Variant report

Variant	nsv598654
Chromosome Location	chr5:74345369-74351228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:787)
CpG islands
(count:795)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:74345596-74346055	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:74349551-74350155	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:74348686-74350492	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:74346230-74346497	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr5:74349196-74349715	HepG2	liver:	n/a	chr5:74349390-74349406 chr5:74349377-74349393 chr5:74349389-74349405
6	BRCA1	chr5:74348656-74348704	HepG2	liver:	n/a	n/a
7	BRCA1	chr5:74349979-74350422	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr5:74349319-74349422	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:74345544-74345965	A549	lung:	n/a	chr5:74345780-74345791
10	CEBPB	chr5:74348978-74349139	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:74345612-74345984	K562	blood:	n/a	chr5:74345780-74345791
12	CEBPB	chr5:74345612-74345943	ECC-1	luminal epithelium:	n/a	chr5:74345780-74345791
13	CEBPB	chr5:74351209-74352017	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:74345611-74346027	Hela-S3	cervix:	n/a	chr5:74345780-74345791
15	CEBPB	chr5:74345625-74345985	K562	blood:	n/a	chr5:74345780-74345791
16	CEBPB	chr5:74345526-74346089	MCF-7	breast:	n/a	chr5:74345780-74345791
17	CEBPB	chr5:74345627-74345992	HepG2	liver:	n/a	chr5:74345780-74345791
18	CEBPB	chr5:74345609-74346093	MCF-7	breast:	n/a	chr5:74345780-74345791
19	CEBPB	chr5:74345493-74346108	A549	lung:	n/a	chr5:74345780-74345791
20	CEBPB	chr5:74348623-74348748	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:74345636-74346047	H1-hESC	embryonic stem cell:	n/a	chr5:74345780-74345791
22	CEBPB	chr5:74345620-74345983	A549	lung:	n/a	chr5:74345780-74345791
23	CEBPB	chr5:74345604-74345984	IMR90	lung:	n/a	chr5:74345780-74345791
24	CHD1	chr5:74347519-74350428	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr5:74350645-74351820	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr5:74349147-74349199	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr5:74349347-74349703	HepG2	liver:	n/a	n/a
28	CHD2	chr5:74350149-74350361	HepG2	liver:	n/a	n/a
29	CHD2	chr5:74348665-74348815	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr5:74350013-74350679	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr5:74345576-74346508	H1-hESC	embryonic stem cell:	n/a	chr5:74346307-74346317
32	CREB1	chr5:74349249-74349726	A549	lung:	n/a	n/a
33	CREB1	chr5:74349380-74349941	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr5:74349300-74350258	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr5:74346320-74346470	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr5:74345660-74345810	GM12801	blood:	n/a	n/a
37	CTCF	chr5:74349120-74349270	HBMEC	blood vessel:	n/a	chr5:74349166-74349179
38	CTCF	chr5:74346320-74346470	HMF	breast:	n/a	n/a
39	CTCF	chr5:74348660-74348810	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr5:74345676-74345950	LNCaP	prostate:	n/a	n/a
41	CTCF	chr5:74349097-74349258	GM10266	blood:	n/a	chr5:74349166-74349179
42	CTCF	chr5:74345720-74345870	GM12868	blood:	n/a	n/a
43	CTCF	chr5:74345579-74346045	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr5:74349080-74349230	Hela-S3	cervix:	n/a	chr5:74349084-74349097 chr5:74349166-74349179
45	CTCF	chr5:74349400-74349550	WI-38	lung:	n/a	n/a
46	CTCF	chr5:74349086-74349294	GM12891	blood:	n/a	chr5:74349166-74349179
47	CTCF	chr5:74349081-74349305	NHEK	skin:	n/a	chr5:74349084-74349097 chr5:74349166-74349179
48	CTCF	chr5:74345760-74345910	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr5:74346303-74346461	GM19238	blood:	n/a	n/a
50	CTCF	chr5:74349514-74349558	HepG2	liver:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74346730-74346780	HCM	heart:	n/a
2	chr5:74350132-74350182	K562	blood:	n/a
3	chr5:74346730-74346780	HCM	heart:	n/a
4	chr5:74350132-74350182	K562	blood:	n/a
5	chr5:74349644-74349694	GM06990	blood:	n/a
6	chr5:74348903-74348953	HNPCEpiC	eye:	n/a
7	chr5:74350132-74350182	BJ	skin:	n/a
8	chr5:74349644-74349694	HL-60	blood:	n/a
9	chr5:74350214-74350264	NT2-D1	testis:	n/a
10	chr5:74348187-74348237	NH-A	brain:	n/a
11	chr5:74348903-74348953	AG09309	skin:	n/a
12	chr5:74350214-74350264	PANC-1	pancreas:	n/a
13	chr5:74346260-74346310	BE2_C	brain:	n/a
14	chr5:74349804-74349854	NHBE	bronchial:	n/a
15	chr5:74348187-74348237	NHBE	bronchial:	n/a
16	chr5:74348187-74348237	SKMC	muscle:	n/a
17	chr5:74346260-74346310	NB4	blood:	n/a
18	chr5:74350815-74350865	HRPEpiC	eye:	n/a
19	chr5:74348903-74348953	HL-60	blood:	n/a
20	chr5:74346260-74346310	SAEC	small airway:	n/a
21	chr5:74348187-74348237	BE2_C	brain:	n/a
22	chr5:74349993-74350043	PANC-1	pancreas:	n/a
23	chr5:74348373-74348423	HNPCEpiC	eye:	n/a
24	chr5:74347539-74347589	HL-60	blood:	n/a
25	chr5:74348187-74348237	Hepatocyte	liver:	n/a
26	chr5:74348373-74348423	IMR90	lung:	fetal
27	chr5:74348373-74348423	HRPEpiC	eye:	n/a
28	chr5:74346260-74346310	HRCEpiC	kidney:	n/a
29	chr5:74350815-74350865	HCF	heart:	n/a
30	chr5:74350132-74350182	PANC-1	pancreas:	n/a
31	chr5:74346260-74346310	RPTEC	kidney:	n/a
32	chr5:74347539-74347589	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:74349993-74350043	HAEpiC	amniotic membrane:	n/a
34	chr5:74346730-74346780	HRPEpiC	eye:	n/a
35	chr5:74350815-74350865	CMK	blood:	n/a
36	chr5:74346260-74346310	SK-N-SH	brain:	n/a
37	chr5:74350214-74350264	Hela-S3	cervix:	n/a
38	chr5:74349993-74350043	Hela-S3	cervix:	n/a
39	chr5:74350752-74350802	PANC-1	pancreas:	n/a
40	chr5:74350214-74350264	ECC-1	luminal epithelium:	n/a
41	chr5:74350214-74350264	IMR90	lung:	fetal
42	chr5:74349804-74349854	BE2_C	brain:	n/a
43	chr5:74349644-74349694	ProgFib	skin:	n/a
44	chr5:74348187-74348237	HL-60	blood:	n/a
45	chr5:74348187-74348237	BJ	skin:	n/a
46	chr5:74350752-74350802	HCPEpiC	choroid plexus:	n/a
47	chr5:74346730-74346780	NHDF-neo	bronchial:	n/a
48	chr5:74350815-74350865	AG10803	skin:	n/a
49	chr5:74348373-74348423	MCF10A-Er-Src	breast:	n/a
50	chr5:74348373-74348423	AG09319	gingival:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74230526..74231383-chr5:74345361..74346008,2	MCF-7	breast:
2	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:
3	chr5:74343721..74346711-chr5:74348510..74350046,2	MCF-7	breast:
4	chr5:74220860..74221763-chr5:74345733..74346235,2	MCF-7	breast:
5	chr5:74341045..74343910-chr5:74344011..74347485,4	MCF-7	breast:
6	chr5:74346800..74348616-chr5:74350730..74353345,2	MCF-7	breast:
7	chr5:74345325..74346339-chr5:74561197..74562160,5	MCF-7	breast:
8	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
9	chr5:74338841..74341157-chr5:74343981..74347541,4	MCF-7	breast:
10	chr5:74343645..74345260-chr5:74345382..74347449,2	K562	blood:
11	chr5:74349473..74351177-chr5:74531614..74533984,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD31-1	chr5:74348254-74348668	ENSG00000250889
2	lnc-ANKRD31-1	chr5:74349340-74349594	NONHSAT102195
3	lnc-ANKRD31-1	chr5:74347994-74348052	ENSG00000250889
4	lnc-ANKRD31-1	chr5:74347993-74348052	XLOC_004890
5	lnc-ANKRD31-1	chr5:74348254-74348668	XLOC_004890

No data

Variant related genes	Relation type
ENSG00000250889	TF binding region
ENSG00000250889	CpG island
ENSG00000250889	chromatin interactions
ENSG00000145700	chromatin interactions

Extended variants
information (count: 230 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:230 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9293641	chr5:74345369-74345370	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543630728	chr5:74345371-74345372	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563873845	chr5:74345393-74345394	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529469341	chr5:74345399-74345400	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs142696807	chr5:74345420-74345421	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150999911	chr5:74345461-74345462	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527282561	chr5:74345463-74345464	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563384123	chr5:74345481-74345482	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139927769	chr5:74345482-74345483	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570432657	chr5:74345512-74345513	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528184660	chr5:74345565-74345566	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564704062	chr5:74345574-74345575	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78588827	chr5:74345595-74345596	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs569528587	chr5:74345601-74345602	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548765104	chr5:74345633-74345634	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6867172	chr5:74345646-74345647	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557862760	chr5:74345736-74345737	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143347046	chr5:74345754-74345755	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573087601	chr5:74345760-74345761	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574382220	chr5:74345773-74345774	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs4597948	chr5:74345778-74345779	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs146719522	chr5:74345788-74345789	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572408788	chr5:74345792-74345793	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78664563	chr5:74345881-74345882	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4428388	chr5:74345950-74345951	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558157771	chr5:74346002-74346003	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577974532	chr5:74346061-74346062	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141316023	chr5:74346064-74346065	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150218244	chr5:74346084-74346085	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111818169	chr5:74346102-74346103	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145710787	chr5:74346117-74346118	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148918204	chr5:74346130-74346131	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528788949	chr5:74346157-74346158	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143825886	chr5:74346220-74346221	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564073635	chr5:74346221-74346222	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532810005	chr5:74346240-74346241	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538582833	chr5:74346267-74346268	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181157000	chr5:74346326-74346327	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537419441	chr5:74346353-74346354	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569776206	chr5:74346371-74346372	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558489335	chr5:74346391-74346392	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372771081	chr5:74346456-74346457	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557208605	chr5:74346538-74346539	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138522306	chr5:74346570-74346571	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534948564	chr5:74346572-74346573	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557791175	chr5:74346694-74346695	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144068131	chr5:74346702-74346703	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537062533	chr5:74346777-74346778	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs557419480	chr5:74346841-74346842	Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs573842987	chr5:74346864-74346865	Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74328600-74345600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:74329200-74346800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:74330600-74345400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:74330600-74348000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr5:74331400-74345400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr5:74331400-74345600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:74331600-74347000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:74333200-74346000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:74336600-74345600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:74337600-74348200	Weak transcription	Left Ventricle	heart
11	chr5:74338600-74348000	Weak transcription	Psoas Muscle	Psoas
12	chr5:74339000-74347000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:74339200-74345400	Weak transcription	Colonic Mucosa	Colon
14	chr5:74340200-74346000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:74340600-74345400	Weak transcription	Fetal Stomach	stomach
16	chr5:74340600-74347400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:74341000-74346400	Weak transcription	Small Intestine	intestine
18	chr5:74341200-74345400	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:74341400-74347400	Enhancers	HMEC	breast
20	chr5:74342000-74346000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr5:74342200-74345800	Weak transcription	Lung	lung
22	chr5:74342200-74347800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:74342400-74345800	Weak transcription	Esophagus	oesophagus
24	chr5:74342400-74346000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr5:74342800-74345400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:74342800-74345400	Enhancers	Fetal Intestine Large	intestine
27	chr5:74342800-74345600	Weak transcription	Pancreas	Pancrea
28	chr5:74343200-74345600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:74343400-74345600	Weak transcription	NHEK	skin
30	chr5:74343400-74346200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr5:74343600-74345800	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr5:74343600-74345800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr5:74343800-74345400	Enhancers	NH-A	brain
34	chr5:74343800-74346800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr5:74343800-74346800	Enhancers	Fetal Brain Female	brain
36	chr5:74344000-74345600	Enhancers	Primary T cells fromperipheralblood	blood
37	chr5:74344000-74345600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr5:74344000-74345600	Enhancers	Colon Smooth Muscle	Colon
39	chr5:74344000-74345800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:74344000-74346800	Enhancers	Stomach Mucosa	stomach
41	chr5:74344200-74345600	Genic enhancers	Fetal Thymus	thymus
42	chr5:74344200-74345600	Flanking Active TSS	GM12878-XiMat	blood
43	chr5:74344200-74347200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:74344400-74345600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr5:74344400-74345800	Weak transcription	Gastric	stomach
46	chr5:74344400-74346200	Genic enhancers	Fetal Intestine Small	intestine
47	chr5:74344400-74346400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr5:74344400-74346800	Enhancers	Rectal Smooth Muscle	rectum
49	chr5:74344400-74347200	Enhancers	Fetal Brain Male	brain
50	chr5:74344400-74348000	Weak transcription	Right Atrium	heart

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