Variant report

Variant	nsv901009
Chromosome Location	chr13:111134780-111176393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:769)
CpG islands
(count:2137)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111161798-111162280	K562	blood:	n/a	n/a
2	ARID3A	chr13:111137921-111138251	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:111159493-111159911	K562	blood:	n/a	n/a
4	ARID3A	chr13:111142737-111143030	HepG2	liver:	n/a	n/a
5	ATF1	chr13:111161881-111162845	K562	blood:	n/a	n/a
6	ATF2	chr13:111137856-111138239	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr13:111167915-111168366	GM12878	blood:	n/a	n/a
8	ATF2	chr13:111137790-111138286	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr13:111167970-111168377	GM12878	blood:	n/a	chr13:111168111-111168119
10	BATF	chr13:111156491-111156790	GM12878	blood:	n/a	chr13:111156656-111156666 chr13:111156655-111156666
11	BCL11A	chr13:111137948-111138194	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr13:111137913-111138107	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr13:111135652-111136115	GM12878	blood:	n/a	n/a
14	BCL3	chr13:111135723-111135993	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:111159371-111160094	K562	blood:	n/a	n/a
16	BHLHE40	chr13:111167561-111167707	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:111168043-111168267	GM12878	blood:	n/a	n/a
18	BHLHE40	chr13:111155839-111156135	K562	blood:	n/a	n/a
19	BHLHE40	chr13:111161881-111163113	K562	blood:	n/a	n/a
20	BHLHE40	chr13:111163922-111164155	K562	blood:	n/a	n/a
21	BHLHE40	chr13:111137892-111138185	HepG2	liver:	n/a	n/a
22	BHLHE40	chr13:111156449-111156785	K562	blood:	n/a	n/a
23	CBX3	chr13:111161867-111162192	K562	blood:	n/a	n/a
24	CBX3	chr13:111158789-111159233	K562	blood:	n/a	n/a
25	CBX3	chr13:111162464-111163146	K562	blood:	n/a	n/a
26	CBX3	chr13:111156498-111156841	K562	blood:	n/a	n/a
27	CBX3	chr13:111161794-111162310	K562	blood:	n/a	n/a
28	CBX3	chr13:111159277-111159973	K562	blood:	n/a	n/a
29	CCNT2	chr13:111162614-111162895	K562	blood:	n/a	chr13:111162674-111162683
30	CCNT2	chr13:111159493-111160053	K562	blood:	n/a	n/a
31	CCNT2	chr13:111163810-111164238	K562	blood:	n/a	n/a
32	CCNT2	chr13:111161872-111162172	K562	blood:	n/a	n/a
33	CEBPB	chr13:111159552-111159908	K562	blood:	n/a	n/a
34	CEBPB	chr13:111174270-111174621	K562	blood:	n/a	chr13:111174440-111174453
35	CEBPB	chr13:111174304-111174611	A549	lung:	n/a	chr13:111174440-111174453
36	CEBPB	chr13:111174332-111174559	K562	blood:	n/a	chr13:111174440-111174453
37	CEBPB	chr13:111161898-111162206	K562	blood:	n/a	n/a
38	CEBPB	chr13:111174304-111174565	MCF-7	breast:	n/a	chr13:111174440-111174453
39	CEBPB	chr13:111169860-111170247	Hela-S3	cervix:	n/a	chr13:111170038-111170049 chr13:111170040-111170051
40	CEBPB	chr13:111174294-111174581	H1-hESC	embryonic stem cell:	n/a	chr13:111174440-111174453
41	CEBPB	chr13:111169887-111170243	IMR90	lung:	n/a	chr13:111170038-111170049 chr13:111170040-111170051
42	CEBPB	chr13:111161870-111162167	K562	blood:	n/a	n/a
43	CEBPB	chr13:111161844-111162175	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:111159457-111159819	K562	blood:	n/a	n/a
45	CEBPB	chr13:111156454-111156936	K562	blood:	n/a	n/a
46	CEBPB	chr13:111174281-111174614	IMR90	lung:	n/a	chr13:111174440-111174453
47	CEBPB	chr13:111169949-111170210	K562	blood:	n/a	chr13:111170038-111170049 chr13:111170040-111170051
48	CEBPB	chr13:111137851-111138212	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr13:111173062-111173435	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:111169867-111170213	HepG2	liver:	n/a	chr13:111170038-111170049 chr13:111170040-111170051

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111165457-111165507	HL-60	blood:	n/a
2	chr13:111144447-111144497	HAEpiC	amniotic membrane:	n/a
3	chr13:111165457-111165507	HL-60	blood:	n/a
4	chr13:111144447-111144497	HAEpiC	amniotic membrane:	n/a
5	chr13:111138063-111138113	NH-A	brain:	n/a
6	chr13:111158919-111158969	HCT-116	colon:	n/a
7	chr13:111143644-111143694	T-47D	breast:	n/a
8	chr13:111164546-111164596	ovcar-3	ovarian:	n/a
9	chr13:111165457-111165507	BE2_C	brain:	n/a
10	chr13:111144464-111144514	PANC-1	pancreas:	n/a
11	chr13:111164546-111164596	GM12878	blood:	n/a
12	chr13:111141854-111141904	Caco-2	colon:	n/a
13	chr13:111143644-111143694	LNCaP	prostate:	n/a
14	chr13:111159111-111159161	BE2_C	brain:	n/a
15	chr13:111145583-111145633	PANC-1	pancreas:	n/a
16	chr13:111144447-111144497	AG04449	skin:	fetal
17	chr13:111138063-111138113	BJ	skin:	n/a
18	chr13:111145581-111145631	PrEC	prostate:	n/a
19	chr13:111166833-111166883	BJ	skin:	n/a
20	chr13:111145572-111145622	HL-60	blood:	n/a
21	chr13:111137257-111137307	NH-A	brain:	n/a
22	chr13:111145564-111145614	AG09319	gingival:	n/a
23	chr13:111164702-111164752	IMR90	lung:	fetal
24	chr13:111165419-111165469	NT2-D1	testis:	n/a
25	chr13:111141854-111141904	HCPEpiC	choroid plexus:	n/a
26	chr13:111141868-111141918	HUVEC	blood vessel:	n/a
27	chr13:111144447-111144497	GM06990	blood:	n/a
28	chr13:111145583-111145633	NHDF-neo	bronchial:	n/a
29	chr13:111161943-111161993	GM06990	blood:	n/a
30	chr13:111145564-111145614	PrEC	prostate:	n/a
31	chr13:111145583-111145633	SKMC	muscle:	n/a
32	chr13:111175670-111175720	SAEC	small airway:	n/a
33	chr13:111141868-111141918	SK-N-SH_RA	brain:	n/a
34	chr13:111141854-111141904	CMK	blood:	n/a
35	chr13:111144464-111144514	NHBE	bronchial:	n/a
36	chr13:111141841-111141891	Hepatocyte	liver:	n/a
37	chr13:111141830-111141880	PrEC	prostate:	n/a
38	chr13:111164966-111165016	GM19239	blood:	n/a
39	chr13:111145770-111145820	PFSK-1	brain:	n/a
40	chr13:111164702-111164752	GM12878	blood:	n/a
41	chr13:111160399-111160449	PFSK-1	brain:	n/a
42	chr13:111141868-111141918	NHBE	bronchial:	n/a
43	chr13:111165419-111165469	BE2_C	brain:	n/a
44	chr13:111145770-111145820	HCF	heart:	n/a
45	chr13:111142065-111142115	K562	blood:	n/a
46	chr13:111138063-111138113	Hepatocyte	liver:	n/a
47	chr13:111164367-111164417	AG09319	gingival:	n/a
48	chr13:111137257-111137307	AG04450	lung:	fetal
49	chr13:111145592-111145642	SK-N-SH_RA	brain:	n/a
50	chr13:111160399-111160449	MCF10A-Er-Src	breast:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:111161146..111163590-chr13:111168306..111171101,3	K562	blood:
2	chr13:111152581..111154203-chr13:111156626..111159489,2	MCF-7	breast:
3	chr13:111161146..111163590-chr13:111168306..111171101,3	K562	blood:
4	chr13:111156722..111158386-chr13:111162360..111164730,2	MCF-7	breast:
5	chr13:111158122..111160358-chr13:111366408..111368725,2	MCF-7	breast:
6	chr13:111164951..111166469-chr13:111366583..111368150,2	K562	blood:
7	chr13:111171406..111173667-chr13:111365704..111368151,2	K562	blood:
8	chr13:111145123..111148050-chr13:111150419..111153433,3	K562	blood:
9	chr13:111171438..111174386-chr13:111180872..111182991,2	MCF-7	breast:
10	chr13:111146736..111149122-chr13:111366104..111368314,2	K562	blood:
11	chr13:111160586..111163300-chr13:111242800..111244422,2	MCF-7	breast:
12	chr13:111155981..111156623-chr13:111173427..111174132,2	NB4	blood:
13	chr13:111146550..111148284-chr13:111150740..111153734,2	K562	blood:
14	chr13:111149836..111151933-chr13:111211909..111213452,2	K562	blood:
15	chr13:111155981..111156623-chr13:111173427..111174132,2	NB4	blood:
16	chr13:111162545..111165671-chr13:111172658..111175880,3	MCF-7	breast:
17	chr13:111137982..111139929-chr13:111150615..111152724,2	K562	blood:
18	chr13:111155022..111158226-chr13:111364288..111368980,5	K562	blood:
19	chr1:227922456..227923342-chr13:111156032..111156739,2	NB4	blood:
20	chr13:111145900..111148026-chr13:111158293..111160990,2	MCF-7	breast:
21	chr13:111162545..111165671-chr13:111172658..111175880,3	MCF-7	breast:
22	chr13:111158284..111162693-chr13:111363847..111368622,9	K562	blood:
23	chr13:111146550..111148284-chr13:111150740..111153734,2	K562	blood:
24	chr13:111123579..111125936-chr13:111162097..111164181,2	K562	blood:
25	chr13:111132025..111133976-chr13:111134676..111137349,2	MCF-7	breast:
26	chr13:111158296..111161279-chr13:111366588..111368622,2	K562	blood:
27	chr13:111147183..111148852-chr13:111151910..111153653,2	MCF-7	breast:
28	chr13:111160457..111163590-chr13:111168306..111171101,4	K562	blood:
29	chr13:111161352..111163541-chr13:111207330..111209869,3	MCF-7	breast:
30	chr13:111136194..111138390-chr13:111154257..111156579,2	K562	blood:
31	chr13:111159545..111161201-chr13:111212465..111215084,2	MCF-7	breast:
32	chr13:111107007..111108826-chr13:111174960..111176925,2	MCF-7	breast:
33	chr13:111148436..111150454-chr13:111154372..111156484,2	K562	blood:
34	chr13:111158315..111162369-chr13:111211913..111215301,3	MCF-7	breast:
35	chr13:111128717..111130651-chr13:111161918..111164704,2	K562	blood:
36	chr13:111141148..111142734-chr13:111213143..111215554,2	K562	blood:
37	chr13:111156722..111158386-chr13:111162360..111164730,2	MCF-7	breast:
38	chr13:111175360..111178796-chr13:111180023..111183032,3	MCF-7	breast:
39	chr13:111137005..111139926-chr13:111365403..111367570,2	K562	blood:
40	chr13:111134838..111136595-chr13:111159284..111162082,2	MCF-7	breast:
41	chr13:111159158..111160698-chr13:111176140..111178279,2	MCF-7	breast:
42	chr13:111148436..111150454-chr13:111154372..111156484,2	K562	blood:
43	chr13:111175089..111177508-chr13:111178295..111180453,3	MCF-7	breast:
44	chr13:111166149..111167793-chr13:111205225..111207566,2	MCF-7	breast:
45	chr13:111145936..111148236-chr13:111366104..111367856,2	K562	blood:
46	chr13:111160160..111164294-chr13:111174560..111180121,5	MCF-7	breast:
47	chr13:111160382..111162246-chr13:111163776..111165316,2	MCF-7	breast:
48	chr13:111145123..111148050-chr13:111150419..111153433,3	K562	blood:
49	chr13:111166073..111168474-chr13:111201353..111203309,2	MCF-7	breast:
50	chr13:111152980..111156957-chr13:111159190..111161050,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-4	chr13:111166518-111166932	NONHSAT035153

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	COL4A2	hsa-miR-29b-3p	chr13:111164551-111164573
2	COL4A2	hsa-miR-29c-3p	chr13:111164556-111164573
3	COL4A2	hsa-miR-29a-3p	chr13:111164566-111164572
4	COL4A2	hsa-miR-29b-3p	chr13:111164566-111164572
5	COL4A2	hsa-miR-29c-3p	chr13:111164566-111164572
6	COL4A2	hsa-miR-29a-3p	chr13:111164556-111164573
7	COL4A2	hsa-miR-26b-5p	chr13:111165202-111165221

Variant related genes	Relation type
COL4A2	TF binding region
COL4A2-AS1	TF binding region
COL4A2	CpG island
COL4A2-AS1	CpG island
ENSG00000081692	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000232814	chromatin interactions
ENSG00000139832	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000134871	chromatin interactions
ENSG00000143740	chromatin interactions
ENSG00000213995	chromatin interactions

Extended variants
information (count: 2199 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3803229	chr13:111134780-111134781	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534176403	chr13:111134785-111134786	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78589207	chr13:111134789-111134790	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544732591	chr13:111134809-111134810	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188827003	chr13:111134825-111134826	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370306986	chr13:111134827-111134828	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541632438	chr13:111134830-111134831	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3803228	chr13:111134858-111134859	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369814664	chr13:111134866-111134867	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181283055	chr13:111134877-111134878	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145040676	chr13:111134883-111134884	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372108933	chr13:111134918-111134919	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374749394	chr13:111134924-111134925	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199678709	chr13:111134946-111134947	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372961760	chr13:111135009-111135010	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377140964	chr13:111135011-111135012	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369736820	chr13:111135035-111135036	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs369736501	chr13:111135039-111135040	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373605735	chr13:111135052-111135053	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs536480845	chr13:111135060-111135061	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553026578	chr13:111135072-111135073	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566496704	chr13:111135086-111135087	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568964324	chr13:111135094-111135095	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs114140846	chr13:111135108-111135109	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71419776	chr13:111135250-111135251	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9583505	chr13:111135251-111135252	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs534084080	chr13:111135284-111135285	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs141592511	chr13:111135303-111135304	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs34997070	chr13:111135318-111135319	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563766417	chr13:111135340-111135341	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs7990038	chr13:111135353-111135354	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs538270953	chr13:111135414-111135415	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs145344648	chr13:111135425-111135426	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540617302	chr13:111135429-111135430	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574915642	chr13:111135430-111135431	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147702264	chr13:111135432-111135433	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560739135	chr13:111135465-111135466	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs9521804	chr13:111135466-111135467	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs546106621	chr13:111135478-111135479	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374028579	chr13:111135502-111135503	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564514706	chr13:111135503-111135504	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531963035	chr13:111135557-111135558	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550585153	chr13:111135578-111135579	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs11616507	chr13:111135593-111135594	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs529845480	chr13:111135613-111135614	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs138762732	chr13:111135618-111135619	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142409059	chr13:111135669-111135670	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200085046	chr13:111135710-111135711	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566686813	chr13:111135722-111135723	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527554399	chr13:111135731-111135732	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111078200-111136800	Weak transcription	Colonic Mucosa	Colon
2	chr13:111105800-111138000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr13:111108200-111138400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr13:111108600-111138200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:111108600-111149200	Strong transcription	Fetal Stomach	stomach
6	chr13:111108600-111150600	Weak transcription	NHDF-Ad	bronchial
7	chr13:111108800-111148800	Weak transcription	Brain Angular Gyrus	brain
8	chr13:111108800-111152200	Strong transcription	Fetal Intestine Small	intestine
9	chr13:111109000-111158800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:111109600-111155800	Strong transcription	Fetal Intestine Large	intestine
11	chr13:111109600-111158800	Strong transcription	Ovary	ovary
12	chr13:111109800-111152600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr13:111109800-111168000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr13:111114200-111138800	Strong transcription	Aorta	Aorta
15	chr13:111117200-111152000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr13:111119000-111142600	Weak transcription	Stomach Mucosa	stomach
17	chr13:111119000-111143600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr13:111119200-111138200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:111119200-111150400	Weak transcription	Brain Anterior Caudate	brain
20	chr13:111119200-111159200	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr13:111119600-111139800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr13:111119600-111160400	Weak transcription	Brain Germinal Matrix	brain
23	chr13:111124200-111137400	Strong transcription	NH-A	brain
24	chr13:111124200-111144600	Weak transcription	Liver	Liver
25	chr13:111124400-111136200	Strong transcription	HSMM	muscle
26	chr13:111124400-111139000	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr13:111124400-111152000	Strong transcription	Osteobl	bone
28	chr13:111124400-111167400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr13:111125200-111136800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr13:111125600-111157800	Weak transcription	Small Intestine	intestine
31	chr13:111127400-111147400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr13:111127400-111148200	Weak transcription	Brain Hippocampus Middle	brain
33	chr13:111127400-111148600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr13:111127600-111136800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr13:111127600-111144600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr13:111127600-111148600	Strong transcription	Lung	lung
37	chr13:111127600-111153000	Weak transcription	Brain Substantia Nigra	brain
38	chr13:111127600-111156200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr13:111127800-111147800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr13:111128600-111137200	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr13:111128800-111146000	Strong transcription	Fetal Lung	lung
42	chr13:111129000-111138000	Weak transcription	A549	lung
43	chr13:111129200-111142400	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr13:111130000-111137200	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr13:111130200-111138000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:111130600-111137200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr13:111130600-111137800	Weak transcription	Fetal Heart	heart
48	chr13:111130600-111139400	Strong transcription	Spleen	Spleen
49	chr13:111130600-111155400	Strong transcription	Left Ventricle	heart
50	chr13:111130800-111138400	Strong transcription	Rectal Smooth Muscle	rectum

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