Variant report

Variant	esv2759694
Chromosome Location	chr9:72018246-72048098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72037187-72037443	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:72027632-72027832	HepG2	liver:	n/a	n/a
3	BACH1	chr9:72044969-72045003	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr9:72027757-72027957	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr9:72046604-72047163	K562	blood:	n/a	n/a
6	CBX3	chr9:72046628-72046987	K562	blood:	n/a	n/a
7	CEBPB	chr9:72037167-72037438	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr9:72027580-72027806	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPD	chr9:72046517-72047194	K562	blood:	n/a	n/a
10	CEBPD	chr9:72046554-72047083	K562	blood:	n/a	n/a
11	CHD2	chr9:72027645-72027655	HepG2	liver:	n/a	n/a
12	CHD2	chr9:72036898-72036903	GM12878	blood:	n/a	n/a
13	CHD2	chr9:72027662-72027923	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr9:72027620-72027770	GM12864	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
15	CTCF	chr9:72037220-72037370	GM06990	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
16	CTCF	chr9:72037200-72037350	GM12873	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
17	CTCF	chr9:72037200-72037350	WERI-Rb-1	eye:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
18	CTCF	chr9:72027657-72027808	GM19240	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
19	CTCF	chr9:72027640-72027790	RPTEC	kidney:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
20	CTCF	chr9:72040380-72040648	MCF-7	breast:	n/a	n/a
21	CTCF	chr9:72027622-72027878	MCF-7	breast:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
22	CTCF	chr9:72037220-72037370	HRE	kidney:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
23	CTCF	chr9:72037120-72037270	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr9:72027618-72027877	ProgFib	skin:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
25	CTCF	chr9:72040456-72040537	LNCaP	prostate:	n/a	n/a
26	CTCF	chr9:72040361-72040584	MCF-7	breast:	n/a	n/a
27	CTCF	chr9:72043396-72043519	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:72027640-72027790	GM12865	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
29	CTCF	chr9:72040377-72040593	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:72027618-72027891	Gliobla	brain:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
31	CTCF	chr9:72027647-72027866	Kidney_OC	kidney:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
32	CTCF	chr9:72027619-72027905	GM12878	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
33	CTCF	chr9:72027561-72027967	MCF-7	breast:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
34	CTCF	chr9:72027652-72027820	A549	lung:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
35	CTCF	chr9:72037180-72037458	GM19239	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
36	CTCF	chr9:72037160-72037310	GM12875	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
37	CTCF	chr9:72027680-72027830	K562	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
38	CTCF	chr9:72037200-72037350	SAEC	small airway:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
39	CTCF	chr9:72037160-72037407	LNCaP	prostate:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
40	CTCF	chr9:72037158-72037434	MCF-7	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
41	CTCF	chr9:72027630-72027933	K562	blood:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
42	CTCF	chr9:72037180-72037330	HepG2	liver:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
43	CTCF	chr9:72037101-72037448	K562	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
44	CTCF	chr9:72037160-72037310	GM12866	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
45	CTCF	chr9:72036961-72037044	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:72036900-72037050	SAEC	small airway:	n/a	n/a
47	CTCF	chr9:72027700-72027850	AG04450	lung:	n/a	chr9:72027736-72027754 chr9:72027741-72027751 chr9:72027739-72027748 chr9:72027739-72027752
48	CTCF	chr9:72040369-72040615	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:72037240-72037390	Hela-S3	cervix:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
50	CTCF	chr9:72037121-72037431	GM12878	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72027019-72027069	HCT-116	colon:	n/a
2	chr9:72027409-72027459	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:72046240-72046290	SAEC	small airway:	n/a
4	chr9:72027019-72027069	AoSMC	blood vessel:	n/a
5	chr9:72027409-72027459	HIPEpiC	eye:	n/a
6	chr9:72027019-72027069	SK-N-SH	brain:	n/a
7	chr9:72046240-72046290	AG04450	lung:	fetal
8	chr9:72046240-72046290	SK-N-MC	brain:	n/a
9	chr9:72046240-72046290	Jurkat	blood:	n/a
10	chr9:72027409-72027459	HRPEpiC	eye:	n/a
11	chr9:72027019-72027069	HCPEpiC	choroid plexus:	n/a
12	chr9:72046240-72046290	NB4	blood:	n/a
13	chr9:72027019-72027069	AG09309	skin:	n/a
14	chr9:72027019-72027069	PFSK-1	brain:	n/a
15	chr9:72027409-72027459	U87	brain:	n/a
16	chr9:72027019-72027069	PrEC	prostate:	n/a
17	chr9:72046240-72046290	PANC-1	pancreas:	n/a
18	chr9:72046240-72046290	GM06990	blood:	n/a
19	chr9:72027019-72027069	GM12891	blood:	n/a
20	chr9:72046240-72046290	AG09319	gingival:	n/a
21	chr9:72027409-72027459	PrEC	prostate:	n/a
22	chr9:72046240-72046290	HMEC	breast:	n/a
23	chr9:72027019-72027069	AG04449	skin:	fetal
24	chr9:72027409-72027459	HEEpiC	esophagus:	n/a
25	chr9:72027019-72027069	HRE	kidney:	n/a
26	chr9:72046240-72046290	ECC-1	luminal epithelium:	n/a
27	chr9:72027409-72027459	PANC-1	pancreas:	n/a
28	chr9:72027019-72027069	SK-N-MC	brain:	n/a
29	chr9:72027019-72027069	GM06990	blood:	n/a
30	chr9:72027409-72027459	AG10803	skin:	n/a
31	chr9:72027409-72027459	BE2_C	brain:	n/a
32	chr9:72046240-72046290	HPAEpiC	pulmonary alveolar:	n/a
33	chr9:72046240-72046290	Hela-S3	cervix:	n/a
34	chr9:72027409-72027459	GM06990	blood:	n/a
35	chr9:72027409-72027459	AoSMC	blood vessel:	n/a
36	chr9:72046240-72046290	IMR90	lung:	fetal
37	chr9:72027019-72027069	HRCEpiC	kidney:	n/a
38	chr9:72027409-72027459	MCF10A-Er-Src	breast:	n/a
39	chr9:72046240-72046290	HRPEpiC	eye:	n/a
40	chr9:72027019-72027069	BE2_C	brain:	n/a
41	chr9:72046240-72046290	HRE	kidney:	n/a
42	chr9:72027019-72027069	HUVEC	blood vessel:	n/a
43	chr9:72046240-72046290	HepG2	liver:	n/a
44	chr9:72046240-72046290	PFSK-1	brain:	n/a
45	chr9:72027409-72027459	SAEC	small airway:	n/a
46	chr9:72027019-72027069	ProgFib	skin:	n/a
47	chr9:72027409-72027459	ovcar-3	ovarian:	n/a
48	chr9:72046240-72046290	MCF-7	breast:	n/a
49	chr9:72027409-72027459	GM12892	blood:	n/a
50	chr9:72027019-72027069	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:71907137..71907714-chr9:72027328..72028069,2	MCF-7	breast:
2	chr9:72027335..72027966-chr9:72164135..72164934,2	MCF-7	breast:
3	chr9:72036807..72037778-chr9:72056686..72057333,2	MCF-7	breast:
4	chr9:72039845..72040903-chr9:72160889..72161458,4	MCF-7	breast:
5	chr9:72036812..72037787-chr9:72160880..72161856,6	MCF-7	breast:
6	chr9:72036664..72037777-chr9:72163377..72165001,9	K562	blood:
7	chr9:71939359..71941808-chr9:72025736..72028094,2	MCF-7	breast:
8	chr9:72036895..72038079-chr9:72163773..72164881,7	MCF-7	breast:
9	chr9:72000714..72007830-chr9:72009954..72019278,14	MCF-7	breast:
10	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
11	chr9:71650287..71651089-chr9:72027660..72028217,2	K562	blood:
12	chr9:72038579..72040872-chr9:72161729..72164338,3	MCF-7	breast:
13	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
14	chr9:72005489..72008452-chr9:72026108..72027745,2	K562	blood:
15	chr9:72027288..72028201-chr9:72161004..72161637,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBA1-1	chr9:72042449-72044751	NONHSAT131778
2	lnc-APBA1-1	chr9:72043544-72043637	ENSG00000243888
3	lnc-APBA1-1	chr9:72043164-72043467	ENSG00000243888

Variant related genes	Relation type
ENSG00000243888	TF binding region
ENSG00000243888	CpG island
ENSG00000135063	chromatin interactions
ENSG00000165060	chromatin interactions

Extended variants
information (count: 1258 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7024302	chr9:72018246-72018247	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529490166	chr9:72018292-72018293	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79020438	chr9:72018333-72018334	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371904593	chr9:72018340-72018341	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141856495	chr9:72018367-72018368	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79761912	chr9:72018445-72018446	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189768764	chr9:72018457-72018458	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376653682	chr9:72018513-72018514	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2781526	chr9:72018519-72018520	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs180675118	chr9:72018570-72018571	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573807523	chr9:72018580-72018581	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146265161	chr9:72018583-72018584	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555907570	chr9:72018619-72018620	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117161314	chr9:72018723-72018724	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185985201	chr9:72018735-72018736	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113993384	chr9:72018754-72018755	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564190004	chr9:72018764-72018765	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139321626	chr9:72018768-72018769	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192158440	chr9:72018778-72018779	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371476317	chr9:72018878-72018879	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142635004	chr9:72018885-72018886	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150978364	chr9:72018918-72018919	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2777877	chr9:72018961-72018962	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114936952	chr9:72018976-72018977	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139331605	chr9:72018984-72018985	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566403280	chr9:72019014-72019015	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533786111	chr9:72019038-72019039	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555035022	chr9:72019039-72019040	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567568966	chr9:72019040-72019041	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539366139	chr9:72019049-72019050	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537734834	chr9:72019078-72019079	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555970848	chr9:72019086-72019087	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577415556	chr9:72019108-72019109	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546870558	chr9:72019119-72019120	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566919662	chr9:72019138-72019139	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557843118	chr9:72019167-72019168	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573225513	chr9:72019172-72019173	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141092989	chr9:72019180-72019181	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561917471	chr9:72019235-72019236	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181993747	chr9:72019243-72019244	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544916965	chr9:72019244-72019245	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563115255	chr9:72019251-72019252	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186533282	chr9:72019252-72019253	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142327728	chr9:72019266-72019267	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560214548	chr9:72019267-72019268	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527362276	chr9:72019268-72019269	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548998019	chr9:72019280-72019281	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs575629437	chr9:72019283-72019284	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs538311538	chr9:72019286-72019287	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs146908590	chr9:72019289-72019290	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72003600-72026200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:72007600-72026800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr9:72009000-72024400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:72010000-72027800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:72011000-72026800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:72012400-72018600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr9:72012800-72018400	Weak transcription	Right Atrium	heart
8	chr9:72013200-72027800	Weak transcription	Brain Substantia Nigra	brain
9	chr9:72017000-72024800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:72017800-72018400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:72018200-72019000	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
12	chr9:72018400-72018600	Enhancers	Right Atrium	heart
13	chr9:72018600-72018800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr9:72018600-72019800	Weak transcription	Right Atrium	heart
15	chr9:72018800-72019600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:72019000-72024800	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr9:72020000-72020200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:72020600-72020800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:72020600-72021000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:72020800-72023800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:72023800-72025000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:72024200-72024400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr9:72024400-72024600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr9:72024400-72024800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:72024400-72027000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr9:72024600-72025000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
27	chr9:72024600-72025400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr9:72024600-72025400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr9:72024800-72025000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:72024800-72025000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr9:72024800-72025000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr9:72024800-72025400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr9:72025000-72025200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr9:72025000-72025200	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr9:72025000-72025400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:72025000-72027000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:72025000-72027400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr9:72025200-72025600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr9:72025400-72027200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr9:72025400-72027400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr9:72025600-72027600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr9:72026200-72027000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:72026400-72026600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr9:72026400-72027800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr9:72026600-72027800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr9:72026800-72028000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr9:72026800-72028400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:72027000-72027400	Active TSS	Primary hematopoietic stem cells	blood
49	chr9:72027000-72027400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:72027000-72027400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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