Variant report

Variant	nsv873879
Chromosome Location	chr2:37200033-37299145
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	chr2:37287122-37287354	K562	blood:	n/a	n/a
2	ARID3A	chr2:37200534-37200833	K562	blood:	n/a	n/a
3	ARID3A	chr2:37215196-37215467	HepG2	liver:	n/a	n/a
4	ATF1	chr2:37200535-37200833	K562	blood:	n/a	n/a
5	ATF2	chr2:37239989-37240618	GM12878	blood:	n/a	n/a
6	ATF2	chr2:37232207-37232802	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:37240105-37240439	GM12878	blood:	n/a	n/a
8	BCLAF1	chr2:37239997-37240602	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:37232209-37232835	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:37240130-37240517	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:37232378-37232794	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:37200552-37200885	K562	blood:	n/a	n/a
13	BRCA1	chr2:37275816-37275880	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr2:37200436-37200844	K562	blood:	n/a	n/a
15	CEBPB	chr2:37219228-37219428	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:37200481-37200826	K562	blood:	n/a	n/a
17	CEBPB	chr2:37264938-37265297	HepG2	liver:	n/a	chr2:37265111-37265122
18	CEBPB	chr2:37232250-37232480	A549	lung:	n/a	n/a
19	CEBPB	chr2:37200526-37200868	K562	blood:	n/a	n/a
20	CEBPB	chr2:37279918-37280329	HepG2	liver:	n/a	chr2:37280024-37280035
21	CEBPB	chr2:37264958-37265193	MCF-7	breast:	n/a	chr2:37265111-37265122
22	CEBPB	chr2:37265046-37265146	H1-hESC	embryonic stem cell:	n/a	chr2:37265111-37265122
23	CEBPB	chr2:37202248-37202274	K562	blood:	n/a	n/a
24	CEBPB	chr2:37298131-37298395	A549	lung:	n/a	n/a
25	CEBPB	chr2:37246316-37246520	Hela-S3	cervix:	n/a	chr2:37246387-37246398 chr2:37246387-37246398 chr2:37246387-37246400 chr2:37246388-37246399 chr2:37246409-37246420
26	CEBPB	chr2:37264957-37265276	A549	lung:	n/a	chr2:37265111-37265122
27	CEBPB	chr2:37246254-37246589	A549	lung:	n/a	chr2:37246387-37246398 chr2:37246387-37246398 chr2:37246387-37246400 chr2:37246388-37246399 chr2:37246409-37246420
28	CEBPB	chr2:37227698-37227946	A549	lung:	n/a	n/a
29	CEBPB	chr2:37285054-37285066	K562	blood:	n/a	n/a
30	CEBPB	chr2:37232234-37232555	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:37246381-37246531	IMR90	lung:	n/a	chr2:37246387-37246398 chr2:37246387-37246398 chr2:37246387-37246400 chr2:37246388-37246399 chr2:37246409-37246420
32	CEBPB	chr2:37264954-37265270	IMR90	lung:	n/a	chr2:37265111-37265122
33	CEBPB	chr2:37269316-37269583	HepG2	liver:	n/a	chr2:37269437-37269448
34	CEBPB	chr2:37246325-37246586	K562	blood:	n/a	chr2:37246387-37246398 chr2:37246387-37246398 chr2:37246387-37246400 chr2:37246388-37246399 chr2:37246409-37246420
35	CEBPB	chr2:37275785-37275975	A549	lung:	n/a	chr2:37275932-37275949 chr2:37275935-37275947
36	CEBPB	chr2:37264945-37265299	K562	blood:	n/a	chr2:37265111-37265122
37	CEBPB	chr2:37226277-37226376	K562	blood:	n/a	n/a
38	CEBPB	chr2:37279874-37280161	K562	blood:	n/a	chr2:37280024-37280035
39	CEBPB	chr2:37265024-37265238	Hela-S3	cervix:	n/a	chr2:37265111-37265122
40	CEBPB	chr2:37248053-37248604	HepG2	liver:	n/a	chr2:37248429-37248440 chr2:37248084-37248097
41	CEBPB	chr2:37247617-37248603	IMR90	lung:	n/a	chr2:37248429-37248440 chr2:37248084-37248097
42	CEBPB	chr2:37209348-37209432	A549	lung:	n/a	chr2:37209390-37209403
43	CEBPB	chr2:37232072-37232906	GM12878	blood:	n/a	n/a
44	CEBPB	chr2:37232229-37232541	K562	blood:	n/a	n/a
45	CEBPB	chr2:37246278-37246570	HepG2	liver:	n/a	chr2:37246387-37246398 chr2:37246387-37246398 chr2:37246387-37246400 chr2:37246388-37246399 chr2:37246409-37246420
46	CEBPB	chr2:37215151-37215482	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:37279880-37280061	A549	lung:	n/a	chr2:37280024-37280035
48	CEBPD	chr2:37200459-37200886	K562	blood:	n/a	n/a
49	CEBPD	chr2:37200481-37200885	K562	blood:	n/a	n/a
50	CHD1	chr2:37232612-37232907	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:37237050..37239169-chr2:37241274..37243867,2	K562	blood:
2	chr2:37288334..37292049-chr2:37300310..37302436,3	K562	blood:
3	chr2:37251052..37253037-chr2:37255174..37257744,2	K562	blood:
4	chr2:37268003..37270548-chr2:37276680..37278983,2	K562	blood:
5	chr2:37192081..37194283-chr2:37200274..37202081,2	MCF-7	breast:
6	chr2:37192024..37194292-chr2:37227624..37230036,2	MCF-7	breast:
7	chr2:37005040..37005587-chr2:37231880..37232793,2	MCF-7	breast:
8	chr2:37286149..37287887-chr2:37310266..37312882,2	K562	blood:
9	chr2:37251052..37253037-chr2:37255174..37257744,2	K562	blood:
10	chr2:37227746..37229597-chr2:37231248..37232780,2	K562	blood:
11	chr2:37212231..37214849-chr2:37242255..37244987,2	K562	blood:
12	chr2:37263179..37264825-chr2:37269498..37271219,2	K562	blood:
13	chr2:37275982..37277521-chr2:37277722..37279319,2	K562	blood:
14	chr2:37219829..37222181-chr2:37235362..37237238,2	K562	blood:
15	chr2:37237050..37239169-chr2:37241274..37243867,2	K562	blood:
16	chr2:37200625..37203059-chr2:37207408..37209806,2	MCF-7	breast:
17	chr2:37275245..37277976-chr2:37283983..37286805,2	K562	blood:
18	chr2:37275245..37277976-chr2:37283983..37286805,2	K562	blood:
19	chr2:37219829..37222181-chr2:37235362..37237238,2	K562	blood:
20	chr2:37232752..37235418-chr2:37239434..37241635,2	K562	blood:
21	chr2:37204760..37206841-chr2:37210799..37212478,2	K562	blood:
22	chr2:37212231..37214849-chr2:37242255..37244987,2	K562	blood:
23	chr2:37190637..37196620-chr2:37200622..37205629,7	K562	blood:
24	chr2:37192475..37194046-chr2:37274865..37276412,2	K562	blood:
25	chr2:37295135..37296941-chr2:37382697..37385623,2	MCF-7	breast:
26	chr2:37193009..37195682-chr2:37250815..37252662,2	K562	blood:
27	chr2:37200625..37203059-chr2:37207408..37209806,2	MCF-7	breast:
28	chr2:37204760..37206841-chr2:37210799..37212478,2	K562	blood:
29	chr2:37266157..37269087-chr2:37341136..37344012,2	K562	blood:
30	chr2:37293488..37295304-chr2:37309858..37311799,2	MCF-7	breast:
31	chr2:37194014..37195839-chr2:37202260..37204776,2	MCF-7	breast:
32	chr2:37195981..37197530-chr2:37208433..37209942,2	K562	blood:
33	chr2:37291968..37296809-chr2:37296827..37300511,4	K562	blood:
34	chr2:37218150..37220358-chr2:37221248..37224159,2	K562	blood:
35	chr2:37273282..37277482-chr2:37277722..37281272,4	K562	blood:
36	chr2:37297161..37300083-chr2:37309727..37312346,2	K562	blood:
37	chr2:37275982..37277521-chr2:37277722..37279319,2	K562	blood:
38	chr2:37227746..37229597-chr2:37231248..37232780,2	K562	blood:
39	chr2:37194465..37196285-chr2:37212369..37214230,2	K562	blood:
40	chr2:37274910..37276585-chr2:37282399..37284618,2	MCF-7	breast:
41	chr2:37258831..37261022-chr2:37271777..37274021,2	MCF-7	breast:
42	chr2:37045354..37047713-chr2:37230824..37232867,2	MCF-7	breast:
43	chr2:37191677..37193362-chr2:37233119..37235779,2	K562	blood:
44	chr2:37284639..37287706-chr2:37310103..37313648,3	K562	blood:
45	chr2:37268003..37270548-chr2:37276680..37278983,2	K562	blood:
46	chr2:37250519..37253429-chr2:85770477..85772159,2	MCF-7	breast:
47	chr2:37214250..37217213-chr2:37218281..37220281,2	K562	blood:
48	chr2:37193659..37195188-chr2:37231958..37233613,2	MCF-7	breast:
49	chr2:37206126..37208242-chr2:37214233..37216058,2	K562	blood:
50	chr2:37291968..37296809-chr2:37296827..37300511,4	K562	blood:

Variant related genes	Relation type
HEATR5B	TF binding region
ENSG00000152133	chromatin interactions
ENSG00000115808	chromatin interactions
ENSG00000055332	chromatin interactions
ENSG00000008869	chromatin interactions

Extended variants
information (count: 4286 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4286 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6739171	chr2:37200033-37200034	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192486834	chr2:37200074-37200075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547527018	chr2:37200078-37200079	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs566290560	chr2:37200100-37200101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs533741360	chr2:37200106-37200107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs558402252	chr2:37200119-37200120	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576740808	chr2:37200144-37200145	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs538173903	chr2:37200152-37200153	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs555861810	chr2:37200189-37200190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs146195746	chr2:37200259-37200260	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs541548473	chr2:37200303-37200304	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553911713	chr2:37200334-37200335	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544694763	chr2:37200404-37200405	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75793046	chr2:37200468-37200469	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184533255	chr2:37200554-37200555	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531891293	chr2:37200602-37200603	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544143036	chr2:37200669-37200670	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561927653	chr2:37200675-37200676	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567335826	chr2:37200691-37200692	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529297874	chr2:37200717-37200718	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10181959	chr2:37200739-37200740	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551392408	chr2:37200746-37200747	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13426552	chr2:37200752-37200753	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377002840	chr2:37200753-37200754	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527449488	chr2:37200768-37200769	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551935393	chr2:37200798-37200799	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs80143191	chr2:37200852-37200853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs6758058	chr2:37200859-37200860	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs371611665	chr2:37200875-37200876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117985034	chr2:37200967-37200968	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189369925	chr2:37200972-37200973	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535444087	chr2:37201003-37201004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373079006	chr2:37201105-37201106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs199800383	chr2:37201107-37201108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553870846	chr2:37201108-37201109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550496607	chr2:37201121-37201122	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200559022	chr2:37201122-37201123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs3080787	chr2:37201124-37201125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373004188	chr2:37201125-37201126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192838472	chr2:37201155-37201156	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185382496	chr2:37201183-37201184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558382270	chr2:37201207-37201208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551903228	chr2:37201217-37201218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189493650	chr2:37201245-37201246	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181559565	chr2:37201288-37201289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374522900	chr2:37201328-37201329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185931096	chr2:37201330-37201331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114406103	chr2:37201356-37201357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559354473	chr2:37201362-37201363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs137882506	chr2:37201440-37201441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2586 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37194400-37214200	Weak transcription	Pancreas	Pancrea
2	chr2:37194400-37229000	Weak transcription	Gastric	stomach
3	chr2:37194800-37206200	Weak transcription	Brain Germinal Matrix	brain
4	chr2:37194800-37211600	Weak transcription	HSMM	muscle
5	chr2:37194800-37226400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr2:37194800-37232400	Weak transcription	NHLF	lung
7	chr2:37195000-37206200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:37195000-37206400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:37195000-37206800	Weak transcription	Primary B cells from cord blood	blood
10	chr2:37195000-37206800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr2:37195000-37213800	Weak transcription	Right Ventricle	heart
12	chr2:37195000-37224200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr2:37195200-37202600	Weak transcription	Right Atrium	heart
14	chr2:37195200-37202600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr2:37195200-37205600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr2:37195200-37206000	Weak transcription	Primary T cells from cord blood	blood
17	chr2:37195200-37206200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr2:37195200-37206200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr2:37195200-37206400	Weak transcription	Fetal Brain Female	brain
20	chr2:37195200-37206600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr2:37195200-37206800	Weak transcription	Adipose Nuclei	Adipose
22	chr2:37195200-37207600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr2:37195200-37211200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:37195200-37214000	Weak transcription	Brain Anterior Caudate	brain
25	chr2:37195200-37217400	Weak transcription	NHDF-Ad	bronchial
26	chr2:37195200-37225400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr2:37195200-37252800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:37195400-37206400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr2:37195400-37206600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr2:37195400-37207400	Weak transcription	GM12878-XiMat	blood
31	chr2:37195400-37207800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:37195400-37208600	Weak transcription	Osteobl	bone
33	chr2:37195400-37213800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr2:37195400-37215000	Weak transcription	Brain Hippocampus Middle	brain
35	chr2:37195400-37217600	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:37195400-37227400	Weak transcription	A549	lung
37	chr2:37195400-37227600	Weak transcription	HUVEC	blood vessel
38	chr2:37195400-37248600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr2:37195600-37205800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:37195600-37206600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr2:37195600-37215200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:37195600-37231400	Weak transcription	Brain Angular Gyrus	brain
43	chr2:37195800-37206000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr2:37195800-37206400	Weak transcription	Fetal Muscle Leg	muscle
45	chr2:37195800-37207000	Weak transcription	Fetal Lung	lung
46	chr2:37195800-37208800	Weak transcription	Fetal Intestine Large	intestine
47	chr2:37195800-37229000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr2:37196000-37206800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:37196000-37206800	Weak transcription	Fetal Intestine Small	intestine
50	chr2:37196000-37207800	Weak transcription	Duodenum Mucosa	Duodenum

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