Variant report

Variant	nsv1001542
Chromosome Location	chr2:115920847-116082585
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	ATF1	chr2:116043088-116043252	K562	blood:	n/a	n/a
2	ATF3	chr2:115940796-115941033	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:116035173-116035405	K562	blood:	n/a	chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035272-116035285 chr2:116035272-116035285
4	CEBPB	chr2:115972484-115972684	A549	lung:	n/a	n/a
5	CEBPB	chr2:116005814-116005967	H1-hESC	embryonic stem cell:	n/a	chr2:116005889-116005900
6	CEBPB	chr2:115927410-115927757	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:116005744-116005988	A549	lung:	n/a	chr2:116005889-116005900
8	CEBPB	chr2:115926661-115926928	A549	lung:	n/a	chr2:115926802-115926813
9	CEBPB	chr2:116005729-116006041	HepG2	liver:	n/a	chr2:116005889-116005900
10	CEBPB	chr2:115932181-115932471	HepG2	liver:	n/a	chr2:115932314-115932323 chr2:115932312-115932325 chr2:115932314-115932323 chr2:115932314-115932323 chr2:115932312-115932323 chr2:115932312-115932325 chr2:115932312-115932325 chr2:115932314-115932323 chr2:115932313-115932324 chr2:115932312-115932323
11	CEBPB	chr2:115926629-115926972	HepG2	liver:	n/a	chr2:115926802-115926813 chr2:115926631-115926642
12	CEBPB	chr2:115927422-115927757	K562	blood:	n/a	n/a
13	CEBPB	chr2:116035135-116035335	IMR90	lung:	n/a	chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035272-116035285 chr2:116035272-116035285
14	CEBPB	chr2:116051147-116051306	H1-hESC	embryonic stem cell:	n/a	chr2:116051277-116051286 chr2:116051277-116051286
15	CEBPB	chr2:115932283-115932339	K562	blood:	n/a	chr2:115932314-115932323 chr2:115932312-115932325 chr2:115932314-115932323 chr2:115932314-115932323 chr2:115932312-115932323 chr2:115932312-115932325 chr2:115932312-115932325 chr2:115932314-115932323 chr2:115932313-115932324 chr2:115932312-115932323
16	CEBPB	chr2:116006280-116006565	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:116005750-116006051	IMR90	lung:	n/a	chr2:116005889-116005900
18	CEBPB	chr2:115927400-115927763	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:115971660-115972044	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:115926634-115926963	IMR90	lung:	n/a	chr2:115926802-115926813
21	CEBPB	chr2:115956080-115956322	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:115972531-115972787	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:116051097-116051409	HepG2	liver:	n/a	chr2:116051277-116051286 chr2:116051277-116051286
24	CEBPB	chr2:115920841-115921055	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:115927400-115927773	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:116035154-116035389	HepG2	liver:	n/a	chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035272-116035285 chr2:116035272-116035285
27	CEBPB	chr2:115927428-115927759	A549	lung:	n/a	n/a
28	CEBPB	chr2:116035211-116035324	H1-hESC	embryonic stem cell:	n/a	chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035274-116035283 chr2:116035272-116035285 chr2:116035272-116035285
29	CTCF	chr2:115923180-115923420	A549	lung:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
30	CTCF	chr2:115952333-115952446	HepG2	liver:	n/a	chr2:115952386-115952404 chr2:115952381-115952402 chr2:115952387-115952403
31	CTCF	chr2:115940919-115940979	MCF-7	breast:	n/a	chr2:115940958-115940974
32	CTCF	chr2:115923220-115923370	SAEC	small airway:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
33	CTCF	chr2:115922260-115922340	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:115923280-115923430	K562	blood:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
35	CTCF	chr2:115923114-115923400	H1-hESC	embryonic stem cell:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
36	CTCF	chr2:115923194-115923414	MCF-7	breast:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
37	CTCF	chr2:115923180-115923330	GM12869	blood:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
38	CTCF	chr2:115922923-115923673	SK-N-SH	brain:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
39	CTCF	chr2:115921320-115921470	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:115923188-115923396	Pancreas_OC	pancreas:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
41	CTCF	chr2:115940960-115941110	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:115923075-115923496	GM12878	blood:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
43	CTCF	chr2:115923220-115923370	GM12865	blood:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
44	CTCF	chr2:115921326-115921437	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr2:115947960-115948110	HepG2	liver:	n/a	n/a
46	CTCF	chr2:115969486-115969545	GM20000	blood:	n/a	n/a
47	CTCF	chr2:115923240-115923390	GM12868	blood:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
48	CTCF	chr2:115923220-115923370	HPF	lung:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
49	CTCF	chr2:115923227-115923365	NHEK	skin:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300
50	CTCF	chr2:115923240-115923390	HRPEpiC	eye:	n/a	chr2:115923285-115923294 chr2:115923287-115923297 chr2:115923283-115923299 chr2:115923284-115923305 chr2:115923285-115923298 chr2:115923282-115923300

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:115920825-115920875	Jurkat	blood:	n/a
2	chr2:115972042-115972092	HUVEC	blood vessel:	n/a
3	chr2:115920825-115920875	HIPEpiC	eye:	n/a
4	chr2:115972042-115972092	GM12892	blood:	n/a
5	chr2:115972042-115972092	K562	blood:	n/a
6	chr2:115972042-115972092	AG09309	skin:	n/a
7	chr2:115972042-115972092	Jurkat	blood:	n/a
8	chr2:115972042-115972092	AoSMC	blood vessel:	n/a
9	chr2:115921258-115921308	HAEpiC	amniotic membrane:	n/a
10	chr2:115920825-115920875	NH-A	brain:	n/a
11	chr2:115972042-115972092	NT2-D1	testis:	n/a
12	chr2:115921258-115921308	NH-A	brain:	n/a
13	chr2:115920825-115920875	HEK293	kidney:	embryo
14	chr2:115921258-115921308	ECC-1	luminal epithelium:	n/a
15	chr2:115920825-115920875	NT2-D1	testis:	n/a
16	chr2:115921258-115921308	HCT-116	colon:	n/a
17	chr2:115920825-115920875	MCF10A-Er-Src	breast:	n/a
18	chr2:115921258-115921308	AG10803	skin:	n/a
19	chr2:115920825-115920875	HCPEpiC	choroid plexus:	n/a
20	chr2:115972042-115972092	HEK293	kidney:	embryo
21	chr2:115920825-115920875	CMK	blood:	n/a
22	chr2:115921258-115921308	HIPEpiC	eye:	n/a
23	chr2:115921258-115921308	SK-N-SH	brain:	n/a
24	chr2:115920825-115920875	BJ	skin:	n/a
25	chr2:115920825-115920875	PrEC	prostate:	n/a
26	chr2:115920825-115920875	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:115920825-115920875	PANC-1	pancreas:	n/a
28	chr2:115921258-115921308	NT2-D1	testis:	n/a
29	chr2:115921258-115921308	MCF10A-Er-Src	breast:	n/a
30	chr2:115972042-115972092	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:115920825-115920875	HCF	heart:	n/a
32	chr2:115921258-115921308	GM12878	blood:	n/a
33	chr2:115972042-115972092	HCM	heart:	n/a
34	chr2:115972042-115972092	ovcar-3	ovarian:	n/a
35	chr2:115972042-115972092	GM12878	blood:	n/a
36	chr2:115921258-115921308	HRPEpiC	eye:	n/a
37	chr2:115972042-115972092	T-47D	breast:	n/a
38	chr2:115920825-115920875	SKMC	muscle:	n/a
39	chr2:115972042-115972092	PANC-1	pancreas:	n/a
40	chr2:115921258-115921308	RPTEC	kidney:	n/a
41	chr2:115972042-115972092	PFSK-1	brain:	n/a
42	chr2:115920825-115920875	HepG2	liver:	n/a
43	chr2:115920825-115920875	BE2_C	brain:	n/a
44	chr2:115920825-115920875	RPTEC	kidney:	n/a
45	chr2:115920825-115920875	PFSK-1	brain:	n/a
46	chr2:115972042-115972092	HepG2	liver:	n/a
47	chr2:115921258-115921308	CMK	blood:	n/a
48	chr2:115972042-115972092	U87	brain:	n/a
49	chr2:115921258-115921308	ovcar-3	ovarian:	n/a
50	chr2:115921258-115921308	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:115922401..115925088-chr2:115925771..115928554,2	MCF-7	breast:
2	chr2:115933713..115935600-chr2:115936141..115938782,2	MCF-7	breast:
3	chr2:115486408..115487261-chr2:115951872..115952594,3	MCF-7	breast:
4	chr2:115486382..115487273-chr2:115940531..115941348,2	MCF-7	breast:
5	chr2:116069793..116071338-chr2:116297492..116299171,2	K562	blood:
6	chr2:115891632..115893895-chr2:116010152..116012412,2	K562	blood:
7	chr2:115922401..115925088-chr2:115925771..115928554,2	MCF-7	breast:
8	chr2:115933713..115935600-chr2:115936141..115938782,2	MCF-7	breast:

Variant related genes	Relation type
DPP10	TF binding region
DPP10-AS1	TF binding region
DPP10	CpG island
DPP10-AS1	CpG island

Extended variants
information (count: 5027 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:5027 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144290650	chr2:115920859-115920860	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs184821542	chr2:115920865-115920866	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs560780800	chr2:115920921-115920922	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs58110812	chr2:115920938-115920939	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs542659176	chr2:115921008-115921009	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12615811	chr2:115921098-115921099	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375724575	chr2:115921104-115921105	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146578111	chr2:115921122-115921123	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs140111714	chr2:115921124-115921125	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564769780	chr2:115921207-115921208	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs527506814	chr2:115921225-115921226	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189289347	chr2:115921238-115921239	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567224275	chr2:115921269-115921270	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs536238961	chr2:115921292-115921293	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs549549241	chr2:115921293-115921294	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs181019519	chr2:115921297-115921298	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs185771350	chr2:115921325-115921326	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs558707816	chr2:115921368-115921369	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs578191384	chr2:115921379-115921380	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs189876386	chr2:115921393-115921394	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs137919792	chr2:115921412-115921413	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370828011	chr2:115921426-115921427	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554460771	chr2:115921449-115921450	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574434307	chr2:115921558-115921559	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs542999636	chr2:115921631-115921632	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562778003	chr2:115921745-115921746	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576462656	chr2:115921797-115921798	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545147348	chr2:115921805-115921806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202009434	chr2:115921826-115921827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565056883	chr2:115921858-115921859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527445508	chr2:115921864-115921865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142415592	chr2:115921886-115921887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181147098	chr2:115921912-115921913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529975120	chr2:115921923-115921924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187051024	chr2:115921924-115921925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs151307226	chr2:115921927-115921928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372918550	chr2:115921940-115921941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538643642	chr2:115921999-115922000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552260608	chr2:115922001-115922002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565783208	chr2:115922065-115922066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567689801	chr2:115922073-115922074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191700386	chr2:115922139-115922140	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs542941329	chr2:115922176-115922177	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs554448716	chr2:115922358-115922359	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79382638	chr2:115922366-115922367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536574417	chr2:115922367-115922368	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs77212001	chr2:115922376-115922377	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs140594782	chr2:115922378-115922379	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182969739	chr2:115922390-115922391	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs553544620	chr2:115922394-115922395	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17621639	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115918000-115921200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr2:115918200-115921200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr2:115918600-115921000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:115918600-115921000	Active TSS	Pancreas	Pancrea
5	chr2:115919600-115921000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr2:115919800-115921000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr2:115919800-115921000	Bivalent Enhancer	Liver	Liver
8	chr2:115919800-115921200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:115920000-115921000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
10	chr2:115920000-115921000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:115920000-115921000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
12	chr2:115920000-115921000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr2:115920000-115921200	Bivalent/Poised TSS	Fetal Brain Female	brain
14	chr2:115920000-115921200	Bivalent/Poised TSS	Fetal Kidney	kidney
15	chr2:115920200-115921000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:115920200-115921000	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
17	chr2:115920200-115921200	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
18	chr2:115920200-115921600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:115920400-115921800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:115920600-115921000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:115920600-115921200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr2:115920600-115921600	Active TSS	Brain Angular Gyrus	brain
23	chr2:115920600-115921600	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr2:115920600-115921600	Bivalent/Poised TSS	Fetal Brain Male	brain
25	chr2:115920800-115921000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:115920800-115921000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
27	chr2:115920800-115921000	Active TSS	Rectal Smooth Muscle	rectum
28	chr2:115920800-115921200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr2:115920800-115921200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
30	chr2:115920800-115921200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr2:115920800-115921200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
32	chr2:115920800-115921200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
33	chr2:115920800-115921200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
34	chr2:115920800-115921400	Active TSS	Brain Hippocampus Middle	brain
35	chr2:115920800-115921400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr2:115920800-115921400	Bivalent Enhancer	Fetal Stomach	stomach
37	chr2:115921000-115921200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
38	chr2:115921000-115921200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:115921000-115921400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
40	chr2:115921000-115921400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
41	chr2:115921000-115921600	Bivalent Enhancer	Fetal Intestine Large	intestine
42	chr2:115921200-115921400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr2:115921200-115921400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:115921200-115921400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr2:115921200-115921400	Bivalent Enhancer	Brain Germinal Matrix	brain
46	chr2:115921200-115921600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
47	chr2:115921200-115921600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:115921200-115921600	Active TSS	Fetal Brain Female	brain
49	chr2:115921400-115921800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
50	chr2:115921400-115922400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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