Variant report

Variant	nsv1037878
Chromosome Location	chr15:92713130-92739827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:92714142-92714591	HepG2	liver:	n/a	n/a
2	BHLHE40	chr15:92728231-92728455	K562	blood:	n/a	chr15:92728318-92728334
3	CEBPB	chr15:92714120-92714568	HepG2	liver:	n/a	n/a
4	CEBPB	chr15:92714145-92714562	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:92714252-92714455	HepG2	liver:	n/a	n/a
6	CEBPB	chr15:92733949-92734207	HepG2	liver:	n/a	chr15:92734067-92734078
7	CHD2	chr15:92714354-92714509	HepG2	liver:	n/a	n/a
8	CTCF	chr15:92718740-92718890	GM12866	blood:	n/a	n/a
9	CTCF	chr15:92726620-92726770	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr15:92725420-92725570	SK-N-SH_RA	brain:	n/a	n/a
11	ELF1	chr15:92731179-92731738	MCF-7	breast:	n/a	n/a
12	EP300	chr15:92714035-92714562	HepG2	liver:	n/a	n/a
13	EP300	chr15:92731166-92731764	MCF-7	breast:	n/a	n/a
14	EP300	chr15:92714192-92714524	HepG2	liver:	n/a	n/a
15	ESR1	chr15:92731370-92731733	T-47D	breast:	n/a	chr15:92731569-92731586
16	ESR1	chr15:92731341-92731753	T-47D	breast:	n/a	chr15:92731569-92731586
17	ESR1	chr15:92731395-92731665	T-47D	breast:	n/a	chr15:92731569-92731586
18	ESR1	chr15:92731400-92731712	T-47D	breast:	n/a	chr15:92731569-92731586
19	ESR1	chr15:92731319-92731749	T-47D	breast:	n/a	chr15:92731569-92731586
20	ESR1	chr15:92731367-92731704	T-47D	breast:	n/a	chr15:92731569-92731586
21	FOSL2	chr15:92714074-92714646	HepG2	liver:	n/a	n/a
22	FOSL2	chr15:92714124-92714578	HepG2	liver:	n/a	n/a
23	FOXA1	chr15:92714146-92714556	HepG2	liver:	n/a	n/a
24	FOXA1	chr15:92714076-92714522	HepG2	liver:	n/a	n/a
25	FOXA1	chr15:92714163-92714501	HepG2	liver:	n/a	n/a
26	FOXA1	chr15:92714022-92714461	HepG2	liver:	n/a	n/a
27	FOXA2	chr15:92714116-92714435	HepG2	liver:	n/a	n/a
28	FOXM1	chr15:92731163-92731860	MCF-7	breast:	n/a	n/a
29	GATA3	chr15:92731150-92732183	MCF-7	breast:	n/a	chr15:92731546-92731553
30	GATA3	chr15:92731252-92732045	MCF-7	breast:	n/a	chr15:92731546-92731553
31	GATA3	chr15:92731259-92731756	MCF-7	breast:	n/a	chr15:92731546-92731553
32	GATA3	chr15:92731011-92732036	MCF-7	breast:	n/a	chr15:92731546-92731553
33	HA-E2F1	chr15:92731174-92731854	MCF-7	breast:	n/a	n/a
34	HDAC2	chr15:92714125-92714480	HepG2	liver:	n/a	n/a
35	HDAC2	chr15:92731196-92731817	MCF-7	breast:	n/a	n/a
36	HNF4A	chr15:92714126-92714498	HepG2	liver:	n/a	chr15:92714298-92714313 chr15:92714299-92714311 chr15:92714296-92714314 chr15:92714297-92714312 chr15:92714299-92714311 chr15:92714298-92714313 chr15:92714299-92714312 chr15:92714298-92714312 chr15:92714298-92714313
37	HNF4A	chr15:92714090-92714495	HepG2	liver:	n/a	chr15:92714298-92714313 chr15:92714299-92714311 chr15:92714296-92714314 chr15:92714297-92714312 chr15:92714299-92714311 chr15:92714298-92714313 chr15:92714299-92714312 chr15:92714298-92714312 chr15:92714298-92714313
38	HNF4G	chr15:92714019-92714540	HepG2	liver:	n/a	chr15:92714298-92714313 chr15:92714299-92714311 chr15:92714296-92714314 chr15:92714299-92714311 chr15:92714298-92714313 chr15:92714299-92714312 chr15:92714298-92714312 chr15:92714296-92714311 chr15:92714298-92714313
39	HNF4G	chr15:92714061-92714527	HepG2	liver:	n/a	chr15:92714298-92714313 chr15:92714299-92714311 chr15:92714296-92714314 chr15:92714299-92714311 chr15:92714298-92714313 chr15:92714299-92714312 chr15:92714298-92714312 chr15:92714296-92714311 chr15:92714298-92714313
40	JUN	chr15:92714252-92714545	HepG2	liver:	n/a	n/a
41	JUND	chr15:92714184-92714577	HepG2	liver:	n/a	n/a
42	MAFF	chr15:92737286-92737441	HepG2	liver:	n/a	n/a
43	MAFF	chr15:92721698-92721913	HepG2	liver:	n/a	n/a
44	MAFF	chr15:92713997-92714531	HepG2	liver:	n/a	n/a
45	MAFK	chr15:92737221-92737494	HepG2	liver:	n/a	n/a
46	MAFK	chr15:92737263-92737475	HepG2	liver:	n/a	n/a
47	MAFK	chr15:92721641-92721934	IMR90	lung:	n/a	n/a
48	MAFK	chr15:92714027-92714413	HepG2	liver:	n/a	chr15:92714404-92714413
49	MAFK	chr15:92714018-92714374	HepG2	liver:	n/a	n/a
50	MAX	chr15:92731353-92731747	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:92715189-92715239	MCF10A-Er-Src	breast:	n/a
2	chr15:92715189-92715239	HRCEpiC	kidney:	n/a
3	chr15:92715189-92715239	HEK293	kidney:	embryo
4	chr15:92715189-92715239	LNCaP	prostate:	n/a
5	chr15:92715189-92715239	A549	lung:	n/a
6	chr15:92715189-92715239	PANC-1	pancreas:	n/a
7	chr15:92715189-92715239	SKMC	muscle:	n/a
8	chr15:92715189-92715239	T-47D	breast:	n/a
9	chr15:92715189-92715239	NH-A	brain:	n/a
10	chr15:92715189-92715239	AG09309	skin:	n/a
11	chr15:92715189-92715239	HMEC	breast:	n/a
12	chr15:92715189-92715239	AG09319	gingival:	n/a
13	chr15:92715189-92715239	HNPCEpiC	eye:	n/a
14	chr15:92715189-92715239	NB4	blood:	n/a
15	chr15:92715189-92715239	AG10803	skin:	n/a
16	chr15:92715189-92715239	BJ	skin:	n/a
17	chr15:92715189-92715239	AoSMC	blood vessel:	n/a
18	chr15:92715189-92715239	SK-N-SH_RA	brain:	n/a
19	chr15:92715189-92715239	GM12891	blood:	n/a
20	chr15:92715189-92715239	HRPEpiC	eye:	n/a
21	chr15:92715189-92715239	U87	brain:	n/a
22	chr15:92715189-92715239	HCM	heart:	n/a
23	chr15:92715189-92715239	HEEpiC	esophagus:	n/a
24	chr15:92715189-92715239	GM12878	blood:	n/a
25	chr15:92715189-92715239	HepG2	liver:	n/a
26	chr15:92715189-92715239	ProgFib	skin:	n/a
27	chr15:92715189-92715239	SK-N-MC	brain:	n/a
28	chr15:92715189-92715239	SK-N-SH	brain:	n/a
29	chr15:92715189-92715239	PFSK-1	brain:	n/a
30	chr15:92715189-92715239	HIPEpiC	eye:	n/a
31	chr15:92715189-92715239	CMK	blood:	n/a
32	chr15:92715189-92715239	Jurkat	blood:	n/a
33	chr15:92715189-92715239	AG04449	skin:	fetal
34	chr15:92715189-92715239	HAEpiC	amniotic membrane:	n/a
35	chr15:92715189-92715239	HRE	kidney:	n/a
36	chr15:92715189-92715239	HCPEpiC	choroid plexus:	n/a
37	chr15:92715189-92715239	Hela-S3	cervix:	n/a
38	chr15:92715189-92715239	HCF	heart:	n/a
39	chr15:92715189-92715239	HL-60	blood:	n/a
40	chr15:92715189-92715239	SAEC	small airway:	n/a
41	chr15:92715189-92715239	AG04450	lung:	fetal
42	chr15:92715189-92715239	K562	blood:	n/a
43	chr15:92715189-92715239	PrEC	prostate:	n/a
44	chr15:92715189-92715239	H1-hESC	embryonic stem cell:	embryo
45	chr15:92715189-92715239	NHBE	bronchial:	n/a
46	chr15:92715189-92715239	IMR90	lung:	fetal
47	chr15:92715189-92715239	BE2_C	brain:	n/a
48	chr15:92715189-92715239	RPTEC	kidney:	n/a
49	chr15:92715189-92715239	MCF-7	breast:	n/a
50	chr15:92715189-92715239	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:92736484..92738328-chr15:92738601..92741490,2	MCF-7	breast:
2	chr15:92720415..92722812-chr15:92730710..92732386,2	MCF-7	breast:
3	chr15:92711407..92714704-chr15:92715302..92716979,3	K562	blood:
4	chr15:92645092..92647412-chr15:92726254..92727975,2	MCF-7	breast:
5	chr15:92736484..92738328-chr15:92738601..92741490,2	MCF-7	breast:
6	chr15:92702907..92704729-chr15:92722855..92724927,2	K562	blood:
7	chr15:92724157..92727098-chr15:92727915..92730383,2	MCF-7	breast:
8	chr15:92720415..92722812-chr15:92730710..92732386,2	MCF-7	breast:
9	chr15:92724157..92727098-chr15:92727915..92730383,2	MCF-7	breast:
10	chr15:92715714..92718386-chr15:92718766..92720334,3	MCF-7	breast:
11	chr15:92715714..92718386-chr15:92718766..92720334,3	MCF-7	breast:
12	chr15:92711407..92714704-chr15:92715302..92716979,3	K562	blood:
13	chr15:92709419..92711582-chr15:92716283..92718037,2	MCF-7	breast:
14	chr15:92731070..92731782-chr15:93188599..93189119,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM174B-4	chr15:92715250-92715666	ENSG00000258761.1
2	lnc-SLCO3A1-2	chr15:92714102-92715665	NONHSAT048516

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLCO3A1	hsa-let-7e-5p	chr15:92715364-92715385

Variant related genes	Relation type
ENSG00000258761	TF binding region
SLCO3A1	TF binding region
ENSG00000258761	CpG island
SLCO3A1	CpG island
ENSG00000185442	chromatin interactions
ENSG00000176463	chromatin interactions
ENSG00000258761	chromatin interactions

Extended variants
information (count: 1214 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16946485	chr15:92713130-92713131	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531082161	chr15:92713163-92713164	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191875039	chr15:92713168-92713169	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184468752	chr15:92713174-92713175	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535219764	chr15:92713176-92713177	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548781712	chr15:92713179-92713180	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187398461	chr15:92713194-92713195	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534531601	chr15:92713205-92713206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192246736	chr15:92713228-92713229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555259799	chr15:92713246-92713247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs577999630	chr15:92713271-92713272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573581578	chr15:92713297-92713298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537305014	chr15:92713349-92713350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553071592	chr15:92713356-92713357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557434618	chr15:92713417-92713418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114619626	chr15:92713428-92713429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543138583	chr15:92713481-92713482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374960942	chr15:92713486-92713487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559577889	chr15:92713493-92713494	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139526070	chr15:92713580-92713581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545294663	chr15:92713584-92713585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs565090821	chr15:92713586-92713587	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75372489	chr15:92713615-92713616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145065183	chr15:92713646-92713647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185376599	chr15:92713647-92713648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562972084	chr15:92713674-92713675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528865722	chr15:92713681-92713682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548926498	chr15:92713705-92713706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs9744294	chr15:92713710-92713711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs200112162	chr15:92713722-92713723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs17696325	chr15:92713735-92713736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536021995	chr15:92713795-92713796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs377740052	chr15:92713802-92713803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190663081	chr15:92713819-92713820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367863209	chr15:92713861-92713862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537393444	chr15:92713865-92713866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542878944	chr15:92713893-92713894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557273413	chr15:92713894-92713895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372065527	chr15:92713946-92713947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs180814998	chr15:92713962-92713963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184662346	chr15:92714011-92714012	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553304721	chr15:92714018-92714019	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371125594	chr15:92714025-92714026	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573260215	chr15:92714094-92714095	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563421882	chr15:92714106-92714107	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs147556753	chr15:92714124-92714125	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs375047992	chr15:92714132-92714133	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs565184834	chr15:92714141-92714142	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs116010263	chr15:92714148-92714149	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs561260235	chr15:92714150-92714151	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Epilepsy	19486360	CNVD
Acute myeloid leukemia	17237825	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92684000-92713200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr15:92684400-92713200	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr15:92687600-92719400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr15:92690600-92714600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr15:92692800-92715200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr15:92704200-92713200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:92706200-92714800	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:92706400-92713400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr15:92706400-92714800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr15:92708000-92718400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr15:92708200-92719000	Weak transcription	Lung	lung
12	chr15:92708600-92716000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:92709000-92715400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:92709400-92714800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr15:92709800-92714000	Weak transcription	Esophagus	oesophagus
16	chr15:92710800-92713600	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr15:92710800-92713600	Weak transcription	Stomach Mucosa	stomach
18	chr15:92711000-92714800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr15:92711600-92713400	Weak transcription	Fetal Intestine Small	intestine
20	chr15:92711600-92727200	Weak transcription	Left Ventricle	heart
21	chr15:92712000-92713400	Weak transcription	Liver	Liver
22	chr15:92712000-92713400	Weak transcription	HepG2	liver
23	chr15:92712400-92716400	Weak transcription	Fetal Heart	heart
24	chr15:92713000-92717400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr15:92713200-92714000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr15:92713200-92714800	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr15:92713200-92714800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr15:92713400-92714200	Enhancers	GM12878-XiMat	blood
29	chr15:92713400-92715200	Enhancers	Liver	Liver
30	chr15:92713400-92715400	Enhancers	HepG2	liver
31	chr15:92713600-92713800	Enhancers	Fetal Intestine Small	intestine
32	chr15:92713600-92714400	Enhancers	Stomach Mucosa	stomach
33	chr15:92714000-92714200	Enhancers	Esophagus	oesophagus
34	chr15:92714000-92715400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr15:92714400-92714600	Enhancers	Fetal Intestine Large	intestine
36	chr15:92715200-92715400	Enhancers	Fetal Muscle Trunk	muscle
37	chr15:92716400-92717000	Enhancers	Fetal Heart	heart
38	chr15:92718400-92720400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr15:92719400-92719800	Enhancers	Primary hematopoietic stem cells	blood
40	chr15:92719600-92719800	Enhancers	Lung	lung
41	chr15:92722000-92722400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr15:92722000-92722400	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr15:92725600-92725800	Enhancers	HSMMtube	muscle
44	chr15:92725800-92726800	Weak transcription	HSMMtube	muscle
45	chr15:92726000-92728000	Enhancers	Fetal Heart	heart
46	chr15:92726600-92727200	Enhancers	Psoas Muscle	Psoas
47	chr15:92726800-92728400	Enhancers	Fetal Thymus	thymus
48	chr15:92726800-92728400	Enhancers	Thymus	Thymus
49	chr15:92726800-92728800	Enhancers	HSMMtube	muscle
50	chr15:92726800-92729000	Enhancers	Fetal Muscle Leg	muscle

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