Variant report

Variant	esv2761506
Chromosome Location	chr9:16040491-16093736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:16060750-16061133	GM12878	blood:	n/a	n/a
2	ATF2	chr9:16060647-16061176	GM12878	blood:	n/a	n/a
3	ATF3	chr9:16062908-16063301	HCT-116	colon:	n/a	n/a
4	ATF3	chr9:16062763-16063305	HCT-116	colon:	n/a	n/a
5	ATF3	chr9:16062761-16063303	A549	lung:	n/a	n/a
6	BATF	chr9:16060743-16061148	GM12878	blood:	n/a	n/a
7	BATF	chr9:16062567-16062863	GM12878	blood:	n/a	n/a
8	BATF	chr9:16046711-16046966	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:16060792-16061149	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:16060676-16061037	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:16069309-16069354	HepG2	liver:	n/a	n/a
12	CBX3	chr9:16062787-16063294	HCT-116	colon:	n/a	n/a
13	CEBPB	chr9:16062757-16063382	HCT-116	colon:	n/a	chr9:16063016-16063027
14	CEBPB	chr9:16040364-16040850	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr9:16049018-16049283	Hela-S3	cervix:	n/a	chr9:16049185-16049196
16	CEBPB	chr9:16062861-16063167	HepG2	liver:	n/a	chr9:16063016-16063027
17	CEBPB	chr9:16049057-16049343	HepG2	liver:	n/a	chr9:16049185-16049196
18	CEBPB	chr9:16053187-16053402	HepG2	liver:	n/a	chr9:16053306-16053317
19	CEBPB	chr9:16091287-16091577	IMR90	lung:	n/a	chr9:16091443-16091456
20	CEBPB	chr9:16064950-16065163	IMR90	lung:	n/a	chr9:16065064-16065075
21	CEBPB	chr9:16062761-16063670	A549	lung:	n/a	chr9:16063449-16063466 chr9:16063016-16063027 chr9:16063450-16063461 chr9:16063450-16063463 chr9:16063450-16063461
22	CEBPB	chr9:16049066-16049267	IMR90	lung:	n/a	chr9:16049185-16049196
23	CEBPB	chr9:16062813-16063608	Hela-S3	cervix:	n/a	chr9:16063449-16063466 chr9:16063016-16063027 chr9:16063450-16063461 chr9:16063450-16063463 chr9:16063450-16063461
24	CEBPB	chr9:16049017-16049349	A549	lung:	n/a	chr9:16049185-16049196
25	CEBPB	chr9:16062812-16063626	IMR90	lung:	n/a	chr9:16063449-16063466 chr9:16063016-16063027 chr9:16063450-16063461 chr9:16063450-16063463 chr9:16063450-16063461
26	CEBPB	chr9:16058124-16058404	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:16062695-16063727	A549	lung:	n/a	chr9:16063449-16063466 chr9:16063016-16063027 chr9:16063450-16063461 chr9:16063450-16063463 chr9:16063450-16063461
28	CEBPB	chr9:16062769-16063273	MCF-7	breast:	n/a	chr9:16063016-16063027
29	CEBPB	chr9:16064893-16065151	HepG2	liver:	n/a	chr9:16065064-16065075
30	CEBPB	chr9:16062837-16063527	A549	lung:	n/a	chr9:16063449-16063466 chr9:16063016-16063027 chr9:16063450-16063461 chr9:16063450-16063463 chr9:16063450-16063461
31	CEBPB	chr9:16064962-16065202	A549	lung:	n/a	chr9:16065064-16065075
32	CEBPB	chr9:16062698-16063381	HCT-116	colon:	n/a	chr9:16063016-16063027
33	CEBPB	chr9:16053308-16053347	A549	lung:	n/a	n/a
34	CHD2	chr9:16040292-16040680	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr9:16062868-16063231	Hela-S3	cervix:	n/a	n/a
36	CTBP2	chr9:16040059-16040654	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr9:16058330-16058462	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:16058440-16058498	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:16058360-16058510	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr9:16058380-16058530	AG04450	lung:	n/a	n/a
41	CTCF	chr9:16058458-16058502	GM12878	blood:	n/a	n/a
42	CTCF	chr9:16058400-16058550	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:16058500-16058650	AG10803	skin:	n/a	n/a
44	CTCF	chr9:16062069-16062124	NHEK	skin:	n/a	n/a
45	CTCF	chr9:16062280-16062430	HPF	lung:	n/a	n/a
46	CTCF	chr9:16062097-16062130	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr9:16083020-16083170	NB4	blood:	n/a	n/a
48	CTCF	chr9:16058340-16058490	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr9:16063246-16063385	NHEK	skin:	n/a	n/a
50	CTCF	chr9:16058440-16058590	AG04450	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16069562-16069612	HRE	kidney:	n/a
2	chr9:16091885-16091935	HCF	heart:	n/a
3	chr9:16044344-16044394	NHBE	bronchial:	n/a
4	chr9:16044344-16044394	AG10803	skin:	n/a
5	chr9:16040625-16040675	SAEC	small airway:	n/a
6	chr9:16069562-16069612	ECC-1	luminal epithelium:	n/a
7	chr9:16044344-16044394	NHDF-neo	bronchial:	n/a
8	chr9:16040625-16040675	T-47D	breast:	n/a
9	chr9:16069562-16069612	SK-N-MC	brain:	n/a
10	chr9:16044344-16044394	HRPEpiC	eye:	n/a
11	chr9:16091885-16091935	K562	blood:	n/a
12	chr9:16091885-16091935	ProgFib	skin:	n/a
13	chr9:16044344-16044394	HCT-116	colon:	n/a
14	chr9:16091885-16091935	HPAEpiC	pulmonary alveolar:	n/a
15	chr9:16040625-16040675	HIPEpiC	eye:	n/a
16	chr9:16069562-16069612	GM12892	blood:	n/a
17	chr9:16069562-16069612	HEEpiC	esophagus:	n/a
18	chr9:16040625-16040675	IMR90	lung:	fetal
19	chr9:16044344-16044394	Jurkat	blood:	n/a
20	chr9:16091885-16091935	AoSMC	blood vessel:	n/a
21	chr9:16069562-16069612	HMEC	breast:	n/a
22	chr9:16069562-16069612	SKMC	muscle:	n/a
23	chr9:16044344-16044394	AG09309	skin:	n/a
24	chr9:16091885-16091935	H1-hESC	embryonic stem cell:	embryo
25	chr9:16040625-16040675	Jurkat	blood:	n/a
26	chr9:16040625-16040675	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:16069562-16069612	SK-N-SH_RA	brain:	n/a
28	chr9:16044344-16044394	AG09319	gingival:	n/a
29	chr9:16040625-16040675	HNPCEpiC	eye:	n/a
30	chr9:16044344-16044394	HIPEpiC	eye:	n/a
31	chr9:16069562-16069612	Hela-S3	cervix:	n/a
32	chr9:16040625-16040675	RPTEC	kidney:	n/a
33	chr9:16069562-16069612	PrEC	prostate:	n/a
34	chr9:16040625-16040675	SK-N-SH	brain:	n/a
35	chr9:16069562-16069612	AG10803	skin:	n/a
36	chr9:16040625-16040675	AG04450	lung:	fetal
37	chr9:16040625-16040675	AG09309	skin:	n/a
38	chr9:16044344-16044394	HEK293	kidney:	embryo
39	chr9:16069562-16069612	HNPCEpiC	eye:	n/a
40	chr9:16091885-16091935	AG10803	skin:	n/a
41	chr9:16044344-16044394	HPAEpiC	pulmonary alveolar:	n/a
42	chr9:16091885-16091935	RPTEC	kidney:	n/a
43	chr9:16091885-16091935	HEK293	kidney:	embryo
44	chr9:16044344-16044394	HNPCEpiC	eye:	n/a
45	chr9:16069562-16069612	HCT-116	colon:	n/a
46	chr9:16069562-16069612	RPTEC	kidney:	n/a
47	chr9:16040625-16040675	GM12878	blood:	n/a
48	chr9:16069562-16069612	HCPEpiC	choroid plexus:	n/a
49	chr9:16069562-16069612	A549	lung:	n/a
50	chr9:16040625-16040675	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:16074686..16077163-chr9:16077255..16078933,2	MCF-7	breast:
2	chr9:16080126..16081905-chr9:16084168..16087016,2	MCF-7	breast:
3	chr9:16080117..16082951-chr9:16084939..16087066,2	K562	blood:
4	chr9:16063712..16066364-chr9:16092575..16094646,2	MCF-7	breast:
5	chr9:16063712..16066364-chr9:16092575..16094646,2	MCF-7	breast:
6	chr9:16080126..16081905-chr9:16084168..16087016,2	MCF-7	breast:
7	chr9:16064268..16067195-chr9:16080044..16082356,2	MCF-7	breast:
8	chr9:16074686..16077163-chr9:16077255..16078933,2	MCF-7	breast:
9	chr9:16080117..16082951-chr9:16084939..16087066,2	K562	blood:
10	chr9:16064268..16067195-chr9:16080044..16082356,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-1	chr9:16060644-16061318	NONHSAT130282
2	lnc-SNAPC3-1	chr9:16042796-16042918	XLOC_007290
3	lnc-SNAPC3-1	chr9:16060644-16061661	NONHSAT130279
4	lnc-SNAPC3-1	chr9:16060644-16060851	XLOC_007290
5	lnc-SNAPC3-1	chr9:16042796-16042918	XLOC_007290
6	lnc-SNAPC3-1	chr9:16042796-16042884	NONHSAT130282
7	lnc-SNAPC3-1	chr9:16042796-16042918	NONHSAT130279
8	lnc-SNAPC3-1	chr9:16060644-16061855	XLOC_007290

No data

Variant related genes	Relation type
CCDC171	TF binding region
CCDC171	CpG island
RAB6A	miRNA target sites
DACT1	miRNA target sites
PEMT	miRNA target sites
MLL3	miRNA target sites

Extended variants
information (count: 2081 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560534036	chr9:16040562-16040563	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs527638222	chr9:16040612-16040613	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs543313958	chr9:16040625-16040626	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs184645951	chr9:16040626-16040627	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs189010539	chr9:16040635-16040636	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs3008705	chr9:16040663-16040664	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs377611750	chr9:16040736-16040737	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs550385096	chr9:16040737-16040738	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs117274976	chr9:16040745-16040746	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs372382545	chr9:16040819-16040820	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs373880408	chr9:16040824-16040825	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs533056900	chr9:16040831-16040832	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181492513	chr9:16040843-16040844	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184255690	chr9:16040851-16040852	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557383695	chr9:16040862-16040863	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs138577073	chr9:16040873-16040874	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs145586533	chr9:16040877-16040878	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs201541680	chr9:16040879-16040880	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370151672	chr9:16040895-16040896	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73415878	chr9:16040918-16040919	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555654818	chr9:16040932-16040933	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs538169593	chr9:16040977-16040978	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73415882	chr9:16041026-16041027	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138318284	chr9:16041036-16041037	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374666309	chr9:16041052-16041053	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs16933985	chr9:16041053-16041054	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs572957590	chr9:16041069-16041070	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs555927986	chr9:16041070-16041071	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200017454	chr9:16041078-16041079	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147659695	chr9:16041105-16041106	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs111365330	chr9:16041169-16041170	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs545099617	chr9:16041181-16041182	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs553933559	chr9:16041186-16041187	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs572427734	chr9:16041221-16041222	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs79631794	chr9:16041275-16041276	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs180890481	chr9:16041395-16041396	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs10810526	chr9:16041399-16041400	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs186041711	chr9:16041417-16041418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565482708	chr9:16041419-16041420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192113846	chr9:16041429-16041430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551470832	chr9:16041441-16041442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558256611	chr9:16041475-16041476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566415447	chr9:16041497-16041498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527309526	chr9:16041540-16041541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548686494	chr9:16041550-16041551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10738425	chr9:16041576-16041577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10738426	chr9:16041615-16041616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142305624	chr9:16041644-16041645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77984311	chr9:16041672-16041673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35839166	chr9:16041683-16041684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16023600-16040600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:16030800-16050000	Weak transcription	Aorta	Aorta
3	chr9:16034000-16043600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:16039000-16041400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:16039000-16041400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:16039000-16041400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:16039000-16041400	Enhancers	Fetal Kidney	kidney
8	chr9:16039000-16041400	Enhancers	Rectal Smooth Muscle	rectum
9	chr9:16039000-16041600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:16039000-16041600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:16039200-16040600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:16039200-16040800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:16039200-16040800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr9:16039200-16041200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr9:16039200-16041400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr9:16039200-16041400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:16039200-16041400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:16039200-16041400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:16039200-16041400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:16039200-16041400	Enhancers	Fetal Lung	lung
21	chr9:16039200-16041400	Enhancers	Ovary	ovary
22	chr9:16039200-16041400	Enhancers	NH-A	brain
23	chr9:16039200-16041600	Enhancers	Fetal Muscle Leg	muscle
24	chr9:16039200-16042800	Enhancers	Fetal Stomach	stomach
25	chr9:16039400-16041000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr9:16039400-16041400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:16039600-16041200	Enhancers	Colon Smooth Muscle	Colon
28	chr9:16039600-16042400	Enhancers	Adipose Nuclei	Adipose
29	chr9:16039800-16040600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr9:16039800-16040600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:16039800-16040600	Enhancers	Fetal Muscle Trunk	muscle
32	chr9:16039800-16042600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr9:16039800-16043400	Weak transcription	Osteobl	bone
34	chr9:16040000-16043600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:16040200-16040800	Flanking Active TSS	Stomach Smooth Muscle	stomach
36	chr9:16040200-16041200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr9:16040400-16040600	Enhancers	Fetal Intestine Large	intestine
38	chr9:16040400-16040800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr9:16040400-16041000	Enhancers	A549	lung
40	chr9:16040400-16041400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr9:16040400-16043600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:16040600-16041000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:16040600-16041200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr9:16040600-16041200	Weak transcription	Fetal Intestine Large	intestine
45	chr9:16040600-16042000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr9:16040600-16057600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:16040800-16041000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr9:16040800-16041200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:16040800-16041200	Enhancers	Stomach Smooth Muscle	stomach
50	chr9:16040800-16043400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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