Variant report

Variant	nsv895394
Chromosome Location	chr10:52793177-52866503
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	chr10:52823525-52823717	HepG2	liver:	n/a	n/a
2	ATF1	chr10:52852243-52852266	K562	blood:	n/a	n/a
3	BACH1	chr10:52833419-52834110	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:52846737-52846747	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:52842750-52843001	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:52795098-52795411	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr10:52797776-52798103	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:52835575-52835945	A549	lung:	n/a	n/a
9	CEBPB	chr10:52835578-52835941	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:52835669-52835943	A549	lung:	n/a	n/a
11	CEBPB	chr10:52835646-52835901	K562	blood:	n/a	n/a
12	CEBPB	chr10:52835579-52835951	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:52840318-52840628	H1-hESC	embryonic stem cell:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
14	CEBPB	chr10:52840363-52840576	Hela-S3	cervix:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
15	CEBPB	chr10:52807306-52807523	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:52840279-52840625	IMR90	lung:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
17	CEBPB	chr10:52816932-52817206	IMR90	lung:	n/a	chr10:52817043-52817054 chr10:52817042-52817053 chr10:52817044-52817053
18	CEBPB	chr10:52816909-52817121	HepG2	liver:	n/a	chr10:52817043-52817054 chr10:52817042-52817053 chr10:52817044-52817053
19	CEBPB	chr10:52860110-52860230	IMR90	lung:	n/a	chr10:52860125-52860136
20	CEBPB	chr10:52837397-52837550	IMR90	lung:	n/a	chr10:52837492-52837505
21	CEBPB	chr10:52835645-52835906	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:52797803-52798077	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:52835586-52835897	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr10:52835577-52835949	IMR90	lung:	n/a	n/a
25	CEBPB	chr10:52831766-52832006	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:52824024-52824139	A549	lung:	n/a	chr10:52824068-52824079
27	CEBPB	chr10:52823914-52824238	IMR90	lung:	n/a	chr10:52824068-52824079
28	CEBPB	chr10:52840302-52840573	HepG2	liver:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
29	CEBPB	chr10:52840299-52840579	A549	lung:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
30	CHD2	chr10:52834171-52834724	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr10:52833324-52833754	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr10:52833262-52834832	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:52807780-52807930	AG09319	gingival:	n/a	chr10:52807814-52807835
34	CTCF	chr10:52823540-52823690	HRE	kidney:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
35	CTCF	chr10:52833557-52833644	A549	lung:	n/a	n/a
36	CTCF	chr10:52823395-52823800	T-47D	breast:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
37	CTCF	chr10:52833460-52833610	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr10:52823520-52823670	AG09319	gingival:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
39	CTCF	chr10:52823520-52823670	NHEK	skin:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
40	CTCF	chr10:52816382-52816396	GM10248	blood:	n/a	n/a
41	CTCF	chr10:52834572-52834576	ProgFib	skin:	n/a	n/a
42	CTCF	chr10:52807760-52807910	AG09319	gingival:	n/a	chr10:52807814-52807835
43	CTCF	chr10:52843460-52843610	HepG2	liver:	n/a	n/a
44	CTCF	chr10:52823560-52823710	GM12801	blood:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
45	CTCF	chr10:52807760-52807910	HCM	heart:	n/a	chr10:52807814-52807835
46	CTCF	chr10:52843401-52843696	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr10:52807760-52807910	HFF-Myc	foreskin:	n/a	chr10:52807814-52807835
48	CTCF	chr10:52834578-52834581	ProgFib	skin:	n/a	n/a
49	CTCF	chr10:52823520-52823670	GM06990	blood:	n/a	chr10:52823603-52823619 chr10:52823602-52823620 chr10:52823604-52823625
50	CTCF	chr10:52834540-52834690	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52834093-52834143	PFSK-1	brain:	n/a
2	chr10:52834093-52834143	PFSK-1	brain:	n/a
3	chr10:52840377-52840427	HRPEpiC	eye:	n/a
4	chr10:52835002-52835052	A549	lung:	n/a
5	chr10:52835002-52835052	HCF	heart:	n/a
6	chr10:52843235-52843285	CMK	blood:	n/a
7	chr10:52833909-52833959	K562	blood:	n/a
8	chr10:52834676-52834726	ProgFib	skin:	n/a
9	chr10:52834121-52834171	GM12878	blood:	n/a
10	chr10:52833909-52833959	HNPCEpiC	eye:	n/a
11	chr10:52833610-52833660	HEK293	kidney:	embryo
12	chr10:52833902-52833952	K562	blood:	n/a
13	chr10:52834121-52834171	BE2_C	brain:	n/a
14	chr10:52834121-52834171	BJ	skin:	n/a
15	chr10:52840377-52840427	HEK293	kidney:	embryo
16	chr10:52840377-52840427	HRCEpiC	kidney:	n/a
17	chr10:52834676-52834726	T-47D	breast:	n/a
18	chr10:52829575-52829625	HL-60	blood:	n/a
19	chr10:52829575-52829625	HIPEpiC	eye:	n/a
20	chr10:52834093-52834143	SAEC	small airway:	n/a
21	chr10:52834498-52834548	HRE	kidney:	n/a
22	chr10:52834850-52834900	BE2_C	brain:	n/a
23	chr10:52834676-52834726	SK-N-MC	brain:	n/a
24	chr10:52834850-52834900	SKMC	muscle:	n/a
25	chr10:52834498-52834548	A549	lung:	n/a
26	chr10:52834850-52834900	HNPCEpiC	eye:	n/a
27	chr10:52834498-52834548	HRCEpiC	kidney:	n/a
28	chr10:52834121-52834171	Hela-S3	cervix:	n/a
29	chr10:52840377-52840427	HNPCEpiC	eye:	n/a
30	chr10:52840377-52840427	SKMC	muscle:	n/a
31	chr10:52843235-52843285	HepG2	liver:	n/a
32	chr10:52840377-52840427	SK-N-SH	brain:	n/a
33	chr10:52829575-52829625	NT2-D1	testis:	n/a
34	chr10:52833444-52833494	HNPCEpiC	eye:	n/a
35	chr10:52834498-52834548	RPTEC	kidney:	n/a
36	chr10:52834498-52834548	K562	blood:	n/a
37	chr10:52834093-52834143	GM19239	blood:	n/a
38	chr10:52835078-52835128	HL-60	blood:	n/a
39	chr10:52833902-52833952	Jurkat	blood:	n/a
40	chr10:52843235-52843285	GM06990	blood:	n/a
41	chr10:52835078-52835128	HRPEpiC	eye:	n/a
42	chr10:52834850-52834900	HEK293	kidney:	embryo
43	chr10:52834850-52834900	HL-60	blood:	n/a
44	chr10:52829575-52829625	NHBE	bronchial:	n/a
45	chr10:52834498-52834548	HL-60	blood:	n/a
46	chr10:52834850-52834900	HepG2	liver:	n/a
47	chr10:52833444-52833494	NB4	blood:	n/a
48	chr10:52835078-52835128	AG10803	skin:	n/a
49	chr10:52834676-52834726	U87	brain:	n/a
50	chr10:52834067-52834117	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:52823455..52824113-chr10:53182409..53182910,2	MCF-7	breast:
2	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
3	chr10:52852996..52855697-chr10:52862209..52864368,2	MCF-7	breast:
4	chr10:52839499..52841510-chr10:52846608..52849576,2	K562	blood:
5	chr10:52823519..52824020-chr10:53763789..53764326,2	MCF-7	breast:
6	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:
7	chr10:52860891..52863860-chr11:62621758..62623546,2	K562	blood:
8	chr10:52832484..52833988-chr10:52835992..52837513,2	K562	blood:
9	chr10:52845255..52847999-chr10:52848856..52851821,2	K562	blood:
10	chr10:52823077..52823678-chr10:53719716..53720617,2	MCF-7	breast:
11	chr10:52805100..52807814-chr2:220435282..220438038,2	MCF-7	breast:
12	chr10:52761120..52762328-chr10:52807357..52808643,3	MCF-7	breast:
13	chr10:52845255..52847999-chr10:52848856..52851821,2	K562	blood:
14	chr10:52852996..52855697-chr10:52862209..52864368,2	MCF-7	breast:
15	chr10:52824508..52825384-chr17:56387619..56388193,2	MCF-7	breast:
16	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
17	chr10:52839499..52841510-chr10:52846608..52849576,2	K562	blood:
18	chr10:52770484..52771339-chr10:52807377..52808118,3	MCF-7	breast:
19	chr10:52770367..52771306-chr10:52807728..52808411,3	MCF-7	breast:
20	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A1CF-1	chr10:52822339-52822690	ENSG00000223502.1
2	lnc-A1CF-1	chr10:52828245-52828313	ENSG00000223502.1

Variant related genes	Relation type
ENSG00000223502	TF binding region
PRKG1	TF binding region
ENSG00000223502	CpG island
PRKG1	CpG island
ENSG00000168003	chromatin interactions
ENSG00000185532	chromatin interactions
ENSG00000123999	chromatin interactions
ENSG00000005379	chromatin interactions
ENSG00000124006	chromatin interactions
ENSG00000255717	chromatin interactions

Extended variants
information (count: 2673 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2673 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2339680	chr10:52793177-52793178	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552405687	chr10:52793274-52793275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569071010	chr10:52793313-52793314	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs538012415	chr10:52793341-52793342	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145087919	chr10:52793370-52793371	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs568298524	chr10:52793382-52793383	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs534281620	chr10:52793399-52793400	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554021377	chr10:52793440-52793441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs374130851	chr10:52793461-52793462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs368828083	chr10:52793479-52793480	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs149121921	chr10:52793547-52793548	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs539460123	chr10:52793549-52793550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs549740912	chr10:52793587-52793588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs138446763	chr10:52793604-52793605	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs35637704	chr10:52793605-52793606	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs386371340	chr10:52793608-52793609	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs398069788	chr10:52793609-52793610	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs370327182	chr10:52793635-52793636	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187365017	chr10:52793643-52793644	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs191712272	chr10:52793768-52793769	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs544751079	chr10:52793773-52793774	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs376743999	chr10:52793797-52793798	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs117164226	chr10:52793892-52793893	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs144569509	chr10:52793893-52793894	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540273198	chr10:52793916-52793917	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs559998622	chr10:52793987-52793988	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532096108	chr10:52794008-52794009	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs551905683	chr10:52794059-52794060	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs533384775	chr10:52794088-52794089	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs957717	chr10:52794124-52794125	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs560403763	chr10:52794136-52794137	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs531624689	chr10:52794148-52794149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529211225	chr10:52794208-52794209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373950433	chr10:52794281-52794282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370416213	chr10:52794300-52794301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548762759	chr10:52794338-52794339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568259322	chr10:52794359-52794360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74884599	chr10:52794380-52794381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146666051	chr10:52794393-52794394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199524579	chr10:52794424-52794425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs5784854	chr10:52794426-52794427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367664918	chr10:52794428-52794429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35034911	chr10:52794429-52794430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535491758	chr10:52794430-52794431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557212554	chr10:52794448-52794449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570874149	chr10:52794481-52794482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140272432	chr10:52794571-52794572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368443363	chr10:52794583-52794584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556266611	chr10:52794622-52794623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371836223	chr10:52794628-52794629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:870 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52756800-52794800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:52788000-52793600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:52790600-52794600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:52791800-52795400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr10:52792000-52793200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:52792000-52793400	Weak transcription	Fetal Lung	lung
7	chr10:52792200-52793200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:52792200-52794800	Weak transcription	Aorta	Aorta
9	chr10:52792400-52793600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:52792400-52796400	Weak transcription	Fetal Stomach	stomach
11	chr10:52792600-52793400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr10:52792600-52796400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr10:52792800-52793400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr10:52792800-52795200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr10:52792800-52795800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr10:52793000-52793200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:52793000-52794200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr10:52793000-52795400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr10:52793000-52795600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr10:52793000-52796200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr10:52793200-52793400	Enhancers	Fetal Kidney	kidney
22	chr10:52793200-52794200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr10:52793400-52793600	Enhancers	Rectal Smooth Muscle	rectum
24	chr10:52793400-52793600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr10:52793400-52794600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr10:52793600-52793800	Enhancers	Fetal Lung	lung
27	chr10:52793600-52794000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr10:52793600-52794200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr10:52793600-52795000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:52793800-52794400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr10:52794200-52796000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr10:52794200-52796600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr10:52794600-52795400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr10:52794600-52795600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr10:52794800-52795000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr10:52794800-52795000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr10:52794800-52795200	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr10:52794800-52795400	Enhancers	Aorta	Aorta
39	chr10:52795000-52796000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr10:52795000-52796200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr10:52795400-52801200	Weak transcription	Aorta	Aorta
42	chr10:52795600-52796000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr10:52795600-52796200	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr10:52796000-52796400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr10:52796000-52796600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr10:52796200-52796400	Enhancers	H9 Cell Line	embryonic stem cell
47	chr10:52796200-52796600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:52796400-52796600	Enhancers	Fetal Stomach	stomach
49	chr10:52796600-52806800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr10:52796600-52806800	Weak transcription	Fetal Stomach	stomach

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