Variant report

Variant	nsv1023259
Chromosome Location	chr5:12483982-12578638
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:230)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:230 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:12573954-12574062	K562	blood:	n/a	n/a
2	BCL11A	chr5:12505213-12505415	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:12574678-12575143	K562	blood:	n/a	n/a
4	CBX3	chr5:12574582-12575256	K562	blood:	n/a	n/a
5	CCNT2	chr5:12574035-12574280	K562	blood:	n/a	n/a
6	CCNT2	chr5:12574667-12575084	K562	blood:	n/a	n/a
7	CEBPB	chr5:12566667-12566990	HepG2	liver:	n/a	chr5:12566765-12566776
8	CEBPB	chr5:12503100-12503364	A549	lung:	n/a	chr5:12503277-12503288
9	CEBPB	chr5:12503180-12503352	HepG2	liver:	n/a	chr5:12503277-12503288
10	CEBPB	chr5:12575018-12575331	K562	blood:	n/a	n/a
11	CEBPB	chr5:12566709-12566868	A549	lung:	n/a	chr5:12566765-12566776
12	CEBPB	chr5:12566709-12566828	H1-hESC	embryonic stem cell:	n/a	chr5:12566765-12566776
13	CEBPB	chr5:12505166-12505427	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:12566600-12566907	Hela-S3	cervix:	n/a	chr5:12566765-12566776
15	CEBPB	chr5:12540762-12541082	HepG2	liver:	n/a	chr5:12540898-12540909
16	CEBPB	chr5:12501654-12501824	HepG2	liver:	n/a	chr5:12501682-12501693 chr5:12501680-12501691
17	CHD2	chr5:12574604-12575169	K562	blood:	n/a	n/a
18	CTCF	chr5:12505852-12505885	GM10248	blood:	n/a	n/a
19	CTCF	chr5:12541880-12542030	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr5:12486616-12486651	ProgFib	skin:	n/a	n/a
21	CTCF	chr5:12535540-12535690	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:12532680-12532830	GM12867	blood:	n/a	n/a
23	CTCF	chr5:12530620-12530770	GM12864	blood:	n/a	n/a
24	CTCF	chr5:12574029-12574111	K562	blood:	n/a	n/a
25	CTCF	chr5:12573949-12574147	K562	blood:	n/a	n/a
26	CTCF	chr5:12510211-12510275	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:12538324-12538394	Lung_OC	lung:	n/a	n/a
28	CTCF	chr5:12574000-12574150	K562	blood:	n/a	n/a
29	E2F4	chr5:12570967-12571208	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr5:12566638-12566925	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr5:12522352-12522485	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F6	chr5:12574021-12574203	K562	blood:	n/a	n/a
33	E2F6	chr5:12574510-12575158	K562	blood:	n/a	chr5:12574962-12574973 chr5:12574947-12574958
34	E2F6	chr5:12574526-12575252	K562	blood:	n/a	chr5:12574962-12574973 chr5:12574947-12574958
35	E2F6	chr5:12574594-12575135	K562	blood:	n/a	chr5:12574962-12574973 chr5:12574947-12574958
36	EGR1	chr5:12574580-12575024	K562	blood:	n/a	n/a
37	EGR1	chr5:12574545-12574914	K562	blood:	n/a	n/a
38	EGR1	chr5:12573991-12574213	K562	blood:	n/a	n/a
39	ELF1	chr5:12574639-12575189	K562	blood:	n/a	chr5:12574920-12574933
40	ELF1	chr5:12574634-12575134	K562	blood:	n/a	chr5:12574920-12574933
41	ELK1	chr5:12574717-12575112	K562	blood:	n/a	n/a
42	EP300	chr5:12574788-12574977	K562	blood:	n/a	n/a
43	EP300	chr5:12573055-12573209	GM12878	blood:	n/a	n/a
44	EP300	chr5:12574704-12575037	T-47D	breast:	n/a	n/a
45	ETS1	chr5:12574770-12575099	K562	blood:	n/a	n/a
46	ETS1	chr5:12574653-12574905	GM12878	blood:	n/a	n/a
47	FOS	chr5:12526247-12526613	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr5:12522204-12522606	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr5:12522180-12522843	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:12526253-12526596	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:12574688-12574738	PrEC	prostate:	n/a
2	chr5:12574688-12574738	HCF	heart:	n/a
3	chr5:12574872-12574922	HAEpiC	amniotic membrane:	n/a
4	chr5:12574872-12574922	PrEC	prostate:	n/a
5	chr5:12574872-12574922	MCF10A-Er-Src	breast:	n/a
6	chr5:12574688-12574738	AG09319	gingival:	n/a
7	chr5:12574872-12574922	SK-N-SH	brain:	n/a
8	chr5:12574872-12574922	NHBE	bronchial:	n/a
9	chr5:12574688-12574738	HNPCEpiC	eye:	n/a
10	chr5:12574872-12574922	T-47D	breast:	n/a
11	chr5:12574688-12574738	NHDF-neo	bronchial:	n/a
12	chr5:12574872-12574922	HL-60	blood:	n/a
13	chr5:12574688-12574738	SK-N-MC	brain:	n/a
14	chr5:12574872-12574922	SAEC	small airway:	n/a
15	chr5:12574872-12574922	BJ	skin:	n/a
16	chr5:12574688-12574738	AoSMC	blood vessel:	n/a
17	chr5:12574688-12574738	AG04449	skin:	fetal
18	chr5:12574688-12574738	AG04450	lung:	fetal
19	chr5:12574688-12574738	IMR90	lung:	fetal
20	chr5:12574872-12574922	H1-hESC	embryonic stem cell:	embryo
21	chr5:12574872-12574922	Jurkat	blood:	n/a
22	chr5:12574872-12574922	HUVEC	blood vessel:	n/a
23	chr5:12574872-12574922	HCT-116	colon:	n/a
24	chr5:12574872-12574922	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:12574688-12574738	GM12878	blood:	n/a
26	chr5:12574872-12574922	HRCEpiC	kidney:	n/a
27	chr5:12574872-12574922	NHDF-neo	bronchial:	n/a
28	chr5:12574872-12574922	GM19239	blood:	n/a
29	chr5:12574688-12574738	HMEC	breast:	n/a
30	chr5:12574872-12574922	AoSMC	blood vessel:	n/a
31	chr5:12574688-12574738	GM19239	blood:	n/a
32	chr5:12574688-12574738	RPTEC	kidney:	n/a
33	chr5:12574872-12574922	NT2-D1	testis:	n/a
34	chr5:12574688-12574738	HIPEpiC	eye:	n/a
35	chr5:12574688-12574738	K562	blood:	n/a
36	chr5:12574688-12574738	ovcar-3	ovarian:	n/a
37	chr5:12574872-12574922	CMK	blood:	n/a
38	chr5:12574688-12574738	HEEpiC	esophagus:	n/a
39	chr5:12574688-12574738	Jurkat	blood:	n/a
40	chr5:12574688-12574738	HCT-116	colon:	n/a
41	chr5:12574872-12574922	HMEC	breast:	n/a
42	chr5:12574688-12574738	HCPEpiC	choroid plexus:	n/a
43	chr5:12574688-12574738	PANC-1	pancreas:	n/a
44	chr5:12574872-12574922	ProgFib	skin:	n/a
45	chr5:12574872-12574922	Hepatocyte	liver:	n/a
46	chr5:12574872-12574922	ECC-1	luminal epithelium:	n/a
47	chr5:12574872-12574922	K562	blood:	n/a
48	chr5:12574688-12574738	GM12891	blood:	n/a
49	chr5:12574688-12574738	AG09309	skin:	n/a
50	chr5:12574872-12574922	HCF	heart:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:12569399..12571855-chr5:12571987..12574855,2	K562	blood:
2	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
3	chr5:12566855..12569678-chr5:12570834..12573967,4	MCF-7	breast:
4	chr5:12577735..12580318-chr5:12581576..12583762,3	K562	blood:
5	chr5:12542323..12544151-chr5:12547320..12550095,2	K562	blood:
6	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
7	chr5:12542323..12544151-chr5:12547320..12550095,2	K562	blood:
8	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
9	chr5:12562087..12563881-chr5:12566086..12568996,3	K562	blood:
10	chr5:12560874..12562617-chr5:12573988..12576942,2	K562	blood:
11	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
12	chr5:12566855..12569678-chr5:12570834..12573967,4	MCF-7	breast:
13	chr5:12537002..12539656-chr5:12586201..12588814,2	K562	blood:
14	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
15	chr5:12572185..12574233-chr5:12590584..12592577,2	K562	blood:
16	chr5:12562087..12563881-chr5:12566086..12568996,3	K562	blood:
17	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
18	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
19	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
20	chr5:12573778..12576984-chr5:12577746..12580874,3	K562	blood:
21	chr5:12576312..12579149-chr5:12776108..12778231,2	K562	blood:
22	chr5:12474522..12476679-chr5:12488826..12490778,2	MCF-7	breast:
23	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
2	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
3	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
4	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100511
5	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100514

No data

Variant related genes	Relation type
ENSG00000248783	TF binding region
CT49	TF binding region
ENSG00000248783	CpG island
CT49	CpG island
ENSG00000248131	chromatin interactions
ENSG00000248783	chromatin interactions
ABL2	miRNA target sites
ARHGEF7	miRNA target sites
PSMD7	miRNA target sites

Extended variants
information (count: 1608 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35327802	chr5:12488204-12488205	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573134400	chr5:12488217-12488218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541451176	chr5:12488244-12488245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190471922	chr5:12488269-12488270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377344265	chr5:12488294-12488295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540794104	chr5:12488314-12488315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182201490	chr5:12488347-12488348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6554712	chr5:12488397-12488398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs532820457	chr5:12488403-12488404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551024749	chr5:12488404-12488405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562866954	chr5:12488405-12488406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73744668	chr5:12488408-12488409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs377160434	chr5:12488418-12488419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562161194	chr5:12488442-12488443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185204727	chr5:12488443-12488444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566978483	chr5:12488489-12488490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534328621	chr5:12488501-12488502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377483827	chr5:12488541-12488542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546811450	chr5:12488588-12488589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571377840	chr5:12488589-12488590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542851125	chr5:12501623-12501624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374665472	chr5:12501708-12501709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565308407	chr5:12501733-12501734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555174688	chr5:12501775-12501776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573443080	chr5:12501776-12501777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540939540	chr5:12501815-12501816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183344539	chr5:12501827-12501828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532555984	chr5:12501872-12501873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2022092	chr5:12501892-12501893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs372144147	chr5:12501969-12501970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79760805	chr5:12502002-12502003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6554714	chr5:12502067-12502068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561168374	chr5:12502069-12502070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144395758	chr5:12502076-12502077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546895439	chr5:12502106-12502107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187603159	chr5:12502119-12502120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538255218	chr5:12502123-12502124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550209091	chr5:12502142-12502143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80254115	chr5:12502195-12502196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536382178	chr5:12502241-12502242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537139374	chr5:12502245-12502246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377041381	chr5:12502357-12502358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554830918	chr5:12502362-12502363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558661665	chr5:12502405-12502406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2052522	chr5:12502417-12502418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576608742	chr5:12502421-12502422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193072387	chr5:12502422-12502423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550151069	chr5:12502430-12502431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114688548	chr5:12502469-12502470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544612209	chr5:12502504-12502505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:12488200-12488400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:12488200-12488600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:12501600-12505600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:12503400-12504600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr5:12504000-12505000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:12504200-12505000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:12504200-12507000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:12504400-12506200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:12504600-12505000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:12504600-12507400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr5:12505000-12505200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr5:12505000-12505200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr5:12505000-12506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr5:12505200-12505400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr5:12505200-12505400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:12505400-12505600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr5:12505400-12505800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr5:12505600-12505800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:12505600-12506400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:12505800-12506000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:12505800-12506400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:12507200-12507400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:12507600-12522400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:12509800-12511800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr5:12532200-12532800	ZNF genes & repeats	Pancreas	Pancrea
26	chr5:12535400-12535600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr5:12535600-12535800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr5:12562600-12569200	Weak transcription	Placenta	Placenta
29	chr5:12565600-12570400	Weak transcription	K562	blood
30	chr5:12567600-12568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:12569200-12570800	Strong transcription	Placenta	Placenta
32	chr5:12570400-12572400	Strong transcription	K562	blood
33	chr5:12570800-12573800	Weak transcription	Placenta	Placenta
34	chr5:12572400-12573000	Weak transcription	K562	blood
35	chr5:12573000-12576200	Active TSS	K562	blood
36	chr5:12573800-12575400	Active TSS	Placenta	Placenta
37	chr5:12576200-12577600	Weak transcription	K562	blood
38	chr5:12577800-12578000	ZNF genes & repeats	K562	blood
39	chr5:12578000-12581200	Weak transcription	K562	blood

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