Variant report

Variant	nsv600670
Chromosome Location	chr5:180047412-180063743
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	CREB1	chr5:180058933-180059230	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr5:180057425-180057500	H1-hESC	embryonic stem cell:	n/a	chr5:180057427-180057440 chr5:180057482-180057495
3	CTCF	chr5:180062384-180062431	GM19239	blood:	n/a	n/a
4	CTCF	chr5:180057580-180057730	GM12865	blood:	n/a	n/a
5	CTCF	chr5:180060903-180061058	K562	blood:	n/a	n/a
6	CTCF	chr5:180051640-180051790	HEK293	kidney:	n/a	chr5:180051657-180051670 chr5:180051664-180051677
7	CTCF	chr5:180051660-180051774	H1-hESC	embryonic stem cell:	n/a	chr5:180051664-180051677
8	CTCF	chr5:180051672-180051766	GM12891	blood:	n/a	n/a
9	CTCF	chr5:180051580-180051730	MCF-7	breast:	n/a	chr5:180051657-180051670 chr5:180051664-180051677
10	CTCF	chr5:180051679-180051730	MCF-7	breast:	n/a	n/a
11	CTCF	chr5:180060900-180061050	HepG2	liver:	n/a	n/a
12	CTCF	chr5:180051718-180051778	GM10266	blood:	n/a	n/a
13	CTCF	chr5:180060860-180061010	K562	blood:	n/a	n/a
14	E2F6	chr5:180048580-180048713	K562	blood:	n/a	n/a
15	EGR1	chr5:180047580-180047868	K562	blood:	n/a	chr5:180047717-180047727
16	EGR1	chr5:180056713-180056931	K562	blood:	n/a	chr5:180056854-180056868 chr5:180056856-180056867
17	ELF1	chr5:180050410-180050691	K562	blood:	n/a	chr5:180050509-180050522 chr5:180050511-180050522 chr5:180050479-180050490 chr5:180050510-180050521 chr5:180050478-180050491
18	ELF1	chr5:180050383-180050661	K562	blood:	n/a	chr5:180050509-180050522 chr5:180050511-180050522 chr5:180050479-180050490 chr5:180050510-180050521 chr5:180050478-180050491
19	FOSL2	chr5:180063326-180063936	SK-N-SH	brain:	n/a	n/a
20	FOXP2	chr5:180059565-180060038	PFSK-1	brain:	n/a	n/a
21	JUND	chr5:180063364-180063962	SK-N-SH	brain:	n/a	n/a
22	MAX	chr5:180053648-180053853	K562	blood:	n/a	n/a
23	MAX	chr5:180058776-180059089	K562	blood:	n/a	chr5:180058910-180058920 chr5:180058910-180058919 chr5:180058910-180058917
24	NFIC	chr5:180051521-180052077	ECC-1	luminal epithelium:	n/a	chr5:180051814-180051830 chr5:180051813-180051830
25	POLR2A	chr5:180047870-180047893	MCF-7	breast:	n/a	n/a
26	POLR2A	chr5:180057015-180057092	MCF-7	breast:	n/a	n/a
27	RAD21	chr5:180060908-180061074	K562	blood:	n/a	n/a
28	SPI1	chr5:180050427-180050636	K562	blood:	n/a	chr5:180050484-180050497 chr5:180050509-180050522 chr5:180050512-180050521 chr5:180050510-180050523
29	SPI1	chr5:180050272-180050755	HL-60	blood:	n/a	chr5:180050484-180050497 chr5:180050509-180050522 chr5:180050512-180050521 chr5:180050510-180050523
30	SPI1	chr5:180050379-180050595	K562	blood:	n/a	chr5:180050484-180050497 chr5:180050509-180050522 chr5:180050512-180050521 chr5:180050510-180050523
31	TCF12	chr5:180063264-180064019	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180050565-180050615	GM12891	blood:	n/a
2	chr5:180050565-180050615	GM12891	blood:	n/a
3	chr5:180050565-180050615	NB4	blood:	n/a
4	chr5:180057594-180057644	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:180047407-180047457	AoSMC	blood vessel:	n/a
6	chr5:180055850-180055900	T-47D	breast:	n/a
7	chr5:180057303-180057353	GM19239	blood:	n/a
8	chr5:180047686-180047736	PFSK-1	brain:	n/a
9	chr5:180052364-180052414	A549	lung:	n/a
10	chr5:180056580-180056630	Hepatocyte	liver:	n/a
11	chr5:180056522-180056572	SAEC	small airway:	n/a
12	chr5:180055850-180055900	Hepatocyte	liver:	n/a
13	chr5:180055850-180055900	PrEC	prostate:	n/a
14	chr5:180055982-180056032	NHBE	bronchial:	n/a
15	chr5:180048155-180048205	IMR90	lung:	fetal
16	chr5:180057034-180057084	LNCaP	prostate:	n/a
17	chr5:180056522-180056572	HCT-116	colon:	n/a
18	chr5:180059096-180059146	HEK293	kidney:	embryo
19	chr5:180056580-180056630	HCT-116	colon:	n/a
20	chr5:180057303-180057353	Hepatocyte	liver:	n/a
21	chr5:180056301-180056351	Hela-S3	cervix:	n/a
22	chr5:180056522-180056572	SK-N-SH_RA	brain:	n/a
23	chr5:180057034-180057084	GM12892	blood:	n/a
24	chr5:180057594-180057644	LNCaP	prostate:	n/a
25	chr5:180056040-180056090	SK-N-SH_RA	brain:	n/a
26	chr5:180056522-180056572	AG04450	lung:	fetal
27	chr5:180055982-180056032	RPTEC	kidney:	n/a
28	chr5:180056522-180056572	HMEC	breast:	n/a
29	chr5:180047686-180047736	U87	brain:	n/a
30	chr5:180052364-180052414	HepG2	liver:	n/a
31	chr5:180047798-180047848	K562	blood:	n/a
32	chr5:180048893-180048943	NT2-D1	testis:	n/a
33	chr5:180057303-180057353	NT2-D1	testis:	n/a
34	chr5:180055850-180055900	Caco-2	colon:	n/a
35	chr5:180056040-180056090	GM12891	blood:	n/a
36	chr5:180048893-180048943	PFSK-1	brain:	n/a
37	chr5:180050565-180050615	MCF10A-Er-Src	breast:	n/a
38	chr5:180057034-180057084	Hela-S3	cervix:	n/a
39	chr5:180055850-180055900	HRPEpiC	eye:	n/a
40	chr5:180059096-180059146	AG04450	lung:	fetal
41	chr5:180053982-180054032	HNPCEpiC	eye:	n/a
42	chr5:180056301-180056351	HEEpiC	esophagus:	n/a
43	chr5:180047407-180047457	AG09309	skin:	n/a
44	chr5:180056580-180056630	HNPCEpiC	eye:	n/a
45	chr5:180050565-180050615	AG04450	lung:	fetal
46	chr5:180057034-180057084	ovcar-3	ovarian:	n/a
47	chr5:180057303-180057353	IMR90	lung:	fetal
48	chr5:180050565-180050615	K562	blood:	n/a
49	chr5:180048155-180048205	Jurkat	blood:	n/a
50	chr5:180056522-180056572	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr5:180047660..180049691-chr5:180056996..180059691,2	K562	blood:
2	chr5:180048663..180050730-chr5:180113911..180116171,2	K562	blood:
3	chr5:180046012..180054191-chr5:180056996..180060440,8	K562	blood:
4	chr5:179799196..179802015-chr5:180050331..180053003,2	MCF-7	breast:
5	chr5:180051235..180053741-chr5:180054610..180058069,3	K562	blood:
6	chr5:180047630..180050366-chr5:180050889..180052970,2	K562	blood:
7	chr5:179921107..179922607-chr5:180049466..180050983,2	MCF-7	breast:
8	chr5:180047630..180050366-chr5:180050889..180052970,2	K562	blood:
9	chr5:180048401..180050293-chr5:180059742..180062204,2	MCF-7	breast:
10	chr5:180030276..180031977-chr5:180049658..180052103,2	MCF-7	breast:
11	chr5:180048401..180050293-chr5:180059742..180062204,2	MCF-7	breast:
12	chr5:180044847..180047372-chr5:180048996..180050512,2	K562	blood:
13	chr5:180052176..180054289-chr5:180056133..180059074,3	MCF-7	breast:
14	chr5:180047660..180049691-chr5:180056996..180059691,2	K562	blood:

Variant related genes	Relation type
FLT4	TF binding region
FLT4	CpG island
ENSG00000037280	chromatin interactions
ENSG00000113300	chromatin interactions

Extended variants
information (count: 1076 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1076 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs382266	chr5:180047412-180047413	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545911664	chr5:180047414-180047415	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs562745219	chr5:180047429-180047430	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs142502226	chr5:180047448-180047449	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs576142860	chr5:180047449-180047450	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs151017458	chr5:180047450-180047451	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs371285234	chr5:180047472-180047473	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575203390	chr5:180047473-180047474	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146582558	chr5:180047553-180047554	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376696560	chr5:180047560-180047561	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35096491	chr5:180047564-180047565	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140880453	chr5:180047570-180047571	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143420734	chr5:180047584-180047585	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542137668	chr5:180047586-180047587	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs146726877	chr5:180047587-180047588	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs140327027	chr5:180047588-180047589	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs145063070	chr5:180047599-180047600	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs138792259	chr5:180047601-180047602	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs148937087	chr5:180047607-180047608	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143655361	chr5:180047620-180047621	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148178465	chr5:180047621-180047622	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs561809492	chr5:180047632-180047633	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs140668517	chr5:180047639-180047640	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs371032164	chr5:180047666-180047667	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs527697511	chr5:180047668-180047669	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200449328	chr5:180047669-180047670	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs144102777	chr5:180047674-180047675	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs147312865	chr5:180047685-180047686	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139263798	chr5:180047687-180047688	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs143171174	chr5:180047702-180047703	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs144822344	chr5:180047710-180047711	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs150754113	chr5:180047716-180047717	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs139080773	chr5:180047732-180047733	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs141972439	chr5:180047739-180047740	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs66507436	chr5:180047740-180047741	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs68082749	chr5:180047747-180047748	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs67805218	chr5:180047749-180047750	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs148914380	chr5:180047754-180047755	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs57822329	chr5:180047757-180047758	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199518698	chr5:180047764-180047765	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs149890433	chr5:180047771-180047772	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs143867526	chr5:180047774-180047775	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs34419336	chr5:180047793-180047794	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs143507539	chr5:180047808-180047809	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs535644501	chr5:180047809-180047810	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs146745741	chr5:180047823-180047824	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs143550381	chr5:180047824-180047825	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs561291886	chr5:180047834-180047835	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs201357576	chr5:180047835-180047836	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs374635802	chr5:180047838-180047839	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180040000-180061200	Weak transcription	Gastric	stomach
2	chr5:180046000-180047600	Strong transcription	Lung	lung
3	chr5:180046000-180049600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr5:180046000-180050200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr5:180046200-180071800	Weak transcription	Liver	Liver
6	chr5:180046400-180049800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr5:180046400-180050000	Weak transcription	Primary T cells from cord blood	blood
8	chr5:180046400-180050600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr5:180046400-180051400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:180046400-180072200	Weak transcription	Right Atrium	heart
11	chr5:180046600-180049200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr5:180046800-180047800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:180046800-180048800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:180046800-180050200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr5:180046800-180050600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:180046800-180059600	Weak transcription	Pancreas	Pancrea
17	chr5:180047000-180047800	Strong transcription	Spleen	Spleen
18	chr5:180047000-180048800	Bivalent Enhancer	Placenta	Placenta
19	chr5:180047600-180048400	Weak transcription	Lung	lung
20	chr5:180047800-180048000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:180047800-180048000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:180047800-180048800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:180047800-180048800	ZNF genes & repeats	Spleen	Spleen
24	chr5:180048000-180048400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:180048400-180048800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:180048400-180048800	Strong transcription	Lung	lung
27	chr5:180048800-180049600	Weak transcription	Lung	lung
28	chr5:180048800-180049800	Weak transcription	Spleen	Spleen
29	chr5:180048800-180050200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:180048800-180050400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:180048800-180052200	Enhancers	Placenta	Placenta
32	chr5:180049200-180051200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr5:180049200-180051600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr5:180049600-180049800	Enhancers	Lung	lung
35	chr5:180049600-180051200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr5:180049600-180051800	Enhancers	Primary T cells fromperipheralblood	blood
37	chr5:180049800-180050800	Genic enhancers	Lung	lung
38	chr5:180049800-180051200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr5:180049800-180051600	Enhancers	Fetal Muscle Trunk	muscle
40	chr5:180049800-180051800	Enhancers	Spleen	Spleen
41	chr5:180050000-180050800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr5:180050000-180050800	Enhancers	Dnd41	blood
43	chr5:180050000-180051000	Enhancers	Primary T cells from cord blood	blood
44	chr5:180050000-180051200	Enhancers	HUVEC	blood vessel
45	chr5:180050000-180051600	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr5:180050000-180051800	Enhancers	Fetal Muscle Leg	muscle
47	chr5:180050000-180051800	Enhancers	Left Ventricle	heart
48	chr5:180050000-180052800	Enhancers	Adipose Nuclei	Adipose
49	chr5:180050000-180052800	Enhancers	Right Ventricle	heart
50	chr5:180050200-180050800	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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