Variant report

Variant	nsv974566
Chromosome Location	chr15:43423478-43426186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:549)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43424959-43425100	K562	blood:	n/a	n/a
2	ARID3A	chr15:43425386-43425955	HepG2	liver:	n/a	n/a
3	ATF2	chr15:43425478-43425941	GM12878	blood:	n/a	n/a
4	ATF2	chr15:43425489-43425993	GM12878	blood:	n/a	n/a
5	ATF3	chr15:43425798-43426027	K562	blood:	n/a	n/a
6	BACH1	chr15:43425909-43425912	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr15:43425519-43425881	GM12878	blood:	n/a	n/a
8	BCLAF1	chr15:43425383-43426120	GM12878	blood:	n/a	chr15:43425430-43425439 chr15:43425914-43425923
9	BHLHE40	chr15:43425319-43426331	GM12878	blood:	n/a	chr15:43425797-43425813 chr15:43425933-43425949 chr15:43426202-43426218
10	BHLHE40	chr15:43425480-43426609	K562	blood:	n/a	chr15:43425797-43425813 chr15:43425933-43425949 chr15:43426202-43426218
11	BRCA1	chr15:43426165-43426227	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr15:43424722-43425096	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr15:43425788-43426354	GM12878	blood:	n/a	n/a
14	BRCA1	chr15:43425381-43425942	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr15:43425076-43426017	K562	blood:	n/a	n/a
16	CCNT2	chr15:43425533-43426350	K562	blood:	n/a	n/a
17	CEBPB	chr15:43424973-43425186	A549	lung:	n/a	chr15:43425039-43425050
18	CEBPB	chr15:43425665-43425725	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr15:43424899-43425949	Hela-S3	cervix:	n/a	chr15:43425039-43425050
20	CEBPB	chr15:43425676-43425921	K562	blood:	n/a	n/a
21	CEBPB	chr15:43424921-43425135	HepG2	liver:	n/a	chr15:43425039-43425050
22	CEBPB	chr15:43424931-43425208	K562	blood:	n/a	chr15:43425039-43425050
23	CEBPD	chr15:43425569-43425968	HepG2	liver:	n/a	n/a
24	CHD1	chr15:43425358-43426427	GM12878	blood:	n/a	n/a
25	CHD2	chr15:43425222-43426416	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr15:43425732-43425870	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:43425226-43425397	K562	blood:	n/a	n/a
28	CHD2	chr15:43425651-43426432	K562	blood:	n/a	n/a
29	CHD2	chr15:43425796-43426023	HepG2	liver:	n/a	n/a
30	CHD2	chr15:43425506-43426073	GM12878	blood:	n/a	n/a
31	CREB1	chr15:43425430-43426047	GM12878	blood:	n/a	n/a
32	CREB1	chr15:43425561-43426118	A549	lung:	n/a	n/a
33	CTBP2	chr15:43425207-43426707	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr15:43425920-43426070	GM12875	blood:	n/a	n/a
35	CTCF	chr15:43425660-43425810	AG04449	skin:	n/a	n/a
36	CTCF	chr15:43425880-43426030	GM12875	blood:	n/a	n/a
37	CTCF	chr15:43426020-43426170	HCM	heart:	n/a	n/a
38	CTCF	chr15:43426020-43426170	GM12872	blood:	n/a	n/a
39	CTCF	chr15:43426060-43426210	NHEK	skin:	n/a	n/a
40	CTCF	chr15:43426080-43426230	Caco-2	colon:	n/a	n/a
41	CTCF	chr15:43426160-43426310	SAEC	small airway:	n/a	n/a
42	CTCF	chr15:43425780-43425930	K562	blood:	n/a	n/a
43	CTCF	chr15:43425860-43426010	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr15:43426140-43426290	GM06990	blood:	n/a	n/a
45	CTCF	chr15:43426150-43426221	GM19238	blood:	n/a	n/a
46	CTCF	chr15:43425675-43425711	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr15:43425820-43425970	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr15:43426040-43426190	GM12874	blood:	n/a	n/a
49	CTCF	chr15:43426100-43426250	GM12867	blood:	n/a	n/a
50	CTCF	chr15:43425360-43425510	SAEC	small airway:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43425883-43425933	RPTEC	kidney:	n/a
2	chr15:43425462-43425512	BJ	skin:	n/a
3	chr15:43425949-43425999	NH-A	brain:	n/a
4	chr15:43425568-43425618	HEK293	kidney:	embryo
5	chr15:43425524-43425574	H1-hESC	embryonic stem cell:	embryo
6	chr15:43425883-43425933	Caco-2	colon:	n/a
7	chr15:43425462-43425512	HIPEpiC	eye:	n/a
8	chr15:43425698-43425748	RPTEC	kidney:	n/a
9	chr15:43425524-43425574	HepG2	liver:	n/a
10	chr15:43425698-43425748	ovcar-3	ovarian:	n/a
11	chr15:43425524-43425574	AG09319	gingival:	n/a
12	chr15:43425698-43425748	HNPCEpiC	eye:	n/a
13	chr15:43425568-43425618	HCM	heart:	n/a
14	chr15:43425568-43425618	GM12891	blood:	n/a
15	chr15:43425883-43425933	GM12892	blood:	n/a
16	chr15:43425591-43425641	GM12891	blood:	n/a
17	chr15:43425285-43425335	GM12892	blood:	n/a
18	chr15:43425524-43425574	BJ	skin:	n/a
19	chr15:43425285-43425335	AG09319	gingival:	n/a
20	chr15:43425644-43425694	H1-hESC	embryonic stem cell:	embryo
21	chr15:43425644-43425694	U87	brain:	n/a
22	chr15:43425883-43425933	AG04449	skin:	fetal
23	chr15:43425568-43425618	ProgFib	skin:	n/a
24	chr15:43425568-43425618	K562	blood:	n/a
25	chr15:43425644-43425694	HMEC	breast:	n/a
26	chr15:43425591-43425641	A549	lung:	n/a
27	chr15:43425524-43425574	T-47D	breast:	n/a
28	chr15:43425591-43425641	AG04450	lung:	fetal
29	chr15:43425949-43425999	HRCEpiC	kidney:	n/a
30	chr15:43425524-43425574	GM12878	blood:	n/a
31	chr15:43425644-43425694	MCF-7	breast:	n/a
32	chr15:43425883-43425933	HCPEpiC	choroid plexus:	n/a
33	chr15:43425568-43425618	GM12878	blood:	n/a
34	chr15:43425591-43425641	Hela-S3	cervix:	n/a
35	chr15:43425462-43425512	HCT-116	colon:	n/a
36	chr15:43425698-43425748	IMR90	lung:	fetal
37	chr15:43425285-43425335	AG10803	skin:	n/a
38	chr15:43425644-43425694	ProgFib	skin:	n/a
39	chr15:43425698-43425748	U87	brain:	n/a
40	chr15:43425698-43425748	K562	blood:	n/a
41	chr15:43425285-43425335	HCM	heart:	n/a
42	chr15:43425591-43425641	NB4	blood:	n/a
43	chr15:43425524-43425574	GM12892	blood:	n/a
44	chr15:43425524-43425574	AG04449	skin:	fetal
45	chr15:43425949-43425999	GM12878	blood:	n/a
46	chr15:43425698-43425748	AoSMC	blood vessel:	n/a
47	chr15:43425462-43425512	GM19239	blood:	n/a
48	chr15:43425644-43425694	HEEpiC	esophagus:	n/a
49	chr15:43425285-43425335	RPTEC	kidney:	n/a
50	chr15:43425524-43425574	AoSMC	blood vessel:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:43425568..43426223-chr6:30584868..30585413,2	Hela-S3	cervix:
2	chr15:43395932..43399418-chr15:43425897..43428585,4	K562	blood:
3	chr15:43424687..43428034-chr15:43433131..43438698,7	K562	blood:
4	chr15:43396979..43399675-chr15:43425245..43427228,2	MCF-7	breast:
5	chr15:43425791..43426365-chr9:74525585..74526547,2	NB4	blood:
6	chr15:43412581..43417001-chr15:43422670..43429913,10	K562	blood:
7	chr15:43411554..43416767-chr15:43424269..43426823,6	K562	blood:
8	chr15:43424637..43426187-chr15:43437128..43439640,2	K562	blood:
9	chr15:43424880..43427064-chr15:51913097..51915072,2	MCF-7	breast:
10	chr15:43406517..43409330-chr15:43424584..43426379,2	MCF-7	breast:
11	chr15:43397983..43399514-chr15:43421683..43423629,2	K562	blood:

No data

Variant related genes	Relation type
TMEM62	TF binding region
TMEM62	CpG island
ENSG00000204569	chromatin interactions
ENSG00000205871	chromatin interactions
ENSG00000107362	chromatin interactions
ENSG00000104093	chromatin interactions
ENSG00000155621	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000137842	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148162729	chr15:43423559-43423560	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544543999	chr15:43423569-43423570	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561013131	chr15:43423619-43423620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs574115470	chr15:43423640-43423641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181968244	chr15:43423659-43423660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559752603	chr15:43423672-43423673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528611261	chr15:43423780-43423781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551543286	chr15:43423868-43423869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141961081	chr15:43423893-43423894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568466033	chr15:43423898-43423899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531008130	chr15:43423932-43423933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535817305	chr15:43423972-43423973	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551292709	chr15:43423981-43423982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543501099	chr15:43423994-43423995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149709856	chr15:43423997-43423998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371987220	chr15:43424025-43424026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567598859	chr15:43424064-43424065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536520671	chr15:43424083-43424084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs551105533	chr15:43424089-43424090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546205179	chr15:43424090-43424091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566094235	chr15:43424097-43424098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538733023	chr15:43424114-43424115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558367747	chr15:43424120-43424121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs6493078	chr15:43424122-43424123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs539937069	chr15:43424130-43424131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558372639	chr15:43424152-43424153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550945310	chr15:43424165-43424166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372923262	chr15:43424166-43424167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186952764	chr15:43424181-43424182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565115599	chr15:43424182-43424183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554930394	chr15:43424183-43424184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377573833	chr15:43424187-43424188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7173005	chr15:43424193-43424194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2899075	chr15:43424197-43424198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574803150	chr15:43424204-43424205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568833286	chr15:43424231-43424232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559795126	chr15:43424264-43424265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573106468	chr15:43424294-43424295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142730301	chr15:43424335-43424336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191747951	chr15:43424355-43424356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs60435696	chr15:43424365-43424366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573341130	chr15:43424378-43424379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147353745	chr15:43424408-43424409	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561112768	chr15:43424438-43424439	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555749738	chr15:43424444-43424445	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546845441	chr15:43424488-43424489	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566179953	chr15:43424618-43424619	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532004338	chr15:43424670-43424671	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199836043	chr15:43424693-43424694	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536746515	chr15:43424861-43424862	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	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
Renal cell carcinoma	18765545	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

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43415600-43425200	Weak transcription	Gastric	stomach
2	chr15:43415800-43425000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:43415800-43425000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr15:43415800-43425000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:43415800-43425000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:43415800-43425000	Weak transcription	Aorta	Aorta
7	chr15:43415800-43425000	Weak transcription	Brain Anterior Caudate	brain
8	chr15:43415800-43425200	Weak transcription	Esophagus	oesophagus
9	chr15:43416200-43425000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr15:43417600-43425000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:43417600-43425000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr15:43418400-43425200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:43419800-43425000	Weak transcription	Colonic Mucosa	Colon
14	chr15:43420000-43425000	Weak transcription	Pancreas	Pancrea
15	chr15:43420000-43425000	Weak transcription	Stomach Mucosa	stomach
16	chr15:43420200-43424600	Weak transcription	A549	lung
17	chr15:43420200-43425000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr15:43420400-43424400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr15:43420400-43425000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr15:43421000-43424800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr15:43422000-43425000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr15:43422000-43425000	Weak transcription	Fetal Intestine Large	intestine
23	chr15:43422000-43425000	Weak transcription	Small Intestine	intestine
24	chr15:43422000-43425000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr15:43422200-43424600	Weak transcription	HepG2	liver
26	chr15:43422200-43425000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:43423400-43424400	Weak transcription	Fetal Intestine Small	intestine
28	chr15:43423600-43425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr15:43423800-43424000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr15:43424000-43425000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr15:43424400-43424600	Active TSS	Colon Smooth Muscle	Colon
32	chr15:43424400-43424800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr15:43424400-43424800	Enhancers	K562	blood
34	chr15:43424400-43425000	Active TSS	Liver	Liver
35	chr15:43424400-43425000	Enhancers	Fetal Intestine Small	intestine
36	chr15:43424400-43425000	Weak transcription	Thymus	Thymus
37	chr15:43424400-43425000	Enhancers	Hela-S3	cervix
38	chr15:43424600-43424800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:43424600-43424800	Enhancers	A549	lung
40	chr15:43424600-43424800	Enhancers	HepG2	liver
41	chr15:43424800-43425000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr15:43424800-43425000	Enhancers	Primary hematopoietic stem cells	blood
43	chr15:43424800-43425000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr15:43424800-43425000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr15:43424800-43425000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:43424800-43425000	Enhancers	Adipose Nuclei	Adipose
47	chr15:43424800-43425000	Enhancers	Duodenum Mucosa	Duodenum
48	chr15:43424800-43425000	Enhancers	Placenta	Placenta
49	chr15:43424800-43425000	Enhancers	Rectal Smooth Muscle	rectum
50	chr15:43424800-43425000	Enhancers	Dnd41	blood

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