Variant report

Variant	nsv1008620
Chromosome Location	chr1:175430808-175760752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2556)
CpG islands
(count:1587)
Chromatin interactive
region (count:89)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2556 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:175450223-175450578	K562	blood:	n/a	n/a
2	ARID3A	chr1:175712067-175712270	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:175677993-175678220	K562	blood:	n/a	n/a
4	ATF1	chr1:175560566-175560845	K562	blood:	n/a	n/a
5	ATF1	chr1:175530746-175530820	K562	blood:	n/a	n/a
6	ATF1	chr1:175702938-175703247	K562	blood:	n/a	n/a
7	ATF1	chr1:175567614-175567771	K562	blood:	n/a	n/a
8	ATF1	chr1:175440318-175440593	K562	blood:	n/a	n/a
9	ATF1	chr1:175694946-175695151	K562	blood:	n/a	n/a
10	ATF2	chr1:175567111-175567613	GM12878	blood:	n/a	n/a
11	ATF2	chr1:175569870-175570603	GM12878	blood:	n/a	n/a
12	ATF2	chr1:175546050-175546351	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:175567113-175567630	GM12878	blood:	n/a	n/a
14	BACH1	chr1:175712123-175712541	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:175659425-175659778	GM12878	blood:	n/a	chr1:175659590-175659601
16	BATF	chr1:175440148-175440454	GM12878	blood:	n/a	chr1:175440280-175440291
17	BATF	chr1:175570238-175570573	GM12878	blood:	n/a	n/a
18	BATF	chr1:175570278-175570496	GM12878	blood:	n/a	n/a
19	BATF	chr1:175659507-175659689	GM12878	blood:	n/a	chr1:175659590-175659601
20	BATF	chr1:175567105-175567461	GM12878	blood:	n/a	n/a
21	BATF	chr1:175601806-175602145	GM12878	blood:	n/a	chr1:175601977-175601988
22	BATF	chr1:175567143-175567484	GM12878	blood:	n/a	n/a
23	BATF	chr1:175601811-175602154	GM12878	blood:	n/a	chr1:175601977-175601988
24	BCL11A	chr1:175545989-175546282	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCLAF1	chr1:175569764-175570602	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:175568409-175568632	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:175570039-175570625	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:175702931-175703343	K562	blood:	n/a	n/a
29	BHLHE40	chr1:175560446-175560858	K562	blood:	n/a	n/a
30	BRCA1	chr1:175440161-175440685	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr1:175560458-175560815	K562	blood:	n/a	n/a
32	CBX3	chr1:175702890-175703263	K562	blood:	n/a	n/a
33	CCNT2	chr1:175560540-175560861	K562	blood:	n/a	n/a
34	CCNT2	chr1:175702945-175703389	K562	blood:	n/a	n/a
35	CCNT2	chr1:175726668-175726976	K562	blood:	n/a	n/a
36	CEBPB	chr1:175450185-175450598	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:175716502-175716663	HepG2	liver:	n/a	chr1:175716563-175716574
38	CEBPB	chr1:175467218-175467472	A549	lung:	n/a	n/a
39	CEBPB	chr1:175440085-175440861	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:175501194-175501532	HepG2	liver:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
41	CEBPB	chr1:175570730-175570860	K562	blood:	n/a	chr1:175570824-175570835
42	CEBPB	chr1:175733888-175734188	A549	lung:	n/a	n/a
43	CEBPB	chr1:175467135-175467496	MCF-7	breast:	n/a	n/a
44	CEBPB	chr1:175757114-175757387	Hela-S3	cervix:	n/a	chr1:175757236-175757247
45	CEBPB	chr1:175505509-175505801	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:175456170-175456208	IMR90	lung:	n/a	chr1:175456177-175456188
47	CEBPB	chr1:175456167-175456194	HepG2	liver:	n/a	chr1:175456177-175456188
48	CEBPB	chr1:175569846-175570607	GM12878	blood:	n/a	n/a
49	CEBPB	chr1:175757097-175757411	HepG2	liver:	n/a	chr1:175757236-175757247
50	CEBPB	chr1:175440252-175440453	K562	blood:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175713219-175713269	HepG2	liver:	n/a
2	chr1:175713219-175713269	HepG2	liver:	n/a
3	chr1:175474533-175474583	GM06990	blood:	n/a
4	chr1:175683971-175684021	SK-N-SH	brain:	n/a
5	chr1:175568710-175568760	HUVEC	blood vessel:	n/a
6	chr1:175549030-175549080	MCF-7	breast:	n/a
7	chr1:175571970-175572020	K562	blood:	n/a
8	chr1:175533566-175533616	NT2-D1	testis:	n/a
9	chr1:175712871-175712921	GM06990	blood:	n/a
10	chr1:175490611-175490661	HUVEC	blood vessel:	n/a
11	chr1:175568710-175568760	PrEC	prostate:	n/a
12	chr1:175525106-175525156	HEK293	kidney:	embryo
13	chr1:175568216-175568266	PANC-1	pancreas:	n/a
14	chr1:175712382-175712432	NHDF-neo	bronchial:	n/a
15	chr1:175568710-175568760	Caco-2	colon:	n/a
16	chr1:175568216-175568266	AoSMC	blood vessel:	n/a
17	chr1:175525244-175525294	AG04449	skin:	fetal
18	chr1:175565371-175565421	Hela-S3	cervix:	n/a
19	chr1:175474533-175474583	GM12892	blood:	n/a
20	chr1:175511259-175511309	ProgFib	skin:	n/a
21	chr1:175525244-175525294	H1-hESC	embryonic stem cell:	embryo
22	chr1:175525244-175525294	ECC-1	luminal epithelium:	n/a
23	chr1:175571970-175572020	NHDF-neo	bronchial:	n/a
24	chr1:175712382-175712432	HCT-116	colon:	n/a
25	chr1:175568559-175568609	MCF-7	breast:	n/a
26	chr1:175712871-175712921	RPTEC	kidney:	n/a
27	chr1:175712382-175712432	AG09309	skin:	n/a
28	chr1:175712871-175712921	HIPEpiC	eye:	n/a
29	chr1:175671657-175671707	NT2-D1	testis:	n/a
30	chr1:175712871-175712921	LNCaP	prostate:	n/a
31	chr1:175490611-175490661	AG09309	skin:	n/a
32	chr1:175490611-175490661	SKMC	muscle:	n/a
33	chr1:175570022-175570072	HMEC	breast:	n/a
34	chr1:175549030-175549080	GM12892	blood:	n/a
35	chr1:175525244-175525294	HL-60	blood:	n/a
36	chr1:175525106-175525156	GM12891	blood:	n/a
37	chr1:175474471-175474521	ECC-1	luminal epithelium:	n/a
38	chr1:175474533-175474583	AG10803	skin:	n/a
39	chr1:175683971-175684021	NB4	blood:	n/a
40	chr1:175713219-175713269	HIPEpiC	eye:	n/a
41	chr1:175712382-175712432	ovcar-3	ovarian:	n/a
42	chr1:175533566-175533616	SK-N-SH	brain:	n/a
43	chr1:175490611-175490661	GM12891	blood:	n/a
44	chr1:175571970-175572020	GM19239	blood:	n/a
45	chr1:175525986-175526036	HAEpiC	amniotic membrane:	n/a
46	chr1:175713219-175713269	NB4	blood:	n/a
47	chr1:175653121-175653171	Hepatocyte	liver:	n/a
48	chr1:175525986-175526036	GM12892	blood:	n/a
49	chr1:175474437-175474487	AG09309	skin:	n/a
50	chr1:175549030-175549080	HL-60	blood:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:175623612..175625312-chr1:175626921..175628780,2	K562	blood:
2	chr1:175439998..175440746-chr20:52740037..52740572,2	MCF-7	breast:
3	chr1:175450058..175450683-chr1:175793398..175794082,2	MCF-7	breast:
4	chr1:175515953..175518588-chr1:175527952..175530742,2	MCF-7	breast:
5	chr1:175759186..175762304-chr1:175765098..175768230,3	K562	blood:
6	chr1:175592287..175594796-chr1:175597956..175600571,2	K562	blood:
7	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
8	chr1:175742229..175743888-chr1:175748692..175751512,2	K562	blood:
9	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
10	chr1:175630324..175632456-chr1:175632718..175635511,2	MCF-7	breast:
11	chr1:175450451..175451287-chr1:175647331..175647999,2	MCF-7	breast:
12	chr1:175345040..175345574-chr1:175450603..175451457,2	MCF-7	breast:
13	chr1:175521179..175523999-chr1:175667216..175668901,2	K562	blood:
14	chr1:175623612..175626086-chr1:175627280..175629192,2	K562	blood:
15	chr1:175437981..175439964-chr1:175464237..175467168,2	K562	blood:
16	chr1:175548057..175550584-chr1:175551957..175553666,2	K562	blood:
17	chr1:175342681..175343454-chr1:175450088..175451392,6	MCF-7	breast:
18	chr1:175619703..175621428-chr1:175631712..175633665,2	K562	blood:
19	chr1:175479902..175482193-chr1:175482223..175485139,2	K562	blood:
20	chr1:175722601..175724520-chr1:175811862..175813377,2	K562	blood:
21	chr1:175695673..175698499-chr1:175710964..175712851,2	MCF-7	breast:
22	chr1:175619488..175620053-chr2:29991948..29992448,2	NB4	blood:
23	chr1:175714332..175717213-chr1:175717860..175720283,2	K562	blood:
24	chr1:175518429..175521323-chr1:175522798..175524454,2	K562	blood:
25	chr1:175677536..175679863-chr1:175684649..175686890,2	K562	blood:
26	chr1:175512204..175514383-chr1:175514961..175517684,2	K562	blood:
27	chr1:175555708..175557465-chr1:175560630..175563099,2	MCF-7	breast:
28	chr1:175593287..175595749-chr1:175606302..175608362,2	K562	blood:
29	chr1:175514239..175516178-chr1:175518743..175521414,2	MCF-7	breast:
30	chr1:175450010..175450941-chr1:175813865..175814693,2	MCF-7	breast:
31	chr1:175703408..175708282-chr1:175710356..175712842,4	K562	blood:
32	chr1:175596398..175599153-chr1:175609947..175612782,2	K562	blood:
33	chr1:175712269..175713164-chr1:175726366..175727326,3	MCF-7	breast:
34	chr1:175528817..175531396-chr1:175532065..175533684,2	MCF-7	breast:
35	chr1:175685957..175688244-chr1:175716194..175717776,2	MCF-7	breast:
36	chr1:175636404..175638015-chr1:175641711..175644234,2	MCF-7	breast:
37	chr1:175521179..175523999-chr1:175667216..175668901,2	K562	blood:
38	chr1:175479902..175482193-chr1:175482223..175485139,2	K562	blood:
39	chr1:175685957..175688244-chr1:175716194..175717776,2	MCF-7	breast:
40	chr1:175709353..175712316-chr1:175718100..175722074,3	MCF-7	breast:
41	chr1:175514377..175516679-chr1:175519088..175521360,2	K562	blood:
42	chr1:175713728..175714591-chr1:175856822..175857663,2	MCF-7	breast:
43	chr1:175586743..175589262-chr1:175590428..175592846,2	MCF-7	breast:
44	chr1:175450085..175451047-chr1:175712257..175712999,4	MCF-7	breast:
45	chr1:175732717..175735663-chr1:175737285..175738902,2	MCF-7	breast:
46	chr1:175437981..175439964-chr1:175464237..175467168,2	K562	blood:
47	chr1:175623612..175626086-chr1:175627280..175629192,2	K562	blood:
48	chr1:175120874..175121520-chr1:175449995..175450848,2	MCF-7	breast:
49	chr1:175450451..175451287-chr1:175647331..175647999,2	MCF-7	breast:
50	chr1:175638168..175641161-chr1:175648590..175650196,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNR-3	chr1:175712362-175712766	NONHSAT007755
2	lnc-TNN-3	chr1:175535772-175537384	NONHSAT007758
3	lnc-TNR-3	chr1:175712773-175712906	NONHSAT007755
4	lnc-TNN-4	chr1:175592606-175592824	NONHSAT007759
5	lnc-TNR-3	chr1:175497405-175497505	NONHSAT007755
6	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007757
7	lnc-RFWD2-2	chr1:175525727-175525954	ENSG00000235628.1
8	lnc-TNN-4	chr1:175587345-175587409	NONHSAT007759
9	lnc-RFWD2-2	chr1:175507911-175508312	ENSG00000235628.1
10	lnc-TNN-3	chr1:175531373-175533005	NONHSAT007757
11	lnc-TNN-4	chr1:175601928-175602031	NONHSAT007759
12	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007758
13	lnc-TNR-5	chr1:175629438-175629547	NONHSAT007760
14	lnc-TNN-4	chr1:175599198-175599300	NONHSAT007759

No data

Variant related genes	Relation type
TNR-IT1	TF binding region
TNR	TF binding region
TNR-IT1	CpG island
TNR	CpG island
ENSG00000116147	chromatin interactions
ENSG00000146147	chromatin interactions

Extended variants
information (count: 12437 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:12437 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12119698	chr1:175430808-175430809	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7547439	chr1:175430855-175430856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
3	rs549254465	chr1:175430907-175430908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199917706	chr1:175430918-175430919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10673738	chr1:175430919-175430920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56902551	chr1:175430920-175430921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs58335312	chr1:175430922-175430923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531631051	chr1:175430982-175430983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531680028	chr1:175431029-175431030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs859374	chr1:175431064-175431065	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs571250424	chr1:175431155-175431156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76345756	chr1:175431180-175431181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs16848469	chr1:175431215-175431216	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs373126341	chr1:175431229-175431230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189380481	chr1:175431233-175431234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368343762	chr1:175431300-175431301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536450332	chr1:175431340-175431341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76985481	chr1:175431430-175431431	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs148087110	chr1:175431448-175431449	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs538980778	chr1:175431461-175431462	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs76880228	chr1:175431466-175431467	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs541130136	chr1:175431482-175431483	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs555052396	chr1:175431504-175431505	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs575036252	chr1:175431508-175431509	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs192378070	chr1:175431509-175431510	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs562710064	chr1:175431511-175431512	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs376303619	chr1:175431519-175431520	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs184374457	chr1:175431520-175431521	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs545310863	chr1:175431533-175431534	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs564691801	chr1:175431537-175431538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs190154453	chr1:175431573-175431574	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs181865723	chr1:175431607-175431608	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs567018300	chr1:175431612-175431613	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs554305088	chr1:175431613-175431614	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs529777824	chr1:175431646-175431647	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs549946000	chr1:175431707-175431708	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs569942854	chr1:175431712-175431713	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs538915028	chr1:175431737-175431738	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs61808379	chr1:175431768-175431769	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186478987	chr1:175431809-175431810	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535016603	chr1:175431821-175431822	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189795610	chr1:175431822-175431823	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574973250	chr1:175431869-175431870	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75931710	chr1:175431945-175431946	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs180937483	chr1:175432012-175432013	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs61808380	chr1:175432039-175432040	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73044438	chr1:175432070-175432071	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs76840829	chr1:175432100-175432101	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576276497	chr1:175432108-175432109	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527634918	chr1:175432109-175432110	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
Retinoblastoma	19183342	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
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	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
Trisomy 5 syndrome	21098271	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
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1677 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175428200-175432200	Enhancers	Fetal Brain Male	brain
2	chr1:175429400-175431200	Weak transcription	Fetal Brain Female	brain
3	chr1:175429600-175432600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:175429800-175435800	Weak transcription	Pancreas	Pancrea
5	chr1:175431000-175432200	Enhancers	Brain Germinal Matrix	brain
6	chr1:175431200-175432000	Enhancers	Fetal Brain Female	brain
7	chr1:175431400-175432800	Bivalent Enhancer	Fetal Lung	lung
8	chr1:175431800-175434200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:175431800-175434200	Enhancers	Fetal Intestine Small	intestine
10	chr1:175432000-175432200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:175432400-175434400	Enhancers	Fetal Intestine Large	intestine
12	chr1:175432600-175433400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:175434400-175439200	Weak transcription	Fetal Intestine Large	intestine
14	chr1:175435800-175436000	Enhancers	Pancreas	Pancrea
15	chr1:175436000-175436400	Weak transcription	Pancreas	Pancrea
16	chr1:175436400-175436800	Enhancers	Pancreas	Pancrea
17	chr1:175438800-175440000	Enhancers	NHEK	skin
18	chr1:175438800-175442000	Enhancers	Hela-S3	cervix
19	chr1:175439000-175439200	Bivalent Enhancer	HMEC	breast
20	chr1:175439000-175440800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:175439200-175440000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:175439200-175440600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:175439200-175440800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:175439200-175440800	Enhancers	Fetal Intestine Small	intestine
25	chr1:175439200-175440800	Enhancers	HMEC	breast
26	chr1:175439200-175441400	Enhancers	Fetal Intestine Large	intestine
27	chr1:175439400-175440400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:175439400-175441000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:175439800-175440200	Enhancers	Brain Angular Gyrus	brain
30	chr1:175439800-175440600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:175440000-175440200	Flanking Active TSS	NHEK	skin
32	chr1:175440000-175440400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr1:175440200-175440400	Enhancers	NHEK	skin
34	chr1:175440400-175440600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:175440400-175440600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:175440400-175440600	Flanking Active TSS	NHEK	skin
37	chr1:175440600-175441400	Enhancers	NHEK	skin
38	chr1:175440800-175447000	Weak transcription	Fetal Intestine Small	intestine
39	chr1:175441000-175443800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:175441400-175446400	Weak transcription	Fetal Intestine Large	intestine
41	chr1:175442000-175446400	Weak transcription	Hela-S3	cervix
42	chr1:175443800-175444000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:175444000-175445200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:175445200-175445800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:175445400-175445800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:175445800-175446800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr1:175446000-175446800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:175446400-175447200	Enhancers	Brain Germinal Matrix	brain
49	chr1:175446400-175448400	Enhancers	Hela-S3	cervix
50	chr1:175446400-175451000	Enhancers	Fetal Intestine Large	intestine

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