Variant report

Variant	nsv960928
Chromosome Location	chr19:38790012-38822380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1901)
CpG islands
(count:2198)
Chromatin interactive
region (count:95)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:38806857-38807135	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:38804182-38804600	K562	blood:	n/a	n/a
3	ARID3A	chr19:38806277-38806573	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:38812633-38812933	K562	blood:	n/a	n/a
5	ARID3A	chr19:38807469-38808195	K562	blood:	n/a	n/a
6	ARID3A	chr19:38795692-38795935	K562	blood:	n/a	n/a
7	ARID3A	chr19:38806755-38807222	K562	blood:	n/a	n/a
8	ARID3A	chr19:38791340-38791757	HepG2	liver:	n/a	n/a
9	ATF1	chr19:38806354-38807135	K562	blood:	n/a	n/a
10	ATF1	chr19:38807689-38808131	K562	blood:	n/a	n/a
11	ATF1	chr19:38793477-38793753	K562	blood:	n/a	n/a
12	ATF2	chr19:38804133-38804425	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr19:38804094-38804345	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr19:38791029-38791872	A549	lung:	n/a	n/a
15	ATF3	chr19:38794088-38796300	A549	lung:	n/a	n/a
16	ATF3	chr19:38791075-38791857	A549	lung:	n/a	n/a
17	ATF3	chr19:38805786-38806512	A549	lung:	n/a	n/a
18	BACH1	chr19:38806437-38806524	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:38810781-38810913	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr19:38804215-38804375	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr19:38794376-38794504	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr19:38807736-38808062	K562	blood:	n/a	n/a
23	BACH1	chr19:38795613-38795885	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr19:38794737-38794893	H1-hESC	embryonic stem cell:	n/a	chr19:38794752-38794766
25	BCL3	chr19:38791148-38791533	GM12878	blood:	n/a	n/a
26	BCL3	chr19:38801412-38802382	A549	lung:	n/a	n/a
27	BCL3	chr19:38790948-38791875	A549	lung:	n/a	n/a
28	BCL3	chr19:38805922-38806593	A549	lung:	n/a	n/a
29	BCL3	chr19:38789050-38790238	A549	lung:	n/a	n/a
30	BCL3	chr19:38790918-38792043	A549	lung:	n/a	n/a
31	BCL3	chr19:38793007-38793866	A549	lung:	n/a	n/a
32	BCL3	chr19:38797589-38800656	A549	lung:	n/a	n/a
33	BCL3	chr19:38794056-38796560	A549	lung:	n/a	chr19:38794754-38794763 chr19:38794532-38794541 chr19:38796292-38796305
34	BCL3	chr19:38798688-38800758	A549	lung:	n/a	n/a
35	BCL3	chr19:38805728-38807472	A549	lung:	n/a	n/a
36	BCL3	chr19:38791146-38791626	GM12878	blood:	n/a	n/a
37	BCL3	chr19:38809796-38811002	A549	lung:	n/a	n/a
38	BCL3	chr19:38800999-38801761	A549	lung:	n/a	n/a
39	BCL3	chr19:38794125-38796665	A549	lung:	n/a	chr19:38794754-38794763 chr19:38794532-38794541 chr19:38796292-38796305
40	BCLAF1	chr19:38806376-38806673	GM12878	blood:	n/a	n/a
41	BHLHE40	chr19:38791138-38791759	A549	lung:	n/a	n/a
42	BHLHE40	chr19:38795441-38795990	K562	blood:	n/a	n/a
43	BHLHE40	chr19:38806202-38806895	HepG2	liver:	n/a	n/a
44	BHLHE40	chr19:38807604-38808181	K562	blood:	n/a	n/a
45	BHLHE40	chr19:38805861-38807154	K562	blood:	n/a	n/a
46	BHLHE40	chr19:38791221-38791745	HepG2	liver:	n/a	n/a
47	BHLHE40	chr19:38812288-38812657	K562	blood:	n/a	n/a
48	BHLHE40	chr19:38793475-38793771	K562	blood:	n/a	n/a
49	BHLHE40	chr19:38804289-38804604	K562	blood:	n/a	n/a
50	BHLHE40	chr19:38794338-38795860	A549	lung:	n/a	chr19:38794500-38794516 chr19:38795353-38795362 chr19:38795353-38795362 chr19:38795354-38795363

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:38794598-38794648	NHDF-neo	bronchial:	n/a
2	chr19:38806779-38806829	AG10803	skin:	n/a
3	chr19:38794598-38794648	NHDF-neo	bronchial:	n/a
4	chr19:38806779-38806829	AG10803	skin:	n/a
5	chr19:38794598-38794648	HCM	heart:	n/a
6	chr19:38806457-38806507	GM12891	blood:	n/a
7	chr19:38794845-38794895	H1-hESC	embryonic stem cell:	embryo
8	chr19:38806834-38806884	A549	lung:	n/a
9	chr19:38810284-38810334	HEEpiC	esophagus:	n/a
10	chr19:38795051-38795101	GM06990	blood:	n/a
11	chr19:38810227-38810277	AG04450	lung:	fetal
12	chr19:38801388-38801438	NT2-D1	testis:	n/a
13	chr19:38806411-38806461	SK-N-SH	brain:	n/a
14	chr19:38794598-38794648	HEEpiC	esophagus:	n/a
15	chr19:38811036-38811086	HepG2	liver:	n/a
16	chr19:38810437-38810487	RPTEC	kidney:	n/a
17	chr19:38794845-38794895	IMR90	lung:	fetal
18	chr19:38811027-38811077	HMEC	breast:	n/a
19	chr19:38794814-38794864	HCT-116	colon:	n/a
20	chr19:38806375-38806425	PFSK-1	brain:	n/a
21	chr19:38810212-38810262	K562	blood:	n/a
22	chr19:38801506-38801556	SK-N-SH	brain:	n/a
23	chr19:38795051-38795101	SK-N-SH	brain:	n/a
24	chr19:38813802-38813852	SK-N-SH	brain:	n/a
25	chr19:38810212-38810262	AG10803	skin:	n/a
26	chr19:38796094-38796144	RPTEC	kidney:	n/a
27	chr19:38806411-38806461	NHDF-neo	bronchial:	n/a
28	chr19:38810434-38810484	HepG2	liver:	n/a
29	chr19:38806457-38806507	GM06990	blood:	n/a
30	chr19:38806834-38806884	SAEC	small airway:	n/a
31	chr19:38810162-38810212	IMR90	lung:	fetal
32	chr19:38813802-38813852	ovcar-3	ovarian:	n/a
33	chr19:38794598-38794648	A549	lung:	n/a
34	chr19:38810166-38810216	GM19239	blood:	n/a
35	chr19:38811036-38811086	LNCaP	prostate:	n/a
36	chr19:38806874-38806924	GM12892	blood:	n/a
37	chr19:38806846-38806896	GM12891	blood:	n/a
38	chr19:38801388-38801438	Caco-2	colon:	n/a
39	chr19:38795051-38795101	MCF10A-Er-Src	breast:	n/a
40	chr19:38818130-38818180	HepG2	liver:	n/a
41	chr19:38810284-38810334	AG04450	lung:	fetal
42	chr19:38794664-38794714	AoSMC	blood vessel:	n/a
43	chr19:38796094-38796144	K562	blood:	n/a
44	chr19:38806834-38806884	GM12878	blood:	n/a
45	chr19:38794814-38794864	HRE	kidney:	n/a
46	chr19:38806874-38806924	HRPEpiC	eye:	n/a
47	chr19:38806411-38806461	NB4	blood:	n/a
48	chr19:38806145-38806195	GM12892	blood:	n/a
49	chr19:38810437-38810487	K562	blood:	n/a
50	chr19:38806834-38806884	HepG2	liver:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:38819188..38821432-chr19:38824241..38826346,2	K562	blood:
2	chr19:38804503..38806796-chr19:38878549..38880159,2	K562	blood:
3	chr19:38789522..38790555-chr19:38811884..38812916,56	MCF-7	breast:
4	chr19:38746686..38748655-chr19:38804241..38806513,3	K562	blood:
5	chr19:38806332..38809400-chr19:38825014..38828541,5	K562	blood:
6	chr19:38793475..38795482-chr19:38826442..38828638,2	K562	blood:
7	chr19:38767240..38769774-chr19:38804248..38806367,2	K562	blood:
8	chr19:38815734..38818245-chr19:38825001..38828035,3	K562	blood:
9	chr19:38771059..38771781-chr19:38789868..38790376,2	MCF-7	breast:
10	chr19:13262824..13265095-chr19:38789559..38791383,2	MCF-7	breast:
11	chr19:38789573..38790446-chr19:39205149..39205721,3	MCF-7	breast:
12	chr19:38800007..38802686-chr19:38805252..38808238,5	K562	blood:
13	chr19:38791429..38792070-chr19:38812011..38812528,2	MCF-7	breast:
14	chr14:64108540..64109428-chr19:38794685..38795598,2	Hela-S3	cervix:
15	chr19:38796381..38798650-chr19:38799992..38801610,2	K562	blood:
16	chr19:38809370..38811650-chr19:38819162..38821932,2	K562	blood:
17	chr19:38745470..38748025-chr19:38806544..38809528,4	K562	blood:
18	chr19:38811920..38812880-chr19:39204810..39205833,6	MCF-7	breast:
19	chr19:38755234..38758154-chr19:38804246..38806924,3	K562	blood:
20	chr19:13951028..13952754-chr19:38788444..38790834,2	MCF-7	breast:
21	chr19:38811920..38812880-chr19:39204762..39205833,7	MCF-7	breast:
22	chr19:38789196..38790974-chr19:38800428..38802782,2	K562	blood:
23	chr12:46762605..46765177-chr19:38791168..38793279,2	MCF-7	breast:
24	chr19:38789524..38790548-chr19:38811945..38812916,35	MCF-7	breast:
25	chr1:149223898..149224411-chr19:38794775..38795700,2	Hela-S3	cervix:
26	chr19:38765937..38769216-chr19:38788492..38791727,3	MCF-7	breast:
27	chr19:38791429..38792070-chr19:38812011..38812528,2	MCF-7	breast:
28	chr19:38806188..38807107-chr7:6414078..6414612,2	Hela-S3	cervix:
29	chr19:38793175..38794787-chr19:38818413..38820106,2	MCF-7	breast:
30	chr19:38779327..38783351-chr19:38794485..38798006,3	K562	blood:
31	chr19:38795298..38801659-chr19:38801673..38807893,10	K562	blood:
32	chr19:38712075..38714163-chr19:38804604..38806382,2	K562	blood:
33	chr19:38759354..38761774-chr19:38815692..38818427,2	K562	blood:
34	chr19:38753031..38764322-chr19:38787496..38798494,54	MCF-7	breast:
35	chr19:38789522..38790555-chr19:38811884..38812916,56	MCF-7	breast:
36	chr19:38802009..38804221-chr19:38806405..38809236,2	K562	blood:
37	chr19:38808796..38810665-chr19:38878393..38880605,3	MCF-7	breast:
38	chr19:38794775..38795460-chr3:119814356..119814863,2	Hela-S3	cervix:
39	chr19:38810024..38812525-chr19:38892478..38895075,3	MCF-7	breast:
40	chr15:43662884..43663770-chr19:38795192..38796060,2	Hela-S3	cervix:
41	chr19:38746805..38747381-chr19:38795459..38796438,2	K562	blood:
42	chr19:38718266..38721870-chr19:38794040..38798765,4	MCF-7	breast:
43	chr19:38806279..38807928-chr19:38863720..38866328,2	K562	blood:
44	chr19:38805296..38807779-chr19:38877097..38880049,2	K562	blood:
45	chr19:38755242..38758154-chr19:38804246..38806924,2	K562	blood:
46	chr19:38795165..38795875-chrX:100650150..100651016,2	Hela-S3	cervix:
47	chr19:38744771..38747370-chr19:38793659..38796631,3	MCF-7	breast:
48	chr19:38746183..38748575-chr19:38806704..38809483,2	K562	blood:
49	chr19:38793175..38794787-chr19:38818413..38820106,2	MCF-7	breast:
50	chr19:38789246..38790528-chr19:38811922..38812923,16	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPINT2-1	chr19:38794995-38795130	NONHSAT066202
2	lnc-KCNK6-1	chr19:38822274-38822716	ENSG00000268913.1
3	lnc-SPINT2-1	chr19:38795486-38795677	NONHSAT066202
4	lnc-SPINT2-1	chr19:38795485-38795646	NONHSAT066201
5	lnc-SPINT2-1	chr19:38795205-38795326	NONHSAT066201
6	lnc-SPINT2-1	chr19:38794913-38795130	NONHSAT066201
7	lnc-SPINT2-1	chr19:38795206-38795326	NONHSAT066202

No data

Variant related genes	Relation type
CATSPERG	TF binding region
YIF1B	TF binding region
ENSG00000268913	TF binding region
KCNK6	TF binding region
C19orf33	TF binding region
CATSPERG	CpG island
YIF1B	CpG island
ENSG00000268913	CpG island
KCNK6	CpG island
C19orf33	CpG island
ENSG00000267598	chromatin interactions
ENSG00000104823	chromatin interactions
ENSG00000099338	chromatin interactions
ENSG00000267090	chromatin interactions
ENSG00000266963	chromatin interactions
ENSG00000179168	chromatin interactions
ENSG00000099337	chromatin interactions
ENSG00000188766	chromatin interactions
ENSG00000140006	chromatin interactions
ENSG00000105738	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000006704	chromatin interactions
ENSG00000136238	chromatin interactions
ENSG00000099341	chromatin interactions
ENSG00000200209	chromatin interactions
ENSG00000011332	chromatin interactions
ENSG00000130244	chromatin interactions
ENSG00000137822	chromatin interactions
ENSG00000140265	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000167641	chromatin interactions
ENSG00000272195	chromatin interactions
ENSG00000267748	chromatin interactions
ENSG00000171804	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000167645	chromatin interactions
ENSG00000167644	chromatin interactions
ENSG00000167642	chromatin interactions
ENSG00000175087	chromatin interactions
ENSG00000242622	chromatin interactions

Extended variants
information (count: 1381 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1381 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532142028	chr19:38790015-38790016	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs141550730	chr19:38790023-38790024	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs187410897	chr19:38790048-38790049	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs146171696	chr19:38790098-38790099	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs537588872	chr19:38790152-38790153	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs139205244	chr19:38790201-38790202	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs536131667	chr19:38790232-38790233	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs569792763	chr19:38790254-38790255	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs530643219	chr19:38790308-38790309	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs375077444	chr19:38790318-38790319	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs549197980	chr19:38790321-38790322	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs191750454	chr19:38790338-38790339	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs144041639	chr19:38790358-38790359	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs553439183	chr19:38790413-38790414	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs75394771	chr19:38790500-38790501	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs568728765	chr19:38790539-38790540	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs535518069	chr19:38790579-38790580	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs556915473	chr19:38790589-38790590	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs201070743	chr19:38790629-38790630	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs35436012	chr19:38790635-38790636	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534686775	chr19:38790740-38790741	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs545908133	chr19:38790741-38790742	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs150888339	chr19:38790770-38790771	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs183163680	chr19:38790777-38790778	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs187053643	chr19:38790786-38790787	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs556256314	chr19:38790799-38790800	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs34966655	chr19:38790800-38790801	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs541211082	chr19:38790824-38790825	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs374196966	chr19:38790828-38790829	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs529978464	chr19:38790829-38790830	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs375226524	chr19:38790840-38790841	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs563286478	chr19:38790855-38790856	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs553302514	chr19:38790872-38790873	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs139348936	chr19:38790879-38790880	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs190338524	chr19:38790895-38790896	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs557136179	chr19:38790899-38790900	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs528723024	chr19:38790908-38790909	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs547158322	chr19:38790913-38790914	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs368280930	chr19:38790919-38790920	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs536169491	chr19:38790929-38790930	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs113205923	chr19:38790930-38790931	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs550828733	chr19:38790935-38790936	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs568920858	chr19:38790971-38790972	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs539444282	chr19:38791017-38791018	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs575430747	chr19:38791044-38791045	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs34992016	chr19:38791055-38791056	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150068237	chr19:38791082-38791083	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs182109290	chr19:38791083-38791084	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs577948529	chr19:38791106-38791107	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs71165533	chr19:38791125-38791126	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2152 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38765800-38794800	Weak transcription	Small Intestine	intestine
2	chr19:38769200-38791200	Weak transcription	Fetal Kidney	kidney
3	chr19:38769400-38795200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr19:38771400-38805800	Weak transcription	Right Atrium	heart
5	chr19:38775800-38791000	Weak transcription	Liver	Liver
6	chr19:38777000-38791200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:38781000-38794400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr19:38781200-38795800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr19:38781200-38805800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr19:38781400-38795400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr19:38781400-38797800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr19:38781600-38795600	Weak transcription	Right Ventricle	heart
13	chr19:38782000-38806000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr19:38782200-38791200	Weak transcription	NHDF-Ad	bronchial
15	chr19:38782400-38798000	Weak transcription	Fetal Thymus	thymus
16	chr19:38782600-38796400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr19:38782800-38791200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr19:38782800-38791200	Weak transcription	Stomach Mucosa	stomach
19	chr19:38783000-38794200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr19:38783000-38795600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr19:38783200-38794200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr19:38783400-38797000	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr19:38783600-38791400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr19:38783600-38795200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:38784000-38791200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr19:38784000-38794600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr19:38784000-38797200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr19:38784000-38805800	Weak transcription	Primary B cells from cord blood	blood
29	chr19:38784200-38790400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr19:38784200-38790800	Weak transcription	Colonic Mucosa	Colon
31	chr19:38784200-38791200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr19:38784200-38791200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr19:38784200-38793400	Weak transcription	Lung	lung
34	chr19:38784200-38794200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr19:38784200-38794400	Weak transcription	Thymus	Thymus
36	chr19:38784400-38791200	Weak transcription	Pancreas	Pancrea
37	chr19:38784400-38794400	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr19:38785200-38791200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr19:38785200-38795200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:38785200-38795400	Weak transcription	Primary T cells from cord blood	blood
41	chr19:38785200-38795400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:38785400-38791200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:38785400-38791200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr19:38785400-38791400	Weak transcription	Spleen	Spleen
45	chr19:38785400-38794200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr19:38785400-38794400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr19:38785400-38794600	Weak transcription	Brain Substantia Nigra	brain
48	chr19:38785400-38794800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr19:38785400-38795400	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr19:38785400-38797000	Weak transcription	Brain Anterior Caudate	brain

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