Variant report

Variant	nsv817861
Chromosome Location	chr19:53484032-53505860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:794)
Chromatin interactive
region (count:6)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53497019-53497409	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr19:53497048-53497179	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr19:53487980-53488326	K562	blood:	n/a	n/a
4	CBX3	chr19:53490152-53490462	K562	blood:	n/a	n/a
5	CBX3	chr19:53496785-53497423	K562	blood:	n/a	n/a
6	CEBPB	chr19:53503344-53503663	HepG2	liver:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
7	CEBPB	chr19:53494299-53494580	HepG2	liver:	n/a	chr19:53494449-53494460
8	CEBPB	chr19:53494294-53494605	K562	blood:	n/a	chr19:53494449-53494460
9	CEBPB	chr19:53494404-53494593	H1-hESC	embryonic stem cell:	n/a	chr19:53494449-53494460
10	CEBPB	chr19:53499048-53499248	K562	blood:	n/a	n/a
11	CEBPB	chr19:53503339-53503575	IMR90	lung:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
12	CEBPB	chr19:53494277-53495058	Hela-S3	cervix:	n/a	chr19:53494449-53494460
13	CEBPB	chr19:53494284-53494605	IMR90	lung:	n/a	chr19:53494449-53494460
14	CEBPB	chr19:53503242-53503648	K562	blood:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
15	CHD2	chr19:53496834-53497202	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr19:53496660-53497280	K562	blood:	n/a	n/a
17	CTCF	chr19:53496960-53497110	BE2_C	brain:	n/a	n/a
18	CTCF	chr19:53496980-53497130	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr19:53496855-53497092	ProgFib	skin:	n/a	n/a
20	CTCF	chr19:53497232-53497429	ProgFib	skin:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
21	CTCF	chr19:53496892-53497057	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:53497240-53497390	AG04449	skin:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
23	CTCF	chr19:53484700-53484850	HCPEpiC	choroid plexus:	n/a	chr19:53484768-53484781
24	CTCF	chr19:53497220-53497370	K562	blood:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
25	CTCF	chr19:53496700-53496850	NHEK	skin:	n/a	n/a
26	CTCF	chr19:53496980-53497130	AG10803	skin:	n/a	n/a
27	CTCF	chr19:53496720-53496870	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr19:53497195-53497392	SK-N-SH_RA	brain:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
29	CTCF	chr19:53496960-53497110	GM12868	blood:	n/a	n/a
30	CTCF	chr19:53497000-53497150	HMF	breast:	n/a	n/a
31	CTCF	chr19:53496860-53497150	HRE	kidney:	n/a	n/a
32	CTCF	chr19:53496853-53497088	GM10248	blood:	n/a	n/a
33	CTCF	chr19:53496785-53497085	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr19:53496980-53497130	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr19:53497000-53497150	GM12872	blood:	n/a	n/a
36	CTCF	chr19:53497266-53497379	MCF-7	breast:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
37	CTCF	chr19:53485340-53485382	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr19:53496940-53497090	GM12869	blood:	n/a	n/a
39	CTCF	chr19:53485274-53485470	K562	blood:	n/a	n/a
40	CTCF	chr19:53496980-53497130	GM12870	blood:	n/a	n/a
41	CTCF	chr19:53497240-53497390	HL-60	blood:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
42	CTCF	chr19:53497400-53497409	LNCaP	prostate:	n/a	n/a
43	CTCF	chr19:53496960-53497110	GM12867	blood:	n/a	n/a
44	CTCF	chr19:53497292-53497349	MCF-7	breast:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
45	CTCF	chr19:53496740-53496890	HCT-116	colon:	n/a	n/a
46	CTCF	chr19:53497220-53497370	AG04450	lung:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
47	CTCF	chr19:53496766-53497078	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr19:53497220-53497370	AoAF	blood vessel:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
49	CTCF	chr19:53496720-53496870	GM12873	blood:	n/a	n/a
50	CTCF	chr19:53497220-53497370	WERI-Rb-1	eye:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53493775-53493825	HAEpiC	amniotic membrane:	n/a
2	chr19:53493775-53493825	HAEpiC	amniotic membrane:	n/a
3	chr19:53497281-53497331	NHDF-neo	bronchial:	n/a
4	chr19:53493775-53493825	PANC-1	pancreas:	n/a
5	chr19:53493775-53493825	ovcar-3	ovarian:	n/a
6	chr19:53496846-53496896	SK-N-MC	brain:	n/a
7	chr19:53496835-53496885	AG04449	skin:	fetal
8	chr19:53496738-53496788	SK-N-MC	brain:	n/a
9	chr19:53496695-53496745	T-47D	breast:	n/a
10	chr19:53496440-53496490	HEK293	kidney:	embryo
11	chr19:53496738-53496788	SK-N-SH	brain:	n/a
12	chr19:53496893-53496943	Jurkat	blood:	n/a
13	chr19:53496440-53496490	HAEpiC	amniotic membrane:	n/a
14	chr19:53496695-53496745	HEEpiC	esophagus:	n/a
15	chr19:53496695-53496745	H1-hESC	embryonic stem cell:	embryo
16	chr19:53496664-53496714	SK-N-MC	brain:	n/a
17	chr19:53496738-53496788	HEEpiC	esophagus:	n/a
18	chr19:53496846-53496896	HAEpiC	amniotic membrane:	n/a
19	chr19:53496695-53496745	HIPEpiC	eye:	n/a
20	chr19:53496893-53496943	A549	lung:	n/a
21	chr19:53500997-53501047	SKMC	muscle:	n/a
22	chr19:53496664-53496714	HRCEpiC	kidney:	n/a
23	chr19:53493775-53493825	AG10803	skin:	n/a
24	chr19:53497048-53497098	GM12892	blood:	n/a
25	chr19:53497027-53497077	RPTEC	kidney:	n/a
26	chr19:53493775-53493825	Hepatocyte	liver:	n/a
27	chr19:53497027-53497077	Hepatocyte	liver:	n/a
28	chr19:53497281-53497331	BJ	skin:	n/a
29	chr19:53500997-53501047	HRCEpiC	kidney:	n/a
30	chr19:53496440-53496490	HCF	heart:	n/a
31	chr19:53496695-53496745	SAEC	small airway:	n/a
32	chr19:53493775-53493825	RPTEC	kidney:	n/a
33	chr19:53496893-53496943	AG04449	skin:	fetal
34	chr19:53496893-53496943	HepG2	liver:	n/a
35	chr19:53497048-53497098	AG09319	gingival:	n/a
36	chr19:53496738-53496788	AG09309	skin:	n/a
37	chr19:53496695-53496745	ProgFib	skin:	n/a
38	chr19:53497048-53497098	Hela-S3	cervix:	n/a
39	chr19:53496440-53496490	GM06990	blood:	n/a
40	chr19:53496893-53496943	NT2-D1	testis:	n/a
41	chr19:53497281-53497331	NB4	blood:	n/a
42	chr19:53496846-53496896	RPTEC	kidney:	n/a
43	chr19:53493775-53493825	GM19239	blood:	n/a
44	chr19:53496846-53496896	Hela-S3	cervix:	n/a
45	chr19:53493775-53493825	HCT-116	colon:	n/a
46	chr19:53497027-53497077	GM12891	blood:	n/a
47	chr19:53496695-53496745	HepG2	liver:	n/a
48	chr19:53500997-53501047	AoSMC	blood vessel:	n/a
49	chr19:53497281-53497331	SK-N-SH_RA	brain:	n/a
50	chr19:53496835-53496885	PFSK-1	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53482347..53484833-chr19:53488292..53490832,2	K562	blood:
2	chr19:53482347..53484833-chr19:53488292..53490832,2	K562	blood:
3	chr19:53466473..53468381-chr19:53486482..53488386,2	K562	blood:
4	chr19:53478537..53481849-chr19:53482363..53484640,3	K562	blood:
5	chr14:77866421..77867168-chr19:53501795..53502295,2	MCF-7	breast:
6	chr19:53465058..53468377-chr19:53495533..53497921,4	K562	blood:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-2	chr19:53484145-53484225	NONHSAT067611
2	lnc-ZNF816-2	chr19:53489819-53490099	NONHSAT067619
3	lnc-ZNF816-2	chr19:53484195-53484225	NONHSAT067615
4	lnc-VN1R2-11	chr19:53485444-53485548	NONHSAT067616
5	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067618
6	lnc-ZNF816-2	chr19:53496733-53496784	NONHSAT067619
7	lnc-ZNF816-2	chr19:53484775-53484797	NONHSAT067606
8	lnc-ZNF816-2	chr19:53484145-53484225	NONHSAT067606
9	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067614
10	lnc-ZNF816-2	chr19:53496733-53496784	NONHSAT067612
11	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067610
12	lnc-ZNF816-2	chr19:53484013-53484225	NONHSAT067614
13	lnc-ZNF816-2	chr19:53489705-53490099	NONHSAT067618
14	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067609
15	lnc-ZNF816-2	chr19:53496733-53496778	NONHSAT067611
16	lnc-ZNF816-2	chr19:53484775-53484907	ENSG00000269082.1
17	lnc-ZNF816-2	chr19:53484089-53484225	NONHSAT067610
18	lnc-ZNF816-2	chr19:53484145-53484225	NONHSAT067609
19	lnc-ZNF816-2	chr19:53489828-53489972	NONHSAT067617
20	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067612
21	lnc-ZNF816-2	chr19:53484089-53484225	ENSG00000269082.1
22	lnc-ZNF816-2	chr19:53484145-53484225	NONHSAT067612
23	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067619
24	lnc-ZNF816-2	chr19:53484145-53484225	NONHSAT067613
25	lnc-ZNF816-2	chr19:53489828-53490101	NONHSAT067615
26	lnc-ZNF816-2	chr19:53486092-53486512	NONHSAT067617
27	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067613
28	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067618
29	lnc-ZNF816-2	chr19:53493663-53493785	NONHSAT067619
30	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067609
31	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067609
32	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067610
33	lnc-ZNF816-2	chr19:53496733-53496767	NONHSAT067614
34	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067611
35	lnc-VN1R2-11	chr19:53488013-53488207	NONHSAT067616

No data

Variant related genes	Relation type
ENSG00000268282	TF binding region
ENSG00000267943	TF binding region
ENSG00000269082	TF binding region
ZNF702P	TF binding region
ENSG00000268282	CpG island
ENSG00000267943	CpG island
ENSG00000269082	CpG island
ZNF702P	CpG island
ENSG00000221874	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000180257	chromatin interactions

Extended variants
information (count: 1013 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2015565	chr19:53484032-53484033	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563715155	chr19:53484039-53484040	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs145074322	chr19:53484040-53484041	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs549527405	chr19:53484055-53484056	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs150981458	chr19:53484062-53484063	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs375635087	chr19:53484071-53484072	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs35901395	chr19:53484076-53484077	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs374040028	chr19:53484081-53484082	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs376167474	chr19:53484083-53484084	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs546487299	chr19:53484087-53484088	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs571470387	chr19:53484126-53484127	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs538601347	chr19:53484127-53484128	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs329728	chr19:53484142-53484143	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs568545227	chr19:53484155-53484156	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs535918276	chr19:53484164-53484165	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs183377508	chr19:53484195-53484196	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs111415990	chr19:53484202-53484203	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs146287450	chr19:53484234-53484235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs370400312	chr19:53484235-53484236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs398121084	chr19:53484246-53484247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188386501	chr19:53484318-53484319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs369393612	chr19:53484332-53484333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs329727	chr19:53484360-53484361	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs371347915	chr19:53484377-53484378	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs578190782	chr19:53484412-53484413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545752434	chr19:53484413-53484414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4803029	chr19:53484455-53484456	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575681910	chr19:53484481-53484482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs140855558	chr19:53484485-53484486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150154894	chr19:53484487-53484488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528578921	chr19:53484547-53484548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192700471	chr19:53484577-53484578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564972126	chr19:53484578-53484579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532419053	chr19:53484586-53484587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550487318	chr19:53484589-53484590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568831302	chr19:53484591-53484592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369584045	chr19:53484614-53484615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142636338	chr19:53484761-53484762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375611393	chr19:53484765-53484766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535807611	chr19:53484793-53484794	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs547788484	chr19:53484797-53484798	Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs184645543	chr19:53484798-53484799	Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs533693855	chr19:53484805-53484806	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs115499805	chr19:53484812-53484813	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs189215211	chr19:53484819-53484820	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs372290711	chr19:53484827-53484828	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs329726	chr19:53484845-53484846	Strong transcription Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs576017831	chr19:53484893-53484894	Strong transcription Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs544270212	chr19:53484908-53484909	Strong transcription Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs540518763	chr19:53484927-53484928	Strong transcription Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53467000-53489000	Weak transcription	Right Ventricle	heart
2	chr19:53467000-53494600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr19:53467200-53488600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr19:53467200-53489200	Weak transcription	Colon Smooth Muscle	Colon
5	chr19:53467200-53495400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:53471600-53487600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr19:53472600-53489000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr19:53472800-53487800	Weak transcription	Adipose Nuclei	Adipose
9	chr19:53472800-53495800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:53473000-53488000	Weak transcription	K562	blood
11	chr19:53473000-53488600	Weak transcription	Colonic Mucosa	Colon
12	chr19:53473000-53489400	Weak transcription	Brain Anterior Caudate	brain
13	chr19:53473600-53488600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:53473600-53495800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr19:53473800-53487800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr19:53474000-53488200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr19:53474000-53488800	Weak transcription	Fetal Kidney	kidney
18	chr19:53474000-53495800	Weak transcription	Fetal Lung	lung
19	chr19:53474200-53488000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr19:53474200-53488000	Weak transcription	HUVEC	blood vessel
21	chr19:53480200-53487800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr19:53480400-53488200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr19:53481200-53495400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr19:53481400-53484200	Weak transcription	Brain Germinal Matrix	brain
25	chr19:53481800-53487600	Weak transcription	Aorta	Aorta
26	chr19:53482000-53487600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:53482000-53487600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr19:53482000-53487800	Weak transcription	Gastric	stomach
29	chr19:53482000-53489800	Weak transcription	NHLF	lung
30	chr19:53482000-53491200	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr19:53482200-53484200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr19:53482200-53485200	Weak transcription	Pancreas	Pancrea
33	chr19:53482200-53485400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr19:53482200-53485800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr19:53482200-53487600	Weak transcription	Left Ventricle	heart
36	chr19:53482200-53487600	Weak transcription	Spleen	Spleen
37	chr19:53482400-53487400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:53482400-53487600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr19:53482400-53487600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr19:53482600-53487200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr19:53482600-53487200	Weak transcription	Fetal Intestine Small	intestine
42	chr19:53482600-53487600	Weak transcription	Ovary	ovary
43	chr19:53482600-53487800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr19:53482600-53488600	Weak transcription	Fetal Stomach	stomach
45	chr19:53483200-53487400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr19:53483200-53487600	Weak transcription	Placenta	Placenta
47	chr19:53484000-53484800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr19:53484000-53487600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:53484000-53487800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr19:53484200-53487600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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