Variant report

Variant	nsv1027845
Chromosome Location	chr8:10959666-10995565
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	ATF2	chr8:10981506-10982207	GM12878	blood:	n/a	n/a
2	ATF2	chr8:10981488-10982324	GM12878	blood:	n/a	n/a
3	BACH1	chr8:10962868-10963169	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr8:10981539-10982080	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:10981392-10982182	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:10984322-10984480	HepG2	liver:	n/a	chr8:10984400-10984411
7	CEBPB	chr8:10969507-10969750	HepG2	liver:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
8	CEBPB	chr8:10969452-10969699	K562	blood:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
9	CEBPB	chr8:10969442-10969756	IMR90	lung:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
10	CEBPB	chr8:10986551-10986831	IMR90	lung:	n/a	n/a
11	CHD1	chr8:10981485-10982120	GM12878	blood:	n/a	n/a
12	CHD2	chr8:10981673-10981992	GM12878	blood:	n/a	n/a
13	CTCF	chr8:10962800-10962950	HMF	breast:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
14	CTCF	chr8:10962916-10962955	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:10965940-10966090	GM12878	blood:	n/a	chr8:10966022-10966040
16	CTCF	chr8:10965982-10966052	GM10248	blood:	n/a	chr8:10966022-10966040
17	CTCF	chr8:10962860-10963010	HA-sp	spinal cord:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
18	CTCF	chr8:10962880-10963030	Caco-2	colon:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
19	CTCF	chr8:10962793-10962996	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
20	CTCF	chr8:10962840-10962990	SK-N-SH_RA	brain:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
21	CTCF	chr8:10962820-10962970	HBMEC	blood vessel:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
22	CTCF	chr8:10966039-10966073	GM19238	blood:	n/a	n/a
23	CTCF	chr8:10962812-10963078	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
24	CTCF	chr8:10962760-10962910	GM12864	blood:	n/a	n/a
25	CTCF	chr8:10962820-10962970	AG04450	lung:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
26	CTCF	chr8:10965982-10966079	K562	blood:	n/a	chr8:10966022-10966040
27	CTCF	chr8:10962866-10962988	MCF-7	breast:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
28	CTCF	chr8:10977247-10977292	GM13977	blood:	n/a	n/a
29	CTCF	chr8:10982701-10982751	GM19239	blood:	n/a	n/a
30	CTCF	chr8:10962840-10962990	GM12868	blood:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
31	CTCF	chr8:10985140-10985290	GM06990	blood:	n/a	n/a
32	CTCF	chr8:10966100-10966250	GM12867	blood:	n/a	n/a
33	CTCF	chr8:10962760-10962910	GM06990	blood:	n/a	n/a
34	CTCF	chr8:10962800-10962950	HFF-Myc	foreskin:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
35	CTCF	chr8:10977243-10977296	GM10266	blood:	n/a	n/a
36	CTCF	chr8:10962780-10962930	RPTEC	kidney:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
37	CTCF	chr8:10962820-10962970	HEK293	kidney:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
38	CTCF	chr8:10962800-10962950	AG04449	skin:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
39	CTCF	chr8:10977240-10977269	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr8:10971467-10971489	GM19239	blood:	n/a	n/a
41	CTCF	chr8:10962820-10962970	Caco-2	colon:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
42	CTCF	chr8:10962850-10963009	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
43	CTCF	chr8:10962760-10962910	HCT-116	colon:	n/a	n/a
44	CTCF	chr8:10962887-10962969	MCF-7	breast:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
45	CTCF	chr8:10965980-10966130	BE2_C	brain:	n/a	chr8:10966022-10966040
46	CTCF	chr8:10962840-10962990	HBMEC	blood vessel:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
47	CTCF	chr8:10977237-10977346	LNCaP	prostate:	n/a	n/a
48	CTCF	chr8:10965020-10965170	GM12868	blood:	n/a	n/a
49	CTCF	chr8:10962780-10962930	HRE	kidney:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
50	CTCF	chr8:10962980-10963130	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10982332-10982382	HUVEC	blood vessel:	n/a
2	chr8:10982332-10982382	HUVEC	blood vessel:	n/a
3	chr8:10982836-10982886	AG09309	skin:	n/a
4	chr8:10988117-10988167	GM12878	blood:	n/a
5	chr8:10966192-10966242	HCT-116	colon:	n/a
6	chr8:10966192-10966242	Jurkat	blood:	n/a
7	chr8:10966192-10966242	ovcar-3	ovarian:	n/a
8	chr8:10965533-10965583	CMK	blood:	n/a
9	chr8:10966224-10966274	GM19239	blood:	n/a
10	chr8:10988117-10988167	GM19239	blood:	n/a
11	chr8:10982332-10982382	IMR90	lung:	fetal
12	chr8:10966224-10966274	SK-N-SH	brain:	n/a
13	chr8:10982836-10982886	HIPEpiC	eye:	n/a
14	chr8:10965533-10965583	BE2_C	brain:	n/a
15	chr8:10966224-10966274	AG09319	gingival:	n/a
16	chr8:10987869-10987919	NHDF-neo	bronchial:	n/a
17	chr8:10982668-10982718	Caco-2	colon:	n/a
18	chr8:10965533-10965583	SK-N-SH_RA	brain:	n/a
19	chr8:10966251-10966301	SK-N-MC	brain:	n/a
20	chr8:10982836-10982886	NB4	blood:	n/a
21	chr8:10982332-10982382	GM12878	blood:	n/a
22	chr8:10965533-10965583	ovcar-3	ovarian:	n/a
23	chr8:10982836-10982886	HCPEpiC	choroid plexus:	n/a
24	chr8:10966251-10966301	HL-60	blood:	n/a
25	chr8:10988117-10988167	PFSK-1	brain:	n/a
26	chr8:10965533-10965583	HRPEpiC	eye:	n/a
27	chr8:10965430-10965480	HepG2	liver:	n/a
28	chr8:10982332-10982382	Hela-S3	cervix:	n/a
29	chr8:10965430-10965480	SK-N-MC	brain:	n/a
30	chr8:10982668-10982718	NB4	blood:	n/a
31	chr8:10966224-10966274	H1-hESC	embryonic stem cell:	embryo
32	chr8:10966192-10966242	HCPEpiC	choroid plexus:	n/a
33	chr8:10966224-10966274	HRPEpiC	eye:	n/a
34	chr8:10982332-10982382	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:10966224-10966274	HL-60	blood:	n/a
36	chr8:10965430-10965480	HL-60	blood:	n/a
37	chr8:10965430-10965480	NB4	blood:	n/a
38	chr8:10966192-10966242	HCF	heart:	n/a
39	chr8:10966251-10966301	HEEpiC	esophagus:	n/a
40	chr8:10987869-10987919	PFSK-1	brain:	n/a
41	chr8:10982836-10982886	AG04449	skin:	fetal
42	chr8:10982332-10982382	H1-hESC	embryonic stem cell:	embryo
43	chr8:10966251-10966301	SAEC	small airway:	n/a
44	chr8:10987869-10987919	HL-60	blood:	n/a
45	chr8:10965430-10965480	Hepatocyte	liver:	n/a
46	chr8:10966251-10966301	NHBE	bronchial:	n/a
47	chr8:10965430-10965480	Jurkat	blood:	n/a
48	chr8:10982836-10982886	T-47D	breast:	n/a
49	chr8:10982668-10982718	RPTEC	kidney:	n/a
50	chr8:10966251-10966301	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:
2	chr8:10953851..10956299-chr8:10959068..10961747,2	MCF-7	breast:
3	chr5:138973431..138974207-chr8:10970599..10971381,2	MCF-7	breast:
4	chr8:10890969..10893547-chr8:10959450..10962216,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131215.3.1-2	chr8:10986134-10987275	NONHSAT125039
2	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3
3	lnc-AF131215.3.1-1	chr8:10980891-10982327	NONHSAT125036
4	lnc-AF131215.4.1-1	chr8:10994408-10996117	ENSG00000254556.1
5	lnc-AF131215.3.1-2	chr8:10984315-10984600	NONHSAT125039
6	lnc-AF131215.2.1-1	chr8:10964720-10967428	ENSG00000255310.1
7	lnc-AF131215.2.1-1	chr8:10962201-10964214	ENSG00000269918.1
8	lnc-AF131215.2.1-1	chr8:10965298-10967236	ENSG00000255310.2
9	lnc-MTMR9-1	chr8:10983268-10983574	ENSG00000247665
10	lnc-MTMR9-1	chr8:10980891-10982326	ENSG00000247665
11	lnc-AF131215.2.1-1	chr8:10965064-10965184	NONHSAT125034
12	lnc-AF131215.3.1-1	chr8:10983268-10983574	ENSG00000254936.3
13	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3
14	lnc-AF131215.2.1-1	chr8:10962658-10964223	NONHSAT125034
15	lnc-AF131215.3.1-1	chr8:10983271-10983574	ENSG00000254936.3

Variant related genes	Relation type
ENSG00000269918	TF binding region
ENSG00000254936	TF binding region
ENSG00000255310	TF binding region
ENSG00000215346	TF binding region
ENSG00000269918	CpG island
ENSG00000254936	CpG island
ENSG00000255310	CpG island
ENSG00000215346	CpG island
ENSG00000207600	chromatin interactions
ZFYVE20	miRNA target sites
KIF5C	miRNA target sites

Extended variants
information (count: 2073 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:2073 , 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	rs7000695	chr8:10959666-10959667	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568640640	chr8:10959672-10959673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567165722	chr8:10959689-10959690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537432117	chr8:10959695-10959696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534262420	chr8:10959742-10959743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181675144	chr8:10959746-10959747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557350594	chr8:10959775-10959776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs5889359	chr8:10959780-10959781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567994222	chr8:10959813-10959814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139532469	chr8:10959819-10959820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186208036	chr8:10959831-10959832	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575004846	chr8:10959879-10959880	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540161683	chr8:10959898-10959899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373641240	chr8:10959899-10959900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545547644	chr8:10959906-10959907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149718874	chr8:10959922-10959923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2409705	chr8:10959932-10959933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs75782340	chr8:10960019-10960020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115302488	chr8:10960035-10960036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375140434	chr8:10960142-10960143	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553892517	chr8:10960151-10960152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562036156	chr8:10960160-10960161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529236671	chr8:10960173-10960174	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs544626388	chr8:10960175-10960176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562920614	chr8:10960217-10960218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533509948	chr8:10960233-10960234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573750629	chr8:10960235-10960236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114597816	chr8:10960262-10960263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566985704	chr8:10960295-10960296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs527965701	chr8:10960313-10960314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549386131	chr8:10960324-10960325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145587790	chr8:10960334-10960335	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556542332	chr8:10960338-10960339	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148879856	chr8:10960359-10960360	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542869876	chr8:10960367-10960368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377226121	chr8:10960391-10960392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539189596	chr8:10960414-10960415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145270643	chr8:10960415-10960416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572922776	chr8:10960437-10960438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs534006668	chr8:10960440-10960441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147646376	chr8:10960464-10960465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562146330	chr8:10960471-10960472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377083091	chr8:10960483-10960484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10503413	chr8:10960495-10960496	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115799310	chr8:10960496-10960497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12543056	chr8:10960497-10960498	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7843934	chr8:10960506-10960507	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs79242232	chr8:10960518-10960519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533634593	chr8:10960554-10960555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4840544	chr8:10960572-10960573	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:138)

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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10950600-10965000	Weak transcription	Gastric	stomach
2	chr8:10955200-10968000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:10956800-10964800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr8:10957200-10964800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr8:10958200-10965000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr8:10958200-10967200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr8:10958200-10970200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:10958400-10965200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr8:10958400-10974800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr8:10958600-10964800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr8:10958600-10965000	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr8:10958600-10971200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr8:10958600-10971200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr8:10958800-10967400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr8:10959600-10964800	Weak transcription	Pancreas	Pancrea
16	chr8:10960400-10963800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:10960400-10967000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr8:10960400-10968400	Weak transcription	Spleen	Spleen
19	chr8:10960800-10961800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:10960800-10965200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:10960800-10970800	Weak transcription	HSMM	muscle
22	chr8:10961200-10961800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:10961200-10964600	Weak transcription	Fetal Intestine Small	intestine
24	chr8:10961200-10964800	Weak transcription	Fetal Stomach	stomach
25	chr8:10961200-10975400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr8:10961600-10970600	Weak transcription	Fetal Intestine Large	intestine
27	chr8:10961800-10962800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:10961800-10963600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:10961800-10968800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr8:10961800-10971400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:10962000-10968000	Weak transcription	GM12878-XiMat	blood
32	chr8:10962200-10964400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:10962400-10964800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:10962400-10964800	Weak transcription	HMEC	breast
35	chr8:10962400-10967600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr8:10962400-10969600	Weak transcription	NH-A	brain
37	chr8:10962600-10964000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:10962800-10965000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:10963000-10963400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:10963000-10964800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:10963000-10981200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr8:10963200-10967200	Weak transcription	Primary T cells from cord blood	blood
43	chr8:10963200-10970400	Weak transcription	Primary B cells from cord blood	blood
44	chr8:10963400-10965000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr8:10963400-10965000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr8:10963400-10971400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:10963600-10964000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:10963600-10966600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr8:10963600-10971200	Weak transcription	HSMMtube	muscle
50	chr8:10963600-10973600	Weak transcription	Lung	lung

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