Variant report

Variant	nsv442088
Chromosome Location	chr8:5854296-5950848
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	BRCA1	chr8:5934404-5934557	HepG2	liver:	n/a	n/a
2	BRCA1	chr8:5875790-5876111	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr8:5934620-5934703	GM12878	blood:	n/a	n/a
4	CEBPB	chr8:5943713-5943758	IMR90	lung:	n/a	n/a
5	CEBPB	chr8:5875401-5876188	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr8:5931821-5932072	K562	blood:	n/a	n/a
7	CEBPB	chr8:5883252-5883353	A549	lung:	n/a	n/a
8	CEBPB	chr8:5871257-5871567	A549	lung:	n/a	chr8:5871421-5871434
9	CEBPB	chr8:5923529-5923871	H1-hESC	embryonic stem cell:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
10	CEBPB	chr8:5855136-5855336	HepG2	liver:	n/a	chr8:5855245-5855256
11	CEBPB	chr8:5903426-5903622	A549	lung:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
12	CEBPB	chr8:5871254-5871589	IMR90	lung:	n/a	chr8:5871421-5871434
13	CEBPB	chr8:5877716-5878268	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:5871279-5871583	K562	blood:	n/a	chr8:5871421-5871434
15	CEBPB	chr8:5930436-5930514	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:5917232-5917357	HepG2	liver:	n/a	chr8:5917295-5917306
17	CEBPB	chr8:5871276-5871564	H1-hESC	embryonic stem cell:	n/a	chr8:5871421-5871434
18	CEBPB	chr8:5920888-5921158	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:5923557-5923830	HepG2	liver:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
20	CEBPB	chr8:5923564-5923858	IMR90	lung:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
21	CEBPB	chr8:5871244-5871593	HepG2	liver:	n/a	chr8:5871421-5871434
22	CEBPB	chr8:5879099-5879536	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:5923536-5923736	K562	blood:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
24	CEBPB	chr8:5903392-5903683	K562	blood:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
25	CEBPB	chr8:5903414-5903669	HepG2	liver:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
26	CEBPB	chr8:5917160-5917474	H1-hESC	embryonic stem cell:	n/a	chr8:5917295-5917306
27	CEBPD	chr8:5934299-5934456	HepG2	liver:	n/a	n/a
28	CHD1	chr8:5917698-5917701	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr8:5877874-5878141	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr8:5934360-5934510	BJ	skin:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
31	CTCF	chr8:5934380-5934530	NHDF-neo	bronchial:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
32	CTCF	chr8:5939820-5939970	GM12869	blood:	n/a	n/a
33	CTCF	chr8:5934733-5934750	GM12878	blood:	n/a	n/a
34	CTCF	chr8:5934240-5934390	A549	lung:	n/a	n/a
35	CTCF	chr8:5934360-5934510	AG04449	skin:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
36	CTCF	chr8:5917516-5917708	LNCaP	prostate:	n/a	chr8:5917622-5917643
37	CTCF	chr8:5934400-5934550	GM12878	blood:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
38	CTCF	chr8:5934360-5934510	HAc	cerebellar:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
39	CTCF	chr8:5934360-5934510	SK-N-SH_RA	brain:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
40	CTCF	chr8:5934316-5934599	MCF-7	breast:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
41	CTCF	chr8:5934380-5934530	SK-N-SH_RA	brain:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
42	CTCF	chr8:5934400-5934550	GM12873	blood:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
43	CTCF	chr8:5934325-5934557	GM10248	blood:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
44	CTCF	chr8:5934380-5934530	GM12872	blood:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
45	CTCF	chr8:5934340-5934490	MCF-7	breast:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
46	CTCF	chr8:5934321-5934573	GM12892	blood:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
47	CTCF	chr8:5934380-5934530	HUVEC	blood vessel:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
48	CTCF	chr8:5949512-5949553	GM10266	blood:	n/a	n/a
49	CTCF	chr8:5934360-5934510	HCT-116	colon:	n/a	chr8:5934436-5934445 chr8:5934425-5934446 chr8:5934431-5934447 chr8:5934430-5934448
50	CTCF	chr8:5934820-5934970	GM12870	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5909880-5909930	GM19239	blood:	n/a
2	chr8:5909880-5909930	GM19239	blood:	n/a
3	chr8:5909945-5909995	PANC-1	pancreas:	n/a
4	chr8:5909945-5909995	Hepatocyte	liver:	n/a
5	chr8:5909880-5909930	AG04450	lung:	fetal
6	chr8:5909880-5909930	AG09319	gingival:	n/a
7	chr8:5909880-5909930	IMR90	lung:	fetal
8	chr8:5909880-5909930	SKMC	muscle:	n/a
9	chr8:5902873-5902923	HRPEpiC	eye:	n/a
10	chr8:5910061-5910111	SK-N-SH_RA	brain:	n/a
11	chr8:5909945-5909995	NB4	blood:	n/a
12	chr8:5902873-5902923	HEEpiC	esophagus:	n/a
13	chr8:5909880-5909930	HepG2	liver:	n/a
14	chr8:5949290-5949340	ECC-1	luminal epithelium:	n/a
15	chr8:5902873-5902923	AG04450	lung:	fetal
16	chr8:5902873-5902923	U87	brain:	n/a
17	chr8:5902873-5902923	ovcar-3	ovarian:	n/a
18	chr8:5902873-5902923	AG09319	gingival:	n/a
19	chr8:5909880-5909930	HAEpiC	amniotic membrane:	n/a
20	chr8:5909945-5909995	LNCaP	prostate:	n/a
21	chr8:5902873-5902923	BJ	skin:	n/a
22	chr8:5909880-5909930	GM12892	blood:	n/a
23	chr8:5909880-5909930	GM06990	blood:	n/a
24	chr8:5909945-5909995	MCF-7	breast:	n/a
25	chr8:5902873-5902923	NHDF-neo	bronchial:	n/a
26	chr8:5902873-5902923	BE2_C	brain:	n/a
27	chr8:5949290-5949340	HepG2	liver:	n/a
28	chr8:5909945-5909995	HepG2	liver:	n/a
29	chr8:5949290-5949340	HEEpiC	esophagus:	n/a
30	chr8:5910061-5910111	AG04450	lung:	fetal
31	chr8:5902873-5902923	Hela-S3	cervix:	n/a
32	chr8:5910061-5910111	ovcar-3	ovarian:	n/a
33	chr8:5909880-5909930	LNCaP	prostate:	n/a
34	chr8:5949290-5949340	PrEC	prostate:	n/a
35	chr8:5910061-5910111	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:5949290-5949340	SK-N-SH	brain:	n/a
37	chr8:5909880-5909930	NH-A	brain:	n/a
38	chr8:5902873-5902923	HCM	heart:	n/a
39	chr8:5949290-5949340	HPAEpiC	pulmonary alveolar:	n/a
40	chr8:5902873-5902923	HL-60	blood:	n/a
41	chr8:5910061-5910111	PrEC	prostate:	n/a
42	chr8:5949290-5949340	ProgFib	skin:	n/a
43	chr8:5909945-5909995	SK-N-MC	brain:	n/a
44	chr8:5909880-5909930	GM12878	blood:	n/a
45	chr8:5909880-5909930	Hepatocyte	liver:	n/a
46	chr8:5909880-5909930	BE2_C	brain:	n/a
47	chr8:5909880-5909930	HUVEC	blood vessel:	n/a
48	chr8:5949290-5949340	HRE	kidney:	n/a
49	chr8:5902873-5902923	AoSMC	blood vessel:	n/a
50	chr8:5909945-5909995	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
2	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:
3	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
4	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
5	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
6	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
7	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
8	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:5901875-5902047	ENSG00000253880
2	lnc-ANGPT2-4	chr8:5893955-5893990	ENSG00000253189
3	lnc-ANGPT2-4	chr8:5894372-5894496	ENSG00000253189
4	lnc-ANGPT2-5	chr8:5858959-5859084	XLOC_006983
5	lnc-ANGPT2-3	chr8:5916281-5916302	XLOC_006984
6	lnc-ANGPT2-5	chr8:5860524-5860623	XLOC_006983
7	lnc-ANGPT2-4	chr8:5894123-5894292	ENSG00000253189
8	lnc-ANGPT2-3	chr8:5916524-5916659	XLOC_006984
9	lnc-ANGPT2-3	chr8:5923520-5923650	XLOC_006984
10	lnc-ANGPT2-3	chr8:5917266-5917339	XLOC_006984
11	lnc-ANGPT2-3	chr8:5917266-5917339	ENSG00000253880
12	lnc-ANGPT2-3	chr8:5916524-5916600	ENSG00000253880

Variant related genes	Relation type
ENSG00000253189	TF binding region
ENSG00000253189	CpG island
ACVR1B	miRNA target sites
ACVR2A	miRNA target sites

Extended variants
information (count: 4136 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:4136 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2703194	chr8:5858800-5858801	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs578096686	chr8:5858822-5858823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545204864	chr8:5858831-5858832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2700732	chr8:5858840-5858841	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs151001521	chr8:5858851-5858852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2816480	chr8:5858890-5858891	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs112523784	chr8:5858920-5858921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183736020	chr8:5858923-5858924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73660274	chr8:5858924-5858925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571388087	chr8:5858928-5858929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79993768	chr8:5858936-5858937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550448944	chr8:5858940-5858941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545684731	chr8:5858948-5858949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142285150	chr8:5858984-5858985	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs145910058	chr8:5859021-5859022	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs566102789	chr8:5859029-5859030	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs535021528	chr8:5859034-5859035	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs187132188	chr8:5859039-5859040	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs147823493	chr8:5859046-5859047	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs79047642	chr8:5859052-5859053	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs192413028	chr8:5859083-5859084	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs141376920	chr8:5859085-5859086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543118667	chr8:5859086-5859087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2700733	chr8:5859089-5859090	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528481118	chr8:5859099-5859100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540188312	chr8:5859107-5859108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533488673	chr8:5859110-5859111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs137996906	chr8:5859114-5859115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78610124	chr8:5859121-5859122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149449973	chr8:5859151-5859152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143035123	chr8:5859156-5859157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182282575	chr8:5859173-5859174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138456063	chr8:5859218-5859219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186944445	chr8:5859231-5859232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75704471	chr8:5859234-5859235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189877004	chr8:5859237-5859238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs66529264	chr8:5859242-5859243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182496638	chr8:5859249-5859250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117632926	chr8:5859262-5859263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575876312	chr8:5859299-5859300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563488385	chr8:5859304-5859305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543179670	chr8:5859306-5859307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114937272	chr8:5859319-5859320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573205173	chr8:5859333-5859334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77113655	chr8:5859341-5859342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540609437	chr8:5859369-5859370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2703195	chr8:5859384-5859385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs552055580	chr8:5859411-5859412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544149264	chr8:5859416-5859417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562357437	chr8:5859417-5859418	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

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
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20688739	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5858800-5860000	Enhancers	Placenta Amnion	Placenta Amnion
2	chr8:5859000-5859400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:5860000-5860600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr8:5863000-5870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:5865600-5866200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:5865600-5866200	Enhancers	Fetal Heart	heart
7	chr8:5865600-5866200	Enhancers	Hela-S3	cervix
8	chr8:5865800-5866200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:5865800-5866200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr8:5866000-5866200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:5866200-5875000	Weak transcription	Hela-S3	cervix
12	chr8:5866600-5869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:5869400-5870400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:5870200-5870400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:5871200-5871600	Enhancers	NHEK	skin
16	chr8:5871400-5871600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:5871600-5872200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:5871600-5875000	Weak transcription	NHEK	skin
19	chr8:5872200-5872400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:5872400-5875000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:5872800-5874000	Enhancers	Fetal Brain Male	brain
22	chr8:5874000-5875000	Weak transcription	Fetal Brain Male	brain
23	chr8:5874400-5876800	Enhancers	Fetal Heart	heart
24	chr8:5874600-5874800	Enhancers	Aorta	Aorta
25	chr8:5874600-5876000	Enhancers	Fetal Muscle Leg	muscle
26	chr8:5874800-5875800	Weak transcription	Aorta	Aorta
27	chr8:5874800-5876000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:5874800-5876400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:5874800-5876600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr8:5874800-5876600	Enhancers	HMEC	breast
31	chr8:5875000-5875800	Enhancers	Fetal Brain Male	brain
32	chr8:5875000-5876600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:5875000-5878200	Enhancers	NHEK	skin
34	chr8:5875000-5878800	Enhancers	HUVEC	blood vessel
35	chr8:5875000-5879000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:5875000-5879800	Enhancers	Hela-S3	cervix
37	chr8:5875200-5875600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:5875200-5875600	Enhancers	NH-A	brain
39	chr8:5875200-5876200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:5875400-5875800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr8:5875400-5876000	Enhancers	NHDF-Ad	bronchial
42	chr8:5875600-5876000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr8:5875600-5876000	Flanking Active TSS	NH-A	brain
44	chr8:5875800-5876000	Enhancers	Aorta	Aorta
45	chr8:5875800-5876200	Enhancers	Osteobl	bone
46	chr8:5875800-5876600	Enhancers	NHLF	lung
47	chr8:5876000-5876600	Enhancers	NH-A	brain
48	chr8:5876000-5877200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:5876000-5878000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:5876400-5876600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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