Variant report

Variant	nsv890025
Chromosome Location	chr8:5818412-6055638
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	BACH1	chr8:5850953-5851324	K562	blood:	n/a	n/a
2	BACH1	chr8:5997567-5997673	K562	blood:	n/a	n/a
3	BHLHE40	chr8:5851096-5851152	K562	blood:	n/a	n/a
4	BHLHE40	chr8:5833612-5833750	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:5851125-5851150	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:5997564-5997834	K562	blood:	n/a	n/a
7	BRCA1	chr8:5934620-5934703	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:5934404-5934557	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:5875790-5876111	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr8:5850952-5851325	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr8:5848023-5848042	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:5877716-5878268	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:6038065-6038396	K562	blood:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
14	CEBPB	chr8:6038040-6038412	A549	lung:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
15	CEBPB	chr8:5931821-5932072	K562	blood:	n/a	n/a
16	CEBPB	chr8:6026333-6026694	A549	lung:	n/a	chr8:6026509-6026520 chr8:6026351-6026363
17	CEBPB	chr8:5943713-5943758	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:5903426-5903622	A549	lung:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
19	CEBPB	chr8:6038057-6038393	IMR90	lung:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
20	CEBPB	chr8:5871254-5871589	IMR90	lung:	n/a	chr8:5871421-5871434
21	CEBPB	chr8:5992348-5992622	Hela-S3	cervix:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
22	CEBPB	chr8:6026433-6026617	H1-hESC	embryonic stem cell:	n/a	chr8:6026509-6026520
23	CEBPB	chr8:6038148-6038455	A549	lung:	n/a	chr8:6038225-6038236
24	CEBPB	chr8:5992308-5992620	IMR90	lung:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
25	CEBPB	chr8:5871279-5871583	K562	blood:	n/a	chr8:5871421-5871434
26	CEBPB	chr8:5930436-5930514	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:5923557-5923830	HepG2	liver:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
28	CEBPB	chr8:5917232-5917357	HepG2	liver:	n/a	chr8:5917295-5917306
29	CEBPB	chr8:5871276-5871564	H1-hESC	embryonic stem cell:	n/a	chr8:5871421-5871434
30	CEBPB	chr8:5920888-5921158	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:6026345-6026672	IMR90	lung:	n/a	chr8:6026509-6026520 chr8:6026351-6026363
32	CEBPB	chr8:5875401-5876188	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:5992332-5992648	A549	lung:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
34	CEBPB	chr8:5850585-5850618	HepG2	liver:	n/a	chr8:5850591-5850602
35	CEBPB	chr8:5871244-5871593	HepG2	liver:	n/a	chr8:5871421-5871434
36	CEBPB	chr8:5871257-5871567	A549	lung:	n/a	chr8:5871421-5871434
37	CEBPB	chr8:5992286-5992654	HepG2	liver:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
38	CEBPB	chr8:5879099-5879536	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:5923529-5923871	H1-hESC	embryonic stem cell:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
40	CEBPB	chr8:5978204-5978460	HepG2	liver:	n/a	chr8:5978303-5978315 chr8:5978298-5978309
41	CEBPB	chr8:5923536-5923736	K562	blood:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
42	CEBPB	chr8:5992318-5992636	H1-hESC	embryonic stem cell:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
43	CEBPB	chr8:5917160-5917474	H1-hESC	embryonic stem cell:	n/a	chr8:5917295-5917306
44	CEBPB	chr8:5855136-5855336	HepG2	liver:	n/a	chr8:5855245-5855256
45	CEBPB	chr8:5903414-5903669	HepG2	liver:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
46	CEBPB	chr8:5903392-5903683	K562	blood:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
47	CEBPB	chr8:5883252-5883353	A549	lung:	n/a	n/a
48	CEBPB	chr8:5923564-5923858	IMR90	lung:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
49	CEBPB	chr8:6037962-6038464	A549	lung:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
50	CEBPB	chr8:6026359-6026690	HepG2	liver:	n/a	chr8:6026509-6026520

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5909945-5909995	BJ	skin:	n/a
2	chr8:5909945-5909995	BJ	skin:	n/a
3	chr8:5909880-5909930	AG04450	lung:	fetal
4	chr8:5902873-5902923	SKMC	muscle:	n/a
5	chr8:5949290-5949340	ovcar-3	ovarian:	n/a
6	chr8:6010199-6010249	AG04450	lung:	fetal
7	chr8:6010199-6010249	GM12878	blood:	n/a
8	chr8:6010288-6010338	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:5992822-5992872	Caco-2	colon:	n/a
10	chr8:6010199-6010249	GM12891	blood:	n/a
11	chr8:5910061-5910111	HepG2	liver:	n/a
12	chr8:5910061-5910111	K562	blood:	n/a
13	chr8:5902873-5902923	AG04449	skin:	fetal
14	chr8:5909945-5909995	SK-N-SH	brain:	n/a
15	chr8:5992822-5992872	ovcar-3	ovarian:	n/a
16	chr8:6010199-6010249	NH-A	brain:	n/a
17	chr8:6010288-6010338	AG09319	gingival:	n/a
18	chr8:5909945-5909995	IMR90	lung:	fetal
19	chr8:6010288-6010338	NB4	blood:	n/a
20	chr8:5949290-5949340	HIPEpiC	eye:	n/a
21	chr8:5909880-5909930	HRPEpiC	eye:	n/a
22	chr8:5992822-5992872	SKMC	muscle:	n/a
23	chr8:5910061-5910111	AG10803	skin:	n/a
24	chr8:6010288-6010338	SK-N-SH_RA	brain:	n/a
25	chr8:5949290-5949340	Caco-2	colon:	n/a
26	chr8:6010288-6010338	HL-60	blood:	n/a
27	chr8:5909880-5909930	HCM	heart:	n/a
28	chr8:5909880-5909930	PFSK-1	brain:	n/a
29	chr8:6010288-6010338	ECC-1	luminal epithelium:	n/a
30	chr8:6010288-6010338	Caco-2	colon:	n/a
31	chr8:6010199-6010249	ProgFib	skin:	n/a
32	chr8:6010288-6010338	SK-N-MC	brain:	n/a
33	chr8:6010199-6010249	BE2_C	brain:	n/a
34	chr8:5949290-5949340	Hepatocyte	liver:	n/a
35	chr8:5902873-5902923	PFSK-1	brain:	n/a
36	chr8:5909945-5909995	HRCEpiC	kidney:	n/a
37	chr8:5992822-5992872	SK-N-SH	brain:	n/a
38	chr8:5902873-5902923	SK-N-SH	brain:	n/a
39	chr8:5992822-5992872	GM12891	blood:	n/a
40	chr8:5992822-5992872	ECC-1	luminal epithelium:	n/a
41	chr8:5910061-5910111	BE2_C	brain:	n/a
42	chr8:6010199-6010249	NT2-D1	testis:	n/a
43	chr8:5909880-5909930	MCF-7	breast:	n/a
44	chr8:5949290-5949340	BJ	skin:	n/a
45	chr8:5949290-5949340	GM12891	blood:	n/a
46	chr8:6010288-6010338	HepG2	liver:	n/a
47	chr8:5902873-5902923	GM06990	blood:	n/a
48	chr8:6010199-6010249	Hela-S3	cervix:	n/a
49	chr8:5910061-5910111	GM12878	blood:	n/a
50	chr8:5910061-5910111	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
2	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:
3	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
4	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
5	chr10:132324298..132325038-chr8:6023084..6023812,2	MCF-7	breast:
6	chr8:4919838..4920394-chr8:5997449..5998189,2	K562	blood:
7	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
8	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
9	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
10	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
11	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
12	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
13	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
14	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
15	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
16	chr8:4919533..4920406-chr8:5997153..5998101,2	MCF-7	breast:
17	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:5916524-5916659	XLOC_006984
2	lnc-ANGPT2-4	chr8:5893955-5893990	ENSG00000253189
3	lnc-ANGPT2-5	chr8:5858959-5859084	XLOC_006983
4	lnc-ANGPT2-3	chr8:5901875-5902047	ENSG00000253880
5	lnc-ANGPT2-5	chr8:5860524-5860623	XLOC_006983
6	lnc-ANGPT2-3	chr8:5916281-5916302	XLOC_006984
7	lnc-ANGPT2-3	chr8:5957850-5957973	ENSG00000253880
8	lnc-ANGPT2-3	chr8:5923520-5923650	XLOC_006984
9	lnc-ANGPT2-3	chr8:5917266-5917339	XLOC_006984
10	lnc-ANGPT2-4	chr8:5894372-5894496	ENSG00000253189
11	lnc-ANGPT2-3	chr8:5916524-5916600	ENSG00000253880
12	lnc-ANGPT2-3	chr8:5917266-5917339	ENSG00000253880
13	lnc-ANGPT2-4	chr8:5894123-5894292	ENSG00000253189

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

Extended variants
information (count: 9437 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:9437 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17365733	chr8:5818412-5818413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555170265	chr8:5818419-5818420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573625021	chr8:5818448-5818449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144537154	chr8:5818455-5818456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370549632	chr8:5818471-5818472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572418730	chr8:5818496-5818497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568156592	chr8:5818505-5818506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546045340	chr8:5818514-5818515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564702646	chr8:5818515-5818516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35905782	chr8:5818517-5818518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199781380	chr8:5818520-5818521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs398067533	chr8:5818524-5818525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557274494	chr8:5818534-5818535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577286454	chr8:5818538-5818539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2703313	chr8:5818550-5818551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs150688605	chr8:5818582-5818583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529331822	chr8:5818618-5818619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547832489	chr8:5818637-5818638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139714952	chr8:5818638-5818639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533275191	chr8:5818644-5818645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7015774	chr8:5818671-5818672	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs569879779	chr8:5818680-5818681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536846976	chr8:5818695-5818696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558818512	chr8:5818721-5818722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567229976	chr8:5818730-5818731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534377865	chr8:5818758-5818759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552556516	chr8:5818792-5818793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117013746	chr8:5818800-5818801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371973442	chr8:5818819-5818820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4614019	chr8:5818830-5818831	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576609848	chr8:5818834-5818835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543631049	chr8:5818838-5818839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114975401	chr8:5818839-5818840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529424341	chr8:5818842-5818843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4506241	chr8:5818843-5818844	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs114381611	chr8:5818867-5818868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191186470	chr8:5818876-5818877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533362630	chr8:5818907-5818908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182285380	chr8:5818908-5818909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569837895	chr8:5818910-5818911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111950699	chr8:5818916-5818917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561158758	chr8:5818924-5818925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78935094	chr8:5818933-5818934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149771497	chr8:5818945-5818946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567080223	chr8:5818951-5818952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145680593	chr8:5818972-5818973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552644904	chr8:5818981-5818982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528147523	chr8:5819013-5819014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570947638	chr8:5819021-5819022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548246694	chr8:5819022-5819023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20688739	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5816000-5818600	Weak transcription	Fetal Heart	heart
2	chr8:5816000-5819200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:5816000-5819400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:5818600-5820600	Enhancers	Fetal Heart	heart
5	chr8:5819200-5820600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:5819400-5820600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:5819600-5820800	Enhancers	Fetal Brain Male	brain
8	chr8:5819800-5820200	Enhancers	Fetal Lung	lung
9	chr8:5819800-5820800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr8:5820000-5821600	Enhancers	Primary hematopoietic stem cells	blood
11	chr8:5820200-5820600	Enhancers	Brain Germinal Matrix	brain
12	chr8:5820200-5820600	Enhancers	Fetal Brain Female	brain
13	chr8:5820200-5820600	Weak transcription	Fetal Lung	lung
14	chr8:5820600-5820800	Enhancers	Fetal Lung	lung
15	chr8:5820600-5821000	Enhancers	Brain Anterior Caudate	brain
16	chr8:5820600-5821000	Active TSS	Fetal Brain Female	brain
17	chr8:5820600-5821200	Flanking Active TSS	Brain Germinal Matrix	brain
18	chr8:5820600-5821200	Enhancers	Brain Substantia Nigra	brain
19	chr8:5820600-5821200	Flanking Active TSS	Fetal Heart	heart
20	chr8:5820600-5821400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:5820600-5821600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:5820600-5821600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:5820800-5821000	Enhancers	Brain Cingulate Gyrus	brain
24	chr8:5820800-5821000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:5820800-5821200	Active TSS	Adipose Nuclei	Adipose
26	chr8:5820800-5821200	Enhancers	Aorta	Aorta
27	chr8:5820800-5821200	Enhancers	Brain Angular Gyrus	brain
28	chr8:5820800-5821200	Active TSS	Brain Hippocampus Middle	brain
29	chr8:5820800-5821200	Flanking Active TSS	Fetal Brain Male	brain
30	chr8:5820800-5821200	Enhancers	Lung	lung
31	chr8:5820800-5821200	Enhancers	NH-A	brain
32	chr8:5820800-5821400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr8:5820800-5821400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:5820800-5821400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:5820800-5821400	Flanking Active TSS	Fetal Lung	lung
36	chr8:5820800-5821400	Enhancers	Fetal Stomach	stomach
37	chr8:5820800-5821600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:5821000-5821400	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr8:5821000-5821400	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr8:5821000-5821400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:5821000-5821400	Flanking Active TSS	Fetal Brain Female	brain
42	chr8:5821000-5821600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:5821200-5821400	Enhancers	Adipose Nuclei	Adipose
44	chr8:5821200-5821400	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr8:5821200-5821400	Enhancers	Fetal Brain Male	brain
46	chr8:5821200-5822200	Enhancers	Fetal Heart	heart
47	chr8:5821400-5821800	Enhancers	Fetal Lung	lung
48	chr8:5821400-5822200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr8:5821600-5822200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:5821800-5827000	Weak transcription	Fetal Lung	lung

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