Variant report

Variant	nsv890371
Chromosome Location	chr8:11771089-11896831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1807)
CpG islands
(count:3235)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
5	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
6	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
7	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
8	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
9	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
13	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:11783650-11783829	GM12878	blood:	n/a	n/a
15	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
17	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
18	BHLHE40	chr8:11799584-11800147	K562	blood:	n/a	n/a
19	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
20	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
21	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
22	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372
23	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
24	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372
25	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
26	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
27	BRCA1	chr8:11801145-11801480	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:11801202-11801448	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr8:11805093-11805433	K562	blood:	n/a	n/a
30	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
31	CBX3	chr8:11796176-11796816	K562	blood:	n/a	n/a
32	CBX3	chr8:11796463-11796779	K562	blood:	n/a	n/a
33	CBX3	chr8:11799688-11800155	K562	blood:	n/a	n/a
34	CCNT2	chr8:11807053-11807488	K562	blood:	n/a	chr8:11807360-11807369 chr8:11807248-11807268
35	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
36	CCNT2	chr8:11799474-11800136	K562	blood:	n/a	n/a
37	CCNT2	chr8:11843856-11844050	K562	blood:	n/a	n/a
38	CEBPB	chr8:11854216-11854508	IMR90	lung:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
39	CEBPB	chr8:11816243-11816470	K562	blood:	n/a	chr8:11816330-11816341
40	CEBPB	chr8:11852658-11853061	IMR90	lung:	n/a	chr8:11852980-11852993
41	CEBPB	chr8:11816146-11816527	MCF-7	breast:	n/a	chr8:11816330-11816341
42	CEBPB	chr8:11813778-11814105	IMR90	lung:	n/a	chr8:11813929-11813940
43	CEBPB	chr8:11858243-11858418	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:11813806-11814094	Hela-S3	cervix:	n/a	chr8:11813929-11813940
45	CEBPB	chr8:11772699-11772818	IMR90	lung:	n/a	chr8:11772799-11772812 chr8:11772800-11772811
46	CEBPB	chr8:11813757-11814093	K562	blood:	n/a	chr8:11813929-11813940
47	CEBPB	chr8:11775490-11775787	IMR90	lung:	n/a	chr8:11775632-11775643
48	CEBPB	chr8:11816162-11816603	IMR90	lung:	n/a	chr8:11816330-11816341
49	CEBPB	chr8:11816146-11816622	A549	lung:	n/a	chr8:11816330-11816341
50	CEBPB	chr8:11816229-11816539	HepG2	liver:	n/a	chr8:11816330-11816341

(count:3235 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11872778-11872828	LNCaP	prostate:	n/a
2	chr8:11774336-11774386	SK-N-SH_RA	brain:	n/a
3	chr8:11872778-11872828	LNCaP	prostate:	n/a
4	chr8:11774336-11774386	SK-N-SH_RA	brain:	n/a
5	chr8:11882897-11882947	NT2-D1	testis:	n/a
6	chr8:11772734-11772784	HEK293	kidney:	embryo
7	chr8:11835607-11835657	CMK	blood:	n/a
8	chr8:11771498-11771548	HMEC	breast:	n/a
9	chr8:11870338-11870388	RPTEC	kidney:	n/a
10	chr8:11772734-11772784	Hela-S3	cervix:	n/a
11	chr8:11895252-11895302	HEK293	kidney:	embryo
12	chr8:11853920-11853970	CMK	blood:	n/a
13	chr8:11794716-11794766	ovcar-3	ovarian:	n/a
14	chr8:11832039-11832089	IMR90	lung:	fetal
15	chr8:11771244-11771294	MCF10A-Er-Src	breast:	n/a
16	chr8:11839844-11839894	HCT-116	colon:	n/a
17	chr8:11771244-11771294	Hepatocyte	liver:	n/a
18	chr8:11790326-11790376	Hepatocyte	liver:	n/a
19	chr8:11774336-11774386	HL-60	blood:	n/a
20	chr8:11813211-11813261	SAEC	small airway:	n/a
21	chr8:11872659-11872709	AG09309	skin:	n/a
22	chr8:11838843-11838893	ECC-1	luminal epithelium:	n/a
23	chr8:11771498-11771548	SKMC	muscle:	n/a
24	chr8:11882897-11882947	GM06990	blood:	n/a
25	chr8:11772119-11772169	GM12892	blood:	n/a
26	chr8:11838843-11838893	Hela-S3	cervix:	n/a
27	chr8:11773969-11774019	GM19239	blood:	n/a
28	chr8:11772734-11772784	BE2_C	brain:	n/a
29	chr8:11795262-11795312	BE2_C	brain:	n/a
30	chr8:11853878-11853928	K562	blood:	n/a
31	chr8:11832039-11832089	AG04450	lung:	fetal
32	chr8:11841980-11842030	HRPEpiC	eye:	n/a
33	chr8:11839138-11839188	AG04449	skin:	fetal
34	chr8:11832261-11832311	CMK	blood:	n/a
35	chr8:11772734-11772784	GM12878	blood:	n/a
36	chr8:11771244-11771294	NHDF-neo	bronchial:	n/a
37	chr8:11838532-11838582	NHBE	bronchial:	n/a
38	chr8:11801320-11801370	GM12891	blood:	n/a
39	chr8:11839138-11839188	IMR90	lung:	fetal
40	chr8:11771244-11771294	SK-N-SH	brain:	n/a
41	chr8:11773969-11774019	HAEpiC	amniotic membrane:	n/a
42	chr8:11794716-11794766	HAEpiC	amniotic membrane:	n/a
43	chr8:11832762-11832812	GM12891	blood:	n/a
44	chr8:11835607-11835657	IMR90	lung:	fetal
45	chr8:11882897-11882947	NHDF-neo	bronchial:	n/a
46	chr8:11795273-11795323	HEK293	kidney:	embryo
47	chr8:11876646-11876696	SAEC	small airway:	n/a
48	chr8:11843807-11843857	HMEC	breast:	n/a
49	chr8:11853920-11853970	SK-N-MC	brain:	n/a
50	chr8:11872882-11872932	Hela-S3	cervix:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:
2	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
3	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
4	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
5	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
6	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
7	chr8:11622652..11623752-chr8:11800899..11801806,5	MCF-7	breast:
8	chr8:11619764..11620442-chr8:11816053..11817012,3	K562	blood:
9	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
10	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
11	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
12	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:
13	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
14	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
15	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
16	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
17	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
18	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
19	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
20	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
21	chr8:11622669..11623564-chr8:11800869..11801753,3	K562	blood:
22	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
23	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
24	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
25	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
26	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
27	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
28	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
29	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
30	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
31	chr8:11710424..11713168-chr8:11798660..11801424,2	K562	blood:
32	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
33	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
34	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
35	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
36	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
37	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
38	chr8:11723911..11726339-chr8:11798413..11801274,2	K562	blood:
39	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
40	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
41	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
42	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
43	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105
2	lnc-CTSB-2	chr8:11777409-11778318	NONHSAT125102
3	lnc-DEFB134-1	chr8:11860909-11861591	NONHSAT125106

No data

Variant related genes	Relation type
DEFB134	TF binding region
DEFB136	TF binding region
ENSG00000254507	TF binding region
DEFB135	TF binding region
OR7E161P	TF binding region
ENSG00000255098	TF binding region
ENSG00000255016	TF binding region
ENSG00000255174	TF binding region
OR7E160P	TF binding region
OR7E158P	TF binding region
DEFB134	CpG island
DEFB136	CpG island
ENSG00000254507	CpG island
DEFB135	CpG island
OR7E161P	CpG island
ENSG00000255098	CpG island
ENSG00000255016	CpG island
ENSG00000255174	CpG island
OR7E160P	CpG island
OR7E158P	CpG island
ENSG00000205883	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000205882	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000079459	chromatin interactions

Extended variants
information (count: 6171 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:6171 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377538083	chr8:11771089-11771090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190727268	chr8:11771090-11771091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575622651	chr8:11771098-11771099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182545473	chr8:11771115-11771116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184172279	chr8:11771116-11771117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112759635	chr8:11771123-11771124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200772750	chr8:11771133-11771134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6992288	chr8:11771162-11771163	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534129948	chr8:11771204-11771205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373887506	chr8:11771221-11771222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567501351	chr8:11771222-11771223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187180442	chr8:11771242-11771243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377506065	chr8:11771277-11771278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529277740	chr8:11771278-11771279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536455799	chr8:11771279-11771280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550544820	chr8:11771287-11771288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145301539	chr8:11771290-11771291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566802006	chr8:11771335-11771336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533460910	chr8:11771352-11771353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192050711	chr8:11771357-11771358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566996108	chr8:11771363-11771364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534402417	chr8:11771385-11771386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552823098	chr8:11771391-11771392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568149559	chr8:11771392-11771393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373030022	chr8:11771409-11771410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200256411	chr8:11771424-11771425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397961140	chr8:11771427-11771428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11779722	chr8:11771441-11771442	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183475353	chr8:11771459-11771460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187218590	chr8:11771461-11771462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11786381	chr8:11771467-11771468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558022661	chr8:11771468-11771469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572999932	chr8:11771475-11771476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538217775	chr8:11771482-11771483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561881084	chr8:11771499-11771500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191742800	chr8:11771511-11771512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558163777	chr8:11771513-11771514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544251982	chr8:11771517-11771518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182470116	chr8:11771518-11771519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578178808	chr8:11771523-11771524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533353490	chr8:11771527-11771528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112667510	chr8:11771528-11771529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540966204	chr8:11771529-11771530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560818611	chr8:11771548-11771549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374569120	chr8:11771562-11771563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186752203	chr8:11771570-11771571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114934924	chr8:11771574-11771575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535543962	chr8:11771575-11771576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550652730	chr8:11771578-11771579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141804037	chr8:11771590-11771591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

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
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11770800-11772000	Weak transcription	K562	blood
2	chr8:11772000-11772200	Enhancers	K562	blood
3	chr8:11779000-11780000	Enhancers	Placenta	Placenta
4	chr8:11781000-11781200	Enhancers	NHEK	skin
5	chr8:11783600-11783800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:11783600-11784000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:11783600-11784600	Enhancers	Dnd41	blood
8	chr8:11783600-11785000	Enhancers	HMEC	breast
9	chr8:11783600-11787000	Enhancers	NHEK	skin
10	chr8:11783800-11784000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:11783800-11785000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:11784000-11786000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:11784200-11786200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:11784400-11784800	Enhancers	GM12878-XiMat	blood
15	chr8:11785000-11785200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:11785000-11786000	Weak transcription	HMEC	breast
17	chr8:11785200-11786000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:11786000-11786400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:11786000-11786800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:11786000-11787000	Enhancers	HMEC	breast
21	chr8:11786000-11799400	Weak transcription	Right Atrium	heart
22	chr8:11786200-11786600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:11786600-11788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:11786800-11790600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:11787000-11790600	Weak transcription	NHEK	skin
26	chr8:11789200-11789400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:11790600-11790800	Enhancers	Placenta	Placenta
28	chr8:11790600-11791400	Enhancers	NHEK	skin
29	chr8:11790600-11791600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:11791000-11791200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:11791200-11791400	Enhancers	HepG2	liver
32	chr8:11791200-11791600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr8:11791200-11792200	Enhancers	Pancreas	Pancrea
34	chr8:11791200-11792200	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:11791200-11793600	Enhancers	Duodenum Mucosa	Duodenum
36	chr8:11791400-11791600	Enhancers	Placenta	Placenta
37	chr8:11791400-11791800	Enhancers	K562	blood
38	chr8:11791400-11792000	Flanking Active TSS	HepG2	liver
39	chr8:11791400-11792200	Enhancers	Fetal Intestine Small	intestine
40	chr8:11791400-11793200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr8:11791400-11793600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:11791400-11794200	Enhancers	Stomach Mucosa	stomach
43	chr8:11791600-11792800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:11791800-11792000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:11791800-11793400	Weak transcription	K562	blood
46	chr8:11792000-11793600	Enhancers	HepG2	liver
47	chr8:11792000-11794000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:11792200-11793600	Weak transcription	Fetal Intestine Small	intestine
49	chr8:11793000-11793400	Enhancers	Gastric	stomach
50	chr8:11793000-11794000	Enhancers	Primary hematopoietic stem cells	blood

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