Variant report

Variant	nsv1016749
Chromosome Location	chr8:11422571-11466745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:979)
CpG islands
(count:306)
Chromatin interactive
region (count:40)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11446987-11447268	HepG2	liver:	n/a	n/a
2	ATF2	chr8:11446931-11447251	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:11421987-11422609	GM12878	blood:	n/a	n/a
4	ATF2	chr8:11421419-11423115	GM12878	blood:	n/a	n/a
5	ATF2	chr8:11446925-11447218	GM12878	blood:	n/a	n/a
6	ATF2	chr8:11446903-11447247	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:11446945-11447320	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:11463287-11463625	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr8:11423267-11423719	GM12878	blood:	n/a	n/a
10	BCL3	chr8:11421305-11422586	GM12878	blood:	n/a	chr8:11422235-11422243
11	BCL3	chr8:11422664-11423817	GM12878	blood:	n/a	n/a
12	BCLAF1	chr8:11424543-11425004	GM12878	blood:	n/a	chr8:11424896-11424905
13	BCLAF1	chr8:11423452-11423876	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:11421273-11422842	GM12878	blood:	n/a	chr8:11422235-11422243
15	BCLAF1	chr8:11446898-11447345	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:11446764-11446808	K562	blood:	n/a	n/a
17	BHLHE40	chr8:11447046-11447259	K562	blood:	n/a	chr8:11447205-11447221
18	BHLHE40	chr8:11446852-11447323	HepG2	liver:	n/a	chr8:11447205-11447221
19	BHLHE40	chr8:11446896-11447329	GM12878	blood:	n/a	chr8:11447205-11447221
20	BHLHE40	chr8:11424742-11424860	GM12878	blood:	n/a	n/a
21	BRCA1	chr8:11425163-11425294	HepG2	liver:	n/a	n/a
22	BRCA1	chr8:11446830-11447356	HepG2	liver:	n/a	n/a
23	BRCA1	chr8:11447027-11447358	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr8:11446906-11447230	K562	blood:	n/a	n/a
25	CEBPB	chr8:11446939-11447141	K562	blood:	n/a	n/a
26	CEBPB	chr8:11430353-11430648	HepG2	liver:	n/a	chr8:11430495-11430506 chr8:11430496-11430507 chr8:11430495-11430508
27	CEBPB	chr8:11446943-11447184	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:11430283-11430749	MCF-7	breast:	n/a	chr8:11430495-11430506 chr8:11430496-11430507 chr8:11430495-11430508
29	CEBPB	chr8:11430317-11430742	Hela-S3	cervix:	n/a	chr8:11430495-11430506 chr8:11430496-11430507 chr8:11430495-11430508
30	CEBPB	chr8:11442062-11442294	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:11423676-11423968	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:11448254-11448528	HepG2	liver:	n/a	chr8:11448432-11448443
33	CEBPB	chr8:11448344-11448584	Hela-S3	cervix:	n/a	chr8:11448432-11448443
34	CEBPB	chr8:11463927-11464075	HepG2	liver:	n/a	chr8:11463999-11464010
35	CEBPB	chr8:11426257-11426416	HepG2	liver:	n/a	chr8:11426284-11426295
36	CEBPB	chr8:11461345-11461439	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:11448258-11448640	HepG2	liver:	n/a	chr8:11448432-11448443
38	CEBPB	chr8:11433042-11433213	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:11446953-11447240	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:11448342-11448547	HepG2	liver:	n/a	chr8:11448432-11448443
41	CEBPB	chr8:11425141-11425455	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:11455157-11455301	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:11430263-11430785	MCF-7	breast:	n/a	chr8:11430495-11430506 chr8:11430496-11430507 chr8:11430495-11430508
44	CEBPB	chr8:11448250-11448602	A549	lung:	n/a	chr8:11448432-11448443
45	CEBPB	chr8:11429395-11429804	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:11448301-11448573	K562	blood:	n/a	chr8:11448432-11448443
47	CEBPB	chr8:11444350-11444646	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:11448272-11448603	IMR90	lung:	n/a	chr8:11448432-11448443
49	CHD2	chr8:11446852-11447190	GM12878	blood:	n/a	n/a
50	CHD2	chr8:11422994-11422995	HepG2	liver:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11451194-11451244	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:11451194-11451244	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:11451041-11451091	SK-N-SH_RA	brain:	n/a
4	chr8:11451194-11451244	LNCaP	prostate:	n/a
5	chr8:11451194-11451244	HEK293	kidney:	embryo
6	chr8:11451194-11451244	Hepatocyte	liver:	n/a
7	chr8:11424789-11424839	AG04450	lung:	fetal
8	chr8:11451194-11451244	BE2_C	brain:	n/a
9	chr8:11424789-11424839	AG09309	skin:	n/a
10	chr8:11451194-11451244	GM12878	blood:	n/a
11	chr8:11451194-11451244	GM19239	blood:	n/a
12	chr8:11451194-11451244	U87	brain:	n/a
13	chr8:11422730-11422780	NH-A	brain:	n/a
14	chr8:11424789-11424839	AG10803	skin:	n/a
15	chr8:11422730-11422780	HL-60	blood:	n/a
16	chr8:11451041-11451091	U87	brain:	n/a
17	chr8:11451041-11451091	ECC-1	luminal epithelium:	n/a
18	chr8:11422730-11422780	HEEpiC	esophagus:	n/a
19	chr8:11451194-11451244	HCM	heart:	n/a
20	chr8:11422730-11422780	ProgFib	skin:	n/a
21	chr8:11451194-11451244	GM12891	blood:	n/a
22	chr8:11422730-11422780	GM19239	blood:	n/a
23	chr8:11451041-11451091	HEK293	kidney:	embryo
24	chr8:11422730-11422780	NHBE	bronchial:	n/a
25	chr8:11451194-11451244	HRCEpiC	kidney:	n/a
26	chr8:11424789-11424839	NT2-D1	testis:	n/a
27	chr8:11451312-11451362	HCT-116	colon:	n/a
28	chr8:11451312-11451362	GM12891	blood:	n/a
29	chr8:11422730-11422780	AG10803	skin:	n/a
30	chr8:11424789-11424839	IMR90	lung:	fetal
31	chr8:11424789-11424839	HRCEpiC	kidney:	n/a
32	chr8:11451041-11451091	HEEpiC	esophagus:	n/a
33	chr8:11422730-11422780	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:11451312-11451362	IMR90	lung:	fetal
35	chr8:11451194-11451244	ovcar-3	ovarian:	n/a
36	chr8:11424789-11424839	A549	lung:	n/a
37	chr8:11422730-11422780	HEK293	kidney:	embryo
38	chr8:11451194-11451244	AG04450	lung:	fetal
39	chr8:11451312-11451362	HAEpiC	amniotic membrane:	n/a
40	chr8:11451312-11451362	HRCEpiC	kidney:	n/a
41	chr8:11422730-11422780	NB4	blood:	n/a
42	chr8:11424789-11424839	HCT-116	colon:	n/a
43	chr8:11451312-11451362	H1-hESC	embryonic stem cell:	embryo
44	chr8:11422730-11422780	AG09309	skin:	n/a
45	chr8:11424789-11424839	MCF10A-Er-Src	breast:	n/a
46	chr8:11422730-11422780	GM12891	blood:	n/a
47	chr8:11424789-11424839	MCF-7	breast:	n/a
48	chr8:11451194-11451244	Hela-S3	cervix:	n/a
49	chr8:11422730-11422780	ECC-1	luminal epithelium:	n/a
50	chr8:11451312-11451362	HRE	kidney:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11429899..11432844-chr8:11444265..11445875,2	MCF-7	breast:
2	chr8:11421842..11422772-chr8:11603355..11604431,7	MCF-7	breast:
3	chr8:11422187..11423813-chr8:11429710..11432078,2	MCF-7	breast:
4	chr8:11446870..11447723-chr8:11603904..11604616,2	K562	blood:
5	chr17:62223347..62226304-chr8:11454133..11456749,2	MCF-7	breast:
6	chr8:11444228..11446493-chr8:11461211..11463347,2	K562	blood:
7	chr8:11430263..11432062-chr8:11433287..11435276,2	K562	blood:
8	chr8:11424324..11425489-chr8:11573800..11574792,3	MCF-7	breast:
9	chr8:11446527..11447418-chr8:11587991..11588812,3	MCF-7	breast:
10	chr8:11422289..11424857-chr8:11598109..11600598,2	MCF-7	breast:
11	chr8:11421781..11422781-chr8:11603539..11604516,9	K562	blood:
12	chr8:11433178..11433693-chr8:11488566..11489368,2	MCF-7	breast:
13	chr8:11444228..11446493-chr8:11461211..11463347,2	K562	blood:
14	chr8:11411028..11411558-chr8:11446874..11447601,2	K562	blood:
15	chr8:11448479..11450712-chr8:11450788..11453218,2	K562	blood:
16	chr8:11430194..11430977-chr8:11603626..11604340,2	MCF-7	breast:
17	chr8:11424667..11425261-chr8:11603180..11604185,3	MCF-7	breast:
18	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
19	chr8:11429899..11432844-chr8:11444265..11445875,2	MCF-7	breast:
20	chr8:11448415..11450264-chr8:11463470..11466297,2	K562	blood:
21	chr8:11421719..11422643-chr8:11446645..11447610,4	K562	blood:
22	chr8:11448415..11450264-chr8:11463470..11466297,2	K562	blood:
23	chr8:11448479..11450712-chr8:11450788..11453218,2	K562	blood:
24	chr8:11459957..11462868-chr8:11472194..11474715,2	K562	blood:
25	chr8:11432773..11433729-chr8:11587844..11588900,10	MCF-7	breast:
26	chr8:11426984..11428613-chr8:11595138..11596810,2	K562	blood:
27	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
28	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
29	chr8:11422187..11423813-chr8:11429710..11432078,2	MCF-7	breast:
30	chr8:11410226..11416148-chr8:11417699..11422629,5	K562	blood:
31	chr8:11462808..11463594-chr8:11587916..11588873,3	MCF-7	breast:
32	chr8:11429172..11431915-chr8:11433216..11435875,2	MCF-7	breast:
33	chr8:11268286..11268904-chr8:11447156..11448012,2	K562	blood:
34	chr8:11421719..11422643-chr8:11446645..11447610,4	K562	blood:
35	chr8:11433477..11436325-chr8:11437296..11440162,3	MCF-7	breast:
36	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
37	chr8:11428917..11429796-chr8:11587902..11588451,3	MCF-7	breast:
38	chr8:11422237..11424811-chr8:11602615..11604781,2	MCF-7	breast:
39	chr8:11379820..11382247-chr8:11420170..11422972,2	MCF-7	breast:
40	chr8:11430122..11430693-chr8:11587796..11588653,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLK-1	chr8:11435879-11436150	NR_040035
2	lnc-BLK-1	chr8:11437979-11438850	NR_040035
3	lnc-BLK-1	chr8:11434044-11434826	XLOC_006711
4	lnc-BLK-1	chr8:11437979-11438851	ENSG00000170983
5	lnc-BLK-1	chr8:11434044-11434826	NR_040035
6	lnc-BLK-1	chr8:11437979-11438851	XLOC_006711
7	lnc-BLK-1	chr8:11435879-11436150	XLOC_006711
8	lnc-BLK-1	chr8:11433822-11434826	ENSG00000170983
9	lnc-BLK-1	chr8:11435879-11436150	ENSG00000170983

No data

Variant related genes	Relation type
LINC00208	TF binding region
LINC00208	CpG island
ENSG00000255518	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000254774	chromatin interactions
ENSG00000170983	chromatin interactions
ENSG00000269954	chromatin interactions

Extended variants
information (count: 2396 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371264032	chr8:11422595-11422596	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs116694331	chr8:11422665-11422666	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547764176	chr8:11422714-11422715	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs571663267	chr8:11422744-11422745	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs376036621	chr8:11422773-11422774	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542238382	chr8:11422779-11422780	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs141751941	chr8:11422799-11422800	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs575916632	chr8:11422813-11422814	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs543729297	chr8:11422825-11422826	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs28715042	chr8:11422832-11422833	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs12549144	chr8:11422861-11422862	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs4460336	chr8:11422894-11422895	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs547525745	chr8:11422909-11422910	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs189797548	chr8:11422910-11422911	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs12549150	chr8:11422936-11422937	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs566018696	chr8:11422943-11422944	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs142946315	chr8:11422950-11422951	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs184077001	chr8:11422951-11422952	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs537339296	chr8:11422983-11422984	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs111277816	chr8:11423015-11423016	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552877224	chr8:11423019-11423020	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570919278	chr8:11423032-11423033	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112059768	chr8:11423035-11423036	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189002997	chr8:11423065-11423066	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12541800	chr8:11423072-11423073	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs368507600	chr8:11423077-11423078	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11985709	chr8:11423083-11423084	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs568570528	chr8:11423092-11423093	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193038811	chr8:11423109-11423110	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562580547	chr8:11423123-11423124	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183763558	chr8:11423140-11423141	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12541802	chr8:11423142-11423143	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73197313	chr8:11423143-11423144	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35964286	chr8:11423156-11423157	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571110628	chr8:11423182-11423183	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541078035	chr8:11423274-11423275	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554724981	chr8:11423275-11423276	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376604102	chr8:11423282-11423283	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576934045	chr8:11423288-11423289	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547280968	chr8:11423293-11423294	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565673363	chr8:11423335-11423336	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541234767	chr8:11423352-11423353	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10094362	chr8:11423381-11423382	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs375218435	chr8:11423385-11423386	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530193436	chr8:11423391-11423392	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548743691	chr8:11423433-11423434	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34379689	chr8:11423434-11423435	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs755320	chr8:11423439-11423440	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs552549786	chr8:11423469-11423470	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373793514	chr8:11423496-11423497	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Gastric cancer	22315472	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11421000-11422600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr8:11421200-11422600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
3	chr8:11421200-11422600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
4	chr8:11421200-11422600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:11421200-11422800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr8:11421200-11422800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:11421400-11422600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:11421400-11422600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr8:11421400-11422600	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr8:11421400-11422600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:11421400-11422600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:11421400-11422600	Bivalent Enhancer	Fetal Brain Male	brain
13	chr8:11421400-11422600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
14	chr8:11421400-11422600	Active TSS	Right Atrium	heart
15	chr8:11421400-11422800	Bivalent Enhancer	Liver	Liver
16	chr8:11421400-11422800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
17	chr8:11421400-11423000	Bivalent Enhancer	Esophagus	oesophagus
18	chr8:11421400-11423000	Enhancers	Fetal Heart	heart
19	chr8:11421600-11422600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr8:11421600-11422600	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:11421600-11422600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:11421600-11422600	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
23	chr8:11421600-11422600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
24	chr8:11421600-11422600	Bivalent/Poised TSS	NHLF	lung
25	chr8:11421600-11422600	Flanking Bivalent TSS/Enh	Osteobl	bone
26	chr8:11421600-11422800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
27	chr8:11421600-11422800	Bivalent Enhancer	Placenta	Placenta
28	chr8:11421600-11422800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
29	chr8:11421800-11422600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:11421800-11422600	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
31	chr8:11421800-11422600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
32	chr8:11421800-11422600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
33	chr8:11421800-11422600	Bivalent Enhancer	Fetal Lung	lung
34	chr8:11421800-11422600	Flanking Active TSS	HSMM	muscle
35	chr8:11421800-11422600	Active TSS	K562	blood
36	chr8:11421800-11422800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
37	chr8:11421800-11422800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
38	chr8:11421800-11422800	Active TSS	A549	lung
39	chr8:11421800-11423000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
40	chr8:11421800-11423000	Bivalent Enhancer	Stomach Mucosa	stomach
41	chr8:11422000-11422600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr8:11422000-11422600	Bivalent/Poised TSS	Fetal Brain Female	brain
43	chr8:11422000-11422600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
44	chr8:11422000-11422600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
45	chr8:11422000-11422800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
46	chr8:11422200-11422600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:11422200-11422600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr8:11422200-11422600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
49	chr8:11422200-11422600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr8:11422200-11422600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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