Variant report

Variant	nsv569155
Chromosome Location	chr15:35371869-35408386
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:119)
CpG islands
(count:977)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:119 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:35382126-35382748	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:35393584-35393809	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:35375349-35375384	HepG2	liver:	n/a	n/a
4	BHLHE40	chr15:35397564-35397568	GM12878	blood:	n/a	n/a
5	CEBPB	chr15:35402877-35402953	HepG2	liver:	n/a	chr15:35402884-35402895 chr15:35402884-35402897
6	CTCF	chr15:35381060-35381210	GM12873	blood:	n/a	n/a
7	CTCF	chr15:35376460-35376610	HepG2	liver:	n/a	n/a
8	CTCF	chr15:35376744-35376778	GM13977	blood:	n/a	n/a
9	CTCF	chr15:35377037-35377136	GM13976	blood:	n/a	n/a
10	CTCF	chr15:35375372-35375450	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr15:35398860-35399010	HMF	breast:	n/a	n/a
12	CTCF	chr15:35405560-35405710	GM06990	blood:	n/a	n/a
13	CTCF	chr15:35398951-35398953	K562	blood:	n/a	n/a
14	CTCF	chr15:35375378-35375462	GM10248	blood:	n/a	n/a
15	CTCF	chr15:35376717-35376736	GM13977	blood:	n/a	n/a
16	CTCF	chr15:35377944-35378007	MCF-7	breast:	n/a	n/a
17	E2F4	chr15:35397208-35397303	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr15:35398239-35398248	GM12878	blood:	n/a	n/a
19	EP300	chr15:35382303-35382729	HepG2	liver:	n/a	n/a
20	EP300	chr15:35382267-35382649	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr15:35390912-35391283	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr15:35378258-35378429	GM12878	blood:	n/a	n/a
23	EP300	chr15:35382286-35382685	HepG2	liver:	n/a	n/a
24	EP300	chr15:35382286-35382666	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr15:35407337-35407632	HepG2	liver:	n/a	n/a
26	EP300	chr15:35377654-35377856	HepG2	liver:	n/a	n/a
27	FAM48A	chr15:35393725-35393765	GM12878	blood:	n/a	n/a
28	FOS	chr15:35380103-35380153	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr15:35399488-35399622	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr15:35399422-35399589	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL2	chr15:35382338-35382639	HepG2	liver:	n/a	n/a
32	FOXA1	chr15:35382188-35382672	HepG2	liver:	n/a	n/a
33	FOXA1	chr15:35382279-35382798	HepG2	liver:	n/a	n/a
34	FOXA1	chr15:35375097-35375595	HepG2	liver:	n/a	n/a
35	FOXA1	chr15:35402762-35403162	HepG2	liver:	n/a	n/a
36	FOXA1	chr15:35393495-35393938	HepG2	liver:	n/a	n/a
37	FOXA1	chr15:35402861-35403107	HepG2	liver:	n/a	n/a
38	FOXA1	chr15:35402832-35403166	HepG2	liver:	n/a	n/a
39	FOXA1	chr15:35382209-35382734	HepG2	liver:	n/a	n/a
40	FOXA1	chr15:35393574-35393887	HepG2	liver:	n/a	n/a
41	FOXA1	chr15:35402771-35403090	HepG2	liver:	n/a	n/a
42	FOXA1	chr15:35393562-35393858	HepG2	liver:	n/a	n/a
43	FOXA1	chr15:35382221-35382709	HepG2	liver:	n/a	n/a
44	FOXA1	chr15:35374957-35375631	HepG2	liver:	n/a	n/a
45	FOXA2	chr15:35375092-35375514	A549	lung:	n/a	n/a
46	FOXA2	chr15:35375189-35375480	HepG2	liver:	n/a	n/a
47	FOXA2	chr15:35393584-35393833	HepG2	liver:	n/a	n/a
48	FOXA2	chr15:35382266-35382890	HepG2	liver:	n/a	n/a
49	FOXA2	chr15:35402865-35403057	HepG2	liver:	n/a	n/a
50	FOXA2	chr15:35382326-35382698	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35384714-35384764	SK-N-MC	brain:	n/a
2	chr15:35384714-35384764	SK-N-MC	brain:	n/a
3	chr15:35385240-35385290	BJ	skin:	n/a
4	chr15:35374148-35374198	SAEC	small airway:	n/a
5	chr15:35388805-35388855	HCM	heart:	n/a
6	chr15:35384129-35384179	NHBE	bronchial:	n/a
7	chr15:35372947-35372997	AG09309	skin:	n/a
8	chr15:35384714-35384764	HRE	kidney:	n/a
9	chr15:35384648-35384698	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:35384648-35384698	NH-A	brain:	n/a
11	chr15:35385240-35385290	HCF	heart:	n/a
12	chr15:35388805-35388855	Hela-S3	cervix:	n/a
13	chr15:35372947-35372997	NHDF-neo	bronchial:	n/a
14	chr15:35396612-35396662	HUVEC	blood vessel:	n/a
15	chr15:35384650-35384700	Jurkat	blood:	n/a
16	chr15:35372947-35372997	RPTEC	kidney:	n/a
17	chr15:35384864-35384914	GM06990	blood:	n/a
18	chr15:35375018-35375068	HMEC	breast:	n/a
19	chr15:35384864-35384914	LNCaP	prostate:	n/a
20	chr15:35384864-35384914	ECC-1	luminal epithelium:	n/a
21	chr15:35384654-35384704	Jurkat	blood:	n/a
22	chr15:35388805-35388855	HAEpiC	amniotic membrane:	n/a
23	chr15:35384654-35384704	MCF-7	breast:	n/a
24	chr15:35384650-35384700	HIPEpiC	eye:	n/a
25	chr15:35375018-35375068	PrEC	prostate:	n/a
26	chr15:35385101-35385151	HepG2	liver:	n/a
27	chr15:35385353-35385403	NHBE	bronchial:	n/a
28	chr15:35384654-35384704	A549	lung:	n/a
29	chr15:35385240-35385290	HCM	heart:	n/a
30	chr15:35372947-35372997	PANC-1	pancreas:	n/a
31	chr15:35385101-35385151	IMR90	lung:	fetal
32	chr15:35384648-35384698	HNPCEpiC	eye:	n/a
33	chr15:35384864-35384914	NH-A	brain:	n/a
34	chr15:35384714-35384764	PrEC	prostate:	n/a
35	chr15:35396612-35396662	NHDF-neo	bronchial:	n/a
36	chr15:35372947-35372997	BE2_C	brain:	n/a
37	chr15:35381318-35381368	GM06990	blood:	n/a
38	chr15:35372947-35372997	LNCaP	prostate:	n/a
39	chr15:35384648-35384698	Jurkat	blood:	n/a
40	chr15:35384648-35384698	HepG2	liver:	n/a
41	chr15:35396612-35396662	MCF10A-Er-Src	breast:	n/a
42	chr15:35396612-35396662	SAEC	small airway:	n/a
43	chr15:35396612-35396662	AoSMC	blood vessel:	n/a
44	chr15:35385101-35385151	HCPEpiC	choroid plexus:	n/a
45	chr15:35374148-35374198	GM12891	blood:	n/a
46	chr15:35396612-35396662	PrEC	prostate:	n/a
47	chr15:35372947-35372997	HUVEC	blood vessel:	n/a
48	chr15:35384648-35384698	PrEC	prostate:	n/a
49	chr15:35385240-35385290	SKMC	muscle:	n/a
50	chr15:35384714-35384764	HEK293	kidney:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:35405163..35407322-chr15:35410998..35413747,2	K562	blood:
2	chr15:35371050..35372574-chr15:35610805..35612927,2	K562	blood:
3	chr15:35372169..35374065-chr15:35837227..35839807,2	K562	blood:
4	chr15:35398374..35400467-chr15:35402747..35404431,2	K562	blood:
5	chr15:35398374..35400467-chr15:35402747..35404431,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114546.1-6	chr15:35373345-35373714	NONHSAT041616
2	lnc-AC114546.1-6	chr15:35374996-35375071	NONHSAT041617
3	lnc-ATPBD4-1	chr15:35391223-35392490	ENSG00000259336.1
4	lnc-AC114546.1-6	chr15:35373528-35373750	NONHSAT041617

No data

Variant related genes	Relation type
ENSG00000259665	TF binding region
ENSG00000259397	TF binding region
NANOGP8	TF binding region
ENSG00000259665	CpG island
ENSG00000259397	CpG island
NANOGP8	CpG island
ENSG00000134146	chromatin interactions
ENSG00000248079	chromatin interactions

Extended variants
information (count: 1279 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8030031	chr15:35371869-35371870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80199448	chr15:35371948-35371949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs8035211	chr15:35371962-35371963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370044995	chr15:35371972-35371973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556517215	chr15:35372013-35372014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs55800503	chr15:35372014-35372015	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536506050	chr15:35372037-35372038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182914870	chr15:35372072-35372073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533820178	chr15:35372107-35372108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572670991	chr15:35372117-35372118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7175331	chr15:35372179-35372180	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs558362978	chr15:35372221-35372222	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576851980	chr15:35372246-35372247	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs142682742	chr15:35372258-35372259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562497632	chr15:35372316-35372317	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529669011	chr15:35372337-35372338	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs542495343	chr15:35372422-35372423	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs560788979	chr15:35372457-35372458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527854658	chr15:35372460-35372461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552780925	chr15:35372503-35372504	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs186925857	chr15:35372517-35372518	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs150909290	chr15:35372528-35372529	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs550015908	chr15:35372567-35372568	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs376775131	chr15:35372645-35372646	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs898125	chr15:35372686-35372687	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191413484	chr15:35372738-35372739	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs562265225	chr15:35372753-35372754	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs139403213	chr15:35372850-35372851	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2279069	chr15:35372893-35372894	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185075096	chr15:35372933-35372934	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113988117	chr15:35372950-35372951	ZNF genes & repeats Enhancers Weak transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544257457	chr15:35372977-35372978	ZNF genes & repeats Enhancers Weak transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs551223446	chr15:35373038-35373039	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs2279068	chr15:35373063-35373064	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555594610	chr15:35373102-35373103	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574347581	chr15:35373126-35373127	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs187719431	chr15:35373133-35373134	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376553631	chr15:35373159-35373160	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs118129699	chr15:35373164-35373165	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527986622	chr15:35373223-35373224	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs546560204	chr15:35373229-35373230	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4923897	chr15:35373235-35373236	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs531815069	chr15:35373276-35373277	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550217649	chr15:35373291-35373292	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568475475	chr15:35373316-35373317	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs529421822	chr15:35373349-35373350	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs111371661	chr15:35373357-35373358	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs576058354	chr15:35373382-35373383	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs565784863	chr15:35373396-35373397	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs73377079	chr15:35373403-35373404	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35357000-35379400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:35370600-35372800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr15:35370600-35373600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:35371000-35373200	Enhancers	Fetal Stomach	stomach
5	chr15:35371200-35372600	Weak transcription	Ovary	ovary
6	chr15:35371600-35373000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr15:35371600-35373000	Enhancers	Fetal Lung	lung
8	chr15:35372000-35372400	Enhancers	NHLF	lung
9	chr15:35372200-35372800	Enhancers	Rectal Smooth Muscle	rectum
10	chr15:35372600-35372800	Enhancers	Ovary	ovary
11	chr15:35372800-35373000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr15:35373000-35380800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr15:35373600-35375200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr15:35374000-35375000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr15:35374400-35375200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:35374400-35375200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:35375000-35375200	Enhancers	HepG2	liver
18	chr15:35375200-35377800	Weak transcription	HepG2	liver
19	chr15:35375200-35379400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:35375600-35377400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr15:35375600-35381000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr15:35377800-35378000	Enhancers	Left Ventricle	heart
23	chr15:35377800-35378200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr15:35377800-35378400	Enhancers	HepG2	liver
25	chr15:35378000-35378200	Enhancers	Right Atrium	heart
26	chr15:35378000-35396400	Weak transcription	Left Ventricle	heart
27	chr15:35378400-35379800	Weak transcription	HepG2	liver
28	chr15:35379400-35379600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:35379400-35379600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:35379600-35380400	Enhancers	Fetal Kidney	kidney
31	chr15:35379600-35385000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr15:35379800-35383400	Enhancers	HepG2	liver
33	chr15:35380600-35381200	Enhancers	Liver	Liver
34	chr15:35381000-35381200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr15:35381000-35381400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr15:35381200-35382400	Weak transcription	Liver	Liver
37	chr15:35382200-35386600	Weak transcription	Ovary	ovary
38	chr15:35382400-35382600	Enhancers	Liver	Liver
39	chr15:35383000-35384600	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr15:35383400-35390400	Weak transcription	Right Ventricle	heart
41	chr15:35384200-35384800	Weak transcription	Aorta	Aorta
42	chr15:35384600-35385200	Weak transcription	Fetal Stomach	stomach
43	chr15:35384600-35385200	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr15:35384800-35385200	ZNF genes & repeats	Aorta	Aorta
45	chr15:35384800-35385200	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr15:35385000-35385200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:35385000-35385400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:35385200-35385400	Strong transcription	Aorta	Aorta
49	chr15:35385200-35386800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr15:35385400-35389200	Weak transcription	Aorta	Aorta

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