Variant report

Variant	nsv1019693
Chromosome Location	chr8:6999220-7323551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1684)
CpG islands
(count:3177)
Chromatin interactive
region (count:3)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1684 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:7277768-7278018	K562	blood:	n/a	n/a
2	ATF1	chr8:7255409-7255636	K562	blood:	n/a	n/a
3	BACH1	chr8:7085606-7085806	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:7265686-7265994	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:7065329-7065744	GM12878	blood:	n/a	chr8:7065585-7065596
6	BATF	chr8:7220356-7220781	GM12878	blood:	n/a	n/a
7	BATF	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
8	BATF	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
9	BATF	chr8:7215685-7216141	GM12878	blood:	n/a	n/a
10	BATF	chr8:7105978-7106319	GM12878	blood:	n/a	n/a
11	BATF	chr8:7215669-7216199	GM12878	blood:	n/a	n/a
12	BATF	chr8:7255357-7255599	GM12878	blood:	n/a	n/a
13	BATF	chr8:7065286-7065896	GM12878	blood:	n/a	chr8:7065585-7065596
14	BATF	chr8:7106013-7106321	GM12878	blood:	n/a	n/a
15	BATF	chr8:7281851-7282075	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:7220370-7220830	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:7078884-7079047	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:7065268-7065674	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:7096016-7096195	GM12878	blood:	n/a	chr8:7096138-7096151
20	BCL11A	chr8:7059717-7059897	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:7213997-7214166	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:7212700-7212924	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:7228613-7228840	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:7215704-7215862	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:7065285-7065931	GM12878	blood:	n/a	n/a
26	BCL3	chr8:7199106-7199270	GM12878	blood:	n/a	chr8:7199138-7199147
27	BHLHE40	chr8:7079428-7079694	HepG2	liver:	n/a	chr8:7079551-7079567
28	BHLHE40	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:7212724-7213120	K562	blood:	n/a	n/a
30	BRCA1	chr8:7255419-7255821	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr8:7212733-7213463	GM12878	blood:	n/a	n/a
32	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
33	CEBPB	chr8:7252439-7252682	HepG2	liver:	n/a	chr8:7252592-7252609
34	CEBPB	chr8:7178817-7179042	K562	blood:	n/a	n/a
35	CEBPB	chr8:7216733-7216933	HepG2	liver:	n/a	chr8:7216873-7216886 chr8:7216873-7216886 chr8:7216873-7216884
36	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
37	CEBPB	chr8:7247541-7247907	IMR90	lung:	n/a	chr8:7247717-7247726 chr8:7247717-7247728
38	CEBPB	chr8:7281546-7281777	K562	blood:	n/a	n/a
39	CEBPB	chr8:7281458-7281820	A549	lung:	n/a	n/a
40	CEBPB	chr8:7281458-7281828	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:7252446-7252801	H1-hESC	embryonic stem cell:	n/a	chr8:7252592-7252609
42	CEBPB	chr8:7247544-7247875	A549	lung:	n/a	chr8:7247717-7247726 chr8:7247717-7247728
43	CEBPB	chr8:7281563-7281826	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr8:7252300-7252814	A549	lung:	n/a	chr8:7252592-7252609
45	CEBPB	chr8:7255340-7255633	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
47	CEBPB	chr8:7281556-7281783	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:7252287-7252800	Hela-S3	cervix:	n/a	chr8:7252592-7252609
49	CEBPB	chr8:7247547-7247867	H1-hESC	embryonic stem cell:	n/a	chr8:7247717-7247726 chr8:7247717-7247728
50	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a

(count:3177 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7083881-7083931	NB4	blood:	n/a
2	chr8:7151550-7151600	HUVEC	blood vessel:	n/a
3	chr8:7155667-7155717	Jurkat	blood:	n/a
4	chr8:7128706-7128756	MCF10A-Er-Src	breast:	n/a
5	chr8:7078402-7078452	SK-N-SH	brain:	n/a
6	chr8:7083881-7083931	NB4	blood:	n/a
7	chr8:7151550-7151600	HUVEC	blood vessel:	n/a
8	chr8:7155667-7155717	Jurkat	blood:	n/a
9	chr8:7128706-7128756	MCF10A-Er-Src	breast:	n/a
10	chr8:7078402-7078452	SK-N-SH	brain:	n/a
11	chr8:7005011-7005061	SK-N-SH	brain:	n/a
12	chr8:7189580-7189630	HIPEpiC	eye:	n/a
13	chr8:7213526-7213576	ProgFib	skin:	n/a
14	chr8:7221471-7221521	HEK293	kidney:	embryo
15	chr8:7005011-7005061	PrEC	prostate:	n/a
16	chr8:7191953-7192003	HCF	heart:	n/a
17	chr8:7156743-7156793	Hepatocyte	liver:	n/a
18	chr8:7153933-7153983	GM19239	blood:	n/a
19	chr8:7015931-7015981	BE2_C	brain:	n/a
20	chr8:7154895-7154945	HCT-116	colon:	n/a
21	chr8:7221471-7221521	GM12878	blood:	n/a
22	chr8:7155667-7155717	HRPEpiC	eye:	n/a
23	chr8:7009699-7009749	NHBE	bronchial:	n/a
24	chr8:7212941-7212991	ovcar-3	ovarian:	n/a
25	chr8:7079106-7079156	IMR90	lung:	fetal
26	chr8:7009699-7009749	HMEC	breast:	n/a
27	chr8:7113462-7113512	GM12891	blood:	n/a
28	chr8:7305465-7305515	AG10803	skin:	n/a
29	chr8:7191920-7191970	PFSK-1	brain:	n/a
30	chr8:7311130-7311180	NH-A	brain:	n/a
31	chr8:7113462-7113512	SK-N-SH_RA	brain:	n/a
32	chr8:7213522-7213572	U87	brain:	n/a
33	chr8:7079106-7079156	HUVEC	blood vessel:	n/a
34	chr8:7015931-7015981	SK-N-MC	brain:	n/a
35	chr8:7216871-7216921	MCF-7	breast:	n/a
36	chr8:7212941-7212991	SAEC	small airway:	n/a
37	chr8:7079761-7079811	NT2-D1	testis:	n/a
38	chr8:7191273-7191323	ProgFib	skin:	n/a
39	chr8:7208812-7208862	HEEpiC	esophagus:	n/a
40	chr8:7212941-7212991	HRPEpiC	eye:	n/a
41	chr8:7213526-7213576	PFSK-1	brain:	n/a
42	chr8:7083881-7083931	SK-N-SH	brain:	n/a
43	chr8:7212954-7213004	NHDF-neo	bronchial:	n/a
44	chr8:7085814-7085864	HNPCEpiC	eye:	n/a
45	chr8:7005678-7005728	ovcar-3	ovarian:	n/a
46	chr8:7015931-7015981	NT2-D1	testis:	n/a
47	chr8:7212954-7213004	HCPEpiC	choroid plexus:	n/a
48	chr8:7015931-7015981	MCF-7	breast:	n/a
49	chr8:7004819-7004869	HRCEpiC	kidney:	n/a
50	chr8:7155667-7155717	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:
2	chr8:7255181..7256067-chr8:7770740..7771265,2	MCF-7	breast:
3	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
2	lnc-ZNF705G-1	chr8:7212333-7212574	NONHSAT124826
3	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823
4	lnc-ZNF705G-1	chr8:7212333-7212511	NONHSAT124824
5	lnc-ZNF705G-1	chr8:7206605-7206668	NONHSAT124824
6	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
7	lnc-ZNF705G-1	chr8:7206593-7206668	NONHSAT124826
8	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
9	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813
10	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824
11	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
12	lnc-DEFB105B-1	chr8:7234859-7235022	NONHSAT124827
13	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
14	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
15	lnc-DEFB105B-1	chr8:7230636-7230723	NONHSAT124827

No data

Variant related genes	Relation type
FAM90A13P	TF binding region
SPAG11B	TF binding region
FAM90A20P	TF binding region
DEFB109P1B	TF binding region
ENSG00000235778	TF binding region
ENSG00000221567	TF binding region
ENSG00000230106	TF binding region
ENSG00000216194	TF binding region
ENSG00000255025	TF binding region
FAM90A3P	TF binding region
RPS3AP33	TF binding region
FAM90A4P	TF binding region
DEFB103B	TF binding region
FAM90A15P	TF binding region
DEFB108P2	TF binding region
ENSG00000254683	TF binding region
FAM90A5P	TF binding region
ZNF705G	TF binding region
ENSG00000231930	TF binding region
OR7E125P	TF binding region
DEFB4B	TF binding region
FAM66B	TF binding region
USP17L1P	TF binding region
USP17L4	TF binding region
HSPD1P3	TF binding region
FAM90A13P	CpG island
SPAG11B	CpG island
FAM90A20P	CpG island
DEFB109P1B	CpG island
ENSG00000235778	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
ENSG00000216194	CpG island
ENSG00000255025	CpG island
FAM90A3P	CpG island
RPS3AP33	CpG island
FAM90A4P	CpG island
DEFB103B	CpG island
FAM90A15P	CpG island
DEFB108P2	CpG island
ENSG00000254683	CpG island
FAM90A5P	CpG island
ZNF705G	CpG island
ENSG00000231930	CpG island
OR7E125P	CpG island
DEFB4B	CpG island
FAM66B	CpG island
USP17L1P	CpG island
USP17L4	CpG island
HSPD1P3	CpG island
ENSG00000226711	chromatin interactions

Extended variants
information (count: 4650 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:4650 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4840673	chr8:6999220-6999221	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs543018547	chr8:6999234-6999235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs59148681	chr8:6999243-6999244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71214994	chr8:6999257-6999258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563322766	chr8:6999259-6999260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528964928	chr8:6999262-6999263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549102459	chr8:6999267-6999268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12677885	chr8:6999283-6999284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373114242	chr8:6999289-6999290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146669790	chr8:6999313-6999314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370416796	chr8:6999322-6999323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191340475	chr8:6999349-6999350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182857339	chr8:6999357-6999358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537769984	chr8:6999361-6999362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4240692	chr8:6999423-6999424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567688264	chr8:6999436-6999437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186155503	chr8:6999442-6999443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553098519	chr8:6999444-6999445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573007212	chr8:6999449-6999450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534472184	chr8:6999473-6999474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563445420	chr8:6999477-6999478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190454805	chr8:6999481-6999482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577492189	chr8:6999486-6999487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138904418	chr8:6999494-6999495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183555832	chr8:6999504-6999505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573625213	chr8:6999518-6999519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542260113	chr8:6999530-6999531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559450275	chr8:6999531-6999532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528209914	chr8:6999538-6999539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552160053	chr8:6999562-6999563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187854269	chr8:6999564-6999565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565507999	chr8:6999571-6999572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199699732	chr8:6999578-6999579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531096244	chr8:6999600-6999601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373493434	chr8:6999621-6999622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200653180	chr8:6999629-6999630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536604280	chr8:6999631-6999632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192451844	chr8:6999632-6999633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566593895	chr8:6999662-6999663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202068492	chr8:6999684-6999685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200055691	chr8:6999690-6999691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538770938	chr8:6999694-6999695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557512659	chr8:6999714-6999715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571457902	chr8:6999720-6999721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377310243	chr8:6999723-6999724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536941295	chr8:6999737-6999738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182736891	chr8:6999751-6999752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573862111	chr8:6999756-6999757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370165774	chr8:6999757-6999758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553024316	chr8:6999763-6999764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:158)

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
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	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
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	23813976	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Developmental disorder	20461109	CNVD
Pancreatic cancer	17952125	CNVD
Crohn''s disease	17953491	CNVD
Immune disease	21076436	CNVD
Crohn''s disease	21956041	CNVD
Autism	21865298	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6997000-7002200	Weak transcription	Dnd41	blood
2	chr8:7001600-7004800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:7002200-7005000	Strong transcription	Dnd41	blood
4	chr8:7004800-7005000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:7005000-7011600	Weak transcription	Dnd41	blood
6	chr8:7006000-7011400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr8:7008800-7009200	Enhancers	Fetal Heart	heart
8	chr8:7009200-7010200	Weak transcription	Fetal Heart	heart
9	chr8:7009200-7011600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:7009800-7010400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:7010200-7010400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:7010200-7010400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr8:7010400-7010600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:7010400-7010600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr8:7010400-7010600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:7010400-7010600	Enhancers	Fetal Heart	heart
17	chr8:7010400-7014600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:7010400-7014600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr8:7010600-7011600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr8:7010600-7014600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr8:7010600-7014600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr8:7011200-7013400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:7011400-7012600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:7011400-7012600	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr8:7011600-7012200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr8:7011600-7012400	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:7011600-7012400	Strong transcription	Dnd41	blood
28	chr8:7012200-7014600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr8:7012400-7012600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:7012400-7014200	Weak transcription	Dnd41	blood
31	chr8:7012400-7015000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr8:7012600-7014800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr8:7012600-7015000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:7014600-7014800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:7014600-7014800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr8:7014600-7015800	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr8:7014600-7015800	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr8:7014600-7016000	Active TSS	H9 Cell Line	embryonic stem cell
39	chr8:7014800-7015000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:7014800-7016000	Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr8:7014800-7016000	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr8:7015000-7015800	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:7015000-7015800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:7015000-7015800	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr8:7015000-7016000	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr8:7015400-7016000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:7016000-7016800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr8:7016800-7017200	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr8:7078600-7079600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr8:7078800-7079000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links