Variant report

Variant	nsv1007718
Chromosome Location	chr2:99542281-99729107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1146)
CpG islands
(count:916)
Chromatin interactive
region (count:46)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99682514-99682773	K562	blood:	n/a	n/a
2	ARID3A	chr2:99682462-99683411	HepG2	liver:	n/a	n/a
3	ATF1	chr2:99704644-99704755	K562	blood:	n/a	n/a
4	ATF1	chr2:99564634-99564637	K562	blood:	n/a	n/a
5	ATF1	chr2:99683108-99683403	K562	blood:	n/a	n/a
6	BACH1	chr2:99723482-99723804	K562	blood:	n/a	n/a
7	BACH1	chr2:99553086-99554164	H1-hESC	embryonic stem cell:	n/a	chr2:99554105-99554119
8	BHLHE40	chr2:99704525-99704982	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:99553623-99553785	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr2:99682781-99683058	GM12878	blood:	n/a	n/a
11	CBX3	chr2:99682494-99682955	HCT-116	colon:	n/a	n/a
12	CEBPB	chr2:99718218-99718544	Hela-S3	cervix:	n/a	chr2:99718391-99718402
13	CEBPB	chr2:99569490-99569773	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:99718222-99718527	HepG2	liver:	n/a	chr2:99718391-99718402
15	CEBPB	chr2:99684154-99684307	HepG2	liver:	n/a	chr2:99684260-99684271
16	CEBPB	chr2:99718224-99718502	A549	lung:	n/a	chr2:99718391-99718402
17	CEBPB	chr2:99639240-99639388	K562	blood:	n/a	chr2:99639344-99639355
18	CEBPB	chr2:99629824-99629911	K562	blood:	n/a	n/a
19	CEBPB	chr2:99718243-99718466	HepG2	liver:	n/a	chr2:99718391-99718402
20	CEBPB	chr2:99718199-99718513	H1-hESC	embryonic stem cell:	n/a	chr2:99718391-99718402
21	CEBPB	chr2:99718198-99718536	K562	blood:	n/a	chr2:99718391-99718402
22	CEBPB	chr2:99718206-99718582	HepG2	liver:	n/a	chr2:99718391-99718402
23	CEBPB	chr2:99688468-99688576	HepG2	liver:	n/a	chr2:99688563-99688574
24	CEBPB	chr2:99612083-99612214	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:99683620-99683944	HepG2	liver:	n/a	chr2:99683790-99683801 chr2:99683789-99683802 chr2:99683789-99683802 chr2:99683789-99683802
26	CEBPB	chr2:99718201-99718576	K562	blood:	n/a	chr2:99718391-99718402
27	CEBPB	chr2:99639246-99639463	HepG2	liver:	n/a	chr2:99639344-99639355
28	CEBPB	chr2:99718227-99718522	IMR90	lung:	n/a	chr2:99718391-99718402
29	CEBPD	chr2:99720462-99720897	K562	blood:	n/a	n/a
30	CEBPD	chr2:99720459-99720920	K562	blood:	n/a	n/a
31	CHD1	chr2:99657346-99657507	GM12878	blood:	n/a	n/a
32	CHD1	chr2:99553780-99553835	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr2:99700769-99700991	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:99553204-99553214	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:99701900-99702139	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:99549540-99549690	HepG2	liver:	n/a	n/a
37	CTCF	chr2:99701940-99702090	BJ	skin:	n/a	n/a
38	CTCF	chr2:99682560-99682710	AoAF	blood vessel:	n/a	chr2:99682652-99682670 chr2:99682647-99682668 chr2:99682653-99682669
39	CTCF	chr2:99701940-99702090	HVMF	connective:	n/a	n/a
40	CTCF	chr2:99552880-99553030	RPTEC	kidney:	n/a	n/a
41	CTCF	chr2:99682460-99683497	GM12878	blood:	n/a	chr2:99682652-99682670 chr2:99682647-99682668 chr2:99682653-99682669
42	CTCF	chr2:99718100-99718250	AG04450	lung:	n/a	n/a
43	CTCF	chr2:99682580-99682730	GM12869	blood:	n/a	chr2:99682652-99682670 chr2:99682647-99682668 chr2:99682653-99682669
44	CTCF	chr2:99718300-99718450	RPTEC	kidney:	n/a	n/a
45	CTCF	chr2:99701910-99702131	GM19240	blood:	n/a	n/a
46	CTCF	chr2:99683220-99683370	HMEC	breast:	n/a	n/a
47	CTCF	chr2:99701900-99702050	GM12878	blood:	n/a	n/a
48	CTCF	chr2:99683220-99683370	SAEC	small airway:	n/a	n/a
49	CTCF	chr2:99683260-99683410	GM12873	blood:	n/a	n/a
50	CTCF	chr2:99701976-99702104	Pancreas_OC	pancreas:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99553406-99553456	Hepatocyte	liver:	n/a
2	chr2:99553406-99553456	Hepatocyte	liver:	n/a
3	chr2:99552737-99552787	NT2-D1	testis:	n/a
4	chr2:99549050-99549100	T-47D	breast:	n/a
5	chr2:99549050-99549100	HCT-116	colon:	n/a
6	chr2:99553141-99553191	NB4	blood:	n/a
7	chr2:99553055-99553105	NH-A	brain:	n/a
8	chr2:99553830-99553880	LNCaP	prostate:	n/a
9	chr2:99553406-99553456	PrEC	prostate:	n/a
10	chr2:99552109-99552159	GM12892	blood:	n/a
11	chr2:99553642-99553692	CMK	blood:	n/a
12	chr2:99553055-99553105	IMR90	lung:	fetal
13	chr2:99552737-99552787	HEK293	kidney:	embryo
14	chr2:99553078-99553128	HL-60	blood:	n/a
15	chr2:99553442-99553492	NHDF-neo	bronchial:	n/a
16	chr2:99553141-99553191	HRE	kidney:	n/a
17	chr2:99613938-99613988	NHBE	bronchial:	n/a
18	chr2:99552633-99552683	HAEpiC	amniotic membrane:	n/a
19	chr2:99552737-99552787	ovcar-3	ovarian:	n/a
20	chr2:99552261-99552311	K562	blood:	n/a
21	chr2:99613938-99613988	HEEpiC	esophagus:	n/a
22	chr2:99552261-99552311	AoSMC	blood vessel:	n/a
23	chr2:99553442-99553492	CMK	blood:	n/a
24	chr2:99552737-99552787	HNPCEpiC	eye:	n/a
25	chr2:99554416-99554466	LNCaP	prostate:	n/a
26	chr2:99613938-99613988	Hela-S3	cervix:	n/a
27	chr2:99553642-99553692	HepG2	liver:	n/a
28	chr2:99553141-99553191	NT2-D1	testis:	n/a
29	chr2:99553406-99553456	NHBE	bronchial:	n/a
30	chr2:99553830-99553880	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:99553830-99553880	AG04450	lung:	fetal
32	chr2:99553406-99553456	HUVEC	blood vessel:	n/a
33	chr2:99553830-99553880	GM12892	blood:	n/a
34	chr2:99553442-99553492	U87	brain:	n/a
35	chr2:99553442-99553492	GM06990	blood:	n/a
36	chr2:99553442-99553492	HCPEpiC	choroid plexus:	n/a
37	chr2:99552737-99552787	HIPEpiC	eye:	n/a
38	chr2:99553141-99553191	SKMC	muscle:	n/a
39	chr2:99613938-99613988	MCF10A-Er-Src	breast:	n/a
40	chr2:99613938-99613988	ECC-1	luminal epithelium:	n/a
41	chr2:99552827-99552877	HepG2	liver:	n/a
42	chr2:99553642-99553692	SK-N-SH_RA	brain:	n/a
43	chr2:99552633-99552683	HMEC	breast:	n/a
44	chr2:99552827-99552877	U87	brain:	n/a
45	chr2:99553442-99553492	HCT-116	colon:	n/a
46	chr2:99553642-99553692	A549	lung:	n/a
47	chr2:99553055-99553105	K562	blood:	n/a
48	chr2:99552737-99552787	HepG2	liver:	n/a
49	chr2:99552261-99552311	CMK	blood:	n/a
50	chr2:99553078-99553128	PANC-1	pancreas:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:99718937..99720867-chr2:99770483..99773115,2	K562	blood:
2	chr2:99343906..99346771-chr2:99682642..99684272,2	MCF-7	breast:
3	chr2:99720605..99722311-chr2:99723972..99725744,2	K562	blood:
4	chr2:99683250..99685988-chr2:99756129..99759687,3	MCF-7	breast:
5	chr2:99721431..99723129-chr2:99723599..99725832,2	MCF-7	breast:
6	chr2:99678573..99681466-chr2:99681524..99683363,2	MCF-7	breast:
7	chr2:99265627..99266606-chr2:99681933..99683499,6	MCF-7	breast:
8	chr2:99651571..99653300-chr2:99794305..99796617,2	K562	blood:
9	chr2:99223859..99226826-chr2:99680320..99683264,2	MCF-7	breast:
10	chr2:99724735..99727280-chr2:99755994..99759484,3	MCF-7	breast:
11	chr2:99567888..99569888-chr2:99587161..99588849,2	MCF-7	breast:
12	chr2:99224528..99226809-chr2:99681520..99684338,2	MCF-7	breast:
13	chr2:99552279..99554160-chr2:99555590..99558457,2	MCF-7	breast:
14	chr2:99185380..99185885-chr2:99682836..99683668,2	MCF-7	breast:
15	chr2:99701627..99702172-chr2:99814711..99815368,2	MCF-7	breast:
16	chr2:99682196..99683733-chr2:99690104..99693098,2	K562	blood:
17	chr2:99678684..99681017-chr2:99686725..99688659,2	MCF-7	breast:
18	chr2:99265511..99266529-chr2:99682139..99682979,3	K562	blood:
19	chr2:99681346..99684760-chr2:99690104..99692439,3	K562	blood:
20	chr2:99347012..99347636-chr2:99682209..99682753,2	MCF-7	breast:
21	chr2:99681346..99684760-chr2:99690104..99692439,3	K562	blood:
22	chr2:99525536..99528520-chr2:99541090..99543085,2	MCF-7	breast:
23	chr2:99721431..99723129-chr2:99723599..99725832,2	MCF-7	breast:
24	chr2:99452886..99453651-chr2:99682645..99683214,2	MCF-7	breast:
25	chr2:99682196..99683733-chr2:99690104..99693098,2	K562	blood:
26	chr2:99689213..99690975-chr2:99692608..99694533,2	MCF-7	breast:
27	chr2:99633286..99635570-chr2:99636929..99639924,2	K562	blood:
28	chr2:99630915..99633529-chr2:99638709..99640411,2	MCF-7	breast:
29	chr2:99694874..99697753-chr2:99797016..99799140,2	MCF-7	breast:
30	chr2:99689213..99690975-chr2:99692608..99694533,2	MCF-7	breast:
31	chr2:99678573..99681466-chr2:99681524..99683363,2	MCF-7	breast:
32	chr2:99720605..99722311-chr2:99723972..99725744,2	K562	blood:
33	chr2:99523789..99526225-chr2:99550557..99552954,3	MCF-7	breast:
34	chr2:99265613..99266542-chr2:99682479..99683707,4	MCF-7	breast:
35	chr2:99567888..99569888-chr2:99587161..99588849,2	MCF-7	breast:
36	chr2:99633286..99635570-chr2:99636929..99639924,2	K562	blood:
37	chr2:99630915..99633529-chr2:99638709..99640411,2	MCF-7	breast:
38	chr2:99695561..99698102-chr2:99771046..99772619,2	MCF-7	breast:
39	chr2:99552080..99554137-chr2:99681642..99683151,2	MCF-7	breast:
40	chr2:99703138..99704885-chr2:99770602..99772136,2	MCF-7	breast:
41	chr2:99701798..99702298-chr2:100170503..100171309,2	K562	blood:
42	chr2:99532387..99535858-chr2:99543640..99546629,3	MCF-7	breast:
43	chr2:99551050..99554031-chr2:99555882..99558658,3	MCF-7	breast:
44	chr2:99678684..99681017-chr2:99686725..99688659,2	MCF-7	breast:
45	chr2:99728152..99730874-chr2:99731119..99733166,2	MCF-7	breast:
46	chr2:99345574..99348199-chr2:99652477..99654603,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MITD1-2	chr2:99727313-99727378	NONHSAT072730
2	lnc-MITD1-2	chr2:99725977-99726019	NONHSAT072730

No data

Variant related genes	Relation type
ENSG00000231822	TF binding region
KIAA1211L	TF binding region
TSGA10	TF binding region
ENSG00000231822	CpG island
KIAA1211L	CpG island
TSGA10	CpG island
ENSG00000241962	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000273155	chromatin interactions
ENSG00000196872	chromatin interactions
ENSG00000071073	chromatin interactions
ENSG00000273045	chromatin interactions
ENSG00000115446	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000144182	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000183513	chromatin interactions

Extended variants
information (count: 3773 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3773 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554332423	chr2:99542300-99542301	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192503375	chr2:99542338-99542339	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577830510	chr2:99542365-99542366	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563320284	chr2:99542369-99542370	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545941555	chr2:99542387-99542388	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562921935	chr2:99542389-99542390	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576310023	chr2:99542401-99542402	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147405066	chr2:99542412-99542413	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201783596	chr2:99542467-99542468	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199871335	chr2:99542470-99542471	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560839394	chr2:99542521-99542522	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529867135	chr2:99542529-99542530	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372425017	chr2:99542572-99542573	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559882273	chr2:99542586-99542587	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532257863	chr2:99542596-99542597	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551940437	chr2:99542629-99542630	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568846628	chr2:99542651-99542652	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377002119	chr2:99542689-99542690	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557268291	chr2:99542709-99542710	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548949794	chr2:99542735-99542736	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139970955	chr2:99542788-99542789	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184638034	chr2:99542794-99542795	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78950011	chr2:99542796-99542797	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149912238	chr2:99542812-99542813	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570927444	chr2:99542815-99542816	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367987616	chr2:99542844-99542845	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114480515	chr2:99542899-99542900	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116530122	chr2:99542916-99542917	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78666624	chr2:99542942-99542943	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75813557	chr2:99542966-99542967	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574408411	chr2:99542982-99542983	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190174358	chr2:99543050-99543051	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181331098	chr2:99543071-99543072	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1607255	chr2:99543105-99543106	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs117592945	chr2:99543109-99543110	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562442905	chr2:99543201-99543202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74329987	chr2:99543207-99543208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12467504	chr2:99543208-99543209	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565587655	chr2:99543227-99543228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145489544	chr2:99543245-99543246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112946243	chr2:99543288-99543289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533626214	chr2:99543289-99543290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528012128	chr2:99543316-99543317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548062578	chr2:99543317-99543318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545368961	chr2:99543384-99543385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539635644	chr2:99543410-99543411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556664505	chr2:99543418-99543419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563672984	chr2:99543423-99543424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557746678	chr2:99543428-99543429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569985098	chr2:99543432-99543433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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	17483303	CNVD
Medulloblastoma	20607354	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
Ovarian cancer	21781307	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	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	chr2:99532400-99542800	Weak transcription	Pancreas	Pancrea
2	chr2:99538000-99550800	Weak transcription	Gastric	stomach
3	chr2:99538400-99542600	Weak transcription	NHEK	skin
4	chr2:99538400-99551400	Weak transcription	Esophagus	oesophagus
5	chr2:99540600-99542800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:99541600-99542800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:99542000-99543200	Active TSS	Brain Anterior Caudate	brain
8	chr2:99542000-99543200	Enhancers	HSMM	muscle
9	chr2:99542200-99543200	Enhancers	HSMMtube	muscle
10	chr2:99542600-99543000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr2:99542600-99543400	Enhancers	NHEK	skin
12	chr2:99542600-99543800	Enhancers	HMEC	breast
13	chr2:99542800-99543200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:99542800-99543400	Enhancers	Brain Germinal Matrix	brain
15	chr2:99542800-99543600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr2:99542800-99543600	Enhancers	A549	lung
17	chr2:99542800-99543600	Enhancers	NH-A	brain
18	chr2:99542800-99543600	Enhancers	Osteobl	bone
19	chr2:99542800-99543800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:99542800-99543800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:99542800-99543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:99542800-99543800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:99542800-99543800	Enhancers	Pancreas	Pancrea
24	chr2:99542800-99544000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:99542800-99545000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:99543000-99543400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:99543000-99544200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:99543000-99548200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:99543600-99543800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr2:99543600-99545400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr2:99543600-99545400	Weak transcription	A549	lung
32	chr2:99543800-99545600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:99543800-99551200	Weak transcription	HMEC	breast
34	chr2:99543800-99551400	Weak transcription	Pancreas	Pancrea
35	chr2:99544000-99544200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:99544000-99549600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:99544800-99545000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr2:99544800-99545200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:99545000-99548800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:99545400-99545600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr2:99545400-99545600	Enhancers	A549	lung
42	chr2:99545600-99545800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:99545800-99548400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:99548200-99548600	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr2:99548600-99548800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:99548600-99551200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr2:99548800-99549000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:99548800-99550200	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr2:99549000-99549200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr2:99549000-99549200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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