Variant report

Variant	esv3392751
Chromosome Location	chr5:179560495-179563780
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	BACH1	chr5:179561454-179561491	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr5:179560620-179560770	MCF-7	breast:	n/a	n/a
3	CTCF	chr5:179562440-179562590	HMEC	breast:	n/a	n/a
4	CTCF	chr5:179561460-179561610	GM12871	blood:	n/a	chr5:179561463-179561481
5	CTCF	chr5:179561534-179561544	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr5:179562474-179562546	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:179562460-179562610	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:179561180-179561330	GM12866	blood:	n/a	n/a
9	CTCF	chr5:179560700-179560850	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr5:179561429-179561526	K562	blood:	n/a	chr5:179561463-179561481
11	CTCF	chr5:179561428-179561587	K562	blood:	n/a	chr5:179561463-179561481
12	E2F4	chr5:179562286-179562376	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F6	chr5:179563699-179564357	H1-hESC	embryonic stem cell:	n/a	n/a
14	EGR1	chr5:179562094-179562745	MCF-7	breast:	n/a	chr5:179562472-179562486 chr5:179562474-179562483 chr5:179562474-179562484 chr5:179562474-179562485 chr5:179562473-179562486
15	EGR1	chr5:179561920-179562634	HCT-116	colon:	n/a	chr5:179562472-179562486 chr5:179562474-179562483 chr5:179562474-179562484 chr5:179562474-179562485 chr5:179562473-179562486
16	EGR1	chr5:179562123-179562601	ECC-1	luminal epithelium:	n/a	chr5:179562472-179562486 chr5:179562474-179562483 chr5:179562474-179562484 chr5:179562474-179562485 chr5:179562473-179562486
17	EGR1	chr5:179562082-179562687	ECC-1	luminal epithelium:	n/a	chr5:179562472-179562486 chr5:179562474-179562483 chr5:179562474-179562484 chr5:179562474-179562485 chr5:179562473-179562486
18	ELF1	chr5:179561913-179563218	MCF-7	breast:	n/a	n/a
19	ESR1	chr5:179562077-179562707	ECC-1	luminal epithelium:	n/a	n/a
20	ESR1	chr5:179562138-179562433	ECC-1	luminal epithelium:	n/a	n/a
21	FOS	chr5:179562107-179562433	MCF10A-Er-Src	breast:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562248-179562259
22	FOS	chr5:179562092-179562450	HUVEC	blood vessel:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562248-179562259
23	FOS	chr5:179562080-179562434	MCF10A-Er-Src	breast:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562248-179562259
24	FOS	chr5:179562118-179562415	MCF10A-Er-Src	breast:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562248-179562259
25	FOS	chr5:179562111-179562459	MCF10A-Er-Src	breast:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562248-179562259
26	FOSL2	chr5:179562023-179562579	MCF-7	breast:	n/a	chr5:179562250-179562258 chr5:179562249-179562259 chr5:179562249-179562259 chr5:179562249-179562259
27	GABPA	chr5:179562004-179562545	MCF-7	breast:	n/a	chr5:179562472-179562481
28	HMGN3	chr5:179563598-179563662	K562	blood:	n/a	n/a
29	MAFF	chr5:179561381-179561450	K562	blood:	n/a	n/a
30	MAFK	chr5:179562198-179562324	IMR90	lung:	n/a	n/a
31	MAX	chr5:179562121-179562500	NB4	blood:	n/a	chr5:179562471-179562481
32	MAX	chr5:179561955-179562772	MCF-7	breast:	n/a	chr5:179562471-179562481
33	MAX	chr5:179563731-179564129	K562	blood:	n/a	n/a
34	MAZ	chr5:179561524-179562553	IMR90	lung:	n/a	chr5:179561566-179561576 chr5:179561567-179561576 chr5:179562471-179562481 chr5:179561567-179561576 chr5:179561566-179561577 chr5:179561568-179561575 chr5:179561566-179561577 chr5:179561567-179561577 chr5:179561566-179561577
35	MYC	chr5:179562246-179562560	MCF-7	breast:	n/a	chr5:179562471-179562481
36	MYC	chr5:179562216-179562498	MCF-7	breast:	n/a	chr5:179562471-179562481
37	MYC	chr5:179562031-179562560	MCF10A-Er-Src	breast:	n/a	chr5:179562471-179562481
38	MYC	chr5:179562074-179562434	NB4	blood:	n/a	n/a
39	NFYA	chr5:179563706-179563993	K562	blood:	n/a	chr5:179563837-179563855 chr5:179563907-179563925
40	NFYB	chr5:179563692-179564013	K562	blood:	n/a	n/a
41	NR2F2	chr5:179561974-179563355	MCF-7	breast:	n/a	n/a
42	POLR2A	chr5:179562071-179562478	HCT-116	colon:	n/a	n/a
43	POLR2A	chr5:179562686-179562785	MCF-7	breast:	n/a	n/a
44	POLR2A	chr5:179562249-179562301	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr5:179562171-179562601	MCF-7	breast:	n/a	n/a
46	POLR2A	chr5:179562355-179562443	Gliobla	brain:	n/a	n/a
47	POLR2A	chr5:179562090-179562417	U87	brain:	n/a	n/a
48	POLR2A	chr5:179562228-179562513	ECC-1	luminal epithelium:	n/a	n/a
49	POLR2A	chr5:179562069-179562511	HCT-116	colon:	n/a	n/a
50	RCOR1	chr5:179560391-179560518	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179562118-179562168	AG09319	gingival:	n/a
2	chr5:179563200-179563250	GM12891	blood:	n/a
3	chr5:179562118-179562168	AG09319	gingival:	n/a
4	chr5:179563200-179563250	GM12891	blood:	n/a
5	chr5:179562118-179562168	GM12878	blood:	n/a
6	chr5:179563200-179563250	GM06990	blood:	n/a
7	chr5:179562620-179562670	H1-hESC	embryonic stem cell:	embryo
8	chr5:179563745-179563795	Caco-2	colon:	n/a
9	chr5:179563738-179563788	T-47D	breast:	n/a
10	chr5:179563738-179563788	MCF-7	breast:	n/a
11	chr5:179563200-179563250	K562	blood:	n/a
12	chr5:179562118-179562168	HMEC	breast:	n/a
13	chr5:179563745-179563795	NB4	blood:	n/a
14	chr5:179563200-179563250	NT2-D1	testis:	n/a
15	chr5:179562118-179562168	ovcar-3	ovarian:	n/a
16	chr5:179563745-179563795	IMR90	lung:	fetal
17	chr5:179563200-179563250	NHDF-neo	bronchial:	n/a
18	chr5:179562118-179562168	ProgFib	skin:	n/a
19	chr5:179562620-179562670	HCPEpiC	choroid plexus:	n/a
20	chr5:179562118-179562168	PANC-1	pancreas:	n/a
21	chr5:179562620-179562670	NT2-D1	testis:	n/a
22	chr5:179563497-179563547	HCM	heart:	n/a
23	chr5:179563200-179563250	AG04449	skin:	fetal
24	chr5:179563745-179563795	AoSMC	blood vessel:	n/a
25	chr5:179562620-179562670	T-47D	breast:	n/a
26	chr5:179563497-179563547	HUVEC	blood vessel:	n/a
27	chr5:179562620-179562670	HCT-116	colon:	n/a
28	chr5:179562620-179562670	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:179563738-179563788	SK-N-SH	brain:	n/a
30	chr5:179562118-179562168	HCM	heart:	n/a
31	chr5:179562118-179562168	Jurkat	blood:	n/a
32	chr5:179563738-179563788	HepG2	liver:	n/a
33	chr5:179563745-179563795	HCF	heart:	n/a
34	chr5:179563200-179563250	SK-N-SH	brain:	n/a
35	chr5:179562118-179562168	Hepatocyte	liver:	n/a
36	chr5:179562118-179562168	AG04450	lung:	fetal
37	chr5:179562620-179562670	ECC-1	luminal epithelium:	n/a
38	chr5:179563738-179563788	HCT-116	colon:	n/a
39	chr5:179562118-179562168	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:179563745-179563795	HCT-116	colon:	n/a
41	chr5:179563200-179563250	CMK	blood:	n/a
42	chr5:179563745-179563795	ovcar-3	ovarian:	n/a
43	chr5:179563738-179563788	CMK	blood:	n/a
44	chr5:179562118-179562168	ECC-1	luminal epithelium:	n/a
45	chr5:179563497-179563547	A549	lung:	n/a
46	chr5:179563738-179563788	HL-60	blood:	n/a
47	chr5:179563738-179563788	AG04450	lung:	fetal
48	chr5:179563497-179563547	AG09309	skin:	n/a
49	chr5:179563200-179563250	AG09309	skin:	n/a
50	chr5:179562118-179562168	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:179560653..179562263-chr5:179716326..179719288,2	MCF-7	breast:
2	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
3	chr5:179551435..179553864-chr5:179559199..179562159,2	K562	blood:
4	chr5:179551929..179554732-chr5:179557989..179560690,2	K562	blood:
5	chr5:179558293..179560674-chr5:179562402..179565370,2	MCF-7	breast:

Variant related genes	Relation type
RASGEF1C	TF binding region
RASGEF1C	CpG island
ENSG00000146090	chromatin interactions
ENSG00000050748	chromatin interactions

Extended variants
information (count: 169 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:169 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182846303	chr5:179560513-179560514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561628242	chr5:179560536-179560537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530458384	chr5:179560574-179560575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548599744	chr5:179560587-179560588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568701113	chr5:179560625-179560626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534579076	chr5:179560626-179560627	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534117607	chr5:179560641-179560642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368796084	chr5:179560655-179560656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs186992869	chr5:179560691-179560692	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570636989	chr5:179560709-179560710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147385445	chr5:179560719-179560720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs137994972	chr5:179560802-179560803	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574486537	chr5:179560834-179560835	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557707496	chr5:179560835-179560836	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553765065	chr5:179560908-179560909	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572269363	chr5:179560973-179560974	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577582680	chr5:179560979-179560980	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559998954	chr5:179560996-179560997	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs143458978	chr5:179561021-179561022	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs59917820	chr5:179561041-179561042	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs191467124	chr5:179561078-179561079	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538029090	chr5:179561095-179561096	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs55766469	chr5:179561103-179561104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs369201631	chr5:179561106-179561107	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561713181	chr5:179561122-179561123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528874318	chr5:179561126-179561127	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548899936	chr5:179561140-179561141	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11738961	chr5:179561189-179561190	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147138997	chr5:179561263-179561264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552502669	chr5:179561325-179561326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115964400	chr5:179561329-179561330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556654510	chr5:179561359-179561360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376652197	chr5:179561365-179561366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537994314	chr5:179561374-179561375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139623532	chr5:179561420-179561421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374304056	chr5:179561423-179561424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183682083	chr5:179561448-179561449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113881439	chr5:179561494-179561495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554106865	chr5:179561500-179561501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144556783	chr5:179561519-179561520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368206515	chr5:179561589-179561590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539678289	chr5:179561595-179561596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558025245	chr5:179561627-179561628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200400509	chr5:179561644-179561645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6883804	chr5:179561647-179561648	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543572486	chr5:179561653-179561654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148448111	chr5:179561693-179561694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201431696	chr5:179561732-179561733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13176496	chr5:179561836-179561837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186967325	chr5:179561838-179561839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Acute lymphoblastic leukemia	20435627	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
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	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179555400-179560800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:179555400-179571000	Weak transcription	Right Atrium	heart
3	chr5:179556800-179562400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr5:179556800-179566600	Weak transcription	Brain Angular Gyrus	brain
5	chr5:179557000-179562000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:179557000-179562200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr5:179557200-179562000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:179559600-179565800	Weak transcription	Fetal Brain Female	brain
9	chr5:179560000-179561400	Enhancers	Placenta	Placenta
10	chr5:179560800-179561200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:179561200-179562200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:179561800-179562200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:179561800-179562800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr5:179561800-179563000	Enhancers	Osteobl	bone
15	chr5:179561800-179563200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:179561800-179563200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:179562000-179562200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:179562000-179562400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:179562000-179562600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:179562000-179562600	Enhancers	Primary hematopoietic stem cells	blood
21	chr5:179562000-179562600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:179562000-179562600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:179562000-179562600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr5:179562000-179562600	Enhancers	Gastric	stomach
25	chr5:179562000-179562600	Enhancers	HUVEC	blood vessel
26	chr5:179562000-179562800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:179562000-179562800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr5:179562000-179562800	Enhancers	NH-A	brain
29	chr5:179562000-179563200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:179562000-179563200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr5:179562000-179564200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr5:179562200-179562600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:179562200-179562600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr5:179562200-179562600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:179562200-179562600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr5:179562200-179562600	Enhancers	Esophagus	oesophagus
37	chr5:179562200-179562600	Enhancers	NHEK	skin
38	chr5:179562200-179562800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:179562200-179562800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chr5:179562200-179562800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:179562200-179562800	Enhancers	Brain Hippocampus Middle	brain
42	chr5:179562200-179562800	Enhancers	Brain Substantia Nigra	brain
43	chr5:179562200-179562800	Enhancers	HMEC	breast
44	chr5:179562200-179562800	Enhancers	HSMM	muscle
45	chr5:179562200-179563000	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:179562200-179563200	Enhancers	Fetal Muscle Leg	muscle
47	chr5:179562200-179564000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:179562400-179562600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr5:179562400-179562600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
50	chr5:179562400-179562800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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