Variant report

Variant	nsv873903
Chromosome Location	chr2:40285145-40382712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:305)
Chromatin interactive
region (count:13)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:40351612-40351729	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr2:40323608-40323787	HepG2	liver:	n/a	n/a
3	CCNT2	chr2:40376631-40376865	K562	blood:	n/a	n/a
4	CEBPB	chr2:40324645-40325431	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:40351906-40352261	HepG2	liver:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
6	CEBPB	chr2:40299334-40299453	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:40381145-40381361	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:40319735-40319825	A549	lung:	n/a	n/a
9	CEBPB	chr2:40326107-40326546	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:40319866-40319890	HepG2	liver:	n/a	chr2:40319879-40319890
11	CEBPB	chr2:40324858-40325242	A549	lung:	n/a	n/a
12	CEBPB	chr2:40324822-40325151	A549	lung:	n/a	n/a
13	CEBPB	chr2:40339141-40339430	HepG2	liver:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
14	CEBPB	chr2:40324907-40325147	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:40355036-40355623	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:40288200-40288530	HepG2	liver:	n/a	chr2:40288341-40288352
17	CEBPB	chr2:40324745-40325354	A549	lung:	n/a	n/a
18	CEBPB	chr2:40288194-40288467	IMR90	lung:	n/a	chr2:40288341-40288352
19	CEBPB	chr2:40330231-40331193	IMR90	lung:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
20	CEBPB	chr2:40339108-40339410	IMR90	lung:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
21	CEBPB	chr2:40329747-40329985	H1-hESC	embryonic stem cell:	n/a	chr2:40329843-40329856
22	CEBPB	chr2:40381128-40381404	A549	lung:	n/a	n/a
23	CEBPB	chr2:40330290-40330603	H1-hESC	embryonic stem cell:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
24	CEBPB	chr2:40351972-40352202	A549	lung:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
25	CEBPB	chr2:40332438-40332720	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:40330267-40330599	Hela-S3	cervix:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
27	CEBPB	chr2:40351880-40352226	MCF-7	breast:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
28	CEBPB	chr2:40330299-40330611	HepG2	liver:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
29	CEBPB	chr2:40339221-40339389	Hela-S3	cervix:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
30	CEBPB	chr2:40286576-40286696	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:40339184-40339384	A549	lung:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
32	CEBPB	chr2:40351937-40352262	MCF-7	breast:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
33	CEBPB	chr2:40330341-40330569	A549	lung:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
34	CEBPB	chr2:40336603-40336904	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr2:40315227-40315355	A549	lung:	n/a	n/a
36	CTCF	chr2:40294115-40294149	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr2:40299429-40299468	GM10266	blood:	n/a	n/a
38	CTCF	chr2:40366640-40366790	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr2:40329960-40330110	AG10803	skin:	n/a	n/a
40	CTCF	chr2:40315262-40315355	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:40315238-40315355	GM12891	blood:	n/a	n/a
42	CTCF	chr2:40315257-40315349	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:40315215-40315355	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:40315250-40315351	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:40310880-40311030	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:40365440-40365590	A549	lung:	n/a	n/a
47	CTCF	chr2:40315270-40315342	NHEK	skin:	n/a	n/a
48	CTCF	chr2:40299460-40299610	A549	lung:	n/a	n/a
49	CTCF	chr2:40315237-40315351	Gliobla	brain:	n/a	n/a
50	CTCF	chr2:40315266-40315310	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40370829-40370879	T-47D	breast:	n/a
2	chr2:40377776-40377826	GM12878	blood:	n/a
3	chr2:40351367-40351417	NHDF-neo	bronchial:	n/a
4	chr2:40370829-40370879	CMK	blood:	n/a
5	chr2:40356782-40356832	GM19239	blood:	n/a
6	chr2:40356782-40356832	GM12892	blood:	n/a
7	chr2:40370829-40370879	HEEpiC	esophagus:	n/a
8	chr2:40370829-40370879	HCF	heart:	n/a
9	chr2:40377776-40377826	Hela-S3	cervix:	n/a
10	chr2:40342248-40342298	HIPEpiC	eye:	n/a
11	chr2:40370829-40370879	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:40377776-40377826	PrEC	prostate:	n/a
13	chr2:40356782-40356832	AG09309	skin:	n/a
14	chr2:40356782-40356832	HRE	kidney:	n/a
15	chr2:40377776-40377826	SKMC	muscle:	n/a
16	chr2:40370829-40370879	HIPEpiC	eye:	n/a
17	chr2:40351367-40351417	SAEC	small airway:	n/a
18	chr2:40351367-40351417	T-47D	breast:	n/a
19	chr2:40342248-40342298	Caco-2	colon:	n/a
20	chr2:40370829-40370879	PFSK-1	brain:	n/a
21	chr2:40370829-40370879	MCF-7	breast:	n/a
22	chr2:40377776-40377826	HPAEpiC	pulmonary alveolar:	n/a
23	chr2:40356782-40356832	HRCEpiC	kidney:	n/a
24	chr2:40351367-40351417	AG04450	lung:	fetal
25	chr2:40377776-40377826	MCF-7	breast:	n/a
26	chr2:40342248-40342298	GM19239	blood:	n/a
27	chr2:40351367-40351417	AG10803	skin:	n/a
28	chr2:40377776-40377826	HCM	heart:	n/a
29	chr2:40370829-40370879	SKMC	muscle:	n/a
30	chr2:40377776-40377826	SK-N-MC	brain:	n/a
31	chr2:40351367-40351417	HCM	heart:	n/a
32	chr2:40370829-40370879	PANC-1	pancreas:	n/a
33	chr2:40342248-40342298	H1-hESC	embryonic stem cell:	embryo
34	chr2:40356782-40356832	GM12891	blood:	n/a
35	chr2:40342248-40342298	SK-N-SH	brain:	n/a
36	chr2:40356782-40356832	Jurkat	blood:	n/a
37	chr2:40356782-40356832	GM12878	blood:	n/a
38	chr2:40351367-40351417	AG09319	gingival:	n/a
39	chr2:40377776-40377826	PANC-1	pancreas:	n/a
40	chr2:40356782-40356832	HepG2	liver:	n/a
41	chr2:40342248-40342298	AG04449	skin:	fetal
42	chr2:40377776-40377826	AG04449	skin:	fetal
43	chr2:40351367-40351417	HNPCEpiC	eye:	n/a
44	chr2:40377776-40377826	AG09309	skin:	n/a
45	chr2:40356782-40356832	HIPEpiC	eye:	n/a
46	chr2:40356782-40356832	HEEpiC	esophagus:	n/a
47	chr2:40342248-40342298	NH-A	brain:	n/a
48	chr2:40370829-40370879	K562	blood:	n/a
49	chr2:40377776-40377826	NHBE	bronchial:	n/a
50	chr2:40370829-40370879	HAEpiC	amniotic membrane:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:40334175..40336560-chr2:40339727..40341466,2	MCF-7	breast:
2	chr2:40358744..40360269-chr2:40362071..40363765,2	K562	blood:
3	chr2:40319121..40321528-chr2:40332638..40334554,2	K562	blood:
4	chr2:40340588..40343446-chr2:40344341..40345880,2	K562	blood:
5	chr2:40358658..40360428-chr2:40361170..40364164,2	MCF-7	breast:
6	chr2:40365962..40367921-chr2:40369317..40371065,2	MCF-7	breast:
7	chr2:40358658..40360428-chr2:40361170..40364164,2	MCF-7	breast:
8	chr2:40319121..40321528-chr2:40332638..40334554,2	K562	blood:
9	chr2:40317100..40319815-chr2:40339611..40341990,2	MCF-7	breast:
10	chr2:40322332..40325510-chr2:40329886..40332730,3	MCF-7	breast:
11	chr2:40365962..40367921-chr2:40369317..40371065,2	MCF-7	breast:
12	chr2:40334175..40336560-chr2:40339727..40341466,2	MCF-7	breast:
13	chr2:40358744..40360269-chr2:40362071..40363765,2	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
2	lnc-TMEM178-2	chr2:40342169-40342293	ENSG00000227028.1
3	lnc-TMEM178-2	chr2:40345452-40345645	ENSG00000227028.2
4	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
5	lnc-TMEM178-2	chr2:40350286-40350414	ENSG00000227028.2
6	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
7	lnc-TMEM178-2	chr2:40341678-40342293	ENSG00000227028.2
8	lnc-TMEM178-2	chr2:40350286-40350414	ENSG00000227028.2
9	lnc-TMEM178-2	chr2:40332328-40332418	ucscGeneNc_uc002rrw_2
10	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.1
11	lnc-TMEM178-2	chr2:40328301-40328397	ENSG00000227028.2
12	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
13	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
14	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
15	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
16	lnc-TMEM178-2	chr2:40299893-40300140	ENSG00000227028.2
17	lnc-TMEM178-2	chr2:40332049-40332102	NONHSAT070261
18	lnc-TMEM178-2	chr2:40345529-40345645	ENSG00000227028.2
19	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
20	lnc-TMEM178-2	chr2:40292493-40292612	ENSG00000227028.2
21	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
22	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
23	lnc-TMEM178-2	chr2:40332049-40332102	NONHSAT070263
24	lnc-TMEM178-2	chr2:40332301-40332562	ENSG00000227028.1
25	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
26	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
27	lnc-TMEM178-2	chr2:40292487-40292995	ENSG00000227028.2
28	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
29	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
30	lnc-TMEM178-2	chr2:40335064-40335843	ucscGeneNc_uc002rrw_2
31	lnc-TMEM178-2	chr2:40342075-40342293	ENSG00000227028.2
32	lnc-SLC8A1-1	chr2:40324916-40328505	NONHSAT070272
33	lnc-TMEM178-2	chr2:40347844-40347940	ENSG00000227028.2
34	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.1
35	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
36	lnc-TMEM178-2	chr2:40332049-40332461	ENSG00000227028.1

No data

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
SLC8A1-AS1	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 4224 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4224 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13028070	chr2:40285145-40285146	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77464447	chr2:40285163-40285164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189017816	chr2:40285164-40285165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149930030	chr2:40285198-40285199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs985058	chr2:40285224-40285225	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549484688	chr2:40285227-40285228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs985057	chr2:40285231-40285232	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs985056	chr2:40285239-40285240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs546436218	chr2:40285241-40285242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77539289	chr2:40285270-40285271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538982387	chr2:40285271-40285272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557283982	chr2:40285272-40285273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575346248	chr2:40285275-40285276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536236005	chr2:40285290-40285291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142205514	chr2:40285295-40285296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs58712614	chr2:40285325-40285326	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs117409714	chr2:40285334-40285335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559741260	chr2:40285338-40285339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146761137	chr2:40285342-40285343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140213641	chr2:40285349-40285350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144055275	chr2:40285391-40285392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561510140	chr2:40285398-40285399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182081108	chr2:40285399-40285400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78998886	chr2:40285402-40285403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187128404	chr2:40285411-40285412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145249142	chr2:40285420-40285421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146453700	chr2:40285459-40285460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547070208	chr2:40285473-40285474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571508466	chr2:40285476-40285477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532331420	chr2:40285498-40285499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192464990	chr2:40285517-40285518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562430374	chr2:40285526-40285527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569147659	chr2:40285528-40285529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113424162	chr2:40285581-40285582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536263039	chr2:40285603-40285604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79784865	chr2:40285606-40285607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373165853	chr2:40285608-40285609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182560455	chr2:40285627-40285628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533689638	chr2:40285642-40285643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558602604	chr2:40285652-40285653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577842111	chr2:40285666-40285667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545169003	chr2:40285671-40285672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550804682	chr2:40285676-40285677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186096581	chr2:40285689-40285690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150451131	chr2:40285692-40285693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543009945	chr2:40285711-40285712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560153701	chr2:40285719-40285720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138286296	chr2:40285720-40285721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190111906	chr2:40285738-40285739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540406608	chr2:40285757-40285758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40269400-40299200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:40276000-40287400	Weak transcription	HSMM	muscle
3	chr2:40284800-40285600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:40285600-40290600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:40287400-40288000	ZNF genes & repeats	Dnd41	blood
6	chr2:40287400-40288000	ZNF genes & repeats	HSMM	muscle
7	chr2:40289600-40290000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:40289800-40290000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:40289800-40290000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:40289800-40290200	Enhancers	Osteobl	bone
11	chr2:40289800-40290400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:40289800-40291200	Enhancers	HSMMtube	muscle
13	chr2:40290000-40292000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:40290400-40291800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:40291800-40292600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:40292000-40292400	Enhancers	Right Ventricle	heart
17	chr2:40292000-40293400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:40299600-40299800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:40303400-40304200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:40304200-40308600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr2:40308600-40308800	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr2:40313000-40313200	Enhancers	Left Ventricle	heart
23	chr2:40313000-40314600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:40313000-40315200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:40313200-40314200	Weak transcription	Left Ventricle	heart
26	chr2:40313400-40313800	Enhancers	NHDF-Ad	bronchial
27	chr2:40313600-40314600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:40313600-40315200	Enhancers	Osteobl	bone
29	chr2:40313800-40314800	Weak transcription	NHDF-Ad	bronchial
30	chr2:40314200-40315200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:40314200-40315200	Enhancers	Right Ventricle	heart
32	chr2:40314200-40315400	Enhancers	Left Ventricle	heart
33	chr2:40314400-40315000	Enhancers	Right Atrium	heart
34	chr2:40314600-40315000	Enhancers	Esophagus	oesophagus
35	chr2:40314600-40315200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:40314600-40320000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:40314800-40315200	Enhancers	NHDF-Ad	bronchial
38	chr2:40314800-40316400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:40315200-40317200	Weak transcription	Osteobl	bone
40	chr2:40315200-40320000	Weak transcription	NHDF-Ad	bronchial
41	chr2:40315200-40320400	Weak transcription	Right Ventricle	heart
42	chr2:40315200-40321800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:40316400-40319800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:40317200-40317600	Enhancers	Osteobl	bone
45	chr2:40317600-40321800	Weak transcription	Osteobl	bone
46	chr2:40319000-40319800	Enhancers	Dnd41	blood
47	chr2:40319800-40320200	Weak transcription	Dnd41	blood
48	chr2:40319800-40320400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:40319800-40321200	Enhancers	Fetal Brain Male	brain
50	chr2:40320000-40320600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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