Variant report

Variant	esv3344281
Chromosome Location	chr3:46923473-46926321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:732)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr3:46923951-46924441	K562	blood:	n/a	chr3:46923962-46923971
2	CEBPB	chr3:46923360-46923502	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr3:46924036-46924271	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr3:46922694-46924513	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr3:46923920-46924070	SK-N-SH_RA	brain:	n/a	n/a
6	EGR1	chr3:46923526-46923722	K562	blood:	n/a	chr3:46923533-46923543 chr3:46923533-46923546 chr3:46923613-46923626
7	EGR1	chr3:46923473-46923842	K562	blood:	n/a	chr3:46923533-46923543 chr3:46923533-46923546 chr3:46923613-46923626
8	HMGN3	chr3:46923910-46924346	K562	blood:	n/a	n/a
9	MAZ	chr3:46924755-46924995	GM12878	blood:	n/a	chr3:46924951-46924961 chr3:46924948-46924957
10	MAZ	chr3:46923993-46924210	GM12878	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	chr3:46923480-46924335	K562	blood:	n/a	n/a
14	MXI1	chr3:46924194-46924315	GM12878	blood:	n/a	n/a
15	MYC	chr3:46924124-46924220	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr3:46925919-46926117	K562	blood:	n/a	n/a
17	REST	chr3:46924671-46924724	PANC-1	pancreas:	n/a	n/a
18	SIN3A	chr3:46923964-46924439	H1-hESC	embryonic stem cell:	n/a	n/a
19	SIN3A	chr3:46923024-46923569	H1-hESC	embryonic stem cell:	n/a	chr3:46923038-46923051 chr3:46923040-46923051
20	SPI1	chr3:46923924-46924026	K562	blood:	n/a	n/a
21	TBP	chr3:46924070-46924200	H1-hESC	embryonic stem cell:	n/a	n/a
22	UBTF	chr3:46923406-46924245	K562	blood:	n/a	n/a
23	UBTF	chr3:46925683-46925693	K562	blood:	n/a	n/a
24	UBTF	chr3:46923292-46924415	K562	blood:	n/a	n/a
25	UBTF	chr3:46925082-46925282	K562	blood:	n/a	n/a
26	ZBTB7A	chr3:46924679-46924823	K562	blood:	n/a	n/a
27	ZBTB7A	chr3:46924260-46924578	K562	blood:	n/a	chr3:46924477-46924486
28	ZBTB7A	chr3:46923151-46923686	ECC-1	luminal epithelium:	n/a	n/a
29	ZBTB7A	chr3:46924833-46924959	K562	blood:	n/a	n/a
30	ZBTB7A	chr3:46923273-46923677	K562	blood:	n/a	n/a
31	ZBTB7A	chr3:46923158-46923696	K562	blood:	n/a	n/a
32	ZBTB7A	chr3:46923706-46924608	ECC-1	luminal epithelium:	n/a	chr3:46924477-46924486 chr3:46923905-46923913
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	ZNF143	chr3:46923965-46924358	H1-hESC	embryonic stem cell:	n/a	n/a
36	ZNF263	chr3:46923869-46924334	HEK293-T-REx	kidney:	n/a	chr3:46924001-46924010
37	ZNF384	chr3:46923387-46923486	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46925524-46925574	K562	blood:	n/a
2	chr3:46924401-46924451	HUVEC	blood vessel:	n/a
3	chr3:46925081-46925131	HCPEpiC	choroid plexus:	n/a
4	chr3:46925524-46925574	HUVEC	blood vessel:	n/a
5	chr3:46924401-46924451	BE2_C	brain:	n/a
6	chr3:46924113-46924163	AoSMC	blood vessel:	n/a
7	chr3:46924401-46924451	U87	brain:	n/a
8	chr3:46924956-46925006	GM12878	blood:	n/a
9	chr3:46923433-46923483	ovcar-3	ovarian:	n/a
10	chr3:46924050-46924100	U87	brain:	n/a
11	chr3:46924768-46924818	AG04449	skin:	fetal
12	chr3:46925181-46925231	GM12878	blood:	n/a
13	chr3:46925181-46925231	HAEpiC	amniotic membrane:	n/a
14	chr3:46925081-46925131	HepG2	liver:	n/a
15	chr3:46924956-46925006	SKMC	muscle:	n/a
16	chr3:46925181-46925231	NH-A	brain:	n/a
17	chr3:46923503-46923553	GM12891	blood:	n/a
18	chr3:46924050-46924100	AoSMC	blood vessel:	n/a
19	chr3:46924401-46924451	SK-N-SH	brain:	n/a
20	chr3:46924050-46924100	SKMC	muscle:	n/a
21	chr3:46924768-46924818	SK-N-MC	brain:	n/a
22	chr3:46925181-46925231	HCT-116	colon:	n/a
23	chr3:46923503-46923553	BJ	skin:	n/a
24	chr3:46925081-46925131	GM12892	blood:	n/a
25	chr3:46924113-46924163	Jurkat	blood:	n/a
26	chr3:46924401-46924451	RPTEC	kidney:	n/a
27	chr3:46924401-46924451	MCF10A-Er-Src	breast:	n/a
28	chr3:46923433-46923483	HEK293	kidney:	embryo
29	chr3:46924113-46924163	BE2_C	brain:	n/a
30	chr3:46925181-46925231	BE2_C	brain:	n/a
31	chr3:46924050-46924100	HepG2	liver:	n/a
32	chr3:46923937-46923987	SAEC	small airway:	n/a
33	chr3:46925181-46925231	SAEC	small airway:	n/a
34	chr3:46923937-46923987	HRE	kidney:	n/a
35	chr3:46924768-46924818	SK-N-SH	brain:	n/a
36	chr3:46925081-46925131	AG09319	gingival:	n/a
37	chr3:46924401-46924451	HNPCEpiC	eye:	n/a
38	chr3:46924050-46924100	Caco-2	colon:	n/a
39	chr3:46923433-46923483	IMR90	lung:	fetal
40	chr3:46925081-46925131	AG10803	skin:	n/a
41	chr3:46924768-46924818	HAEpiC	amniotic membrane:	n/a
42	chr3:46923503-46923553	NHBE	bronchial:	n/a
43	chr3:46925081-46925131	SK-N-SH_RA	brain:	n/a
44	chr3:46924768-46924818	BE2_C	brain:	n/a
45	chr3:46924401-46924451	SK-N-SH_RA	brain:	n/a
46	chr3:46923937-46923987	A549	lung:	n/a
47	chr3:46923937-46923987	RPTEC	kidney:	n/a
48	chr3:46924956-46925006	HCF	heart:	n/a
49	chr3:46923503-46923553	A549	lung:	n/a
50	chr3:46924113-46924163	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:46921853..46924302-chr3:46929528..46931190,2	K562	blood:
2	chr3:46763658..46765267-chr3:46926020..46928200,2	MCF-7	breast:
3	chr3:46917885..46923537-chr3:46925586..46931315,6	MCF-7	breast:
4	chr3:46917885..46923537-chr3:46925586..46931315,6	MCF-7	breast:
5	chr3:46917376..46920621-chr3:46922888..46926605,5	K562	blood:
6	chr3:46733801..46735413-chr3:46924430..46926212,2	MCF-7	breast:
7	chr3:46924894..46926955-chr3:46938452..46941314,2	K562	blood:
8	chr3:46919067..46921668-chr3:46922191..46925334,3	K562	blood:
9	chr3:46923291..46931131-chr3:46931662..46935716,9	K562	blood:

No data

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

Extended variants
information (count: 60 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	rs200710310	chr3:46925133-46925134	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
31	rs200603325	chr3:46925136-46925137	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
32	rs571514959	chr3:46925151-46925152	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
33	rs199993250	chr3:46925165-46925166	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
34	rs200851488	chr3:46925166-46925167	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
35	rs565913864	chr3:46925206-46925207	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs149087775	chr3:46925234-46925235	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs539245231	chr3:46925292-46925293	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs577466875	chr3:46925300-46925301	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs535912660	chr3:46925360-46925361	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11922659	chr3:46925525-46925526	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11926707	chr3:46925539-46925540	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543984152	chr3:46925546-46925547	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs140341993	chr3:46925599-46925600	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536668798	chr3:46925648-46925649	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554909365	chr3:46925767-46925768	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114316645	chr3:46925839-46925840	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs367579525	chr3:46925851-46925852	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs541103592	chr3:46925854-46925855	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78098070	chr3:46925874-46925875	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577730924	chr3:46925886-46925887	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 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:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46920400-46923800	Weak transcription	Liver	Liver
2	chr3:46922400-46924000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:46922400-46925000	Active TSS	Fetal Kidney	kidney
4	chr3:46922400-46925400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
5	chr3:46922600-46923600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
6	chr3:46922600-46924000	Active TSS	Left Ventricle	heart
7	chr3:46922600-46925000	Active TSS	Pancreas	Pancrea
8	chr3:46922600-46925200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
9	chr3:46922600-46925200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr3:46922600-46925400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr3:46922600-46925400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:46922600-46925400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:46922600-46925600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
14	chr3:46922600-46926000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr3:46922800-46923600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
16	chr3:46922800-46923600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
17	chr3:46922800-46924000	Bivalent/Poised TSS	Colonic Mucosa	Colon
18	chr3:46922800-46924000	Active TSS	Right Ventricle	heart
19	chr3:46922800-46925000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr3:46922800-46925200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr3:46922800-46925200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
22	chr3:46922800-46925200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
23	chr3:46922800-46925200	Active TSS	Placenta Amnion	Placenta Amnion
24	chr3:46922800-46925400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr3:46922800-46925600	Active TSS	Brain Cingulate Gyrus	brain
26	chr3:46923000-46923600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:46923000-46923600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr3:46923000-46923600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr3:46923000-46923600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
30	chr3:46923000-46923600	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr3:46923000-46923800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
32	chr3:46923000-46923800	Bivalent/Poised TSS	Psoas Muscle	Psoas
33	chr3:46923000-46924000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:46923000-46924000	Enhancers	Primary B cells from cord blood	blood
35	chr3:46923000-46924000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
36	chr3:46923000-46924000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
37	chr3:46923000-46924000	Active TSS	Brain Anterior Caudate	brain
38	chr3:46923000-46924000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
39	chr3:46923000-46924200	Active TSS	Brain Angular Gyrus	brain
40	chr3:46923000-46924200	Bivalent Enhancer	Fetal Brain Male	brain
41	chr3:46923000-46924600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:46923000-46925200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:46923000-46925200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:46923000-46925200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
45	chr3:46923000-46925400	Active TSS	Aorta	Aorta
46	chr3:46923000-46925600	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
47	chr3:46923200-46923600	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
48	chr3:46923200-46923600	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
49	chr3:46923200-46923600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:46923200-46923600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin

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