Variant report

Variant	nsv535681
Chromosome Location	chr2:48421389-48492090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:48446581-48447667	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:48433217-48433475	K562	blood:	n/a	n/a
3	ARID3A	chr2:48484484-48484520	K562	blood:	n/a	n/a
4	ARID3A	chr2:48475747-48476038	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:48430164-48430486	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:48448813-48449551	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:48477046-48478513	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:48463565-48464093	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:48427791-48428233	K562	blood:	n/a	n/a
10	ARID3A	chr2:48432221-48433107	HepG2	liver:	n/a	chr2:48432400-48432416
11	ATF1	chr2:48491931-48493102	K562	blood:	n/a	n/a
12	ATF2	chr2:48478029-48478492	GM12878	blood:	n/a	n/a
13	ATF2	chr2:48475608-48476169	GM12878	blood:	n/a	n/a
14	ATF2	chr2:48454572-48455439	GM12878	blood:	n/a	n/a
15	ATF2	chr2:48454623-48455253	GM12878	blood:	n/a	n/a
16	ATF2	chr2:48475582-48476108	GM12878	blood:	n/a	n/a
17	ATF3	chr2:48448870-48449538	HepG2	liver:	n/a	n/a
18	ATF3	chr2:48475723-48476146	HCT-116	colon:	n/a	n/a
19	BACH1	chr2:48475704-48476068	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr2:48454704-48455022	GM12878	blood:	n/a	n/a
21	BATF	chr2:48475730-48476062	GM12878	blood:	n/a	chr2:48475910-48475921 chr2:48475882-48475890
22	BATF	chr2:48460150-48460423	GM12878	blood:	n/a	n/a
23	BATF	chr2:48478102-48478372	GM12878	blood:	n/a	n/a
24	BATF	chr2:48475749-48476094	GM12878	blood:	n/a	chr2:48475910-48475921 chr2:48475882-48475890
25	BCL11A	chr2:48475759-48476096	GM12878	blood:	n/a	chr2:48475946-48475954
26	BCL11A	chr2:48475758-48476036	GM12878	blood:	n/a	chr2:48475946-48475954
27	BCL11A	chr2:48454672-48455139	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:48454785-48455079	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:48460148-48460384	GM12878	blood:	n/a	n/a
30	BCL3	chr2:48475733-48476014	GM12878	blood:	n/a	chr2:48475946-48475954
31	BCLAF1	chr2:48455381-48455759	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:48422434-48422515	K562	blood:	n/a	n/a
33	BHLHE40	chr2:48432815-48432958	K562	blood:	n/a	n/a
34	BHLHE40	chr2:48434518-48434748	K562	blood:	n/a	n/a
35	BHLHE40	chr2:48454747-48455103	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:48448860-48449489	HepG2	liver:	n/a	n/a
37	BHLHE40	chr2:48446906-48447658	HepG2	liver:	n/a	n/a
38	CCNT2	chr2:48427785-48428096	K562	blood:	n/a	chr2:48428042-48428051
39	CCNT2	chr2:48433392-48433460	K562	blood:	n/a	n/a
40	CCNT2	chr2:48480165-48480611	K562	blood:	n/a	n/a
41	CEBPB	chr2:48447052-48447286	K562	blood:	n/a	chr2:48447170-48447181
42	CEBPB	chr2:48475731-48476029	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:48477109-48477516	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:48478160-48478479	K562	blood:	n/a	chr2:48478348-48478359
45	CEBPB	chr2:48477166-48477470	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:48485932-48486292	HepG2	liver:	n/a	chr2:48486112-48486123 chr2:48486111-48486122
47	CEBPB	chr2:48447005-48447283	HepG2	liver:	n/a	chr2:48447170-48447181
48	CEBPB	chr2:48472099-48472254	Hela-S3	cervix:	n/a	chr2:48472193-48472204
49	CEBPB	chr2:48446923-48447436	HepG2	liver:	n/a	chr2:48447170-48447181
50	CEBPB	chr2:48478181-48478401	HepG2	liver:	n/a	chr2:48478348-48478359

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48434367-48434417	AG10803	skin:	n/a
2	chr2:48434367-48434417	HAEpiC	amniotic membrane:	n/a
3	chr2:48434367-48434417	GM19239	blood:	n/a
4	chr2:48434367-48434417	NH-A	brain:	n/a
5	chr2:48434367-48434417	SAEC	small airway:	n/a
6	chr2:48434367-48434417	AG04450	lung:	fetal
7	chr2:48434367-48434417	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:48434367-48434417	HepG2	liver:	n/a
9	chr2:48434367-48434417	BE2_C	brain:	n/a
10	chr2:48434367-48434417	K562	blood:	n/a
11	chr2:48434367-48434417	AG04449	skin:	fetal
12	chr2:48434367-48434417	SK-N-MC	brain:	n/a
13	chr2:48434367-48434417	AG09309	skin:	n/a
14	chr2:48434367-48434417	IMR90	lung:	fetal
15	chr2:48434367-48434417	GM12878	blood:	n/a
16	chr2:48434367-48434417	SKMC	muscle:	n/a
17	chr2:48434367-48434417	ECC-1	luminal epithelium:	n/a
18	chr2:48434367-48434417	LNCaP	prostate:	n/a
19	chr2:48434367-48434417	HL-60	blood:	n/a
20	chr2:48434367-48434417	HEK293	kidney:	embryo
21	chr2:48434367-48434417	HUVEC	blood vessel:	n/a
22	chr2:48434367-48434417	MCF10A-Er-Src	breast:	n/a
23	chr2:48434367-48434417	HCM	heart:	n/a
24	chr2:48434367-48434417	ProgFib	skin:	n/a
25	chr2:48434367-48434417	PrEC	prostate:	n/a
26	chr2:48434367-48434417	HRE	kidney:	n/a
27	chr2:48434367-48434417	BJ	skin:	n/a
28	chr2:48434367-48434417	HCT-116	colon:	n/a
29	chr2:48434367-48434417	CMK	blood:	n/a
30	chr2:48434367-48434417	GM06990	blood:	n/a
31	chr2:48434367-48434417	Hela-S3	cervix:	n/a
32	chr2:48434367-48434417	HCPEpiC	choroid plexus:	n/a
33	chr2:48434367-48434417	GM12891	blood:	n/a
34	chr2:48434367-48434417	HMEC	breast:	n/a
35	chr2:48434367-48434417	MCF-7	breast:	n/a
36	chr2:48434367-48434417	H1-hESC	embryonic stem cell:	embryo
37	chr2:48434367-48434417	Caco-2	colon:	n/a
38	chr2:48434367-48434417	NB4	blood:	n/a
39	chr2:48434367-48434417	AG09319	gingival:	n/a
40	chr2:48434367-48434417	T-47D	breast:	n/a
41	chr2:48434367-48434417	HRPEpiC	eye:	n/a
42	chr2:48434367-48434417	NHDF-neo	bronchial:	n/a
43	chr2:48434367-48434417	PANC-1	pancreas:	n/a
44	chr2:48434367-48434417	A549	lung:	n/a
45	chr2:48434367-48434417	HCF	heart:	n/a
46	chr2:48434367-48434417	Hepatocyte	liver:	n/a
47	chr2:48434367-48434417	HRCEpiC	kidney:	n/a
48	chr2:48434367-48434417	ovcar-3	ovarian:	n/a
49	chr2:48434367-48434417	SK-N-SH	brain:	n/a
50	chr2:48434367-48434417	RPTEC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:48475464..48477949-chr2:48504616..48506328,2	K562	blood:
2	chr2:48457105..48459838-chr2:48462699..48465520,3	K562	blood:
3	chr2:48456981..48457558-chr8:144780788..144781293,2	MCF-7	breast:
4	chr2:48431668..48433629-chr2:48442154..48444145,2	MCF-7	breast:
5	chr2:48463548..48466435-chr2:48483353..48486334,2	K562	blood:
6	chr2:48444859..48447446-chr2:48460629..48462297,2	K562	blood:
7	chr2:48432585..48437809-chr2:48438116..48442314,6	K562	blood:
8	chr2:48434273..48436933-chr2:48509087..48510604,2	K562	blood:
9	chr2:48487519..48489450-chr2:48489934..48492138,2	K562	blood:
10	chr2:48436276..48438962-chr2:48439621..48441170,3	K562	blood:
11	chr2:48487519..48489450-chr2:48489934..48492138,2	K562	blood:
12	chr2:48444197..48446382-chr2:48474210..48475992,2	MCF-7	breast:
13	chr2:48432585..48437809-chr2:48438116..48442314,6	K562	blood:
14	chr2:48457105..48459838-chr2:48462699..48465520,3	K562	blood:
15	chr2:48420748..48422643-chr2:48628237..48631229,2	K562	blood:
16	chr2:48430653..48432447-chr2:48432583..48435502,2	K562	blood:
17	chr2:48442344..48444202-chr2:48446205..48448068,2	K562	blood:
18	chr2:48475740..48478459-chr2:48481350..48483573,2	K562	blood:
19	chr1:8360834..8361754-chr2:48483082..48483582,2	NB4	blood:
20	chr2:48430653..48432447-chr2:48432583..48435502,2	K562	blood:
21	chr2:48415132..48417658-chr2:48422363..48423907,2	MCF-7	breast:
22	chr2:48463548..48466435-chr2:48483353..48486334,2	K562	blood:
23	chr2:48444859..48447446-chr2:48460629..48462297,2	K562	blood:
24	chr2:48442344..48444202-chr2:48446205..48448068,2	K562	blood:
25	chr14:81611696..81613196-chr2:48488940..48490546,2	MCF-7	breast:
26	chr2:48475740..48478459-chr2:48481350..48483573,2	K562	blood:
27	chr2:48436276..48438962-chr2:48439621..48441170,3	K562	blood:
28	chr2:48480909..48483204-chr2:48540042..48542458,2	K562	blood:
29	chr2:48431668..48433629-chr2:48442154..48444145,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO11-1	chr2:48468067-48468141	NONHSAT070610
2	lnc-FOXN2-4	chr2:48423238-48423721	NONHSAT070616
3	lnc-FOXN2-4	chr2:48425532-48425603	NONHSAT070616
4	lnc-FOXN2-3	chr2:48444714-48445038	NONHSAT070617
5	lnc-FBXO11-1	chr2:48468067-48468122	ENSG00000230773

No data

Variant related genes	Relation type
RN7SKP224	TF binding region
ENSG00000230773	TF binding region
RN7SKP224	CpG island
ENSG00000230773	CpG island
ENSG00000170802	chromatin interactions
ENSG00000201010	chromatin interactions

Extended variants
information (count: 2845 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2845 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547632882	chr2:48421424-48421425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139618803	chr2:48421425-48421426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530362788	chr2:48421444-48421445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548877402	chr2:48421454-48421455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540875669	chr2:48421476-48421477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569921054	chr2:48421493-48421494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116402250	chr2:48421504-48421505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184948698	chr2:48421535-48421536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570995888	chr2:48421582-48421583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189881917	chr2:48421604-48421605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149752169	chr2:48421689-48421690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572287730	chr2:48421693-48421694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145699590	chr2:48421700-48421701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554854770	chr2:48421735-48421736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141570236	chr2:48421738-48421739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569251269	chr2:48421753-48421754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147050771	chr2:48421802-48421803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181938446	chr2:48421874-48421875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34908565	chr2:48421908-48421909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72885740	chr2:48421931-48421932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs186935780	chr2:48421950-48421951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191021131	chr2:48421967-48421968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201186946	chr2:48421999-48422000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530338006	chr2:48422017-48422018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548551787	chr2:48422048-48422049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147696536	chr2:48422076-48422077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530802658	chr2:48422120-48422121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142478679	chr2:48422168-48422169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570934399	chr2:48422250-48422251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369963939	chr2:48422259-48422260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535156212	chr2:48422287-48422288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547140199	chr2:48422305-48422306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376549516	chr2:48422311-48422312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143340697	chr2:48422317-48422318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367874973	chr2:48422348-48422349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371650880	chr2:48422376-48422377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554561552	chr2:48422416-48422417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533206872	chr2:48422419-48422420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576332913	chr2:48422427-48422428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536628261	chr2:48422433-48422434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558164934	chr2:48422457-48422458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148358341	chr2:48422467-48422468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141567672	chr2:48422484-48422485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559026081	chr2:48422526-48422527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372515137	chr2:48422543-48422544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182007374	chr2:48422546-48422547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542449516	chr2:48422569-48422570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150487138	chr2:48422595-48422596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185251552	chr2:48422609-48422610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552587597	chr2:48422617-48422618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
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
Breast cancer	17603634	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
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48415000-48423200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:48417600-48423400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr2:48418000-48423200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr2:48418200-48422000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr2:48418200-48423200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr2:48418800-48423200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:48419000-48423200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:48419000-48423200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:48419000-48423200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:48419000-48423400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr2:48419000-48423600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:48421200-48421600	Enhancers	Brain Substantia Nigra	brain
13	chr2:48421400-48421600	Enhancers	Brain Anterior Caudate	brain
14	chr2:48421400-48422200	Enhancers	Fetal Brain Male	brain
15	chr2:48421400-48424600	Enhancers	Brain Hippocampus Middle	brain
16	chr2:48421600-48422000	Weak transcription	Brain Substantia Nigra	brain
17	chr2:48421800-48422000	Enhancers	Brain Cingulate Gyrus	brain
18	chr2:48421800-48422600	Enhancers	Lung	lung
19	chr2:48422000-48422200	Enhancers	Brain Angular Gyrus	brain
20	chr2:48422000-48425200	Enhancers	Brain Substantia Nigra	brain
21	chr2:48422000-48426400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr2:48422200-48422400	Enhancers	Fetal Brain Female	brain
23	chr2:48422200-48423200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr2:48422200-48423200	Weak transcription	Fetal Brain Male	brain
25	chr2:48422400-48422600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:48422400-48422600	Enhancers	Pancreas	Pancrea
27	chr2:48422400-48423400	Weak transcription	Fetal Brain Female	brain
28	chr2:48422400-48423600	Weak transcription	Brain Angular Gyrus	brain
29	chr2:48422400-48424000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:48422400-48424600	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr2:48422600-48423400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:48422600-48423400	Weak transcription	Pancreas	Pancrea
33	chr2:48422600-48424400	Weak transcription	Lung	lung
34	chr2:48422600-48425000	Enhancers	Fetal Muscle Leg	muscle
35	chr2:48423200-48423600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr2:48423200-48424000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:48423200-48424000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:48423200-48424000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:48423200-48424000	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:48423200-48424000	Enhancers	Fetal Intestine Large	intestine
41	chr2:48423200-48424000	Enhancers	Stomach Mucosa	stomach
42	chr2:48423200-48424200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:48423200-48424200	Enhancers	Fetal Brain Male	brain
44	chr2:48423200-48424600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr2:48423200-48424600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:48423200-48424600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:48423200-48424600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:48423200-48424600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:48423200-48424600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:48423200-48424600	Enhancers	Brain Anterior Caudate	brain

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