Variant report

Variant	nsv1026344
Chromosome Location	chr8:11786255-11897177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1737)
CpG islands
(count:2565)
Chromatin interactive
region (count:43)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
3	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11872669-11872691	HepG2	liver:	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	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
10	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
11	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
14	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
16	BHLHE40	chr8:11799584-11800147	K562	blood:	n/a	n/a
17	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
18	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
19	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
20	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372
21	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
22	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
23	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372
24	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
25	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
26	BRCA1	chr8:11801202-11801448	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr8:11801145-11801480	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr8:11796176-11796816	K562	blood:	n/a	n/a
29	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
30	CBX3	chr8:11805093-11805433	K562	blood:	n/a	n/a
31	CBX3	chr8:11799688-11800155	K562	blood:	n/a	n/a
32	CBX3	chr8:11796463-11796779	K562	blood:	n/a	n/a
33	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
34	CCNT2	chr8:11807053-11807488	K562	blood:	n/a	chr8:11807360-11807369 chr8:11807248-11807268
35	CCNT2	chr8:11799474-11800136	K562	blood:	n/a	n/a
36	CCNT2	chr8:11843856-11844050	K562	blood:	n/a	n/a
37	CEBPB	chr8:11795384-11795418	HepG2	liver:	n/a	chr8:11795407-11795418
38	CEBPB	chr8:11854216-11854508	IMR90	lung:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
39	CEBPB	chr8:11852501-11853120	HCT-116	colon:	n/a	chr8:11852980-11852993
40	CEBPB	chr8:11854282-11854495	HepG2	liver:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
41	CEBPB	chr8:11816168-11816706	Hela-S3	cervix:	n/a	chr8:11816330-11816341
42	CEBPB	chr8:11813814-11814090	A549	lung:	n/a	chr8:11813929-11813940
43	CEBPB	chr8:11816229-11816539	HepG2	liver:	n/a	chr8:11816330-11816341
44	CEBPB	chr8:11813744-11814114	HepG2	liver:	n/a	chr8:11813929-11813940
45	CEBPB	chr8:11816152-11816521	HepG2	liver:	n/a	chr8:11816330-11816341
46	CEBPB	chr8:11795337-11795460	IMR90	lung:	n/a	chr8:11795407-11795418
47	CEBPB	chr8:11813778-11814109	A549	lung:	n/a	chr8:11813929-11813940
48	CEBPB	chr8:11816144-11816589	K562	blood:	n/a	chr8:11816330-11816341
49	CEBPB	chr8:11813806-11814094	Hela-S3	cervix:	n/a	chr8:11813929-11813940
50	CEBPB	chr8:11854319-11854398	H1-hESC	embryonic stem cell:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11795273-11795323	HRE	kidney:	n/a
2	chr8:11843971-11844021	IMR90	lung:	fetal
3	chr8:11853920-11853970	HCT-116	colon:	n/a
4	chr8:11795273-11795323	HRE	kidney:	n/a
5	chr8:11843971-11844021	IMR90	lung:	fetal
6	chr8:11853920-11853970	HCT-116	colon:	n/a
7	chr8:11841980-11842030	AG09309	skin:	n/a
8	chr8:11853920-11853970	BE2_C	brain:	n/a
9	chr8:11882897-11882947	AG04449	skin:	fetal
10	chr8:11872882-11872932	LNCaP	prostate:	n/a
11	chr8:11876646-11876696	HCPEpiC	choroid plexus:	n/a
12	chr8:11831823-11831873	PFSK-1	brain:	n/a
13	chr8:11790559-11790609	RPTEC	kidney:	n/a
14	chr8:11813211-11813261	HL-60	blood:	n/a
15	chr8:11839844-11839894	SK-N-SH	brain:	n/a
16	chr8:11853121-11853171	Jurkat	blood:	n/a
17	chr8:11843816-11843866	HUVEC	blood vessel:	n/a
18	chr8:11835607-11835657	MCF-7	breast:	n/a
19	chr8:11790639-11790689	GM12891	blood:	n/a
20	chr8:11870063-11870113	MCF-7	breast:	n/a
21	chr8:11790559-11790609	SAEC	small airway:	n/a
22	chr8:11841980-11842030	HCT-116	colon:	n/a
23	chr8:11839764-11839814	HCT-116	colon:	n/a
24	chr8:11790559-11790609	AoSMC	blood vessel:	n/a
25	chr8:11835607-11835657	MCF10A-Er-Src	breast:	n/a
26	chr8:11831823-11831873	MCF10A-Er-Src	breast:	n/a
27	chr8:11843971-11844021	HCM	heart:	n/a
28	chr8:11841980-11842030	HUVEC	blood vessel:	n/a
29	chr8:11839780-11839830	GM19239	blood:	n/a
30	chr8:11813211-11813261	AG10803	skin:	n/a
31	chr8:11872778-11872828	Jurkat	blood:	n/a
32	chr8:11872659-11872709	NT2-D1	testis:	n/a
33	chr8:11839138-11839188	AG10803	skin:	n/a
34	chr8:11835607-11835657	GM12878	blood:	n/a
35	chr8:11832039-11832089	Caco-2	colon:	n/a
36	chr8:11895252-11895302	Caco-2	colon:	n/a
37	chr8:11853920-11853970	IMR90	lung:	fetal
38	chr8:11870338-11870388	SKMC	muscle:	n/a
39	chr8:11882962-11883012	HRPEpiC	eye:	n/a
40	chr8:11882897-11882947	NHDF-neo	bronchial:	n/a
41	chr8:11839764-11839814	LNCaP	prostate:	n/a
42	chr8:11872778-11872828	SK-N-SH_RA	brain:	n/a
43	chr8:11839138-11839188	NH-A	brain:	n/a
44	chr8:11843816-11843866	BJ	skin:	n/a
45	chr8:11838843-11838893	HRE	kidney:	n/a
46	chr8:11801365-11801415	MCF-7	breast:	n/a
47	chr8:11790326-11790376	PrEC	prostate:	n/a
48	chr8:11813211-11813261	ovcar-3	ovarian:	n/a
49	chr8:11838532-11838582	GM12891	blood:	n/a
50	chr8:11839844-11839894	HAEpiC	amniotic membrane:	n/a

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

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

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105
2	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
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
ENSG00000205882	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000205883	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000149823	chromatin interactions

Extended variants
information (count: 5675 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:5675 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12719915	chr8:11786255-11786256	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539187976	chr8:11786279-11786280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557441079	chr8:11786284-11786285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114380413	chr8:11786300-11786301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113138444	chr8:11786301-11786302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555026937	chr8:11786316-11786317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112143484	chr8:11786330-11786331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544155077	chr8:11786338-11786339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs118124527	chr8:11786352-11786353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543464315	chr8:11786374-11786375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577750290	chr8:11786378-11786379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563655396	chr8:11786386-11786387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144746020	chr8:11786436-11786437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560592578	chr8:11786437-11786438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191749160	chr8:11786465-11786466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543080450	chr8:11786489-11786490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367777955	chr8:11786498-11786499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532078806	chr8:11786508-11786509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577168422	chr8:11786513-11786514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115258116	chr8:11786530-11786531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371218073	chr8:11786542-11786543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532571255	chr8:11786547-11786548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547556067	chr8:11786562-11786563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566245096	chr8:11786577-11786578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182484228	chr8:11786584-11786585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555367167	chr8:11786586-11786587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186761983	chr8:11786607-11786608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191279120	chr8:11786608-11786609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556190969	chr8:11786625-11786626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577980321	chr8:11786635-11786636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545242960	chr8:11786642-11786643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185856776	chr8:11786648-11786649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572603005	chr8:11786657-11786658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542753027	chr8:11786658-11786659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188780671	chr8:11786666-11786667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375422689	chr8:11786687-11786688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543753964	chr8:11786737-11786738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs193223701	chr8:11786760-11786761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532633400	chr8:11786772-11786773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547618079	chr8:11786778-11786779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35890869	chr8:11786781-11786782	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs527429556	chr8:11786802-11786803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542339901	chr8:11786831-11786832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567311462	chr8:11786840-11786841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537442889	chr8:11786848-11786849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185223891	chr8:11786854-11786855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147475183	chr8:11786861-11786862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548772284	chr8:11786865-11786866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78799009	chr8:11786878-11786879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538915249	chr8:11786880-11786881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
Schizophrenia	20967226	CNVD

Chromatin state (count:1104 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11783600-11787000	Enhancers	NHEK	skin
2	chr8:11786000-11786400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:11786000-11786800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:11786000-11787000	Enhancers	HMEC	breast
5	chr8:11786000-11799400	Weak transcription	Right Atrium	heart
6	chr8:11786200-11786600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:11786600-11788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:11786800-11790600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:11787000-11790600	Weak transcription	NHEK	skin
10	chr8:11789200-11789400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:11790600-11790800	Enhancers	Placenta	Placenta
12	chr8:11790600-11791400	Enhancers	NHEK	skin
13	chr8:11790600-11791600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:11791000-11791200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:11791200-11791400	Enhancers	HepG2	liver
16	chr8:11791200-11791600	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr8:11791200-11792200	Enhancers	Pancreas	Pancrea
18	chr8:11791200-11792200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr8:11791200-11793600	Enhancers	Duodenum Mucosa	Duodenum
20	chr8:11791400-11791600	Enhancers	Placenta	Placenta
21	chr8:11791400-11791800	Enhancers	K562	blood
22	chr8:11791400-11792000	Flanking Active TSS	HepG2	liver
23	chr8:11791400-11792200	Enhancers	Fetal Intestine Small	intestine
24	chr8:11791400-11793200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:11791400-11793600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:11791400-11794200	Enhancers	Stomach Mucosa	stomach
27	chr8:11791600-11792800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:11791800-11792000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:11791800-11793400	Weak transcription	K562	blood
30	chr8:11792000-11793600	Enhancers	HepG2	liver
31	chr8:11792000-11794000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr8:11792200-11793600	Weak transcription	Fetal Intestine Small	intestine
33	chr8:11793000-11793400	Enhancers	Gastric	stomach
34	chr8:11793000-11794000	Enhancers	Primary hematopoietic stem cells	blood
35	chr8:11793200-11793400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:11793200-11793600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:11793200-11793800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
38	chr8:11793200-11793800	Bivalent Enhancer	Small Intestine	intestine
39	chr8:11793200-11794200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
40	chr8:11793200-11794200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:11793400-11793600	Enhancers	K562	blood
42	chr8:11793400-11793800	Enhancers	Esophagus	oesophagus
43	chr8:11793400-11794000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:11793600-11793800	Enhancers	Fetal Intestine Small	intestine
45	chr8:11793600-11793800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
46	chr8:11793600-11794200	Enhancers	A549	lung
47	chr8:11793600-11794200	Weak transcription	K562	blood
48	chr8:11793800-11794000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr8:11794000-11794200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:11794200-11794400	Enhancers	K562	blood

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