Variant report

Variant	esv1794309
Chromosome Location	chr17:59861640-59907952
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	chr17:59873066-59873082	K562	blood:	n/a	n/a
2	ATF1	chr17:59867383-59867517	K562	blood:	n/a	n/a
3	ATF1	chr17:59887540-59887852	K562	blood:	n/a	n/a
4	ATF2	chr17:59861070-59862129	GM12878	blood:	n/a	n/a
5	BATF	chr17:59899793-59900416	GM12878	blood:	n/a	n/a
6	BATF	chr17:59877431-59877718	GM12878	blood:	n/a	n/a
7	BATF	chr17:59899782-59900304	GM12878	blood:	n/a	n/a
8	BCLAF1	chr17:59861041-59862233	GM12878	blood:	n/a	n/a
9	CEBPB	chr17:59887485-59887739	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
10	CEBPB	chr17:59887499-59887855	Hela-S3	cervix:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
11	CEBPB	chr17:59887414-59887886	HCT-116	colon:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
12	CEBPB	chr17:59887479-59887843	A549	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
13	CEBPB	chr17:59884175-59889134	MCF-7	breast:	n/a	chr17:59887671-59887688 chr17:59886328-59886341 chr17:59887673-59887684 chr17:59887672-59887685 chr17:59884651-59884662
14	CEBPB	chr17:59887243-59887914	ECC-1	luminal epithelium:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
15	CEBPB	chr17:59887431-59887885	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
16	CEBPB	chr17:59867828-59872635	MCF-7	breast:	n/a	chr17:59871260-59871271 chr17:59871260-59871271 chr17:59868340-59868353 chr17:59871258-59871271 chr17:59871258-59871271
17	CEBPB	chr17:59887494-59887853	HepG2	liver:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
18	CEBPB	chr17:59887091-59887874	K562	blood:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
19	CEBPB	chr17:59905901-59906407	HepG2	liver:	n/a	n/a
20	CEBPB	chr17:59887415-59887877	ECC-1	luminal epithelium:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
21	CEBPB	chr17:59887662-59887709	H1-hESC	embryonic stem cell:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
22	CEBPB	chr17:59861047-59861763	GM12878	blood:	n/a	n/a
23	CEBPB	chr17:59905997-59906318	A549	lung:	n/a	n/a
24	CEBPB	chr17:59904328-59907370	MCF-7	breast:	n/a	n/a
25	CEBPB	chr17:59887096-59887870	IMR90	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
26	CEBPB	chr17:59887068-59887960	MCF-7	breast:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
27	CEBPB	chr17:59859730-59863951	MCF-7	breast:	n/a	n/a
28	CEBPB	chr17:59887401-59887934	A549	lung:	n/a	chr17:59887671-59887688 chr17:59887673-59887684 chr17:59887672-59887685
29	CEBPB	chr17:59884572-59884745	IMR90	lung:	n/a	chr17:59884651-59884662
30	CEBPD	chr17:59887511-59887889	K562	blood:	n/a	chr17:59887672-59887683
31	CTCF	chr17:59893480-59893630	MCF-7	breast:	n/a	n/a
32	CTCF	chr17:59874540-59874690	MCF-7	breast:	n/a	n/a
33	CTCF	chr17:59869520-59869556	ProgFib	skin:	n/a	n/a
34	CTCF	chr17:59883440-59883590	MCF-7	breast:	n/a	n/a
35	CTCF	chr17:59907521-59907570	GM13976	blood:	n/a	n/a
36	CTCF	chr17:59887480-59887630	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:59876480-59876630	MCF-7	breast:	n/a	n/a
38	CTCF	chr17:59863600-59863750	MCF-7	breast:	n/a	n/a
39	CTCF	chr17:59893521-59893530	K562	blood:	n/a	n/a
40	CTCF	chr17:59874800-59874950	MCF-7	breast:	n/a	n/a
41	CTCF	chr17:59898440-59898590	MCF-7	breast:	n/a	n/a
42	CTCF	chr17:59893380-59893530	MCF-7	breast:	n/a	chr17:59893456-59893464
43	CTCF	chr17:59868094-59868112	MCF-7	breast:	n/a	n/a
44	CTCF	chr17:59883360-59883510	GM12874	blood:	n/a	n/a
45	CTCF	chr17:59885920-59886070	MCF-7	breast:	n/a	n/a
46	CTCF	chr17:59869360-59869510	MCF-7	breast:	n/a	n/a
47	CTCF	chr17:59863537-59863593	MCF-7	breast:	n/a	n/a
48	CTCF	chr17:59871284-59871341	GM20000	blood:	n/a	n/a
49	CUX1	chr17:59861296-59861955	GM12878	blood:	n/a	n/a
50	E2F4	chr17:59882793-59883050	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:59477516..59480504-chr17:59906468..59908816,2	MCF-7	breast:
2	chr17:59800397..59801337-chr17:59877348..59878274,6	MCF-7	breast:
3	chr17:59878729..59881613-chr17:59885443..59887044,2	K562	blood:
4	chr17:59858750..59861674-chr6:83070524..83072969,2	MCF-7	breast:
5	chr17:59876155..59878975-chr7:26238906..26240517,2	MCF-7	breast:
6	chr17:59606709..59608528-chr17:59876673..59878930,2	MCF-7	breast:
7	chr17:59877060..59879935-chr20:55851000..55853475,2	MCF-7	breast:
8	chr17:59907737..59910025-chr20:55839076..55841532,2	MCF-7	breast:
9	chr17:59862782..59863461-chr3:64008914..64009596,2	MCF-7	breast:
10	chr17:59889939..59890716-chr18:62012536..62013241,2	MCF-7	breast:
11	chr17:59764767..59767595-chr17:59891834..59893836,2	MCF-7	breast:
12	chr17:59655980..59658048-chr17:59890809..59893274,2	MCF-7	breast:
13	chr17:59889894..59892041-chr2:101925111..101926799,2	MCF-7	breast:
14	chr17:59738960..59741122-chr17:59903243..59905163,2	MCF-7	breast:
15	chr17:58677576..58679804-chr17:59895961..59897997,2	MCF-7	breast:
16	chr1:116235935..116238608-chr17:59873371..59874879,2	MCF-7	breast:
17	chr17:59800856..59804163-chr17:59876065..59879949,4	MCF-7	breast:
18	chr17:59800395..59801174-chr17:59877584..59878511,3	MCF-7	breast:
19	chr17:59801899..59802799-chr17:59877268..59878115,2	MCF-7	breast:
20	chr17:59905219..59908191-chr17:62224835..62227533,2	MCF-7	breast:
21	chr17:59875243..59877912-chr17:59882843..59885260,2	K562	blood:
22	chr1:107598419..107600523-chr17:59895411..59897981,2	MCF-7	breast:
23	chr17:59713070..59714030-chr17:59904455..59905249,2	MCF-7	breast:
24	chr1:121484542..121485203-chr17:59874419..59875382,2	MCF-7	breast:
25	chr17:59493147..59495448-chr17:59892097..59894543,2	MCF-7	breast:
26	chr17:59787606..59790047-chr17:59879549..59882493,2	MCF-7	breast:
27	chr17:59892093..59894768-chr8:103186539..103188242,2	MCF-7	breast:
28	chr17:59477279..59479183-chr17:59870460..59872520,2	MCF-7	breast:
29	chr17:59485300..59495746-chr17:59906301..59920408,36	MCF-7	breast:
30	chr17:59890246..59897512-chr17:59906301..59911865,9	MCF-7	breast:
31	chr17:59706037..59708264-chr17:59889035..59891024,2	MCF-7	breast:
32	chr17:59890049..59891797-chr3:75078865..75080866,2	MCF-7	breast:
33	chr17:59870008..59870511-chr3:172015804..172016695,2	MCF-7	breast:
34	chr17:59526831..59528449-chr17:59861163..59863891,2	MCF-7	breast:
35	chr17:59890842..59893130-chr17:59894180..59895735,2	K562	blood:
36	chr17:59864218..59867206-chr17:59938344..59939974,2	MCF-7	breast:
37	chr17:59875217..59877001-chr20:52186479..52188206,2	MCF-7	breast:
38	chr17:59898858..59900358-chr17:59911804..59913981,2	MCF-7	breast:
39	chr17:59866718..59868702-chr17:59911534..59913402,2	MCF-7	breast:
40	chr17:59901501..59904462-chr20:52238183..52241107,2	MCF-7	breast:
41	chr17:59884431..59885001-chr4:80544092..80544675,2	MCF-7	breast:
42	chr17:57969150..57971912-chr17:59907118..59908695,2	MCF-7	breast:
43	chr17:59890439..59893207-chr6:64345789..64347919,2	MCF-7	breast:
44	chr17:59853761..59854400-chr17:59866223..59867007,2	MCF-7	breast:
45	chr17:59876623..59877141-chr17:59884142..59884839,2	MCF-7	breast:
46	chr17:59876462..59878052-chr6:21599536..21601804,2	MCF-7	breast:
47	chr17:59878944..59880921-chr17:59881668..59883370,2	K562	blood:
48	chr17:59800446..59802720-chr17:59893670..59895500,2	MCF-7	breast:
49	chr17:59883764..59885405-chr20:60640568..60643018,2	MCF-7	breast:
50	chr17:16254890..16255689-chr17:59860995..59861816,2	MCF-7	breast:

Variant related genes	Relation type
BRIP1	TF binding region
ENSG00000123427	chromatin interactions
ENSG00000264857	chromatin interactions
ENSG00000155850	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000130699	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000257921	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000198890	chromatin interactions
ENSG00000228395	chromatin interactions
ENSG00000153944	chromatin interactions
ENSG00000037897	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000197694	chromatin interactions
ENSG00000146242	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000163162	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000108506	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000136492	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000233449	chromatin interactions
ENSG00000118482	chromatin interactions
ENSG00000200795	chromatin interactions

Extended variants
information (count: 1435 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4988349	chr17:59861640-59861641	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs199616792	chr17:59861643-59861644	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs56024614	chr17:59861654-59861655	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs4988350	chr17:59861668-59861669	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs138784299	chr17:59861673-59861674	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370658123	chr17:59861774-59861775	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536081549	chr17:59861775-59861776	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552752779	chr17:59861788-59861789	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375084607	chr17:59861813-59861814	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374100914	chr17:59861815-59861816	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs182302236	chr17:59861864-59861865	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs545188400	chr17:59861908-59861909	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185030456	chr17:59861958-59861959	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs191057166	chr17:59861965-59861966	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575580069	chr17:59861975-59861976	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs140395804	chr17:59861979-59861980	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183872183	chr17:59861986-59861987	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs561611846	chr17:59862066-59862067	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs72842992	chr17:59862082-59862083	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547265260	chr17:59862086-59862087	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560674304	chr17:59862087-59862088	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs8078977	chr17:59862099-59862100	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs554242685	chr17:59862139-59862140	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs374279653	chr17:59862140-59862141	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs111379355	chr17:59862147-59862148	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs79429591	chr17:59862186-59862187	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs71355194	chr17:59862208-59862209	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs6504070	chr17:59862209-59862210	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs568602415	chr17:59862273-59862274	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377704842	chr17:59862274-59862275	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs188874692	chr17:59862316-59862317	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs192923808	chr17:59862324-59862325	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs552815970	chr17:59862337-59862338	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs535258804	chr17:59862344-59862345	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538806694	chr17:59862351-59862352	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs113619683	chr17:59862353-59862354	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs367947784	chr17:59862387-59862388	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558819569	chr17:59862459-59862460	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575686917	chr17:59862505-59862506	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs556769992	chr17:59862542-59862543	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372017436	chr17:59862558-59862559	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs183540264	chr17:59862622-59862623	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373395139	chr17:59862641-59862642	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532172913	chr17:59862653-59862654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140929663	chr17:59862657-59862658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559607484	chr17:59862857-59862858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187253367	chr17:59862903-59862904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78603262	chr17:59863005-59863006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376080115	chr17:59863185-59863186	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540941201	chr17:59863195-59863196	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Williams-Beuren syndrome	16971481	CNVD
Breast cancer	21958427	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr17:59850000-59865000	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr17:59850000-59866000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr17:59850000-59869400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr17:59850000-59870800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr17:59850000-59871000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr17:59850000-59872200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr17:59850000-59873200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr17:59850000-59887000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr17:59850000-59887000	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr17:59851200-59902600	Weak transcription	Fetal Stomach	stomach
29	chr17:59852600-59869400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr17:59852600-59898000	Weak transcription	Fetal Intestine Small	intestine
31	chr17:59853800-59869400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr17:59854000-59866000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr17:59854000-59868600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr17:59854000-59873000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr17:59856400-59872800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr17:59856800-59868000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr17:59857000-59888600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:59857400-59866000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr17:59857800-59868200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr17:59858000-59872800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr17:59858200-59866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr17:59858200-59869400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr17:59860000-59863600	Strong transcription	Dnd41	blood
44	chr17:59860200-59883200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr17:59860800-59868000	Weak transcription	A549	lung
46	chr17:59861200-59862600	Enhancers	Primary B cells from peripheral blood	blood
47	chr17:59861400-59862000	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr17:59861600-59862000	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr17:59861600-59862600	Flanking Active TSS	GM12878-XiMat	blood
50	chr17:59862000-59864000	Enhancers	Primary B cells from cord blood	blood

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