Variant report

Variant	esv1830113
Chromosome Location	chr3:20200232-20430932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1901)
CpG islands
(count:1343)
Chromatin interactive
region (count:137)
LncRNA
region (count:23)
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	chr3:20371522-20371864	K562	blood:	n/a	n/a
2	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
3	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
4	ARID3A	chr3:20227329-20228186	K562	blood:	n/a	n/a
5	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
6	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
7	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:20267278-20267600	K562	blood:	n/a	n/a
9	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
11	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
12	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
13	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
14	ARID3A	chr3:20227487-20228388	HepG2	liver:	n/a	n/a
15	ATF1	chr3:20226994-20228147	K562	blood:	n/a	n/a
16	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
17	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
18	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
19	ATF2	chr3:20227637-20228238	GM12878	blood:	n/a	n/a
20	ATF2	chr3:20227207-20228211	GM12878	blood:	n/a	n/a
21	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
22	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
23	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr3:20227535-20227966	K562	blood:	n/a	n/a
25	ATF3	chr3:20227425-20228037	HepG2	liver:	n/a	n/a
26	ATF3	chr3:20227505-20227918	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr3:20227527-20228058	GM12878	blood:	n/a	n/a
28	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
29	ATF3	chr3:20227605-20227903	HepG2	liver:	n/a	n/a
30	ATF3	chr3:20227575-20227873	GM12878	blood:	n/a	n/a
31	ATF3	chr3:20227448-20228043	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr3:20227585-20227975	K562	blood:	n/a	n/a
33	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
35	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
36	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
37	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
38	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
39	BATF	chr3:20277379-20277647	GM12878	blood:	n/a	n/a
40	BATF	chr3:20277377-20277645	GM12878	blood:	n/a	n/a
41	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
42	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:20263785-20264058	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:20263779-20264109	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL3	chr3:20227304-20227885	A549	lung:	n/a	n/a
49	BCLAF1	chr3:20227123-20228281	GM12878	blood:	n/a	n/a
50	BCLAF1	chr3:20227146-20228169	GM12878	blood:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20227925-20227975	SAEC	small airway:	n/a
2	chr3:20227925-20227975	SAEC	small airway:	n/a
3	chr3:20223923-20223973	NHDF-neo	bronchial:	n/a
4	chr3:20226994-20227044	BE2_C	brain:	n/a
5	chr3:20371290-20371340	PFSK-1	brain:	n/a
6	chr3:20412342-20412392	HMEC	breast:	n/a
7	chr3:20227059-20227109	HMEC	breast:	n/a
8	chr3:20226964-20227014	HEK293	kidney:	embryo
9	chr3:20228976-20229026	MCF-7	breast:	n/a
10	chr3:20227801-20227851	NHBE	bronchial:	n/a
11	chr3:20418856-20418906	HRPEpiC	eye:	n/a
12	chr3:20227091-20227141	SK-N-MC	brain:	n/a
13	chr3:20227091-20227141	GM06990	blood:	n/a
14	chr3:20227059-20227109	AoSMC	blood vessel:	n/a
15	chr3:20227925-20227975	HRPEpiC	eye:	n/a
16	chr3:20227801-20227851	HCT-116	colon:	n/a
17	chr3:20227925-20227975	HCPEpiC	choroid plexus:	n/a
18	chr3:20231061-20231111	BJ	skin:	n/a
19	chr3:20227940-20227990	HCM	heart:	n/a
20	chr3:20228976-20229026	HepG2	liver:	n/a
21	chr3:20202403-20202453	PANC-1	pancreas:	n/a
22	chr3:20227822-20227872	HCPEpiC	choroid plexus:	n/a
23	chr3:20227397-20227447	NH-A	brain:	n/a
24	chr3:20227670-20227720	RPTEC	kidney:	n/a
25	chr3:20227789-20227839	Hela-S3	cervix:	n/a
26	chr3:20227059-20227109	AG10803	skin:	n/a
27	chr3:20412342-20412392	NT2-D1	testis:	n/a
28	chr3:20226964-20227014	Jurkat	blood:	n/a
29	chr3:20371290-20371340	HCT-116	colon:	n/a
30	chr3:20227516-20227566	IMR90	lung:	fetal
31	chr3:20227059-20227109	GM12891	blood:	n/a
32	chr3:20227663-20227713	HRE	kidney:	n/a
33	chr3:20227516-20227566	T-47D	breast:	n/a
34	chr3:20227925-20227975	Jurkat	blood:	n/a
35	chr3:20231061-20231111	ECC-1	luminal epithelium:	n/a
36	chr3:20321584-20321634	IMR90	lung:	fetal
37	chr3:20227670-20227720	HUVEC	blood vessel:	n/a
38	chr3:20228976-20229026	HL-60	blood:	n/a
39	chr3:20227940-20227990	SK-N-SH	brain:	n/a
40	chr3:20227516-20227566	Hela-S3	cervix:	n/a
41	chr3:20231061-20231111	CMK	blood:	n/a
42	chr3:20226964-20227014	PrEC	prostate:	n/a
43	chr3:20227059-20227109	HCM	heart:	n/a
44	chr3:20227059-20227109	NT2-D1	testis:	n/a
45	chr3:20202403-20202453	IMR90	lung:	fetal
46	chr3:20418856-20418906	U87	brain:	n/a
47	chr3:20226964-20227014	GM19239	blood:	n/a
48	chr3:20227809-20227859	HAEpiC	amniotic membrane:	n/a
49	chr3:20223923-20223973	HL-60	blood:	n/a
50	chr3:20227822-20227872	HNPCEpiC	eye:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:20255206..20257186-chr3:20272224..20273896,2	K562	blood:
2	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
3	chr3:20227937..20230614-chr3:20238703..20240365,2	K562	blood:
4	chr3:20215671..20219222-chr3:20225067..20228168,4	MCF-7	breast:
5	chr3:20216479..20218064-chr3:20218704..20221260,2	K562	blood:
6	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
7	chr3:20212391..20215096-chr3:20215867..20218986,3	K562	blood:
8	chr3:20240283..20242142-chr3:20254913..20256935,2	K562	blood:
9	chr3:20223638..20225446-chr3:20225885..20227918,2	MCF-7	breast:
10	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
11	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
12	chr3:20226448..20228980-chr3:20231144..20234755,4	MCF-7	breast:
13	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
14	chr3:20227831..20229515-chr3:20229924..20231692,2	MCF-7	breast:
15	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
16	chr3:20219250..20222131-chr3:20228592..20230370,2	K562	blood:
17	chr3:20225982..20227551-chr3:20349845..20352725,2	K562	blood:
18	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
19	chr3:19991248..19993079-chr3:20225987..20227552,2	MCF-7	breast:
20	chr15:42565172..42565968-chr3:20227231..20227766,2	Hela-S3	cervix:
21	chr3:20202636..20204189-chr3:20204811..20206613,2	MCF-7	breast:
22	chr3:20266881..20267830-chr3:21935770..21936618,4	MCF-7	breast:
23	chr3:19985145..19990136-chr3:20225418..20228312,6	K562	blood:
24	chr3:19987439..19992261-chr3:20226257..20229350,4	K562	blood:
25	chr3:20202636..20204189-chr3:20204811..20206613,2	MCF-7	breast:
26	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
27	chr3:20231614..20234175-chr3:20236441..20238488,2	K562	blood:
28	chr3:20226448..20228980-chr3:20231144..20234755,4	MCF-7	breast:
29	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
30	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
31	chr3:20218894..20221253-chr3:20226177..20229116,2	MCF-7	breast:
32	chr3:20228018..20229588-chr3:20240700..20242261,2	K562	blood:
33	chr3:20225377..20229978-chr3:20232761..20235716,5	K562	blood:
34	chr3:20197490..20199260-chr3:20227955..20230018,2	K562	blood:
35	chr3:20209340..20212001-chr3:20214407..20216140,2	K562	blood:
36	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
37	chr3:20079693..20081472-chr3:20203928..20206383,2	K562	blood:
38	chr3:20079993..20081743-chr3:20205055..20207823,2	MCF-7	breast:
39	chr3:20248922..20251335-chr3:20323167..20325698,2	K562	blood:
40	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
41	chr3:20053872..20056558-chr3:20225792..20227888,2	K562	blood:
42	chr3:20199507..20201505-chr3:20225585..20228159,2	MCF-7	breast:
43	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
44	chr3:20215671..20219222-chr3:20225067..20228168,4	MCF-7	breast:
45	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
46	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
47	chr3:19987980..19990853-chr3:20225710..20227616,2	MCF-7	breast:
48	chr3:20201533..20203572-chr3:20204589..20206739,2	K562	blood:
49	chr3:20228018..20229588-chr3:20240700..20242261,2	K562	blood:
50	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
2	lnc-KAT2B-1	chr3:20227726-20230848	NONHSAT088617
3	lnc-PP2D1-2	chr3:20212535-20212759	NONHSAT088614
4	lnc-KAT2B-1	chr3:20218709-20218742	ENSG00000237485.1
5	lnc-KAT2B-1	chr3:20215736-20216017	ENSG00000237485.1
6	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
7	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
8	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
9	lnc-KAT2B-5	chr3:20202876-20203154	l_2328_chr3:20202875-20210905_testes
10	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
11	lnc-KAT2B-1	chr3:20227467-20227607	ENSG00000237485.1
12	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
13	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
14	lnc-PP2D1-2	chr3:20211553-20212307	NONHSAT088614
15	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
16	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
17	lnc-KAT2B-1	chr3:20215778-20216017	ENSG00000237485.1
18	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
19	lnc-KAT2B-5	chr3:20210846-20210905	l_2328_chr3:20202875-20210905_testes
20	lnc-KAT2B-1	chr3:20227467-20227919	ENSG00000237485.1
21	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
22	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
23	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1

No data

Variant related genes	Relation type
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
RNY4P22	TF binding region
ENSG00000261734	TF binding region
SGOL1-AS1	TF binding region
SGOL1	TF binding region
RNU6-822P	CpG island
ENSG00000231304	CpG island
RNY4P22	CpG island
ENSG00000261734	CpG island
SGOL1-AS1	CpG island
SGOL1	CpG island
ENSG00000229468	chromatin interactions
ENSG00000117625	chromatin interactions
ENSG00000158158	chromatin interactions
ENSG00000234779	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000237485	chromatin interactions
ENSG00000163576	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000252442	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000126226	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000103978	chromatin interactions

Extended variants
information (count: 8504 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:8504 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10865760	chr3:20200232-20200233	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144330426	chr3:20200275-20200276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148751658	chr3:20200296-20200297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571820842	chr3:20200299-20200300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144718010	chr3:20200311-20200312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs539165459	chr3:20200321-20200322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566101628	chr3:20200329-20200330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546638890	chr3:20200341-20200342	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530382926	chr3:20200452-20200453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548637088	chr3:20200462-20200463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs1828080	chr3:20200472-20200473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs369561111	chr3:20200487-20200488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200186589	chr3:20200498-20200499	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10596926	chr3:20200502-20200503	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554936110	chr3:20200519-20200520	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs193280565	chr3:20200539-20200540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147887841	chr3:20200546-20200547	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76122929	chr3:20200547-20200548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553321521	chr3:20200571-20200572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571722949	chr3:20200572-20200573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542891320	chr3:20200577-20200578	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554594509	chr3:20200582-20200583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575193151	chr3:20200598-20200599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71634898	chr3:20200602-20200603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576182151	chr3:20200609-20200610	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543292676	chr3:20200619-20200620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1828079	chr3:20200636-20200637	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs532624476	chr3:20200644-20200645	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs4273391	chr3:20200696-20200697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577383791	chr3:20200818-20200819	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372582834	chr3:20200828-20200829	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530147171	chr3:20200839-20200840	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548862831	chr3:20200891-20200892	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570296304	chr3:20200900-20200901	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141557755	chr3:20200905-20200906	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184777124	chr3:20200937-20200938	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7629055	chr3:20200939-20200940	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538310399	chr3:20200943-20200944	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7651985	chr3:20200955-20200956	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368916145	chr3:20200981-20200982	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200736045	chr3:20200985-20200986	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565313274	chr3:20200988-20200989	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs535914283	chr3:20201026-20201027	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554838682	chr3:20201065-20201066	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142874715	chr3:20201074-20201075	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs17627750	chr3:20201077-20201078	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs537373767	chr3:20201221-20201222	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558751046	chr3:20201259-20201260	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543046995	chr3:20201292-20201293	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562866047	chr3:20201295-20201296	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20141200-20222400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:20159200-20201400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:20164400-20204400	Weak transcription	Small Intestine	intestine
4	chr3:20164800-20211400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:20167800-20226000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr3:20168800-20200800	Weak transcription	GM12878-XiMat	blood
7	chr3:20169800-20201600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:20169800-20202000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:20182600-20201400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:20183600-20201000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr3:20184600-20220200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:20187400-20201000	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr3:20187600-20201200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr3:20188400-20204800	Weak transcription	Fetal Brain Female	brain
15	chr3:20188400-20212400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr3:20189600-20200800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:20189800-20201600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr3:20190200-20201400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr3:20190200-20201800	Weak transcription	Fetal Intestine Large	intestine
20	chr3:20190400-20202400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr3:20190600-20220200	Weak transcription	Fetal Muscle Leg	muscle
22	chr3:20191200-20200800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:20191600-20201200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr3:20191600-20201400	Weak transcription	Left Ventricle	heart
25	chr3:20191800-20200800	Weak transcription	HSMM	muscle
26	chr3:20191800-20201800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr3:20191800-20201800	Weak transcription	Adipose Nuclei	Adipose
28	chr3:20191800-20202400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr3:20191800-20202600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr3:20192400-20200800	Weak transcription	Fetal Heart	heart
31	chr3:20192400-20201800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr3:20192800-20220600	Weak transcription	Fetal Lung	lung
33	chr3:20193000-20201800	Weak transcription	Colon Smooth Muscle	Colon
34	chr3:20193200-20204000	Strong transcription	Fetal Thymus	thymus
35	chr3:20193400-20200600	Weak transcription	Hela-S3	cervix
36	chr3:20193800-20226600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr3:20194000-20220400	Weak transcription	NH-A	brain
38	chr3:20194200-20201600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr3:20194200-20205400	Strong transcription	Dnd41	blood
40	chr3:20194800-20215200	Weak transcription	HepG2	liver
41	chr3:20195000-20212400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr3:20195000-20226000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:20195200-20201000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr3:20195200-20201400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr3:20195200-20201400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr3:20195200-20201600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr3:20195200-20203800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr3:20195200-20221800	Weak transcription	NHEK	skin
49	chr3:20195400-20201000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr3:20195400-20226000	Weak transcription	NHDF-Ad	bronchial

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