Variant report

Variant	nsv884054
Chromosome Location	chr6:30061361-30069525
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:1281)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:30068295-30068660	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:30063318-30063773	HepG2	liver:	n/a	n/a
3	ATF1	chr6:30065754-30065986	K562	blood:	n/a	n/a
4	BACH1	chr6:30068640-30068840	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr6:30068530-30068837	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:30069294-30069423	K562	blood:	n/a	n/a
7	BRCA1	chr6:30061983-30062063	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:30068512-30068718	Hela-S3	cervix:	n/a	n/a
9	CEBPD	chr6:30068391-30068962	HepG2	liver:	n/a	n/a
10	CHD2	chr6:30068579-30068612	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr6:30068550-30068689	HepG2	liver:	n/a	n/a
12	CREB1	chr6:30068194-30071311	HepG2	liver:	n/a	n/a
13	CTCF	chr6:30068680-30068830	SAEC	small airway:	n/a	n/a
14	CTCF	chr6:30068460-30068610	HMEC	breast:	n/a	n/a
15	CTCF	chr6:30068720-30068870	HCFaa	heart:	n/a	n/a
16	CTCF	chr6:30068760-30068910	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr6:30068700-30068850	Caco-2	colon:	n/a	n/a
18	CTCF	chr6:30069480-30069630	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr6:30068725-30068815	Fibrobl	skin:	n/a	n/a
20	CTCF	chr6:30068600-30068750	GM12873	blood:	n/a	n/a
21	CTCF	chr6:30069520-30069670	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr6:30062542-30062613	GM10248	blood:	n/a	n/a
23	CTCF	chr6:30069080-30069230	BJ	skin:	n/a	n/a
24	CTCF	chr6:30068640-30068790	GM12875	blood:	n/a	n/a
25	CTCF	chr6:30068903-30068917	GM10248	blood:	n/a	n/a
26	CTCF	chr6:30063700-30063850	GM12873	blood:	n/a	n/a
27	CTCF	chr6:30068740-30068890	HCM	heart:	n/a	n/a
28	CTCF	chr6:30068620-30068770	AG04449	skin:	n/a	n/a
29	CTCF	chr6:30068734-30068825	GM19238	blood:	n/a	n/a
30	CTCF	chr6:30068762-30068798	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:30068660-30068810	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr6:30068714-30068864	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:30069500-30069650	HMEC	breast:	n/a	n/a
34	CTCF	chr6:30068734-30068815	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr6:30068640-30068790	Caco-2	colon:	n/a	n/a
36	CTCF	chr6:30068689-30068852	NHEK	skin:	n/a	n/a
37	CTCF	chr6:30068780-30068930	SAEC	small airway:	n/a	n/a
38	CTCF	chr6:30068760-30068910	HepG2	liver:	n/a	n/a
39	CTCF	chr6:30068763-30068902	GM10248	blood:	n/a	n/a
40	CTCF	chr6:30068620-30068770	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr6:30068780-30068930	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr6:30068600-30068750	RPTEC	kidney:	n/a	n/a
43	CTCF	chr6:30065620-30065770	GM06990	blood:	n/a	n/a
44	CTCF	chr6:30068660-30068810	NHEK	skin:	n/a	n/a
45	CTCF	chr6:30068680-30068830	GM12875	blood:	n/a	n/a
46	CTCF	chr6:30068685-30068872	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:30068760-30068910	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:30068760-30068910	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr6:30068500-30068650	HMEC	breast:	n/a	n/a
50	CTCF	chr6:30068756-30068772	GM10266	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30067108-30067158	HepG2	liver:	n/a
2	chr6:30068493-30068543	GM12891	blood:	n/a
3	chr6:30068493-30068543	AoSMC	blood vessel:	n/a
4	chr6:30068667-30068717	PFSK-1	brain:	n/a
5	chr6:30068851-30068901	LNCaP	prostate:	n/a
6	chr6:30066428-30066478	Caco-2	colon:	n/a
7	chr6:30069319-30069369	AG09309	skin:	n/a
8	chr6:30068471-30068521	SAEC	small airway:	n/a
9	chr6:30069296-30069346	HMEC	breast:	n/a
10	chr6:30069213-30069263	PFSK-1	brain:	n/a
11	chr6:30068818-30068868	AoSMC	blood vessel:	n/a
12	chr6:30068832-30068882	MCF-7	breast:	n/a
13	chr6:30068942-30068992	U87	brain:	n/a
14	chr6:30068656-30068706	HRPEpiC	eye:	n/a
15	chr6:30068899-30068949	HCF	heart:	n/a
16	chr6:30066428-30066478	HRPEpiC	eye:	n/a
17	chr6:30068851-30068901	AG04449	skin:	fetal
18	chr6:30069250-30069300	U87	brain:	n/a
19	chr6:30068934-30068984	U87	brain:	n/a
20	chr6:30068493-30068543	HAEpiC	amniotic membrane:	n/a
21	chr6:30069213-30069263	SK-N-SH_RA	brain:	n/a
22	chr6:30069250-30069300	Hela-S3	cervix:	n/a
23	chr6:30068501-30068551	AoSMC	blood vessel:	n/a
24	chr6:30067108-30067158	H1-hESC	embryonic stem cell:	embryo
25	chr6:30069065-30069115	Jurkat	blood:	n/a
26	chr6:30068667-30068717	SK-N-SH_RA	brain:	n/a
27	chr6:30069250-30069300	HCM	heart:	n/a
28	chr6:30069065-30069115	HL-60	blood:	n/a
29	chr6:30069065-30069115	HRPEpiC	eye:	n/a
30	chr6:30069213-30069263	NB4	blood:	n/a
31	chr6:30068818-30068868	HCT-116	colon:	n/a
32	chr6:30068656-30068706	GM12891	blood:	n/a
33	chr6:30067855-30067905	SK-N-MC	brain:	n/a
34	chr6:30069319-30069369	Hela-S3	cervix:	n/a
35	chr6:30069213-30069263	CMK	blood:	n/a
36	chr6:30068656-30068706	GM12878	blood:	n/a
37	chr6:30067108-30067158	Hela-S3	cervix:	n/a
38	chr6:30069296-30069346	AG04449	skin:	fetal
39	chr6:30068501-30068551	Hepatocyte	liver:	n/a
40	chr6:30067108-30067158	HCM	heart:	n/a
41	chr6:30068934-30068984	HCM	heart:	n/a
42	chr6:30068818-30068868	HepG2	liver:	n/a
43	chr6:30068471-30068521	AoSMC	blood vessel:	n/a
44	chr6:30068899-30068949	ovcar-3	ovarian:	n/a
45	chr6:30069250-30069300	HL-60	blood:	n/a
46	chr6:30068934-30068984	SAEC	small airway:	n/a
47	chr6:30066428-30066478	GM06990	blood:	n/a
48	chr6:30068851-30068901	GM06990	blood:	n/a
49	chr6:30068493-30068543	HCPEpiC	choroid plexus:	n/a
50	chr6:30067855-30067905	AG09309	skin:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30067195..30070112-chr6:30098151..30100617,2	MCF-7	breast:
2	chr6:30067592..30070049-chr6:30312859..30314391,2	K562	blood:
3	chr6:30041751..30043519-chr6:30060494..30062224,2	K562	blood:
4	chr17:73720378..73720925-chr6:30069323..30069983,2	HCT-116	colon:
5	chr6:30028086..30030535-chr6:30068315..30071049,3	MCF-7	breast:
6	chr6:30058600..30061539-chr6:30062741..30064895,3	MCF-7	breast:
7	chr6:30063791..30066840-chr6:30067476..30070156,3	MCF-7	breast:
8	chr6:30059663..30061808-chr6:30067229..30070058,2	K562	blood:
9	chr6:30058142..30060356-chr6:30062997..30064640,2	MCF-7	breast:
10	chr6:30027872..30030809-chr6:30069511..30072907,4	K562	blood:
11	chr6:30033726..30035867-chr6:30063166..30065210,2	MCF-7	breast:
12	chr6:30046314..30047956-chr6:30068316..30070912,2	MCF-7	breast:
13	chr6:30039276..30042217-chr6:30067253..30069841,2	K562	blood:
14	chr6:30027986..30030809-chr6:30067690..30071011,4	K562	blood:
15	chr6:30034219..30034740-chr6:30069488..30070083,2	Hela-S3	cervix:
16	chr6:30004933..30007814-chr6:30068168..30069816,2	MCF-7	breast:
17	chr6:30040732..30043488-chr6:30062276..30064354,2	K562	blood:
18	chr6:30069286..30070342-chr6:30364378..30364933,3	K562	blood:
19	chr6:30068376..30069897-chr6:30103951..30105962,2	MCF-7	breast:
20	chr20:43514111..43515072-chr6:30069397..30070319,2	Hela-S3	cervix:
21	chr6:30058600..30061539-chr6:30062741..30064895,3	MCF-7	breast:
22	chr6:30039673..30045870-chr6:30065915..30071954,9	MCF-7	breast:
23	chr6:30039555..30048654-chr6:30056865..30065735,15	MCF-7	breast:
24	chr6:30053423..30056076-chr6:30062128..30065252,3	MCF-7	breast:
25	chr6:30031856..30036259-chr6:30064937..30071315,10	MCF-7	breast:
26	chr6:30068684..30075353-chr6:30179679..30184952,7	MCF-7	breast:
27	chr6:30036068..30037732-chr6:30063349..30066200,2	MCF-7	breast:
28	chr6:30069516..30071040-chr6:30137847..30139463,2	MCF-7	breast:
29	chr6:30041901..30046365-chr6:30059553..30065121,9	MCF-7	breast:
30	chr6:30059663..30061808-chr6:30067229..30070058,2	K562	blood:
31	chr6:30059482..30063646-chr6:30064744..30071169,8	MCF-7	breast:
32	chr6:30068547..30070487-chr6:30073986..30076858,2	K562	blood:
33	chr6:30063791..30066840-chr6:30067476..30070156,3	MCF-7	breast:
34	chr6:30043035..30044565-chr6:30066202..30069074,2	MCF-7	breast:
35	chr6:30029240..30031636-chr6:30067690..30069434,2	K562	blood:
36	chr6:30037077..30039641-chr6:30068261..30070312,3	MCF-7	breast:
37	chr6:30034665..30036494-chr6:30061234..30063128,2	MCF-7	breast:
38	chr17:70636264..70637244-chr6:30069427..30070287,2	Hela-S3	cervix:
39	chr6:30027914..30030220-chr6:30065122..30067982,3	MCF-7	breast:
40	chr10:72575478..72576318-chr6:30069366..30070276,2	Hela-S3	cervix:
41	chr11:65195679..65196336-chr6:30069510..30070292,2	Hela-S3	cervix:
42	chr6:30054838..30057804-chr6:30069131..30071158,2	MCF-7	breast:
43	chr6:30031338..30034907-chr6:30068673..30070684,4	MCF-7	breast:
44	chr6:30024946..30027912-chr6:30068442..30070614,2	MCF-7	breast:
45	chr6:30039304..30041261-chr6:30060958..30063803,2	MCF-7	breast:
46	chr6:30059482..30063646-chr6:30064744..30071169,8	MCF-7	breast:
47	chr6:30027765..30030437-chr6:30060037..30061710,2	MCF-7	breast:

No data

Variant related genes	Relation type
TRIM31-AS1	TF binding region
ENSG00000252901	TF binding region
TRIM31-AS1	CpG island
ENSG00000252901	CpG island
ENSG00000241370	chromatin interactions
ENSG00000204610	chromatin interactions
ENSG00000166224	chromatin interactions
ENSG00000204616	chromatin interactions
ENSG00000252901	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000204614	chromatin interactions
ENSG00000204618	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000227036	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000166913	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000234127	chromatin interactions

Extended variants
information (count: 293 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9261387	chr6:30061361-30061362	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551882213	chr6:30061362-30061363	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs7754777	chr6:30061398-30061399	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs144091254	chr6:30061484-30061485	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs9261388	chr6:30061500-30061501	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs551155022	chr6:30061532-30061533	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs9261389	chr6:30061555-30061556	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs554247394	chr6:30061582-30061583	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs536966168	chr6:30061689-30061690	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs553361557	chr6:30061707-30061708	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573302164	chr6:30061732-30061733	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115513366	chr6:30061749-30061750	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559134798	chr6:30061820-30061821	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148270608	chr6:30061886-30061887	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141305147	chr6:30061888-30061889	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs17194174	chr6:30061910-30061911	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187498085	chr6:30061913-30061914	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377346346	chr6:30061954-30061955	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs116580055	chr6:30061964-30061965	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6923832	chr6:30062058-30062059	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs529967108	chr6:30062065-30062066	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532016647	chr6:30062132-30062133	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2394736	chr6:30062133-30062134	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs569841457	chr6:30062162-30062163	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs6149502	chr6:30062166-30062167	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562096145	chr6:30062175-30062176	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs56214003	chr6:30062201-30062202	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547940307	chr6:30062233-30062234	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs115238975	chr6:30062257-30062258	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536424002	chr6:30062279-30062280	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547304083	chr6:30062284-30062285	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12661731	chr6:30062345-30062346	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs191875395	chr6:30062463-30062464	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113147989	chr6:30062500-30062501	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575669536	chr6:30062578-30062579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538352488	chr6:30062581-30062582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111687450	chr6:30062590-30062591	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs534079792	chr6:30062625-30062626	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs68008510	chr6:30062627-30062628	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs9280887	chr6:30062628-30062629	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs28780078	chr6:30062650-30062651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs201763687	chr6:30062662-30062663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376669721	chr6:30062664-30062665	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs574606254	chr6:30062731-30062732	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540040237	chr6:30062739-30062740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183959282	chr6:30062740-30062741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374258784	chr6:30062750-30062751	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7764464	chr6:30062765-30062766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368473896	chr6:30062782-30062783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372170415	chr6:30062787-30062788	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30058400-30062200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:30058600-30061400	Enhancers	Fetal Intestine Large	intestine
3	chr6:30060000-30063000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:30060000-30063000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:30060000-30063000	Weak transcription	A549	lung
6	chr6:30060000-30064800	Weak transcription	Gastric	stomach
7	chr6:30060200-30063000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:30060200-30063000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:30060200-30063000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:30060200-30063000	Weak transcription	NHEK	skin
11	chr6:30060200-30063200	Weak transcription	HMEC	breast
12	chr6:30060200-30065600	Weak transcription	Spleen	Spleen
13	chr6:30060400-30063000	Weak transcription	Hela-S3	cervix
14	chr6:30060400-30065200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr6:30061000-30062000	Weak transcription	Fetal Intestine Small	intestine
16	chr6:30061000-30062400	Bivalent Enhancer	HepG2	liver
17	chr6:30061000-30066800	Enhancers	Stomach Mucosa	stomach
18	chr6:30061200-30062000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:30061400-30062600	Weak transcription	Fetal Intestine Large	intestine
20	chr6:30062000-30062200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:30062000-30063800	Enhancers	Duodenum Mucosa	Duodenum
22	chr6:30062000-30067000	Enhancers	Fetal Intestine Small	intestine
23	chr6:30062200-30067800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:30062400-30063000	Enhancers	HepG2	liver
25	chr6:30062600-30064800	Enhancers	Fetal Intestine Large	intestine
26	chr6:30062800-30064000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr6:30063000-30063200	Enhancers	A549	lung
28	chr6:30063000-30063400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:30063000-30063400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:30063000-30063600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:30063000-30063600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:30063000-30063600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:30063000-30063600	Bivalent Enhancer	HUVEC	blood vessel
34	chr6:30063000-30063800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:30063000-30063800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:30063000-30063800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:30063000-30063800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:30063000-30063800	Bivalent Enhancer	Brain Hippocampus Middle	brain
39	chr6:30063000-30063800	Enhancers	Placenta	Placenta
40	chr6:30063000-30063800	Bivalent Enhancer	Small Intestine	intestine
41	chr6:30063000-30063800	Enhancers	Hela-S3	cervix
42	chr6:30063000-30063800	Bivalent Enhancer	NHDF-Ad	bronchial
43	chr6:30063000-30063800	Enhancers	NHEK	skin
44	chr6:30063000-30063800	Enhancers	Osteobl	bone
45	chr6:30063000-30064000	Flanking Active TSS	HepG2	liver
46	chr6:30063200-30063600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:30063200-30063600	Bivalent Enhancer	Brain Substantia Nigra	brain
48	chr6:30063200-30063600	Enhancers	HMEC	breast
49	chr6:30063200-30063600	Enhancers	HSMMtube	muscle
50	chr6:30063200-30063800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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