Variant report

Variant	nsv2974
Chromosome Location	chr2:152401495-152499455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:978)
CpG islands
(count:244)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:978 , 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	chr2:152475918-152476168	K562	blood:	n/a	n/a
2	ARID3A	chr2:152486946-152487254	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:152498461-152498920	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:152489561-152490014	K562	blood:	n/a	n/a
5	ARID3A	chr2:152475908-152476156	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:152495081-152495492	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:152489716-152490090	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:152471221-152471756	K562	blood:	n/a	n/a
9	ARID3A	chr2:152473538-152473689	K562	blood:	n/a	n/a
10	ARID3A	chr2:152496581-152496778	HepG2	liver:	n/a	n/a
11	ATF1	chr2:152471227-152471887	K562	blood:	n/a	n/a
12	ATF1	chr2:152475782-152476352	K562	blood:	n/a	n/a
13	ATF1	chr2:152416770-152417027	K562	blood:	n/a	n/a
14	ATF1	chr2:152470680-152470976	K562	blood:	n/a	n/a
15	ATF3	chr2:152475830-152476205	K562	blood:	n/a	n/a
16	BATF	chr2:152437230-152437561	GM12878	blood:	n/a	n/a
17	BATF	chr2:152471501-152471796	GM12878	blood:	n/a	chr2:152471623-152471634
18	BATF	chr2:152447781-152448112	GM12878	blood:	n/a	n/a
19	BATF	chr2:152458334-152458665	GM12878	blood:	n/a	n/a
20	BATF	chr2:152471516-152471727	GM12878	blood:	n/a	chr2:152471623-152471634
21	BCL11A	chr2:152458352-152458651	GM12878	blood:	n/a	n/a
22	BCL11A	chr2:152447799-152448098	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:152437248-152437547	GM12878	blood:	n/a	n/a
24	BHLHE40	chr2:152498473-152498783	HepG2	liver:	n/a	n/a
25	BHLHE40	chr2:152494780-152495471	HepG2	liver:	n/a	n/a
26	BHLHE40	chr2:152495080-152495371	K562	blood:	n/a	n/a
27	BHLHE40	chr2:152495104-152495407	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:152494144-152494283	K562	blood:	n/a	n/a
29	BHLHE40	chr2:152475839-152476343	K562	blood:	n/a	n/a
30	BHLHE40	chr2:152495106-152495390	HepG2	liver:	n/a	n/a
31	BHLHE40	chr2:152495071-152495356	HepG2	liver:	n/a	n/a
32	CCNT2	chr2:152471521-152471693	K562	blood:	n/a	n/a
33	CEBPB	chr2:152443187-152443552	K562	blood:	n/a	n/a
34	CEBPB	chr2:152495609-152495795	Hela-S3	cervix:	n/a	chr2:152495623-152495636
35	CEBPB	chr2:152418839-152418984	HepG2	liver:	n/a	chr2:152418915-152418926
36	CEBPB	chr2:152414468-152414617	K562	blood:	n/a	n/a
37	CEBPB	chr2:152475871-152476156	K562	blood:	n/a	n/a
38	CEBPB	chr2:152443242-152443477	K562	blood:	n/a	n/a
39	CEBPB	chr2:152453747-152454114	K562	blood:	n/a	n/a
40	CEBPB	chr2:152453798-152454061	K562	blood:	n/a	n/a
41	CEBPB	chr2:152475835-152476240	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:152464307-152464657	K562	blood:	n/a	n/a
43	CEBPB	chr2:152464347-152464575	K562	blood:	n/a	n/a
44	CEBPB	chr2:152498482-152498890	HepG2	liver:	n/a	chr2:152498872-152498885
45	CEBPB	chr2:152494065-152494408	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr2:152494020-152494413	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPD	chr2:152448226-152448506	K562	blood:	n/a	n/a
48	CHD2	chr2:152470178-152470276	K562	blood:	n/a	n/a
49	CREB1	chr2:152475848-152476152	GM12878	blood:	n/a	n/a
50	CREB1	chr2:152475837-152476093	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152440445-152440495	HRPEpiC	eye:	n/a
2	chr2:152440445-152440495	LNCaP	prostate:	n/a
3	chr2:152440445-152440495	GM12891	blood:	n/a
4	chr2:152497119-152497169	IMR90	lung:	fetal
5	chr2:152402878-152402928	ovcar-3	ovarian:	n/a
6	chr2:152440445-152440495	AG10803	skin:	n/a
7	chr2:152497119-152497169	AoSMC	blood vessel:	n/a
8	chr2:152497119-152497169	LNCaP	prostate:	n/a
9	chr2:152402878-152402928	GM12891	blood:	n/a
10	chr2:152497119-152497169	RPTEC	kidney:	n/a
11	chr2:152496744-152496794	HCPEpiC	choroid plexus:	n/a
12	chr2:152440445-152440495	BJ	skin:	n/a
13	chr2:152402878-152402928	HAEpiC	amniotic membrane:	n/a
14	chr2:152402878-152402928	GM12878	blood:	n/a
15	chr2:152496744-152496794	Hepatocyte	liver:	n/a
16	chr2:152496744-152496794	Caco-2	colon:	n/a
17	chr2:152402878-152402928	Hepatocyte	liver:	n/a
18	chr2:152496744-152496794	Hela-S3	cervix:	n/a
19	chr2:152440445-152440495	CMK	blood:	n/a
20	chr2:152440445-152440495	K562	blood:	n/a
21	chr2:152440445-152440495	HIPEpiC	eye:	n/a
22	chr2:152496744-152496794	HepG2	liver:	n/a
23	chr2:152440445-152440495	PANC-1	pancreas:	n/a
24	chr2:152402878-152402928	PrEC	prostate:	n/a
25	chr2:152497119-152497169	HL-60	blood:	n/a
26	chr2:152496744-152496794	AoSMC	blood vessel:	n/a
27	chr2:152402878-152402928	HRPEpiC	eye:	n/a
28	chr2:152440445-152440495	SK-N-SH	brain:	n/a
29	chr2:152497119-152497169	NH-A	brain:	n/a
30	chr2:152496744-152496794	NH-A	brain:	n/a
31	chr2:152440445-152440495	PFSK-1	brain:	n/a
32	chr2:152402878-152402928	SK-N-SH_RA	brain:	n/a
33	chr2:152402878-152402928	HCT-116	colon:	n/a
34	chr2:152440445-152440495	GM12878	blood:	n/a
35	chr2:152497119-152497169	GM12891	blood:	n/a
36	chr2:152402878-152402928	GM06990	blood:	n/a
37	chr2:152497119-152497169	HepG2	liver:	n/a
38	chr2:152496744-152496794	AG09319	gingival:	n/a
39	chr2:152402878-152402928	IMR90	lung:	fetal
40	chr2:152440445-152440495	NT2-D1	testis:	n/a
41	chr2:152497119-152497169	GM19239	blood:	n/a
42	chr2:152440445-152440495	IMR90	lung:	fetal
43	chr2:152497119-152497169	PFSK-1	brain:	n/a
44	chr2:152497119-152497169	HIPEpiC	eye:	n/a
45	chr2:152497119-152497169	Jurkat	blood:	n/a
46	chr2:152496744-152496794	U87	brain:	n/a
47	chr2:152440445-152440495	GM06990	blood:	n/a
48	chr2:152402878-152402928	AG04450	lung:	fetal
49	chr2:152496744-152496794	PANC-1	pancreas:	n/a
50	chr2:152497119-152497169	ECC-1	luminal epithelium:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:152398924..152401108-chr2:152404034..152405550,2	K562	blood:
2	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
3	chr2:152396825..152398789-chr2:152409057..152411603,2	K562	blood:
4	chr2:152120609..152121411-chr2:152475693..152476303,2	MCF-7	breast:
5	chr2:152467390..152469082-chr2:152475969..152477688,2	MCF-7	breast:
6	chr2:152470745..152473720-chr2:152480140..152483557,3	K562	blood:
7	chr2:152394167..152396602-chr2:152404193..152405928,2	K562	blood:
8	chr2:152402480..152405227-chr2:152409026..152411315,2	K562	blood:
9	chr2:152470745..152473899-chr2:152481197..152482872,3	K562	blood:
10	chr2:152467390..152469082-chr2:152475969..152477688,2	MCF-7	breast:
11	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
12	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
13	chr2:152499221..152501472-chr2:152507320..152509759,2	K562	blood:
14	chr2:152479591..152483516-chr2:152681949..152685103,4	K562	blood:
15	chr2:152474324..152476009-chr2:152481234..152483014,2	K562	blood:
16	chr2:152470745..152473720-chr2:152480140..152483557,3	K562	blood:
17	chr2:152478231..152481133-chr2:152482062..152484946,3	K562	blood:
18	chr2:152474324..152476009-chr2:152481234..152483014,2	K562	blood:
19	chr2:152470745..152473899-chr2:152481197..152482872,3	K562	blood:
20	chr2:152414320..152417036-chr2:152422973..152425873,2	K562	blood:
21	chr2:152494240..152495902-chr2:152684868..152686810,2	K562	blood:
22	chr2:152423732..152425326-chr2:152425773..152428506,2	K562	blood:
23	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
24	chr2:152420725..152422914-chr2:152422923..152425843,3	MCF-7	breast:
25	chr2:152420294..152421848-chr2:152423349..152426128,2	K562	blood:
26	chr2:152478231..152481133-chr2:152482062..152484946,3	K562	blood:
27	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
28	chr2:152485006..152487630-chr2:152562456..152564501,2	K562	blood:
29	chr2:152392901..152394420-chr2:152407078..152409911,2	K562	blood:
30	chr2:152398754..152402722-chr2:152404309..152407409,3	K562	blood:
31	chr2:152471974..152472482-chr2:152882224..152882926,2	K562	blood:
32	chr2:152402480..152405227-chr2:152409026..152411315,2	K562	blood:
33	chr2:152492617..152495101-chr2:152500321..152502341,2	K562	blood:

No data

Variant related genes	Relation type
NEB	TF binding region
NEB	CpG island
ENSG00000183091	chromatin interactions
ENSG00000162980	chromatin interactions

Extended variants
information (count: 2984 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2984 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113491623	chr2:152401495-152401496	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147262394	chr2:152401521-152401522	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117457833	chr2:152401559-152401560	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560490281	chr2:152401563-152401564	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140838871	chr2:152401577-152401578	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4664485	chr2:152401679-152401680	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs189799843	chr2:152401725-152401726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375345535	chr2:152401795-152401796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113192566	chr2:152401819-152401820	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370294616	chr2:152401842-152401843	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374682217	chr2:152401889-152401890	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181443897	chr2:152401945-152401946	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561592841	chr2:152401959-152401960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184439256	chr2:152402024-152402025	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566474049	chr2:152402090-152402091	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369771510	chr2:152402104-152402105	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151243988	chr2:152402131-152402132	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560160030	chr2:152402156-152402157	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4664055	chr2:152402171-152402172	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs531781478	chr2:152402184-152402185	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552598372	chr2:152402258-152402259	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372252328	chr2:152402362-152402363	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377243130	chr2:152402414-152402415	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201539722	chr2:152402446-152402447	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201001168	chr2:152402475-152402476	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370098540	chr2:152402476-152402477	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368914782	chr2:152402516-152402517	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74780321	chr2:152402530-152402531	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10687343	chr2:152402532-152402533	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375181005	chr2:152402591-152402592	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550520536	chr2:152402613-152402614	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189217946	chr2:152402656-152402657	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536581512	chr2:152402659-152402660	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13413290	chr2:152402663-152402664	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs376488706	chr2:152402690-152402691	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3213818	chr2:152402711-152402712	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs538647271	chr2:152402712-152402713	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558577048	chr2:152402808-152402809	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568451191	chr2:152402822-152402823	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11436329	chr2:152402823-152402824	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374422239	chr2:152402826-152402827	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544775500	chr2:152402847-152402848	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181826071	chr2:152402848-152402849	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201684605	chr2:152402852-152402853	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374662309	chr2:152402871-152402872	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199875722	chr2:152402878-152402879	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370764959	chr2:152402891-152402892	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373276952	chr2:152402895-152402896	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534443920	chr2:152402900-152402901	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111994546	chr2:152402958-152402959	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	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
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
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152343200-152422200	Weak transcription	Primary B cells from cord blood	blood
2	chr2:152360800-152424400	Weak transcription	Brain Anterior Caudate	brain
3	chr2:152365200-152415600	Weak transcription	Fetal Intestine Small	intestine
4	chr2:152370400-152403600	Strong transcription	Skeletal Muscle Male	skeletal muscle
5	chr2:152371400-152421000	Weak transcription	Pancreas	Pancrea
6	chr2:152381000-152410200	Weak transcription	Placenta	Placenta
7	chr2:152383200-152424000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr2:152385800-152426800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:152389800-152412000	Strong transcription	HSMMtube	muscle
10	chr2:152391000-152405600	Weak transcription	Left Ventricle	heart
11	chr2:152392000-152405200	Weak transcription	Brain Angular Gyrus	brain
12	chr2:152392600-152414200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr2:152395000-152411800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr2:152395800-152411800	Strong transcription	Fetal Muscle Leg	muscle
15	chr2:152397000-152403600	Weak transcription	Psoas Muscle	Psoas
16	chr2:152400800-152401600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:152401000-152401600	Enhancers	Aorta	Aorta
18	chr2:152401200-152401600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:152401200-152401600	Enhancers	Adipose Nuclei	Adipose
20	chr2:152401200-152401600	Flanking Active TSS	NHDF-Ad	bronchial
21	chr2:152401400-152402400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:152401400-152405400	Strong transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:152401600-152402400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:152401600-152405600	Weak transcription	Aorta	Aorta
25	chr2:152402200-152402800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:152402200-152403000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:152402400-152402800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:152402400-152402800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:152402600-152402800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr2:152402600-152402800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:152402600-152403000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:152402600-152403000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:152403000-152408600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:152403600-152404000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
35	chr2:152403600-152404200	Strong transcription	Psoas Muscle	Psoas
36	chr2:152404000-152405400	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr2:152404200-152405600	Weak transcription	Psoas Muscle	Psoas
38	chr2:152405400-152406200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
39	chr2:152405400-152408400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
40	chr2:152405600-152405800	ZNF genes & repeats	Aorta	Aorta
41	chr2:152405600-152406400	Strong transcription	Psoas Muscle	Psoas
42	chr2:152405800-152406000	Strong transcription	Aorta	Aorta
43	chr2:152406000-152425800	Weak transcription	Aorta	Aorta
44	chr2:152406200-152409800	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:152406400-152408400	Weak transcription	Psoas Muscle	Psoas
46	chr2:152408000-152410600	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr2:152408200-152408400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:152408200-152408400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr2:152408400-152409400	Strong transcription	Psoas Muscle	Psoas
50	chr2:152408400-152409400	Strong transcription	Skeletal Muscle Male	skeletal muscle

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