Variant report

Variant	nsv875456
Chromosome Location	chr2:179775893-179896787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:954)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:954 , 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	ATF1	chr2:179822029-179822138	K562	blood:	n/a	n/a
2	ATF2	chr2:179896288-179897163	GM12878	blood:	n/a	n/a
3	ATF2	chr2:179896233-179897238	GM12878	blood:	n/a	n/a
4	ATF2	chr2:179885897-179886437	GM12878	blood:	n/a	n/a
5	ATF2	chr2:179885852-179886432	GM12878	blood:	n/a	n/a
6	ATF2	chr2:179792712-179793308	GM12878	blood:	n/a	n/a
7	ATF2	chr2:179792721-179793253	GM12878	blood:	n/a	n/a
8	BATF	chr2:179855315-179855664	GM12878	blood:	n/a	n/a
9	BATF	chr2:179885882-179886408	GM12878	blood:	n/a	n/a
10	BATF	chr2:179792891-179793179	GM12878	blood:	n/a	n/a
11	BATF	chr2:179885953-179886337	GM12878	blood:	n/a	n/a
12	BATF	chr2:179855311-179855592	GM12878	blood:	n/a	n/a
13	BATF	chr2:179792774-179793269	GM12878	blood:	n/a	n/a
14	BATF	chr2:179896385-179897191	GM12878	blood:	n/a	chr2:179896815-179896825 chr2:179896814-179896825
15	BCL11A	chr2:179885866-179886395	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:179792876-179793143	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:179885932-179886385	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:179896464-179896913	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:179896398-179897128	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:179792828-179793280	GM12878	blood:	n/a	n/a
21	BCL3	chr2:179896426-179897244	GM12878	blood:	n/a	n/a
22	BCLAF1	chr2:179885964-179886450	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:179896411-179897213	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:179885813-179886511	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:179896181-179897435	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:179888995-179889074	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:179885721-179886428	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:179896442-179896875	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:179779091-179779331	K562	blood:	n/a	n/a
30	BRCA1	chr2:179886019-179886139	GM12878	blood:	n/a	n/a
31	BRCA1	chr2:179779076-179779308	HepG2	liver:	n/a	n/a
32	CBX3	chr2:179778967-179779359	K562	blood:	n/a	n/a
33	CEBPB	chr2:179884005-179884332	A549	lung:	n/a	chr2:179884163-179884174
34	CEBPB	chr2:179779041-179779269	K562	blood:	n/a	n/a
35	CEBPB	chr2:179824567-179824773	IMR90	lung:	n/a	chr2:179824626-179824637
36	CEBPB	chr2:179867933-179868107	HepG2	liver:	n/a	chr2:179868015-179868026
37	CEBPB	chr2:179845656-179845895	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:179883997-179884337	IMR90	lung:	n/a	chr2:179884163-179884174
39	CEBPB	chr2:179794025-179794223	HepG2	liver:	n/a	chr2:179794176-179794187
40	CEBPB	chr2:179824508-179824783	HepG2	liver:	n/a	chr2:179824626-179824637
41	CEBPB	chr2:179884975-179885140	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:179845472-179845929	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:179779099-179779372	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:179884063-179884320	H1-hESC	embryonic stem cell:	n/a	chr2:179884163-179884174
45	CEBPB	chr2:179813967-179814201	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:179845572-179845925	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:179796391-179796595	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:179794465-179794531	HepG2	liver:	n/a	chr2:179794487-179794496 chr2:179794485-179794498 chr2:179794487-179794496 chr2:179794485-179794496 chr2:179794487-179794496 chr2:179794487-179794496 chr2:179794486-179794497
49	CEBPB	chr2:179883991-179884359	HepG2	liver:	n/a	chr2:179884163-179884174
50	CEBPB	chr2:179845588-179845908	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179847360-179847410	NT2-D1	testis:	n/a
2	chr2:179828541-179828591	NHDF-neo	bronchial:	n/a
3	chr2:179828541-179828591	HCPEpiC	choroid plexus:	n/a
4	chr2:179828541-179828591	MCF-7	breast:	n/a
5	chr2:179828541-179828591	ovcar-3	ovarian:	n/a
6	chr2:179828541-179828591	ProgFib	skin:	n/a
7	chr2:179828541-179828591	GM12892	blood:	n/a
8	chr2:179828541-179828591	AG04449	skin:	fetal
9	chr2:179847360-179847410	NB4	blood:	n/a
10	chr2:179847360-179847410	T-47D	breast:	n/a
11	chr2:179847360-179847410	Caco-2	colon:	n/a
12	chr2:179828541-179828591	HL-60	blood:	n/a
13	chr2:179828541-179828591	BJ	skin:	n/a
14	chr2:179828541-179828591	H1-hESC	embryonic stem cell:	embryo
15	chr2:179847360-179847410	AoSMC	blood vessel:	n/a
16	chr2:179847360-179847410	PFSK-1	brain:	n/a
17	chr2:179847360-179847410	RPTEC	kidney:	n/a
18	chr2:179847360-179847410	ovcar-3	ovarian:	n/a
19	chr2:179847360-179847410	HCM	heart:	n/a
20	chr2:179828541-179828591	A549	lung:	n/a
21	chr2:179847360-179847410	SAEC	small airway:	n/a
22	chr2:179847360-179847410	AG09309	skin:	n/a
23	chr2:179847360-179847410	GM12891	blood:	n/a
24	chr2:179847360-179847410	SK-N-MC	brain:	n/a
25	chr2:179828541-179828591	AG04450	lung:	fetal
26	chr2:179847360-179847410	AG10803	skin:	n/a
27	chr2:179847360-179847410	GM12878	blood:	n/a
28	chr2:179847360-179847410	Jurkat	blood:	n/a
29	chr2:179847360-179847410	PrEC	prostate:	n/a
30	chr2:179847360-179847410	BJ	skin:	n/a
31	chr2:179828541-179828591	HepG2	liver:	n/a
32	chr2:179828541-179828591	Jurkat	blood:	n/a
33	chr2:179847360-179847410	HIPEpiC	eye:	n/a
34	chr2:179847360-179847410	NHDF-neo	bronchial:	n/a
35	chr2:179828541-179828591	BE2_C	brain:	n/a
36	chr2:179828541-179828591	PrEC	prostate:	n/a
37	chr2:179847360-179847410	HNPCEpiC	eye:	n/a
38	chr2:179828541-179828591	GM12891	blood:	n/a
39	chr2:179847360-179847410	MCF-7	breast:	n/a
40	chr2:179847360-179847410	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:179828541-179828591	LNCaP	prostate:	n/a
42	chr2:179847360-179847410	Hela-S3	cervix:	n/a
43	chr2:179847360-179847410	SK-N-SH	brain:	n/a
44	chr2:179847360-179847410	SK-N-SH_RA	brain:	n/a
45	chr2:179828541-179828591	HNPCEpiC	eye:	n/a
46	chr2:179828541-179828591	SKMC	muscle:	n/a
47	chr2:179847360-179847410	AG09319	gingival:	n/a
48	chr2:179828541-179828591	NH-A	brain:	n/a
49	chr2:179847360-179847410	HCT-116	colon:	n/a
50	chr2:179828541-179828591	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr2:179839245..179841547-chr2:179841885..179844119,2	MCF-7	breast:
2	chr2:179753736..179754555-chr2:179779013..179779601,2	K562	blood:
3	chr2:179825079..179826748-chr2:179827040..179829506,2	MCF-7	breast:
4	chr2:179759499..179761617-chr2:179773864..179776480,2	MCF-7	breast:
5	chr2:179660554..179661360-chr2:179778610..179779597,4	MCF-7	breast:
6	chr2:179812060..179813972-chr2:179815546..179817287,2	K562	blood:
7	chr2:179839245..179841547-chr2:179841885..179844119,2	MCF-7	breast:
8	chr2:179660895..179661817-chr2:179778782..179780213,7	MCF-7	breast:
9	chr2:179809785..179813560-chr2:179814171..179817287,4	K562	blood:
10	chr2:179882961..179884886-chr2:179892703..179894826,2	K562	blood:
11	chr2:179625849..179626645-chr2:179778697..179779282,2	MCF-7	breast:
12	chr2:179809785..179813560-chr2:179814171..179817287,4	K562	blood:
13	chr2:179788003..179790590-chr2:179803122..179805955,2	K562	blood:
14	chr2:179664555..179665445-chr2:179778727..179779258,2	MCF-7	breast:
15	chr2:179626672..179627866-chr2:179778732..179779655,4	MCF-7	breast:
16	chr2:179882961..179884886-chr2:179892703..179894826,2	K562	blood:
17	chr2:179812060..179813972-chr2:179815546..179817287,2	K562	blood:
18	chr2:179825079..179826748-chr2:179827040..179829506,2	MCF-7	breast:
19	chr2:179755889..179756631-chr2:179779117..179779892,4	MCF-7	breast:
20	chr2:179771628..179773744-chr2:179775367..179777094,2	K562	blood:
21	chr2:179769183..179772111-chr2:179772237..179776036,4	K562	blood:
22	chr2:179788003..179790590-chr2:179803122..179805955,2	K562	blood:
23	chr2:179660662..179661438-chr2:179778754..179779666,2	K562	blood:
24	chr2:179664498..179665287-chr2:179884587..179885536,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA3-17	chr2:179866849-179867487	NONHSAT075822
2	lnc-PLEKHA3-17	chr2:179866483-179866548	NONHSAT075822

No data

Variant related genes	Relation type
CCDC141	TF binding region
RPS6P2	TF binding region
ENSG00000252000	TF binding region
CCDC141	CpG island
RPS6P2	CpG island
ENSG00000252000	CpG island

Extended variants
information (count: 4699 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4699 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10179812	chr2:179775893-179775894	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545137387	chr2:179775898-179775899	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565301529	chr2:179775912-179775913	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377462781	chr2:179775940-179775941	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375100759	chr2:179775942-179775943	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532629935	chr2:179775981-179775982	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182250235	chr2:179776016-179776017	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544603640	chr2:179776020-179776021	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536378409	chr2:179776021-179776022	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187636974	chr2:179776116-179776117	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530414819	chr2:179776246-179776247	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113396412	chr2:179776279-179776280	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10167882	chr2:179776290-179776291	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs192616749	chr2:179776312-179776313	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528209258	chr2:179776324-179776325	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76645685	chr2:179776339-179776340	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571300919	chr2:179776383-179776384	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537034695	chr2:179776407-179776408	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78123462	chr2:179776408-179776409	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556534147	chr2:179776458-179776459	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567224096	chr2:179776463-179776464	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536099543	chr2:179776484-179776485	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10167919	chr2:179776492-179776493	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572922957	chr2:179776536-179776537	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538804337	chr2:179776557-179776558	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114560537	chr2:179776592-179776593	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567982820	chr2:179776623-179776624	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185108588	chr2:179776648-179776649	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544664996	chr2:179776699-179776700	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561220189	chr2:179776717-179776718	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575223297	chr2:179776861-179776862	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58397865	chr2:179776864-179776865	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536948837	chr2:179776927-179776928	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372620898	chr2:179776985-179776986	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188825431	chr2:179777032-179777033	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74911159	chr2:179777035-179777036	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143897500	chr2:179777067-179777068	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564684342	chr2:179777079-179777080	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530473602	chr2:179777125-179777126	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200793860	chr2:179777229-179777230	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374205095	chr2:179777257-179777258	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12999923	chr2:179777279-179777280	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs80178659	chr2:179777292-179777293	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566887878	chr2:179777307-179777308	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536162685	chr2:179777335-179777336	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546604097	chr2:179777383-179777384	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147251949	chr2:179777389-179777390	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538498795	chr2:179777414-179777415	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377710583	chr2:179777430-179777431	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192701812	chr2:179777446-179777447	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179710800-179782800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr2:179713400-179778600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr2:179717000-179790600	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr2:179733200-179779200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr2:179749800-179785200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr2:179761200-179782800	Weak transcription	Right Ventricle	heart
7	chr2:179770000-179788600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:179770000-179848200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr2:179770200-179789200	Weak transcription	Primary B cells from cord blood	blood
10	chr2:179771600-179781600	Weak transcription	Lung	lung
11	chr2:179772200-179779800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr2:179773200-179776200	Enhancers	HSMMtube	muscle
13	chr2:179774000-179776200	Enhancers	Fetal Heart	heart
14	chr2:179774600-179776200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr2:179774600-179776600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr2:179775000-179779000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:179775200-179776000	Enhancers	Psoas Muscle	Psoas
18	chr2:179775200-179776200	Strong transcription	Primary T cells from cord blood	blood
19	chr2:179775400-179776200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:179775400-179777000	Weak transcription	HSMM	muscle
21	chr2:179775600-179780200	Weak transcription	Right Atrium	heart
22	chr2:179775600-179782400	Weak transcription	Fetal Muscle Leg	muscle
23	chr2:179775600-179824200	Weak transcription	Left Ventricle	heart
24	chr2:179775600-179826400	Weak transcription	Pancreas	Pancrea
25	chr2:179775800-179777000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:179776000-179776200	Enhancers	Aorta	Aorta
27	chr2:179776000-179776400	Weak transcription	Psoas Muscle	Psoas
28	chr2:179776200-179777400	Weak transcription	HSMMtube	muscle
29	chr2:179776200-179777600	Weak transcription	Aorta	Aorta
30	chr2:179776200-179777800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:179776200-179780400	Weak transcription	Primary T cells from cord blood	blood
32	chr2:179776200-179783000	Weak transcription	Fetal Heart	heart
33	chr2:179776400-179776600	Enhancers	Psoas Muscle	Psoas
34	chr2:179776600-179777400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr2:179776600-179777600	Weak transcription	Psoas Muscle	Psoas
36	chr2:179776800-179777800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr2:179776800-179778000	Enhancers	HMEC	breast
38	chr2:179777000-179777800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:179777000-179778000	Enhancers	NHDF-Ad	bronchial
40	chr2:179777000-179778800	Enhancers	HSMM	muscle
41	chr2:179777200-179777600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr2:179777400-179777800	Enhancers	NHEK	skin
43	chr2:179777400-179777800	Enhancers	NHLF	lung
44	chr2:179777400-179778000	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr2:179777400-179778000	Enhancers	HSMMtube	muscle
46	chr2:179777400-179778000	Enhancers	Osteobl	bone
47	chr2:179777400-179778600	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr2:179777400-179779400	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr2:179777600-179777800	Enhancers	Psoas Muscle	Psoas
50	chr2:179777600-179778000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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