Variant report

Variant	nsv1004148
Chromosome Location	chr1:166951869-167016311
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	ATF1	chr1:167013300-167013645	K562	blood:	n/a	n/a
2	ATF2	chr1:167013031-167013739	GM12878	blood:	n/a	chr1:167013480-167013491
3	ATF3	chr1:167013381-167013608	K562	blood:	n/a	chr1:167013479-167013490 chr1:167013480-167013491 chr1:167013482-167013489 chr1:167013480-167013493 chr1:167013478-167013493 chr1:167013482-167013492 chr1:167013478-167013489 chr1:167013482-167013490 chr1:167013480-167013491
4	ATF3	chr1:167013224-167013687	K562	blood:	n/a	chr1:167013479-167013490 chr1:167013480-167013491 chr1:167013482-167013489 chr1:167013480-167013493 chr1:167013478-167013493 chr1:167013482-167013492 chr1:167013478-167013489 chr1:167013482-167013490 chr1:167013480-167013491
5	BACH1	chr1:166965155-166965166	K562	blood:	n/a	n/a
6	BHLHE40	chr1:167013303-167013633	K562	blood:	n/a	n/a
7	BRCA1	chr1:167013471-167013493	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr1:167013171-167013672	K562	blood:	n/a	n/a
9	CCNT2	chr1:167013435-167013594	K562	blood:	n/a	n/a
10	CEBPB	chr1:166958088-166958463	IMR90	lung:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
11	CEBPB	chr1:166958146-166958419	HepG2	liver:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
12	CEBPB	chr1:166985424-166985627	ECC-1	luminal epithelium:	n/a	chr1:166985595-166985606
13	CEBPB	chr1:166958122-166958456	HepG2	liver:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
14	CEBPB	chr1:166985346-166985703	IMR90	lung:	n/a	chr1:166985595-166985606
15	CEBPB	chr1:166958065-166958406	A549	lung:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
16	CEBPB	chr1:166958090-166958496	MCF-7	breast:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
17	CEBPB	chr1:166959841-166959881	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:166980888-166981198	Hela-S3	cervix:	n/a	chr1:166981035-166981046
19	CEBPB	chr1:166980911-166981184	H1-hESC	embryonic stem cell:	n/a	chr1:166981035-166981046
20	CEBPB	chr1:166985417-166985678	MCF-7	breast:	n/a	chr1:166985595-166985606
21	CEBPB	chr1:166980855-166981217	IMR90	lung:	n/a	chr1:166981035-166981046
22	CEBPB	chr1:166980841-166981215	HepG2	liver:	n/a	chr1:166981035-166981046
23	CEBPB	chr1:166958027-166958543	A549	lung:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
24	CEBPB	chr1:166958077-166958403	K562	blood:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
25	CEBPB	chr1:166958081-166958470	A549	lung:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
26	CEBPB	chr1:166958173-166958374	HepG2	liver:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
27	CEBPB	chr1:166958081-166958495	H1-hESC	embryonic stem cell:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
28	CEBPB	chr1:166957971-166958571	K562	blood:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
29	CEBPB	chr1:166980853-166981221	A549	lung:	n/a	chr1:166981035-166981046
30	CEBPB	chr1:166985434-166985695	H1-hESC	embryonic stem cell:	n/a	chr1:166985595-166985606
31	CEBPB	chr1:166985332-166985694	HepG2	liver:	n/a	chr1:166985595-166985606
32	CEBPB	chr1:167013460-167013524	K562	blood:	n/a	n/a
33	CEBPB	chr1:166985360-166985693	A549	lung:	n/a	chr1:166985595-166985606
34	CEBPB	chr1:166958080-166958464	Hela-S3	cervix:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
35	CEBPB	chr1:166958050-166958475	MCF-7	breast:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
36	CEBPB	chr1:166958085-166958412	ECC-1	luminal epithelium:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
37	CEBPB	chr1:166980856-166981219	K562	blood:	n/a	chr1:166981035-166981046
38	CEBPB	chr1:166958071-166958476	ECC-1	luminal epithelium:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
39	CEBPB	chr1:166958003-166958585	K562	blood:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
40	CEBPB	chr1:166989333-166989414	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:166958083-166958471	HepG2	liver:	n/a	chr1:166958338-166958346 chr1:166958268-166958279 chr1:166958269-166958278 chr1:166958269-166958278 chr1:166958267-166958280 chr1:166958269-166958278
42	CEBPB	chr1:166985358-166985679	K562	blood:	n/a	chr1:166985595-166985606
43	CEBPD	chr1:166958075-166958493	K562	blood:	n/a	chr1:166958269-166958278
44	CHD1	chr1:166972697-166972787	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr1:167013450-167013619	K562	blood:	n/a	n/a
46	CHD2	chr1:167013444-167013454	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr1:167013498-167013641	HepG2	liver:	n/a	n/a
48	CREB1	chr1:167013323-167013585	A549	lung:	n/a	chr1:167013479-167013492
49	CREB1	chr1:167013172-167013699	GM12878	blood:	n/a	chr1:167013479-167013492
50	CREB1	chr1:167013330-167013593	H1-hESC	embryonic stem cell:	n/a	chr1:167013479-167013492

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:166958389-166958439	MCF10A-Er-Src	breast:	n/a
2	chr1:166958389-166958439	MCF10A-Er-Src	breast:	n/a
3	chr1:166958406-166958456	HRE	kidney:	n/a
4	chr1:166955898-166955948	AG10803	skin:	n/a
5	chr1:166958581-166958631	NT2-D1	testis:	n/a
6	chr1:166958439-166958489	LNCaP	prostate:	n/a
7	chr1:166958406-166958456	K562	blood:	n/a
8	chr1:166958439-166958489	HRE	kidney:	n/a
9	chr1:166958406-166958456	GM06990	blood:	n/a
10	chr1:166958401-166958451	AG09309	skin:	n/a
11	chr1:166958273-166958323	HCF	heart:	n/a
12	chr1:166958221-166958271	NH-A	brain:	n/a
13	chr1:166958581-166958631	BJ	skin:	n/a
14	chr1:166958583-166958633	NT2-D1	testis:	n/a
15	chr1:166959030-166959080	H1-hESC	embryonic stem cell:	embryo
16	chr1:166959030-166959080	HCF	heart:	n/a
17	chr1:166958389-166958439	Hela-S3	cervix:	n/a
18	chr1:166962376-166962426	AoSMC	blood vessel:	n/a
19	chr1:166958221-166958271	AG04449	skin:	fetal
20	chr1:166958581-166958631	GM12892	blood:	n/a
21	chr1:166958389-166958439	CMK	blood:	n/a
22	chr1:166958308-166958358	LNCaP	prostate:	n/a
23	chr1:166959030-166959080	HCPEpiC	choroid plexus:	n/a
24	chr1:166958583-166958633	HAEpiC	amniotic membrane:	n/a
25	chr1:166958233-166958283	HEK293	kidney:	embryo
26	chr1:166958233-166958283	AG09309	skin:	n/a
27	chr1:166958221-166958271	HepG2	liver:	n/a
28	chr1:166958401-166958451	PANC-1	pancreas:	n/a
29	chr1:166958322-166958372	Hela-S3	cervix:	n/a
30	chr1:166962376-166962426	AG04449	skin:	fetal
31	chr1:166958439-166958489	AG04449	skin:	fetal
32	chr1:166958273-166958323	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:166958389-166958439	AG09319	gingival:	n/a
34	chr1:166958583-166958633	SKMC	muscle:	n/a
35	chr1:166958233-166958283	HCPEpiC	choroid plexus:	n/a
36	chr1:167013332-167013382	SAEC	small airway:	n/a
37	chr1:167013332-167013382	GM12891	blood:	n/a
38	chr1:166958583-166958633	GM06990	blood:	n/a
39	chr1:166958233-166958283	GM19239	blood:	n/a
40	chr1:166958308-166958358	AG04450	lung:	fetal
41	chr1:166955898-166955948	HIPEpiC	eye:	n/a
42	chr1:166958401-166958451	NHBE	bronchial:	n/a
43	chr1:166958273-166958323	SK-N-MC	brain:	n/a
44	chr1:166958322-166958372	Hepatocyte	liver:	n/a
45	chr1:166955898-166955948	HRPEpiC	eye:	n/a
46	chr1:166962376-166962426	Jurkat	blood:	n/a
47	chr1:166959030-166959080	PFSK-1	brain:	n/a
48	chr1:166958233-166958283	K562	blood:	n/a
49	chr1:166958308-166958358	HepG2	liver:	n/a
50	chr1:166958439-166958489	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:166806409..166808484-chr1:167002328..167004286,2	K562	blood:
2	chr1:167002101..167004859-chr1:167007151..167009265,2	MCF-7	breast:
3	chr1:167012979..167014978-chr1:167017542..167019812,2	K562	blood:
4	chr1:166970676..166973500-chr1:166976279..166979134,2	K562	blood:
5	chr1:166958430..166961533-chr1:166963618..166965813,3	K562	blood:
6	chr1:166945300..166947626-chr1:166953556..166955132,2	K562	blood:
7	chr1:166844981..166846791-chr1:167011977..167013580,2	MCF-7	breast:
8	chr1:166953493..166955548-chr1:167027824..167030715,2	K562	blood:
9	chr1:166844307..166846188-chr1:167015555..167017418,2	K562	blood:
10	chr1:167015895..167019634-chr1:167023562..167026888,4	K562	blood:
11	chr1:167002101..167004859-chr1:167007151..167009265,2	MCF-7	breast:
12	chr1:166959072..166963031-chr1:166963279..166965118,3	K562	blood:
13	chr1:166970676..166973500-chr1:166976279..166979134,2	K562	blood:
14	chr1:166954507..166957391-chr1:166978145..166980426,2	K562	blood:
15	chr1:166807506..166810186-chr1:167012787..167014455,2	MCF-7	breast:
16	chr1:166954507..166957391-chr1:166978145..166980426,2	K562	blood:
17	chr1:167012456..167017091-chr1:167019887..167022128,4	K562	blood:
18	chr1:167009577..167010118-chr1:167021584..167022369,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPA33-2	chr1:166999227-166999478	NONHSAT007377
2	lnc-GPA33-2	chr1:167010187-167010352	NONHSAT007377

Variant related genes	Relation type
ENSG00000238325	TF binding region
MAEL	TF binding region
RNA5SP65	TF binding region
ENSG00000238325	CpG island
MAEL	CpG island
RNA5SP65	CpG island
ENSG00000152382	chromatin interactions
ENSG00000143194	chromatin interactions
ENSG00000143157	chromatin interactions
ENSG00000227907	chromatin interactions

Extended variants
information (count: 1115 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145823155	chr1:166953843-166953844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs6695609	chr1:166953866-166953867	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs574888359	chr1:166953893-166953894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs542418676	chr1:166953894-166953895	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181040925	chr1:166953939-166953940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs148973812	chr1:166953959-166953960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546546151	chr1:166953980-166953981	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564856779	chr1:166954012-166954013	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532183745	chr1:166954038-166954039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs72689320	chr1:166954057-166954058	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146456914	chr1:166954480-166954481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532140177	chr1:166956673-166956674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142575989	chr1:166958006-166958007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs80132679	chr1:166958019-166958020	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370432964	chr1:166958037-166958038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574927984	chr1:166958083-166958084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139363882	chr1:166958086-166958087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs557475852	chr1:166958214-166958215	Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs572652516	chr1:166958232-166958233	Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs540060616	chr1:166958354-166958355	Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs561985084	chr1:166958366-166958367	Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs529199083	chr1:166958367-166958368	Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs185297654	chr1:166958380-166958381	Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs562857566	chr1:166958402-166958403	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs533407293	chr1:166958407-166958408	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs551903079	chr1:166958434-166958435	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs531300048	chr1:166958435-166958436	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs566974864	chr1:166958455-166958456	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs150046632	chr1:166958460-166958461	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs549333054	chr1:166958476-166958477	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs188784403	chr1:166958514-166958515	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs538139762	chr1:166958531-166958532	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550100670	chr1:166958534-166958535	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs367546837	chr1:166958538-166958539	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs371448725	chr1:166958542-166958543	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200229017	chr1:166958544-166958545	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs199628429	chr1:166958545-166958546	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572864312	chr1:166958547-166958548	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191751530	chr1:166958550-166958551	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369323097	chr1:166958554-166958555	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373094105	chr1:166958557-166958558	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs375758244	chr1:166958566-166958567	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376351090	chr1:166958569-166958570	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562819345	chr1:166958573-166958574	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147719038	chr1:166958581-166958582	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs201592441	chr1:166958582-166958583	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs560543252	chr1:166958585-166958586	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs368453105	chr1:166958594-166958595	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs2296837	chr1:166958601-166958602	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs113297248	chr1:166958607-166958608	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Lung cancer	18438408	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166958200-166958400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:166958200-166958600	ZNF genes & repeats	Placenta	Placenta
3	chr1:166958400-166958600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:166958400-166958800	Active TSS	Spleen	Spleen
5	chr1:166958400-166959000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:166958400-166964600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:166958600-166959200	Active TSS	Placenta	Placenta
8	chr1:166960200-166960400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:166961400-166961800	Enhancers	Fetal Heart	heart
10	chr1:166964600-166964800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:166965200-166965600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:166965200-166965800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:166965200-166965800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr1:166968000-166968800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:166968600-166970000	Enhancers	GM12878-XiMat	blood
16	chr1:166978200-166978600	Enhancers	Liver	Liver
17	chr1:166978600-166980200	Weak transcription	Liver	Liver
18	chr1:166979800-166980000	Enhancers	Primary T cells from cord blood	blood
19	chr1:166979800-166980400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:166979800-166980400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:166979800-166980400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:166980000-166980400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:166980200-166980800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:166980200-166982400	Enhancers	Liver	Liver
25	chr1:166980400-166985000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:166980400-166985400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr1:166980600-166980800	Enhancers	Primary T cells from cord blood	blood
28	chr1:166980800-166985200	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr1:166982200-166982600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr1:166982200-166982600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:166982200-166982800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:166982200-166983200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:166982200-166983200	Enhancers	HMEC	breast
34	chr1:166982400-166982800	Enhancers	NHEK	skin
35	chr1:166982400-166983000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:166982400-166983200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr1:166982400-166983400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:166982400-166983400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:166982600-166983200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:166982800-166983200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:166983000-166983400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:166983000-166983600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:166983200-166984200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:166984400-166984600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:166985000-166985800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:166985200-166985400	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr1:166985200-166986000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:166985400-166986000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr1:166985400-166986000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr1:166985400-166986200	Enhancers	Fetal Heart	heart

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