Variant report

Variant	nsv521972
Chromosome Location	chr15:72859770-72878772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:245 , 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	BRCA1	chr15:72864294-72864303	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr15:72872212-72872513	HepG2	liver:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
3	CEBPB	chr15:72872214-72872522	Hela-S3	cervix:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
4	CEBPB	chr15:72862480-72862677	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:72872181-72872536	IMR90	lung:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
6	CEBPB	chr15:72862462-72862634	IMR90	lung:	n/a	n/a
7	CEBPB	chr15:72872214-72872539	A549	lung:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
8	CEBPB	chr15:72872202-72872378	H1-hESC	embryonic stem cell:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
9	CEBPB	chr15:72866020-72866245	IMR90	lung:	n/a	chr15:72866088-72866101 chr15:72866090-72866101 chr15:72866088-72866101
10	CEBPB	chr15:72872186-72872509	K562	blood:	n/a	chr15:72872341-72872352 chr15:72872303-72872314
11	CTCF	chr15:72878180-72878236	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr15:72878111-72878295	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr15:72878140-72878290	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr15:72878110-72878315	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr15:72878100-72878250	NHEK	skin:	n/a	n/a
16	CTCF	chr15:72878217-72878251	MCF-7	breast:	n/a	n/a
17	CTCF	chr15:72878140-72878290	HVMF	connective:	n/a	n/a
18	CTCF	chr15:72877980-72878501	MCF-7	breast:	n/a	n/a
19	CTCF	chr15:72878027-72878272	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr15:72878100-72878250	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr15:72878080-72878230	HMF	breast:	n/a	n/a
22	CTCF	chr15:72878100-72878250	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr15:72878140-72878290	AG09309	skin:	n/a	n/a
24	CTCF	chr15:72878120-72878270	GM12872	blood:	n/a	n/a
25	CTCF	chr15:72878120-72878270	AG10803	skin:	n/a	n/a
26	CTCF	chr15:72878100-72878250	BE2_C	brain:	n/a	n/a
27	CTCF	chr15:72861544-72861598	GM10248	blood:	n/a	n/a
28	CTCF	chr15:72878114-72878306	Gliobla	brain:	n/a	n/a
29	CTCF	chr15:72878099-72878313	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr15:72878020-72878170	HVMF	connective:	n/a	n/a
31	CTCF	chr15:72878120-72878270	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr15:72878096-72878317	MCF-7	breast:	n/a	n/a
33	CTCF	chr15:72878142-72878262	GM13977	blood:	n/a	n/a
34	CTCF	chr15:72878180-72878330	HCT-116	colon:	n/a	n/a
35	CTCF	chr15:72878080-72878230	NHLF	lung:	n/a	n/a
36	CTCF	chr15:72878140-72878290	HEK293	kidney:	n/a	n/a
37	CTCF	chr15:72878140-72878290	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr15:72878092-72878306	A549	lung:	n/a	n/a
39	CTCF	chr15:72878140-72878290	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr15:72878080-72878230	WI-38	lung:	n/a	n/a
41	CTCF	chr15:72878160-72878310	SAEC	small airway:	n/a	n/a
42	CTCF	chr15:72873060-72873210	GM12872	blood:	n/a	n/a
43	CTCF	chr15:72878120-72878270	A549	lung:	n/a	n/a
44	CTCF	chr15:72878080-72878230	HAc	cerebellar:	n/a	n/a
45	CTCF	chr15:72878032-72878221	A549	lung:	n/a	n/a
46	CTCF	chr15:72878220-72878370	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr15:72878040-72878190	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr15:72878120-72878270	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr15:72878120-72878270	RPTEC	kidney:	n/a	n/a
50	CTCF	chr15:72878180-72878330	GM12866	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72876508-72876558	HRCEpiC	kidney:	n/a
2	chr15:72876508-72876558	HRE	kidney:	n/a
3	chr15:72876508-72876558	SK-N-SH_RA	brain:	n/a
4	chr15:72876508-72876558	HAEpiC	amniotic membrane:	n/a
5	chr15:72876508-72876558	A549	lung:	n/a
6	chr15:72876508-72876558	GM06990	blood:	n/a
7	chr15:72876508-72876558	Hepatocyte	liver:	n/a
8	chr15:72876508-72876558	RPTEC	kidney:	n/a
9	chr15:72876508-72876558	HepG2	liver:	n/a
10	chr15:72876508-72876558	ovcar-3	ovarian:	n/a
11	chr15:72876508-72876558	MCF10A-Er-Src	breast:	n/a
12	chr15:72876508-72876558	MCF-7	breast:	n/a
13	chr15:72876508-72876558	PrEC	prostate:	n/a
14	chr15:72876508-72876558	HCT-116	colon:	n/a
15	chr15:72876508-72876558	NB4	blood:	n/a
16	chr15:72876508-72876558	SK-N-MC	brain:	n/a
17	chr15:72876508-72876558	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:72876508-72876558	Caco-2	colon:	n/a
19	chr15:72876508-72876558	Hela-S3	cervix:	n/a
20	chr15:72876508-72876558	K562	blood:	n/a
21	chr15:72876508-72876558	GM12892	blood:	n/a
22	chr15:72876508-72876558	HNPCEpiC	eye:	n/a
23	chr15:72876508-72876558	AG09309	skin:	n/a
24	chr15:72876508-72876558	BE2_C	brain:	n/a
25	chr15:72876508-72876558	LNCaP	prostate:	n/a
26	chr15:72876508-72876558	ECC-1	luminal epithelium:	n/a
27	chr15:72876508-72876558	PANC-1	pancreas:	n/a
28	chr15:72876508-72876558	SK-N-SH	brain:	n/a
29	chr15:72876508-72876558	HUVEC	blood vessel:	n/a
30	chr15:72876508-72876558	AoSMC	blood vessel:	n/a
31	chr15:72876508-72876558	IMR90	lung:	fetal
32	chr15:72876508-72876558	U87	brain:	n/a
33	chr15:72876508-72876558	SAEC	small airway:	n/a
34	chr15:72876508-72876558	BJ	skin:	n/a
35	chr15:72876508-72876558	HMEC	breast:	n/a
36	chr15:72876508-72876558	CMK	blood:	n/a
37	chr15:72876508-72876558	HEEpiC	esophagus:	n/a
38	chr15:72876508-72876558	GM12891	blood:	n/a
39	chr15:72876508-72876558	PFSK-1	brain:	n/a
40	chr15:72876508-72876558	AG04449	skin:	fetal
41	chr15:72876508-72876558	GM12878	blood:	n/a
42	chr15:72876508-72876558	HCM	heart:	n/a
43	chr15:72876508-72876558	H1-hESC	embryonic stem cell:	embryo
44	chr15:72876508-72876558	GM19239	blood:	n/a
45	chr15:72876508-72876558	HL-60	blood:	n/a
46	chr15:72876508-72876558	NHBE	bronchial:	n/a
47	chr15:72876508-72876558	AG04450	lung:	fetal
48	chr15:72876508-72876558	Jurkat	blood:	n/a
49	chr15:72876508-72876558	HRPEpiC	eye:	n/a
50	chr15:72876508-72876558	SKMC	muscle:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72855805..72858326-chr15:72860263..72862647,4	K562	blood:
2	chr15:72875535..72877060-chr15:72880584..72882682,2	K562	blood:
3	chr15:72765119..72768565-chr15:72866514..72869188,4	MCF-7	breast:
4	chr10:14226515..14228688-chr15:72869488..72872468,2	K562	blood:
5	chr15:72860065..72861886-chr15:72865467..72867105,2	K562	blood:
6	chr15:72870050..72872612-chr15:72882296..72884014,2	MCF-7	breast:
7	chr15:72876608..72879489-chr15:72887263..72889049,2	MCF-7	breast:
8	chr15:72871985..72876083-chr15:72877411..72879866,3	K562	blood:
9	chr15:72764608..72767510-chr15:72858916..72862461,3	K562	blood:
10	chr15:72523201..72524932-chr15:72878327..72881016,2	MCF-7	breast:
11	chr10:14227180..14228688-chr15:72870968..72872488,2	K562	blood:
12	chr15:72855852..72858795-chr15:72878278..72880560,2	K562	blood:
13	chr15:72668326..72670574-chr15:72860104..72862462,2	MCF-7	breast:
14	chr15:72867565..72869086-chr15:72877556..72879281,2	MCF-7	breast:
15	chr15:72764026..72766932-chr15:72877151..72879938,2	K562	blood:
16	chr15:72860065..72861886-chr15:72865467..72867105,2	K562	blood:
17	chr15:72875994..72878313-chr15:72882141..72883878,2	MCF-7	breast:
18	chr15:72871985..72876083-chr15:72877411..72879866,3	K562	blood:
19	chr15:72867565..72869086-chr15:72877556..72879281,2	MCF-7	breast:
20	chr15:72674377..72675186-chr15:72877692..72878568,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ARIH1	hsa-miR-425-5p	chr15:72877901-72877921

Variant related genes	Relation type
ENSG00000260534	TF binding region
ARIH1	TF binding region
MIR630	TF binding region
ENSG00000260534	CpG island
ARIH1	CpG island
MIR630	CpG island
ENSG00000260339	chromatin interactions
ENSG00000207690	chromatin interactions
ENSG00000213614	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000260534	chromatin interactions
ENSG00000261423	chromatin interactions

Extended variants
information (count: 603 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2278694	chr15:72859770-72859771	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540702597	chr15:72859822-72859823	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562270704	chr15:72859841-72859842	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571503044	chr15:72859862-72859863	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189258057	chr15:72859863-72859864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35261899	chr15:72859926-72859927	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569533242	chr15:72859938-72859939	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530454499	chr15:72859954-72859955	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs12324013	chr15:72859981-72859982	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12324014	chr15:72859994-72859995	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536171555	chr15:72859998-72859999	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533788865	chr15:72860022-72860023	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149392408	chr15:72860026-72860027	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs73444798	chr15:72860048-72860049	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368821352	chr15:72860091-72860092	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs552607951	chr15:72860111-72860112	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs567952150	chr15:72860127-72860128	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs535266265	chr15:72860134-72860135	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs557000941	chr15:72860179-72860180	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs143710375	chr15:72860206-72860207	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs148111911	chr15:72860208-72860209	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs141859887	chr15:72860251-72860252	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs558153729	chr15:72860300-72860301	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs553548536	chr15:72860313-72860314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs79580042	chr15:72860333-72860334	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs181030031	chr15:72860357-72860358	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs186059700	chr15:72860373-72860374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs191208627	chr15:72860377-72860378	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs181136732	chr15:72860379-72860380	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs533697047	chr15:72860380-72860381	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs551738277	chr15:72860514-72860515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs186163518	chr15:72860518-72860519	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs570119708	chr15:72860549-72860550	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs528066177	chr15:72860558-72860559	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs556259487	chr15:72860596-72860597	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs546334927	chr15:72860704-72860705	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs540044907	chr15:72860707-72860708	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs535514784	chr15:72860716-72860717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs558238064	chr15:72860741-72860742	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs190534581	chr15:72860955-72860956	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs78574393	chr15:72860979-72860980	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs182961966	chr15:72860982-72860983	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs568930571	chr15:72861004-72861005	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375128154	chr15:72861024-72861025	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs10518993	chr15:72861064-72861065	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557727947	chr15:72861123-72861124	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs147240289	chr15:72861188-72861189	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs534182585	chr15:72861235-72861236	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs555926729	chr15:72861252-72861253	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs574168741	chr15:72861338-72861339	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72828600-72869800	Weak transcription	Aorta	Aorta
2	chr15:72829200-72880800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:72830400-72866800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:72830800-72867400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:72833600-72865000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:72833600-72867000	Weak transcription	Right Ventricle	heart
7	chr15:72833600-72870200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:72833600-72870400	Weak transcription	Gastric	stomach
9	chr15:72835200-72876000	Weak transcription	Pancreas	Pancrea
10	chr15:72835600-72870400	Weak transcription	Spleen	Spleen
11	chr15:72836600-72870000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:72838600-72862400	Weak transcription	Fetal Heart	heart
13	chr15:72838800-72870400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr15:72839400-72866600	Weak transcription	Lung	lung
15	chr15:72841000-72909000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr15:72844400-72870000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr15:72844600-72870400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:72846600-72865400	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr15:72846600-72868600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr15:72846600-72878400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr15:72846800-72870200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr15:72847000-72878400	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr15:72847200-72867400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr15:72847200-72870000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr15:72847600-72860800	Strong transcription	Dnd41	blood
26	chr15:72847800-72878000	Strong transcription	Primary B cells from peripheral blood	blood
27	chr15:72847800-72878400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr15:72848800-72863800	Weak transcription	Brain Anterior Caudate	brain
29	chr15:72848800-72867800	Weak transcription	Colonic Mucosa	Colon
30	chr15:72849000-72870200	Weak transcription	Fetal Brain Male	brain
31	chr15:72850200-72880800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr15:72851200-72867400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr15:72851400-72877600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:72851800-72867800	Strong transcription	HepG2	liver
35	chr15:72851800-72868600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:72852000-72878800	Strong transcription	Placenta	Placenta
37	chr15:72852600-72860000	Strong transcription	Osteobl	bone
38	chr15:72852600-72870800	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr15:72852800-72861000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr15:72852800-72868600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr15:72852800-72878400	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr15:72853000-72872600	Weak transcription	Stomach Mucosa	stomach
43	chr15:72853200-72859800	Strong transcription	NHDF-Ad	bronchial
44	chr15:72853200-72867400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr15:72853600-72879800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:72853800-72868600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:72854000-72860200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:72854200-72870600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr15:72854400-72860400	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr15:72854400-72860600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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