Variant report

Variant	nsv979
Chromosome Location	chr13:30122254-30167821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:884)
CpG islands
(count:428)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:30145799-30146289	HepG2	liver:	n/a	n/a
2	BACH1	chr13:30157526-30157911	H1-hESC	embryonic stem cell:	n/a	chr13:30157817-30157831
3	BCL11A	chr13:30132330-30132573	GM12878	blood:	n/a	n/a
4	BCL3	chr13:30133593-30133834	GM12878	blood:	n/a	n/a
5	BCL3	chr13:30132697-30132909	GM12878	blood:	n/a	n/a
6	BCL3	chr13:30124786-30125125	GM12878	blood:	n/a	n/a
7	BHLHE40	chr13:30156407-30156994	K562	blood:	n/a	n/a
8	BHLHE40	chr13:30147304-30147679	K562	blood:	n/a	n/a
9	BHLHE40	chr13:30161910-30162105	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:30164067-30164218	HepG2	liver:	n/a	n/a
11	BHLHE40	chr13:30145988-30146310	HepG2	liver:	n/a	chr13:30146287-30146303
12	BHLHE40	chr13:30161854-30162190	K562	blood:	n/a	n/a
13	BHLHE40	chr13:30144247-30144538	HepG2	liver:	n/a	n/a
14	BRCA1	chr13:30151823-30151918	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:30163262-30163734	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr13:30150479-30150658	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:30157421-30157486	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr13:30157822-30158136	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:30163545-30163653	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:30153384-30153616	K562	blood:	n/a	chr13:30153553-30153564
21	CEBPB	chr13:30146069-30146239	HepG2	liver:	n/a	n/a
22	CEBPB	chr13:30136143-30136465	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:30145959-30146337	HepG2	liver:	n/a	n/a
24	CEBPB	chr13:30143798-30143883	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:30143776-30143878	IMR90	lung:	n/a	n/a
26	CEBPB	chr13:30153483-30153680	HepG2	liver:	n/a	chr13:30153553-30153564
27	CEBPB	chr13:30157679-30158129	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:30153320-30153634	ECC-1	luminal epithelium:	n/a	chr13:30153553-30153564
29	CEBPB	chr13:30136159-30136410	IMR90	lung:	n/a	n/a
30	CEBPB	chr13:30163370-30163669	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr13:30163432-30163713	IMR90	lung:	n/a	n/a
32	CEBPB	chr13:30142884-30143403	MCF-7	breast:	n/a	n/a
33	CHD2	chr13:30146348-30146386	HepG2	liver:	n/a	n/a
34	CHD2	chr13:30139383-30139384	K562	blood:	n/a	n/a
35	CTCF	chr13:30164240-30164390	AG09309	skin:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
36	CTCF	chr13:30164192-30164394	H1-hESC	embryonic stem cell:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
37	CTCF	chr13:30164180-30164330	NHDF-neo	bronchial:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
38	CTCF	chr13:30139085-30139198	Hela-S3	cervix:	n/a	chr13:30139144-30139157 chr13:30139173-30139181
39	CTCF	chr13:30163680-30163879	NHEK	skin:	n/a	n/a
40	CTCF	chr13:30139080-30139230	HPAF	blood vessel:	n/a	chr13:30139144-30139157 chr13:30139173-30139181
41	CTCF	chr13:30139100-30139250	HFF-Myc	foreskin:	n/a	chr13:30139144-30139157 chr13:30139173-30139181
42	CTCF	chr13:30164221-30164364	MCF-7	breast:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
43	CTCF	chr13:30164180-30164330	A549	lung:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
44	CTCF	chr13:30147519-30147598	GM19238	blood:	n/a	n/a
45	CTCF	chr13:30139060-30139210	Caco-2	colon:	n/a	chr13:30139144-30139157 chr13:30139173-30139181
46	CTCF	chr13:30147500-30147650	AG10803	skin:	n/a	n/a
47	CTCF	chr13:30164180-30164330	K562	blood:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
48	CTCF	chr13:30164188-30164398	NHEK	skin:	n/a	chr13:30164289-30164302 chr13:30164293-30164302 chr13:30164287-30164305
49	CTCF	chr13:30139060-30139210	HMF	breast:	n/a	chr13:30139144-30139157 chr13:30139173-30139181
50	CTCF	chr13:30163684-30163895	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30166944-30166994	Hela-S3	cervix:	n/a
2	chr13:30166944-30166994	Hela-S3	cervix:	n/a
3	chr13:30156486-30156536	NH-A	brain:	n/a
4	chr13:30163303-30163353	HCT-116	colon:	n/a
5	chr13:30143971-30144021	NHDF-neo	bronchial:	n/a
6	chr13:30163303-30163353	PFSK-1	brain:	n/a
7	chr13:30156486-30156536	PANC-1	pancreas:	n/a
8	chr13:30156486-30156536	LNCaP	prostate:	n/a
9	chr13:30156486-30156536	U87	brain:	n/a
10	chr13:30146493-30146543	HEEpiC	esophagus:	n/a
11	chr13:30156486-30156536	Hela-S3	cervix:	n/a
12	chr13:30163303-30163353	Hepatocyte	liver:	n/a
13	chr13:30166944-30166994	SK-N-SH	brain:	n/a
14	chr13:30163303-30163353	ECC-1	luminal epithelium:	n/a
15	chr13:30143971-30144021	HepG2	liver:	n/a
16	chr13:30124401-30124451	NB4	blood:	n/a
17	chr13:30146493-30146543	HCM	heart:	n/a
18	chr13:30166944-30166994	HCT-116	colon:	n/a
19	chr13:30166879-30166929	PrEC	prostate:	n/a
20	chr13:30163303-30163353	ProgFib	skin:	n/a
21	chr13:30143971-30144021	MCF-7	breast:	n/a
22	chr13:30163303-30163353	PrEC	prostate:	n/a
23	chr13:30163303-30163353	HMEC	breast:	n/a
24	chr13:30166879-30166929	HRPEpiC	eye:	n/a
25	chr13:30143971-30144021	K562	blood:	n/a
26	chr13:30143971-30144021	T-47D	breast:	n/a
27	chr13:30143971-30144021	HEK293	kidney:	embryo
28	chr13:30146493-30146543	SAEC	small airway:	n/a
29	chr13:30163303-30163353	GM12878	blood:	n/a
30	chr13:30163303-30163353	IMR90	lung:	fetal
31	chr13:30163303-30163353	HRPEpiC	eye:	n/a
32	chr13:30163303-30163353	HRCEpiC	kidney:	n/a
33	chr13:30146493-30146543	Caco-2	colon:	n/a
34	chr13:30166879-30166929	BE2_C	brain:	n/a
35	chr13:30166879-30166929	AoSMC	blood vessel:	n/a
36	chr13:30146493-30146543	NT2-D1	testis:	n/a
37	chr13:30143971-30144021	PFSK-1	brain:	n/a
38	chr13:30143971-30144021	BJ	skin:	n/a
39	chr13:30166944-30166994	AG10803	skin:	n/a
40	chr13:30143971-30144021	ECC-1	luminal epithelium:	n/a
41	chr13:30146493-30146543	ProgFib	skin:	n/a
42	chr13:30156486-30156536	SK-N-SH_RA	brain:	n/a
43	chr13:30143971-30144021	NH-A	brain:	n/a
44	chr13:30166944-30166994	PrEC	prostate:	n/a
45	chr13:30156486-30156536	HEK293	kidney:	embryo
46	chr13:30163303-30163353	HAEpiC	amniotic membrane:	n/a
47	chr13:30124401-30124451	HMEC	breast:	n/a
48	chr13:30143971-30144021	HCT-116	colon:	n/a
49	chr13:30163303-30163353	HIPEpiC	eye:	n/a
50	chr13:30166879-30166929	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:30142186..30144552-chr13:30152474..30154361,2	MCF-7	breast:
2	chr13:30140340..30147664-chr13:30167192..30171255,11	MCF-7	breast:
3	chr13:30125675..30127526-chr13:30168701..30170678,2	MCF-7	breast:
4	chr13:30126094..30127682-chr13:30160999..30163139,2	MCF-7	breast:
5	chr13:30139726..30141978-chr13:30142351..30145103,3	MCF-7	breast:
6	chr13:30124978..30127325-chr13:30144094..30146175,2	MCF-7	breast:
7	chr13:30154508..30157101-chr13:30157805..30160613,2	MCF-7	breast:
8	chr13:30137385..30139177-chr13:30144253..30145908,2	MCF-7	breast:
9	chr13:30163424..30165091-chr13:31039254..31040913,2	K562	blood:
10	chr13:30132857..30135227-chr13:30168652..30170927,2	MCF-7	breast:
11	chr13:30147177..30149389-chr13:30151174..30153674,3	K562	blood:
12	chr13:30157813..30160720-chr13:30181026..30182667,2	K562	blood:
13	chr13:30154508..30157101-chr13:30157805..30160613,2	MCF-7	breast:
14	chr13:30165310..30167432-chr13:30231633..30234187,2	K562	blood:
15	chr13:30147733..30149517-chr13:30152740..30154897,2	MCF-7	breast:
16	chr13:30137385..30139177-chr13:30144253..30145908,2	MCF-7	breast:
17	chr13:30139090..30142290-chr13:30166982..30171178,4	K562	blood:
18	chr13:30156184..30157693-chr13:30157838..30160325,2	MCF-7	breast:
19	chr13:30145040..30147217-chr13:30165008..30167643,2	K562	blood:
20	chr13:30156184..30157693-chr13:30157838..30160325,2	MCF-7	breast:
21	chr13:30086955..30089041-chr13:30166781..30169428,2	MCF-7	breast:
22	chr13:30102776..30104828-chr13:30146774..30149345,2	K562	blood:
23	chr13:30163838..30166172-chr13:30279497..30282436,2	K562	blood:
24	chr13:30116350..30118708-chr13:30122829..30125095,2	K562	blood:
25	chr13:30087328..30089533-chr13:30164162..30166342,2	MCF-7	breast:
26	chr13:30142867..30144693-chr13:30149445..30152081,2	MCF-7	breast:
27	chr13:30142261..30144231-chr13:30163491..30165148,2	MCF-7	breast:
28	chr13:30128754..30131140-chr13:30168189..30170872,2	MCF-7	breast:
29	chr13:30147177..30149389-chr13:30151174..30153674,3	K562	blood:
30	chr13:30164682..30166932-chr13:30278422..30280468,2	MCF-7	breast:
31	chr13:30128662..30130229-chr13:30134308..30136024,2	K562	blood:
32	chr13:30142261..30144231-chr13:30163491..30165148,2	MCF-7	breast:
33	chr13:30128662..30130229-chr13:30134308..30136024,2	K562	blood:
34	chr13:30146852..30149367-chr13:30152203..30154425,2	MCF-7	breast:
35	chr13:30124978..30127325-chr13:30144094..30146175,2	MCF-7	breast:
36	chr13:30146852..30149367-chr13:30152203..30154425,2	MCF-7	breast:
37	chr13:30126094..30127682-chr13:30160999..30163139,2	MCF-7	breast:
38	chr13:30142186..30144552-chr13:30152474..30154361,2	MCF-7	breast:
39	chr13:30137163..30140178-chr13:30141147..30143927,3	K562	blood:
40	chr13:30122738..30124853-chr13:30133655..30135999,2	MCF-7	breast:
41	chr13:30164095..30165741-chr13:30171298..30173970,2	MCF-7	breast:
42	chr13:30139726..30141978-chr13:30142351..30145103,3	MCF-7	breast:
43	chr13:30147733..30149517-chr13:30152740..30154897,2	MCF-7	breast:
44	chr13:30142867..30144693-chr13:30149445..30152081,2	MCF-7	breast:
45	chr13:30137163..30140178-chr13:30141147..30143927,3	K562	blood:
46	chr13:30145938..30148491-chr13:30169335..30172186,4	K562	blood:
47	chr13:30122738..30124853-chr13:30133655..30135999,2	MCF-7	breast:
48	chr13:30124073..30126477-chr13:30167606..30170454,3	MCF-7	breast:
49	chr13:30145040..30147217-chr13:30165008..30167643,2	K562	blood:
50	chr13:30141734..30150637-chr13:30164575..30171336,12	MCF-7	breast:

No data

Variant related genes	Relation type
SLC7A1	TF binding region
SLC7A1	CpG island
ENSG00000189403	chromatin interactions
ENSG00000139514	chromatin interactions

Extended variants
information (count: 1870 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565667296	chr13:30122275-30122276	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534554737	chr13:30122316-30122317	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184502694	chr13:30122324-30122325	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536446386	chr13:30122326-30122327	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116039569	chr13:30122338-30122339	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147760760	chr13:30122372-30122373	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141121930	chr13:30122393-30122394	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551175037	chr13:30122431-30122432	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs576703208	chr13:30122457-30122458	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs545375566	chr13:30122472-30122473	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs146938470	chr13:30122492-30122493	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs188522678	chr13:30122565-30122566	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs114822238	chr13:30122580-30122581	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs540997925	chr13:30122583-30122584	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs561062027	chr13:30122587-30122588	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs77882366	chr13:30122588-30122589	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs549975354	chr13:30122593-30122594	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs563332629	chr13:30122676-30122677	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs369201881	chr13:30122737-30122738	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs552506400	chr13:30122749-30122750	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs138079522	chr13:30122771-30122772	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570097807	chr13:30122772-30122773	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs149116522	chr13:30122803-30122804	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs181278629	chr13:30122877-30122878	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs533668168	chr13:30122906-30122907	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs548177215	chr13:30122920-30122921	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs551138977	chr13:30122957-30122958	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs143118060	chr13:30122972-30122973	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536728241	chr13:30122988-30122989	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566467670	chr13:30122996-30122997	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546833010	chr13:30122997-30122998	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs556764548	chr13:30123027-30123028	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184274798	chr13:30123146-30123147	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75685898	chr13:30123241-30123242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148248180	chr13:30123299-30123300	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142826946	chr13:30123306-30123307	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558844398	chr13:30123312-30123313	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572369498	chr13:30123324-30123325	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188812168	chr13:30123338-30123339	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114725642	chr13:30123367-30123368	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374727712	chr13:30123405-30123406	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs116602085	chr13:30123439-30123440	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs574921856	chr13:30123452-30123453	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs555061454	chr13:30123459-30123460	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs57383892	chr13:30123481-30123482	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563759167	chr13:30123492-30123493	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs371579794	chr13:30123499-30123500	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs113351802	chr13:30123526-30123527	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs532207835	chr13:30123534-30123535	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs552374715	chr13:30123535-30123536	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:1913 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30071000-30128800	Strong transcription	Dnd41	blood
2	chr13:30092200-30133000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr13:30097200-30138400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr13:30098800-30129000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr13:30103800-30137200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:30104200-30135400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:30104800-30124600	Weak transcription	Right Ventricle	heart
8	chr13:30105200-30136800	Weak transcription	Brain Germinal Matrix	brain
9	chr13:30106600-30125400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr13:30107000-30123200	Weak transcription	K562	blood
11	chr13:30107200-30123200	Weak transcription	A549	lung
12	chr13:30107200-30124200	Weak transcription	Placenta	Placenta
13	chr13:30107400-30122600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr13:30107400-30129200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr13:30108000-30122600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr13:30110400-30123200	Weak transcription	Lung	lung
17	chr13:30110400-30123400	Weak transcription	Spleen	Spleen
18	chr13:30110400-30123400	Weak transcription	NHLF	lung
19	chr13:30110400-30124200	Weak transcription	HMEC	breast
20	chr13:30110400-30127200	Weak transcription	Brain Angular Gyrus	brain
21	chr13:30110600-30123200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:30111200-30123200	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr13:30112400-30122400	Weak transcription	Fetal Intestine Small	intestine
24	chr13:30112800-30122800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr13:30112800-30127200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr13:30112800-30129200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr13:30113200-30123000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr13:30113200-30124600	Weak transcription	Brain Anterior Caudate	brain
29	chr13:30113200-30141600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr13:30113600-30123200	Weak transcription	Brain Hippocampus Middle	brain
31	chr13:30113600-30124200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr13:30113600-30129200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr13:30113800-30136200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr13:30114400-30123200	Weak transcription	Fetal Brain Female	brain
35	chr13:30114400-30126000	Weak transcription	Colon Smooth Muscle	Colon
36	chr13:30115000-30122600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:30115200-30123000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr13:30115200-30123400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr13:30115200-30125600	Weak transcription	Left Ventricle	heart
40	chr13:30115600-30123000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr13:30115600-30123000	Weak transcription	Thymus	Thymus
42	chr13:30115600-30124600	Weak transcription	Aorta	Aorta
43	chr13:30115600-30125800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr13:30115800-30124800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr13:30117600-30122400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr13:30117800-30124600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr13:30117800-30129000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr13:30118000-30122400	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr13:30118000-30123200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr13:30118000-30124600	Weak transcription	Placenta Amnion	Placenta Amnion

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