Variant report

Variant	esv3357649
Chromosome Location	chr10:94607197-94609745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:592)
CpG islands
(count:856)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94607190-94607759	HepG2	liver:	n/a	n/a
2	BACH1	chr10:94608204-94609014	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:94608874-94609012	K562	blood:	n/a	n/a
4	BCLAF1	chr10:94608193-94608716	GM12878	blood:	n/a	chr10:94608697-94608710 chr10:94608669-94608682 chr10:94608422-94608431
5	BHLHE40	chr10:94607382-94607394	K562	blood:	n/a	n/a
6	BHLHE40	chr10:94608161-94608594	HepG2	liver:	n/a	chr10:94608578-94608594
7	BHLHE40	chr10:94607787-94608653	K562	blood:	n/a	chr10:94608112-94608128 chr10:94608578-94608594
8	BHLHE40	chr10:94607896-94608638	GM12878	blood:	n/a	chr10:94608112-94608128 chr10:94608578-94608594
9	BRCA1	chr10:94606920-94607306	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr10:94607912-94609050	K562	blood:	n/a	n/a
11	CEBPB	chr10:94607015-94607408	HepG2	liver:	n/a	chr10:94607150-94607161
12	CEBPB	chr10:94606923-94607313	ECC-1	luminal epithelium:	n/a	chr10:94607150-94607161
13	CEBPB	chr10:94606993-94607332	H1-hESC	embryonic stem cell:	n/a	chr10:94607150-94607161
14	CEBPB	chr10:94606808-94607680	Hela-S3	cervix:	n/a	chr10:94607150-94607161
15	CEBPB	chr10:94606965-94607347	A549	lung:	n/a	chr10:94607150-94607161
16	CEBPB	chr10:94606873-94607427	K562	blood:	n/a	chr10:94607150-94607161
17	CEBPB	chr10:94606962-94607591	HepG2	liver:	n/a	chr10:94607150-94607161
18	CEBPB	chr10:94606828-94607456	A549	lung:	n/a	chr10:94607150-94607161
19	CEBPB	chr10:94607950-94608610	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:94607019-94607274	HepG2	liver:	n/a	chr10:94607150-94607161
21	CEBPB	chr10:94606974-94607336	HepG2	liver:	n/a	chr10:94607150-94607161
22	CEBPB	chr10:94606889-94607425	MCF-7	breast:	n/a	chr10:94607150-94607161
23	CEBPB	chr10:94606849-94607535	MCF-7	breast:	n/a	chr10:94607150-94607161
24	CEBPB	chr10:94606953-94607368	IMR90	lung:	n/a	chr10:94607150-94607161
25	CEBPB	chr10:94606923-94607339	K562	blood:	n/a	chr10:94607150-94607161
26	CEBPB	chr10:94606896-94607586	ECC-1	luminal epithelium:	n/a	chr10:94607150-94607161
27	CEBPB	chr10:94606923-94607303	A549	lung:	n/a	chr10:94607150-94607161
28	CEBPB	chr10:94606886-94607441	K562	blood:	n/a	chr10:94607150-94607161
29	CEBPD	chr10:94606891-94607406	K562	blood:	n/a	chr10:94607151-94607162
30	CEBPD	chr10:94607019-94607287	HepG2	liver:	n/a	chr10:94607151-94607162
31	CHD1	chr10:94608673-94608819	GM12878	blood:	n/a	n/a
32	CHD2	chr10:94608377-94608572	GM12878	blood:	n/a	n/a
33	CHD2	chr10:94608332-94609162	K562	blood:	n/a	n/a
34	CHD2	chr10:94606836-94607344	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr10:94608909-94609086	HepG2	liver:	n/a	n/a
36	CHD2	chr10:94607702-94609187	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr10:94608267-94608406	HepG2	liver:	n/a	n/a
38	CHD2	chr10:94607973-94607997	K562	blood:	n/a	n/a
39	CREB1	chr10:94608061-94608706	A549	lung:	n/a	n/a
40	CTBP2	chr10:94608427-94609018	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr10:94608160-94608310	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr10:94608903-94609001	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:94608480-94608630	GM12878	blood:	n/a	n/a
44	CTCF	chr10:94608740-94608890	GM12873	blood:	n/a	n/a
45	CTCF	chr10:94608540-94608690	AG10803	skin:	n/a	n/a
46	CTCF	chr10:94608880-94609030	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr10:94609000-94609150	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr10:94608520-94608670	SAEC	small airway:	n/a	n/a
49	CTCF	chr10:94608420-94608570	AG09319	gingival:	n/a	n/a
50	CTCF	chr10:94608500-94608650	AG04449	skin:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94608593-94608643	AG09309	skin:	n/a
2	chr10:94607939-94607989	AoSMC	blood vessel:	n/a
3	chr10:94608593-94608643	AG09309	skin:	n/a
4	chr10:94607939-94607989	AoSMC	blood vessel:	n/a
5	chr10:94609038-94609088	GM12878	blood:	n/a
6	chr10:94608038-94608088	HAEpiC	amniotic membrane:	n/a
7	chr10:94607950-94608000	A549	lung:	n/a
8	chr10:94607950-94608000	NH-A	brain:	n/a
9	chr10:94608593-94608643	HEK293	kidney:	embryo
10	chr10:94607950-94608000	Jurkat	blood:	n/a
11	chr10:94608189-94608239	HRCEpiC	kidney:	n/a
12	chr10:94607950-94608000	PFSK-1	brain:	n/a
13	chr10:94608070-94608120	IMR90	lung:	fetal
14	chr10:94609401-94609451	BJ	skin:	n/a
15	chr10:94609038-94609088	AG04450	lung:	fetal
16	chr10:94607950-94608000	H1-hESC	embryonic stem cell:	embryo
17	chr10:94608593-94608643	HCF	heart:	n/a
18	chr10:94607950-94608000	HAEpiC	amniotic membrane:	n/a
19	chr10:94608077-94608127	HAEpiC	amniotic membrane:	n/a
20	chr10:94609038-94609088	AoSMC	blood vessel:	n/a
21	chr10:94608258-94608308	ProgFib	skin:	n/a
22	chr10:94608332-94608382	H1-hESC	embryonic stem cell:	embryo
23	chr10:94607950-94608000	HIPEpiC	eye:	n/a
24	chr10:94609401-94609451	HL-60	blood:	n/a
25	chr10:94609036-94609086	IMR90	lung:	fetal
26	chr10:94609401-94609451	NHDF-neo	bronchial:	n/a
27	chr10:94608038-94608088	GM12892	blood:	n/a
28	chr10:94608038-94608088	PANC-1	pancreas:	n/a
29	chr10:94608593-94608643	HEEpiC	esophagus:	n/a
30	chr10:94608070-94608120	AG09309	skin:	n/a
31	chr10:94608189-94608239	BE2_C	brain:	n/a
32	chr10:94608332-94608382	Hepatocyte	liver:	n/a
33	chr10:94608040-94608090	HRCEpiC	kidney:	n/a
34	chr10:94608040-94608090	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:94609036-94609086	HAEpiC	amniotic membrane:	n/a
36	chr10:94608593-94608643	NB4	blood:	n/a
37	chr10:94607948-94607998	IMR90	lung:	fetal
38	chr10:94607950-94608000	HNPCEpiC	eye:	n/a
39	chr10:94608332-94608382	HepG2	liver:	n/a
40	chr10:94607948-94607998	H1-hESC	embryonic stem cell:	embryo
41	chr10:94609401-94609451	NHBE	bronchial:	n/a
42	chr10:94609036-94609086	HCPEpiC	choroid plexus:	n/a
43	chr10:94607948-94607998	AoSMC	blood vessel:	n/a
44	chr10:94608593-94608643	HCT-116	colon:	n/a
45	chr10:94608258-94608308	HAEpiC	amniotic membrane:	n/a
46	chr10:94609401-94609451	MCF10A-Er-Src	breast:	n/a
47	chr10:94609038-94609088	HEEpiC	esophagus:	n/a
48	chr10:94609401-94609451	AG10803	skin:	n/a
49	chr10:94608593-94608643	ECC-1	luminal epithelium:	n/a
50	chr10:94608038-94608088	HEK293	kidney:	embryo

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94604476..94607331-chr10:94608009..94611387,4	K562	blood:
2	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
3	chr10:94332956..94335217-chr10:94607050..94609174,2	MCF-7	breast:
4	chr10:94607085..94609622-chr3:12881442..12883571,2	MCF-7	breast:
5	chr10:94607840..94608395-chr12:58329411..58330143,2	NB4	blood:
6	chr10:94607070..94611530-chr10:94637347..94641279,5	MCF-7	breast:
7	chr10:94351156..94354361-chr10:94606648..94609927,3	MCF-7	breast:
8	chr10:94331601..94334574-chr10:94607928..94609540,2	MCF-7	breast:
9	chr10:94351135..94353608-chr10:94605711..94608172,2	K562	blood:
10	chr1:151512334..151513279-chr10:94608004..94608822,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
EXOC6	TF binding region
EXOC6	CpG island
ENSG00000119912	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000144713	chromatin interactions
ENSG00000225118	chromatin interactions
ENSG00000152804	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000257698	chromatin interactions
ENSG00000207496	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138362475	chr10:94607223-94607224	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs547832940	chr10:94607261-94607262	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs564015267	chr10:94607287-94607288	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs544653458	chr10:94607326-94607327	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs564890901	chr10:94607396-94607397	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs536648189	chr10:94607425-94607426	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs61860811	chr10:94607452-94607453	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs4291588	chr10:94607528-94607529	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs149247360	chr10:94607552-94607553	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs386372105	chr10:94607593-94607594	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs546430377	chr10:94607611-94607612	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs3078184	chr10:94607612-94607613	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs577453927	chr10:94607722-94607723	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs539713074	chr10:94607738-94607739	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs112013707	chr10:94607774-94607775	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs75962189	chr10:94607783-94607784	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs573310660	chr10:94607851-94607852	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs542354361	chr10:94607881-94607882	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs11187190	chr10:94607923-94607924	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs562156443	chr10:94607951-94607952	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs575754414	chr10:94607992-94607993	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs4933747	chr10:94608083-94608084	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563468638	chr10:94608103-94608104	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs532450072	chr10:94608122-94608123	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs146199230	chr10:94608126-94608127	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs559500079	chr10:94608154-94608155	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs528229335	chr10:94608248-94608249	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs201154201	chr10:94608267-94608268	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs200138547	chr10:94608283-94608284	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs151243420	chr10:94608308-94608309	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs536685797	chr10:94608317-94608318	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs139196824	chr10:94608319-94608320	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs147113843	chr10:94608390-94608391	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs188445802	chr10:94608428-94608429	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs553350719	chr10:94608458-94608459	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs567111551	chr10:94608463-94608464	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs536051654	chr10:94608493-94608494	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs555924516	chr10:94608526-94608527	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs575793042	chr10:94608533-94608534	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs544683432	chr10:94608584-94608585	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs558151439	chr10:94608586-94608587	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs550601343	chr10:94608598-94608599	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs369694820	chr10:94608663-94608664	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs559375983	chr10:94608705-94608706	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs528299941	chr10:94608709-94608710	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs192878970	chr10:94608727-94608728	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs144065352	chr10:94608749-94608750	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs370641308	chr10:94608768-94608769	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs530544366	chr10:94608815-94608816	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs550357415	chr10:94608828-94608829	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94596800-94607800	Weak transcription	HSMMtube	muscle
2	chr10:94598600-94607200	Weak transcription	Primary T cells from cord blood	blood
3	chr10:94599400-94607200	Weak transcription	Osteobl	bone
4	chr10:94599400-94607400	Weak transcription	Spleen	Spleen
5	chr10:94599600-94607600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:94600600-94607800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr10:94602600-94607600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr10:94602800-94607400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr10:94603200-94607200	Weak transcription	Liver	Liver
10	chr10:94603200-94607400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr10:94603200-94607400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr10:94603400-94607200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr10:94603400-94607200	Weak transcription	A549	lung
14	chr10:94603400-94607400	Weak transcription	Adipose Nuclei	Adipose
15	chr10:94604200-94607200	Weak transcription	Placenta	Placenta
16	chr10:94604200-94607400	Weak transcription	Fetal Muscle Leg	muscle
17	chr10:94604200-94607400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr10:94604200-94607600	Weak transcription	Brain Hippocampus Middle	brain
19	chr10:94605400-94608000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr10:94605600-94607600	Enhancers	Primary B cells from peripheral blood	blood
21	chr10:94605800-94607200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr10:94605800-94607200	Genic enhancers	HUVEC	blood vessel
23	chr10:94605800-94607400	Enhancers	HepG2	liver
24	chr10:94606000-94607200	Enhancers	Primary B cells from cord blood	blood
25	chr10:94606200-94607400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr10:94606200-94607400	Weak transcription	Fetal Thymus	thymus
27	chr10:94606200-94607800	Weak transcription	Thymus	Thymus
28	chr10:94606600-94607200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr10:94606600-94607400	Enhancers	Primary hematopoietic stem cells	blood
30	chr10:94606600-94607400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr10:94606600-94607600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr10:94606600-94607800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr10:94606600-94607800	Enhancers	GM12878-XiMat	blood
34	chr10:94606800-94607200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr10:94606800-94607200	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr10:94606800-94607400	Weak transcription	Lung	lung
37	chr10:94606800-94607600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr10:94606800-94607600	Genic enhancers	K562	blood
39	chr10:94606800-94608000	Flanking Active TSS	Hela-S3	cervix
40	chr10:94607000-94607200	Enhancers	Fetal Kidney	kidney
41	chr10:94607000-94607400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr10:94607000-94607600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr10:94607000-94607600	Enhancers	Fetal Intestine Large	intestine
44	chr10:94607000-94607600	Enhancers	Dnd41	blood
45	chr10:94607000-94607800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr10:94607000-94607800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr10:94607000-94607800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr10:94607000-94607800	Bivalent Enhancer	NHEK	skin
49	chr10:94607200-94607400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr10:94607200-94607400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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