Variant report

Variant	nsv1031685
Chromosome Location	chr5:17472891-17625621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1717)
CpG islands
(count:1037)
Chromatin interactive
region (count:4)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1717 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17526839-17526866	K562	blood:	n/a	n/a
2	ARID3A	chr5:17517830-17517852	K562	blood:	n/a	n/a
3	ATF1	chr5:17517811-17517870	K562	blood:	n/a	n/a
4	ATF1	chr5:17492224-17492379	K562	blood:	n/a	n/a
5	ATF3	chr5:17517759-17517894	K562	blood:	n/a	n/a
6	BACH1	chr5:17526845-17526876	K562	blood:	n/a	n/a
7	BATF	chr5:17528689-17530680	GM12878	blood:	n/a	n/a
8	BATF	chr5:17595530-17597898	GM12878	blood:	n/a	n/a
9	BATF	chr5:17581407-17582352	GM12878	blood:	n/a	n/a
10	BATF	chr5:17599128-17599665	GM12878	blood:	n/a	n/a
11	BATF	chr5:17583178-17585829	GM12878	blood:	n/a	n/a
12	BATF	chr5:17518382-17520848	GM12878	blood:	n/a	n/a
13	BATF	chr5:17525255-17528049	GM12878	blood:	n/a	n/a
14	BATF	chr5:17595471-17597904	GM12878	blood:	n/a	n/a
15	BATF	chr5:17521816-17524282	GM12878	blood:	n/a	n/a
16	BATF	chr5:17581436-17582365	GM12878	blood:	n/a	n/a
17	BATF	chr5:17586589-17586869	GM12878	blood:	n/a	n/a
18	BATF	chr5:17581115-17581413	GM12878	blood:	n/a	n/a
19	BATF	chr5:17525250-17527716	GM12878	blood:	n/a	n/a
20	BATF	chr5:17588369-17588646	GM12878	blood:	n/a	n/a
21	BATF	chr5:17520861-17521352	GM12878	blood:	n/a	n/a
22	BATF	chr5:17591814-17594470	GM12878	blood:	n/a	n/a
23	BATF	chr5:17583462-17585828	GM12878	blood:	n/a	n/a
24	BATF	chr5:17527729-17528285	GM12878	blood:	n/a	n/a
25	BATF	chr5:17581121-17581401	GM12878	blood:	n/a	n/a
26	BATF	chr5:17588661-17591031	GM12878	blood:	n/a	n/a
27	BATF	chr5:17524295-17524851	GM12878	blood:	n/a	n/a
28	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
29	BATF	chr5:17586875-17587277	GM12878	blood:	n/a	n/a
30	BATF	chr5:17599390-17599669	GM12878	blood:	n/a	n/a
31	BATF	chr5:17580902-17581080	GM12878	blood:	n/a	n/a
32	BATF	chr5:17518387-17521181	GM12878	blood:	n/a	n/a
33	BATF	chr5:17587321-17587686	GM12878	blood:	n/a	n/a
34	BATF	chr5:17528684-17530686	GM12878	blood:	n/a	n/a
35	BATF	chr5:17595225-17595440	GM12878	blood:	n/a	n/a
36	BATF	chr5:17588662-17591030	GM12878	blood:	n/a	n/a
37	BATF	chr5:17524307-17524569	GM12878	blood:	n/a	n/a
38	BATF	chr5:17592098-17594464	GM12878	blood:	n/a	n/a
39	BATF	chr5:17591806-17592083	GM12878	blood:	n/a	n/a
40	BATF	chr5:17583170-17583447	GM12878	blood:	n/a	n/a
41	BATF	chr5:17586583-17586881	GM12878	blood:	n/a	n/a
42	BATF	chr5:17586894-17587691	GM12878	blood:	n/a	n/a
43	BATF	chr5:17521821-17524301	GM12878	blood:	n/a	n/a
44	BATF	chr5:17595045-17595501	GM12878	blood:	n/a	n/a
45	BATF	chr5:17588377-17588634	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:17599180-17599635	GM12878	blood:	n/a	n/a
47	BCL11A	chr5:17586591-17587689	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:17528686-17530695	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:17525182-17528231	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:17591642-17594553	GM12878	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17485435-17485485	GM12878	blood:	n/a
2	chr5:17517201-17517251	GM12878	blood:	n/a
3	chr5:17517201-17517251	HIPEpiC	eye:	n/a
4	chr5:17604867-17604917	H1-hESC	embryonic stem cell:	embryo
5	chr5:17491941-17491991	IMR90	lung:	fetal
6	chr5:17485435-17485485	BE2_C	brain:	n/a
7	chr5:17491941-17491991	PFSK-1	brain:	n/a
8	chr5:17527430-17527480	HNPCEpiC	eye:	n/a
9	chr5:17495781-17495831	H1-hESC	embryonic stem cell:	embryo
10	chr5:17485435-17485485	HRE	kidney:	n/a
11	chr5:17527430-17527480	CMK	blood:	n/a
12	chr5:17485435-17485485	SK-N-MC	brain:	n/a
13	chr5:17604867-17604917	GM12878	blood:	n/a
14	chr5:17491586-17491636	RPTEC	kidney:	n/a
15	chr5:17491469-17491519	HCM	heart:	n/a
16	chr5:17527430-17527480	AG04450	lung:	fetal
17	chr5:17595441-17595491	SKMC	muscle:	n/a
18	chr5:17491604-17491654	GM12892	blood:	n/a
19	chr5:17495781-17495831	BJ	skin:	n/a
20	chr5:17491469-17491519	GM19239	blood:	n/a
21	chr5:17491941-17491991	GM12892	blood:	n/a
22	chr5:17519013-17519063	NB4	blood:	n/a
23	chr5:17519013-17519063	HAEpiC	amniotic membrane:	n/a
24	chr5:17519013-17519063	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:17604867-17604917	HCF	heart:	n/a
26	chr5:17580826-17580876	SKMC	muscle:	n/a
27	chr5:17517201-17517251	SK-N-SH	brain:	n/a
28	chr5:17528991-17529041	H1-hESC	embryonic stem cell:	embryo
29	chr5:17524561-17524611	PFSK-1	brain:	n/a
30	chr5:17485435-17485485	HepG2	liver:	n/a
31	chr5:17522582-17522632	GM19239	blood:	n/a
32	chr5:17495781-17495831	HIPEpiC	eye:	n/a
33	chr5:17524561-17524611	CMK	blood:	n/a
34	chr5:17527430-17527480	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:17517201-17517251	HL-60	blood:	n/a
36	chr5:17528991-17529041	GM19239	blood:	n/a
37	chr5:17528991-17529041	HEEpiC	esophagus:	n/a
38	chr5:17524561-17524611	AG09309	skin:	n/a
39	chr5:17604867-17604917	PANC-1	pancreas:	n/a
40	chr5:17595441-17595491	NHBE	bronchial:	n/a
41	chr5:17604867-17604917	SAEC	small airway:	n/a
42	chr5:17491586-17491636	HepG2	liver:	n/a
43	chr5:17485435-17485485	LNCaP	prostate:	n/a
44	chr5:17490778-17490828	NHDF-neo	bronchial:	n/a
45	chr5:17491469-17491519	BE2_C	brain:	n/a
46	chr5:17528991-17529041	HepG2	liver:	n/a
47	chr5:17527430-17527480	ProgFib	skin:	n/a
48	chr5:17604867-17604917	RPTEC	kidney:	n/a
49	chr5:17517201-17517251	HEEpiC	esophagus:	n/a
50	chr5:17580826-17580876	HUVEC	blood vessel:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
2	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
3	chr5:17482145..17483996-chr5:17485919..17488626,2	MCF-7	breast:
4	chr5:17223492..17225946-chr5:17474747..17476783,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-4	chr5:17483841-17484055	XLOC_004309
2	lnc-MYO10-12	chr5:17587399-17587632	NONHSAT100653
3	lnc-BASP1-4	chr5:17483931-17484068	XLOC_004309
4	lnc-BASP1-4	chr5:17477724-17477865	XLOC_004309
5	lnc-BASP1-4	chr5:17485639-17485937	XLOC_004309
6	lnc-BASP1-11	chr5:17494578-17494846	l_2885_chr5:17456969-17494846_brain

No data

Variant related genes	Relation type
ENSG00000251304	TF binding region
ENSG00000249427	TF binding region
ENSG00000249282	TF binding region
ENSG00000250558	TF binding region
ENSG00000250807	TF binding region
ENSG00000250296	TF binding region
ENSG00000250055	TF binding region
ENSG00000249339	TF binding region
ENSG00000249329	TF binding region
ENSG00000249156	TF binding region
ENSG00000268799	TF binding region
ENSG00000249620	TF binding region
ENSG00000248861	TF binding region
ENSG00000248205	TF binding region
ENSG00000250667	TF binding region
ENSG00000248422	TF binding region
ENSG00000271296	TF binding region
ENSG00000250351	TF binding region
ENSG00000249357	TF binding region
ENSG00000250088	TF binding region
ENSG00000185041	TF binding region
ENSG00000251304	CpG island
ENSG00000249427	CpG island
ENSG00000249282	CpG island
ENSG00000250558	CpG island
ENSG00000250807	CpG island
ENSG00000250296	CpG island
ENSG00000250055	CpG island
ENSG00000249339	CpG island
ENSG00000249329	CpG island
ENSG00000249156	CpG island
ENSG00000268799	CpG island
ENSG00000249620	CpG island
ENSG00000248861	CpG island
ENSG00000248205	CpG island
ENSG00000250667	CpG island
ENSG00000248422	CpG island
ENSG00000271296	CpG island
ENSG00000250351	CpG island
ENSG00000249357	CpG island
ENSG00000250088	CpG island
ENSG00000185041	CpG island
ENSG00000268799	chromatin interactions
ENSG00000250667	chromatin interactions
ENSG00000251304	chromatin interactions

Extended variants
information (count: 1987 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540018498	chr5:17475120-17475121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116061017	chr5:17475123-17475124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116343749	chr5:17475138-17475139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552094012	chr5:17475179-17475180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376856184	chr5:17475212-17475213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369872702	chr5:17475217-17475218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531625299	chr5:17475303-17475304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548649733	chr5:17475327-17475328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568428846	chr5:17475379-17475380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62348782	chr5:17475400-17475401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111970289	chr5:17475401-17475402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554029516	chr5:17475402-17475403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571068498	chr5:17475403-17475404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4701689	chr5:17475410-17475411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76139739	chr5:17475426-17475427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556946840	chr5:17475440-17475441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575293235	chr5:17475455-17475456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562735690	chr5:17475495-17475496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528477055	chr5:17475650-17475651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190529298	chr5:17475660-17475661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111468482	chr5:17475695-17475696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540326413	chr5:17475728-17475729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs193234091	chr5:17475740-17475741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184541213	chr5:17475741-17475742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545670291	chr5:17475773-17475774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562476442	chr5:17475802-17475803	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531515681	chr5:17475808-17475809	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189424824	chr5:17475849-17475850	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143612104	chr5:17475929-17475930	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568443379	chr5:17475954-17475955	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527742109	chr5:17475982-17475983	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547908734	chr5:17475985-17475986	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180703143	chr5:17475987-17475988	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540069653	chr5:17475989-17475990	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556881797	chr5:17476012-17476013	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374265105	chr5:17476018-17476019	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556311231	chr5:17476024-17476025	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148636997	chr5:17476025-17476026	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185717523	chr5:17476028-17476029	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142081856	chr5:17476033-17476034	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6877829	chr5:17476065-17476066	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533641038	chr5:17476085-17476086	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530279619	chr5:17476088-17476089	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576612638	chr5:17476096-17476097	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4701690	chr5:17476113-17476114	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188539844	chr5:17476116-17476117	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576208262	chr5:17476135-17476136	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369221573	chr5:17476144-17476145	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542113463	chr5:17476168-17476169	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150707799	chr5:17476204-17476205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Cervical squamous cell carcinoma	21590768	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
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17475000-17475800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:17475800-17476200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:17475800-17476400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr5:17475800-17476400	Enhancers	Primary B cells from peripheral blood	blood
5	chr5:17476200-17478800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:17476400-17486200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr5:17480600-17480800	Enhancers	Fetal Kidney	kidney
8	chr5:17481400-17481600	Enhancers	Fetal Kidney	kidney
9	chr5:17481400-17482000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:17481400-17482000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:17481400-17482000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:17481400-17482000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:17481400-17482000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr5:17481400-17482200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:17481400-17483000	Enhancers	A549	lung
16	chr5:17481600-17481800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:17481600-17482000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:17481600-17482000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:17481600-17482000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:17483000-17487000	Weak transcription	A549	lung
21	chr5:17486200-17487800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr5:17487000-17487600	Enhancers	A549	lung
23	chr5:17487200-17487400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:17487200-17487600	Enhancers	Hela-S3	cervix
25	chr5:17487400-17488200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:17488200-17489000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:17494400-17496200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr5:17500600-17500800	Enhancers	A549	lung
29	chr5:17500600-17500800	Enhancers	Hela-S3	cervix
30	chr5:17500600-17501000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:17500600-17501000	Active TSS	NHDF-Ad	bronchial
32	chr5:17502200-17503000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:17509000-17509400	Enhancers	Fetal Brain Male	brain
34	chr5:17512000-17512200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:17512200-17512400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:17512200-17512400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:17512400-17512600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:17512600-17517600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:17512600-17519400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:17513600-17514600	Enhancers	A549	lung
41	chr5:17517400-17517600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:17517600-17518000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:17517600-17518000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:17517800-17518000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
45	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Lung	lung
46	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
47	chr5:17517800-17518000	Bivalent/Poised TSS	Small Intestine	intestine
48	chr5:17517800-17518000	Bivalent/Poised TSS	Hela-S3	cervix
49	chr5:17526600-17527000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
50	chr5:17526600-17527000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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