Variant report

Variant	nsv969357
Chromosome Location	chr6:26321434-26323580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:556)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26322814-26323512	K562	blood:	n/a	n/a
2	ARID3A	chr6:26322150-26323650	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:26321345-26321501	K562	blood:	n/a	n/a
4	ARID3A	chr6:26322193-26322540	K562	blood:	n/a	n/a
5	ATF1	chr6:26322938-26323459	K562	blood:	n/a	n/a
6	ATF2	chr6:26322154-26322657	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:26322752-26323434	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:26322825-26323431	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:26322812-26323420	GM12878	blood:	n/a	n/a
10	ATF3	chr6:26322161-26322698	A549	lung:	n/a	n/a
11	ATF3	chr6:26322783-26323487	HCT-116	colon:	n/a	n/a
12	ATF3	chr6:26322573-26323714	A549	lung:	n/a	n/a
13	ATF3	chr6:26322740-26323653	K562	blood:	n/a	n/a
14	ATF3	chr6:26322748-26323657	A549	lung:	n/a	n/a
15	BACH1	chr6:26322181-26322450	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr6:26322885-26323198	GM12878	blood:	n/a	n/a
17	BATF	chr6:26322291-26322469	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:26322109-26322624	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:26322749-26323442	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:26322808-26323429	GM12878	blood:	n/a	n/a
21	BDP1	chr6:26322762-26323210	K562	blood:	n/a	n/a
22	BDP1	chr6:26322788-26323318	Hela-S3	cervix:	n/a	n/a
23	BHLHE40	chr6:26322969-26323464	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:26322141-26322538	K562	blood:	n/a	n/a
25	BHLHE40	chr6:26322061-26322261	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:26322937-26323335	K562	blood:	n/a	n/a
27	BRCA1	chr6:26322850-26323409	Hela-S3	cervix:	n/a	n/a
28	BRF1	chr6:26322851-26323188	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr6:26322193-26323467	HCT-116	colon:	n/a	n/a
30	CBX3	chr6:26322212-26323662	K562	blood:	n/a	n/a
31	CBX3	chr6:26322043-26323729	K562	blood:	n/a	n/a
32	CCNT2	chr6:26322437-26322637	K562	blood:	n/a	n/a
33	CCNT2	chr6:26322985-26323224	K562	blood:	n/a	n/a
34	CEBPB	chr6:26322804-26323587	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr6:26322933-26323519	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:26322255-26323286	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:26322842-26323664	K562	blood:	n/a	n/a
38	CEBPB	chr6:26322867-26323229	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:26322836-26323183	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:26322819-26323357	A549	lung:	n/a	n/a
41	CEBPB	chr6:26322345-26322422	K562	blood:	n/a	n/a
42	CEBPB	chr6:26322850-26323188	A549	lung:	n/a	n/a
43	CEBPB	chr6:26322916-26323736	K562	blood:	n/a	n/a
44	CEBPD	chr6:26322870-26323504	K562	blood:	n/a	n/a
45	CHD1	chr6:26322523-26322568	GM12878	blood:	n/a	n/a
46	CHD2	chr6:26322390-26322633	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr6:26322455-26322486	K562	blood:	n/a	n/a
48	CHD2	chr6:26322930-26323491	K562	blood:	n/a	n/a
49	CREB1	chr6:26322322-26323870	K562	blood:	n/a	n/a
50	CREB1	chr6:26322344-26323791	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26323437-26323487	AG04450	lung:	fetal
2	chr6:26323563-26323613	NB4	blood:	n/a
3	chr6:26322291-26322341	AG09319	gingival:	n/a
4	chr6:26322387-26322437	NB4	blood:	n/a
5	chr6:26322387-26322437	GM12878	blood:	n/a
6	chr6:26323563-26323613	BE2_C	brain:	n/a
7	chr6:26322291-26322341	GM12891	blood:	n/a
8	chr6:26322387-26322437	A549	lung:	n/a
9	chr6:26322387-26322437	GM12891	blood:	n/a
10	chr6:26323437-26323487	GM19239	blood:	n/a
11	chr6:26322387-26322437	BJ	skin:	n/a
12	chr6:26323437-26323487	HRPEpiC	eye:	n/a
13	chr6:26323563-26323613	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:26322488-26322538	GM06990	blood:	n/a
15	chr6:26323437-26323487	HIPEpiC	eye:	n/a
16	chr6:26322291-26322341	AoSMC	blood vessel:	n/a
17	chr6:26323437-26323487	HCM	heart:	n/a
18	chr6:26322488-26322538	HCT-116	colon:	n/a
19	chr6:26322387-26322437	SK-N-SH_RA	brain:	n/a
20	chr6:26323563-26323613	BJ	skin:	n/a
21	chr6:26322291-26322341	GM06990	blood:	n/a
22	chr6:26322488-26322538	SK-N-MC	brain:	n/a
23	chr6:26322488-26322538	HMEC	breast:	n/a
24	chr6:26322488-26322538	NB4	blood:	n/a
25	chr6:26322488-26322538	HCM	heart:	n/a
26	chr6:26322488-26322538	NH-A	brain:	n/a
27	chr6:26322387-26322437	ECC-1	luminal epithelium:	n/a
28	chr6:26323437-26323487	K562	blood:	n/a
29	chr6:26323437-26323487	HEK293	kidney:	embryo
30	chr6:26322387-26322437	SKMC	muscle:	n/a
31	chr6:26322488-26322538	SK-N-SH_RA	brain:	n/a
32	chr6:26322488-26322538	NHBE	bronchial:	n/a
33	chr6:26322488-26322538	Caco-2	colon:	n/a
34	chr6:26322488-26322538	HAEpiC	amniotic membrane:	n/a
35	chr6:26322488-26322538	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:26322387-26322437	CMK	blood:	n/a
37	chr6:26322387-26322437	HRCEpiC	kidney:	n/a
38	chr6:26322387-26322437	SK-N-SH	brain:	n/a
39	chr6:26322488-26322538	MCF-7	breast:	n/a
40	chr6:26323563-26323613	A549	lung:	n/a
41	chr6:26322291-26322341	HNPCEpiC	eye:	n/a
42	chr6:26322488-26322538	AG10803	skin:	n/a
43	chr6:26323563-26323613	NHDF-neo	bronchial:	n/a
44	chr6:26322387-26322437	GM06990	blood:	n/a
45	chr6:26323563-26323613	ovcar-3	ovarian:	n/a
46	chr6:26322488-26322538	ovcar-3	ovarian:	n/a
47	chr6:26323563-26323613	SK-N-MC	brain:	n/a
48	chr6:26323437-26323487	GM12878	blood:	n/a
49	chr6:26323563-26323613	AG10803	skin:	n/a
50	chr6:26323563-26323613	HNPCEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26323439..26325517-chr6:27099019..27100610,2	K562	blood:
2	chr6:26273199..26275817-chr6:26322608..26324495,2	MCF-7	breast:
3	chr1:226250046..226250889-chr6:26322132..26323073,2	NB4	blood:
4	chr6:26250927..26253821-chr6:26323382..26326014,4	MCF-7	breast:
5	chr6:26321606..26324992-chr6:26518176..26520933,3	K562	blood:
6	chr6:26322866..26325773-chr6:26327005..26329096,3	MCF-7	breast:
7	chr6:26317773..26322423-chr6:26326646..26329657,4	MCF-7	breast:
8	chr16:57480084..57480953-chr6:26321593..26322348,2	Hela-S3	cervix:
9	chr6:26323184..26324056-chr6:26341539..26342363,2	K562	blood:
10	chr6:26319791..26322184-chr6:26520367..26521947,2	K562	blood:
11	chr6:26319791..26321443-chr6:26520367..26522578,2	K562	blood:
12	chr6:26323417..26326776-chr6:26326785..26329865,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTN3A2-3	chr6:26320984-26321555	NONHSAT108259

No data

Variant related genes	Relation type
HIST1H3PS1	TF binding region
HIST1H3PS1	CpG island
ENSG00000124635	chromatin interactions
ENSG00000163041	chromatin interactions
ENSG00000199289	chromatin interactions
ENSG00000197459	chromatin interactions
ENSG00000228223	chromatin interactions

Extended variants
information (count: 123 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:123 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184541411	chr6:26321504-26321505	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs113394260	chr6:26321507-26321508	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs527305021	chr6:26321575-26321576	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs10046318	chr6:26321586-26321587	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570537578	chr6:26321590-26321591	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190553399	chr6:26321626-26321627	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556836602	chr6:26321630-26321631	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572274973	chr6:26321649-26321650	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs55822642	chr6:26321668-26321669	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144609158	chr6:26321673-26321674	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536182695	chr6:26321713-26321714	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556116547	chr6:26321737-26321738	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200376812	chr6:26321763-26321764	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537214317	chr6:26321781-26321782	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143918132	chr6:26321782-26321783	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201082719	chr6:26321792-26321793	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541423309	chr6:26321805-26321806	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557817676	chr6:26321809-26321810	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181988065	chr6:26321840-26321841	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543545444	chr6:26321848-26321849	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562380432	chr6:26321880-26321881	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577185403	chr6:26321901-26321902	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531381895	chr6:26321907-26321908	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113683551	chr6:26321953-26321954	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs539873146	chr6:26322023-26322024	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs55776062	chr6:26322055-26322056	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185724293	chr6:26322112-26322113	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs6902392	chr6:26322115-26322116	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs543590864	chr6:26322122-26322123	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs6902389	chr6:26322153-26322154	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs148372112	chr6:26322176-26322177	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189022156	chr6:26322234-26322235	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141548306	chr6:26322237-26322238	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs74455078	chr6:26322242-26322243	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112743764	chr6:26322253-26322254	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs536070004	chr6:26322316-26322317	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs549556157	chr6:26322337-26322338	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370861686	chr6:26322370-26322371	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535001180	chr6:26322385-26322386	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558175856	chr6:26322388-26322389	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs532191819	chr6:26322430-26322431	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577945989	chr6:26322434-26322435	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs537178134	chr6:26322436-26322437	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557056608	chr6:26322459-26322460	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs9358924	chr6:26322473-26322474	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541633352	chr6:26322496-26322497	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138403925	chr6:26322511-26322512	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559272642	chr6:26322516-26322517	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572353445	chr6:26322518-26322519	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs6903015	chr6:26322526-26322527	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:104)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	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
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
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	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
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	20531469	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26314200-26321800	Weak transcription	NH-A	brain
2	chr6:26314200-26322000	Weak transcription	Right Atrium	heart
3	chr6:26314400-26322000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr6:26314400-26322200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:26318600-26323400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr6:26318800-26323200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:26319000-26322800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr6:26319000-26323000	Active TSS	H1 Cell Line	embryonic stem cell
9	chr6:26319000-26323000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:26319400-26321800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:26320400-26322000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:26320600-26321600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr6:26320600-26321600	Flanking Active TSS	K562	blood
14	chr6:26320600-26321800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:26320600-26321800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:26320600-26322000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:26320800-26321600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr6:26320800-26321600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:26320800-26321800	Flanking Active TSS	Dnd41	blood
20	chr6:26321000-26321600	Flanking Active TSS	A549	lung
21	chr6:26321000-26321600	Flanking Active TSS	Hela-S3	cervix
22	chr6:26321000-26321600	Enhancers	NHEK	skin
23	chr6:26321000-26321800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
24	chr6:26321000-26322000	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr6:26321000-26322200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:26321200-26321600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
27	chr6:26321200-26321600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:26321200-26321800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:26321200-26321800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:26321200-26321800	Bivalent Enhancer	Primary T cells from cord blood	blood
31	chr6:26321200-26321800	Enhancers	Primary T cells fromperipheralblood	blood
32	chr6:26321200-26321800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:26321200-26322000	Bivalent Enhancer	Primary B cells from cord blood	blood
34	chr6:26321200-26322000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr6:26321200-26322000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr6:26321200-26323000	Active TSS	HUVEC	blood vessel
37	chr6:26321200-26323800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:26321400-26321600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr6:26321400-26321600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:26321400-26321600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:26321400-26321600	Enhancers	NHDF-Ad	bronchial
42	chr6:26321400-26321800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:26321400-26321800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr6:26321400-26321800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:26321400-26322000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:26321400-26322000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr6:26321400-26322000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr6:26321400-26322000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr6:26321400-26322000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
50	chr6:26321400-26322800	Active TSS	NHLF	lung

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