Variant report

Variant	esv1827960
Chromosome Location	chr17:59869069-59897455
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	chr17:59887540-59887852	K562	blood:	n/a	n/a
2	ATF1	chr17:59873066-59873082	K562	blood:	n/a	n/a
3	BATF	chr17:59877431-59877718	GM12878	blood:	n/a	n/a
4	CEBPB	chr17:59887414-59887886	HCT-116	colon:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
5	CEBPB	chr17:59884175-59889134	MCF-7	breast:	n/a	chr17:59887671-59887688 chr17:59886328-59886341 chr17:59887673-59887684 chr17:59887672-59887685 chr17:59884651-59884662
6	CEBPB	chr17:59887091-59887874	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
7	CEBPB	chr17:59867828-59872635	MCF-7	breast:	n/a	chr17:59871260-59871271 chr17:59871260-59871271 chr17:59868340-59868353 chr17:59871258-59871271 chr17:59871258-59871271
8	CEBPB	chr17:59887494-59887853	HepG2	liver:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
9	CEBPB	chr17:59887096-59887870	IMR90	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
10	CEBPB	chr17:59887431-59887885	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
11	CEBPB	chr17:59887415-59887877	ECC-1	luminal epithelium:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
12	CEBPB	chr17:59884572-59884745	IMR90	lung:	n/a	chr17:59884651-59884662
13	CEBPB	chr17:59887485-59887739	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
14	CEBPB	chr17:59887401-59887934	A549	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
15	CEBPB	chr17:59887499-59887855	Hela-S3	cervix:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
16	CEBPB	chr17:59887243-59887914	ECC-1	luminal epithelium:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
17	CEBPB	chr17:59887662-59887709	H1-hESC	embryonic stem cell:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
18	CEBPB	chr17:59887479-59887843	A549	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
19	CEBPB	chr17:59887068-59887960	MCF-7	breast:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
20	CEBPD	chr17:59887511-59887889	K562	blood:	n/a	chr17:59887672-59887683
21	CTCF	chr17:59876480-59876630	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:59893480-59893630	MCF-7	breast:	n/a	n/a
23	CTCF	chr17:59869520-59869556	ProgFib	skin:	n/a	n/a
24	CTCF	chr17:59883360-59883510	GM12874	blood:	n/a	n/a
25	CTCF	chr17:59874540-59874690	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:59869360-59869510	MCF-7	breast:	n/a	n/a
27	CTCF	chr17:59885920-59886070	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:59883440-59883590	MCF-7	breast:	n/a	n/a
29	CTCF	chr17:59887480-59887630	MCF-7	breast:	n/a	n/a
30	CTCF	chr17:59871284-59871341	GM20000	blood:	n/a	n/a
31	CTCF	chr17:59893521-59893530	K562	blood:	n/a	n/a
32	CTCF	chr17:59893380-59893530	MCF-7	breast:	n/a	chr17:59893456-59893464
33	CTCF	chr17:59874800-59874950	MCF-7	breast:	n/a	n/a
34	E2F4	chr17:59887469-59887722	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr17:59876559-59876625	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr17:59882793-59883050	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr17:59869318-59869490	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr17:59877412-59878093	GM12878	blood:	n/a	chr17:59877809-59877818 chr17:59877807-59877818
39	ELF1	chr17:59889223-59896384	MCF-7	breast:	n/a	n/a
40	ELK1	chr17:59883446-59883448	GM12878	blood:	n/a	n/a
41	EP300	chr17:59887072-59887805	ECC-1	luminal epithelium:	n/a	chr17:59887722-59887730 chr17:59887670-59887684
42	EP300	chr17:59886972-59888094	SK-N-SH	brain:	n/a	chr17:59887722-59887730 chr17:59887021-59887028 chr17:59886990-59886999 chr17:59887670-59887684 chr17:59887866-59887880
43	EP300	chr17:59883486-59883755	GM12878	blood:	n/a	chr17:59883633-59883643
44	EP300	chr17:59877837-59878294	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr17:59878012-59878019	HepG2	liver:	n/a	n/a
46	EP300	chr17:59890641-59890968	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr17:59887455-59887750	K562	blood:	n/a	chr17:59887722-59887730 chr17:59887670-59887684
48	EP300	chr17:59877428-59877870	GM12878	blood:	n/a	n/a
49	EP300	chr17:59889989-59891292	SK-N-SH	brain:	n/a	chr17:59890550-59890564 chr17:59890548-59890562
50	EP300	chr17:59887196-59888030	SK-N-SH	brain:	n/a	chr17:59887722-59887730 chr17:59887670-59887684 chr17:59887866-59887880

No.	Distal block	Cell Line	Cell type
1	chr17:59760845..59762772-chr17:59875907..59878098,2	MCF-7	breast:
2	chr17:59878729..59881613-chr17:59885443..59887044,2	K562	blood:
3	chr17:59892093..59894768-chr8:103186539..103188242,2	MCF-7	breast:
4	chr17:59875243..59877912-chr17:59882843..59885260,2	K562	blood:
5	chr12:58165203..58167229-chr17:59893286..59895128,2	MCF-7	breast:
6	chr17:59722327..59722830-chr17:59891396..59892068,2	MCF-7	breast:
7	chr17:59876155..59878975-chr7:26238906..26240517,2	MCF-7	breast:
8	chr17:59606709..59608528-chr17:59876673..59878930,2	MCF-7	breast:
9	chr1:115210634..115212515-chr17:59866930..59869846,2	MCF-7	breast:
10	chr17:59895734..59897496-chr17:59940156..59941958,2	K562	blood:
11	chr17:59834895..59837098-chr17:59871256..59875287,3	MCF-7	breast:
12	chr17:59895324..59898456-chr17:59898526..59902353,6	MCF-7	breast:
13	chr17:59892648..59894518-chr17:60003995..60006632,2	MCF-7	breast:
14	chr17:59884431..59885001-chr4:80544092..80544675,2	MCF-7	breast:
15	chr1:121484542..121485203-chr17:59874419..59875382,2	MCF-7	breast:
16	chr17:59798054..59800022-chr17:59888680..59890864,2	MCF-7	breast:
17	chr12:120729403..120731557-chr17:59876926..59879782,2	MCF-7	breast:
18	chr1:149818397..149820490-chr17:59879716..59882504,2	MCF-7	breast:
19	chr17:59873836..59876528-chr5:149338569..149340876,2	MCF-7	breast:
20	chr17:59493147..59495448-chr17:59892097..59894543,2	MCF-7	breast:
21	chr17:59488207..59489907-chr17:59897197..59900125,2	MCF-7	breast:
22	chr17:59889894..59892041-chr2:101925111..101926799,2	MCF-7	breast:
23	chr17:59893102..59895072-chr20:47897778..47899643,2	MCF-7	breast:
24	chr17:59893952..59894805-chr7:50993100..50993946,2	MCF-7	breast:
25	chr17:59875217..59877001-chr20:52186479..52188206,2	MCF-7	breast:
26	chr17:59876623..59877141-chr17:59884142..59884839,2	MCF-7	breast:
27	chr17:58677576..58679804-chr17:59895961..59897997,2	MCF-7	breast:
28	chr17:57912982..57915628-chr17:59885852..59887538,2	MCF-7	breast:
29	chr17:59876623..59877141-chr17:59884142..59884839,2	MCF-7	breast:
30	chr17:59890439..59893207-chr6:64345789..64347919,2	MCF-7	breast:
31	chr17:59876832..59880358-chr17:59887599..59890424,3	K562	blood:
32	chr17:59800396..59801468-chr17:59877458..59878364,3	MCF-7	breast:
33	chr17:59890842..59893130-chr17:59894180..59895735,2	K562	blood:
34	chr17:59485645..59487157-chr17:59868692..59871677,2	MCF-7	breast:
35	chr17:59876462..59878052-chr6:21599536..21601804,2	MCF-7	breast:
36	chr17:57915238..57918105-chr17:59890802..59892830,2	MCF-7	breast:
37	chr17:59794574..59796740-chr17:59883852..59885570,2	MCF-7	breast:
38	chr17:59887291..59887834-chr4:30717716..30718321,2	MCF-7	breast:
39	chr17:59876832..59880358-chr17:59887599..59890424,3	K562	blood:
40	chr17:59878729..59881613-chr17:59885443..59887044,2	K562	blood:
41	chr17:59706037..59708264-chr17:59889035..59891024,2	MCF-7	breast:
42	chr17:59883764..59885405-chr20:60640568..60643018,2	MCF-7	breast:
43	chr17:59889939..59890716-chr18:62012536..62013241,2	MCF-7	breast:
44	chr17:59887264..59888905-chr17:59890851..59894921,3	K562	blood:
45	chr17:59890049..59891797-chr3:75078865..75080866,2	MCF-7	breast:
46	chr17:59801899..59802799-chr17:59877268..59878115,2	MCF-7	breast:
47	chr17:59890262..59891161-chr3:64135035..64135674,2	MCF-7	breast:
48	chr17:59475570..59477970-chr17:59890311..59892461,2	MCF-7	breast:
49	chr17:59655980..59658048-chr17:59890809..59893274,2	MCF-7	breast:
50	chr17:59777669..59780570-chr17:59890560..59893186,2	MCF-7	breast:

Variant related genes	Relation type
BRIP1	TF binding region
ENSG00000228395	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000118482	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000153944	chromatin interactions
ENSG00000257921	chromatin interactions
ENSG00000264857	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000037897	chromatin interactions
ENSG00000130699	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000136492	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000197694	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000108506	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000155850	chromatin interactions
ENSG00000198890	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000123427	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000163162	chromatin interactions
ENSG00000233449	chromatin interactions

Extended variants
information (count: 871 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7213329	chr17:59869069-59869070	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7212172	chr17:59869081-59869082	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs375563726	chr17:59869086-59869087	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543578032	chr17:59869170-59869171	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543137590	chr17:59869204-59869205	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563496792	chr17:59869249-59869250	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558095412	chr17:59869277-59869278	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563417584	chr17:59869306-59869307	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs193235177	chr17:59869330-59869331	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548954438	chr17:59869338-59869339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs2378905	chr17:59869398-59869399	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs139157557	chr17:59869429-59869430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528782496	chr17:59869441-59869442	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534403495	chr17:59869465-59869466	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs151181620	chr17:59869526-59869527	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553171839	chr17:59869547-59869548	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571763071	chr17:59869564-59869565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537630598	chr17:59869576-59869577	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540334375	chr17:59869586-59869587	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs140545663	chr17:59869587-59869588	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569759674	chr17:59869598-59869599	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535491170	chr17:59869602-59869603	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs574541500	chr17:59869668-59869669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184486188	chr17:59869681-59869682	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371241023	chr17:59869805-59869806	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188933553	chr17:59869836-59869837	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541959834	chr17:59869870-59869871	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558007629	chr17:59869883-59869884	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577787089	chr17:59869912-59869913	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181379451	chr17:59869930-59869931	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563583153	chr17:59870017-59870018	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs111629030	chr17:59870026-59870027	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75643416	chr17:59870034-59870035	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573791575	chr17:59870108-59870109	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542664089	chr17:59870145-59870146	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184026433	chr17:59870162-59870163	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528451761	chr17:59870233-59870234	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543857115	chr17:59870249-59870250	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs551808136	chr17:59870291-59870292	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs565557431	chr17:59870310-59870311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs531051337	chr17:59870511-59870512	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189712909	chr17:59870512-59870513	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs34138656	chr17:59870514-59870515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs367977039	chr17:59870560-59870561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565260523	chr17:59870583-59870584	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1468577	chr17:59870617-59870618	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549062455	chr17:59870809-59870810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111842788	chr17:59870816-59870817	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs534586629	chr17:59870833-59870834	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs185997519	chr17:59870835-59870836	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	20953835	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
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21467264	CNVD
Ovarian neoplasms	16753589	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
XY sex reversal	17503084	CNVD
Sensorineural hearing loss	22052739	CNVD
intellectual deficit	22052739	CNVD
no characteristic dysmorphism	22052739	CNVD
speech delay	22052739	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17899364	CNVD
Multiple myeloma	16616336	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16620391	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59816800-59887800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr17:59820400-59877200	Weak transcription	NH-A	brain
3	chr17:59825800-59898400	Weak transcription	Thymus	Thymus
4	chr17:59844000-59882600	Weak transcription	NHLF	lung
5	chr17:59844600-59882600	Weak transcription	HMEC	breast
6	chr17:59847600-59883400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:59847800-59876200	Weak transcription	Osteobl	bone
8	chr17:59848400-59873600	Weak transcription	K562	blood
9	chr17:59848600-59874000	Weak transcription	Hela-S3	cervix
10	chr17:59848600-59875600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr17:59848800-59872600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr17:59848800-59882600	Weak transcription	NHEK	skin
13	chr17:59848800-59911200	Weak transcription	HUVEC	blood vessel
14	chr17:59849000-59869400	Weak transcription	HepG2	liver
15	chr17:59849400-59871600	Weak transcription	HSMM	muscle
16	chr17:59849400-59872200	Weak transcription	Fetal Thymus	thymus
17	chr17:59849400-59887200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr17:59849800-59887200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr17:59850000-59869400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr17:59850000-59870800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr17:59850000-59871000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr17:59850000-59872200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr17:59850000-59873200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr17:59850000-59887000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr17:59850000-59887000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr17:59851200-59902600	Weak transcription	Fetal Stomach	stomach
27	chr17:59852600-59869400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr17:59852600-59898000	Weak transcription	Fetal Intestine Small	intestine
29	chr17:59853800-59869400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr17:59854000-59873000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr17:59856400-59872800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr17:59857000-59888600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr17:59858000-59872800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr17:59858200-59869400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr17:59860200-59883200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr17:59862000-59869200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr17:59862000-59887200	Weak transcription	Fetal Kidney	kidney
38	chr17:59863200-59869800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr17:59863600-59925000	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr17:59863800-59876200	Weak transcription	GM12878-XiMat	blood
41	chr17:59864000-59871200	Weak transcription	Primary B cells from cord blood	blood
42	chr17:59865400-59873800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr17:59866000-59880800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr17:59866000-59883200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr17:59866200-59869800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr17:59866400-59883400	Weak transcription	Fetal Lung	lung
47	chr17:59866600-59869200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr17:59867200-59881400	Strong transcription	Dnd41	blood
49	chr17:59867400-59875000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr17:59868000-59870000	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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