Variant report

Variant	nsv901010
Chromosome Location	chr13:111165390-111286592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3183)
CpG islands
(count:3975)
Chromatin interactive
region (count:192)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3183 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111245912-111246135	K562	blood:	n/a	n/a
2	ARID3A	chr13:111208191-111208398	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:111214328-111214493	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:111229132-111229578	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:111267685-111267885	K562	blood:	n/a	n/a
6	ARID3A	chr13:111215440-111215806	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:111270041-111270363	K562	blood:	n/a	n/a
8	ARID3A	chr13:111242353-111242710	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:111246487-111246644	K562	blood:	n/a	n/a
10	ARID3A	chr13:111267627-111268132	HepG2	liver:	n/a	n/a
11	ARID3A	chr13:111245908-111246118	HepG2	liver:	n/a	n/a
12	ATF1	chr13:111180780-111181023	K562	blood:	n/a	n/a
13	ATF1	chr13:111212943-111213287	K562	blood:	n/a	n/a
14	ATF2	chr13:111269617-111270029	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
15	ATF2	chr13:111192135-111192676	GM12878	blood:	n/a	n/a
16	ATF2	chr13:111269691-111269959	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
17	ATF2	chr13:111227510-111228465	GM12878	blood:	n/a	chr13:111227886-111227897
18	ATF2	chr13:111167915-111168366	GM12878	blood:	n/a	n/a
19	ATF2	chr13:111263291-111264210	GM12878	blood:	n/a	n/a
20	ATF2	chr13:111263279-111264374	GM12878	blood:	n/a	n/a
21	ATF2	chr13:111212938-111213387	GM12878	blood:	n/a	n/a
22	ATF2	chr13:111268498-111269019	GM12878	blood:	n/a	n/a
23	ATF2	chr13:111214044-111214558	GM12878	blood:	n/a	n/a
24	ATF2	chr13:111267649-111268098	GM12878	blood:	n/a	n/a
25	ATF2	chr13:111177975-111178520	GM12878	blood:	n/a	n/a
26	ATF2	chr13:111227391-111228665	GM12878	blood:	n/a	chr13:111227886-111227897
27	BACH1	chr13:111213708-111214097	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr13:111262346-111262547	K562	blood:	n/a	n/a
29	BACH1	chr13:111214324-111214533	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr13:111249719-111250046	K562	blood:	n/a	n/a
31	BACH1	chr13:111267862-111268018	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr13:111228025-111228302	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr13:111243055-111243185	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr13:111263512-111263938	GM12878	blood:	n/a	n/a
35	BATF	chr13:111268630-111269012	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
36	BATF	chr13:111167970-111168377	GM12878	blood:	n/a	chr13:111168111-111168119
37	BATF	chr13:111260051-111260403	GM12878	blood:	n/a	n/a
38	BATF	chr13:111190999-111191237	GM12878	blood:	n/a	n/a
39	BATF	chr13:111260075-111260366	GM12878	blood:	n/a	n/a
40	BATF	chr13:111263251-111264016	GM12878	blood:	n/a	n/a
41	BATF	chr13:111227509-111227897	GM12878	blood:	n/a	n/a
42	BATF	chr13:111227402-111228554	GM12878	blood:	n/a	chr13:111227885-111227898 chr13:111228142-111228152 chr13:111227496-111227505
43	BATF	chr13:111268661-111268970	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
44	BCL11A	chr13:111268566-111268980	GM12878	blood:	n/a	n/a
45	BCL11A	chr13:111263261-111263935	GM12878	blood:	n/a	n/a
46	BCL11A	chr13:111263323-111263515	GM12878	blood:	n/a	n/a
47	BCL11A	chr13:111182506-111182825	GM12878	blood:	n/a	n/a
48	BCL11A	chr13:111227999-111228504	GM12878	blood:	n/a	n/a
49	BCL11A	chr13:111263531-111263876	GM12878	blood:	n/a	n/a
50	BCL11A	chr13:111227598-111227909	GM12878	blood:	n/a	n/a

(count:3975 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111214096-111214146	GM12878	blood:	n/a
2	chr13:111212174-111212224	AG09309	skin:	n/a
3	chr13:111178359-111178409	ovcar-3	ovarian:	n/a
4	chr13:111280738-111280788	HEEpiC	esophagus:	n/a
5	chr13:111267856-111267906	NB4	blood:	n/a
6	chr13:111214187-111214237	LNCaP	prostate:	n/a
7	chr13:111214187-111214237	NB4	blood:	n/a
8	chr13:111227891-111227941	NB4	blood:	n/a
9	chr13:111281384-111281434	PANC-1	pancreas:	n/a
10	chr13:111220199-111220249	HRE	kidney:	n/a
11	chr13:111214096-111214146	GM12878	blood:	n/a
12	chr13:111212174-111212224	AG09309	skin:	n/a
13	chr13:111178359-111178409	ovcar-3	ovarian:	n/a
14	chr13:111280738-111280788	HEEpiC	esophagus:	n/a
15	chr13:111267856-111267906	NB4	blood:	n/a
16	chr13:111214187-111214237	LNCaP	prostate:	n/a
17	chr13:111214187-111214237	NB4	blood:	n/a
18	chr13:111227891-111227941	NB4	blood:	n/a
19	chr13:111281384-111281434	PANC-1	pancreas:	n/a
20	chr13:111220199-111220249	HRE	kidney:	n/a
21	chr13:111193758-111193808	K562	blood:	n/a
22	chr13:111165457-111165507	HEEpiC	esophagus:	n/a
23	chr13:111278058-111278108	ECC-1	luminal epithelium:	n/a
24	chr13:111227891-111227941	HEEpiC	esophagus:	n/a
25	chr13:111250951-111251001	HIPEpiC	eye:	n/a
26	chr13:111214174-111214224	HCPEpiC	choroid plexus:	n/a
27	chr13:111214187-111214237	GM06990	blood:	n/a
28	chr13:111165419-111165469	NHDF-neo	bronchial:	n/a
29	chr13:111214192-111214242	AG10803	skin:	n/a
30	chr13:111178359-111178409	AoSMC	blood vessel:	n/a
31	chr13:111166833-111166883	HEK293	kidney:	embryo
32	chr13:111281384-111281434	HUVEC	blood vessel:	n/a
33	chr13:111267793-111267843	AG09319	gingival:	n/a
34	chr13:111268017-111268067	SK-N-SH	brain:	n/a
35	chr13:111217611-111217661	HEK293	kidney:	embryo
36	chr13:111280738-111280788	HRCEpiC	kidney:	n/a
37	chr13:111281129-111281179	NH-A	brain:	n/a
38	chr13:111165457-111165507	HNPCEpiC	eye:	n/a
39	chr13:111267979-111268029	HCM	heart:	n/a
40	chr13:111210121-111210171	GM12892	blood:	n/a
41	chr13:111220199-111220249	HRCEpiC	kidney:	n/a
42	chr13:111250951-111251001	ovcar-3	ovarian:	n/a
43	chr13:111214239-111214289	Jurkat	blood:	n/a
44	chr13:111214239-111214289	CMK	blood:	n/a
45	chr13:111275214-111275264	HRE	kidney:	n/a
46	chr13:111281324-111281374	HCPEpiC	choroid plexus:	n/a
47	chr13:111165457-111165507	CMK	blood:	n/a
48	chr13:111214246-111214296	ovcar-3	ovarian:	n/a
49	chr13:111212174-111212224	NHDF-neo	bronchial:	n/a
50	chr13:111267935-111267985	HRPEpiC	eye:	n/a

(count:192 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr12:51157105..51157794-chr13:111267888..111268432,2	Hela-S3	cervix:
2	chr13:111268040..111269954-chr13:111270156..111273298,3	K562	blood:
3	chr13:111176916..111182382-chr13:111206819..111214349,14	MCF-7	breast:
4	chr13:111247981..111253005-chr13:111363451..111368262,7	MCF-7	breast:
5	chr13:111178065..111180954-chr13:111183980..111185741,2	MCF-7	breast:
6	chr13:111205966..111208052-chr13:111364423..111367291,2	MCF-7	breast:
7	chr13:111247650..111249688-chr13:111251638..111253737,2	K562	blood:
8	chr13:111190119..111192322-chr13:111194362..111196366,2	MCF-7	breast:
9	chr13:111270726..111272560-chr13:111277400..111279622,2	MCF-7	breast:
10	chr13:111248805..111250322-chr13:111277318..111279178,2	MCF-7	breast:
11	chr13:111166073..111168474-chr13:111201353..111203309,2	MCF-7	breast:
12	chr13:111278124..111281264-chr13:111364873..111369262,5	MCF-7	breast:
13	chr13:111270148..111271814-chr13:111272109..111273731,2	K562	blood:
14	chr12:49412567..49413110-chr13:111268213..111268896,2	Hela-S3	cervix:
15	chr13:111270726..111272560-chr13:111277400..111279622,2	MCF-7	breast:
16	chr13:111155981..111156623-chr13:111173427..111174132,2	NB4	blood:
17	chr13:111217584..111220349-chr13:111248231..111250917,2	MCF-7	breast:
18	chr13:111180150..111181818-chr13:111197794..111200126,2	MCF-7	breast:
19	chr13:111266737..111268751-chr13:111366724..111368921,2	K562	blood:
20	chr13:111267350..111267981-chr17:56756502..56757440,2	NB4	blood:
21	chr13:111208343..111210898-chr13:111364767..111367709,3	MCF-7	breast:
22	chr13:111189062..111191604-chr13:111205599..111208435,2	MCF-7	breast:
23	chr13:111286170..111289373-chr13:111362877..111366767,3	K562	blood:
24	chr13:111192777..111195379-chr13:111196356..111198456,2	MCF-7	breast:
25	chr13:111189062..111191604-chr13:111205599..111208435,2	MCF-7	breast:
26	chr13:111245045..111250011-chr13:111292249..111295847,5	MCF-7	breast:
27	chr13:111222975..111225415-chr13:111233711..111236362,2	K562	blood:
28	chr13:111284778..111286525-chr13:111522479..111525295,2	K562	blood:
29	chr13:111214986..111217647-chr13:111218744..111220287,2	MCF-7	breast:
30	chr13:111205877..111207739-chr13:111217049..111218978,2	K562	blood:
31	chr13:111178399..111181198-chr13:111366491..111368547,2	MCF-7	breast:
32	chr13:111248805..111250322-chr13:111277318..111279178,2	MCF-7	breast:
33	chr13:111250674..111253201-chr13:111366496..111368756,2	MCF-7	breast:
34	chr13:111213501..111214341-chr6:27114827..27115817,3	Hela-S3	cervix:
35	chr13:111176604..111179029-chr13:111215041..111217071,2	MCF-7	breast:
36	chr13:111226817..111229792-chr13:111230738..111232332,2	K562	blood:
37	chr13:111226642..111228664-chr13:111251915..111253703,2	MCF-7	breast:
38	chr13:111107007..111108826-chr13:111174960..111176925,2	MCF-7	breast:
39	chr13:111213298..111215293-chr13:111263862..111265630,2	MCF-7	breast:
40	chr13:111226642..111228664-chr13:111251915..111253703,2	MCF-7	breast:
41	chr13:111247650..111249688-chr13:111251638..111253737,2	K562	blood:
42	chr13:111260059..111265177-chr13:111265738..111269909,6	K562	blood:
43	chr13:111249993..111251646-chr13:111251671..111254443,2	MCF-7	breast:
44	chr13:111197640..111199252-chr13:111199742..111202683,2	K562	blood:
45	chr13:111249148..111253667-chr13:111266307..111270199,8	MCF-7	breast:
46	chr13:111166073..111168474-chr13:111201353..111203309,2	MCF-7	breast:
47	chr13:111201421..111204692-chr13:111211938..111214450,3	MCF-7	breast:
48	chr13:111267596..111269197-chr13:111364131..111366094,2	K562	blood:
49	chr13:111207188..111209272-chr13:111210508..111214115,3	K562	blood:
50	chr13:111266655..111268705-chr13:111294879..111298471,3	K562	blood:

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

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

No data

Variant related genes	Relation type
CARKD	TF binding region
RAB20	TF binding region
ENSG00000255831	TF binding region
COL4A2-AS1	TF binding region
CARKD	CpG island
RAB20	CpG island
ENSG00000255831	CpG island
COL4A2-AS1	CpG island
ENSG00000104518	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000050405	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000139832	chromatin interactions
ENSG00000132510	chromatin interactions
ENSG00000213995	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000087502	chromatin interactions
ENSG00000181929	chromatin interactions
ENSG00000134871	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000255831	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000140262	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000232814	chromatin interactions

Extended variants
information (count: 5587 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5587 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6492279	chr13:111165390-111165391	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576784453	chr13:111165402-111165403	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs60815314	chr13:111165420-111165421	Strong transcription Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376676054	chr13:111165457-111165458	Strong transcription Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs367911076	chr13:111165519-111165520	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546320450	chr13:111165534-111165535	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73618183	chr13:111165537-111165538	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs371417864	chr13:111165545-111165546	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145243555	chr13:111165582-111165583	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560028783	chr13:111165592-111165593	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12427708	chr13:111165593-111165594	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs149204212	chr13:111165611-111165612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559185837	chr13:111165623-111165624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540097400	chr13:111165637-111165638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189943542	chr13:111165683-111165684	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143330486	chr13:111165684-111165685	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181526315	chr13:111165711-111165712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374385968	chr13:111165717-111165718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs111404317	chr13:111165737-111165738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535521786	chr13:111165754-111165755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554225244	chr13:111165765-111165766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9515239	chr13:111165766-111165767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs551051581	chr13:111165767-111165768	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571871427	chr13:111165786-111165787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576721429	chr13:111165793-111165794	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs202122947	chr13:111165842-111165843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544085334	chr13:111165857-111165858	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs67348422	chr13:111165860-111165861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs57075488	chr13:111165861-111165862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532549465	chr13:111165862-111165863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145869279	chr13:111165876-111165877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574362827	chr13:111165890-111165891	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs118136447	chr13:111165904-111165905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560169791	chr13:111165921-111165922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527366469	chr13:111165951-111165952	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369787289	chr13:111166024-111166025	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs137884462	chr13:111166037-111166038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531406137	chr13:111166040-111166041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542418387	chr13:111166087-111166088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374066852	chr13:111166129-111166130	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs377595118	chr13:111166130-111166131	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561046248	chr13:111166252-111166253	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568049016	chr13:111166258-111166259	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142307416	chr13:111166267-111166268	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs570939402	chr13:111166293-111166294	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs185911171	chr13:111166306-111166307	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs1570908	chr13:111166307-111166308	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7328347	chr13:111166314-111166315	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539511052	chr13:111166329-111166330	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565252691	chr13:111166337-111166338	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 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	22037309	CNVD

Chromatin state (count:4315 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111109800-111168000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr13:111124400-111167400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:111139600-111166400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:111139600-111166600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr13:111140200-111167200	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr13:111140800-111166600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr13:111141600-111165600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:111143400-111166800	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr13:111150800-111167200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:111152600-111168000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:111152800-111165800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr13:111153000-111168000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:111153400-111172800	Weak transcription	Brain Substantia Nigra	brain
14	chr13:111155200-111175600	Weak transcription	Fetal Thymus	thymus
15	chr13:111159600-111166600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:111159600-111166800	Strong transcription	HUVEC	blood vessel
17	chr13:111159600-111167600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr13:111159600-111172200	Weak transcription	Brain Hippocampus Middle	brain
19	chr13:111159600-111176800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr13:111159800-111167800	Strong transcription	NH-A	brain
21	chr13:111159800-111167800	Strong transcription	Osteobl	bone
22	chr13:111159800-111168200	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr13:111160000-111165600	Strong transcription	NHEK	skin
24	chr13:111160000-111167000	Strong transcription	HSMM	muscle
25	chr13:111160000-111167800	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr13:111160000-111172800	Weak transcription	Brain Anterior Caudate	brain
27	chr13:111160200-111165600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr13:111160200-111167600	Strong transcription	Aorta	Aorta
29	chr13:111160600-111165600	Strong transcription	Colon Smooth Muscle	Colon
30	chr13:111160800-111167800	Strong transcription	Lung	lung
31	chr13:111160800-111172200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr13:111160800-111172600	Weak transcription	Esophagus	oesophagus
33	chr13:111160800-111176400	Weak transcription	Psoas Muscle	Psoas
34	chr13:111160800-111209600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr13:111161000-111168000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr13:111161200-111173000	Weak transcription	Brain Germinal Matrix	brain
37	chr13:111162000-111167400	Strong transcription	Ovary	ovary
38	chr13:111162400-111165600	Strong transcription	NHLF	lung
39	chr13:111162400-111173000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr13:111162600-111166400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:111162600-111166400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr13:111162600-111168000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr13:111162600-111169800	Weak transcription	NHDF-Ad	bronchial
44	chr13:111162600-111177200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:111162800-111166800	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr13:111162800-111167000	Strong transcription	Rectal Smooth Muscle	rectum
47	chr13:111162800-111167400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr13:111163000-111167000	Strong transcription	Fetal Lung	lung
49	chr13:111163000-111167400	Strong transcription	Fetal Intestine Small	intestine
50	chr13:111163000-111168000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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