Variant report

Variant	esv3336846
Chromosome Location	chr6:30420111-30432946
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	ATF1	chr6:30431411-30431412	K562	blood:	n/a	n/a
2	ATF2	chr6:30421288-30421733	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:30421398-30421742	K562	blood:	n/a	n/a
4	BACH1	chr6:30421335-30421688	K562	blood:	n/a	n/a
5	BACH1	chr6:30421296-30421790	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr6:30421473-30421672	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:30421423-30421705	K562	blood:	n/a	n/a
8	BRCA1	chr6:30421486-30421637	HepG2	liver:	n/a	n/a
9	BRCA1	chr6:30421443-30421689	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr6:30421367-30421773	K562	blood:	n/a	n/a
11	CBX3	chr6:30421385-30421764	K562	blood:	n/a	n/a
12	CCNT2	chr6:30421487-30421691	K562	blood:	n/a	n/a
13	CEBPB	chr6:30428127-30428138	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:30421438-30421652	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:30431944-30432234	HepG2	liver:	n/a	n/a
16	CHD2	chr6:30421481-30421615	GM12878	blood:	n/a	n/a
17	CHD2	chr6:30421426-30421638	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr6:30421481-30421629	K562	blood:	n/a	n/a
19	CREB1	chr6:30421455-30421746	A549	lung:	n/a	n/a
20	CREB1	chr6:30421316-30421764	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr6:30432460-30432610	GM12872	blood:	n/a	chr6:30432482-30432495
22	CTCF	chr6:30421303-30421834	K562	blood:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
23	CTCF	chr6:30421020-30421310	GM12873	blood:	n/a	n/a
24	CTCF	chr6:30432580-30432730	HRPEpiC	eye:	n/a	chr6:30432600-30432618 chr6:30432603-30432612
25	CTCF	chr6:30421060-30421210	NB4	blood:	n/a	n/a
26	CTCF	chr6:30421394-30421775	ProgFib	skin:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
27	CTCF	chr6:30420760-30420910	HCFaa	heart:	n/a	n/a
28	CTCF	chr6:30432608-30432618	GM10248	blood:	n/a	n/a
29	CTCF	chr6:30420760-30420910	GM06990	blood:	n/a	n/a
30	CTCF	chr6:30431520-30431670	GM12865	blood:	n/a	chr6:30431623-30431636
31	CTCF	chr6:30421520-30421670	HPAF	blood vessel:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
32	CTCF	chr6:30421300-30421365	GM10248	blood:	n/a	n/a
33	CTCF	chr6:30421286-30421752	H1-hESC	embryonic stem cell:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
34	CTCF	chr6:30421285-30421742	HepG2	liver:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
35	CTCF	chr6:30421440-30421763	GM20000	blood:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
36	CTCF	chr6:30421346-30421738	T-47D	breast:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
37	CTCF	chr6:30432540-30432690	GM12866	blood:	n/a	chr6:30432600-30432618 chr6:30432603-30432612
38	CTCF	chr6:30421520-30421670	SAEC	small airway:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
39	CTCF	chr6:30421418-30421759	LNCaP	prostate:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
40	CTCF	chr6:30421500-30421650	GM12866	blood:	n/a	n/a
41	CTCF	chr6:30421350-30421799	A549	lung:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
42	CTCF	chr6:30432560-30432710	GM12878	blood:	n/a	chr6:30432600-30432618 chr6:30432603-30432612
43	CTCF	chr6:30421520-30421670	GM12864	blood:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
44	CTCF	chr6:30421480-30421630	HFF	foreskin:	n/a	n/a
45	CTCF	chr6:30421520-30421670	AoAF	blood vessel:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
46	CTCF	chr6:30421540-30421690	GM12866	blood:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
47	CTCF	chr6:30421480-30421630	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr6:30431520-30431670	HCPEpiC	choroid plexus:	n/a	chr6:30431623-30431636
49	CTCF	chr6:30421313-30421821	GM19240	blood:	n/a	chr6:30421635-30421653 chr6:30421637-30421658 chr6:30421636-30421652 chr6:30421638-30421651
50	CTCF	chr6:30421480-30421630	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30421275-30421325	Caco-2	colon:	n/a
2	chr6:30431782-30431832	NHDF-neo	bronchial:	n/a
3	chr6:30431724-30431774	HMEC	breast:	n/a
4	chr6:30431563-30431613	HCPEpiC	choroid plexus:	n/a
5	chr6:30421532-30421582	Jurkat	blood:	n/a
6	chr6:30421376-30421426	HL-60	blood:	n/a
7	chr6:30431782-30431832	PrEC	prostate:	n/a
8	chr6:30431770-30431820	GM06990	blood:	n/a
9	chr6:30421218-30421268	HepG2	liver:	n/a
10	chr6:30421655-30421705	HepG2	liver:	n/a
11	chr6:30430828-30430878	HEK293	kidney:	embryo
12	chr6:30421091-30421141	Caco-2	colon:	n/a
13	chr6:30431563-30431613	SK-N-MC	brain:	n/a
14	chr6:30421649-30421699	GM12878	blood:	n/a
15	chr6:30421189-30421239	PrEC	prostate:	n/a
16	chr6:30421526-30421576	AG04449	skin:	fetal
17	chr6:30421107-30421157	ProgFib	skin:	n/a
18	chr6:30431596-30431646	GM19239	blood:	n/a
19	chr6:30431699-30431749	GM12892	blood:	n/a
20	chr6:30421649-30421699	SK-N-SH	brain:	n/a
21	chr6:30421275-30421325	U87	brain:	n/a
22	chr6:30432200-30432250	BJ	skin:	n/a
23	chr6:30421091-30421141	HRCEpiC	kidney:	n/a
24	chr6:30421091-30421141	HEEpiC	esophagus:	n/a
25	chr6:30431592-30431642	NHDF-neo	bronchial:	n/a
26	chr6:30421649-30421699	ovcar-3	ovarian:	n/a
27	chr6:30421376-30421426	HMEC	breast:	n/a
28	chr6:30421463-30421513	PrEC	prostate:	n/a
29	chr6:30430828-30430878	GM12891	blood:	n/a
30	chr6:30431770-30431820	NH-A	brain:	n/a
31	chr6:30431563-30431613	HL-60	blood:	n/a
32	chr6:30420981-30421031	SK-N-SH_RA	brain:	n/a
33	chr6:30431770-30431820	Hepatocyte	liver:	n/a
34	chr6:30431596-30431646	Hepatocyte	liver:	n/a
35	chr6:30421275-30421325	K562	blood:	n/a
36	chr6:30431584-30431634	NT2-D1	testis:	n/a
37	chr6:30431577-30431627	T-47D	breast:	n/a
38	chr6:30431274-30431324	AoSMC	blood vessel:	n/a
39	chr6:30431577-30431627	BE2_C	brain:	n/a
40	chr6:30420981-30421031	HL-60	blood:	n/a
41	chr6:30431577-30431627	IMR90	lung:	fetal
42	chr6:30431590-30431640	Jurkat	blood:	n/a
43	chr6:30431590-30431640	GM19239	blood:	n/a
44	chr6:30431782-30431832	AG04449	skin:	fetal
45	chr6:30421655-30421705	Jurkat	blood:	n/a
46	chr6:30431782-30431832	SK-N-MC	brain:	n/a
47	chr6:30421526-30421576	IMR90	lung:	fetal
48	chr6:30432200-30432250	GM12878	blood:	n/a
49	chr6:30431579-30431629	IMR90	lung:	fetal
50	chr6:30431577-30431627	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:30378981..30379484-chr6:30421470..30421976,2	K562	blood:
2	chr6:30292876..30295211-chr6:30419006..30421683,2	K562	blood:
3	chr6:30420870..30422111-chr6:30449570..30450171,8	MCF-7	breast:
4	chr6:30428115..30430793-chr6:30537147..30539605,2	MCF-7	breast:
5	chr6:30430770..30433095-chr6:30579406..30582231,2	K562	blood:
6	chr6:30098561..30099505-chr6:30421018..30421961,4	K562	blood:
7	chr6:30424289..30426126-chr6:30523378..30525417,2	K562	blood:
8	chr6:30325158..30326032-chr6:30421070..30422057,4	K562	blood:
9	chr6:30421495..30422178-chr6:30512537..30513081,2	K562	blood:
10	chr6:30423219..30426193-chr6:30426415..30429085,2	K562	blood:
11	chr6:30415302..30418095-chr6:30418692..30421060,4	K562	blood:
12	chr6:30423219..30426193-chr6:30426415..30429085,2	K562	blood:
13	chr6:30422351..30425241-chr6:30448232..30450888,2	MCF-7	breast:
14	chr6:30421088..30422240-chr6:30449570..30450644,10	MCF-7	breast:
15	chr6:30420842..30422110-chr6:30449567..30450229,10	K562	blood:
16	chr6:30418502..30422305-chr6:30429667..30432220,3	MCF-7	breast:
17	chr6:30431634..30435485-chr6:30582972..30586314,3	K562	blood:
18	chr6:30414165..30416379-chr6:30427535..30430308,2	MCF-7	breast:
19	chr6:30431267..30434167-chr6:30612886..30615610,2	MCF-7	breast:
20	chr6:30431634..30434565-chr6:30582972..30585070,2	K562	blood:
21	chr6:30418502..30422305-chr6:30429667..30432220,3	MCF-7	breast:
22	chr6:30428958..30430493-chr6:30439620..30441525,2	MCF-7	breast:
23	chr6:30293711..30295719-chr6:30419664..30421683,2	K562	blood:

Variant related genes	Relation type
SUCLA2P1	TF binding region
TMPOP1	TF binding region
SUCLA2P1	CpG island
TMPOP1	CpG island
ENSG00000204569	chromatin interactions
ENSG00000204574	chromatin interactions
ENSG00000204590	chromatin interactions
ENSG00000204564	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000270604	chromatin interactions
ENSG00000204576	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000204599	chromatin interactions

Extended variants
information (count: 607 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565525637	chr6:30420156-30420157	Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs183493535	chr6:30420166-30420167	Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs2524199	chr6:30420187-30420188	Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577079052	chr6:30420200-30420201	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373658904	chr6:30420201-30420202	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs9885622	chr6:30420206-30420207	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143053387	chr6:30420214-30420215	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs373935184	chr6:30420237-30420238	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs562237105	chr6:30420244-30420245	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs9885620	chr6:30420288-30420289	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs541477656	chr6:30420320-30420321	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs564480949	chr6:30420325-30420326	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs9885621	chr6:30420345-30420346	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550122162	chr6:30420360-30420361	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs563305945	chr6:30420369-30420370	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs1077501	chr6:30420386-30420387	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532952431	chr6:30420403-30420404	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs386698760	chr6:30420426-30420427	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs9468770	chr6:30420427-30420428	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs9468771	chr6:30420449-30420450	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs148222157	chr6:30420482-30420483	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570930812	chr6:30420503-30420504	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs386698761	chr6:30420547-30420548	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs9468773	chr6:30420549-30420550	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs377488592	chr6:30420594-30420595	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs9468774	chr6:30420611-30420612	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551093620	chr6:30420639-30420640	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569211928	chr6:30420747-30420748	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2516671	chr6:30420764-30420765	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541540908	chr6:30420774-30420775	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs551455801	chr6:30420778-30420779	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs578081975	chr6:30420808-30420809	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs543726473	chr6:30420844-30420845	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs563630742	chr6:30420867-30420868	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs17411410	chr6:30420907-30420908	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534250617	chr6:30420917-30420918	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs188166748	chr6:30420923-30420924	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs559283356	chr6:30420938-30420939	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs141238763	chr6:30420939-30420940	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs551074356	chr6:30420953-30420954	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs570894037	chr6:30420958-30420959	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530450991	chr6:30420984-30420985	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs573939365	chr6:30420992-30420993	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs538015772	chr6:30421027-30421028	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs575763126	chr6:30421028-30421029	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs192897970	chr6:30421036-30421037	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs72502524	chr6:30421047-30421048	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577638396	chr6:30421081-30421082	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs72502525	chr6:30421082-30421083	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555882670	chr6:30421091-30421092	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	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
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30417200-30421600	Bivalent Enhancer	Fetal Thymus	thymus
2	chr6:30418400-30421600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr6:30418400-30421600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
4	chr6:30419200-30421000	Weak transcription	Right Atrium	heart
5	chr6:30419200-30421200	Weak transcription	Right Ventricle	heart
6	chr6:30419200-30421400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:30419200-30421400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
8	chr6:30419200-30421400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
9	chr6:30419200-30421600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
10	chr6:30419200-30421800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
11	chr6:30419200-30421800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:30419200-30428600	Weak transcription	Pancreas	Pancrea
13	chr6:30419400-30421200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
14	chr6:30419400-30421400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:30419400-30421600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:30419400-30421800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
17	chr6:30419600-30420800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
18	chr6:30419600-30421000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
19	chr6:30419600-30421200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr6:30419600-30421200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
21	chr6:30419600-30421400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr6:30419600-30421600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:30419800-30420400	Bivalent Enhancer	Primary T cells from cord blood	blood
24	chr6:30419800-30420600	Weak transcription	Lung	lung
25	chr6:30419800-30421200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr6:30419800-30421200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr6:30419800-30421400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
28	chr6:30420200-30420400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:30420400-30420800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:30420400-30421200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:30420400-30421400	Bivalent Enhancer	Fetal Heart	heart
32	chr6:30420600-30421000	Enhancers	Lung	lung
33	chr6:30420600-30421600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:30420800-30421000	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
35	chr6:30420800-30421200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
36	chr6:30420800-30421400	Bivalent Enhancer	Adipose Nuclei	Adipose
37	chr6:30420800-30421600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
38	chr6:30420800-30421600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
39	chr6:30420800-30421800	Bivalent Enhancer	Primary B cells from cord blood	blood
40	chr6:30420800-30421800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:30421000-30421200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
42	chr6:30421000-30421200	Flanking Bivalent TSS/Enh	Primary T killer memory cells from peripheral blood	blood
43	chr6:30421000-30421200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:30421000-30421200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr6:30421000-30421400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:30421000-30421400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
47	chr6:30421000-30421600	Bivalent Enhancer	Fetal Intestine Small	intestine
48	chr6:30421000-30421600	Bivalent Enhancer	Spleen	Spleen
49	chr6:30421000-30421800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr6:30421000-30421800	Bivalent Enhancer	Fetal Stomach	stomach

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