Variant report

Variant	nsv872539
Chromosome Location	chr1:169658586-169674590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:169666839-169667373	GM12878	blood:	n/a	n/a
2	BATF	chr1:169666902-169667269	GM12878	blood:	n/a	n/a
3	BATF	chr1:169668150-169668460	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:169661404-169662555	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:169658708-169658717	GM12878	blood:	n/a	n/a
6	BRCA1	chr1:169659659-169660100	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr1:169663513-169663645	GM12878	blood:	n/a	n/a
8	CTCF	chr1:169663500-169663650	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
9	CTCF	chr1:169669060-169669210	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:169663483-169663678	LNCaP	prostate:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
11	CTCF	chr1:169663520-169663670	GM12869	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
12	CTCF	chr1:169663560-169663710	GM12871	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
13	CTCF	chr1:169668620-169668770	GM12874	blood:	n/a	n/a
14	CTCF	chr1:169663354-169663771	HCT-116	colon:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
15	CTCF	chr1:169663420-169663570	RPTEC	kidney:	n/a	n/a
16	CTCF	chr1:169668910-169669291	HCT-116	colon:	n/a	n/a
17	CTCF	chr1:169663513-169663648	HUVEC	blood vessel:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
18	CTCF	chr1:169663516-169663686	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
19	CTCF	chr1:169669040-169669190	Caco-2	colon:	n/a	n/a
20	CTCF	chr1:169663573-169663640	GM10266	blood:	n/a	chr1:169663577-169663585
21	CTCF	chr1:169663560-169663710	GM12873	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
22	CTCF	chr1:169663540-169663690	GM06990	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
23	CTCF	chr1:169663520-169663670	GM12874	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
24	CTCF	chr1:169663480-169663630	HMEC	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
25	CTCF	chr1:169669055-169669142	LNCaP	prostate:	n/a	n/a
26	CTCF	chr1:169663559-169663639	GM10248	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
27	CTCF	chr1:169663460-169663610	A549	lung:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
28	CTCF	chr1:169669120-169669270	GM12873	blood:	n/a	n/a
29	CTCF	chr1:169663493-169663708	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
30	CTCF	chr1:169663489-169663704	Spleen_OC	spleen:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
31	CTCF	chr1:169663400-169663690	GM12871	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
32	CTCF	chr1:169669122-169669176	GM12878	blood:	n/a	n/a
33	CTCF	chr1:169669069-169669188	LNCaP	prostate:	n/a	n/a
34	CTCF	chr1:169663304-169663811	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
35	CTCF	chr1:169669042-169669194	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr1:169663510-169663669	Medullo	brain:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
37	CTCF	chr1:169663480-169663630	GM12867	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
38	CTCF	chr1:169663500-169663650	GM12866	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
39	CTCF	chr1:169669028-169669214	A549	lung:	n/a	n/a
40	CTCF	chr1:169668978-169669282	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:169663480-169663630	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
42	CTCF	chr1:169663560-169663710	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
43	CTCF	chr1:169663540-169663690	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
44	CTCF	chr1:169663540-169663690	GM12873	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
45	CTCF	chr1:169669017-169669198	Medullo	brain:	n/a	n/a
46	CTCF	chr1:169669097-169669182	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:169663570-169663627	K562	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590
48	CTCF	chr1:169663440-169663852	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
49	CTCF	chr1:169663620-169663770	GM12864	blood:	n/a	n/a
50	CTCF	chr1:169663560-169663710	GM06990	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169671116-169671166	SAEC	small airway:	n/a
2	chr1:169671116-169671166	AG10803	skin:	n/a
3	chr1:169660219-169660269	MCF10A-Er-Src	breast:	n/a
4	chr1:169671116-169671166	GM19239	blood:	n/a
5	chr1:169660219-169660269	HepG2	liver:	n/a
6	chr1:169660219-169660269	GM12892	blood:	n/a
7	chr1:169671116-169671166	NHBE	bronchial:	n/a
8	chr1:169660219-169660269	HCT-116	colon:	n/a
9	chr1:169660219-169660269	K562	blood:	n/a
10	chr1:169671116-169671166	NB4	blood:	n/a
11	chr1:169660219-169660269	HCF	heart:	n/a
12	chr1:169660219-169660269	LNCaP	prostate:	n/a
13	chr1:169671116-169671166	PANC-1	pancreas:	n/a
14	chr1:169671116-169671166	LNCaP	prostate:	n/a
15	chr1:169671116-169671166	CMK	blood:	n/a
16	chr1:169660219-169660269	PrEC	prostate:	n/a
17	chr1:169660219-169660269	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:169671116-169671166	ProgFib	skin:	n/a
19	chr1:169660219-169660269	IMR90	lung:	fetal
20	chr1:169671116-169671166	MCF-7	breast:	n/a
21	chr1:169660219-169660269	BE2_C	brain:	n/a
22	chr1:169660219-169660269	HCPEpiC	choroid plexus:	n/a
23	chr1:169660219-169660269	GM12878	blood:	n/a
24	chr1:169660219-169660269	NB4	blood:	n/a
25	chr1:169660219-169660269	Caco-2	colon:	n/a
26	chr1:169660219-169660269	PANC-1	pancreas:	n/a
27	chr1:169660219-169660269	Hepatocyte	liver:	n/a
28	chr1:169671116-169671166	GM12891	blood:	n/a
29	chr1:169671116-169671166	T-47D	breast:	n/a
30	chr1:169671116-169671166	HIPEpiC	eye:	n/a
31	chr1:169671116-169671166	MCF10A-Er-Src	breast:	n/a
32	chr1:169660219-169660269	ProgFib	skin:	n/a
33	chr1:169671116-169671166	SK-N-MC	brain:	n/a
34	chr1:169671116-169671166	HL-60	blood:	n/a
35	chr1:169671116-169671166	HUVEC	blood vessel:	n/a
36	chr1:169660219-169660269	NT2-D1	testis:	n/a
37	chr1:169671116-169671166	SKMC	muscle:	n/a
38	chr1:169660219-169660269	HNPCEpiC	eye:	n/a
39	chr1:169660219-169660269	HRE	kidney:	n/a
40	chr1:169671116-169671166	HCM	heart:	n/a
41	chr1:169671116-169671166	HMEC	breast:	n/a
42	chr1:169660219-169660269	NH-A	brain:	n/a
43	chr1:169671116-169671166	AoSMC	blood vessel:	n/a
44	chr1:169671116-169671166	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:169660219-169660269	Jurkat	blood:	n/a
46	chr1:169660219-169660269	PFSK-1	brain:	n/a
47	chr1:169671116-169671166	HRCEpiC	kidney:	n/a
48	chr1:169671116-169671166	SK-N-SH	brain:	n/a
49	chr1:169671116-169671166	Jurkat	blood:	n/a
50	chr1:169671116-169671166	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169519013..169520404-chr1:169662765..169663989,4	MCF-7	breast:
2	chr1:169668675..169669722-chr1:169778297..169779287,4	MCF-7	breast:
3	chr1:169658516..169660936-chr1:169662078..169664299,2	K562	blood:
4	chr1:169555471..169556167-chr1:169663467..169664121,3	MCF-7	breast:
5	chr1:169668678..169669639-chr1:169778642..169779434,3	MCF-7	breast:
6	chr1:169570098..169571225-chr1:169663167..169664353,5	MCF-7	breast:
7	chr1:169674141..169677050-chr1:169763005..169764633,2	MCF-7	breast:
8	chr1:169658516..169660936-chr1:169662078..169664299,2	K562	blood:
9	chr1:169663115..169663861-chr1:169679931..169680901,2	MCF-7	breast:
10	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SELE-1	chr1:169665676-169665694	NONHSAT007471
2	lnc-SELE-1	chr1:169672396-169672470	NONHSAT007471
3	lnc-SELE-1	chr1:169660822-169660943	NONHSAT007471

Variant related genes	Relation type
SELL	TF binding region
SELL	CpG island
ENSG00000171806	chromatin interactions
ENSG00000000460	chromatin interactions
ENSG00000188404	chromatin interactions
ENSG00000198734	chromatin interactions

Extended variants
information (count: 673 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4987388	chr1:169658586-169658587	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555520848	chr1:169658590-169658591	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs568819689	chr1:169658648-169658649	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544486228	chr1:169658650-169658651	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs574211870	chr1:169658660-169658661	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544373650	chr1:169658675-169658676	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs182075154	chr1:169658680-169658681	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs578039125	chr1:169658711-169658712	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs185482001	chr1:169658761-169658762	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs560495278	chr1:169658774-169658775	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs528370631	chr1:169658787-169658788	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs546948379	chr1:169658799-169658800	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs531230370	chr1:169658880-169658881	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs529133099	chr1:169658898-169658899	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs199770451	chr1:169658917-169658918	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs75144403	chr1:169658918-169658919	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201241240	chr1:169658919-169658920	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190788110	chr1:169658922-169658923	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs4987409	chr1:169658928-169658929	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs147326866	chr1:169658976-169658977	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566159524	chr1:169659021-169659022	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4987387	chr1:169659043-169659044	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144815649	chr1:169659063-169659064	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574150961	chr1:169659066-169659067	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111752235	chr1:169659101-169659102	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548202353	chr1:169659102-169659103	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148529027	chr1:169659123-169659124	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185120584	chr1:169659128-169659129	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4987408	chr1:169659138-169659139	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151028641	chr1:169659153-169659154	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4987386	chr1:169659252-169659253	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs4987407	chr1:169659286-169659287	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189879057	chr1:169659294-169659295	Enhancers Bivalent Enhancer Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs4987385	chr1:169659426-169659427	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs541266789	chr1:169659443-169659444	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs181137671	chr1:169659449-169659450	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs550716829	chr1:169659503-169659504	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs562563519	chr1:169659580-169659581	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs532842634	chr1:169659589-169659590	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs144838954	chr1:169659613-169659614	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs566122797	chr1:169659614-169659615	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs527335095	chr1:169659626-169659627	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs548706834	chr1:169659642-169659643	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs558394367	chr1:169659684-169659685	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs570320132	chr1:169659715-169659716	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs12065232	chr1:169659760-169659761	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs3835455	chr1:169659779-169659780	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs397734000	chr1:169659782-169659783	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs538175004	chr1:169659829-169659830	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs556693100	chr1:169659858-169659859	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169647800-169659600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr1:169647800-169660000	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr1:169648200-169659000	Enhancers	Primary B cells from peripheral blood	blood
4	chr1:169652800-169660200	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr1:169653200-169671600	Weak transcription	Spleen	Spleen
6	chr1:169655000-169658600	Enhancers	Primary T cells from cord blood	blood
7	chr1:169656200-169659400	Enhancers	Primary B cells from cord blood	blood
8	chr1:169656200-169659400	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr1:169656600-169659600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:169656800-169659200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr1:169656800-169662600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr1:169657000-169659400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:169657000-169660200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:169657000-169661800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:169657200-169659200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr1:169657600-169658800	Enhancers	Primary hematopoietic stem cells	blood
17	chr1:169657600-169659200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:169657600-169659400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr1:169657800-169659600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr1:169657800-169659800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr1:169657800-169660200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr1:169657800-169660600	Enhancers	Fetal Thymus	thymus
23	chr1:169658000-169659200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:169658200-169658800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr1:169658200-169659400	Enhancers	Dnd41	blood
26	chr1:169658200-169660600	Enhancers	GM12878-XiMat	blood
27	chr1:169658400-169659000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:169658400-169660200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:169658400-169666200	Enhancers	Thymus	Thymus
30	chr1:169658600-169658800	Flanking Active TSS	Primary T cells from cord blood	blood
31	chr1:169658600-169659600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr1:169658600-169661000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr1:169658800-169659000	Genic enhancers	Primary T cells from cord blood	blood
34	chr1:169658800-169660000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:169658800-169660400	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr1:169659000-169659200	Flanking Active TSS	Primary T cells from cord blood	blood
37	chr1:169659000-169659400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr1:169659000-169660200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:169659000-169661600	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr1:169659200-169659400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr1:169659200-169659600	Enhancers	Primary T cells from cord blood	blood
42	chr1:169659200-169659800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr1:169659200-169660400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
44	chr1:169659200-169660600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:169659200-169660800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr1:169659200-169661000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr1:169659200-169661000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
48	chr1:169659200-169661200	Genic enhancers	Primary T cells fromperipheralblood	blood
49	chr1:169659200-169661400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:169659400-169660000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell

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