Variant report

Variant	nsv998291
Chromosome Location	chr2:231045388-231136278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:795)
Chromatin interactive
region (count:18)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:231084718-231085165	HepG2	liver:	n/a	n/a
2	ATF2	chr2:231070497-231070910	GM12878	blood:	n/a	n/a
3	ATF2	chr2:231122252-231122989	GM12878	blood:	n/a	n/a
4	ATF2	chr2:231121311-231123028	GM12878	blood:	n/a	n/a
5	ATF2	chr2:231099504-231099982	GM12878	blood:	n/a	n/a
6	ATF2	chr2:231121362-231121801	GM12878	blood:	n/a	n/a
7	ATF2	chr2:231084379-231085017	GM12878	blood:	n/a	n/a
8	ATF2	chr2:231099433-231099930	GM12878	blood:	n/a	n/a
9	ATF2	chr2:231090046-231091424	GM12878	blood:	n/a	n/a
10	ATF2	chr2:231067173-231068423	GM12878	blood:	n/a	n/a
11	ATF2	chr2:231090116-231091431	GM12878	blood:	n/a	n/a
12	ATF2	chr2:231087421-231087858	GM12878	blood:	n/a	n/a
13	ATF2	chr2:231067016-231068411	GM12878	blood:	n/a	n/a
14	ATF2	chr2:231091899-231092520	GM12878	blood:	n/a	n/a
15	ATF2	chr2:231131877-231132849	GM12878	blood:	n/a	n/a
16	ATF2	chr2:231132004-231132826	GM12878	blood:	n/a	n/a
17	BACH1	chr2:231094755-231095153	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:231129851-231130015	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr2:231122455-231122835	GM12878	blood:	n/a	n/a
20	BATF	chr2:231132171-231132837	GM12878	blood:	n/a	n/a
21	BATF	chr2:231133535-231133931	GM12878	blood:	n/a	n/a
22	BATF	chr2:231099544-231100002	GM12878	blood:	n/a	chr2:231099806-231099817 chr2:231099807-231099817
23	BATF	chr2:231067192-231067825	GM12878	blood:	n/a	n/a
24	BATF	chr2:231090934-231091313	GM12878	blood:	n/a	n/a
25	BATF	chr2:231132134-231132772	GM12878	blood:	n/a	n/a
26	BATF	chr2:231134418-231134737	GM12878	blood:	n/a	n/a
27	BATF	chr2:231081292-231081652	GM12878	blood:	n/a	n/a
28	BATF	chr2:231098813-231099141	GM12878	blood:	n/a	n/a
29	BATF	chr2:231122423-231122829	GM12878	blood:	n/a	n/a
30	BATF	chr2:231070477-231070805	GM12878	blood:	n/a	n/a
31	BATF	chr2:231070416-231070879	GM12878	blood:	n/a	n/a
32	BATF	chr2:231067082-231068317	GM12878	blood:	n/a	n/a
33	BATF	chr2:231099538-231099979	GM12878	blood:	n/a	chr2:231099806-231099817 chr2:231099807-231099817
34	BATF	chr2:231090235-231090669	GM12878	blood:	n/a	n/a
35	BATF	chr2:231121471-231121833	GM12878	blood:	n/a	n/a
36	BATF	chr2:231090246-231090656	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:231132100-231132730	GM12878	blood:	n/a	chr2:231132711-231132718 chr2:231132487-231132496
38	BCL11A	chr2:231122380-231122948	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:231081280-231081473	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:231067150-231067836	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:231067914-231068366	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:231099606-231099961	GM12878	blood:	n/a	chr2:231099806-231099815
43	BCL11A	chr2:231121407-231121811	GM12878	blood:	n/a	chr2:231121790-231121799
44	BCL11A	chr2:231090889-231091382	GM12878	blood:	n/a	chr2:231091129-231091138
45	BCL11A	chr2:231074124-231074470	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:231099497-231099996	GM12878	blood:	n/a	chr2:231099806-231099815
47	BCL11A	chr2:231132243-231132576	GM12878	blood:	n/a	chr2:231132487-231132496
48	BCL11A	chr2:231074148-231074456	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:231122492-231122920	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:231090994-231091309	GM12878	blood:	n/a	chr2:231091129-231091138

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231090640-231090690	HIPEpiC	eye:	n/a
2	chr2:231085667-231085717	HL-60	blood:	n/a
3	chr2:231090640-231090690	HIPEpiC	eye:	n/a
4	chr2:231085667-231085717	HL-60	blood:	n/a
5	chr2:231089641-231089691	AG04450	lung:	fetal
6	chr2:231084523-231084573	PFSK-1	brain:	n/a
7	chr2:231085725-231085775	GM06990	blood:	n/a
8	chr2:231084523-231084573	K562	blood:	n/a
9	chr2:231090531-231090581	HCF	heart:	n/a
10	chr2:231090745-231090795	LNCaP	prostate:	n/a
11	chr2:231086230-231086280	BE2_C	brain:	n/a
12	chr2:231084523-231084573	LNCaP	prostate:	n/a
13	chr2:231086230-231086280	HIPEpiC	eye:	n/a
14	chr2:231090745-231090795	MCF10A-Er-Src	breast:	n/a
15	chr2:231090376-231090426	Caco-2	colon:	n/a
16	chr2:231085667-231085717	MCF-7	breast:	n/a
17	chr2:231089641-231089691	BJ	skin:	n/a
18	chr2:231085667-231085717	K562	blood:	n/a
19	chr2:231084965-231085015	SK-N-MC	brain:	n/a
20	chr2:231085735-231085785	HCM	heart:	n/a
21	chr2:231090329-231090379	K562	blood:	n/a
22	chr2:231090376-231090426	SKMC	muscle:	n/a
23	chr2:231090329-231090379	Caco-2	colon:	n/a
24	chr2:231084965-231085015	BJ	skin:	n/a
25	chr2:231086230-231086280	HUVEC	blood vessel:	n/a
26	chr2:231084523-231084573	GM06990	blood:	n/a
27	chr2:231090329-231090379	Hepatocyte	liver:	n/a
28	chr2:231090745-231090795	SAEC	small airway:	n/a
29	chr2:231085725-231085775	GM12878	blood:	n/a
30	chr2:231090531-231090581	NHDF-neo	bronchial:	n/a
31	chr2:231090640-231090690	AG04449	skin:	fetal
32	chr2:231090329-231090379	HCT-116	colon:	n/a
33	chr2:231090376-231090426	Hela-S3	cervix:	n/a
34	chr2:231085725-231085775	HCM	heart:	n/a
35	chr2:231090329-231090379	HRCEpiC	kidney:	n/a
36	chr2:231090745-231090795	HAEpiC	amniotic membrane:	n/a
37	chr2:231085725-231085775	HNPCEpiC	eye:	n/a
38	chr2:231084523-231084573	SKMC	muscle:	n/a
39	chr2:231085667-231085717	HCT-116	colon:	n/a
40	chr2:231084523-231084573	PrEC	prostate:	n/a
41	chr2:231089641-231089691	NT2-D1	testis:	n/a
42	chr2:231090329-231090379	HL-60	blood:	n/a
43	chr2:231090640-231090690	ECC-1	luminal epithelium:	n/a
44	chr2:231084523-231084573	PANC-1	pancreas:	n/a
45	chr2:231085667-231085717	RPTEC	kidney:	n/a
46	chr2:231084965-231085015	HCF	heart:	n/a
47	chr2:231084941-231084991	AG04450	lung:	fetal
48	chr2:231084965-231085015	HL-60	blood:	n/a
49	chr2:231090376-231090426	T-47D	breast:	n/a
50	chr2:231085667-231085717	SK-N-MC	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:231072082..231074333-chr2:231080031..231082815,2	MCF-7	breast:
2	chr2:231088013..231089892-chr2:231091301..231094041,2	K562	blood:
3	chr2:231082900..231084679-chr2:231088128..231090414,2	K562	blood:
4	chr2:231112287..231114146-chr2:231116342..231119362,3	MCF-7	breast:
5	chr2:231064688..231066515-chr2:231075264..231078231,2	K562	blood:
6	chr2:231065336..231067742-chr2:231072287..231074738,2	K562	blood:
7	chr2:231112287..231114146-chr2:231116342..231119362,3	MCF-7	breast:
8	chr2:231042254..231045167-chr2:231047833..231049865,3	K562	blood:
9	chr2:231064805..231066676-chr2:231078094..231080853,2	MCF-7	breast:
10	chr2:231080762..231082857-chr2:231083207..231085642,2	K562	blood:
11	chr2:231087067..231089892-chr2:231091301..231094794,3	K562	blood:
12	chr2:231064805..231066676-chr2:231078094..231080853,2	MCF-7	breast:
13	chr2:231087067..231089892-chr2:231091301..231094794,3	K562	blood:
14	chr2:231078945..231080759-chr2:231083081..231084932,2	MCF-7	breast:
15	chr2:231088013..231089892-chr2:231091301..231094041,2	K562	blood:
16	chr2:231081815..231083756-chr2:231088866..231091364,2	MCF-7	breast:
17	chr2:231072082..231074333-chr2:231080031..231082815,2	MCF-7	breast:
18	chr2:231065336..231067742-chr2:231072287..231074738,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP140L-2	chr2:231135301-231135354	NONHSAT077274
2	lnc-SP140-1	chr2:231101799-231101975	NONHSAT077272
3	lnc-SP140-1	chr2:231078369-231078484	ENSG00000243565.1
4	lnc-SP140-1	chr2:231090476-231090618	NONHSAT077272
5	lnc-SP140-1	chr2:231067826-231067995	ENSG00000243565.1
6	lnc-SP140-1	chr2:231078674-231078874	ENSG00000243565.1
7	lnc-SP140-1	chr2:231106120-231106202	NONHSAT077272
8	lnc-SP140-1	chr2:231102929-231103096	NONHSAT077272
9	lnc-SP140-1	chr2:231109704-231109795	NONHSAT077272
10	lnc-SLC16A14-4	chr2:231076185-231076262	NONHSAT077269
11	lnc-SP140-1	chr2:231101798-231102329	NONHSAT077273
12	lnc-SLC16A14-4	chr2:231074646-231074723	NONHSAT077269
13	lnc-SP140-1	chr2:231078369-231078484	ENSG00000243565.1
14	lnc-SP140-1	chr2:231108447-231108526	NONHSAT077272
15	lnc-SP140-1	chr2:231090470-231090618	ENSG00000243565.1
16	lnc-SLC16A14-4	chr2:231065184-231065681	NONHSAT077269
17	lnc-SP140L-2	chr2:231134613-231134668	NONHSAT077274
18	lnc-SLC16A14-4	chr2:231072706-231072774	NONHSAT077269
19	lnc-SP140-1	chr2:231099653-231099681	ENSG00000243565.1
20	lnc-SP140-1	chr2:231068340-231068409	ENSG00000243565.1
21	lnc-SLC16A14-4	chr2:231067295-231067444	NONHSAT077269
22	lnc-SP140-1	chr2:231078674-231078789	ENSG00000243565.1
23	lnc-SP140-1	chr2:231090507-231090618	NONHSAT077273
24	lnc-SP140-1	chr2:231110579-231110628	NONHSAT077272

No data

Variant related genes	Relation type
SP110	TF binding region
SP140	TF binding region
SP110	CpG island
SP140	CpG island
ENSG00000135899	chromatin interactions
ENSG00000079263	chromatin interactions
GOPC	miRNA target sites
GOLT1B	miRNA target sites

Extended variants
information (count: 3515 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3515 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1427292	chr2:231045388-231045389	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144102659	chr2:231045412-231045413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550207080	chr2:231045521-231045522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191734656	chr2:231045528-231045529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572998619	chr2:231045529-231045530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554458024	chr2:231045573-231045574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572922712	chr2:231045621-231045622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541813465	chr2:231045715-231045716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10168057	chr2:231045758-231045759	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs578084276	chr2:231045784-231045785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531959848	chr2:231045790-231045791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573584503	chr2:231045801-231045802	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200497706	chr2:231045901-231045902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545521733	chr2:231045920-231045921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116156957	chr2:231045921-231045922	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575726527	chr2:231045927-231045928	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4973285	chr2:231045943-231045944	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs561655537	chr2:231045961-231045962	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs77807964	chr2:231045978-231045979	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374182916	chr2:231046002-231046003	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs559639233	chr2:231046100-231046101	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs181756812	chr2:231046103-231046104	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs532028819	chr2:231046112-231046113	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146884976	chr2:231046131-231046132	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs58203458	chr2:231046149-231046150	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529661379	chr2:231046159-231046160	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548164596	chr2:231046169-231046170	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs186532511	chr2:231046176-231046177	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs561703220	chr2:231046195-231046196	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs558672282	chr2:231046207-231046208	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs34618178	chr2:231046292-231046293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12618921	chr2:231046312-231046313	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539103581	chr2:231046321-231046322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4327229	chr2:231046328-231046329	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575689930	chr2:231046358-231046359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141625001	chr2:231046395-231046396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191393945	chr2:231046396-231046397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573524627	chr2:231046432-231046433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12615975	chr2:231046438-231046439	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs530804426	chr2:231046465-231046466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565433767	chr2:231046495-231046496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182335265	chr2:231046500-231046501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529329088	chr2:231046522-231046523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543874305	chr2:231046598-231046599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4542839	chr2:231046602-231046603	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs529625387	chr2:231046638-231046639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548216588	chr2:231046717-231046718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371794411	chr2:231046733-231046734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56301614	chr2:231046734-231046735	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535363918	chr2:231046753-231046754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
Breast cancer	22522925	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1961 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231028400-231067000	Strong transcription	Primary B cells from peripheral blood	blood
2	chr2:231028600-231051200	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:231028800-231051600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:231030800-231051000	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr2:231030800-231051000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:231031200-231049800	Weak transcription	HSMMtube	muscle
7	chr2:231031400-231051000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr2:231031400-231051000	Strong transcription	Fetal Thymus	thymus
9	chr2:231031400-231051600	Strong transcription	GM12878-XiMat	blood
10	chr2:231031400-231061200	Strong transcription	Primary B cells from cord blood	blood
11	chr2:231031600-231050800	Strong transcription	Fetal Muscle Leg	muscle
12	chr2:231031600-231052400	Weak transcription	Fetal Brain Male	brain
13	chr2:231031800-231049400	Strong transcription	Liver	Liver
14	chr2:231033800-231050800	Strong transcription	Dnd41	blood
15	chr2:231034800-231047400	Weak transcription	Small Intestine	intestine
16	chr2:231035000-231051800	Strong transcription	Primary T cells from cord blood	blood
17	chr2:231035400-231077000	Weak transcription	HepG2	liver
18	chr2:231035600-231049000	Weak transcription	Brain Angular Gyrus	brain
19	chr2:231035600-231050400	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr2:231035600-231050400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:231035600-231050800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr2:231035600-231050800	Strong transcription	Thymus	Thymus
23	chr2:231035600-231051000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr2:231035600-231051000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:231035600-231051200	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr2:231035600-231051600	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr2:231035800-231049600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr2:231035800-231062800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:231036000-231048400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:231036200-231048800	Strong transcription	Lung	lung
31	chr2:231036200-231049200	Strong transcription	Adipose Nuclei	Adipose
32	chr2:231036200-231050800	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:231036200-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:231036400-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:231036600-231048200	Strong transcription	Stomach Smooth Muscle	stomach
36	chr2:231036600-231048800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr2:231036600-231051200	Strong transcription	Ovary	ovary
38	chr2:231036800-231046400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr2:231036800-231051000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr2:231036800-231071800	Weak transcription	NHEK	skin
41	chr2:231036800-231073600	Weak transcription	HMEC	breast
42	chr2:231037000-231049000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:231037200-231049000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:231037200-231050800	Strong transcription	Spleen	Spleen
45	chr2:231037200-231051000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:231037400-231047200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr2:231037400-231049800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
48	chr2:231038000-231069600	Weak transcription	NHLF	lung
49	chr2:231038800-231049200	Strong transcription	Duodenum Mucosa	Duodenum
50	chr2:231039000-231045400	Weak transcription	HSMM	muscle

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