Variant report

Variant	nsv977712
Chromosome Location	chr15:45501081-45515127
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	BHLHE40	chr15:45504812-45505012	K562	blood:	n/a	n/a
2	CBX3	chr15:45507633-45508025	K562	blood:	n/a	n/a
3	CEBPB	chr15:45504996-45505004	K562	blood:	n/a	n/a
4	CEBPB	chr15:45514460-45514695	HepG2	liver:	n/a	chr15:45514520-45514531
5	CEBPD	chr15:45504708-45504984	K562	blood:	n/a	n/a
6	CEBPD	chr15:45504729-45505135	K562	blood:	n/a	n/a
7	CTCF	chr15:45507720-45507870	RPTEC	kidney:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
8	CTCF	chr15:45514271-45514373	MCF-7	breast:	n/a	n/a
9	CTCF	chr15:45514260-45514392	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr15:45507720-45507926	MCF-7	breast:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
11	CTCF	chr15:45507760-45507910	NHLF	lung:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
12	CTCF	chr15:45507740-45507890	GM12872	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
13	CTCF	chr15:45507720-45507936	GM12878	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
14	CTCF	chr15:45514296-45514368	GM12891	blood:	n/a	n/a
15	CTCF	chr15:45507744-45507864	A549	lung:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
16	CTCF	chr15:45514240-45514390	GM12864	blood:	n/a	n/a
17	CTCF	chr15:45514242-45514356	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr15:45507743-45507951	NHEK	skin:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
19	CTCF	chr15:45507840-45507990	NHEK	skin:	n/a	n/a
20	CTCF	chr15:45507780-45507930	GM12867	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
21	CTCF	chr15:45514140-45514290	HRE	kidney:	n/a	n/a
22	CTCF	chr15:45507758-45507927	MCF-7	breast:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
23	CTCF	chr15:45507700-45507850	HCM	heart:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
24	CTCF	chr15:45507760-45507910	Hela-S3	cervix:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
25	CTCF	chr15:45507760-45507910	K562	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
26	CTCF	chr15:45507760-45507910	HMEC	breast:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
27	CTCF	chr15:45514220-45514370	HRE	kidney:	n/a	n/a
28	CTCF	chr15:45507730-45507948	A549	lung:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
29	CTCF	chr15:45507800-45507950	AG04449	skin:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
30	CTCF	chr15:45507700-45507850	AG09309	skin:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
31	CTCF	chr15:45507737-45507947	ProgFib	skin:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
32	CTCF	chr15:45507780-45507930	HEEpiC	esophagus:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
33	CTCF	chr15:45507680-45507830	AG04450	lung:	n/a	n/a
34	CTCF	chr15:45507780-45507930	HepG2	liver:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
35	CTCF	chr15:45507729-45507951	HepG2	liver:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
36	CTCF	chr15:45507691-45507984	K562	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
37	CTCF	chr15:45507800-45507950	HA-sp	spinal cord:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
38	CTCF	chr15:45514160-45514310	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr15:45507840-45507990	GM06990	blood:	n/a	n/a
40	CTCF	chr15:45507780-45507930	SK-N-SH_RA	brain:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
41	CTCF	chr15:45507760-45507910	GM12871	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
42	CTCF	chr15:45514222-45514434	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr15:45514300-45514450	GM12873	blood:	n/a	n/a
44	CTCF	chr15:45507800-45507950	HFF-Myc	foreskin:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
45	CTCF	chr15:45507660-45507810	A549	lung:	n/a	n/a
46	CTCF	chr15:45514220-45514370	GM12864	blood:	n/a	n/a
47	CTCF	chr15:45507620-45507770	HMEC	breast:	n/a	n/a
48	CTCF	chr15:45507798-45507930	LNCaP	prostate:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
49	CTCF	chr15:45507780-45507930	GM12869	blood:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842
50	CTCF	chr15:45507760-45507910	HPAF	blood vessel:	n/a	chr15:45507828-45507844 chr15:45507829-45507842 chr15:45507822-45507843 chr15:45507827-45507845 chr15:45507829-45507842

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45507695-45507745	HRCEpiC	kidney:	n/a
2	chr15:45507695-45507745	HRCEpiC	kidney:	n/a
3	chr15:45507820-45507870	RPTEC	kidney:	n/a
4	chr15:45507695-45507745	SAEC	small airway:	n/a
5	chr15:45507820-45507870	U87	brain:	n/a
6	chr15:45507820-45507870	ECC-1	luminal epithelium:	n/a
7	chr15:45507695-45507745	U87	brain:	n/a
8	chr15:45507901-45507951	RPTEC	kidney:	n/a
9	chr15:45507695-45507745	T-47D	breast:	n/a
10	chr15:45507695-45507745	AG09319	gingival:	n/a
11	chr15:45507695-45507745	K562	blood:	n/a
12	chr15:45507820-45507870	MCF10A-Er-Src	breast:	n/a
13	chr15:45507695-45507745	HL-60	blood:	n/a
14	chr15:45507820-45507870	GM12878	blood:	n/a
15	chr15:45507695-45507745	PrEC	prostate:	n/a
16	chr15:45507820-45507870	AG10803	skin:	n/a
17	chr15:45507901-45507951	HRE	kidney:	n/a
18	chr15:45507901-45507951	NB4	blood:	n/a
19	chr15:45507901-45507951	HepG2	liver:	n/a
20	chr15:45507820-45507870	HepG2	liver:	n/a
21	chr15:45507695-45507745	AG09309	skin:	n/a
22	chr15:45507820-45507870	AG09319	gingival:	n/a
23	chr15:45507820-45507870	HIPEpiC	eye:	n/a
24	chr15:45507820-45507870	PFSK-1	brain:	n/a
25	chr15:45507901-45507951	PANC-1	pancreas:	n/a
26	chr15:45507695-45507745	HCF	heart:	n/a
27	chr15:45507901-45507951	HIPEpiC	eye:	n/a
28	chr15:45507695-45507745	HMEC	breast:	n/a
29	chr15:45507695-45507745	HRE	kidney:	n/a
30	chr15:45507820-45507870	GM12892	blood:	n/a
31	chr15:45507820-45507870	HMEC	breast:	n/a
32	chr15:45507820-45507870	K562	blood:	n/a
33	chr15:45507820-45507870	HAEpiC	amniotic membrane:	n/a
34	chr15:45507901-45507951	SK-N-MC	brain:	n/a
35	chr15:45507820-45507870	IMR90	lung:	fetal
36	chr15:45507820-45507870	A549	lung:	n/a
37	chr15:45507820-45507870	T-47D	breast:	n/a
38	chr15:45507695-45507745	A549	lung:	n/a
39	chr15:45507901-45507951	SAEC	small airway:	n/a
40	chr15:45507695-45507745	H1-hESC	embryonic stem cell:	embryo
41	chr15:45507820-45507870	Hela-S3	cervix:	n/a
42	chr15:45507695-45507745	AG04450	lung:	fetal
43	chr15:45507695-45507745	HUVEC	blood vessel:	n/a
44	chr15:45507695-45507745	HAEpiC	amniotic membrane:	n/a
45	chr15:45507695-45507745	BJ	skin:	n/a
46	chr15:45507820-45507870	SKMC	muscle:	n/a
47	chr15:45507695-45507745	Hela-S3	cervix:	n/a
48	chr15:45507901-45507951	CMK	blood:	n/a
49	chr15:45507820-45507870	HCM	heart:	n/a
50	chr15:45507820-45507870	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr15:45497672..45499450-chr15:45511651..45513794,2	MCF-7	breast:
2	chr15:45499576..45501512-chr15:45693488..45695611,2	K562	blood:
3	chr15:45491035..45492770-chr15:45505625..45508217,2	K562	blood:
4	chr15:45502112..45504054-chr15:45507904..45509408,2	K562	blood:
5	chr15:45458183..45461229-chr15:45504288..45506472,3	K562	blood:
6	chr15:45512789..45515700-chr15:45518992..45521212,2	MCF-7	breast:
7	chr15:45492950..45494986-chr15:45503176..45505025,2	MCF-7	breast:
8	chr15:45502112..45504054-chr15:45507904..45509408,2	K562	blood:
9	chr15:45514291..45516823-chr15:45570739..45573209,2	MCF-7	breast:
10	chr15:45496656..45498769-chr15:45514443..45516075,2	K562	blood:
11	chr15:45478493..45480559-chr15:45513673..45516315,2	MCF-7	breast:
12	chr15:45494998..45498237-chr15:45508390..45511192,3	K562	blood:
13	chr15:45458183..45460477-chr15:45504288..45505965,2	K562	blood:
14	chr15:45489158..45491324-chr15:45514071..45516738,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHF-1	chr15:45506646-45507242	ENSG00000261709.1
2	lnc-SLC28A2-2	chr15:45507745-45508141	NONHSAT042228

Variant related genes	Relation type
ENSG00000259338	TF binding region
ENSG00000261709	TF binding region
ENSG00000259338	CpG island
ENSG00000261709	CpG island
ENSG00000171763	chromatin interactions
ENSG00000259539	chromatin interactions
ENSG00000138606	chromatin interactions
ENSG00000259520	chromatin interactions
ENSG00000259932	chromatin interactions
ENSG00000171766	chromatin interactions

Extended variants
information (count: 517 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35520687	chr15:45501088-45501089	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs35900730	chr15:45501101-45501102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192517456	chr15:45501104-45501105	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs73427606	chr15:45501145-45501146	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs114116248	chr15:45501164-45501165	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78810182	chr15:45501185-45501186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139970966	chr15:45501189-45501190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114671551	chr15:45501199-45501200	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551699001	chr15:45501212-45501213	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550277337	chr15:45501238-45501239	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs571735886	chr15:45501245-45501246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs369039592	chr15:45501249-45501250	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs184723216	chr15:45501284-45501285	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548887455	chr15:45501311-45501312	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189492869	chr15:45501318-45501319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538623374	chr15:45501319-45501320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571094925	chr15:45501323-45501324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs369542208	chr15:45501345-45501346	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs181516516	chr15:45501352-45501353	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533255259	chr15:45501382-45501383	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549827444	chr15:45501399-45501400	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs145397806	chr15:45501409-45501410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535272337	chr15:45501459-45501460	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534011450	chr15:45501477-45501478	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373364166	chr15:45501506-45501507	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565824597	chr15:45501508-45501509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534648678	chr15:45501509-45501510	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs557787853	chr15:45501513-45501514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201715933	chr15:45501535-45501536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577668834	chr15:45501561-45501562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111541966	chr15:45501567-45501568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148707653	chr15:45501584-45501585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142470098	chr15:45501617-45501618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542044802	chr15:45501624-45501625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569961509	chr15:45501681-45501682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527976668	chr15:45501689-45501690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151320875	chr15:45501745-45501746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564149703	chr15:45501758-45501759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140683762	chr15:45501770-45501771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376376718	chr15:45501840-45501841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs55829262	chr15:45501870-45501871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570035353	chr15:45501906-45501907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529127035	chr15:45501954-45501955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548900129	chr15:45501978-45501979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565818760	chr15:45502032-45502033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146470368	chr15:45502038-45502039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187049464	chr15:45502039-45502040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571286891	chr15:45502061-45502062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112406320	chr15:45502109-45502110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557055758	chr15:45502199-45502200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45493600-45508000	Weak transcription	Right Atrium	heart
2	chr15:45504400-45504800	Enhancers	K562	blood
3	chr15:45504600-45505200	Enhancers	Stomach Mucosa	stomach
4	chr15:45505200-45513400	Weak transcription	Stomach Mucosa	stomach
5	chr15:45507400-45507600	Active TSS	Placenta	Placenta
6	chr15:45507600-45508000	ZNF genes & repeats	Fetal Intestine Small	intestine
7	chr15:45507600-45508000	Flanking Active TSS	Placenta	Placenta
8	chr15:45508000-45508200	Enhancers	Placenta	Placenta
9	chr15:45508000-45510200	Weak transcription	Fetal Intestine Small	intestine
10	chr15:45509600-45510800	Enhancers	Fetal Intestine Large	intestine
11	chr15:45509800-45510400	Enhancers	Hela-S3	cervix
12	chr15:45509800-45510600	Enhancers	Duodenum Mucosa	Duodenum
13	chr15:45509800-45510800	Enhancers	Liver	Liver
14	chr15:45510000-45510200	Active TSS	HepG2	liver
15	chr15:45510200-45510400	Enhancers	Pancreas	Pancrea
16	chr15:45510200-45510400	Flanking Active TSS	HepG2	liver
17	chr15:45510200-45510800	Enhancers	Fetal Intestine Small	intestine
18	chr15:45510200-45510800	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr15:45510200-45511000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr15:45510400-45510800	Enhancers	HepG2	liver
21	chr15:45510400-45516800	Weak transcription	Pancreas	Pancrea
22	chr15:45510800-45514200	Weak transcription	Fetal Intestine Large	intestine
23	chr15:45513400-45513600	Enhancers	Stomach Mucosa	stomach
24	chr15:45513600-45514000	Weak transcription	Stomach Mucosa	stomach
25	chr15:45514000-45514200	Enhancers	Stomach Mucosa	stomach
26	chr15:45514200-45515000	Enhancers	Fetal Intestine Large	intestine
27	chr15:45514200-45515600	Weak transcription	Stomach Mucosa	stomach
28	chr15:45514400-45514600	Enhancers	Gastric	stomach
29	chr15:45514600-45526800	Weak transcription	Gastric	stomach
30	chr15:45514800-45516200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr15:45515000-45516000	Weak transcription	Fetal Intestine Large	intestine

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