Variant report

Variant	esv2758981
Chromosome Location	chr1:185293197-185345771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:122)
Chromatin interactive
region (count:42)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:185318871-185319672	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:185311896-185312614	HepG2	liver:	n/a	n/a
3	ATF1	chr1:185344763-185344993	K562	blood:	n/a	n/a
4	ATF1	chr1:185294576-185294896	K562	blood:	n/a	n/a
5	ATF2	chr1:185333676-185333986	GM12878	blood:	n/a	n/a
6	ATF2	chr1:185307972-185308774	GM12878	blood:	n/a	n/a
7	ATF2	chr1:185307633-185308895	GM12878	blood:	n/a	n/a
8	BACH1	chr1:185336718-185336818	K562	blood:	n/a	n/a
9	BATF	chr1:185308259-185308738	GM12878	blood:	n/a	n/a
10	BATF	chr1:185308365-185308744	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:185333625-185333930	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:185308229-185308773	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:185307806-185308207	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:185308301-185308748	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:185307867-185308176	GM12878	blood:	n/a	n/a
16	BCL3	chr1:185308318-185308785	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:185308276-185308731	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:185307729-185308772	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:185333728-185334001	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:185307622-185308933	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:185315029-185315334	K562	blood:	n/a	n/a
22	BHLHE40	chr1:185319218-185319523	HepG2	liver:	n/a	n/a
23	CBX3	chr1:185294518-185294950	K562	blood:	n/a	n/a
24	CBX3	chr1:185297390-185297847	K562	blood:	n/a	n/a
25	CEBPB	chr1:185293198-185293554	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:185308355-185308735	GM12878	blood:	n/a	n/a
27	CEBPB	chr1:185335767-185335979	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:185307780-185308866	GM12878	blood:	n/a	n/a
29	CEBPB	chr1:185325724-185325950	HepG2	liver:	n/a	chr1:185325861-185325872
30	CEBPB	chr1:185312061-185312311	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:185306387-185306590	K562	blood:	n/a	n/a
32	CEBPB	chr1:185308386-185308465	K562	blood:	n/a	n/a
33	CEBPB	chr1:185306311-185306641	IMR90	lung:	n/a	n/a
34	CHD2	chr1:185307752-185308834	GM12878	blood:	n/a	n/a
35	CTCF	chr1:185328115-185328187	GM19239	blood:	n/a	n/a
36	CTCF	chr1:185325689-185325722	GM13976	blood:	n/a	n/a
37	CTCF	chr1:185312000-185312150	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:185308449-185308801	GM12878	blood:	n/a	n/a
39	CTCF	chr1:185305869-185305892	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:185326020-185326170	Hela-S3	cervix:	n/a	n/a
41	CUX1	chr1:185320612-185320690	K562	blood:	n/a	n/a
42	CUX1	chr1:185307272-185307420	GM12878	blood:	n/a	n/a
43	CUX1	chr1:185307900-185308976	GM12878	blood:	n/a	n/a
44	E2F4	chr1:185335726-185335973	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr1:185308594-185308715	GM12878	blood:	n/a	n/a
46	E2F4	chr1:185342332-185342532	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:185343317-185343623	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:185344673-185344946	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr1:185307763-185308220	GM12878	blood:	n/a	chr1:185307931-185307942
50	EBF1	chr1:185307721-185308780	GM12878	blood:	n/a	chr1:185307931-185307942

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:185302534-185302584	NB4	blood:	n/a
2	chr1:185302534-185302584	HIPEpiC	eye:	n/a
3	chr1:185302534-185302584	IMR90	lung:	fetal
4	chr1:185303447-185303497	Jurkat	blood:	n/a
5	chr1:185303447-185303497	GM06990	blood:	n/a
6	chr1:185302534-185302584	ovcar-3	ovarian:	n/a
7	chr1:185302534-185302584	HMEC	breast:	n/a
8	chr1:185302534-185302584	GM12878	blood:	n/a
9	chr1:185303447-185303497	GM12891	blood:	n/a
10	chr1:185302534-185302584	HCT-116	colon:	n/a
11	chr1:185303447-185303497	Hepatocyte	liver:	n/a
12	chr1:185303447-185303497	HRCEpiC	kidney:	n/a
13	chr1:185303447-185303497	HCM	heart:	n/a
14	chr1:185302534-185302584	PANC-1	pancreas:	n/a
15	chr1:185302534-185302584	Hepatocyte	liver:	n/a
16	chr1:185303447-185303497	AoSMC	blood vessel:	n/a
17	chr1:185303447-185303497	SAEC	small airway:	n/a
18	chr1:185302534-185302584	PrEC	prostate:	n/a
19	chr1:185302534-185302584	ProgFib	skin:	n/a
20	chr1:185302534-185302584	NT2-D1	testis:	n/a
21	chr1:185303447-185303497	PrEC	prostate:	n/a
22	chr1:185303447-185303497	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:185302534-185302584	BJ	skin:	n/a
24	chr1:185303447-185303497	CMK	blood:	n/a
25	chr1:185303447-185303497	T-47D	breast:	n/a
26	chr1:185302534-185302584	HepG2	liver:	n/a
27	chr1:185303447-185303497	SK-N-SH	brain:	n/a
28	chr1:185303447-185303497	NT2-D1	testis:	n/a
29	chr1:185302534-185302584	AoSMC	blood vessel:	n/a
30	chr1:185303447-185303497	H1-hESC	embryonic stem cell:	embryo
31	chr1:185303447-185303497	Caco-2	colon:	n/a
32	chr1:185302534-185302584	LNCaP	prostate:	n/a
33	chr1:185303447-185303497	HCF	heart:	n/a
34	chr1:185302534-185302584	HAEpiC	amniotic membrane:	n/a
35	chr1:185303447-185303497	ProgFib	skin:	n/a
36	chr1:185302534-185302584	PFSK-1	brain:	n/a
37	chr1:185302534-185302584	HEK293	kidney:	embryo
38	chr1:185302534-185302584	HNPCEpiC	eye:	n/a
39	chr1:185303447-185303497	K562	blood:	n/a
40	chr1:185302534-185302584	GM06990	blood:	n/a
41	chr1:185302534-185302584	Caco-2	colon:	n/a
42	chr1:185303447-185303497	RPTEC	kidney:	n/a
43	chr1:185303447-185303497	ECC-1	luminal epithelium:	n/a
44	chr1:185302534-185302584	U87	brain:	n/a
45	chr1:185303447-185303497	SK-N-MC	brain:	n/a
46	chr1:185302534-185302584	HRE	kidney:	n/a
47	chr1:185303447-185303497	IMR90	lung:	fetal
48	chr1:185303447-185303497	NHBE	bronchial:	n/a
49	chr1:185302534-185302584	HEEpiC	esophagus:	n/a
50	chr1:185303447-185303497	HIPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:185294862..185296528-chr1:185308605..185311231,2	K562	blood:
2	chr1:185310478..185312193-chr1:185353516..185355046,2	MCF-7	breast:
3	chr1:185287917..185289698-chr1:185307396..185309858,2	K562	blood:
4	chr1:185302116..185303634-chr1:185304361..185306338,2	K562	blood:
5	chr1:185291465..185294333-chr1:185294415..185297743,3	K562	blood:
6	chr1:185297615..185300332-chr1:185301504..185303093,2	K562	blood:
7	chr1:185284143..185286324-chr1:185309685..185311260,2	K562	blood:
8	chr1:185308094..185310941-chr1:185314344..185316672,2	MCF-7	breast:
9	chr1:185286206..185288234-chr1:185310085..185311597,2	MCF-7	breast:
10	chr1:185319451..185321457-chr1:185323668..185326543,2	K562	blood:
11	chr1:185336579..185338652-chr1:185344761..185346664,3	K562	blood:
12	chr1:185284226..185288398-chr1:185298111..185303024,8	MCF-7	breast:
13	chr1:185336356..185337918-chr1:185339608..185342446,2	K562	blood:
14	chr1:185334258..185337021-chr1:185337463..185339197,2	K562	blood:
15	chr1:185309831..185311372-chr1:185318119..185320699,2	MCF-7	breast:
16	chr1:185273553..185276208-chr1:185318687..185321590,2	K562	blood:
17	chr1:185309831..185311372-chr1:185318119..185320699,2	MCF-7	breast:
18	chr1:185323027..185325964-chr1:185336251..185338084,2	K562	blood:
19	chr1:185323027..185325964-chr1:185336251..185338084,2	K562	blood:
20	chr1:185336579..185338652-chr1:185344761..185346664,3	K562	blood:
21	chr1:185285397..185289190-chr1:185299692..185306897,6	K562	blood:
22	chr1:185285450..185286990-chr1:185317483..185319054,2	MCF-7	breast:
23	chr1:185285756..185288147-chr1:185320973..185323025,2	MCF-7	breast:
24	chr1:185294862..185296528-chr1:185308605..185311231,2	K562	blood:
25	chr1:185308094..185310941-chr1:185314344..185316672,2	MCF-7	breast:
26	chr1:185291465..185294333-chr1:185294415..185297743,3	K562	blood:
27	chr1:185301601..185304149-chr1:185305985..185308630,2	MCF-7	breast:
28	chr1:185283733..185285493-chr1:185317174..185319421,2	K562	blood:
29	chr1:185284682..185286513-chr1:185307599..185309324,2	MCF-7	breast:
30	chr1:185314611..185317426-chr1:185402950..185405222,2	K562	blood:
31	chr1:185286121..185288259-chr1:185293375..185296887,4	MCF-7	breast:
32	chr1:185299843..185302497-chr1:185306799..185309677,2	K562	blood:
33	chr1:185284808..185287790-chr1:185326640..185329248,2	MCF-7	breast:
34	chr1:185285776..185288513-chr1:185317711..185319706,2	K562	blood:
35	chr1:185319451..185321457-chr1:185323668..185326543,2	K562	blood:
36	chr1:185336756..185338388-chr1:185373495..185375950,2	MCF-7	breast:
37	chr1:185334258..185337021-chr1:185337463..185339197,2	K562	blood:
38	chr1:185285222..185287975-chr1:185313401..185316015,2	K562	blood:
39	chr1:185339789..185341634-chr1:185357350..185360310,2	K562	blood:
40	chr1:185284186..185287473-chr1:185329755..185332041,3	K562	blood:
41	chr1:185286292..185288369-chr1:185301648..185303325,2	MCF-7	breast:
42	chr1:185336356..185337918-chr1:185339608..185342446,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IVNS1ABP-1	chr1:185303398-185303519	ENSG00000261024.1
2	lnc-IVNS1ABP-1	chr1:185304093-185304171	ENSG00000261024.1
3	lnc-IVNS1ABP-1	chr1:185303398-185303519	NONHSAT008418
4	lnc-IVNS1ABP-1	chr1:185304093-185304171	NONHSAT008418
5	lnc-IVNS1ABP-1	chr1:185300389-185300513	ENSG00000261024.1
6	lnc-SWT1-1	chr1:185342750-185342860	XLOC_000494
7	lnc-SWT1-1	chr1:185343529-185344123	XLOC_000494
8	lnc-SWT1-5	chr1:185328597-185328701	NONHSAT008420
9	lnc-IVNS1ABP-1	chr1:185303398-185303519	ENSG00000261024.1
10	lnc-IVNS1ABP-1	chr1:185302152-185302434	ENSG00000261024.1
11	lnc-IVNS1ABP-1	chr1:185302152-185302434	ENSG00000261024.1
12	lnc-SWT1-1	chr1:185339834-185339921	XLOC_000494
13	lnc-IVNS1ABP-1	chr1:185304093-185304139	ENSG00000261024.1
14	lnc-IVNS1ABP-1	chr1:185302152-185302200	ENSG00000261024.2
15	lnc-IVNS1ABP-1	chr1:185302152-185302200	ENSG00000261024.1
16	lnc-IVNS1ABP-1	chr1:185302152-185302434	NONHSAT008418

No data

Variant related genes	Relation type
ENSG00000261024	TF binding region
ENSG00000261024	CpG island
ENSG00000261024	chromatin interactions
ENSG00000270920	chromatin interactions
ENSG00000116679	chromatin interactions
ENSG00000252407	chromatin interactions
ENSG00000273004	chromatin interactions
EIF2C1	miRNA target sites
ROCK1	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 1801 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17641003	chr1:185293197-185293198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554353843	chr1:185293275-185293276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189775820	chr1:185293336-185293337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs16823907	chr1:185293352-185293353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552925057	chr1:185293428-185293429	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577994187	chr1:185293514-185293515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369648580	chr1:185293515-185293516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183148526	chr1:185293562-185293563	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558196514	chr1:185293591-185293592	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs151182268	chr1:185293650-185293651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575851017	chr1:185293676-185293677	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140203164	chr1:185293761-185293762	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561481583	chr1:185293768-185293769	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572954154	chr1:185293809-185293810	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150313640	chr1:185293846-185293847	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564718131	chr1:185293853-185293854	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540592883	chr1:185293916-185293917	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74771051	chr1:185293927-185293928	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs115119561	chr1:185293965-185293966	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186385586	chr1:185293976-185293977	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529963024	chr1:185294033-185294034	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs547950989	chr1:185294083-185294084	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs35384668	chr1:185294143-185294144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113442213	chr1:185294205-185294206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529612077	chr1:185294206-185294207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370760121	chr1:185294244-185294245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs191523088	chr1:185294259-185294260	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs534774932	chr1:185294269-185294270	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544821514	chr1:185294282-185294283	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs137892282	chr1:185294309-185294310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs562927552	chr1:185294319-185294320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557085946	chr1:185294322-185294323	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140771977	chr1:185294352-185294353	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535255178	chr1:185294412-185294413	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs183818140	chr1:185294427-185294428	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs536975001	chr1:185294432-185294433	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555187536	chr1:185294479-185294480	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs372981202	chr1:185294489-185294490	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573516907	chr1:185294502-185294503	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs76615895	chr1:185294546-185294547	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564949441	chr1:185294551-185294552	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370390643	chr1:185294580-185294581	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs544162797	chr1:185294597-185294598	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552005808	chr1:185294657-185294658	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs61824149	chr1:185294658-185294659	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374581759	chr1:185294661-185294662	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs397982259	chr1:185294675-185294676	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562369084	chr1:185294737-185294738	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7555243	chr1:185294753-185294754	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548111743	chr1:185294780-185294781	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	19197363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185287600-185298200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:185287800-185298200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:185288400-185294400	Weak transcription	Fetal Heart	heart
4	chr1:185291600-185294400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:185291800-185295000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr1:185292800-185293800	Enhancers	HepG2	liver
7	chr1:185293800-185295600	Weak transcription	HepG2	liver
8	chr1:185294400-185294600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:185294400-185294800	Enhancers	Fetal Heart	heart
10	chr1:185294400-185295000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:185294400-185295000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:185294400-185295200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:185294600-185295000	Enhancers	K562	blood
14	chr1:185295000-185295400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr1:185295000-185302200	Weak transcription	K562	blood
16	chr1:185295400-185296800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr1:185295600-185296800	Enhancers	HepG2	liver
18	chr1:185296600-185297000	Enhancers	Primary B cells from cord blood	blood
19	chr1:185296800-185297800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr1:185297200-185298400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr1:185297800-185298200	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr1:185298200-185298400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr1:185298200-185298600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr1:185298200-185298600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr1:185298200-185298600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:185298200-185298600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:185298200-185298600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:185298200-185298800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr1:185298200-185298800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:185298400-185299800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:185298400-185305200	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr1:185299800-185303000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr1:185301200-185302400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:185301400-185304200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:185302200-185302400	Enhancers	K562	blood
36	chr1:185302400-185303200	Weak transcription	K562	blood
37	chr1:185302400-185307400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:185303000-185303400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr1:185303200-185303400	Enhancers	Duodenum Mucosa	Duodenum
40	chr1:185303200-185303600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:185303200-185303600	Flanking Active TSS	K562	blood
42	chr1:185303400-185305600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr1:185303400-185307800	Weak transcription	Duodenum Mucosa	Duodenum
44	chr1:185303600-185304400	Enhancers	K562	blood
45	chr1:185304200-185310600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:185305000-185305800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr1:185305200-185310200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr1:185305600-185307800	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr1:185305800-185306200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:185305800-185307000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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