Variant report

Variant	esv1803690
Chromosome Location	chr13:48470681-48508091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:48507091-48507891	HepG2	liver:	n/a	n/a
2	CBX3	chr13:48478334-48478745	K562	blood:	n/a	n/a
3	CEBPB	chr13:48470738-48471049	HepG2	liver:	n/a	n/a
4	CEBPB	chr13:48478013-48478293	K562	blood:	n/a	n/a
5	CEBPB	chr13:48477968-48478327	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:48507391-48507955	HepG2	liver:	n/a	n/a
7	CEBPB	chr13:48477973-48478318	Hela-S3	cervix:	n/a	n/a
8	CREB1	chr13:48478335-48478941	K562	blood:	n/a	n/a
9	CTCF	chr13:48477433-48477478	LNCaP	prostate:	n/a	n/a
10	CTCF	chr13:48508080-48508230	AG09319	gingival:	n/a	n/a
11	CTCF	chr13:48502660-48502810	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr13:48475600-48475750	AG04449	skin:	n/a	chr13:48475682-48475691
13	CTCF	chr13:48488028-48488050	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr13:48487533-48487609	LNCaP	prostate:	n/a	n/a
15	CTCF	chr13:48482320-48482470	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr13:48482140-48482290	HepG2	liver:	n/a	n/a
17	CUX1	chr13:48478283-48478394	K562	blood:	n/a	n/a
18	EBF1	chr13:48491388-48491726	GM12878	blood:	n/a	chr13:48491532-48491543 chr13:48491571-48491582
19	EBF1	chr13:48491373-48491736	GM12878	blood:	n/a	chr13:48491532-48491543 chr13:48491571-48491582
20	EBF1	chr13:48491352-48491753	GM12878	blood:	n/a	chr13:48491532-48491543 chr13:48491571-48491582
21	EGR1	chr13:48471494-48471906	MCF-7	breast:	n/a	n/a
22	ELF1	chr13:48478375-48478725	K562	blood:	n/a	n/a
23	ELF1	chr13:48471459-48472026	MCF-7	breast:	n/a	n/a
24	ELK1	chr13:48478510-48478657	K562	blood:	n/a	n/a
25	EP300	chr13:48507117-48507738	HepG2	liver:	n/a	n/a
26	EP300	chr13:48482309-48482801	HepG2	liver:	n/a	n/a
27	EP300	chr13:48471557-48471912	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr13:48472195-48472555	HepG2	liver:	n/a	n/a
29	FOS	chr13:48477996-48478357	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr13:48478879-48479550	HUVEC	blood vessel:	n/a	n/a
31	FOS	chr13:48477996-48478358	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:48507812-48507846	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr13:48477983-48478346	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr13:48471588-48471831	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr13:48477986-48478358	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXA1	chr13:48507134-48507715	HepG2	liver:	n/a	n/a
37	FOXA1	chr13:48507119-48507762	HepG2	liver:	n/a	n/a
38	FOXA1	chr13:48482253-48482816	HepG2	liver:	n/a	n/a
39	FOXA1	chr13:48472311-48472536	HepG2	liver:	n/a	n/a
40	FOXA1	chr13:48482395-48482826	HepG2	liver:	n/a	n/a
41	FOXA1	chr13:48482282-48482755	HepG2	liver:	n/a	n/a
42	FOXA1	chr13:48482281-48482835	HepG2	liver:	n/a	n/a
43	FOXA1	chr13:48507034-48508210	HepG2	liver:	n/a	n/a
44	FOXA1	chr13:48507842-48508209	HepG2	liver:	n/a	n/a
45	FOXA1	chr13:48507883-48508210	HepG2	liver:	n/a	n/a
46	FOXA2	chr13:48507125-48507743	HepG2	liver:	n/a	n/a
47	FOXA2	chr13:48482352-48482785	HepG2	liver:	n/a	n/a
48	FOXA2	chr13:48507838-48508134	HepG2	liver:	n/a	n/a
49	FOXA2	chr13:48472306-48472593	HepG2	liver:	n/a	n/a
50	FOXA2	chr13:48482205-48483015	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:48507440-48507490	Hela-S3	cervix:	n/a
2	chr13:48478591-48478641	HAEpiC	amniotic membrane:	n/a
3	chr13:48478591-48478641	AG09309	skin:	n/a
4	chr13:48507440-48507490	ECC-1	luminal epithelium:	n/a
5	chr13:48478546-48478596	HMEC	breast:	n/a
6	chr13:48507440-48507490	HCF	heart:	n/a
7	chr13:48478546-48478596	PrEC	prostate:	n/a
8	chr13:48507440-48507490	PFSK-1	brain:	n/a
9	chr13:48478591-48478641	NB4	blood:	n/a
10	chr13:48478591-48478641	HEEpiC	esophagus:	n/a
11	chr13:48478546-48478596	HCPEpiC	choroid plexus:	n/a
12	chr13:48478591-48478641	ovcar-3	ovarian:	n/a
13	chr13:48478546-48478596	HCT-116	colon:	n/a
14	chr13:48478546-48478596	T-47D	breast:	n/a
15	chr13:48478591-48478641	MCF10A-Er-Src	breast:	n/a
16	chr13:48478591-48478641	NHDF-neo	bronchial:	n/a
17	chr13:48507440-48507490	CMK	blood:	n/a
18	chr13:48478546-48478596	NH-A	brain:	n/a
19	chr13:48478546-48478596	HEEpiC	esophagus:	n/a
20	chr13:48507440-48507490	HIPEpiC	eye:	n/a
21	chr13:48478591-48478641	HEK293	kidney:	embryo
22	chr13:48478591-48478641	Hela-S3	cervix:	n/a
23	chr13:48507440-48507490	AG09309	skin:	n/a
24	chr13:48478546-48478596	A549	lung:	n/a
25	chr13:48507440-48507490	GM12878	blood:	n/a
26	chr13:48507440-48507490	SAEC	small airway:	n/a
27	chr13:48478546-48478596	H1-hESC	embryonic stem cell:	embryo
28	chr13:48507440-48507490	HRE	kidney:	n/a
29	chr13:48478546-48478596	K562	blood:	n/a
30	chr13:48507440-48507490	HL-60	blood:	n/a
31	chr13:48478591-48478641	SK-N-MC	brain:	n/a
32	chr13:48478591-48478641	HNPCEpiC	eye:	n/a
33	chr13:48478546-48478596	Hepatocyte	liver:	n/a
34	chr13:48478546-48478596	AG09309	skin:	n/a
35	chr13:48507440-48507490	AG10803	skin:	n/a
36	chr13:48507440-48507490	HEEpiC	esophagus:	n/a
37	chr13:48478546-48478596	HRE	kidney:	n/a
38	chr13:48478591-48478641	AG09319	gingival:	n/a
39	chr13:48478546-48478596	HUVEC	blood vessel:	n/a
40	chr13:48478546-48478596	ProgFib	skin:	n/a
41	chr13:48478546-48478596	AG10803	skin:	n/a
42	chr13:48478591-48478641	GM12878	blood:	n/a
43	chr13:48507440-48507490	HCM	heart:	n/a
44	chr13:48478591-48478641	GM12891	blood:	n/a
45	chr13:48478546-48478596	AG09319	gingival:	n/a
46	chr13:48478591-48478641	PFSK-1	brain:	n/a
47	chr13:48478546-48478596	HPAEpiC	pulmonary alveolar:	n/a
48	chr13:48478546-48478596	HepG2	liver:	n/a
49	chr13:48478546-48478596	GM19239	blood:	n/a
50	chr13:48507440-48507490	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:48470064..48472473-chr13:48479999..48482410,2	MCF-7	breast:
2	chr13:48501618..48503669-chr13:48506224..48510200,3	K562	blood:
3	chr13:48480107..48482697-chr13:48488766..48491546,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUCLA2-3	chr13:48481153-48481270	NONHSAT033689
2	lnc-SUCLA2-3	chr13:48481153-48481270	ENSG00000234689
3	lnc-NUDT15-4	chr13:48477761-48477842	NONHSAT033691
4	lnc-SUCLA2-3	chr13:48503273-48504009	NONHSAT033689
5	lnc-SUCLA2-2	chr13:48504290-48506757	ENSG00000260388.1
6	lnc-NUDT15-4	chr13:48478857-48479040	NONHSAT033691
7	lnc-SUCLA2-3	chr13:48479464-48479533	ENSG00000234689
8	lnc-SUCLA2-3	chr13:48481466-48481492	ENSG00000234689
9	lnc-SUCLA2-3	chr13:48506205-48506756	NONHSAT033689

No data

Variant related genes	Relation type
LINC00562	TF binding region
LINC00444	TF binding region
LINC00562	CpG island
LINC00444	CpG island
ENSG00000234689	chromatin interactions
ENSG00000260388	chromatin interactions

Extended variants
information (count: 1465 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9534857	chr13:48470681-48470682	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191346378	chr13:48470700-48470701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs34337565	chr13:48470723-48470724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566294445	chr13:48470734-48470735	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371712514	chr13:48470741-48470742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7317860	chr13:48470742-48470743	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548634344	chr13:48470754-48470755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538012951	chr13:48470770-48470771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148170042	chr13:48470771-48470772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs72147013	chr13:48470780-48470781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7981902	chr13:48470791-48470792	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs35249379	chr13:48470813-48470814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183210012	chr13:48470883-48470884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs118052979	chr13:48470917-48470918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562659736	chr13:48470918-48470919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139582407	chr13:48470930-48470931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs61972220	chr13:48470934-48470935	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs201685546	chr13:48470968-48470969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186906867	chr13:48470971-48470972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377180765	chr13:48470972-48470973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546965413	chr13:48470997-48470998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34906349	chr13:48471001-48471002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4942712	chr13:48471044-48471045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs144540691	chr13:48471052-48471053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372655836	chr13:48471063-48471064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557282312	chr13:48471092-48471093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs72450872	chr13:48471123-48471124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569400177	chr13:48471197-48471198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539766999	chr13:48471201-48471202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558058528	chr13:48471208-48471209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114304730	chr13:48471226-48471227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117973411	chr13:48471237-48471238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182139704	chr13:48471239-48471240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573662865	chr13:48471240-48471241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144143846	chr13:48471298-48471299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs562561495	chr13:48471323-48471324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533188053	chr13:48471449-48471450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146549299	chr13:48471456-48471457	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115412479	chr13:48471470-48471471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527583570	chr13:48471472-48471473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546681805	chr13:48471523-48471524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568404166	chr13:48471570-48471571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529385653	chr13:48471592-48471593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551026294	chr13:48471617-48471618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79983659	chr13:48471673-48471674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114687328	chr13:48471757-48471758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557926270	chr13:48471773-48471774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs118069867	chr13:48471787-48471788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534463123	chr13:48471859-48471860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531136220	chr13:48471863-48471864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	17899364	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
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	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
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	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
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48451000-48480200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:48453800-48471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:48457200-48478000	Weak transcription	Adipose Nuclei	Adipose
4	chr13:48461000-48472200	Weak transcription	Spleen	Spleen
5	chr13:48461000-48472400	Weak transcription	Lung	lung
6	chr13:48461000-48478200	Weak transcription	Left Ventricle	heart
7	chr13:48463600-48474600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr13:48465000-48484000	Weak transcription	Primary T cells from cord blood	blood
9	chr13:48465200-48478200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr13:48466400-48471600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr13:48466600-48471000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr13:48466600-48471600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:48466800-48471800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr13:48468000-48471600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:48468600-48485600	Weak transcription	Gastric	stomach
16	chr13:48468800-48479600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:48468800-48482400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr13:48469000-48478200	Weak transcription	Esophagus	oesophagus
19	chr13:48469200-48471400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:48470400-48478000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:48470600-48471600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr13:48471000-48472600	Enhancers	HepG2	liver
23	chr13:48471400-48472000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:48471400-48472000	Enhancers	HSMM	muscle
25	chr13:48471400-48472200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr13:48471400-48472400	Enhancers	HMEC	breast
27	chr13:48471400-48472600	Enhancers	NH-A	brain
28	chr13:48471600-48472000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr13:48471600-48472000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:48471600-48472000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr13:48471600-48472000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr13:48471600-48472000	Enhancers	Osteobl	bone
33	chr13:48471600-48472200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr13:48471600-48472200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:48471600-48472200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr13:48471600-48472200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:48471600-48472200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr13:48471600-48472200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr13:48471600-48472200	Enhancers	NHEK	skin
40	chr13:48471600-48472600	Enhancers	Placenta	Placenta
41	chr13:48471800-48472000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr13:48471800-48472200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr13:48471800-48472200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr13:48472000-48477800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr13:48472000-48482200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr13:48472200-48473000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr13:48472200-48475600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr13:48472200-48482400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr13:48472200-48482400	Weak transcription	NHEK	skin
50	chr13:48472200-48491400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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