Variant report

Variant	esv3360596
Chromosome Location	chr5:43315646-43336665
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 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	chr5:43321028-43321242	K562	blood:	n/a	n/a
2	ATF1	chr5:43321036-43321339	K562	blood:	n/a	n/a
3	ATF2	chr5:43315431-43315709	GM12878	blood:	n/a	n/a
4	ATF2	chr5:43315422-43315796	GM12878	blood:	n/a	n/a
5	ATF3	chr5:43315330-43315805	A549	lung:	n/a	n/a
6	ATF3	chr5:43336099-43336788	HCT-116	colon:	n/a	n/a
7	ATF3	chr5:43336384-43336694	K562	blood:	n/a	n/a
8	BATF	chr5:43315839-43316130	GM12878	blood:	n/a	n/a
9	BATF	chr5:43315452-43315755	GM12878	blood:	n/a	chr5:43315594-43315605
10	BATF	chr5:43336364-43336691	GM12878	blood:	n/a	chr5:43336565-43336576 chr5:43336548-43336559
11	BATF	chr5:43336468-43336699	GM12878	blood:	n/a	chr5:43336565-43336576 chr5:43336548-43336559
12	BATF	chr5:43315330-43315815	GM12878	blood:	n/a	chr5:43315594-43315605
13	BATF	chr5:43315842-43316193	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:43315866-43316165	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:43315457-43315730	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:43336365-43336661	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:43320977-43321274	K562	blood:	n/a	n/a
18	BRCA1	chr5:43315514-43315786	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr5:43336133-43336464	K562	blood:	n/a	n/a
20	CBX3	chr5:43315416-43315826	HCT-116	colon:	n/a	n/a
21	CBX3	chr5:43336080-43336645	K562	blood:	n/a	n/a
22	CBX3	chr5:43335914-43336787	HCT-116	colon:	n/a	n/a
23	CBX3	chr5:43320811-43321364	K562	blood:	n/a	n/a
24	CBX3	chr5:43336057-43336801	HCT-116	colon:	n/a	n/a
25	CEBPB	chr5:43336470-43336647	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:43315306-43315808	HCT-116	colon:	n/a	n/a
27	CEBPB	chr5:43314768-43315822	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:43321095-43321295	K562	blood:	n/a	n/a
29	CEBPB	chr5:43314647-43315828	A549	lung:	n/a	n/a
30	CEBPB	chr5:43319237-43319428	K562	blood:	n/a	n/a
31	CEBPB	chr5:43315474-43315766	A549	lung:	n/a	n/a
32	CEBPB	chr5:43336126-43336769	HCT-116	colon:	n/a	n/a
33	CEBPB	chr5:43315390-43315908	HCT-116	colon:	n/a	n/a
34	CEBPB	chr5:43336432-43336697	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:43336192-43336768	HCT-116	colon:	n/a	n/a
36	CEBPB	chr5:43336292-43336736	A549	lung:	n/a	n/a
37	CEBPB	chr5:43314300-43315770	A549	lung:	n/a	n/a
38	CEBPD	chr5:43320946-43321339	K562	blood:	n/a	n/a
39	CHD2	chr5:43321044-43321199	K562	blood:	n/a	n/a
40	CHD2	chr5:43315439-43315734	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr5:43336080-43336230	K562	blood:	n/a	n/a
42	CTCF	chr5:43336040-43336190	HEK293	kidney:	n/a	n/a
43	CTCF	chr5:43335980-43336130	GM12869	blood:	n/a	n/a
44	CTCF	chr5:43335980-43336130	HCT-116	colon:	n/a	n/a
45	CTCF	chr5:43336140-43336290	BE2_C	brain:	n/a	n/a
46	CTCF	chr5:43336020-43336170	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:43336100-43336250	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:43318323-43318390	GM13976	blood:	n/a	n/a
49	CTCF	chr5:43335980-43336130	GM12874	blood:	n/a	n/a
50	CTCF	chr5:43336117-43336166	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:43316468-43316518	Caco-2	colon:	n/a
2	chr5:43316468-43316518	HEK293	kidney:	embryo
3	chr5:43316468-43316518	GM06990	blood:	n/a
4	chr5:43316468-43316518	HCT-116	colon:	n/a
5	chr5:43316468-43316518	SAEC	small airway:	n/a
6	chr5:43316468-43316518	HNPCEpiC	eye:	n/a
7	chr5:43316468-43316518	AG09309	skin:	n/a
8	chr5:43316468-43316518	HCPEpiC	choroid plexus:	n/a
9	chr5:43316468-43316518	HRCEpiC	kidney:	n/a
10	chr5:43316468-43316518	PFSK-1	brain:	n/a
11	chr5:43316468-43316518	GM19239	blood:	n/a
12	chr5:43316468-43316518	GM12892	blood:	n/a
13	chr5:43316468-43316518	MCF-7	breast:	n/a
14	chr5:43316468-43316518	BJ	skin:	n/a
15	chr5:43316468-43316518	RPTEC	kidney:	n/a
16	chr5:43316468-43316518	HMEC	breast:	n/a
17	chr5:43316468-43316518	T-47D	breast:	n/a
18	chr5:43316468-43316518	ProgFib	skin:	n/a
19	chr5:43316468-43316518	SK-N-SH_RA	brain:	n/a
20	chr5:43316468-43316518	SK-N-MC	brain:	n/a
21	chr5:43316468-43316518	H1-hESC	embryonic stem cell:	embryo
22	chr5:43316468-43316518	HL-60	blood:	n/a
23	chr5:43316468-43316518	CMK	blood:	n/a
24	chr5:43316468-43316518	HepG2	liver:	n/a
25	chr5:43316468-43316518	GM12891	blood:	n/a
26	chr5:43316468-43316518	GM12878	blood:	n/a
27	chr5:43316468-43316518	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:43316468-43316518	HIPEpiC	eye:	n/a
29	chr5:43316468-43316518	MCF10A-Er-Src	breast:	n/a
30	chr5:43316468-43316518	HRE	kidney:	n/a
31	chr5:43316468-43316518	U87	brain:	n/a
32	chr5:43316468-43316518	SKMC	muscle:	n/a
33	chr5:43316468-43316518	K562	blood:	n/a
34	chr5:43316468-43316518	HCM	heart:	n/a
35	chr5:43316468-43316518	AG10803	skin:	n/a
36	chr5:43316468-43316518	AG09319	gingival:	n/a
37	chr5:43316468-43316518	A549	lung:	n/a
38	chr5:43316468-43316518	Hela-S3	cervix:	n/a
39	chr5:43316468-43316518	NB4	blood:	n/a
40	chr5:43316468-43316518	NHDF-neo	bronchial:	n/a
41	chr5:43316468-43316518	SK-N-SH	brain:	n/a
42	chr5:43316468-43316518	ECC-1	luminal epithelium:	n/a
43	chr5:43316468-43316518	LNCaP	prostate:	n/a
44	chr5:43316468-43316518	PrEC	prostate:	n/a
45	chr5:43316468-43316518	AG04449	skin:	fetal
46	chr5:43316468-43316518	NT2-D1	testis:	n/a
47	chr5:43316468-43316518	HUVEC	blood vessel:	n/a
48	chr5:43316468-43316518	ovcar-3	ovarian:	n/a
49	chr5:43316468-43316518	AG04450	lung:	fetal
50	chr5:43316468-43316518	NHBE	bronchial:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43312302..43315241-chr5:43320244..43322434,2	MCF-7	breast:
2	chr5:43312956..43314498-chr5:43314629..43316286,2	MCF-7	breast:
3	chr5:43317902..43322981-chr5:43481310..43485005,5	K562	blood:
4	chr5:43310462..43313861-chr5:43318500..43321089,4	K562	blood:
5	chr5:43119756..43121419-chr5:43314407..43316423,2	K562	blood:
6	chr5:43314912..43317886-chr5:43482528..43484507,2	K562	blood:
7	chr5:43329470..43332303-chr5:43356763..43358502,2	K562	blood:
8	chr5:43312195..43313861-chr5:43318989..43321314,3	K562	blood:
9	chr5:43313320..43315914-chr5:43513861..43516716,3	MCF-7	breast:
10	chr5:43312181..43314042-chr5:43332862..43335052,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114947.1.1-5	chr5:43336266-43336347	NONHSAT101308

No data

Variant related genes	Relation type
ENSG00000188850	TF binding region
HMGCS1	TF binding region
ENSG00000188850	CpG island
HMGCS1	CpG island
ENSG00000151881	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000112972	chromatin interactions

Extended variants
information (count: 483 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572815851	chr5:43315705-43315706	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs146407644	chr5:43315723-43315724	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs553490242	chr5:43315802-43315803	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs576830281	chr5:43315864-43315865	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs573471961	chr5:43315906-43315907	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs539712501	chr5:43315945-43315946	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs186414665	chr5:43315950-43315951	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs188126091	chr5:43315968-43315969	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs139747899	chr5:43315969-43315970	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs561642025	chr5:43315994-43315995	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs181022462	chr5:43316021-43316022	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs547724419	chr5:43316033-43316034	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs143205180	chr5:43316057-43316058	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs533435457	chr5:43316155-43316156	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs549983258	chr5:43316158-43316159	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs570194769	chr5:43316205-43316206	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs186102992	chr5:43316230-43316231	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs576153474	chr5:43316248-43316249	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs577303590	chr5:43316348-43316349	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146655170	chr5:43316365-43316366	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs2126949	chr5:43316390-43316391	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs2126948	chr5:43316469-43316470	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs72754521	chr5:43316489-43316490	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs370780546	chr5:43316492-43316493	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs114434180	chr5:43316496-43316497	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs542464479	chr5:43316505-43316506	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576786112	chr5:43316506-43316507	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2169781	chr5:43316514-43316515	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs565118445	chr5:43316515-43316516	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs373374746	chr5:43316519-43316520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs111718735	chr5:43316634-43316635	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555825673	chr5:43316709-43316710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142540487	chr5:43316718-43316719	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191021779	chr5:43316739-43316740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561550510	chr5:43316745-43316746	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377321670	chr5:43316793-43316794	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111271525	chr5:43316794-43316795	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs183333827	chr5:43316800-43316801	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564431999	chr5:43316821-43316822	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150985567	chr5:43316838-43316839	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550186961	chr5:43316842-43316843	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563768371	chr5:43316847-43316848	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529410163	chr5:43316851-43316852	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549556169	chr5:43316864-43316865	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186637786	chr5:43316866-43316867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377032201	chr5:43316892-43316893	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140850555	chr5:43316911-43316912	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs551766973	chr5:43316936-43316937	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571942025	chr5:43316947-43316948	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2126947	chr5:43316948-43316949	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21569311	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43314200-43315800	Flanking Active TSS	A549	lung
2	chr5:43314200-43316200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:43314200-43316200	Enhancers	Hela-S3	cervix
4	chr5:43314200-43317000	Enhancers	HMEC	breast
5	chr5:43314400-43316400	Enhancers	NHEK	skin
6	chr5:43314400-43316600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:43314400-43319200	Weak transcription	Fetal Intestine Large	intestine
8	chr5:43314600-43315800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:43314600-43315800	Enhancers	HSMMtube	muscle
10	chr5:43314600-43316000	Weak transcription	Stomach Mucosa	stomach
11	chr5:43314600-43316400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:43314600-43316400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr5:43314600-43316400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr5:43314800-43316000	ZNF genes & repeats	GM12878-XiMat	blood
15	chr5:43315400-43315800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:43315600-43319600	Weak transcription	K562	blood
17	chr5:43315800-43316000	Active TSS	A549	lung
18	chr5:43315800-43316200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:43315800-43316800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:43316000-43316200	Enhancers	Stomach Mucosa	stomach
21	chr5:43316000-43316200	Flanking Active TSS	A549	lung
22	chr5:43316200-43317200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:43316400-43316600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr5:43316600-43317000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr5:43316800-43317000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:43316800-43317000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:43317000-43317800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:43317200-43317400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:43319200-43319600	Enhancers	Fetal Intestine Large	intestine
30	chr5:43319600-43320600	Enhancers	K562	blood
31	chr5:43320600-43321600	Flanking Active TSS	K562	blood
32	chr5:43320800-43321200	Enhancers	HepG2	liver
33	chr5:43321600-43322600	Enhancers	K562	blood
34	chr5:43321800-43322800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr5:43332600-43333800	Enhancers	Hela-S3	cervix
36	chr5:43333000-43333200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr5:43333000-43333800	Enhancers	K562	blood
38	chr5:43335800-43336600	ZNF genes & repeats	Liver	Liver

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