Variant report

Variant	nsv536037
Chromosome Location	chr2:172745597-172780616
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1078)
CpG islands
(count:1406)
Chromatin interactive
region (count:69)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:172778627-172779460	HepG2	liver:	n/a	chr2:172779022-172779037
2	ARID3A	chr2:172778699-172779333	K562	blood:	n/a	chr2:172779022-172779037
3	ARID3A	chr2:172750965-172751421	HepG2	liver:	n/a	n/a
4	ATF1	chr2:172778583-172779625	K562	blood:	n/a	n/a
5	ATF1	chr2:172766410-172766582	K562	blood:	n/a	n/a
6	ATF2	chr2:172778539-172779400	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:172778461-172779599	GM12878	blood:	n/a	n/a
8	ATF2	chr2:172750268-172750816	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:172778638-172779317	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:172778563-172779032	K562	blood:	n/a	chr2:172778894-172778905 chr2:172778893-172778904
11	BACH1	chr2:172779197-172779397	K562	blood:	n/a	n/a
12	BACH1	chr2:172766500-172766666	K562	blood:	n/a	n/a
13	BACH1	chr2:172751659-172751671	K562	blood:	n/a	n/a
14	BACH1	chr2:172750850-172751101	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr2:172767114-172767279	GM12878	blood:	n/a	n/a
16	BCL3	chr2:172750129-172750590	A549	lung:	n/a	chr2:172750443-172750452 chr2:172750574-172750587
17	BCLAF1	chr2:172778464-172779641	GM12878	blood:	n/a	chr2:172778944-172778953
18	BCLAF1	chr2:172750536-172751395	GM12878	blood:	n/a	chr2:172750574-172750587 chr2:172750918-172750931
19	BHLHE40	chr2:172778612-172779071	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:172750385-172751676	K562	blood:	n/a	chr2:172750859-172750875
21	BHLHE40	chr2:172778523-172779438	K562	blood:	n/a	n/a
22	BHLHE40	chr2:172750429-172751255	GM12878	blood:	n/a	chr2:172750859-172750875
23	BHLHE40	chr2:172750285-172751218	HepG2	liver:	n/a	chr2:172750859-172750875
24	BRCA1	chr2:172778613-172779135	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr2:172778886-172778992	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr2:172778955-172778968	GM12878	blood:	n/a	n/a
27	BRCA1	chr2:172778604-172778954	HepG2	liver:	n/a	n/a
28	CBX3	chr2:172754901-172755400	K562	blood:	n/a	n/a
29	CBX3	chr2:172750220-172751418	K562	blood:	n/a	n/a
30	CBX3	chr2:172755013-172755358	K562	blood:	n/a	n/a
31	CBX3	chr2:172778370-172780373	K562	blood:	n/a	n/a
32	CCNT2	chr2:172770550-172770675	K562	blood:	n/a	n/a
33	CCNT2	chr2:172778606-172779341	K562	blood:	n/a	n/a
34	CCNT2	chr2:172750542-172751128	K562	blood:	n/a	n/a
35	CEBPB	chr2:172779831-172780166	K562	blood:	n/a	n/a
36	CEBPB	chr2:172750132-172751232	Hela-S3	cervix:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
37	CEBPB	chr2:172750151-172750434	K562	blood:	n/a	n/a
38	CEBPB	chr2:172752399-172752543	A549	lung:	n/a	n/a
39	CEBPB	chr2:172750035-172751199	A549	lung:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
40	CEBPB	chr2:172776009-172776342	HepG2	liver:	n/a	chr2:172776172-172776183
41	CEBPB	chr2:172778743-172779227	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:172777955-172778156	K562	blood:	n/a	n/a
43	CEBPB	chr2:172750220-172750851	HepG2	liver:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
44	CEBPB	chr2:172750117-172750956	H1-hESC	embryonic stem cell:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
45	CEBPB	chr2:172750166-172750981	GM12878	blood:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
46	CEBPB	chr2:172750093-172750534	A549	lung:	n/a	n/a
47	CEBPB	chr2:172764866-172765050	K562	blood:	n/a	chr2:172764921-172764934 chr2:172764921-172764932
48	CEBPB	chr2:172777801-172778145	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:172750587-172750739	HepG2	liver:	n/a	chr2:172750674-172750685 chr2:172750673-172750686
50	CEBPB	chr2:172750103-172750863	ECC-1	luminal epithelium:	n/a	chr2:172750674-172750685 chr2:172750673-172750686

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:172747482-172747532	HepG2	liver:	n/a
2	chr2:172778750-172778800	HCF	heart:	n/a
3	chr2:172779015-172779065	AG04449	skin:	fetal
4	chr2:172747482-172747532	HepG2	liver:	n/a
5	chr2:172778750-172778800	HCF	heart:	n/a
6	chr2:172779015-172779065	AG04449	skin:	fetal
7	chr2:172778879-172778929	HEEpiC	esophagus:	n/a
8	chr2:172778343-172778393	MCF10A-Er-Src	breast:	n/a
9	chr2:172779015-172779065	RPTEC	kidney:	n/a
10	chr2:172776401-172776451	PANC-1	pancreas:	n/a
11	chr2:172778811-172778861	PFSK-1	brain:	n/a
12	chr2:172779515-172779565	Caco-2	colon:	n/a
13	chr2:172750783-172750833	HL-60	blood:	n/a
14	chr2:172750719-172750769	HMEC	breast:	n/a
15	chr2:172776401-172776451	LNCaP	prostate:	n/a
16	chr2:172779515-172779565	AG09309	skin:	n/a
17	chr2:172751074-172751124	ovcar-3	ovarian:	n/a
18	chr2:172778734-172778784	GM06990	blood:	n/a
19	chr2:172779515-172779565	NB4	blood:	n/a
20	chr2:172776401-172776451	Caco-2	colon:	n/a
21	chr2:172779015-172779065	CMK	blood:	n/a
22	chr2:172750661-172750711	GM12878	blood:	n/a
23	chr2:172778865-172778915	HRE	kidney:	n/a
24	chr2:172750994-172751044	HepG2	liver:	n/a
25	chr2:172779515-172779565	SKMC	muscle:	n/a
26	chr2:172778341-172778391	HepG2	liver:	n/a
27	chr2:172751016-172751066	SK-N-SH_RA	brain:	n/a
28	chr2:172751088-172751138	Hepatocyte	liver:	n/a
29	chr2:172778734-172778784	BJ	skin:	n/a
30	chr2:172778341-172778391	Jurkat	blood:	n/a
31	chr2:172778341-172778391	AG09309	skin:	n/a
32	chr2:172778879-172778929	BJ	skin:	n/a
33	chr2:172750996-172751046	PFSK-1	brain:	n/a
34	chr2:172779111-172779161	RPTEC	kidney:	n/a
35	chr2:172779015-172779065	HMEC	breast:	n/a
36	chr2:172747482-172747532	MCF10A-Er-Src	breast:	n/a
37	chr2:172747482-172747532	AG09309	skin:	n/a
38	chr2:172778343-172778393	SK-N-SH_RA	brain:	n/a
39	chr2:172751074-172751124	NB4	blood:	n/a
40	chr2:172779015-172779065	HL-60	blood:	n/a
41	chr2:172779515-172779565	AoSMC	blood vessel:	n/a
42	chr2:172751088-172751138	A549	lung:	n/a
43	chr2:172776401-172776451	ECC-1	luminal epithelium:	n/a
44	chr2:172778961-172779011	ProgFib	skin:	n/a
45	chr2:172779111-172779161	GM12878	blood:	n/a
46	chr2:172750996-172751046	SKMC	muscle:	n/a
47	chr2:172778734-172778784	NT2-D1	testis:	n/a
48	chr2:172778811-172778861	PANC-1	pancreas:	n/a
49	chr2:172778865-172778915	GM12891	blood:	n/a
50	chr2:172779282-172779332	HIPEpiC	eye:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:172758196..172762608-chr2:172762704..172765555,5	K562	blood:
2	chr2:172749328..172751742-chr2:172775594..172779310,3	MCF-7	breast:
3	chr2:172764440..172768356-chr2:172769175..172774540,8	K562	blood:
4	chr2:172772649..172775409-chr2:172776945..172778838,2	K562	blood:
5	chr2:172749345..172750892-chr2:172948772..172951061,2	MCF-7	breast:
6	chr2:172777448..172780686-chr2:172863264..172866650,5	K562	blood:
7	chr2:172777989..172784973-chr2:172962042..172968003,11	K562	blood:
8	chr2:172749212..172752099-chr2:172863500..172865923,3	MCF-7	breast:
9	chr2:172779206..172781039-chr2:172947710..172950652,2	K562	blood:
10	chr2:172749780..172752389-chr2:172759130..172760701,2	K562	blood:
11	chr2:172749065..172752809-chr2:172776821..172780584,7	K562	blood:
12	chr2:172776047..172778713-chr2:172948688..172950823,3	MCF-7	breast:
13	chr2:172749385..172752362-chr2:172779098..172783248,3	MCF-7	breast:
14	chr2:172769606..172772915-chr2:172967149..172970199,3	K562	blood:
15	chr2:172750934..172752603-chr2:172948877..172950816,2	MCF-7	breast:
16	chr2:172770788..172773001-chr2:172780545..172783443,2	K562	blood:
17	chr2:172772649..172775409-chr2:172776945..172778838,2	K562	blood:
18	chr2:172744007..172746435-chr2:172749737..172751670,2	MCF-7	breast:
19	chr2:172767380..172770009-chr2:172775350..172777979,2	MCF-7	breast:
20	chr2:172765258..172766911-chr2:172774816..172776433,2	K562	blood:
21	chr2:172744693..172746418-chr2:172748270..172750785,2	MCF-7	breast:
22	chr2:172772537..172775890-chr2:172777616..172781028,3	MCF-7	breast:
23	chr2:172720314..172722919-chr2:172744324..172746947,2	K562	blood:
24	chr17:40831691..40832344-chr2:172778820..172779467,2	Hela-S3	cervix:
25	chr2:172780580..172784087-chr2:172788193..172790516,4	K562	blood:
26	chr16:18995213..18995850-chr2:172750648..172751335,2	Hela-S3	cervix:
27	chr2:172771505..172775106-chr2:172777338..172780165,6	K562	blood:
28	chr2:172750125..172752515-chr2:172760872..172762456,2	MCF-7	breast:
29	chr2:172769627..172772363-chr2:172785996..172788506,2	K562	blood:
30	chr2:172750354..172753126-chr2:172762746..172766983,5	MCF-7	breast:
31	chr2:172543765..172545467-chr2:172749369..172751686,2	MCF-7	breast:
32	chr2:172763759..172768235-chr2:172769175..172774540,7	K562	blood:
33	chr2:172777448..172780536-chr2:172864307..172867165,5	K562	blood:
34	chr2:172764440..172768356-chr2:172769175..172774540,8	K562	blood:
35	chr2:172751399..172753053-chr2:172972072..172974852,2	MCF-7	breast:
36	chr2:172778049..172781927-chr2:172965294..172970550,9	K562	blood:
37	chr2:172770788..172773001-chr2:172780545..172783443,2	K562	blood:
38	chr2:172744912..172747525-chr2:172966003..172969811,3	K562	blood:
39	chr2:172763886..172766598-chr2:172776885..172778453,2	MCF-7	breast:
40	chr2:172776261..172781039-chr2:172946394..172953961,9	K562	blood:
41	chr2:172773483..172775547-chr2:172966200..172967761,2	K562	blood:
42	chr2:172763759..172768235-chr2:172769175..172774540,7	K562	blood:
43	chr2:172767380..172770009-chr2:172775350..172777979,2	MCF-7	breast:
44	chr2:172746433..172748218-chr2:172754634..172756631,2	K562	blood:
45	chr2:172777519..172781580-chr2:172819100..172823049,4	K562	blood:
46	chr2:172758196..172760986-chr2:172762704..172765677,2	K562	blood:
47	chr2:172749510..172752866-chr2:172752874..172756053,4	K562	blood:
48	chr2:172745241..172748938-chr2:172777169..172782251,7	K562	blood:
49	chr2:172707276..172709212-chr2:172750786..172752359,2	K562	blood:
50	chr2:172749065..172752809-chr2:172776821..172780584,7	K562	blood:

No data

Variant related genes	Relation type
HAT1	TF binding region
SLC25A12	TF binding region
HAT1	CpG island
SLC25A12	CpG island
ENSG00000267042	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000172878	chromatin interactions
ENSG00000123600	chromatin interactions
ENSG00000115827	chromatin interactions
ENSG00000128708	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000077380	chromatin interactions
ENSG00000236651	chromatin interactions
ENSG00000115844	chromatin interactions
ENSG00000170537	chromatin interactions

Extended variants
information (count: 1269 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74363770	chr2:172745664-172745665	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs550980348	chr2:172745722-172745723	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs78558521	chr2:172745762-172745763	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs6433317	chr2:172745781-172745782	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs142351298	chr2:172746016-172746017	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs146318321	chr2:172746049-172746050	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs548782190	chr2:172746057-172746058	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs139014013	chr2:172746059-172746060	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs117016907	chr2:172746096-172746097	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs568669699	chr2:172746199-172746200	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs10557724	chr2:172746215-172746216	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs202078196	chr2:172746216-172746217	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs577643574	chr2:172746219-172746220	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs548898141	chr2:172746332-172746333	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs544637060	chr2:172746334-172746335	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs368566406	chr2:172746335-172746336	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs556528220	chr2:172746374-172746375	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs140518033	chr2:172746438-172746439	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs542467111	chr2:172746476-172746477	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs369299421	chr2:172746486-172746487	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561145804	chr2:172746500-172746501	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs150427497	chr2:172746526-172746527	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs540401126	chr2:172746531-172746532	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs565271677	chr2:172746539-172746540	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs188555289	chr2:172746585-172746586	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368063427	chr2:172746594-172746595	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs370548102	chr2:172746621-172746622	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs138059936	chr2:172746720-172746721	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs569230021	chr2:172746832-172746833	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs192870446	chr2:172746862-172746863	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs548569076	chr2:172746926-172746927	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs77662255	chr2:172746929-172746930	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs374033955	chr2:172746945-172746946	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs79200378	chr2:172746987-172746988	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs34728188	chr2:172746988-172746989	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201181692	chr2:172746989-172746990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs375427871	chr2:172747009-172747010	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs397986666	chr2:172747011-172747012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs201766596	chr2:172747012-172747013	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs149498472	chr2:172747047-172747048	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs534154771	chr2:172747116-172747117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs535545870	chr2:172747128-172747129	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559090123	chr2:172747156-172747157	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs144156564	chr2:172747169-172747170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs62182403	chr2:172747182-172747183	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556540397	chr2:172747192-172747193	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs574852129	chr2:172747282-172747283	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs542535009	chr2:172747297-172747298	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs34388286	chr2:172747300-172747301	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs184432362	chr2:172747313-172747314	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172690200-172750200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:172709600-172749600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:172709600-172749600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:172710800-172747800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr2:172712200-172749200	Weak transcription	Hela-S3	cervix
6	chr2:172721200-172749600	Weak transcription	Thymus	Thymus
7	chr2:172724000-172749600	Weak transcription	Small Intestine	intestine
8	chr2:172724800-172749600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:172725400-172749800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:172725800-172749600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:172731400-172746400	Weak transcription	Fetal Lung	lung
12	chr2:172731600-172749600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:172731800-172746400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:172732000-172746000	Weak transcription	Fetal Brain Female	brain
15	chr2:172732000-172746400	Weak transcription	Fetal Muscle Leg	muscle
16	chr2:172732000-172746400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr2:172732000-172746600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr2:172732000-172748800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr2:172732000-172749400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr2:172732000-172749400	Weak transcription	A549	lung
21	chr2:172732000-172749600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr2:172732000-172749800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr2:172732000-172749800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr2:172732000-172750000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:172732200-172746400	Weak transcription	Primary B cells from cord blood	blood
26	chr2:172732200-172749600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr2:172732400-172749600	Weak transcription	Fetal Kidney	kidney
28	chr2:172732400-172749800	Weak transcription	Fetal Thymus	thymus
29	chr2:172732600-172747000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:172733000-172746400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:172733000-172749200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:172733000-172749400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr2:172735200-172749600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr2:172735400-172746600	Weak transcription	HSMM	muscle
35	chr2:172735400-172748200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:172735400-172748400	Weak transcription	Brain Anterior Caudate	brain
37	chr2:172735400-172749400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr2:172735400-172749400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr2:172735400-172749400	Weak transcription	Brain Hippocampus Middle	brain
40	chr2:172735400-172749600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr2:172735400-172749600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:172735400-172749600	Weak transcription	NHDF-Ad	bronchial
43	chr2:172735400-172749600	Weak transcription	NHEK	skin
44	chr2:172735600-172746400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:172735600-172749600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr2:172735600-172749600	Weak transcription	Adipose Nuclei	Adipose
47	chr2:172735600-172749600	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr2:172735600-172749600	Weak transcription	Brain Substantia Nigra	brain
49	chr2:172735600-172749600	Weak transcription	HMEC	breast
50	chr2:172735600-172749600	Weak transcription	NHLF	lung

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