Variant report

Variant	esv3438687
Chromosome Location	chr3:46922473-46925321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:42)
CpG islands
(count:793)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:42 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr3:46923207-46923400	K562	blood:	n/a	n/a
2	CCNT2	chr3:46923951-46924441	K562	blood:	n/a	chr3:46923962-46923971
3	CEBPB	chr3:46923360-46923502	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr3:46924036-46924271	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr3:46923232-46923297	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr3:46922694-46924513	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr3:46923920-46924070	SK-N-SH_RA	brain:	n/a	n/a
8	EGR1	chr3:46923473-46923842	K562	blood:	n/a	chr3:46923533-46923543 chr3:46923533-46923546 chr3:46923613-46923626
9	EGR1	chr3:46923526-46923722	K562	blood:	n/a	chr3:46923533-46923543 chr3:46923533-46923546 chr3:46923613-46923626
10	HMGN3	chr3:46923910-46924346	K562	blood:	n/a	n/a
11	MAZ	chr3:46923276-46924587	IMR90	lung:	n/a	chr3:46924575-46924585
12	MAZ	chr3:46924703-46925545	IMR90	lung:	n/a	chr3:46924951-46924961 chr3:46924948-46924957
13	MAZ	chr3:46923993-46924210	GM12878	blood:	n/a	n/a
14	MAZ	chr3:46924755-46924995	GM12878	blood:	n/a	chr3:46924951-46924961 chr3:46924948-46924957
15	MAZ	chr3:46923480-46924335	K562	blood:	n/a	n/a
16	MXI1	chr3:46924194-46924315	GM12878	blood:	n/a	n/a
17	MXI1	chr3:46922475-46922545	H1-hESC	embryonic stem cell:	n/a	n/a
18	MYC	chr3:46924124-46924220	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr3:46923311-46923432	H1-hESC	embryonic stem cell:	n/a	n/a
20	RCOR1	chr3:46922436-46922597	K562	blood:	n/a	n/a
21	REST	chr3:46924671-46924724	PANC-1	pancreas:	n/a	n/a
22	SIN3A	chr3:46923024-46923569	H1-hESC	embryonic stem cell:	n/a	chr3:46923038-46923051 chr3:46923040-46923051
23	SIN3A	chr3:46923964-46924439	H1-hESC	embryonic stem cell:	n/a	n/a
24	SPI1	chr3:46923924-46924026	K562	blood:	n/a	n/a
25	SUZ12	chr3:46921801-46922674	H1-hESC	embryonic stem cell:	n/a	n/a
26	TBP	chr3:46924070-46924200	H1-hESC	embryonic stem cell:	n/a	n/a
27	UBTF	chr3:46923406-46924245	K562	blood:	n/a	n/a
28	UBTF	chr3:46923292-46924415	K562	blood:	n/a	n/a
29	UBTF	chr3:46925082-46925282	K562	blood:	n/a	n/a
30	ZBTB7A	chr3:46922762-46923073	K562	blood:	n/a	n/a
31	ZBTB7A	chr3:46923706-46924608	ECC-1	luminal epithelium:	n/a	chr3:46924477-46924486 chr3:46923905-46923913
32	ZBTB7A	chr3:46924260-46924578	K562	blood:	n/a	chr3:46924477-46924486
33	ZBTB7A	chr3:46923712-46924179	K562	blood:	n/a	chr3:46923905-46923913
34	ZBTB7A	chr3:46923685-46924688	ECC-1	luminal epithelium:	n/a	chr3:46924477-46924486 chr3:46923905-46923913
35	ZBTB7A	chr3:46924833-46924959	K562	blood:	n/a	n/a
36	ZBTB7A	chr3:46923273-46923677	K562	blood:	n/a	n/a
37	ZBTB7A	chr3:46923158-46923696	K562	blood:	n/a	n/a
38	ZBTB7A	chr3:46924679-46924823	K562	blood:	n/a	n/a
39	ZBTB7A	chr3:46923151-46923686	ECC-1	luminal epithelium:	n/a	n/a
40	ZNF143	chr3:46923965-46924358	H1-hESC	embryonic stem cell:	n/a	n/a
41	ZNF263	chr3:46923869-46924334	HEK293-T-REx	kidney:	n/a	chr3:46924001-46924010
42	ZNF384	chr3:46923387-46923486	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46923503-46923553	HEEpiC	esophagus:	n/a
2	chr3:46923503-46923553	GM12878	blood:	n/a
3	chr3:46924050-46924100	HCF	heart:	n/a
4	chr3:46924956-46925006	IMR90	lung:	fetal
5	chr3:46924050-46924100	SKMC	muscle:	n/a
6	chr3:46923546-46923596	GM12878	blood:	n/a
7	chr3:46924768-46924818	RPTEC	kidney:	n/a
8	chr3:46924401-46924451	PANC-1	pancreas:	n/a
9	chr3:46924113-46924163	BJ	skin:	n/a
10	chr3:46924050-46924100	AG09309	skin:	n/a
11	chr3:46925081-46925131	NHDF-neo	bronchial:	n/a
12	chr3:46923546-46923596	HMEC	breast:	n/a
13	chr3:46923937-46923987	HRE	kidney:	n/a
14	chr3:46924956-46925006	K562	blood:	n/a
15	chr3:46925081-46925131	Jurkat	blood:	n/a
16	chr3:46923068-46923118	HCT-116	colon:	n/a
17	chr3:46924401-46924451	HMEC	breast:	n/a
18	chr3:46924401-46924451	HCT-116	colon:	n/a
19	chr3:46924956-46925006	HCM	heart:	n/a
20	chr3:46925081-46925131	NH-A	brain:	n/a
21	chr3:46922486-46922536	GM19239	blood:	n/a
22	chr3:46923546-46923596	NB4	blood:	n/a
23	chr3:46923068-46923118	AG04449	skin:	fetal
24	chr3:46923546-46923596	BE2_C	brain:	n/a
25	chr3:46924113-46924163	T-47D	breast:	n/a
26	chr3:46923433-46923483	HCF	heart:	n/a
27	chr3:46924768-46924818	BJ	skin:	n/a
28	chr3:46925081-46925131	AG09309	skin:	n/a
29	chr3:46924768-46924818	CMK	blood:	n/a
30	chr3:46925081-46925131	U87	brain:	n/a
31	chr3:46924956-46925006	PFSK-1	brain:	n/a
32	chr3:46922486-46922536	GM12891	blood:	n/a
33	chr3:46923937-46923987	HCF	heart:	n/a
34	chr3:46923937-46923987	HIPEpiC	eye:	n/a
35	chr3:46923546-46923596	HRPEpiC	eye:	n/a
36	chr3:46925081-46925131	HRE	kidney:	n/a
37	chr3:46924401-46924451	SKMC	muscle:	n/a
38	chr3:46923068-46923118	HRCEpiC	kidney:	n/a
39	chr3:46925181-46925231	HAEpiC	amniotic membrane:	n/a
40	chr3:46924768-46924818	U87	brain:	n/a
41	chr3:46925081-46925131	SK-N-SH	brain:	n/a
42	chr3:46924050-46924100	GM12878	blood:	n/a
43	chr3:46925081-46925131	A549	lung:	n/a
44	chr3:46923546-46923596	AoSMC	blood vessel:	n/a
45	chr3:46923068-46923118	HCPEpiC	choroid plexus:	n/a
46	chr3:46923546-46923596	HEK293	kidney:	embryo
47	chr3:46923546-46923596	HIPEpiC	eye:	n/a
48	chr3:46924956-46925006	HCF	heart:	n/a
49	chr3:46923433-46923483	U87	brain:	n/a
50	chr3:46924768-46924818	AG09319	gingival:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46917376..46920621-chr3:46922888..46926605,5	K562	blood:
2	chr3:46923291..46931131-chr3:46931662..46935716,9	K562	blood:
3	chr3:46921853..46924302-chr3:46929528..46931190,2	K562	blood:
4	chr3:46733801..46735413-chr3:46924430..46926212,2	MCF-7	breast:
5	chr3:46919067..46921668-chr3:46922191..46925334,3	K562	blood:
6	chr3:46924894..46926955-chr3:46938452..46941314,2	K562	blood:
7	chr3:46917885..46923537-chr3:46925586..46931315,6	MCF-7	breast:

No data

Variant related genes	Relation type
MYL3	TF binding region
PTH1R	TF binding region
MYL3	CpG island
PTH1R	CpG island
ENSG00000160801	chromatin interactions
ENSG00000178038	chromatin interactions
ENSG00000268537	chromatin interactions

Extended variants
information (count: 59 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534092040	chr3:46922563-46922564	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs545734452	chr3:46922615-46922616	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs555742553	chr3:46922620-46922621	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs190387336	chr3:46922645-46922646	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs192644895	chr3:46922658-46922659	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs555871837	chr3:46922691-46922692	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs377661610	chr3:46922716-46922717	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs370215923	chr3:46922769-46922770	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs563818657	chr3:46922849-46922850	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs577684571	chr3:46922904-46922905	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs544749621	chr3:46922928-46922929	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs34407581	chr3:46922941-46922942	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs377707234	chr3:46922946-46922947	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11925356	chr3:46923111-46923112	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530938252	chr3:46923156-46923157	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560741228	chr3:46923176-46923177	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs572345384	chr3:46923190-46923191	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542809292	chr3:46923294-46923295	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs561272770	chr3:46923378-46923379	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116133265	chr3:46923428-46923429	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549352506	chr3:46923437-46923438	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375411771	chr3:46923531-46923532	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs565104652	chr3:46923585-46923586	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs532640048	chr3:46923602-46923603	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547531685	chr3:46923622-46923623	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566171277	chr3:46923651-46923652	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534029713	chr3:46923687-46923688	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs549178924	chr3:46923715-46923716	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs567601733	chr3:46923720-46923721	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs538104514	chr3:46923750-46923751	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs556146665	chr3:46923763-46923764	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs577520011	chr3:46923804-46923805	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs538618862	chr3:46923805-46923806	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs553632104	chr3:46923860-46923861	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs571786426	chr3:46923866-46923867	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs542847778	chr3:46923905-46923906	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs561108773	chr3:46924098-46924099	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs34333904	chr3:46924127-46924128	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs557709840	chr3:46924159-46924160	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs543709113	chr3:46924191-46924192	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs13083011	chr3:46924296-46924297	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs371421960	chr3:46924537-46924538	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs540920290	chr3:46924639-46924640	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs532443298	chr3:46924715-46924716	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs547769292	chr3:46924826-46924827	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs559917886	chr3:46924836-46924837	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs530204092	chr3:46924867-46924868	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs201663714	chr3:46925013-46925014	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs199757613	chr3:46925037-46925038	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs567440911	chr3:46925083-46925084	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46915800-46923000	Weak transcription	Brain Anterior Caudate	brain
2	chr3:46917000-46922800	Weak transcription	Ovary	ovary
3	chr3:46917200-46922800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:46917800-46922600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr3:46920400-46923800	Weak transcription	Liver	Liver
6	chr3:46920600-46922600	Weak transcription	Pancreas	Pancrea
7	chr3:46920800-46922600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:46920800-46922600	Weak transcription	Left Ventricle	heart
9	chr3:46921000-46922800	Weak transcription	Right Ventricle	heart
10	chr3:46921000-46923200	Weak transcription	HSMM	muscle
11	chr3:46921000-46923200	Weak transcription	HSMMtube	muscle
12	chr3:46921200-46923200	Weak transcription	A549	lung
13	chr3:46921600-46922600	Bivalent Enhancer	Fetal Intestine Small	intestine
14	chr3:46921800-46922600	Weak transcription	Brain Hippocampus Middle	brain
15	chr3:46922200-46922600	Flanking Bivalent TSS/Enh	Fetal Lung	lung
16	chr3:46922200-46922600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr3:46922200-46922800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:46922400-46922600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr3:46922400-46922600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
20	chr3:46922400-46922600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:46922400-46922600	Enhancers	Adipose Nuclei	Adipose
22	chr3:46922400-46922600	Bivalent Enhancer	Placenta	Placenta
23	chr3:46922400-46922600	Flanking Active TSS	Spleen	Spleen
24	chr3:46922400-46922800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:46922400-46922800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
26	chr3:46922400-46922800	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr3:46922400-46922800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
28	chr3:46922400-46923000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr3:46922400-46923000	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
30	chr3:46922400-46923000	Active TSS	Right Atrium	heart
31	chr3:46922400-46923200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
32	chr3:46922400-46924000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:46922400-46925000	Active TSS	Fetal Kidney	kidney
34	chr3:46922400-46925400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
35	chr3:46922600-46922800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
36	chr3:46922600-46922800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:46922600-46922800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr3:46922600-46922800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:46922600-46922800	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr3:46922600-46922800	Bivalent Enhancer	Brain Hippocampus Middle	brain
41	chr3:46922600-46922800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr3:46922600-46922800	Flanking Bivalent TSS/Enh	Placenta	Placenta
43	chr3:46922600-46922800	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr3:46922600-46922800	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr3:46922600-46922800	Enhancers	Spleen	Spleen
46	chr3:46922600-46923000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:46922600-46923000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr3:46922600-46923000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:46922600-46923000	Weak transcription	Lung	lung
50	chr3:46922600-46923200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived

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