Variant report

Variant	nsv833894
Chromosome Location	chr20:1519433-1753366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1738)
CpG islands
(count:1647)
Chromatin interactive
region (count:10)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1738 , 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	chr20:1550229-1550409	K562	blood:	n/a	n/a
2	ARID3A	chr20:1617304-1617678	HepG2	liver:	n/a	n/a
3	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
4	ATF1	chr20:1614192-1614501	K562	blood:	n/a	n/a
5	ATF1	chr20:1692944-1693222	K562	blood:	n/a	n/a
6	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
7	ATF2	chr20:1722267-1722650	GM12878	blood:	n/a	n/a
8	ATF2	chr20:1640754-1641281	GM12878	blood:	n/a	n/a
9	ATF2	chr20:1612733-1613271	GM12878	blood:	n/a	n/a
10	ATF2	chr20:1714916-1715539	GM12878	blood:	n/a	n/a
11	ATF2	chr20:1702796-1703222	GM12878	blood:	n/a	n/a
12	ATF2	chr20:1702740-1703371	GM12878	blood:	n/a	n/a
13	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
14	ATF2	chr20:1722240-1722624	GM12878	blood:	n/a	n/a
15	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
16	ATF2	chr20:1640865-1641393	GM12878	blood:	n/a	n/a
17	ATF2	chr20:1645577-1645900	GM12878	blood:	n/a	n/a
18	ATF2	chr20:1645510-1646022	GM12878	blood:	n/a	n/a
19	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
20	ATF2	chr20:1712429-1712884	GM12878	blood:	n/a	n/a
21	ATF2	chr20:1607520-1607935	GM12878	blood:	n/a	n/a
22	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
23	BATF	chr20:1722392-1722620	GM12878	blood:	n/a	n/a
24	BATF	chr20:1642642-1642897	GM12878	blood:	n/a	n/a
25	BATF	chr20:1640943-1641497	GM12878	blood:	n/a	chr20:1641404-1641414
26	BATF	chr20:1628753-1629096	GM12878	blood:	n/a	chr20:1628940-1628951
27	BATF	chr20:1641005-1641263	GM12878	blood:	n/a	n/a
28	BATF	chr20:1715118-1715429	GM12878	blood:	n/a	n/a
29	BATF	chr20:1638736-1639011	GM12878	blood:	n/a	n/a
30	BATF	chr20:1712545-1712765	GM12878	blood:	n/a	n/a
31	BATF	chr20:1633644-1633992	GM12878	blood:	n/a	n/a
32	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
33	BATF	chr20:1744965-1745279	GM12878	blood:	n/a	n/a
34	BATF	chr20:1712492-1712872	GM12878	blood:	n/a	n/a
35	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
36	BATF	chr20:1621158-1621494	GM12878	blood:	n/a	n/a
37	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
38	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
39	BATF	chr20:1702831-1703291	GM12878	blood:	n/a	n/a
40	BATF	chr20:1638679-1639013	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:1702831-1703251	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:1722350-1722625	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:1640981-1641251	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:1722347-1722599	GM12878	blood:	n/a	n/a
47	BCL11A	chr20:1645573-1645931	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
48	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a
49	BCL3	chr20:1603087-1603515	GM12878	blood:	n/a	n/a
50	BCL3	chr20:1628817-1629045	GM12878	blood:	n/a	n/a

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1718648-1718698	PFSK-1	brain:	n/a
2	chr20:1715296-1715346	Caco-2	colon:	n/a
3	chr20:1716510-1716560	AG04450	lung:	fetal
4	chr20:1600705-1600755	GM12891	blood:	n/a
5	chr20:1539641-1539691	HEEpiC	esophagus:	n/a
6	chr20:1538671-1538721	SKMC	muscle:	n/a
7	chr20:1600705-1600755	NH-A	brain:	n/a
8	chr20:1719855-1719905	Jurkat	blood:	n/a
9	chr20:1616387-1616437	K562	blood:	n/a
10	chr20:1538353-1538403	GM12878	blood:	n/a
11	chr20:1712396-1712446	GM06990	blood:	n/a
12	chr20:1712396-1712446	Caco-2	colon:	n/a
13	chr20:1601704-1601754	NHBE	bronchial:	n/a
14	chr20:1639250-1639300	HAEpiC	amniotic membrane:	n/a
15	chr20:1600641-1600691	GM19239	blood:	n/a
16	chr20:1538671-1538721	HMEC	breast:	n/a
17	chr20:1546019-1546069	GM06990	blood:	n/a
18	chr20:1539702-1539752	K562	blood:	n/a
19	chr20:1610358-1610408	GM12878	blood:	n/a
20	chr20:1546019-1546069	ProgFib	skin:	n/a
21	chr20:1718648-1718698	BE2_C	brain:	n/a
22	chr20:1715296-1715346	HUVEC	blood vessel:	n/a
23	chr20:1546019-1546069	Hela-S3	cervix:	n/a
24	chr20:1600705-1600755	AG04449	skin:	fetal
25	chr20:1716510-1716560	HL-60	blood:	n/a
26	chr20:1539702-1539752	H1-hESC	embryonic stem cell:	embryo
27	chr20:1639816-1639866	ECC-1	luminal epithelium:	n/a
28	chr20:1538353-1538403	AG09309	skin:	n/a
29	chr20:1538366-1538416	NH-A	brain:	n/a
30	chr20:1600623-1600673	HUVEC	blood vessel:	n/a
31	chr20:1546019-1546069	HCF	heart:	n/a
32	chr20:1639816-1639866	IMR90	lung:	fetal
33	chr20:1712396-1712446	BE2_C	brain:	n/a
34	chr20:1610358-1610408	IMR90	lung:	fetal
35	chr20:1610358-1610408	SK-N-SH	brain:	n/a
36	chr20:1610358-1610408	HL-60	blood:	n/a
37	chr20:1600623-1600673	SK-N-SH	brain:	n/a
38	chr20:1532543-1532593	Hepatocyte	liver:	n/a
39	chr20:1718648-1718698	HL-60	blood:	n/a
40	chr20:1546019-1546069	HCT-116	colon:	n/a
41	chr20:1538366-1538416	SK-N-MC	brain:	n/a
42	chr20:1639325-1639375	HCM	heart:	n/a
43	chr20:1538671-1538721	AG04450	lung:	fetal
44	chr20:1716510-1716560	K562	blood:	n/a
45	chr20:1616387-1616437	GM12892	blood:	n/a
46	chr20:1719855-1719905	AG04450	lung:	fetal
47	chr20:1538353-1538403	NHDF-neo	bronchial:	n/a
48	chr20:1538671-1538721	U87	brain:	n/a
49	chr20:1716632-1716682	Hepatocyte	liver:	n/a
50	chr20:1600705-1600755	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:
2	chr20:1513747..1514348-chr20:1714921..1715422,2	MCF-7	breast:
3	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:
4	chr20:1715128..1715763-chr21:19211991..19212492,2	MCF-7	breast:
5	chr20:1751934..1753765-chr20:1757216..1759111,2	MCF-7	breast:
6	chr20:1484052..1484617-chr20:1714858..1715446,2	MCF-7	breast:
7	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
8	chr20:1744834..1745679-chr20:2073594..2074454,2	MCF-7	breast:
9	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
10	chr20:1489470..1490474-chr20:1714544..1715733,6	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIRPG-4	chr20:1707166-1707494	NONHSAT078128
2	lnc-SIRPA-3	chr20:1617852-1617996	ENSG00000237914
3	lnc-SIRPG-5	chr20:1716454-1716754	l_2058_chr20:1716453-1746293_testes
4	lnc-SIRPA-3	chr20:1614154-1614366	NR_110090
5	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078123
6	lnc-SIRPG-5	chr20:1735039-1735445	l_2058_chr20:1716453-1746293_testes
7	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
8	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078122
9	lnc-SIRPG-4	chr20:1708308-1708392	NONHSAT078128
10	lnc-SIRPG-4	chr20:1703157-1703311	NONHSAT078128
11	lnc-SIRPG-2	chr20:1609798-1610282	NONHSAT078122
12	lnc-SIRPA-3	chr20:1619056-1619100	ENSG00000237914
13	lnc-SIRPG-5	chr20:1739200-1739320	NONHSAT078130
14	lnc-SIRPG-4	chr20:1702011-1702188	NONHSAT078128
15	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
16	lnc-SIRPA-5	chr20:1647006-1647284	NONHSAT078126
17	lnc-SIRPG-5	chr20:1737402-1739586	NONHSAT078131
18	lnc-SIRPA-3	chr20:1617852-1617996	ENSG00000237914
19	lnc-SIRPA-3	chr20:1618264-1618388	ENSG00000237914
20	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121
21	lnc-SIRPG-5	chr20:1746215-1746252	NONHSAT078130
22	lnc-SIRPG-5	chr20:1739757-1739873	l_2058_chr20:1716453-1746293_testes
23	lnc-SIRPG-5	chr20:1739761-1739870	NONHSAT078130
24	lnc-SIRPG-5	chr20:1732626-1732738	l_2058_chr20:1716453-1746293_testes
25	lnc-SIRPG-2	chr20:1610173-1610282	NONHSAT078123
26	lnc-SIRPG-2	chr20:1611060-1611289	NONHSAT078123
27	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
28	lnc-SIRPA-3	chr20:1617852-1617996	NR_110090
29	lnc-SIRPA-3	chr20:1626682-1629119	NR_110090
30	lnc-SIRPG-5	chr20:1739200-1739323	l_2058_chr20:1716453-1746293_testes
31	lnc-SIRPG-5	chr20:1746215-1746293	l_2058_chr20:1716453-1746293_testes
32	lnc-SIRPA-3	chr20:1626682-1629118	ENSG00000237914
33	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1
34	lnc-SIRPA-3	chr20:1614272-1614366	ENSG00000237914
35	lnc-SIRPA-3	chr20:1614154-1614366	ENSG00000237914
36	lnc-SIRPG-5	chr20:1732662-1732738	NONHSAT078130
37	lnc-SIRPG-2	chr20:1611341-1611482	NONHSAT078122

No data

Variant related genes	Relation type
SIRPB3P	TF binding region
SIRPB1	TF binding region
ENSG00000271461	TF binding region
SIRPD	TF binding region
ENSG00000236550	TF binding region
ENSG00000271523	TF binding region
SIRPG	TF binding region
RN7SL561P	TF binding region
ENSG00000237914	TF binding region
ENSG00000260861	TF binding region
ENSG00000234282	TF binding region
ENSG00000242324	TF binding region
SIRPB3P	CpG island
SIRPB1	CpG island
ENSG00000271461	CpG island
SIRPD	CpG island
ENSG00000236550	CpG island
ENSG00000271523	CpG island
SIRPG	CpG island
RN7SL561P	CpG island
ENSG00000237914	CpG island
ENSG00000260861	CpG island
ENSG00000234282	CpG island
ENSG00000242324	CpG island
ENPP4	miRNA target sites
KIAA0831	miRNA target sites
GOLT1B	miRNA target sites
SOX4	miRNA target sites
BMPR2	miRNA target sites
ETV6	miRNA target sites

Extended variants
information (count: 9027 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9027 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35069620	chr20:1519437-1519438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189769515	chr20:1519472-1519473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76079833	chr20:1519504-1519505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6034006	chr20:1519511-1519512	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs535683113	chr20:1519524-1519525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557584524	chr20:1519530-1519531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575867414	chr20:1519543-1519544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537013052	chr20:1519590-1519591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558111624	chr20:1519686-1519687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576457764	chr20:1519750-1519751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540723839	chr20:1519774-1519775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6110385	chr20:1519805-1519806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530952662	chr20:1519838-1519839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2263656	chr20:1519865-1519866	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs6079527	chr20:1520042-1520043	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs183091186	chr20:1520061-1520062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563565589	chr20:1520088-1520089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75452866	chr20:1520093-1520094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556462031	chr20:1520164-1520165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189061799	chr20:1520224-1520225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2263657	chr20:1520233-1520234	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs528539333	chr20:1520239-1520240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547077062	chr20:1520243-1520244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73076985	chr20:1520245-1520246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs113569508	chr20:1520254-1520255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529460113	chr20:1520259-1520260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2263658	chr20:1520272-1520273	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs569465640	chr20:1520301-1520302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202123315	chr20:1520378-1520379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539721009	chr20:1520455-1520456	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs576266895	chr20:1520465-1520466	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs191555587	chr20:1520472-1520473	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs80106327	chr20:1520475-1520476	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs183813636	chr20:1520509-1520510	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs543048458	chr20:1520513-1520514	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs574465440	chr20:1520551-1520552	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs11905059	chr20:1520606-1520607	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs11906723	chr20:1520669-1520670	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575442763	chr20:1520705-1520706	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs187903518	chr20:1520726-1520727	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs148154360	chr20:1520767-1520768	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs79682096	chr20:1520788-1520789	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs540651148	chr20:1520809-1520810	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs191690442	chr20:1520820-1520821	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529350923	chr20:1520827-1520828	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs551079310	chr20:1520830-1520831	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs113359047	chr20:1520834-1520835	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs569347937	chr20:1520836-1520837	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs182735898	chr20:1520862-1520863	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2256520	chr20:1520883-1520884	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:75)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Prostate cancer	21551127	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
Glioma	20126413	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1989 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1516000-1519600	Enhancers	Primary B cells from peripheral blood	blood
2	chr20:1518400-1520400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr20:1518600-1519800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr20:1518600-1519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr20:1518600-1519800	Enhancers	HMEC	breast
6	chr20:1518800-1519600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr20:1518800-1519800	Enhancers	Primary B cells from cord blood	blood
8	chr20:1519000-1519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr20:1519000-1520400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr20:1519000-1520400	Enhancers	NHEK	skin
11	chr20:1519400-1520400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr20:1519400-1520600	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr20:1519400-1521800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr20:1520000-1520200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr20:1520200-1524000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr20:1520400-1520600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr20:1520400-1521000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
18	chr20:1520400-1521200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
19	chr20:1520600-1529800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr20:1521200-1521600	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr20:1526200-1526400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr20:1527200-1527400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr20:1527400-1529800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr20:1528400-1529600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr20:1529600-1533800	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr20:1529800-1533800	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr20:1529800-1536400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr20:1532600-1532800	Enhancers	Spleen	Spleen
29	chr20:1532800-1545400	Weak transcription	Spleen	Spleen
30	chr20:1533800-1535800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr20:1533800-1536400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr20:1535800-1539200	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr20:1536400-1537400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr20:1536400-1538400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
35	chr20:1536800-1537000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr20:1537000-1541200	Weak transcription	Primary T cells from cord blood	blood
37	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr20:1537400-1542800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr20:1538400-1539600	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr20:1538600-1538800	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr20:1539200-1541200	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr20:1539600-1542600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr20:1540000-1544800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr20:1540200-1543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr20:1541200-1541800	Strong transcription	Primary T cells from cord blood	blood
46	chr20:1541200-1543000	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr20:1541600-1542200	Enhancers	HUVEC	blood vessel
48	chr20:1541800-1545200	Weak transcription	Primary T cells from cord blood	blood
49	chr20:1542400-1543800	Enhancers	Dnd41	blood
50	chr20:1542600-1543200	Genic enhancers	Primary monocytes fromperipheralblood	blood

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