Variant report

Variant	nsv1042623
Chromosome Location	chr15:76863437-76999030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:605)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76865111-76865365	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76935433-76935442	HepG2	liver:	n/a	n/a
3	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
4	ATF2	chr15:76867545-76868188	GM12878	blood:	n/a	n/a
5	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
6	BATF	chr15:76996451-76996676	GM12878	blood:	n/a	n/a
7	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
8	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
9	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
10	BATF	chr15:76867629-76868083	GM12878	blood:	n/a	n/a
11	BATF	chr15:76946672-76946896	GM12878	blood:	n/a	n/a
12	BATF	chr15:76996436-76996655	GM12878	blood:	n/a	n/a
13	BATF	chr15:76946679-76946925	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:76946684-76946864	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:76867571-76868071	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:76867646-76868017	GM12878	blood:	n/a	n/a
17	BCL3	chr15:76867594-76868106	GM12878	blood:	n/a	n/a
18	BCL3	chr15:76867671-76868118	GM12878	blood:	n/a	n/a
19	BCLAF1	chr15:76867350-76868205	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:76867603-76868092	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:76867676-76868010	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:76946680-76946809	GM12878	blood:	n/a	n/a
23	BRCA1	chr15:76969668-76969722	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr15:76928439-76928711	K562	blood:	n/a	n/a
25	CBX3	chr15:76928484-76928676	K562	blood:	n/a	n/a
26	CEBPB	chr15:76960889-76961156	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:76867691-76868041	GM12878	blood:	n/a	n/a
28	CEBPB	chr15:76996963-76996987	A549	lung:	n/a	n/a
29	CEBPB	chr15:76865289-76865622	HepG2	liver:	n/a	chr15:76865442-76865453
30	CEBPB	chr15:76865274-76865637	IMR90	lung:	n/a	chr15:76865442-76865453
31	CEBPB	chr15:76963560-76963674	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr15:76867534-76868241	GM12878	blood:	n/a	n/a
33	CEBPB	chr15:76865278-76865665	Hela-S3	cervix:	n/a	chr15:76865442-76865453
34	CEBPB	chr15:76996796-76997148	HepG2	liver:	n/a	n/a
35	CEBPB	chr15:76869227-76869506	HepG2	liver:	n/a	n/a
36	CEBPB	chr15:76865082-76865698	A549	lung:	n/a	chr15:76865442-76865453
37	CEBPB	chr15:76865304-76865598	K562	blood:	n/a	chr15:76865442-76865453
38	CEBPB	chr15:76953585-76953673	A549	lung:	n/a	n/a
39	CEBPB	chr15:76996894-76997016	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:76865361-76865572	H1-hESC	embryonic stem cell:	n/a	chr15:76865442-76865453
41	CEBPB	chr15:76869014-76869478	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr15:76865196-76865634	A549	lung:	n/a	chr15:76865442-76865453
43	CEBPB	chr15:76960844-76961108	A549	lung:	n/a	n/a
44	CEBPB	chr15:76908855-76909056	HepG2	liver:	n/a	chr15:76908970-76908981
45	CHD1	chr15:76865009-76865537	IMR90	lung:	n/a	n/a
46	CHD2	chr15:76869098-76869401	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr15:76917763-76917765	HepG2	liver:	n/a	n/a
48	CREB1	chr15:76867561-76868169	GM12878	blood:	n/a	n/a
49	CTCF	chr15:76935428-76935439	HepG2	liver:	n/a	n/a
50	CTCF	chr15:76935240-76935390	HBMEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76901065-76901115	Caco-2	colon:	n/a
2	chr15:76868964-76869014	PFSK-1	brain:	n/a
3	chr15:76901065-76901115	MCF10A-Er-Src	breast:	n/a
4	chr15:76901065-76901115	NHBE	bronchial:	n/a
5	chr15:76901065-76901115	NB4	blood:	n/a
6	chr15:76868964-76869014	HCT-116	colon:	n/a
7	chr15:76868964-76869014	IMR90	lung:	fetal
8	chr15:76868964-76869014	NB4	blood:	n/a
9	chr15:76868964-76869014	H1-hESC	embryonic stem cell:	embryo
10	chr15:76901065-76901115	HIPEpiC	eye:	n/a
11	chr15:76868964-76869014	GM06990	blood:	n/a
12	chr15:76901065-76901115	GM06990	blood:	n/a
13	chr15:76868964-76869014	GM12892	blood:	n/a
14	chr15:76901065-76901115	CMK	blood:	n/a
15	chr15:76901065-76901115	HCM	heart:	n/a
16	chr15:76868964-76869014	SK-N-MC	brain:	n/a
17	chr15:76901065-76901115	ProgFib	skin:	n/a
18	chr15:76901065-76901115	T-47D	breast:	n/a
19	chr15:76868964-76869014	AG09319	gingival:	n/a
20	chr15:76901065-76901115	ovcar-3	ovarian:	n/a
21	chr15:76901065-76901115	MCF-7	breast:	n/a
22	chr15:76868964-76869014	CMK	blood:	n/a
23	chr15:76868964-76869014	GM12878	blood:	n/a
24	chr15:76868964-76869014	HCF	heart:	n/a
25	chr15:76868964-76869014	NHDF-neo	bronchial:	n/a
26	chr15:76901065-76901115	Hepatocyte	liver:	n/a
27	chr15:76901065-76901115	ECC-1	luminal epithelium:	n/a
28	chr15:76901065-76901115	AG09319	gingival:	n/a
29	chr15:76901065-76901115	K562	blood:	n/a
30	chr15:76901065-76901115	SAEC	small airway:	n/a
31	chr15:76901065-76901115	HCF	heart:	n/a
32	chr15:76868964-76869014	NT2-D1	testis:	n/a
33	chr15:76868964-76869014	ECC-1	luminal epithelium:	n/a
34	chr15:76901065-76901115	HRPEpiC	eye:	n/a
35	chr15:76868964-76869014	SK-N-SH_RA	brain:	n/a
36	chr15:76901065-76901115	PANC-1	pancreas:	n/a
37	chr15:76868964-76869014	HRPEpiC	eye:	n/a
38	chr15:76901065-76901115	LNCaP	prostate:	n/a
39	chr15:76901065-76901115	HRE	kidney:	n/a
40	chr15:76868964-76869014	U87	brain:	n/a
41	chr15:76901065-76901115	HCPEpiC	choroid plexus:	n/a
42	chr15:76868964-76869014	HAEpiC	amniotic membrane:	n/a
43	chr15:76868964-76869014	HRE	kidney:	n/a
44	chr15:76868964-76869014	BJ	skin:	n/a
45	chr15:76901065-76901115	RPTEC	kidney:	n/a
46	chr15:76901065-76901115	BE2_C	brain:	n/a
47	chr15:76868964-76869014	HIPEpiC	eye:	n/a
48	chr15:76868964-76869014	SAEC	small airway:	n/a
49	chr15:76868964-76869014	HEEpiC	esophagus:	n/a
50	chr15:76868964-76869014	MCF10A-Er-Src	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:
2	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
3	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
4	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
5	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
6	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
7	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
8	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
9	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
10	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
11	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
12	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
13	chr15:76934897..76935640-chr15:77158999..77159764,3	MCF-7	breast:
14	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
15	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
16	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
17	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
SCAPER	TF binding region
MIR3713	TF binding region
SCAPER	CpG island
MIR3713	CpG island
ENSG00000266449	chromatin interactions

Extended variants
information (count: 4725 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4725 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542577199	chr15:76863447-76863448	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs561266031	chr15:76863481-76863482	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs12902174	chr15:76863540-76863541	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs543256926	chr15:76863574-76863575	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs562641726	chr15:76863588-76863589	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs12438077	chr15:76863601-76863602	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs551321884	chr15:76863602-76863603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142149518	chr15:76863667-76863668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527959440	chr15:76863672-76863673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12441550	chr15:76863682-76863683	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs530118855	chr15:76863701-76863702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567989080	chr15:76863721-76863722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2459359	chr15:76863838-76863839	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577868050	chr15:76863892-76863893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1874944	chr15:76863928-76863929	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146023224	chr15:76863994-76863995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534623048	chr15:76864003-76864004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553698717	chr15:76864190-76864191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190919537	chr15:76864254-76864255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201964833	chr15:76864262-76864263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542644177	chr15:76864361-76864362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548173353	chr15:76864415-76864416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62030374	chr15:76864453-76864454	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs182628840	chr15:76864486-76864487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537093664	chr15:76864493-76864494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147848516	chr15:76864588-76864589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572029703	chr15:76864589-76864590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141489661	chr15:76864613-76864614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150377293	chr15:76864648-76864649	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138681623	chr15:76864668-76864669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560669497	chr15:76864766-76864767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs80321981	chr15:76864834-76864835	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs149355045	chr15:76864841-76864842	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561518045	chr15:76864844-76864845	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532050553	chr15:76864872-76864873	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs187698093	chr15:76864891-76864892	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs571889662	chr15:76864999-76865000	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs192610254	chr15:76865019-76865020	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs561661278	chr15:76865101-76865102	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182867682	chr15:76865175-76865176	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs565810651	chr15:76865177-76865178	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs372999259	chr15:76865231-76865232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs67724539	chr15:76865252-76865253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs62030375	chr15:76865254-76865255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376553582	chr15:76865256-76865257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2468115	chr15:76865258-76865259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10467952	chr15:76865260-76865261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71143341	chr15:76865280-76865281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187496187	chr15:76865281-76865282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58395846	chr15:76865286-76865287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	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
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76846000-76869000	Weak transcription	Left Ventricle	heart
2	chr15:76846000-76869000	Weak transcription	Pancreas	Pancrea
3	chr15:76846200-76868800	Weak transcription	Fetal Intestine Small	intestine
4	chr15:76847000-76868200	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr15:76850200-76868400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr15:76852000-76867000	Weak transcription	Primary B cells from peripheral blood	blood
7	chr15:76856400-76863800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:76857000-76868800	Weak transcription	Liver	Liver
9	chr15:76858600-76869000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:76860000-76868400	Weak transcription	Esophagus	oesophagus
11	chr15:76861000-76866400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr15:76861400-76866000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr15:76861600-76869200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr15:76861800-76869000	Weak transcription	Colonic Mucosa	Colon
15	chr15:76861800-76869000	Weak transcription	Placenta	Placenta
16	chr15:76862400-76864800	Weak transcription	Ovary	ovary
17	chr15:76862600-76864000	Strong transcription	Primary B cells from cord blood	blood
18	chr15:76862600-76868800	Weak transcription	Adipose Nuclei	Adipose
19	chr15:76862600-76869000	Weak transcription	Right Ventricle	heart
20	chr15:76862600-76872000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr15:76862800-76863600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr15:76862800-76863600	Strong transcription	Dnd41	blood
23	chr15:76862800-76865400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr15:76863000-76864800	Weak transcription	A549	lung
25	chr15:76863000-76865200	Strong transcription	Primary T cells from cord blood	blood
26	chr15:76863000-76865600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr15:76863000-76867400	Weak transcription	Fetal Heart	heart
28	chr15:76863000-76869000	Weak transcription	Fetal Muscle Leg	muscle
29	chr15:76863200-76867200	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr15:76863400-76864200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr15:76863400-76867800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:76863400-76868600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr15:76863600-76863800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr15:76863600-76865800	Weak transcription	Dnd41	blood
35	chr15:76863600-76867000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:76864000-76868000	Weak transcription	Primary B cells from cord blood	blood
37	chr15:76864200-76867600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:76864600-76864800	Enhancers	Right Atrium	heart
39	chr15:76864800-76865000	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr15:76864800-76865000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr15:76864800-76865000	Enhancers	Osteobl	bone
42	chr15:76864800-76865200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr15:76864800-76865200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:76864800-76865200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:76864800-76865200	Enhancers	Brain Anterior Caudate	brain
46	chr15:76864800-76865200	Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr15:76864800-76865200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr15:76864800-76865200	Enhancers	Fetal Stomach	stomach
49	chr15:76864800-76865200	Flanking Active TSS	Right Atrium	heart
50	chr15:76864800-76865400	Enhancers	Fetal Lung	lung

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