Variant report

Variant	nsv8274
Chromosome Location	chr8:6107278-6165692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

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	chr8:6148528-6148743	HepG2	liver:	n/a	chr8:6148625-6148638 chr8:6148625-6148638 chr8:6148626-6148637 chr8:6148625-6148636
4	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:6132470-6132485	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
8	CTCF	chr8:6115960-6116110	A549	lung:	n/a	n/a
9	CTCF	chr8:6140660-6140810	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
10	CTCF	chr8:6155242-6155309	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr8:6147920-6148070	GM12868	blood:	n/a	n/a
12	CTCF	chr8:6140600-6140750	GM12872	blood:	n/a	n/a
13	CTCF	chr8:6116140-6116290	GM12873	blood:	n/a	n/a
14	CTCF	chr8:6140697-6140827	GM10266	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
15	CTCF	chr8:6116122-6116203	GM13976	blood:	n/a	n/a
16	CTCF	chr8:6116009-6116369	GM12878	blood:	n/a	n/a
17	CTCF	chr8:6116140-6116290	GM12864	blood:	n/a	n/a
18	CTCF	chr8:6115710-6116473	SK-N-SH	brain:	n/a	n/a
19	CTCF	chr8:6115987-6116327	HepG2	liver:	n/a	n/a
20	CTCF	chr8:6116083-6116266	HepG2	liver:	n/a	n/a
21	CTCF	chr8:6116080-6116230	GM12866	blood:	n/a	n/a
22	CTCF	chr8:6140660-6140810	HEK293	kidney:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
23	CTCF	chr8:6116080-6116230	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr8:6140660-6140810	NB4	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
25	CTCF	chr8:6140700-6140850	Hela-S3	cervix:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
26	CTCF	chr8:6160454-6160522	GM10248	blood:	n/a	n/a
27	CTCF	chr8:6140640-6140790	HEEpiC	esophagus:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
28	CTCF	chr8:6116141-6116268	GM19239	blood:	n/a	n/a
29	CTCF	chr8:6115920-6116070	BE2_C	brain:	n/a	n/a
30	CTCF	chr8:6115820-6115970	GM12878	blood:	n/a	n/a
31	CTCF	chr8:6140600-6140750	GM12870	blood:	n/a	n/a
32	CTCF	chr8:6147110-6147473	H1-hESC	embryonic stem cell:	n/a	chr8:6147257-6147270
33	CTCF	chr8:6140640-6140790	GM12866	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
34	CTCF	chr8:6140680-6140830	GM12864	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
35	CTCF	chr8:6147180-6147330	WERI-Rb-1	eye:	n/a	chr8:6147257-6147270
36	CTCF	chr8:6116050-6116354	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:6140700-6140828	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
38	CTCF	chr8:6116080-6116230	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr8:6116046-6116323	T-47D	breast:	n/a	n/a
40	CTCF	chr8:6149920-6150070	GM12873	blood:	n/a	n/a
41	CTCF	chr8:6140713-6140831	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
42	CTCF	chr8:6116064-6116253	GM13977	blood:	n/a	n/a
43	CTCF	chr8:6140600-6140750	GM12871	blood:	n/a	n/a
44	CTCF	chr8:6116081-6116295	LNCaP	prostate:	n/a	n/a
45	CTCF	chr8:6147276-6147301	Gliobla	brain:	n/a	n/a
46	CTCF	chr8:6116140-6116290	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:6116020-6116170	HCT-116	colon:	n/a	n/a
48	CTCF	chr8:6116180-6116330	RPTEC	kidney:	n/a	n/a
49	CTCF	chr8:6115998-6116332	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:6126841-6126881	GM13976	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6118575-6118625	GM12878	blood:	n/a
2	chr8:6118526-6118576	MCF-7	breast:	n/a
3	chr8:6118526-6118576	HL-60	blood:	n/a
4	chr8:6118575-6118625	SAEC	small airway:	n/a
5	chr8:6118575-6118625	MCF-7	breast:	n/a
6	chr8:6118575-6118625	PFSK-1	brain:	n/a
7	chr8:6118526-6118576	SK-N-SH	brain:	n/a
8	chr8:6118575-6118625	SK-N-SH_RA	brain:	n/a
9	chr8:6118526-6118576	SK-N-SH_RA	brain:	n/a
10	chr8:6118526-6118576	NHBE	bronchial:	n/a
11	chr8:6118575-6118625	K562	blood:	n/a
12	chr8:6118575-6118625	HEEpiC	esophagus:	n/a
13	chr8:6118575-6118625	HRPEpiC	eye:	n/a
14	chr8:6118526-6118576	A549	lung:	n/a
15	chr8:6118575-6118625	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:6118526-6118576	CMK	blood:	n/a
17	chr8:6118575-6118625	AG09319	gingival:	n/a
18	chr8:6118575-6118625	AG04449	skin:	fetal
19	chr8:6118575-6118625	HMEC	breast:	n/a
20	chr8:6118526-6118576	PFSK-1	brain:	n/a
21	chr8:6118526-6118576	SKMC	muscle:	n/a
22	chr8:6118526-6118576	HCT-116	colon:	n/a
23	chr8:6118526-6118576	AG09319	gingival:	n/a
24	chr8:6118575-6118625	SKMC	muscle:	n/a
25	chr8:6118526-6118576	Hepatocyte	liver:	n/a
26	chr8:6118526-6118576	HIPEpiC	eye:	n/a
27	chr8:6118526-6118576	HepG2	liver:	n/a
28	chr8:6118575-6118625	U87	brain:	n/a
29	chr8:6118575-6118625	NT2-D1	testis:	n/a
30	chr8:6118575-6118625	HIPEpiC	eye:	n/a
31	chr8:6118526-6118576	AG09309	skin:	n/a
32	chr8:6118575-6118625	T-47D	breast:	n/a
33	chr8:6118526-6118576	HRPEpiC	eye:	n/a
34	chr8:6118526-6118576	ProgFib	skin:	n/a
35	chr8:6118526-6118576	HUVEC	blood vessel:	n/a
36	chr8:6118575-6118625	ovcar-3	ovarian:	n/a
37	chr8:6118526-6118576	HNPCEpiC	eye:	n/a
38	chr8:6118575-6118625	AG04450	lung:	fetal
39	chr8:6118575-6118625	Jurkat	blood:	n/a
40	chr8:6118575-6118625	AG10803	skin:	n/a
41	chr8:6118526-6118576	GM12892	blood:	n/a
42	chr8:6118575-6118625	HRE	kidney:	n/a
43	chr8:6118526-6118576	AoSMC	blood vessel:	n/a
44	chr8:6118575-6118625	NHBE	bronchial:	n/a
45	chr8:6118575-6118625	RPTEC	kidney:	n/a
46	chr8:6118526-6118576	NH-A	brain:	n/a
47	chr8:6118526-6118576	AG04450	lung:	fetal
48	chr8:6118526-6118576	Hela-S3	cervix:	n/a
49	chr8:6118575-6118625	A549	lung:	n/a
50	chr8:6118575-6118625	ECC-1	luminal epithelium:	n/a

(count:10 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 3699 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3699 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67938819	chr8:6107285-6107286	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75236880	chr8:6107293-6107294	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555381265	chr8:6107302-6107303	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571930020	chr8:6107304-6107305	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73522018	chr8:6107323-6107324	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557539834	chr8:6107324-6107325	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377007866	chr8:6107333-6107334	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73522020	chr8:6107335-6107336	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs73522024	chr8:6107372-6107373	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs140227007	chr8:6107382-6107383	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562357287	chr8:6107405-6107406	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542544481	chr8:6107419-6107420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12549028	chr8:6107427-6107428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs188688128	chr8:6107439-6107440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545501770	chr8:6107440-6107441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564995201	chr8:6107449-6107450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371863400	chr8:6107479-6107480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs71525716	chr8:6107480-6107481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs4840559	chr8:6107485-6107486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530457822	chr8:6107503-6107504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568999650	chr8:6107508-6107509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181537372	chr8:6107510-6107511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374089328	chr8:6107527-6107528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539388515	chr8:6107537-6107538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377178435	chr8:6107540-6107541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546955304	chr8:6107543-6107544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565691361	chr8:6107545-6107546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186060709	chr8:6107576-6107577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534288535	chr8:6107608-6107609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190522424	chr8:6107621-6107622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557889960	chr8:6107664-6107665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113501588	chr8:6107676-6107677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546685720	chr8:6107690-6107691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145852169	chr8:6107691-6107692	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183897649	chr8:6107696-6107697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542932485	chr8:6107698-6107699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552960279	chr8:6107711-6107712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541616924	chr8:6107712-6107713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs199690105	chr8:6107715-6107716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs202240136	chr8:6107722-6107723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs66814738	chr8:6107755-6107756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545025266	chr8:6107799-6107800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564932385	chr8:6107856-6107857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530949556	chr8:6107860-6107861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533561736	chr8:6107865-6107866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs56052007	chr8:6107870-6107871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111394877	chr8:6107872-6107873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187270204	chr8:6107877-6107878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs55755015	chr8:6107878-6107879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs547286278	chr8:6107879-6107880	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	chr8:6104400-6107400	Enhancers	Primary hematopoietic stem cells	blood
2	chr8:6105000-6107400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
9	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
17	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
21	chr8:6119400-6120000	Enhancers	Osteobl	bone
22	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
24	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
27	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr8:6132200-6132800	Enhancers	Spleen	Spleen
31	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
32	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
34	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
47	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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