Variant report

Variant	nsv963071
Chromosome Location	chr19:53401720-53480869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1720)
CpG islands
(count:2503)
Chromatin interactive
region (count:70)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53438785-53438996	K562	blood:	n/a	n/a
2	ARID3A	chr19:53427687-53427726	K562	blood:	n/a	n/a
3	ARID3A	chr19:53466088-53466530	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:53448491-53448825	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:53439543-53440078	K562	blood:	n/a	n/a
6	ATF1	chr19:53465981-53466307	K562	blood:	n/a	n/a
7	ATF1	chr19:53427511-53427796	K562	blood:	n/a	n/a
8	ATF1	chr19:53445658-53445970	K562	blood:	n/a	n/a
9	ATF1	chr19:53439468-53440101	K562	blood:	n/a	n/a
10	ATF1	chr19:53426298-53426976	K562	blood:	n/a	n/a
11	ATF2	chr19:53426188-53426746	GM12878	blood:	n/a	n/a
12	ATF2	chr19:53446151-53446509	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr19:53427509-53427761	K562	blood:	n/a	n/a
14	ATF3	chr19:53465957-53466240	K562	blood:	n/a	chr19:53466205-53466214
15	ATF3	chr19:53438666-53438971	K562	blood:	n/a	n/a
16	ATF3	chr19:53439515-53439954	K562	blood:	n/a	n/a
17	BACH1	chr19:53445548-53445553	K562	blood:	n/a	n/a
18	BACH1	chr19:53426291-53426669	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:53426374-53426640	K562	blood:	n/a	n/a
20	BACH1	chr19:53439760-53439843	K562	blood:	n/a	n/a
21	BACH1	chr19:53465691-53466190	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr19:53407016-53407286	GM12878	blood:	n/a	n/a
23	BATF	chr19:53445654-53445924	GM12878	blood:	n/a	n/a
24	BATF	chr19:53439573-53440019	GM12878	blood:	n/a	chr19:53439829-53439840
25	BATF	chr19:53439647-53439948	GM12878	blood:	n/a	chr19:53439829-53439840
26	BCL11A	chr19:53428812-53428959	GM12878	blood:	n/a	n/a
27	BCL3	chr19:53426498-53426869	GM12878	blood:	n/a	chr19:53426812-53426821 chr19:53426810-53426823
28	BCL3	chr19:53439413-53440163	K562	blood:	n/a	n/a
29	BCLAF1	chr19:53426282-53426729	GM12878	blood:	n/a	chr19:53426424-53426433
30	BCLAF1	chr19:53465490-53466576	GM12878	blood:	n/a	n/a
31	BHLHE40	chr19:53446322-53446350	GM12878	blood:	n/a	n/a
32	BHLHE40	chr19:53439408-53439921	GM12878	blood:	n/a	n/a
33	BHLHE40	chr19:53465427-53465574	GM12878	blood:	n/a	n/a
34	BHLHE40	chr19:53445587-53445985	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:53426291-53426835	GM12878	blood:	n/a	n/a
36	BHLHE40	chr19:53465882-53466722	GM12878	blood:	n/a	n/a
37	BHLHE40	chr19:53446241-53446457	K562	blood:	n/a	n/a
38	BHLHE40	chr19:53445617-53445876	K562	blood:	n/a	n/a
39	BHLHE40	chr19:53427608-53427722	K562	blood:	n/a	n/a
40	BHLHE40	chr19:53426214-53426710	K562	blood:	n/a	n/a
41	BHLHE40	chr19:53465669-53466180	K562	blood:	n/a	n/a
42	BHLHE40	chr19:53445643-53445853	HepG2	liver:	n/a	n/a
43	BHLHE40	chr19:53439437-53440064	K562	blood:	n/a	n/a
44	BRCA1	chr19:53426170-53426696	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr19:53465687-53465948	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr19:53446180-53446288	GM12878	blood:	n/a	n/a
47	BRCA1	chr19:53465707-53466366	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr19:53426297-53426678	HepG2	liver:	n/a	n/a
49	BRCA1	chr19:53426334-53426571	GM12878	blood:	n/a	n/a
50	CBX3	chr19:53463851-53464227	K562	blood:	n/a	n/a

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53466188-53466238	BE2_C	brain:	n/a
2	chr19:53446053-53446103	Hepatocyte	liver:	n/a
3	chr19:53466188-53466238	BE2_C	brain:	n/a
4	chr19:53446053-53446103	Hepatocyte	liver:	n/a
5	chr19:53447272-53447322	AG10803	skin:	n/a
6	chr19:53446053-53446103	SK-N-SH_RA	brain:	n/a
7	chr19:53445886-53445936	BJ	skin:	n/a
8	chr19:53466355-53466405	PFSK-1	brain:	n/a
9	chr19:53446053-53446103	AG04450	lung:	fetal
10	chr19:53466322-53466372	IMR90	lung:	fetal
11	chr19:53466924-53466974	LNCaP	prostate:	n/a
12	chr19:53403009-53403059	PANC-1	pancreas:	n/a
13	chr19:53445693-53445743	SAEC	small airway:	n/a
14	chr19:53466924-53466974	NT2-D1	testis:	n/a
15	chr19:53466355-53466405	HMEC	breast:	n/a
16	chr19:53432372-53432422	Caco-2	colon:	n/a
17	chr19:53430697-53430747	SKMC	muscle:	n/a
18	chr19:53466177-53466227	U87	brain:	n/a
19	chr19:53466522-53466572	HEK293	kidney:	embryo
20	chr19:53466313-53466363	CMK	blood:	n/a
21	chr19:53446957-53447007	GM12878	blood:	n/a
22	chr19:53429005-53429055	ECC-1	luminal epithelium:	n/a
23	chr19:53465962-53466012	RPTEC	kidney:	n/a
24	chr19:53449742-53449792	PANC-1	pancreas:	n/a
25	chr19:53429005-53429055	SAEC	small airway:	n/a
26	chr19:53463435-53463485	U87	brain:	n/a
27	chr19:53466322-53466372	LNCaP	prostate:	n/a
28	chr19:53445693-53445743	SK-N-MC	brain:	n/a
29	chr19:53465962-53466012	ProgFib	skin:	n/a
30	chr19:53466210-53466260	NHDF-neo	bronchial:	n/a
31	chr19:53429005-53429055	Hela-S3	cervix:	n/a
32	chr19:53449742-53449792	GM19239	blood:	n/a
33	chr19:53466177-53466227	BJ	skin:	n/a
34	chr19:53466020-53466070	AG04450	lung:	fetal
35	chr19:53424670-53424720	A549	lung:	n/a
36	chr19:53466414-53466464	K562	blood:	n/a
37	chr19:53432372-53432422	AG04450	lung:	fetal
38	chr19:53445886-53445936	AG09309	skin:	n/a
39	chr19:53465759-53465809	H1-hESC	embryonic stem cell:	embryo
40	chr19:53449742-53449792	CMK	blood:	n/a
41	chr19:53466411-53466461	GM06990	blood:	n/a
42	chr19:53426233-53426283	RPTEC	kidney:	n/a
43	chr19:53426802-53426852	GM19239	blood:	n/a
44	chr19:53403009-53403059	AG09309	skin:	n/a
45	chr19:53465759-53465809	ProgFib	skin:	n/a
46	chr19:53466313-53466363	BE2_C	brain:	n/a
47	chr19:53466414-53466464	RPTEC	kidney:	n/a
48	chr19:53465759-53465809	ECC-1	luminal epithelium:	n/a
49	chr19:53463943-53463993	SK-N-SH_RA	brain:	n/a
50	chr19:53466205-53466255	CMK	blood:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:53425712..53428139-chr19:53470752..53473566,2	MCF-7	breast:
2	chr19:53424714..53426568-chr19:53443432..53446550,3	MCF-7	breast:
3	chr19:53424975..53429001-chr19:53430174..53432512,3	K562	blood:
4	chr19:53424791..53427731-chr19:53464365..53467863,4	K562	blood:
5	chr19:53424791..53427731-chr19:53464365..53467863,4	K562	blood:
6	chr19:53399381..53402083-chr19:53412934..53414945,2	K562	blood:
7	chr17:42976466..42977111-chr19:53465593..53466359,2	Hela-S3	cervix:
8	chr19:53400554..53402197-chr19:53402529..53405491,2	MCF-7	breast:
9	chr19:53398490..53401733-chr19:53415760..53419901,4	K562	blood:
10	chr19:53431907..53434266-chr19:53444043..53446544,2	K562	blood:
11	chr19:53437779..53441076-chr19:53444311..53446958,6	K562	blood:
12	chr19:53412333..53414642-chr19:53425536..53427807,2	K562	blood:
13	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
14	chr19:53425069..53426727-chr19:53438910..53441039,3	K562	blood:
15	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
16	chr19:53451271..53453320-chr19:53454303..53456994,2	K562	blood:
17	chr19:53466473..53468381-chr19:53486482..53488386,2	K562	blood:
18	chr19:53449805..53452589-chr19:53464374..53466061,2	K562	blood:
19	chr19:53193334..53193838-chr19:53445297..53445972,2	Hela-S3	cervix:
20	chr19:53425636..53428538-chr19:53430721..53433929,3	K562	blood:
21	chr19:53426133..53428640-chr19:53444456..53447019,4	K562	blood:
22	chr19:53448312..53450113-chr19:53462746..53464266,2	K562	blood:
23	chr19:53451271..53453320-chr19:53454303..53456994,2	K562	blood:
24	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:
25	chr19:53458629..53461334-chr19:53495280..53497421,2	K562	blood:
26	chr19:53400711..53402486-chr19:53463191..53466156,2	K562	blood:
27	chr19:53454155..53456925-chr19:53458863..53460745,2	K562	blood:
28	chr19:53461531..53463196-chr19:53464359..53466216,2	K562	blood:
29	chr19:53418400..53422745-chr19:53423096..53427800,7	K562	blood:
30	chr19:53465551..53467815-chr19:53472678..53475651,2	K562	blood:
31	chr19:53454155..53456925-chr19:53458863..53460745,2	K562	blood:
32	chr19:53458468..53461389-chr19:53462231..53466240,5	K562	blood:
33	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
34	chr19:53431907..53434266-chr19:53444043..53446544,2	K562	blood:
35	chr19:53419869..53422803-chr19:53423217..53426977,4	K562	blood:
36	chr19:53464438..53467826-chr19:53467828..53472633,5	K562	blood:
37	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
38	chr19:53465551..53467815-chr19:53472678..53475651,2	K562	blood:
39	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
40	chr19:53451089..53454198-chr19:53462086..53466975,4	K562	blood:
41	chr19:53399445..53402130-chr19:53440139..53442366,2	K562	blood:
42	chr19:53466302..53467987-chr19:53468520..53470453,2	K562	blood:
43	chr19:53399145..53401987-chr19:53438300..53441406,3	K562	blood:
44	chr19:53448784..53451468-chr19:53451861..53454051,2	K562	blood:
45	chr19:53438104..53442400-chr19:53444179..53446884,10	K562	blood:
46	chr19:53426133..53428140-chr19:53445241..53446971,2	K562	blood:
47	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
48	chr11:62608903..62609637-chr19:53426135..53426686,2	Hela-S3	cervix:
49	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
50	chr19:53478537..53481849-chr19:53482363..53484640,3	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-1	chr19:53445794-53445847	NR_037805
2	lnc-ZNF816-1	chr19:53430388-53432667	NR_037805
3	lnc-ZNF816-2	chr19:53474015-53474095	NONHSAT067609
4	lnc-VN1R2-12	chr19:53426926-53427328	ENSG00000269646.1
5	lnc-VN1R2-12	chr19:53426635-53426717	ENSG00000269646.1
6	lnc-ZNF816-2	chr19:53473636-53474095	NONHSAT067606
7	lnc-ZNF701-2	chr19:53451420-53453256	ucscGeneNc_uc002pik_2
8	lnc-ZNF816-2	chr19:53459294-53459357	ENSG00000269082.1
9	lnc-ZNF816-2	chr19:53477295-53477406	NONHSAT067610
10	lnc-ZNF816-2	chr19:53473877-53474095	ENSG00000269082.1
11	lnc-ZNF701-2	chr19:53452837-53452889	NONHSAT067586
12	lnc-ZNF816-2	chr19:53478626-53479053	NONHSAT067611
13	lnc-ZNF701-2	chr19:53450758-53450863	ucscGeneNc_uc002pik_2

No data

Variant related genes	Relation type
ZNF321P	TF binding region
ZNF320	TF binding region
ENSG00000269646	TF binding region
ZNF888	TF binding region
ZNF816-ZNF321P	TF binding region
ZNF702P	TF binding region
ZNF816	TF binding region
ZNF321P	CpG island
ZNF320	CpG island
ENSG00000269646	CpG island
ZNF888	CpG island
ZNF816-ZNF321P	CpG island
ZNF702P	CpG island
ZNF816	CpG island
ENSG00000180257	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000213801	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000204611	chromatin interactions
ENSG00000108883	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000167131	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000182986	chromatin interactions

Extended variants
information (count: 3764 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3764 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374624288	chr19:53401730-53401731	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs34723703	chr19:53401734-53401735	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs183016692	chr19:53401751-53401752	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs11881877	chr19:53401760-53401761	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs562503161	chr19:53401768-53401769	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs78759530	chr19:53401778-53401779	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs541893796	chr19:53401801-53401802	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs187585408	chr19:53401844-53401845	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs535793374	chr19:53401853-53401854	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs527814030	chr19:53401854-53401855	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs8101252	chr19:53401856-53401857	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs11670402	chr19:53401959-53401960	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531497038	chr19:53401964-53401965	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs146342597	chr19:53401965-53401966	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs117654508	chr19:53401978-53401979	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs535462382	chr19:53402025-53402026	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs537515389	chr19:53402026-53402027	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs547477896	chr19:53402039-53402040	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs565760957	chr19:53402066-53402067	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs371810780	chr19:53402077-53402078	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs193281782	chr19:53402083-53402084	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs184657433	chr19:53402090-53402091	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs537368343	chr19:53402110-53402111	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs544128733	chr19:53402130-53402131	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs59622413	chr19:53402131-53402132	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs28415685	chr19:53402132-53402133	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs556462575	chr19:53402144-53402145	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs574457983	chr19:53402156-53402157	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs541806230	chr19:53402166-53402167	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs8102523	chr19:53402193-53402194	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs550449695	chr19:53402217-53402218	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs568727932	chr19:53402264-53402265	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs371591855	chr19:53402289-53402290	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs377249191	chr19:53402297-53402298	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs143426987	chr19:53402312-53402313	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs8101864	chr19:53402384-53402385	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553769902	chr19:53402390-53402391	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs531535372	chr19:53402440-53402441	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs543710058	chr19:53402443-53402444	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs561976265	chr19:53402453-53402454	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs529235437	chr19:53402468-53402469	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs146270166	chr19:53402479-53402480	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs565722293	chr19:53402483-53402484	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs549693264	chr19:53402490-53402491	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs532850222	chr19:53402538-53402539	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs374201164	chr19:53402544-53402545	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs551460447	chr19:53402564-53402565	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs570929757	chr19:53402602-53402603	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs538449657	chr19:53402623-53402624	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs556373908	chr19:53402631-53402632	Weak transcription Enhancers	Chromatin interactive region	3 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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3286 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53399600-53401800	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr19:53399800-53402000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr19:53400000-53401800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr19:53400200-53402000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr19:53400400-53401800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:53401000-53401800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:53401000-53405200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:53401000-53407200	Weak transcription	Gastric	stomach
9	chr19:53401000-53425600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:53401200-53401800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr19:53401200-53401800	Flanking Active TSS	Brain Cingulate Gyrus	brain
12	chr19:53401200-53402000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr19:53401200-53402000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr19:53401200-53409800	Weak transcription	Small Intestine	intestine
15	chr19:53401400-53401800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr19:53401400-53401800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr19:53401400-53401800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr19:53401400-53401800	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr19:53401400-53401800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr19:53401400-53401800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr19:53401400-53401800	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr19:53401400-53401800	Enhancers	Fetal Brain Male	brain
23	chr19:53401400-53401800	Flanking Active TSS	Fetal Muscle Trunk	muscle
24	chr19:53401400-53401800	Enhancers	Left Ventricle	heart
25	chr19:53401400-53401800	ZNF genes & repeats	HMEC	breast
26	chr19:53401400-53402000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
27	chr19:53401400-53402000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr19:53401400-53402000	ZNF genes & repeats	Fetal Thymus	thymus
29	chr19:53401400-53408800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr19:53401400-53409200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:53401400-53409200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr19:53401400-53409200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr19:53401400-53409200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr19:53401400-53409200	Weak transcription	Ovary	ovary
35	chr19:53401400-53409200	Weak transcription	NH-A	brain
36	chr19:53401400-53409400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr19:53401400-53409400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr19:53401400-53409400	Weak transcription	Fetal Lung	lung
39	chr19:53401400-53409400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr19:53401400-53410400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:53401400-53410600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:53401400-53410600	Weak transcription	Aorta	Aorta
43	chr19:53401400-53410600	Weak transcription	HUVEC	blood vessel
44	chr19:53401400-53411800	Weak transcription	Fetal Intestine Small	intestine
45	chr19:53401400-53425600	Weak transcription	NHDF-Ad	bronchial
46	chr19:53401400-53425800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr19:53401600-53401800	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr19:53401600-53401800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr19:53401600-53401800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr19:53401600-53401800	Enhancers	Primary T helper cells fromperipheralblood	blood

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