Variant report

Variant	nsv824071
Chromosome Location	chr7:38293736-38356741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:554)
CpG islands
(count:1772)
Chromatin interactive
region (count:34)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
2	ARID3A	chr7:38333909-38333936	HepG2	liver:	n/a	n/a
3	ATF1	chr7:38332074-38332345	K562	blood:	n/a	n/a
4	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
5	ATF1	chr7:38319668-38320070	K562	blood:	n/a	n/a
6	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
7	BATF	chr7:38305616-38305913	GM12878	blood:	n/a	n/a
8	BATF	chr7:38335608-38335962	GM12878	blood:	n/a	n/a
9	BATF	chr7:38305659-38305874	GM12878	blood:	n/a	n/a
10	BATF	chr7:38335625-38335952	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38335675-38335915	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38335645-38335867	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:38305612-38305832	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:38305548-38305926	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38330775-38331007	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:38335593-38335955	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:38330740-38331111	K562	blood:	n/a	n/a
18	BHLHE40	chr7:38339818-38340010	K562	blood:	n/a	n/a
19	BHLHE40	chr7:38351349-38351381	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:38313008-38313126	K562	blood:	n/a	n/a
21	BHLHE40	chr7:38351090-38351531	K562	blood:	n/a	n/a
22	CBX3	chr7:38350978-38351579	K562	blood:	n/a	n/a
23	CCNT2	chr7:38350861-38351244	K562	blood:	n/a	n/a
24	CEBPB	chr7:38321770-38322083	HepG2	liver:	n/a	chr7:38321909-38321920
25	CEBPB	chr7:38321761-38322047	K562	blood:	n/a	chr7:38321909-38321920
26	CEBPB	chr7:38312888-38313596	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
28	CEBPB	chr7:38345755-38346111	MCF-7	breast:	n/a	n/a
29	CEBPB	chr7:38330530-38330719	K562	blood:	n/a	n/a
30	CEBPB	chr7:38350358-38350709	K562	blood:	n/a	chr7:38350562-38350575
31	CHD2	chr7:38352615-38352643	GM12878	blood:	n/a	n/a
32	CHD2	chr7:38350904-38351511	GM12878	blood:	n/a	n/a
33	CHD2	chr7:38335609-38335922	GM12878	blood:	n/a	n/a
34	CREB1	chr7:38350990-38351447	A549	lung:	n/a	n/a
35	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
36	CTCF	chr7:38339900-38340050	NB4	blood:	n/a	chr7:38340014-38340027 chr7:38340012-38340030
37	CTCF	chr7:38330620-38330770	K562	blood:	n/a	n/a
38	CTCF	chr7:38330892-38330962	GM12878	blood:	n/a	n/a
39	CTCF	chr7:38330870-38330968	GM12892	blood:	n/a	n/a
40	CTCF	chr7:38351100-38351250	GM06990	blood:	n/a	n/a
41	CTCF	chr7:38353080-38353230	A549	lung:	n/a	n/a
42	CTCF	chr7:38330880-38331030	K562	blood:	n/a	n/a
43	CTCF	chr7:38310342-38310394	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:38330880-38331030	GM12868	blood:	n/a	n/a
45	CTCF	chr7:38330620-38330770	GM12878	blood:	n/a	n/a
46	CTCF	chr7:38330840-38330990	GM06990	blood:	n/a	n/a
47	CTCF	chr7:38330840-38330990	HepG2	liver:	n/a	n/a
48	CTCF	chr7:38330856-38330969	Fibrobl	skin:	n/a	n/a
49	CTCF	chr7:38330840-38330990	GM12873	blood:	n/a	n/a
50	CTCF	chr7:38330880-38331030	BE2_C	brain:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38356729-38356779	AG04450	lung:	fetal
2	chr7:38309984-38310034	NT2-D1	testis:	n/a
3	chr7:38351468-38351518	RPTEC	kidney:	n/a
4	chr7:38356729-38356779	AG04450	lung:	fetal
5	chr7:38309984-38310034	NT2-D1	testis:	n/a
6	chr7:38351468-38351518	RPTEC	kidney:	n/a
7	chr7:38348929-38348979	ovcar-3	ovarian:	n/a
8	chr7:38294113-38294163	HAEpiC	amniotic membrane:	n/a
9	chr7:38331753-38331803	ovcar-3	ovarian:	n/a
10	chr7:38294113-38294163	AG09309	skin:	n/a
11	chr7:38315971-38316021	GM12891	blood:	n/a
12	chr7:38299481-38299531	IMR90	lung:	fetal
13	chr7:38331753-38331803	HRCEpiC	kidney:	n/a
14	chr7:38315971-38316021	IMR90	lung:	fetal
15	chr7:38312366-38312416	HEK293	kidney:	embryo
16	chr7:38340103-38340153	ECC-1	luminal epithelium:	n/a
17	chr7:38344934-38344984	Hela-S3	cervix:	n/a
18	chr7:38351226-38351276	PFSK-1	brain:	n/a
19	chr7:38350921-38350971	ECC-1	luminal epithelium:	n/a
20	chr7:38355100-38355150	HAEpiC	amniotic membrane:	n/a
21	chr7:38344983-38345033	Hela-S3	cervix:	n/a
22	chr7:38344455-38344505	SK-N-SH	brain:	n/a
23	chr7:38312366-38312416	ECC-1	luminal epithelium:	n/a
24	chr7:38303957-38304007	SKMC	muscle:	n/a
25	chr7:38340103-38340153	SAEC	small airway:	n/a
26	chr7:38355100-38355150	HEEpiC	esophagus:	n/a
27	chr7:38350921-38350971	AG10803	skin:	n/a
28	chr7:38312366-38312416	AG10803	skin:	n/a
29	chr7:38332633-38332683	NHBE	bronchial:	n/a
30	chr7:38331871-38331921	AG10803	skin:	n/a
31	chr7:38350921-38350971	HCF	heart:	n/a
32	chr7:38298908-38298958	HCT-116	colon:	n/a
33	chr7:38298966-38299016	HIPEpiC	eye:	n/a
34	chr7:38344455-38344505	BE2_C	brain:	n/a
35	chr7:38316654-38316704	HRPEpiC	eye:	n/a
36	chr7:38331871-38331921	GM06990	blood:	n/a
37	chr7:38351094-38351144	NB4	blood:	n/a
38	chr7:38351094-38351144	BJ	skin:	n/a
39	chr7:38344455-38344505	NB4	blood:	n/a
40	chr7:38356729-38356779	NHBE	bronchial:	n/a
41	chr7:38331753-38331803	AG10803	skin:	n/a
42	chr7:38351226-38351276	HRE	kidney:	n/a
43	chr7:38347775-38347825	SKMC	muscle:	n/a
44	chr7:38296393-38296443	HCM	heart:	n/a
45	chr7:38344934-38344984	AG10803	skin:	n/a
46	chr7:38312366-38312416	MCF-7	breast:	n/a
47	chr7:38351468-38351518	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:38315964-38316014	AG09309	skin:	n/a
49	chr7:38351468-38351518	T-47D	breast:	n/a
50	chr7:38331753-38331803	NB4	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
2	chr7:38325300..38328102-chr7:38356981..38359031,2	K562	blood:
3	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
4	chr19:47892610..47893302-chr7:38314653..38315604,2	NB4	blood:
5	chr7:38316692..38319374-chr7:38324142..38325804,2	MCF-7	breast:
6	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
7	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
8	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
9	chr7:38272138..38275044-chr7:38351799..38354206,2	K562	blood:
10	chr7:38327903..38329443-chr7:38331082..38333824,2	MCF-7	breast:
11	chr7:38329299..38330977-chr7:38349932..38352366,2	K562	blood:
12	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
13	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
14	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
15	chr7:38268526..38271338-chr7:38351636..38353674,2	K562	blood:
16	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
17	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
18	chr5:150068580..150069370-chr7:38338298..38339028,2	NB4	blood:
19	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
20	chr7:38312675..38315674-chr7:38326850..38329772,2	K562	blood:
21	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
22	chr6:31583767..31584372-chr7:38349943..38350554,2	NB4	blood:
23	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
24	chr11:93474211..93474958-chr7:38350865..38351599,2	NB4	blood:
25	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:
26	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
27	chr5:139487048..139487856-chr7:38339265..38339924,2	NB4	blood:
28	chr7:38316692..38319374-chr7:38324142..38325804,2	MCF-7	breast:
29	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
30	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
31	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
32	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
33	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
34	chr7:38350855..38351410-chr9:4679053..4679680,2	NB4	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120170
2	lnc-AMPH-10	chr7:38308874-38309749	ucscGeneNc_uc003tgm_1
3	lnc-AMPH-10	chr7:38310012-38310298	ucscGeneNc_uc003tgm_1
4	lnc-AMPH-10	chr7:38313188-38313242	NONHSAT120170
5	lnc-STARD3NL-1	chr7:38352147-38352253	ucscGeneNc_uc003tgp_1
6	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120162
7	lnc-AMPH-9	chr7:38305937-38306406	ucscGeneNc_uc003tgl_1
8	lnc-STARD3NL-1	chr7:38356472-38356576	ucscGeneNc_uc003tgp_1
9	lnc-AMPH-10	chr7:38310790-38310903	ucscGeneNc_uc003tgm_1
10	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
11	lnc-AMPH-10	chr7:38356616-38356709	NONHSAT120169
12	lnc-AMPH-10	chr7:38356605-38356709	NONHSAT120166
13	lnc-STARD3NL-1	chr7:38347741-38347925	ucscGeneNc_uc003tgp_1
14	lnc-AMPH-10	chr7:38313188-38313238	NONHSAT120169
15	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
16	lnc-AMPH-2	chr7:38343487-38343773	ENSG00000244971
17	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120161
18	lnc-AMPH-2	chr7:38343487-38343773	NONHSAT120173
19	lnc-AMPH-2	chr7:38344265-38344378	NONHSAT120173
20	lnc-AMPH-2	chr7:38342383-38343224	ENSG00000244971
21	lnc-AMPH-8	chr7:38335364-38335834	NONHSAT120172
22	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120169
23	lnc-AMPH-2	chr7:38342349-38343224	NONHSAT120173
24	lnc-AMPH-10	chr7:38356622-38356709	NONHSAT120167
25	lnc-AMPH-2	chr7:38344265-38345247	ENSG00000244971
26	lnc-AMPH-10	chr7:38356623-38356709	NONHSAT120170

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGC1	TF binding region
TRGJP	TF binding region
TRGJP2	TF binding region
TRGV10	TF binding region
TRGV11	TF binding region
TRGJ2	TF binding region
TRGVB	TF binding region
TRGJP1	TF binding region
TRGJ1	TF binding region
ENSG00000231916	TF binding region
TRGC2	CpG island
TRGC1	CpG island
TRGJP	CpG island
TRGJP2	CpG island
TRGV10	CpG island
TRGV11	CpG island
TRGJ2	CpG island
TRGVB	CpG island
TRGJP1	CpG island
TRGJ1	CpG island
ENSG00000231916	CpG island
ENSG00000211689	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000272908	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000106993	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000211693	chromatin interactions
ENSG00000211691	chromatin interactions
ENSG00000204472	chromatin interactions
ENSG00000231202	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000211694	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 2851 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2851 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6462822	chr7:38293786-38293787	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142754203	chr7:38293800-38293801	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533209874	chr7:38293817-38293818	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531513876	chr7:38293818-38293819	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6462823	chr7:38293827-38293828	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561776882	chr7:38293845-38293846	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530121006	chr7:38293871-38293872	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369393726	chr7:38293881-38293882	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139473328	chr7:38293899-38293900	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs141772181	chr7:38293908-38293909	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs538613921	chr7:38293913-38293914	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs187216081	chr7:38293919-38293920	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs117035201	chr7:38293941-38293942	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
14	rs538203051	chr7:38293949-38293950	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs113051061	chr7:38293984-38293985	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
16	rs568703697	chr7:38294071-38294072	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs6462824	chr7:38294079-38294080	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs553872864	chr7:38294100-38294101	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs6462825	chr7:38294114-38294115	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545738996	chr7:38294117-38294118	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
21	rs114106460	chr7:38294118-38294119	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
22	rs114961226	chr7:38294124-38294125	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs2736939	chr7:38294132-38294133	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs2736938	chr7:38294144-38294145	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
25	rs150583144	chr7:38294159-38294160	Weak transcription Enhancers Genic enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
26	rs139652163	chr7:38294171-38294172	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs71558113	chr7:38294185-38294186	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs6462827	chr7:38294186-38294187	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs543002802	chr7:38294193-38294194	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs368636733	chr7:38294194-38294195	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532471904	chr7:38294258-38294259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552539592	chr7:38294261-38294262	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61181871	chr7:38294309-38294310	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs532015777	chr7:38294400-38294401	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113800562	chr7:38294419-38294420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192471312	chr7:38294485-38294486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534353964	chr7:38294523-38294524	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554413932	chr7:38294590-38294591	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559807777	chr7:38294600-38294601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75393462	chr7:38294614-38294615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183424997	chr7:38294621-38294622	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146775400	chr7:38294667-38294668	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7802130	chr7:38294670-38294671	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs541832999	chr7:38294724-38294725	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7802280	chr7:38294780-38294781	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs572018911	chr7:38294785-38294786	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540781014	chr7:38294803-38294804	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563986019	chr7:38294845-38294846	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371362534	chr7:38294862-38294863	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7789316	chr7:38294920-38294921	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD
Neuroblastoma	19536264	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38273800-38305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:38276800-38295600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:38288000-38296200	Weak transcription	Fetal Thymus	thymus
4	chr7:38288200-38295600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr7:38288200-38297000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr7:38288200-38311200	Weak transcription	Primary T cells from cord blood	blood
7	chr7:38292600-38296200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:38293400-38294200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr7:38293600-38294200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:38293600-38294800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:38293600-38298000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:38294200-38295400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:38294200-38295600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:38294800-38296000	Active TSS	Primary T cells fromperipheralblood	blood
15	chr7:38295400-38302600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:38295600-38296200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr7:38295600-38296600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:38295600-38297200	Enhancers	Primary hematopoietic stem cells	blood
19	chr7:38295600-38297600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr7:38295600-38298600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:38295800-38296400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr7:38296000-38305200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr7:38296200-38297200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:38296200-38297400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr7:38296200-38297400	Enhancers	Placenta	Placenta
26	chr7:38296200-38297400	Enhancers	Fetal Thymus	thymus
27	chr7:38296200-38297400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr7:38296400-38297200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
29	chr7:38296600-38296800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:38296600-38297000	Enhancers	GM12878-XiMat	blood
31	chr7:38296600-38297200	Enhancers	Adipose Nuclei	Adipose
32	chr7:38296600-38297400	Enhancers	Primary B cells from cord blood	blood
33	chr7:38296800-38297000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:38296800-38297200	Enhancers	K562	blood
35	chr7:38297000-38297200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr7:38297000-38297200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:38297200-38297400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr7:38297200-38297400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:38297200-38297600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr7:38297200-38312600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr7:38297400-38297800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr7:38297400-38298400	Weak transcription	Fetal Thymus	thymus
43	chr7:38297400-38298600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr7:38297400-38298600	Weak transcription	Placenta	Placenta
45	chr7:38297600-38298000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr7:38297600-38302400	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr7:38297800-38312200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr7:38298000-38298200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr7:38298200-38313000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr7:38298400-38298800	Enhancers	Fetal Thymus	thymus

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