Variant report

Variant	nsv819887
Chromosome Location	chr13:52772113-52926921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1180)
CpG islands
(count:427)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52912177-52912608	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:52917500-52917700	K562	blood:	n/a	n/a
3	ARID3A	chr13:52776095-52776205	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:52775549-52775803	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:52923337-52923432	K562	blood:	n/a	n/a
6	ATF1	chr13:52778134-52778252	K562	blood:	n/a	n/a
7	ATF3	chr13:52777990-52778282	K562	blood:	n/a	n/a
8	BACH1	chr13:52923239-52923415	K562	blood:	n/a	n/a
9	BATF	chr13:52810391-52810616	GM12878	blood:	n/a	n/a
10	BATF	chr13:52898796-52899250	GM12878	blood:	n/a	n/a
11	BATF	chr13:52923181-52923399	GM12878	blood:	n/a	n/a
12	BATF	chr13:52797274-52797490	GM12878	blood:	n/a	n/a
13	BATF	chr13:52853509-52853730	GM12878	blood:	n/a	chr13:52853641-52853652
14	BATF	chr13:52898806-52899037	GM12878	blood:	n/a	n/a
15	BATF	chr13:52809172-52809423	GM12878	blood:	n/a	n/a
16	BCL11A	chr13:52899009-52899322	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:52782513-52782787	HepG2	liver:	n/a	n/a
18	BHLHE40	chr13:52782563-52782573	HepG2	liver:	n/a	n/a
19	BHLHE40	chr13:52923130-52923411	K562	blood:	n/a	n/a
20	BHLHE40	chr13:52923174-52923428	GM12878	blood:	n/a	n/a
21	BRCA1	chr13:52923203-52923515	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr13:52884107-52884381	K562	blood:	n/a	n/a
23	CBX3	chr13:52874759-52875007	K562	blood:	n/a	n/a
24	CBX3	chr13:52884093-52884361	K562	blood:	n/a	n/a
25	CBX3	chr13:52923145-52923428	K562	blood:	n/a	n/a
26	CBX3	chr13:52923026-52923614	HCT-116	colon:	n/a	n/a
27	CBX3	chr13:52923097-52923561	HCT-116	colon:	n/a	n/a
28	CBX3	chr13:52874658-52875125	K562	blood:	n/a	n/a
29	CEBPB	chr13:52778024-52778334	Hela-S3	cervix:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
30	CEBPB	chr13:52781557-52781838	HepG2	liver:	n/a	chr13:52781678-52781695 chr13:52781679-52781690 chr13:52781679-52781692
31	CEBPB	chr13:52778006-52778337	IMR90	lung:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
32	CEBPB	chr13:52781559-52781784	HepG2	liver:	n/a	chr13:52781678-52781695 chr13:52781679-52781690 chr13:52781679-52781692
33	CEBPB	chr13:52781560-52781784	HepG2	liver:	n/a	chr13:52781678-52781695 chr13:52781679-52781690 chr13:52781679-52781692
34	CEBPB	chr13:52834731-52834765	IMR90	lung:	n/a	chr13:52834737-52834748
35	CEBPB	chr13:52864873-52864902	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:52777962-52778367	K562	blood:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
37	CEBPB	chr13:52778027-52778275	K562	blood:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
38	CEBPB	chr13:52781674-52781778	HepG2	liver:	n/a	chr13:52781678-52781695 chr13:52781679-52781690 chr13:52781679-52781692
39	CEBPB	chr13:52834570-52834812	K562	blood:	n/a	chr13:52834737-52834748
40	CEBPB	chr13:52778027-52778306	A549	lung:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
41	CEBPB	chr13:52923160-52923506	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr13:52923205-52923471	IMR90	lung:	n/a	n/a
43	CEBPB	chr13:52834731-52834822	H1-hESC	embryonic stem cell:	n/a	chr13:52834737-52834748
44	CEBPB	chr13:52778051-52778246	K562	blood:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
45	CEBPB	chr13:52778028-52778280	HepG2	liver:	n/a	chr13:52778150-52778161 chr13:52778162-52778173
46	CEBPB	chr13:52776043-52776155	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:52834561-52834763	HepG2	liver:	n/a	chr13:52834737-52834748
48	CEBPD	chr13:52778047-52778301	K562	blood:	n/a	chr13:52778151-52778162 chr13:52778162-52778173
49	CEBPD	chr13:52855570-52855946	K562	blood:	n/a	n/a
50	CTCF	chr13:52917480-52917630	GM12873	blood:	n/a	chr13:52917607-52917628 chr13:52917610-52917618

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52773871-52773921	NHDF-neo	bronchial:	n/a
2	chr13:52909628-52909678	HRCEpiC	kidney:	n/a
3	chr13:52909628-52909678	HUVEC	blood vessel:	n/a
4	chr13:52886181-52886231	HEK293	kidney:	embryo
5	chr13:52909628-52909678	HRPEpiC	eye:	n/a
6	chr13:52912487-52912537	Hela-S3	cervix:	n/a
7	chr13:52886181-52886231	PrEC	prostate:	n/a
8	chr13:52773871-52773921	U87	brain:	n/a
9	chr13:52912487-52912537	A549	lung:	n/a
10	chr13:52866820-52866870	HPAEpiC	pulmonary alveolar:	n/a
11	chr13:52773871-52773921	HNPCEpiC	eye:	n/a
12	chr13:52904816-52904866	PrEC	prostate:	n/a
13	chr13:52907066-52907116	MCF10A-Er-Src	breast:	n/a
14	chr13:52907066-52907116	HCT-116	colon:	n/a
15	chr13:52866820-52866870	HRPEpiC	eye:	n/a
16	chr13:52866820-52866870	PANC-1	pancreas:	n/a
17	chr13:52886181-52886231	HIPEpiC	eye:	n/a
18	chr13:52912487-52912537	GM12892	blood:	n/a
19	chr13:52907066-52907116	AG04449	skin:	fetal
20	chr13:52904816-52904866	PANC-1	pancreas:	n/a
21	chr13:52773871-52773921	PFSK-1	brain:	n/a
22	chr13:52912487-52912537	GM12891	blood:	n/a
23	chr13:52773871-52773921	IMR90	lung:	fetal
24	chr13:52907066-52907116	Hepatocyte	liver:	n/a
25	chr13:52912487-52912537	IMR90	lung:	fetal
26	chr13:52907066-52907116	A549	lung:	n/a
27	chr13:52909628-52909678	CMK	blood:	n/a
28	chr13:52909628-52909678	SK-N-SH_RA	brain:	n/a
29	chr13:52866820-52866870	Hela-S3	cervix:	n/a
30	chr13:52907066-52907116	HL-60	blood:	n/a
31	chr13:52912487-52912537	ovcar-3	ovarian:	n/a
32	chr13:52907066-52907116	MCF-7	breast:	n/a
33	chr13:52773871-52773921	SK-N-SH	brain:	n/a
34	chr13:52866820-52866870	LNCaP	prostate:	n/a
35	chr13:52904816-52904866	GM06990	blood:	n/a
36	chr13:52907066-52907116	SK-N-SH	brain:	n/a
37	chr13:52886181-52886231	Caco-2	colon:	n/a
38	chr13:52907066-52907116	HCM	heart:	n/a
39	chr13:52904816-52904866	NT2-D1	testis:	n/a
40	chr13:52907066-52907116	NH-A	brain:	n/a
41	chr13:52886181-52886231	HNPCEpiC	eye:	n/a
42	chr13:52886181-52886231	NT2-D1	testis:	n/a
43	chr13:52886181-52886231	HRCEpiC	kidney:	n/a
44	chr13:52886181-52886231	CMK	blood:	n/a
45	chr13:52904816-52904866	HMEC	breast:	n/a
46	chr13:52909628-52909678	RPTEC	kidney:	n/a
47	chr13:52904816-52904866	HNPCEpiC	eye:	n/a
48	chr13:52907066-52907116	AG10803	skin:	n/a
49	chr13:52904816-52904866	GM12878	blood:	n/a
50	chr13:52909628-52909678	HIPEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52584314..52586465-chr13:52770402..52772537,2	K562	blood:
2	chr13:52888663..52890246-chr13:52890532..52893511,2	MCF-7	breast:
3	chr13:52912142..52914038-chr13:53027111..53030016,2	K562	blood:
4	chr13:52768256..52771397-chr13:52784460..52787312,3	MCF-7	breast:
5	chr13:52911600..52913908-chr13:53027001..53029186,3	MCF-7	breast:
6	chr13:52921786..52923315-chr13:52926251..52928561,2	K562	blood:
7	chr13:52917176..52917696-chr13:53382727..53383690,2	K562	blood:
8	chr13:52917213..52918202-chr13:53024381..53024988,3	K562	blood:
9	chr13:52885798..52888785-chr13:52889900..52891955,2	MCF-7	breast:
10	chr13:52917335..52918274-chr13:53024499..53025207,3	MCF-7	breast:
11	chr13:52389338..52389872-chr13:52775197..52776130,2	K562	blood:
12	chr13:52917796..52919979-chr13:52922029..52924038,2	MCF-7	breast:
13	chr13:52885798..52888785-chr13:52889900..52891955,2	MCF-7	breast:
14	chr13:52917796..52919979-chr13:52922029..52924038,2	MCF-7	breast:
15	chr13:52917157..52919301-chr13:53024221..53025626,7	MCF-7	breast:
16	chr13:52921786..52923315-chr13:52926251..52928561,2	K562	blood:
17	chr13:52917718..52921216-chr13:53022914..53025768,5	MCF-7	breast:
18	chr13:52888663..52890246-chr13:52890532..52893511,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEK3-1	chr13:52898036-52898302	ENSG00000217576.4
2	lnc-CKAP2-2	chr13:52915028-52915192	ENSG00000271564.1
3	lnc-CKAP2-2	chr13:52908430-52908512	ENSG00000271564.1
4	lnc-THSD1-4	chr13:52889589-52890110	NONHSAT033983
5	lnc-THSD1-4	chr13:52890481-52890534	NONHSAT033983
6	lnc-NEK3-1	chr13:52908062-52908410	ENSG00000217576.4
7	lnc-THSD1-4	chr13:52894685-52894718	NONHSAT033983
8	lnc-NEK3-1	chr13:52907190-52907296	ENSG00000217576.4
9	lnc-CKAP2-2	chr13:52915428-52916031	ENSG00000271564.1

No data

Variant related genes	Relation type
TPTE2P2	TF binding region
MRPS31P5	TF binding region
ENSG00000217576	TF binding region
ENSG00000271564	TF binding region
TPTE2P2	CpG island
MRPS31P5	CpG island
ENSG00000217576	CpG island
ENSG00000271564	CpG island
ENSG00000243406	chromatin interactions
ENSG00000123191	chromatin interactions
ENSG00000136108	chromatin interactions
ENSG00000136100	chromatin interactions

Extended variants
information (count: 2349 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2349 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114355608	chr13:52772190-52772191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536886768	chr13:52772191-52772192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540705663	chr13:52772213-52772214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560762033	chr13:52772260-52772261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143958041	chr13:52772322-52772323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529598274	chr13:52772350-52772351	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575040101	chr13:52772356-52772357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543905596	chr13:52772399-52772400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142072671	chr13:52772498-52772499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs114959419	chr13:52772556-52772557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540128745	chr13:52772604-52772605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560424525	chr13:52772605-52772606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375471601	chr13:52772630-52772631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111284015	chr13:52772646-52772647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180914368	chr13:52772684-52772685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562677248	chr13:52772687-52772688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570487816	chr13:52772693-52772694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551921253	chr13:52772699-52772700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562346722	chr13:52772729-52772730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565106781	chr13:52772764-52772765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527716572	chr13:52772792-52772793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201898232	chr13:52772814-52772815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547759935	chr13:52772833-52772834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567991370	chr13:52772860-52772861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536446403	chr13:52772865-52772866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549913182	chr13:52772866-52772867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368604039	chr13:52772890-52772891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372817184	chr13:52772959-52772960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537511013	chr13:52772984-52772985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376998839	chr13:52773001-52773002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577543982	chr13:52773011-52773012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200227532	chr13:52773208-52773209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139449140	chr13:52773210-52773211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184282686	chr13:52773240-52773241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573833611	chr13:52773241-52773242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542953885	chr13:52773333-52773334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562638616	chr13:52773336-52773337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368297250	chr13:52773398-52773399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571044017	chr13:52773413-52773414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576327986	chr13:52773457-52773458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545499113	chr13:52773475-52773476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79753461	chr13:52773485-52773486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527677629	chr13:52773495-52773496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547819456	chr13:52773496-52773497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189162729	chr13:52773505-52773506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533717355	chr13:52773540-52773541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560311659	chr13:52773549-52773550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530287630	chr13:52773591-52773592	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs550074174	chr13:52773607-52773608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369422034	chr13:52773608-52773609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52769200-52775000	Weak transcription	HepG2	liver
2	chr13:52769400-52778600	Weak transcription	K562	blood
3	chr13:52770000-52774200	Weak transcription	Fetal Heart	heart
4	chr13:52770000-52774200	Weak transcription	Fetal Intestine Large	intestine
5	chr13:52770000-52775800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:52770200-52773400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:52770200-52775000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr13:52770400-52777600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr13:52770600-52775800	Weak transcription	Right Ventricle	heart
10	chr13:52771000-52777600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr13:52773400-52773800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr13:52773800-52775800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr13:52774200-52776400	Enhancers	Fetal Intestine Large	intestine
14	chr13:52774200-52776800	Enhancers	Fetal Heart	heart
15	chr13:52774400-52775000	Enhancers	Fetal Intestine Small	intestine
16	chr13:52775000-52775200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr13:52775000-52775400	Enhancers	HepG2	liver
18	chr13:52775000-52775800	Weak transcription	Fetal Intestine Small	intestine
19	chr13:52775200-52775400	Enhancers	Left Ventricle	heart
20	chr13:52775200-52775800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr13:52775200-52776200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:52775400-52775600	Flanking Active TSS	HepG2	liver
23	chr13:52775400-52776200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr13:52775600-52776000	Enhancers	Brain Cingulate Gyrus	brain
25	chr13:52775600-52776000	Enhancers	Fetal Lung	lung
26	chr13:52775600-52776000	Active TSS	HepG2	liver
27	chr13:52775600-52776200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr13:52775600-52776200	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr13:52775800-52776000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr13:52775800-52776200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr13:52775800-52776200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:52775800-52776200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr13:52775800-52776200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr13:52775800-52776200	Enhancers	Brain Substantia Nigra	brain
35	chr13:52775800-52776200	Enhancers	Fetal Intestine Small	intestine
36	chr13:52775800-52776200	Active TSS	Gastric	stomach
37	chr13:52775800-52776200	Enhancers	Lung	lung
38	chr13:52775800-52776800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr13:52776000-52776200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr13:52776000-52776200	Enhancers	Left Ventricle	heart
41	chr13:52776000-52776200	Enhancers	Right Ventricle	heart
42	chr13:52776000-52776400	Flanking Active TSS	HepG2	liver
43	chr13:52776200-52776400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr13:52776200-52777400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr13:52776200-52778600	Weak transcription	Fetal Intestine Small	intestine
46	chr13:52776200-52783400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:52776400-52776800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr13:52776400-52777600	Weak transcription	Fetal Intestine Large	intestine
49	chr13:52776400-52779400	Enhancers	HepG2	liver
50	chr13:52776800-52777000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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