Variant report

Variant	nsv1023713
Chromosome Location	chr8:9100776-9123940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9106581-9106674	K562	blood:	n/a	n/a
2	ATF1	chr8:9112997-9113254	K562	blood:	n/a	n/a
3	ATF1	chr8:9106470-9106696	K562	blood:	n/a	n/a
4	ATF1	chr8:9117581-9118000	K562	blood:	n/a	n/a
5	ATF2	chr8:9106362-9106824	GM12878	blood:	n/a	n/a
6	ATF2	chr8:9121581-9122231	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:9106397-9106813	GM12878	blood:	n/a	n/a
8	ATF2	chr8:9121573-9122206	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:9106307-9106946	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
10	BATF	chr8:9106372-9106826	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
11	BCL11A	chr8:9106430-9106921	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
12	BCL11A	chr8:9121767-9122132	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr8:9106380-9106943	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
14	BCLAF1	chr8:9106457-9106732	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
15	BHLHE40	chr8:9112909-9113255	K562	blood:	n/a	n/a
16	BHLHE40	chr8:9110612-9110648	K562	blood:	n/a	n/a
17	BHLHE40	chr8:9110246-9110274	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:9110181-9110378	K562	blood:	n/a	n/a
19	BHLHE40	chr8:9117711-9118064	K562	blood:	n/a	n/a
20	BHLHE40	chr8:9106199-9106847	GM12878	blood:	n/a	n/a
21	BRCA1	chr8:9121619-9122124	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:9117691-9118023	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:9100534-9100869	HepG2	liver:	n/a	chr8:9100620-9100631
24	CEBPB	chr8:9100552-9100824	A549	lung:	n/a	chr8:9100620-9100631
25	CEBPB	chr8:9100492-9100818	K562	blood:	n/a	chr8:9100620-9100631
26	CEBPB	chr8:9117816-9117945	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:9117674-9117963	K562	blood:	n/a	n/a
28	CEBPB	chr8:9121074-9121429	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr8:9120610-9120786	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr8:9121198-9122494	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr8:9115053-9115101	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr8:9106307-9106725	GM12878	blood:	n/a	n/a
33	CTCF	chr8:9106540-9106690	GM12874	blood:	n/a	n/a
34	CTCF	chr8:9106340-9106490	GM12866	blood:	n/a	n/a
35	CTCF	chr8:9106520-9106670	HCM	heart:	n/a	n/a
36	CTCF	chr8:9106473-9106684	K562	blood:	n/a	n/a
37	CTCF	chr8:9106506-9106654	GM19240	blood:	n/a	n/a
38	CTCF	chr8:9112800-9112950	A549	lung:	n/a	n/a
39	CTCF	chr8:9106440-9106590	HCT-116	colon:	n/a	n/a
40	CTCF	chr8:9106492-9106653	GM10266	blood:	n/a	n/a
41	CTCF	chr8:9115072-9115119	LNCaP	prostate:	n/a	n/a
42	CTCF	chr8:9112920-9113070	K562	blood:	n/a	n/a
43	CTCF	chr8:9112892-9112988	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:9112860-9113010	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr8:9106480-9106630	GM06990	blood:	n/a	n/a
46	CTCF	chr8:9112920-9113070	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr8:9106487-9106660	GM19239	blood:	n/a	n/a
48	CTCF	chr8:9112860-9113010	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr8:9106390-9106761	GM12878	blood:	n/a	n/a
50	CTCF	chr8:9106369-9106733	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9123484-9123534	NHDF-neo	bronchial:	n/a
2	chr8:9106953-9107003	NT2-D1	testis:	n/a
3	chr8:9106953-9107003	T-47D	breast:	n/a
4	chr8:9106953-9107003	AG09319	gingival:	n/a
5	chr8:9123484-9123534	ProgFib	skin:	n/a
6	chr8:9106953-9107003	GM12891	blood:	n/a
7	chr8:9106953-9107003	HepG2	liver:	n/a
8	chr8:9123484-9123534	HCPEpiC	choroid plexus:	n/a
9	chr8:9123484-9123534	AG09319	gingival:	n/a
10	chr8:9106953-9107003	K562	blood:	n/a
11	chr8:9106953-9107003	SAEC	small airway:	n/a
12	chr8:9106953-9107003	NB4	blood:	n/a
13	chr8:9107382-9107432	NHBE	bronchial:	n/a
14	chr8:9107382-9107432	PANC-1	pancreas:	n/a
15	chr8:9106953-9107003	Hela-S3	cervix:	n/a
16	chr8:9107382-9107432	AG10803	skin:	n/a
17	chr8:9106953-9107003	SK-N-SH	brain:	n/a
18	chr8:9123484-9123534	MCF-7	breast:	n/a
19	chr8:9106953-9107003	SKMC	muscle:	n/a
20	chr8:9106953-9107003	BJ	skin:	n/a
21	chr8:9106953-9107003	H1-hESC	embryonic stem cell:	embryo
22	chr8:9123484-9123534	PFSK-1	brain:	n/a
23	chr8:9107382-9107432	K562	blood:	n/a
24	chr8:9123484-9123534	HEEpiC	esophagus:	n/a
25	chr8:9106953-9107003	A549	lung:	n/a
26	chr8:9123484-9123534	HAEpiC	amniotic membrane:	n/a
27	chr8:9107382-9107432	HCM	heart:	n/a
28	chr8:9106953-9107003	SK-N-SH_RA	brain:	n/a
29	chr8:9107382-9107432	HL-60	blood:	n/a
30	chr8:9123484-9123534	AG04449	skin:	fetal
31	chr8:9107382-9107432	HUVEC	blood vessel:	n/a
32	chr8:9106953-9107003	GM19239	blood:	n/a
33	chr8:9106953-9107003	Jurkat	blood:	n/a
34	chr8:9123484-9123534	IMR90	lung:	fetal
35	chr8:9107382-9107432	IMR90	lung:	fetal
36	chr8:9107382-9107432	Jurkat	blood:	n/a
37	chr8:9106953-9107003	SK-N-MC	brain:	n/a
38	chr8:9107382-9107432	RPTEC	kidney:	n/a
39	chr8:9123484-9123534	AoSMC	blood vessel:	n/a
40	chr8:9107382-9107432	HRCEpiC	kidney:	n/a
41	chr8:9123484-9123534	HRE	kidney:	n/a
42	chr8:9123484-9123534	NT2-D1	testis:	n/a
43	chr8:9107382-9107432	HCT-116	colon:	n/a
44	chr8:9107382-9107432	SK-N-SH_RA	brain:	n/a
45	chr8:9106953-9107003	BE2_C	brain:	n/a
46	chr8:9123484-9123534	GM19239	blood:	n/a
47	chr8:9107382-9107432	ProgFib	skin:	n/a
48	chr8:9107382-9107432	HRPEpiC	eye:	n/a
49	chr8:9106953-9107003	U87	brain:	n/a
50	chr8:9106953-9107003	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
2	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
3	chr8:9121493..9123437-chr8:9133381..9135913,2	K562	blood:
4	chr8:9098947..9101284-chr8:9104230..9106988,2	K562	blood:
5	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
6	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
7	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
8	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
9	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
10	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3B-2	chr8:9112315-9112398	XLOC_006999
2	lnc-PPP1R3B-2	chr8:9115957-9116369	XLOC_006999
3	lnc-PPP1R3B-2	chr8:9117538-9117805	ENSG00000253887
4	lnc-PPP1R3B-2	chr8:9117538-9117788	XLOC_006999
5	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
6	lnc-PPP1R3B-2	chr8:9112893-9113012	XLOC_006999
7	lnc-PPP1R3B-2	chr8:9112859-9113012	ENSG00000253887
8	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999

No data

Variant related genes	Relation type
ENSG00000254235	TF binding region
ENSG00000253887	TF binding region
ENSG00000254235	CpG island
ENSG00000253887	CpG island
ENSG00000254235	chromatin interactions

Extended variants
information (count: 1434 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:1434 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543135092	chr8:9100778-9100779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs147670203	chr8:9100853-9100854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528682201	chr8:9100855-9100856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140666666	chr8:9100862-9100863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35354760	chr8:9100870-9100871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536570548	chr8:9100887-9100888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531213316	chr8:9100888-9100889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4841111	chr8:9100899-9100900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144539943	chr8:9100900-9100901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566911581	chr8:9100910-9100911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549734079	chr8:9100940-9100941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs330033	chr8:9100949-9100950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs67081905	chr8:9100991-9100992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566535571	chr8:9100999-9101000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35666964	chr8:9101009-9101010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151213123	chr8:9101047-9101048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558704428	chr8:9101049-9101050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs28545564	chr8:9101072-9101073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs377466032	chr8:9101097-9101098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575479108	chr8:9101139-9101140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538135072	chr8:9101144-9101145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184286945	chr8:9101172-9101173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76651819	chr8:9101194-9101195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574093614	chr8:9101217-9101218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189192034	chr8:9101239-9101240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565743790	chr8:9101302-9101303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538343082	chr8:9101305-9101306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74365961	chr8:9101347-9101348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375286370	chr8:9101350-9101351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181834397	chr8:9101356-9101357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111771837	chr8:9101373-9101374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111276860	chr8:9101407-9101408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186488252	chr8:9101439-9101440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189572572	chr8:9101454-9101455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550869642	chr8:9101455-9101456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115604544	chr8:9101470-9101471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140333488	chr8:9101509-9101510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571869168	chr8:9101537-9101538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529661146	chr8:9101626-9101627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs330034	chr8:9101627-9101628	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs61046890	chr8:9101633-9101634	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538708282	chr8:9101702-9101703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150344220	chr8:9101710-9101711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569023725	chr8:9101718-9101719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536908086	chr8:9101751-9101752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537998298	chr8:9101773-9101774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs330035	chr8:9101791-9101792	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574757893	chr8:9101836-9101837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1551790	chr8:9101842-9101843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553308733	chr8:9101894-9101895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
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
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
Lung squamous cell carcinoma	22363434	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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9095200-9114400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:9095600-9101800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr8:9095600-9102400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:9095800-9102200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:9097600-9101600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:9097600-9102000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:9097800-9101800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:9098000-9102000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:9098000-9110400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:9098200-9102000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:9098200-9102000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:9099800-9106000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:9100000-9101400	Enhancers	Liver	Liver
14	chr8:9100000-9106200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:9101000-9101400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr8:9101400-9104400	Weak transcription	Liver	Liver
17	chr8:9101400-9106200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr8:9101600-9102800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:9101800-9102800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:9101800-9102800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:9102000-9102400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:9102000-9102600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:9102000-9102600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:9102000-9102800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr8:9102000-9102800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:9102000-9102800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:9102200-9102600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:9102200-9102800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr8:9102200-9103000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:9102400-9102600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:9102600-9103000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:9102600-9106200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:9102600-9110600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:9103000-9107800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:9104400-9106800	Enhancers	Liver	Liver
36	chr8:9104600-9105200	Enhancers	Stomach Smooth Muscle	stomach
37	chr8:9104600-9106200	Enhancers	Colon Smooth Muscle	Colon
38	chr8:9104800-9105200	Enhancers	Fetal Stomach	stomach
39	chr8:9104800-9106000	Enhancers	Rectal Smooth Muscle	rectum
40	chr8:9105000-9105200	Enhancers	Aorta	Aorta
41	chr8:9105000-9105200	Enhancers	Pancreas	Pancrea
42	chr8:9105200-9106200	Weak transcription	Pancreas	Pancrea
43	chr8:9105200-9113200	Weak transcription	Aorta	Aorta
44	chr8:9105400-9106400	Enhancers	Fetal Heart	heart
45	chr8:9105600-9106400	Enhancers	Brain Substantia Nigra	brain
46	chr8:9105600-9106600	Enhancers	Brain Cingulate Gyrus	brain
47	chr8:9106000-9106200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:9106000-9106200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr8:9106000-9106600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:9106000-9106800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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