA1B-1	chr8:6844700-6844945	NONHSAT124804
3	lnc-DEFA1-2	chr8:6817512-6817683	NONHSAT124801
4	lnc-DEFA1-1	chr8:6826461-6826635	NONHSAT124803
5	lnc-DEFA1B-1	chr8:6845622-6845808	NONHSAT124804
6	lnc-DEFA1-1	chr8:6825663-6825769	NONHSAT124802
7	lnc-DEFA1B-1	chr8:6847181-6847243	NONHSAT124804
8	lnc-DEFA1-1	chr8:6826452-6826635	NONHSAT124802
9	lnc-DEFA1-2	chr8:6816811-6816923	NONHSAT124801

No data

Variant related genes	Relation type
DEFA1B	TF binding region
DEFT1P2	TF binding region
DEFA9P	TF binding region
DEFA10P	TF binding region
DEFA1	TF binding region
DEFA3	TF binding region
DEFT1P	TF binding region
DEFA1B	CpG island
DEFT1P2	CpG island
DEFA9P	CpG island
DEFA10P	CpG island
DEFA1	CpG island
DEFA3	CpG island
DEFT1P	CpG island

Extended variants
information (count: 2062 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:2062 , 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	rs190056303	chr8:6816749-6816750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1076577	chr8:6816758-6816759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183036844	chr8:6816759-6816760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555715164	chr8:6816761-6816762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572664117	chr8:6816765-6816766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144776127	chr8:6816775-6816776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574302438	chr8:6816776-6816777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564423871	chr8:6816782-6816783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533377084	chr8:6816790-6816791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187362813	chr8:6816800-6816801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2738079	chr8:6816812-6816813	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192516892	chr8:6816843-6816844	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs548351350	chr8:6816848-6816849	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs371302455	chr8:6816859-6816860	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs534258649	chr8:6816867-6816868	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs184557211	chr8:6816878-6816879	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs148569696	chr8:6816887-6816888	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs144420390	chr8:6816920-6816921	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs531902599	chr8:6816937-6816938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539043955	chr8:6816947-6816948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187652329	chr8:6816988-6816989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117752952	chr8:6816992-6816993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2738078	chr8:6817024-6817025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs527779946	chr8:6817030-6817031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192621437	chr8:6817038-6817039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572553043	chr8:6817063-6817064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541707202	chr8:6817092-6817093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558483982	chr8:6817093-6817094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184230300	chr8:6817096-6817097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567850740	chr8:6817111-6817112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543819446	chr8:6817114-6817115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77025823	chr8:6817129-6817130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369161016	chr8:6817153-6817154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs60520277	chr8:6817158-6817159	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542777361	chr8:6817251-6817252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561874849	chr8:6817254-6817255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527474008	chr8:6817261-6817262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567532034	chr8:6817263-6817264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190006116	chr8:6817276-6817277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570389945	chr8:6817281-6817282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181268987	chr8:6817303-6817304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184542921	chr8:6817327-6817328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs57380867	chr8:6817336-6817337	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188905642	chr8:6817370-6817371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544661314	chr8:6817382-6817383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146569574	chr8:6817383-6817384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565823971	chr8:6817419-6817420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535229758	chr8:6817422-6817423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576028817	chr8:6817443-6817444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181962618	chr8:6817459-6817460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
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
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
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	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
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	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
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Behcet''s disease	22219625	CNVD
Crohn''s disease	21701837	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6794600-6829200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:6811000-6818000	Enhancers	Dnd41	blood
3	chr8:6814600-6817000	Enhancers	Fetal Thymus	thymus
4	chr8:6816200-6817400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr8:6817000-6817600	Weak transcription	Fetal Thymus	thymus
6	chr8:6817400-6818800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr8:6817600-6817800	Enhancers	Fetal Thymus	thymus
8	chr8:6817600-6817800	Flanking Active TSS	Lung	lung
9	chr8:6817800-6820600	Weak transcription	Fetal Thymus	thymus
10	chr8:6818000-6820400	Weak transcription	Dnd41	blood
11	chr8:6818800-6822800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:6820400-6821800	Enhancers	Dnd41	blood
13	chr8:6820600-6821600	Enhancers	Fetal Thymus	thymus
14	chr8:6821400-6821800	Enhancers	Thymus	Thymus
15	chr8:6822800-6830000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr8:6824000-6824800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr8:6824200-6824600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:6824400-6824800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
19	chr8:6824600-6824800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:6824600-6828200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:6826400-6826600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:6826400-6826800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
24	chr8:6826400-6826800	Enhancers	Primary T cells fromperipheralblood	blood
25	chr8:6826400-6826800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
26	chr8:6826400-6826800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:6826400-6827000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
28	chr8:6826600-6826800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
29	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
35	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
38	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood

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