Variant report

Variant	nsv947135
Chromosome Location	chr1:161041002-161050287
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:550)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:161044473-161044777	K562	blood:	n/a	chr1:161044639-161044653
2	ATF3	chr1:161044527-161044753	K562	blood:	n/a	chr1:161044643-161044651 chr1:161044642-161044653 chr1:161044641-161044652 chr1:161044643-161044650 chr1:161044640-161044653 chr1:161044641-161044652 chr1:161044640-161044653 chr1:161044640-161044651 chr1:161044640-161044650 chr1:161044642-161044650 chr1:161044639-161044654 chr1:161044639-161044652 chr1:161044643-161044654 chr1:161044640-161044650
3	ATF3	chr1:161044491-161044768	K562	blood:	n/a	chr1:161044643-161044651 chr1:161044642-161044653 chr1:161044641-161044652 chr1:161044643-161044650 chr1:161044640-161044653 chr1:161044641-161044652 chr1:161044640-161044653 chr1:161044640-161044651 chr1:161044640-161044650 chr1:161044642-161044650 chr1:161044639-161044654 chr1:161044639-161044652 chr1:161044643-161044654 chr1:161044640-161044650
4	BACH1	chr1:161041729-161041969	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:161049693-161049895	GM12878	blood:	n/a	n/a
6	BATF	chr1:161049624-161049992	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:161041741-161041949	K562	blood:	n/a	n/a
8	BRCA1	chr1:161044596-161044796	HepG2	liver:	n/a	n/a
9	CBX3	chr1:161041656-161041970	K562	blood:	n/a	n/a
10	CCNT2	chr1:161041853-161042239	K562	blood:	n/a	n/a
11	CCNT2	chr1:161049405-161049605	K562	blood:	n/a	n/a
12	CEBPB	chr1:161042643-161042780	HepG2	liver:	n/a	n/a
13	CREB1	chr1:161044280-161044975	HepG2	liver:	n/a	chr1:161044803-161044816 chr1:161044640-161044653
14	CTCF	chr1:161041688-161041928	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:161041720-161041870	HMF	breast:	n/a	n/a
16	CTCF	chr1:161041638-161041917	K562	blood:	n/a	n/a
17	CTCF	chr1:161041740-161041890	GM12874	blood:	n/a	n/a
18	CTCF	chr1:161041660-161041810	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr1:161049655-161049821	GM19239	blood:	n/a	n/a
20	CTCF	chr1:161041694-161041942	GM19239	blood:	n/a	n/a
21	CTCF	chr1:161043600-161043750	NHEK	skin:	n/a	chr1:161043719-161043732
22	CTCF	chr1:161049620-161049770	GM12870	blood:	n/a	n/a
23	CTCF	chr1:161042084-161042089	GM12891	blood:	n/a	n/a
24	CTCF	chr1:161041680-161041830	HVMF	connective:	n/a	n/a
25	CTCF	chr1:161049640-161049790	GM12867	blood:	n/a	n/a
26	CTCF	chr1:161049751-161049760	GM10248	blood:	n/a	n/a
27	CTCF	chr1:161042142-161042184	GM12892	blood:	n/a	n/a
28	CTCF	chr1:161041692-161041884	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr1:161041716-161041919	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:161041680-161041830	NHEK	skin:	n/a	n/a
31	CTCF	chr1:161041598-161042050	GM12878	blood:	n/a	n/a
32	CTCF	chr1:161041675-161041922	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:161049680-161049830	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr1:161049711-161049784	NHEK	skin:	n/a	n/a
35	CTCF	chr1:161043647-161043798	H1-hESC	embryonic stem cell:	n/a	chr1:161043719-161043732
36	CTCF	chr1:161043673-161043797	K562	blood:	n/a	chr1:161043719-161043732
37	CTCF	chr1:161041700-161041850	HEK293	kidney:	n/a	n/a
38	CTCF	chr1:161041675-161041939	GM12878	blood:	n/a	n/a
39	CTCF	chr1:161041720-161041870	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr1:161049710-161049776	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr1:161043656-161043783	HepG2	liver:	n/a	chr1:161043719-161043732
42	CTCF	chr1:161041400-161041550	GM12873	blood:	n/a	n/a
43	CTCF	chr1:161041660-161041913	LNCaP	prostate:	n/a	n/a
44	CTCF	chr1:161049656-161049813	GM12891	blood:	n/a	n/a
45	CTCF	chr1:161043640-161043790	WERI-Rb-1	eye:	n/a	chr1:161043719-161043732
46	CTCF	chr1:161049580-161049730	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr1:161049655-161049837	GM19238	blood:	n/a	n/a
48	CTCF	chr1:161041740-161041890	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr1:161041740-161041890	GM06990	blood:	n/a	n/a
50	CTCF	chr1:161041697-161041913	NHEK	skin:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161050227-161050277	SAEC	small airway:	n/a
2	chr1:161050227-161050277	SAEC	small airway:	n/a
3	chr1:161050227-161050277	HRE	kidney:	n/a
4	chr1:161045663-161045713	HL-60	blood:	n/a
5	chr1:161049543-161049593	AG04449	skin:	fetal
6	chr1:161049543-161049593	Hela-S3	cervix:	n/a
7	chr1:161049147-161049197	SK-N-SH_RA	brain:	n/a
8	chr1:161049543-161049593	HCF	heart:	n/a
9	chr1:161049677-161049727	NT2-D1	testis:	n/a
10	chr1:161042063-161042113	ProgFib	skin:	n/a
11	chr1:161042063-161042113	GM06990	blood:	n/a
12	chr1:161049147-161049197	U87	brain:	n/a
13	chr1:161049655-161049705	HMEC	breast:	n/a
14	chr1:161049655-161049705	T-47D	breast:	n/a
15	chr1:161050227-161050277	HL-60	blood:	n/a
16	chr1:161045663-161045713	ProgFib	skin:	n/a
17	chr1:161042063-161042113	HMEC	breast:	n/a
18	chr1:161049147-161049197	HCM	heart:	n/a
19	chr1:161049443-161049493	AG04449	skin:	fetal
20	chr1:161049543-161049593	AG10803	skin:	n/a
21	chr1:161042063-161042113	CMK	blood:	n/a
22	chr1:161042063-161042113	HAEpiC	amniotic membrane:	n/a
23	chr1:161049543-161049593	SAEC	small airway:	n/a
24	chr1:161049579-161049629	PANC-1	pancreas:	n/a
25	chr1:161049677-161049727	NHDF-neo	bronchial:	n/a
26	chr1:161049543-161049593	HRCEpiC	kidney:	n/a
27	chr1:161049543-161049593	HCPEpiC	choroid plexus:	n/a
28	chr1:161049443-161049493	CMK	blood:	n/a
29	chr1:161042063-161042113	ovcar-3	ovarian:	n/a
30	chr1:161049677-161049727	PFSK-1	brain:	n/a
31	chr1:161049579-161049629	IMR90	lung:	fetal
32	chr1:161049443-161049493	PrEC	prostate:	n/a
33	chr1:161049579-161049629	PFSK-1	brain:	n/a
34	chr1:161049543-161049593	SKMC	muscle:	n/a
35	chr1:161049543-161049593	BJ	skin:	n/a
36	chr1:161042063-161042113	BE2_C	brain:	n/a
37	chr1:161049579-161049629	HEEpiC	esophagus:	n/a
38	chr1:161049677-161049727	U87	brain:	n/a
39	chr1:161049443-161049493	ovcar-3	ovarian:	n/a
40	chr1:161045663-161045713	T-47D	breast:	n/a
41	chr1:161050227-161050277	K562	blood:	n/a
42	chr1:161049677-161049727	NB4	blood:	n/a
43	chr1:161049443-161049493	NH-A	brain:	n/a
44	chr1:161049443-161049493	SAEC	small airway:	n/a
45	chr1:161042063-161042113	RPTEC	kidney:	n/a
46	chr1:161050227-161050277	HMEC	breast:	n/a
47	chr1:161049677-161049727	AG04450	lung:	fetal
48	chr1:161049543-161049593	H1-hESC	embryonic stem cell:	embryo
49	chr1:161049579-161049629	Caco-2	colon:	n/a
50	chr1:161049147-161049197	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:161039261..161041594-chr1:161042293..161044565,2	MCF-7	breast:
2	chr1:161041322..161042651-chr1:161108963..161110253,9	K562	blood:
3	chr1:161045029..161046710-chr1:161057509..161060408,2	K562	blood:
4	chr1:161049267..161049804-chr1:161067227..161068374,4	MCF-7	breast:
5	chr1:161039261..161041594-chr1:161042293..161044565,2	MCF-7	breast:
6	chr1:161012288..161019472-chr1:161047717..161055328,13	MCF-7	breast:
7	chr1:161043403..161046292-chr1:161046459..161048840,3	MCF-7	breast:
8	chr1:161049380..161051742-chr1:161085768..161089487,3	MCF-7	breast:
9	chr1:161041307..161042464-chr1:161067079..161068224,19	MCF-7	breast:
10	chr1:161040956..161045180-chr1:161134527..161136918,3	MCF-7	breast:
11	chr1:161015334..161017315-chr1:161043865..161045880,2	MCF-7	breast:
12	chr1:161006354..161009878-chr1:161042497..161045575,4	MCF-7	breast:
13	chr1:161007186..161008951-chr1:161048410..161050017,2	MCF-7	breast:
14	chr1:161041327..161042169-chr1:161066813..161068080,6	MCF-7	breast:
15	chr1:161014829..161016520-chr1:161042176..161043706,2	K562	blood:
16	chr1:161020801..161022470-chr1:161048503..161051319,2	K562	blood:
17	chr1:161013435..161019346-chr1:161039308..161043996,7	MCF-7	breast:
18	chr1:160963404..160964072-chr1:161041337..161041980,2	MCF-7	breast:
19	chr1:160982248..160985015-chr1:161041891..161043731,2	K562	blood:
20	chr1:161043261..161046256-chr1:161047993..161050250,2	K562	blood:
21	chr1:161038298..161040861-chr1:161050005..161051745,3	K562	blood:
22	chr1:161035244..161038070-chr1:161039157..161043697,5	MCF-7	breast:
23	chr1:161041431..161042257-chr1:161128491..161129236,2	K562	blood:
24	chr1:161041308..161041827-chr1:161067091..161067673,2	K562	blood:
25	chr1:161037367..161040150-chr1:161043095..161044825,3	MCF-7	breast:
26	chr1:161049627..161050247-chr1:161067142..161067787,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PVRL4	hsa-miR-181a-5p	chr1:161041816-161041839

Variant related genes	Relation type
PVRL4	TF binding region
ENSG00000228917	TF binding region
ARHGAP30	TF binding region
PVRL4	CpG island
ENSG00000228917	CpG island
ARHGAP30	CpG island
ENSG00000186517	chromatin interactions
ENSG00000158793	chromatin interactions
ENSG00000143256	chromatin interactions
ENSG00000270149	chromatin interactions
ENSG00000215845	chromatin interactions
ENSG00000143217	chromatin interactions
ENSG00000268154	chromatin interactions
ENSG00000162755	chromatin interactions
ENSG00000158773	chromatin interactions
ENSG00000224985	chromatin interactions
ENSG00000143224	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375537125	chr1:161041013-161041014	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs532169466	chr1:161041044-161041045	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs184757561	chr1:161041165-161041166	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs569174746	chr1:161041207-161041208	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs531681970	chr1:161041219-161041220	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs548069699	chr1:161041231-161041232	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs145859289	chr1:161041249-161041250	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs534013378	chr1:161041262-161041263	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs547890655	chr1:161041317-161041318	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs570480171	chr1:161041411-161041412	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs539458638	chr1:161041476-161041477	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs149014831	chr1:161041491-161041492	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs553150310	chr1:161041685-161041686	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs576325428	chr1:161041731-161041732	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs80118484	chr1:161041745-161041746	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs375508679	chr1:161041746-161041747	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs572631106	chr1:161041877-161041878	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs534808314	chr1:161041880-161041881	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs11552341	chr1:161041906-161041907	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs143762939	chr1:161041907-161041908	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs560200648	chr1:161041935-161041936	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs576858901	chr1:161042016-161042017	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs74927936	chr1:161042023-161042024	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs79686183	chr1:161042024-161042025	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs542957566	chr1:161042059-161042060	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs12116949	chr1:161042063-161042064	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs562506176	chr1:161042077-161042078	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs117363341	chr1:161042105-161042106	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs548491230	chr1:161042138-161042139	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs561702889	chr1:161042201-161042202	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs527495166	chr1:161042206-161042207	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs547534513	chr1:161042209-161042210	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs543316888	chr1:161042294-161042295	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs557246132	chr1:161042326-161042327	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs187551945	chr1:161042334-161042335	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs539591539	chr1:161042343-161042344	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs141350553	chr1:161042353-161042354	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs569752525	chr1:161042354-161042355	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs535755638	chr1:161042363-161042364	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs373753089	chr1:161042364-161042365	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs556048786	chr1:161042376-161042377	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs543834963	chr1:161042387-161042388	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs367674230	chr1:161042405-161042406	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs367753351	chr1:161042406-161042407	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs535222169	chr1:161042447-161042448	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs147849290	chr1:161042467-161042468	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs577001042	chr1:161042483-161042484	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs141389274	chr1:161042493-161042494	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs573511829	chr1:161042494-161042495	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs138257801	chr1:161042507-161042508	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161030000-161046200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:161038600-161041200	Enhancers	HMEC	breast
3	chr1:161038800-161041800	Weak transcription	HepG2	liver
4	chr1:161038800-161043400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:161039000-161042000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:161039000-161043400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:161039200-161042400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:161039600-161041800	Weak transcription	Pancreas	Pancrea
9	chr1:161039600-161042000	Weak transcription	Fetal Stomach	stomach
10	chr1:161039600-161042000	Weak transcription	Spleen	Spleen
11	chr1:161039600-161049000	Weak transcription	Lung	lung
12	chr1:161039600-161066800	Weak transcription	Right Atrium	heart
13	chr1:161039800-161041200	Strong transcription	Placenta	Placenta
14	chr1:161039800-161041800	Weak transcription	Adipose Nuclei	Adipose
15	chr1:161039800-161042000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:161039800-161042000	Enhancers	Fetal Thymus	thymus
17	chr1:161039800-161042000	Weak transcription	Gastric	stomach
18	chr1:161039800-161049000	Weak transcription	Fetal Intestine Small	intestine
19	chr1:161039800-161052600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr1:161039800-161053000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:161040000-161041200	Enhancers	Thymus	Thymus
22	chr1:161040000-161041800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr1:161040000-161042000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:161040000-161042000	Strong transcription	Esophagus	oesophagus
25	chr1:161040000-161042200	Enhancers	Primary B cells from peripheral blood	blood
26	chr1:161040000-161042400	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr1:161040000-161044400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr1:161040200-161041800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr1:161040200-161041800	Weak transcription	K562	blood
30	chr1:161040200-161042000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:161040200-161042000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:161040200-161042000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr1:161040200-161042000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:161040200-161042000	Enhancers	GM12878-XiMat	blood
35	chr1:161040200-161042200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr1:161040200-161042200	Enhancers	Primary B cells from cord blood	blood
37	chr1:161040200-161042200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr1:161040200-161042200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr1:161040200-161042400	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr1:161040200-161042400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr1:161040200-161042400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:161040200-161042400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:161040200-161042600	Enhancers	Primary T cells fromperipheralblood	blood
44	chr1:161040200-161042600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:161040200-161045000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:161040200-161052600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:161040200-161052800	Weak transcription	Colonic Mucosa	Colon
48	chr1:161040400-161041400	Enhancers	NHEK	skin
49	chr1:161040400-161042200	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr1:161040600-161042200	Enhancers	Primary T cells from cord blood	blood

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