Variant report

Variant	nsv890045
Chromosome Location	chr8:6108034-6167610
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	BATF	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:6149426-6149734	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:6165750-6165958	HepG2	liver:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
4	CEBPB	chr8:6165750-6165950	IMR90	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
5	CEBPB	chr8:6165763-6166327	K562	blood:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
6	CEBPB	chr8:6132470-6132485	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:6148528-6148743	HepG2	liver:	n/a	chr8:6148625-6148638 chr8:6148625-6148638 chr8:6148626-6148637 chr8:6148625-6148636
8	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
9	CEBPB	chr8:6165771-6165947	A549	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
10	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
12	CTCF	chr8:6140680-6140830	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
13	CTCF	chr8:6115894-6116460	HCT-116	colon:	n/a	n/a
14	CTCF	chr8:6116160-6116310	GM12872	blood:	n/a	n/a
15	CTCF	chr8:6140700-6140828	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
16	CTCF	chr8:6140738-6140800	GM19239	blood:	n/a	n/a
17	CTCF	chr8:6140682-6140798	HepG2	liver:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
18	CTCF	chr8:6116080-6116230	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr8:6116009-6116369	GM12878	blood:	n/a	n/a
20	CTCF	chr8:6140746-6140784	GM19240	blood:	n/a	n/a
21	CTCF	chr8:6140660-6140810	NB4	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
22	CTCF	chr8:6116100-6116250	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr8:6140650-6140833	K562	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
24	CTCF	chr8:6140640-6140790	HEEpiC	esophagus:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
25	CTCF	chr8:6109067-6109110	LNCaP	prostate:	n/a	n/a
26	CTCF	chr8:6116131-6116247	A549	lung:	n/a	n/a
27	CTCF	chr8:6140730-6140797	LNCaP	prostate:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
28	CTCF	chr8:6140640-6140790	Caco-2	colon:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
29	CTCF	chr8:6115928-6116347	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:6140700-6140850	HepG2	liver:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
31	CTCF	chr8:6115998-6116332	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:6140660-6140810	WERI-Rb-1	eye:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
33	CTCF	chr8:6116080-6116230	BE2_C	brain:	n/a	n/a
34	CTCF	chr8:6116180-6116330	RPTEC	kidney:	n/a	n/a
35	CTCF	chr8:6116140-6116290	GM12864	blood:	n/a	n/a
36	CTCF	chr8:6116120-6116270	HEK293	kidney:	n/a	n/a
37	CTCF	chr8:6140686-6140835	GM12892	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
38	CTCF	chr8:6140700-6140850	Hela-S3	cervix:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
39	CTCF	chr8:6116080-6116230	HRE	kidney:	n/a	n/a
40	CTCF	chr8:6116080-6116230	HPF	lung:	n/a	n/a
41	CTCF	chr8:6140640-6140790	HL-60	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
42	CTCF	chr8:6147920-6148070	GM12868	blood:	n/a	n/a
43	CTCF	chr8:6116020-6116170	HCT-116	colon:	n/a	n/a
44	CTCF	chr8:6155242-6155309	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr8:6140653-6140811	HepG2	liver:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
46	CTCF	chr8:6116138-6116263	GM10248	blood:	n/a	n/a
47	CTCF	chr8:6140660-6140810	GM12865	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
48	CTCF	chr8:6140620-6140770	Caco-2	colon:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
49	CTCF	chr8:6160454-6160522	GM10248	blood:	n/a	n/a
50	CTCF	chr8:6116081-6116295	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6118526-6118576	NB4	blood:	n/a
2	chr8:6118526-6118576	AG09309	skin:	n/a
3	chr8:6118526-6118576	ECC-1	luminal epithelium:	n/a
4	chr8:6118575-6118625	GM12878	blood:	n/a
5	chr8:6118575-6118625	AG04449	skin:	fetal
6	chr8:6118526-6118576	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:6118526-6118576	PANC-1	pancreas:	n/a
8	chr8:6118575-6118625	HRCEpiC	kidney:	n/a
9	chr8:6118575-6118625	ECC-1	luminal epithelium:	n/a
10	chr8:6118526-6118576	BE2_C	brain:	n/a
11	chr8:6118526-6118576	MCF10A-Er-Src	breast:	n/a
12	chr8:6118575-6118625	GM19239	blood:	n/a
13	chr8:6118575-6118625	Hepatocyte	liver:	n/a
14	chr8:6118575-6118625	SAEC	small airway:	n/a
15	chr8:6118575-6118625	PrEC	prostate:	n/a
16	chr8:6118575-6118625	NT2-D1	testis:	n/a
17	chr8:6118575-6118625	HCPEpiC	choroid plexus:	n/a
18	chr8:6118526-6118576	H1-hESC	embryonic stem cell:	embryo
19	chr8:6118575-6118625	HCM	heart:	n/a
20	chr8:6118575-6118625	BE2_C	brain:	n/a
21	chr8:6118526-6118576	NH-A	brain:	n/a
22	chr8:6118526-6118576	HRCEpiC	kidney:	n/a
23	chr8:6118526-6118576	U87	brain:	n/a
24	chr8:6118575-6118625	SK-N-SH_RA	brain:	n/a
25	chr8:6118575-6118625	HRPEpiC	eye:	n/a
26	chr8:6118575-6118625	HEEpiC	esophagus:	n/a
27	chr8:6118526-6118576	HUVEC	blood vessel:	n/a
28	chr8:6118526-6118576	Hela-S3	cervix:	n/a
29	chr8:6118526-6118576	AoSMC	blood vessel:	n/a
30	chr8:6118575-6118625	BJ	skin:	n/a
31	chr8:6118575-6118625	HL-60	blood:	n/a
32	chr8:6118526-6118576	NHDF-neo	bronchial:	n/a
33	chr8:6118526-6118576	PrEC	prostate:	n/a
34	chr8:6118575-6118625	GM06990	blood:	n/a
35	chr8:6118575-6118625	Jurkat	blood:	n/a
36	chr8:6118575-6118625	HCF	heart:	n/a
37	chr8:6118526-6118576	SK-N-SH	brain:	n/a
38	chr8:6118526-6118576	AG09319	gingival:	n/a
39	chr8:6118526-6118576	MCF-7	breast:	n/a
40	chr8:6118526-6118576	BJ	skin:	n/a
41	chr8:6118575-6118625	HEK293	kidney:	embryo
42	chr8:6118575-6118625	RPTEC	kidney:	n/a
43	chr8:6118575-6118625	HAEpiC	amniotic membrane:	n/a
44	chr8:6118526-6118576	Caco-2	colon:	n/a
45	chr8:6118526-6118576	IMR90	lung:	fetal
46	chr8:6118575-6118625	PFSK-1	brain:	n/a
47	chr8:6118575-6118625	HRE	kidney:	n/a
48	chr8:6118575-6118625	SK-N-MC	brain:	n/a
49	chr8:6118575-6118625	AoSMC	blood vessel:	n/a
50	chr8:6118526-6118576	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
2	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
3	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
4	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
5	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:
6	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
7	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
8	chr8:6106618..6108795-chr8:6113891..6116770,2	K562	blood:
9	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
10	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:6114933-6115058	ENSG00000253880

Variant related genes	Relation type
ENSG00000253880	TF binding region
ENSG00000253880	CpG island
ENSG00000253880	chromatin interactions

Extended variants
information (count: 3773 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3773 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7018351	chr8:6108034-6108035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7017217	chr8:6108052-6108053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111629419	chr8:6108062-6108063	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4576446	chr8:6108083-6108084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558560849	chr8:6108094-6108095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575211369	chr8:6108128-6108129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182685151	chr8:6108140-6108141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562684148	chr8:6108142-6108143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142050185	chr8:6108145-6108146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561011776	chr8:6108153-6108154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73522038	chr8:6108160-6108161	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540518679	chr8:6108166-6108167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531416338	chr8:6108192-6108193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560728695	chr8:6108193-6108194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532730156	chr8:6108221-6108222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7000342	chr8:6108236-6108237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143839970	chr8:6108247-6108248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187122572	chr8:6108255-6108256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550707141	chr8:6108258-6108259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7017557	chr8:6108260-6108261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs191932499	chr8:6108265-6108266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148138982	chr8:6108267-6108268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs28709256	chr8:6108278-6108279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538573840	chr8:6108284-6108285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544290929	chr8:6108300-6108301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575252538	chr8:6108305-6108306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537806655	chr8:6108311-6108312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs66944953	chr8:6108322-6108323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536929532	chr8:6108341-6108342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs578035530	chr8:6108351-6108352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142565938	chr8:6108356-6108357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540410211	chr8:6108358-6108359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560552448	chr8:6108361-6108362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577342117	chr8:6108404-6108405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546537727	chr8:6108417-6108418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs6984741	chr8:6108423-6108424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs530526575	chr8:6108433-6108434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146517266	chr8:6108443-6108444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117552560	chr8:6108451-6108452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529783504	chr8:6108452-6108453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560321483	chr8:6108453-6108454	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182688452	chr8:6108454-6108455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139154370	chr8:6108468-6108469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552061918	chr8:6108472-6108473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187380963	chr8:6108499-6108500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537739136	chr8:6108503-6108504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554700331	chr8:6108504-6108505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6984891	chr8:6108533-6108534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs7008561	chr8:6108535-6108536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142965409	chr8:6108542-6108543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	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
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
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:134 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
15	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
19	chr8:6119400-6120000	Enhancers	Osteobl	bone
20	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
22	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
25	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:6132200-6132800	Enhancers	Spleen	Spleen
29	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
30	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
32	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
45	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:6147800-6148000	Enhancers	Duodenum Mucosa	Duodenum
50	chr8:6147800-6148200	Enhancers	HUES48 Cell Line	embryonic stem cell

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