Variant report

Variant	nsv908703
Chromosome Location	chr17:66904001-66978319
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	ARID3A	chr17:66903950-66904631	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:66951429-66951869	K562	blood:	n/a	n/a
3	ARID3A	chr17:66934164-66934682	HepG2	liver:	n/a	n/a
4	ATF1	chr17:66905308-66905698	K562	blood:	n/a	n/a
5	ATF1	chr17:66951343-66951843	K562	blood:	n/a	n/a
6	ATF3	chr17:66951415-66951687	K562	blood:	n/a	n/a
7	BATF	chr17:66906318-66906530	GM12878	blood:	n/a	n/a
8	BCL11A	chr17:66977529-66977738	GM12878	blood:	n/a	chr17:66977710-66977719
9	BHLHE40	chr17:66905281-66905526	K562	blood:	n/a	n/a
10	BRCA1	chr17:66957235-66957255	HepG2	liver:	n/a	n/a
11	CBX3	chr17:66904987-66905844	HCT-116	colon:	n/a	n/a
12	CCNT2	chr17:66969489-66969924	K562	blood:	n/a	n/a
13	CEBPB	chr17:66969335-66969976	Hela-S3	cervix:	n/a	chr17:66969894-66969905
14	CEBPB	chr17:66905055-66905747	IMR90	lung:	n/a	n/a
15	CEBPB	chr17:66950744-66951170	K562	blood:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
16	CEBPB	chr17:66950789-66951122	H1-hESC	embryonic stem cell:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
17	CEBPB	chr17:66938012-66938194	HepG2	liver:	n/a	chr17:66938120-66938131
18	CEBPB	chr17:66952202-66952390	K562	blood:	n/a	n/a
19	CEBPB	chr17:66949911-66950058	K562	blood:	n/a	n/a
20	CEBPB	chr17:66969783-66970047	HepG2	liver:	n/a	chr17:66969894-66969905 chr17:66970027-66970040
21	CEBPB	chr17:66950722-66951085	A549	lung:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
22	CEBPB	chr17:66937950-66938271	K562	blood:	n/a	chr17:66938120-66938131
23	CEBPB	chr17:66950794-66951153	HepG2	liver:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
24	CEBPB	chr17:66960200-66960410	K562	blood:	n/a	chr17:66960279-66960292 chr17:66960279-66960290
25	CEBPB	chr17:66973466-66973714	HepG2	liver:	n/a	chr17:66973550-66973561
26	CEBPB	chr17:66950782-66951157	IMR90	lung:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
27	CEBPB	chr17:66977541-66977700	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr17:66924242-66924344	HepG2	liver:	n/a	chr17:66924293-66924304
29	CEBPB	chr17:66946779-66947429	K562	blood:	n/a	chr17:66947347-66947358
30	CEBPB	chr17:66922793-66922820	HepG2	liver:	n/a	chr17:66922798-66922811 chr17:66922800-66922809 chr17:66922799-66922810 chr17:66922798-66922809
31	CEBPB	chr17:66969799-66969935	K562	blood:	n/a	chr17:66969894-66969905
32	CEBPB	chr17:66938010-66938212	A549	lung:	n/a	chr17:66938120-66938131
33	CEBPB	chr17:66916639-66916679	HepG2	liver:	n/a	chr17:66916653-66916664
34	CEBPB	chr17:66950796-66951137	Hela-S3	cervix:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
35	CEBPB	chr17:66924340-66924352	A549	lung:	n/a	n/a
36	CEBPB	chr17:66905340-66905733	K562	blood:	n/a	n/a
37	CEBPB	chr17:66969775-66970045	K562	blood:	n/a	chr17:66969894-66969905 chr17:66970027-66970040
38	CEBPB	chr17:66950544-66951220	K562	blood:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
39	CEBPB	chr17:66950799-66951062	K562	blood:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
40	CEBPB	chr17:66904213-66904629	HepG2	liver:	n/a	n/a
41	CEBPB	chr17:66950797-66951135	A549	lung:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
42	CEBPB	chr17:66973491-66973530	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr17:66934423-66934641	HepG2	liver:	n/a	n/a
44	CEBPB	chr17:66905268-66905672	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr17:66960236-66960396	Hela-S3	cervix:	n/a	chr17:66960279-66960292 chr17:66960279-66960290
46	CREB1	chr17:66951280-66951875	K562	blood:	n/a	n/a
47	CREB1	chr17:66951252-66951984	K562	blood:	n/a	n/a
48	CTCF	chr17:66906600-66906750	HepG2	liver:	n/a	n/a
49	CTCF	chr17:66968403-66968551	GM10266	blood:	n/a	n/a
50	CTCF	chr17:66906557-66906567	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:66905630-66905680	AG09319	gingival:	n/a
2	chr17:66951572-66951622	HCT-116	colon:	n/a
3	chr17:66905630-66905680	ProgFib	skin:	n/a
4	chr17:66926513-66926563	AG09309	skin:	n/a
5	chr17:66925642-66925692	SK-N-SH_RA	brain:	n/a
6	chr17:66942706-66942756	GM12892	blood:	n/a
7	chr17:66951572-66951622	HPAEpiC	pulmonary alveolar:	n/a
8	chr17:66925642-66925692	HCF	heart:	n/a
9	chr17:66951572-66951622	RPTEC	kidney:	n/a
10	chr17:66951572-66951622	AG04449	skin:	fetal
11	chr17:66926513-66926563	A549	lung:	n/a
12	chr17:66971371-66971421	A549	lung:	n/a
13	chr17:66971371-66971421	IMR90	lung:	fetal
14	chr17:66950545-66950595	A549	lung:	n/a
15	chr17:66971371-66971421	HRCEpiC	kidney:	n/a
16	chr17:66950545-66950595	GM12878	blood:	n/a
17	chr17:66950545-66950595	Caco-2	colon:	n/a
18	chr17:66942706-66942756	GM12878	blood:	n/a
19	chr17:66942706-66942756	HPAEpiC	pulmonary alveolar:	n/a
20	chr17:66971371-66971421	LNCaP	prostate:	n/a
21	chr17:66971371-66971421	SK-N-SH	brain:	n/a
22	chr17:66926513-66926563	BE2_C	brain:	n/a
23	chr17:66905630-66905680	ovcar-3	ovarian:	n/a
24	chr17:66905630-66905680	NHDF-neo	bronchial:	n/a
25	chr17:66950545-66950595	HCPEpiC	choroid plexus:	n/a
26	chr17:66950545-66950595	HEEpiC	esophagus:	n/a
27	chr17:66905630-66905680	HIPEpiC	eye:	n/a
28	chr17:66971371-66971421	HCPEpiC	choroid plexus:	n/a
29	chr17:66971371-66971421	HRPEpiC	eye:	n/a
30	chr17:66925642-66925692	HNPCEpiC	eye:	n/a
31	chr17:66942706-66942756	AG04450	lung:	fetal
32	chr17:66925642-66925692	IMR90	lung:	fetal
33	chr17:66971371-66971421	RPTEC	kidney:	n/a
34	chr17:66971371-66971421	GM12891	blood:	n/a
35	chr17:66951572-66951622	HCF	heart:	n/a
36	chr17:66905630-66905680	ECC-1	luminal epithelium:	n/a
37	chr17:66951572-66951622	Caco-2	colon:	n/a
38	chr17:66950545-66950595	RPTEC	kidney:	n/a
39	chr17:66951572-66951622	AG04450	lung:	fetal
40	chr17:66926513-66926563	AG10803	skin:	n/a
41	chr17:66926513-66926563	GM12891	blood:	n/a
42	chr17:66971371-66971421	ProgFib	skin:	n/a
43	chr17:66950545-66950595	GM19239	blood:	n/a
44	chr17:66942706-66942756	HIPEpiC	eye:	n/a
45	chr17:66951572-66951622	HCM	heart:	n/a
46	chr17:66905630-66905680	SAEC	small airway:	n/a
47	chr17:66905630-66905680	PANC-1	pancreas:	n/a
48	chr17:66951572-66951622	HRCEpiC	kidney:	n/a
49	chr17:66905630-66905680	MCF-7	breast:	n/a
50	chr17:66905630-66905680	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:66790371..66791470-chr17:66967983..66969294,6	MCF-7	breast:
2	chr17:66773389..66774236-chr17:66968021..66969271,11	MCF-7	breast:
3	chr1:150945529..150947119-chr17:66926338..66928766,2	MCF-7	breast:
4	chr17:66770128..66770971-chr17:66968392..66969147,2	MCF-7	breast:
5	chr17:66773454..66774157-chr17:66967941..66968651,3	MCF-7	breast:
6	chr17:66898068..66900129-chr17:66902594..66904436,2	K562	blood:
7	chr17:66968043..66969072-chr17:67231311..67232174,4	MCF-7	breast:
8	chr17:66915457..66918410-chr17:66918904..66921689,2	K562	blood:
9	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:
10	chr17:66924075..66929120-chr17:66931843..66935523,4	K562	blood:
11	chr17:66790300..66791288-chr17:66907471..66908085,3	MCF-7	breast:
12	chr17:66771870..66772496-chr17:66967790..66968348,2	MCF-7	breast:
13	chr17:66956572..66959212-chr17:67192982..67195972,2	K562	blood:
14	chr17:66903121..66905132-chr17:66913940..66916268,2	MCF-7	breast:
15	chr17:66773260..66773836-chr17:66907708..66908473,2	MCF-7	breast:
16	chr17:66963587..66965320-chr17:66967793..66970228,2	MCF-7	breast:
17	chr17:66963587..66965320-chr17:66967793..66970228,2	MCF-7	breast:
18	chr17:66767661..66768741-chr17:66968239..66968983,3	MCF-7	breast:

Variant related genes	Relation type
ABCA8	TF binding region
ABCA8	CpG island
ENSG00000143418	chromatin interactions
ENSG00000141338	chromatin interactions
ENSG00000231073	chromatin interactions

Extended variants
information (count: 3083 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3083 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16973424	chr17:66904001-66904002	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201463363	chr17:66904003-66904004	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576252562	chr17:66904030-66904031	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs199770005	chr17:66904031-66904032	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556196309	chr17:66904032-66904033	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572235778	chr17:66904033-66904034	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201773566	chr17:66904038-66904039	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564520518	chr17:66904039-66904040	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs200486985	chr17:66904044-66904045	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs192894780	chr17:66904055-66904056	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540647525	chr17:66904057-66904058	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375594866	chr17:66904058-66904059	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559149490	chr17:66904075-66904076	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9907353	chr17:66904083-66904084	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548446145	chr17:66904090-66904091	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183173739	chr17:66904104-66904105	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144617278	chr17:66904160-66904161	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552932255	chr17:66904165-66904166	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571182713	chr17:66904183-66904184	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs534983954	chr17:66904195-66904196	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs138505442	chr17:66904209-66904210	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556993855	chr17:66904212-66904213	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568416465	chr17:66904220-66904221	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535994354	chr17:66904240-66904241	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115085607	chr17:66904293-66904294	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs74323415	chr17:66904294-66904295	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536922687	chr17:66904323-66904324	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558400302	chr17:66904328-66904329	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144862152	chr17:66904337-66904338	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs111879960	chr17:66904349-66904350	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544186662	chr17:66904401-66904402	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs111364507	chr17:66904405-66904406	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562570682	chr17:66904428-66904429	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191864856	chr17:66904449-66904450	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533030564	chr17:66904490-66904491	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs112096468	chr17:66904497-66904498	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563710613	chr17:66904507-66904508	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567961145	chr17:66904510-66904511	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531099433	chr17:66904525-66904526	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148585051	chr17:66904555-66904556	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs141961849	chr17:66904581-66904582	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184249703	chr17:66904620-66904621	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546677295	chr17:66904625-66904626	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73998574	chr17:66904639-66904640	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374993051	chr17:66904672-66904673	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189025179	chr17:66904693-66904694	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114198819	chr17:66904748-66904749	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs73998575	chr17:66904752-66904753	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs527476670	chr17:66904772-66904773	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79774939	chr17:66904788-66904789	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Congenital generalized hypertrichosis terminalis	19463983	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
XY gonadal dysgenesis	20685758	CNVD
Gingival hyperplasia	19463983	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neuroblastoma	20406844	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Breast cancer	21045282	CNVD
Epilepsy	22083797	CNVD
Sezary syndrome	18413736	CNVD
Honadal dysgenesis	21408189	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66877000-66906200	Weak transcription	Fetal Stomach	stomach
2	chr17:66877800-66918200	Weak transcription	Fetal Brain Male	brain
3	chr17:66881200-66904200	Weak transcription	Psoas Muscle	Psoas
4	chr17:66881400-66906400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr17:66881400-66906400	Weak transcription	Right Ventricle	heart
6	chr17:66893000-66905200	Weak transcription	Fetal Muscle Leg	muscle
7	chr17:66893200-66906400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr17:66893400-66906400	Weak transcription	Fetal Heart	heart
9	chr17:66894000-66904400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr17:66896600-66906200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr17:66898000-66905200	Weak transcription	K562	blood
12	chr17:66899000-66906200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr17:66899600-66904400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr17:66899600-66904400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr17:66899600-66906400	Weak transcription	Left Ventricle	heart
16	chr17:66899600-66906400	Weak transcription	Ovary	ovary
17	chr17:66899800-66904400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr17:66902200-66904400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr17:66902200-66907800	Enhancers	Brain Substantia Nigra	brain
20	chr17:66902400-66907800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr17:66902600-66906400	Enhancers	Brain Hippocampus Middle	brain
22	chr17:66902800-66904400	Enhancers	Brain Cingulate Gyrus	brain
23	chr17:66902800-66908000	Enhancers	HepG2	liver
24	chr17:66903000-66904600	Genic enhancers	Liver	Liver
25	chr17:66903000-66904800	Enhancers	Brain Angular Gyrus	brain
26	chr17:66903000-66906200	Enhancers	Brain Anterior Caudate	brain
27	chr17:66903000-66907800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr17:66903200-66904200	Weak transcription	NHEK	skin
29	chr17:66903200-66904600	Strong transcription	Adipose Nuclei	Adipose
30	chr17:66903200-66907000	Enhancers	HMEC	breast
31	chr17:66903200-66908200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr17:66903400-66904200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr17:66903400-66904400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr17:66903400-66905400	Strong transcription	Fetal Lung	lung
35	chr17:66903600-66905400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr17:66903800-66904200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr17:66903800-66904400	Weak transcription	Osteobl	bone
38	chr17:66903800-66907600	Enhancers	Colon Smooth Muscle	Colon
39	chr17:66904200-66904400	Enhancers	Psoas Muscle	Psoas
40	chr17:66904200-66904600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr17:66904200-66904600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr17:66904200-66904600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:66904200-66905000	Enhancers	NHEK	skin
44	chr17:66904200-66905400	Enhancers	NHDF-Ad	bronchial
45	chr17:66904200-66905800	Enhancers	GM12878-XiMat	blood
46	chr17:66904200-66907200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr17:66904200-66907200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr17:66904200-66907400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr17:66904400-66904600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr17:66904400-66904600	Enhancers	Skeletal Muscle Male	skeletal muscle

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