Variant report

Variant	nsv1004156
Chromosome Location	chr2:36351103-36569122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36566092-36566413	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:36556942-36557316	HepG2	liver:	n/a	chr2:36557242-36557258
4	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
5	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
6	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
7	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
11	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
12	BATF	chr2:36564561-36564770	GM12878	blood:	n/a	n/a
13	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
14	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
15	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
17	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
20	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
21	BCL3	chr2:36565737-36566479	A549	lung:	n/a	n/a
22	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
24	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
25	BRCA1	chr2:36546010-36546093	HepG2	liver:	n/a	n/a
26	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:36556126-36556356	HepG2	liver:	n/a	chr2:36556209-36556220
28	CEBPB	chr2:36521592-36521787	A549	lung:	n/a	n/a
29	CEBPB	chr2:36420124-36420491	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
30	CEBPB	chr2:36556102-36556393	A549	lung:	n/a	chr2:36556209-36556220
31	CEBPB	chr2:36514592-36514954	Hela-S3	cervix:	n/a	chr2:36514780-36514791
32	CEBPB	chr2:36526442-36526614	HepG2	liver:	n/a	chr2:36526529-36526540
33	CEBPB	chr2:36514601-36514964	HepG2	liver:	n/a	chr2:36514780-36514791
34	CEBPB	chr2:36566993-36567410	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr2:36449657-36449993	HepG2	liver:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
36	CEBPB	chr2:36556053-36556379	IMR90	lung:	n/a	chr2:36556209-36556220
37	CEBPB	chr2:36548842-36549024	A549	lung:	n/a	n/a
38	CEBPB	chr2:36434672-36434980	HepG2	liver:	n/a	chr2:36434830-36434841
39	CEBPB	chr2:36437519-36437741	A549	lung:	n/a	chr2:36437627-36437638
40	CEBPB	chr2:36526442-36526637	A549	lung:	n/a	chr2:36526529-36526540
41	CEBPB	chr2:36514610-36514947	A549	lung:	n/a	chr2:36514780-36514791
42	CEBPB	chr2:36556951-36557349	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:36449673-36449993	H1-hESC	embryonic stem cell:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
44	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
45	CEBPB	chr2:36374793-36375473	Hela-S3	cervix:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
46	CEBPB	chr2:36395324-36395659	HepG2	liver:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
47	CEBPB	chr2:36565895-36566334	A549	lung:	n/a	n/a
48	CEBPB	chr2:36374848-36374960	HepG2	liver:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
49	CEBPB	chr2:36379312-36379579	HepG2	liver:	n/a	chr2:36379457-36379468
50	CEBPB	chr2:36556740-36557429	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36565096-36565146	MCF-7	breast:	n/a
2	chr2:36565096-36565146	MCF-7	breast:	n/a
3	chr2:36406592-36406642	GM12878	blood:	n/a
4	chr2:36441749-36441799	ProgFib	skin:	n/a
5	chr2:36565096-36565146	HEK293	kidney:	embryo
6	chr2:36406592-36406642	GM12892	blood:	n/a
7	chr2:36406592-36406642	HepG2	liver:	n/a
8	chr2:36441749-36441799	BJ	skin:	n/a
9	chr2:36467699-36467749	A549	lung:	n/a
10	chr2:36557755-36557805	HRPEpiC	eye:	n/a
11	chr2:36565096-36565146	HCF	heart:	n/a
12	chr2:36441749-36441799	Hepatocyte	liver:	n/a
13	chr2:36406592-36406642	HEEpiC	esophagus:	n/a
14	chr2:36557755-36557805	GM12878	blood:	n/a
15	chr2:36557755-36557805	Caco-2	colon:	n/a
16	chr2:36441749-36441799	AG09309	skin:	n/a
17	chr2:36565096-36565146	U87	brain:	n/a
18	chr2:36467699-36467749	ovcar-3	ovarian:	n/a
19	chr2:36406592-36406642	Hela-S3	cervix:	n/a
20	chr2:36406592-36406642	HRCEpiC	kidney:	n/a
21	chr2:36441749-36441799	A549	lung:	n/a
22	chr2:36467699-36467749	NT2-D1	testis:	n/a
23	chr2:36441749-36441799	HEK293	kidney:	embryo
24	chr2:36557755-36557805	ProgFib	skin:	n/a
25	chr2:36557755-36557805	AG09309	skin:	n/a
26	chr2:36467699-36467749	HIPEpiC	eye:	n/a
27	chr2:36565096-36565146	HNPCEpiC	eye:	n/a
28	chr2:36441749-36441799	HCT-116	colon:	n/a
29	chr2:36441749-36441799	HL-60	blood:	n/a
30	chr2:36557755-36557805	SAEC	small airway:	n/a
31	chr2:36441749-36441799	Caco-2	colon:	n/a
32	chr2:36467699-36467749	HCF	heart:	n/a
33	chr2:36557755-36557805	SKMC	muscle:	n/a
34	chr2:36467699-36467749	SKMC	muscle:	n/a
35	chr2:36406592-36406642	T-47D	breast:	n/a
36	chr2:36565096-36565146	NT2-D1	testis:	n/a
37	chr2:36467699-36467749	T-47D	breast:	n/a
38	chr2:36467699-36467749	HEEpiC	esophagus:	n/a
39	chr2:36467699-36467749	HRPEpiC	eye:	n/a
40	chr2:36557755-36557805	A549	lung:	n/a
41	chr2:36557755-36557805	Hepatocyte	liver:	n/a
42	chr2:36565096-36565146	HIPEpiC	eye:	n/a
43	chr2:36467699-36467749	SAEC	small airway:	n/a
44	chr2:36565096-36565146	NB4	blood:	n/a
45	chr2:36557755-36557805	Hela-S3	cervix:	n/a
46	chr2:36565096-36565146	AG10803	skin:	n/a
47	chr2:36557755-36557805	GM19239	blood:	n/a
48	chr2:36467699-36467749	HRCEpiC	kidney:	n/a
49	chr2:36557755-36557805	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:36565096-36565146	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
2	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
3	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
4	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
5	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
6	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
7	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
8	chr2:36561664..36563772-chr2:36823426..36826394,2	MCF-7	breast:
9	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
10	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-5	chr2:36526531-36526973	NONHSAT070076

Variant related genes	Relation type
ENSG00000233752	TF binding region
ENSG00000233752	CpG island
ENSG00000177410	chromatin interactions
ENSG00000171055	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000124201	chromatin interactions

Extended variants
information (count: 7017 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7017 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17018250	chr2:36351103-36351104	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182838195	chr2:36351112-36351113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566377062	chr2:36351150-36351151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553391718	chr2:36351176-36351177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144625227	chr2:36351216-36351217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187724189	chr2:36351225-36351226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576746689	chr2:36351228-36351229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537972698	chr2:36351254-36351255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555832101	chr2:36351255-36351256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529712912	chr2:36351263-36351264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574156004	chr2:36351270-36351271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7562324	chr2:36351338-36351339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183495916	chr2:36351346-36351347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572322725	chr2:36351367-36351368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545766090	chr2:36351382-36351383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187973237	chr2:36351392-36351393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192025750	chr2:36351513-36351514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547818350	chr2:36351521-36351522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562171100	chr2:36351540-36351541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529356639	chr2:36351547-36351548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548032412	chr2:36351569-36351570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184577150	chr2:36351573-36351574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139647158	chr2:36351614-36351615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375420329	chr2:36351616-36351617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551764849	chr2:36351649-36351650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189675933	chr2:36351655-36351656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369679480	chr2:36351656-36351657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555693078	chr2:36351659-36351660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567837844	chr2:36351660-36351661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535146625	chr2:36351683-36351684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74990311	chr2:36351686-36351687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373179813	chr2:36351689-36351690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572127755	chr2:36351739-36351740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546128483	chr2:36351762-36351763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145260019	chr2:36351779-36351780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12468654	chr2:36351783-36351784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558679725	chr2:36351793-36351794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571036550	chr2:36351831-36351832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576244852	chr2:36351928-36351929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534776523	chr2:36352050-36352051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111299778	chr2:36352071-36352072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529422332	chr2:36352079-36352080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560466978	chr2:36352083-36352084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1397448	chr2:36352095-36352096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs112978183	chr2:36352137-36352138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559922814	chr2:36352199-36352200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533358354	chr2:36352214-36352215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553456022	chr2:36352252-36352253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551911978	chr2:36352297-36352298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369322833	chr2:36352298-36352299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	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	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Autism	22495309	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36350200-36354000	Weak transcription	Fetal Brain Male	brain
2	chr2:36350800-36353200	Weak transcription	Brain Germinal Matrix	brain
3	chr2:36352600-36353200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:36352600-36353600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:36353200-36354000	Enhancers	Brain Germinal Matrix	brain
6	chr2:36353600-36354400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:36354000-36354400	Weak transcription	Brain Germinal Matrix	brain
8	chr2:36354000-36355200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:36354000-36355400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:36354000-36356800	Enhancers	Fetal Brain Male	brain
11	chr2:36354400-36356200	Enhancers	Brain Germinal Matrix	brain
12	chr2:36354800-36355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:36354800-36356200	Enhancers	Fetal Brain Female	brain
14	chr2:36355200-36357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:36355400-36355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:36355800-36356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:36356000-36357600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:36356200-36357200	Weak transcription	Fetal Brain Female	brain
19	chr2:36356200-36357600	Weak transcription	Brain Germinal Matrix	brain
20	chr2:36357400-36357600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:36357400-36357600	Enhancers	Fetal Brain Female	brain
22	chr2:36357600-36357800	Enhancers	Brain Germinal Matrix	brain
23	chr2:36357600-36358000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:36357600-36360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:36358000-36360200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:36360200-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr2:36360800-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:36364400-36365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:36364400-36365200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:36364600-36365000	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr2:36364600-36365200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr2:36364600-36365200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr2:36364600-36365200	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr2:36364600-36365200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr2:36364600-36365400	Enhancers	Primary T cells from cord blood	blood
36	chr2:36364600-36365400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr2:36364800-36365200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr2:36364800-36365200	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr2:36364800-36365200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:36364800-36365200	Enhancers	Thymus	Thymus
41	chr2:36364800-36366000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr2:36365600-36365800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:36365600-36367200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:36365800-36366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:36366200-36366800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:36366400-36367600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:36366600-36367000	Enhancers	Fetal Kidney	kidney
48	chr2:36367000-36367400	Active TSS	Fetal Kidney	kidney
49	chr2:36367200-36367600	Enhancers	Fetal Lung	lung
50	chr2:36367200-36367800	Enhancers	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links