Variant report

Variant	esv6973
Chromosome Location	chr7:38292814-38356689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:1709)
Chromatin interactive
region (count:34)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:555 , 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	chr7:38333909-38333936	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
3	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
4	ATF1	chr7:38319668-38320070	K562	blood:	n/a	n/a
5	ATF1	chr7:38332074-38332345	K562	blood:	n/a	n/a
6	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
7	BATF	chr7:38305659-38305874	GM12878	blood:	n/a	n/a
8	BATF	chr7:38305616-38305913	GM12878	blood:	n/a	n/a
9	BATF	chr7:38335625-38335952	GM12878	blood:	n/a	n/a
10	BATF	chr7:38335608-38335962	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38335645-38335867	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38305548-38305926	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:38335675-38335915	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:38305612-38305832	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38339818-38340010	K562	blood:	n/a	n/a
16	BHLHE40	chr7:38351349-38351381	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:38351090-38351531	K562	blood:	n/a	n/a
18	BHLHE40	chr7:38330775-38331007	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:38313008-38313126	K562	blood:	n/a	n/a
20	BHLHE40	chr7:38335593-38335955	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:38330740-38331111	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	chr7:38345755-38346111	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:38330530-38330719	K562	blood:	n/a	n/a
26	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
27	CEBPB	chr7:38312888-38313596	MCF-7	breast:	n/a	n/a
28	CEBPB	chr7:38350358-38350709	K562	blood:	n/a	chr7:38350562-38350575
29	CEBPB	chr7:38321770-38322083	HepG2	liver:	n/a	chr7:38321909-38321920
30	CEBPB	chr7:38321761-38322047	K562	blood:	n/a	chr7:38321909-38321920
31	CHD2	chr7:38352615-38352643	GM12878	blood:	n/a	n/a
32	CHD2	chr7:38335609-38335922	GM12878	blood:	n/a	n/a
33	CHD2	chr7:38350904-38351511	GM12878	blood:	n/a	n/a
34	CREB1	chr7:38350990-38351447	A549	lung:	n/a	n/a
35	CTCF	chr7:38330893-38330972	GM13977	blood:	n/a	n/a
36	CTCF	chr7:38330860-38331010	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr7:38330699-38331041	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:38330900-38331050	GM12870	blood:	n/a	n/a
39	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
40	CTCF	chr7:38347548-38347588	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:38339862-38340195	K562	blood:	n/a	chr7:38340014-38340027 chr7:38340012-38340030
42	CTCF	chr7:38330880-38331030	HCT-116	colon:	n/a	n/a
43	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
44	CTCF	chr7:38330740-38330890	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr7:38330865-38330993	GM19240	blood:	n/a	n/a
46	CTCF	chr7:38330880-38331030	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:38330840-38330990	GM12873	blood:	n/a	n/a
48	CTCF	chr7:38330800-38330950	HL-60	blood:	n/a	n/a
49	CTCF	chr7:38330900-38331050	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr7:38339900-38340050	NB4	blood:	n/a	chr7:38340014-38340027 chr7:38340012-38340030

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38296393-38296443	MCF-7	breast:	n/a
2	chr7:38296393-38296443	MCF-7	breast:	n/a
3	chr7:38296393-38296443	RPTEC	kidney:	n/a
4	chr7:38344455-38344505	HCF	heart:	n/a
5	chr7:38331871-38331921	NT2-D1	testis:	n/a
6	chr7:38351226-38351276	T-47D	breast:	n/a
7	chr7:38350921-38350971	SK-N-SH	brain:	n/a
8	chr7:38299481-38299531	LNCaP	prostate:	n/a
9	chr7:38351226-38351276	NHDF-neo	bronchial:	n/a
10	chr7:38350921-38350971	NH-A	brain:	n/a
11	chr7:38344934-38344984	SK-N-MC	brain:	n/a
12	chr7:38348929-38348979	HL-60	blood:	n/a
13	chr7:38316654-38316704	BJ	skin:	n/a
14	chr7:38332633-38332683	U87	brain:	n/a
15	chr7:38355100-38355150	Caco-2	colon:	n/a
16	chr7:38350464-38350514	GM12878	blood:	n/a
17	chr7:38298908-38298958	PFSK-1	brain:	n/a
18	chr7:38351468-38351518	RPTEC	kidney:	n/a
19	chr7:38344983-38345033	RPTEC	kidney:	n/a
20	chr7:38355100-38355150	HUVEC	blood vessel:	n/a
21	chr7:38350938-38350988	HIPEpiC	eye:	n/a
22	chr7:38315971-38316021	GM19239	blood:	n/a
23	chr7:38344934-38344984	MCF10A-Er-Src	breast:	n/a
24	chr7:38351468-38351518	HepG2	liver:	n/a
25	chr7:38315964-38316014	HCF	heart:	n/a
26	chr7:38298966-38299016	GM12878	blood:	n/a
27	chr7:38299481-38299531	MCF10A-Er-Src	breast:	n/a
28	chr7:38296393-38296443	ovcar-3	ovarian:	n/a
29	chr7:38351468-38351518	AG10803	skin:	n/a
30	chr7:38298966-38299016	HIPEpiC	eye:	n/a
31	chr7:38332633-38332683	MCF10A-Er-Src	breast:	n/a
32	chr7:38350464-38350514	HNPCEpiC	eye:	n/a
33	chr7:38312366-38312416	HAEpiC	amniotic membrane:	n/a
34	chr7:38344934-38344984	A549	lung:	n/a
35	chr7:38344983-38345033	AG04450	lung:	fetal
36	chr7:38355100-38355150	A549	lung:	n/a
37	chr7:38355100-38355150	AG10803	skin:	n/a
38	chr7:38351468-38351518	HEEpiC	esophagus:	n/a
39	chr7:38315964-38316014	HUVEC	blood vessel:	n/a
40	chr7:38294113-38294163	HepG2	liver:	n/a
41	chr7:38344934-38344984	SAEC	small airway:	n/a
42	chr7:38351226-38351276	AG09319	gingival:	n/a
43	chr7:38299481-38299531	ECC-1	luminal epithelium:	n/a
44	chr7:38350464-38350514	GM06990	blood:	n/a
45	chr7:38309984-38310034	ProgFib	skin:	n/a
46	chr7:38350938-38350988	NT2-D1	testis:	n/a
47	chr7:38350464-38350514	SK-N-SH	brain:	n/a
48	chr7:38312366-38312416	HEEpiC	esophagus:	n/a
49	chr7:38296393-38296443	AG04449	skin:	fetal
50	chr7:38344455-38344505	H1-hESC	embryonic stem cell:	embryo

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

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

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-2	chr7:38342349-38343224	NONHSAT120173
2	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120169
3	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
4	lnc-AMPH-2	chr7:38342383-38343224	ENSG00000244971
5	lnc-AMPH-2	chr7:38343487-38343773	NONHSAT120173
6	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120170
7	lnc-AMPH-10	chr7:38313188-38313238	NONHSAT120169
8	lnc-AMPH-9	chr7:38305937-38306406	ucscGeneNc_uc003tgl_1
9	lnc-AMPH-10	chr7:38356623-38356709	NONHSAT120170
10	lnc-AMPH-10	chr7:38356616-38356709	NONHSAT120169
11	lnc-STARD3NL-1	chr7:38352147-38352253	ucscGeneNc_uc003tgp_1
12	lnc-AMPH-8	chr7:38335364-38335834	NONHSAT120172
13	lnc-AMPH-10	chr7:38310012-38310298	ucscGeneNc_uc003tgm_1
14	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
15	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120162
16	lnc-STARD3NL-1	chr7:38356472-38356576	ucscGeneNc_uc003tgp_1
17	lnc-AMPH-2	chr7:38344265-38344378	NONHSAT120173
18	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
19	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120161
20	lnc-STARD3NL-1	chr7:38347741-38347925	ucscGeneNc_uc003tgp_1
21	lnc-AMPH-10	chr7:38356605-38356709	NONHSAT120166
22	lnc-AMPH-10	chr7:38310790-38310903	ucscGeneNc_uc003tgm_1
23	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
24	lnc-AMPH-2	chr7:38343487-38343773	ENSG00000244971
25	lnc-AMPH-10	chr7:38313188-38313242	NONHSAT120170
26	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
27	lnc-AMPH-10	chr7:38356622-38356709	NONHSAT120167
28	lnc-AMPH-2	chr7:38344265-38345247	ENSG00000244971
29	lnc-AMPH-10	chr7:38308874-38309749	ucscGeneNc_uc003tgm_1

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
ENSG00000106993	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000211691	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000211694	chromatin interactions
ENSG00000211693	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000204472	chromatin interactions
ENSG00000272908	chromatin interactions
ENSG00000231202	chromatin interactions
ENSG00000211689	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000249978	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 2895 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2895 , 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	rs532450570	chr7:38292833-38292834	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs55734725	chr7:38292853-38292854	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12701617	chr7:38292857-38292858	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs144983003	chr7:38292866-38292867	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557454395	chr7:38292867-38292868	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs10267672	chr7:38292890-38292891	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs10252198	chr7:38292916-38292917	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12701618	chr7:38292926-38292927	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368827023	chr7:38292936-38292937	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573200298	chr7:38292941-38292942	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs376187107	chr7:38292944-38292945	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs181312723	chr7:38292971-38292972	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs575823116	chr7:38292972-38292973	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs199756530	chr7:38292991-38292992	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs373590864	chr7:38292999-38293000	Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs561004431	chr7:38293106-38293107	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574457553	chr7:38293125-38293126	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs373087069	chr7:38293140-38293141	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528053283	chr7:38293149-38293150	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560236457	chr7:38293158-38293159	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs532438229	chr7:38293165-38293166	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs552532810	chr7:38293171-38293172	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs562520323	chr7:38293180-38293181	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs58473496	chr7:38293184-38293185	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs548094702	chr7:38293237-38293238	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs567706882	chr7:38293242-38293243	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs536397168	chr7:38293243-38293244	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs546582284	chr7:38293244-38293245	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566563341	chr7:38293246-38293247	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs144981790	chr7:38293315-38293316	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs138813342	chr7:38293316-38293317	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs111895695	chr7:38293337-38293338	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546636249	chr7:38293417-38293418	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113335660	chr7:38293431-38293432	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs58877772	chr7:38293438-38293439	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372549579	chr7:38293479-38293480	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200806308	chr7:38293492-38293493	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs13312658	chr7:38293496-38293497	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs72496139	chr7:38293546-38293547	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs373874735	chr7:38293547-38293548	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184952527	chr7:38293562-38293563	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs13312589	chr7:38293569-38293570	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs13312549	chr7:38293571-38293572	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs78860090	chr7:38293599-38293600	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs13312588	chr7:38293604-38293605	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368641261	chr7:38293605-38293606	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200685219	chr7:38293606-38293607	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13312715	chr7:38293612-38293613	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200709552	chr7:38293654-38293655	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7797364	chr7:38293659-38293660	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

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:747 , 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	chr7:38289000-38293600	Active TSS	Primary T cells fromperipheralblood	blood
8	chr7:38290000-38293400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr7:38291800-38293400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:38292600-38293000	Active TSS	Primary T helper naive cells from peripheral blood	blood
11	chr7:38292600-38293000	Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr7:38292600-38296200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr7:38292800-38293200	Active TSS	Dnd41	blood
14	chr7:38293400-38293600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:38293400-38293600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:38293400-38294200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr7:38293600-38294200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:38293600-38294800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr7:38293600-38298000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:38294200-38295400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:38294200-38295600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr7:38294800-38296000	Active TSS	Primary T cells fromperipheralblood	blood
23	chr7:38295400-38302600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:38295600-38296200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr7:38295600-38296600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:38295600-38297200	Enhancers	Primary hematopoietic stem cells	blood
27	chr7:38295600-38297600	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:38295600-38298600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:38295800-38296400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr7:38296000-38305200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:38296200-38297200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:38296200-38297400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr7:38296200-38297400	Enhancers	Placenta	Placenta
34	chr7:38296200-38297400	Enhancers	Fetal Thymus	thymus
35	chr7:38296200-38297400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr7:38296400-38297200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
37	chr7:38296600-38296800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:38296600-38297000	Enhancers	GM12878-XiMat	blood
39	chr7:38296600-38297200	Enhancers	Adipose Nuclei	Adipose
40	chr7:38296600-38297400	Enhancers	Primary B cells from cord blood	blood
41	chr7:38296800-38297000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:38296800-38297200	Enhancers	K562	blood
43	chr7:38297000-38297200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr7:38297000-38297200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:38297200-38297400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr7:38297200-38297400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:38297200-38297600	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr7:38297200-38312600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr7:38297400-38297800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr7:38297400-38298400	Weak transcription	Fetal Thymus	thymus

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