Variant report

Variant	nsv511436
Chromosome Location	chr10:4700968-4711764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 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	chr10:4705347-4705883	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:4700929-4701323	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:4704133-4704489	HepG2	liver:	n/a	n/a
4	ATF1	chr10:4705297-4705891	K562	blood:	n/a	n/a
5	ATF3	chr10:4705115-4705785	A549	lung:	n/a	n/a
6	ATF3	chr10:4705258-4705685	K562	blood:	n/a	n/a
7	ATF3	chr10:4705088-4705824	A549	lung:	n/a	n/a
8	BCL3	chr10:4705156-4705833	A549	lung:	n/a	n/a
9	BCL3	chr10:4704875-4706233	A549	lung:	n/a	n/a
10	BHLHE40	chr10:4703986-4704503	HepG2	liver:	n/a	n/a
11	BHLHE40	chr10:4700855-4701272	HepG2	liver:	n/a	n/a
12	BHLHE40	chr10:4705275-4705774	K562	blood:	n/a	n/a
13	BHLHE40	chr10:4705303-4705682	HepG2	liver:	n/a	n/a
14	BRCA1	chr10:4705101-4706042	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr10:4705180-4705917	HCT-116	colon:	n/a	n/a
16	CBX3	chr10:4705172-4705705	K562	blood:	n/a	n/a
17	CEBPB	chr10:4705289-4705684	HepG2	liver:	n/a	chr10:4705392-4705403
18	CEBPB	chr10:4705245-4705769	A549	lung:	n/a	chr10:4705392-4705403
19	CEBPB	chr10:4703961-4704746	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:4705177-4706090	HCT-116	colon:	n/a	chr10:4705392-4705403
21	CEBPB	chr10:4705244-4706467	Hela-S3	cervix:	n/a	chr10:4705392-4705403 chr10:4706298-4706309
22	CEBPB	chr10:4705125-4706569	A549	lung:	n/a	chr10:4705392-4705403 chr10:4706298-4706309
23	CEBPB	chr10:4704447-4704768	A549	lung:	n/a	n/a
24	CEBPB	chr10:4706065-4706489	IMR90	lung:	n/a	chr10:4706298-4706309
25	CEBPB	chr10:4705259-4705684	MCF-7	breast:	n/a	chr10:4705392-4705403
26	CEBPB	chr10:4704445-4704718	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:4706107-4706479	K562	blood:	n/a	chr10:4706298-4706309
28	CEBPB	chr10:4705272-4705714	A549	lung:	n/a	chr10:4705392-4705403
29	CEBPB	chr10:4707329-4707876	A549	lung:	n/a	n/a
30	CEBPB	chr10:4707422-4707780	A549	lung:	n/a	n/a
31	CEBPB	chr10:4706137-4706481	HepG2	liver:	n/a	chr10:4706298-4706309
32	CEBPB	chr10:4705270-4705680	IMR90	lung:	n/a	chr10:4705392-4705403
33	CEBPB	chr10:4706125-4706461	A549	lung:	n/a	chr10:4706298-4706309
34	CEBPB	chr10:4705299-4705638	K562	blood:	n/a	chr10:4705392-4705403
35	CEBPZ	chr10:4705192-4705587	HepG2	liver:	n/a	n/a
36	CHD2	chr10:4704136-4704213	HepG2	liver:	n/a	n/a
37	CHD2	chr10:4705250-4705724	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr10:4705370-4705567	K562	blood:	n/a	n/a
39	CREB1	chr10:4705350-4705659	A549	lung:	n/a	n/a
40	CTCF	chr10:4703960-4704110	GM12866	blood:	n/a	n/a
41	CTCF	chr10:4703800-4703950	AG10803	skin:	n/a	n/a
42	CTCF	chr10:4704918-4704930	Gliobla	brain:	n/a	n/a
43	CTCF	chr10:4704100-4704250	SAEC	small airway:	n/a	n/a
44	CTCF	chr10:4704880-4705030	AG10803	skin:	n/a	n/a
45	CTCF	chr10:4703840-4703990	HMF	breast:	n/a	n/a
46	CTCF	chr10:4704861-4704943	Fibrobl	skin:	n/a	n/a
47	CTCF	chr10:4703900-4704050	AG10803	skin:	n/a	n/a
48	CUX1	chr10:4705165-4705528	K562	blood:	n/a	n/a
49	E2F4	chr10:4705214-4705789	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr10:4705208-4705822	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4705434-4705484	K562	blood:	n/a
2	chr10:4705434-4705484	HCF	heart:	n/a
3	chr10:4705434-4705484	AG10803	skin:	n/a
4	chr10:4705434-4705484	GM06990	blood:	n/a
5	chr10:4705434-4705484	HRPEpiC	eye:	n/a
6	chr10:4705434-4705484	HepG2	liver:	n/a
7	chr10:4705434-4705484	HAEpiC	amniotic membrane:	n/a
8	chr10:4705434-4705484	ECC-1	luminal epithelium:	n/a
9	chr10:4705434-4705484	PANC-1	pancreas:	n/a
10	chr10:4705434-4705484	MCF-7	breast:	n/a
11	chr10:4705434-4705484	NH-A	brain:	n/a
12	chr10:4705434-4705484	SK-N-SH	brain:	n/a
13	chr10:4705434-4705484	HMEC	breast:	n/a
14	chr10:4705434-4705484	AG04449	skin:	fetal
15	chr10:4705434-4705484	NHDF-neo	bronchial:	n/a
16	chr10:4705434-4705484	HNPCEpiC	eye:	n/a
17	chr10:4705434-4705484	GM19239	blood:	n/a
18	chr10:4705434-4705484	Hela-S3	cervix:	n/a
19	chr10:4705434-4705484	HRE	kidney:	n/a
20	chr10:4705434-4705484	T-47D	breast:	n/a
21	chr10:4705434-4705484	HEEpiC	esophagus:	n/a
22	chr10:4705434-4705484	HCPEpiC	choroid plexus:	n/a
23	chr10:4705434-4705484	A549	lung:	n/a
24	chr10:4705434-4705484	HL-60	blood:	n/a
25	chr10:4705434-4705484	PrEC	prostate:	n/a
26	chr10:4705434-4705484	GM12892	blood:	n/a
27	chr10:4705434-4705484	BE2_C	brain:	n/a
28	chr10:4705434-4705484	U87	brain:	n/a
29	chr10:4705434-4705484	HIPEpiC	eye:	n/a
30	chr10:4705434-4705484	MCF10A-Er-Src	breast:	n/a
31	chr10:4705434-4705484	HEK293	kidney:	embryo
32	chr10:4705434-4705484	SAEC	small airway:	n/a
33	chr10:4705434-4705484	Jurkat	blood:	n/a
34	chr10:4705434-4705484	AoSMC	blood vessel:	n/a
35	chr10:4705434-4705484	BJ	skin:	n/a
36	chr10:4705434-4705484	Hepatocyte	liver:	n/a
37	chr10:4705434-4705484	H1-hESC	embryonic stem cell:	embryo
38	chr10:4705434-4705484	NHBE	bronchial:	n/a
39	chr10:4705434-4705484	SK-N-MC	brain:	n/a
40	chr10:4705434-4705484	HCM	heart:	n/a
41	chr10:4705434-4705484	AG09319	gingival:	n/a
42	chr10:4705434-4705484	LNCaP	prostate:	n/a
43	chr10:4705434-4705484	RPTEC	kidney:	n/a
44	chr10:4705434-4705484	NT2-D1	testis:	n/a
45	chr10:4705434-4705484	ovcar-3	ovarian:	n/a
46	chr10:4705434-4705484	NB4	blood:	n/a
47	chr10:4705434-4705484	HUVEC	blood vessel:	n/a
48	chr10:4705434-4705484	GM12891	blood:	n/a
49	chr10:4705434-4705484	ProgFib	skin:	n/a
50	chr10:4705434-4705484	SKMC	muscle:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4702583..4705681-chr10:4760032..4763003,3	MCF-7	breast:
2	chr10:4691378..4694078-chr10:4702195..4704638,2	MCF-7	breast:
3	chr10:4703565..4707087-chr10:4805209..4809008,5	MCF-7	breast:
4	chr10:3826531..3829681-chr10:4703609..4706430,7	MCF-7	breast:
5	chr10:4698769..4700286-chr10:4703854..4706647,2	MCF-7	breast:
6	chr10:4582239..4584418-chr10:4702344..4704094,2	MCF-7	breast:
7	chr10:4705429..4707304-chr10:4750266..4753221,2	MCF-7	breast:
8	chr10:4701367..4707262-chr10:4764196..4772300,19	MCF-7	breast:
9	chr10:3928607..3931321-chr10:4704899..4706515,2	MCF-7	breast:
10	chr10:3211964..3214962-chr10:4702105..4703774,2	K562	blood:
11	chr10:3826124..3828322-chr10:4703952..4705855,2	MCF-7	breast:
12	chr10:4702078..4707095-chr10:4773802..4779822,17	MCF-7	breast:
13	chr10:4690809..4692527-chr10:4700264..4703042,2	MCF-7	breast:
14	chr10:4704028..4707695-chr10:4796284..4798657,3	MCF-7	breast:
15	chr10:3873499..3876423-chr10:4703265..4705596,2	MCF-7	breast:
16	chr10:4699032..4701358-chr10:4768674..4770384,2	MCF-7	breast:
17	chr10:4702931..4705070-chr10:4793409..4795730,2	MCF-7	breast:
18	chr10:4694173..4696454-chr10:4704960..4707093,2	K562	blood:
19	chr10:4702023..4704099-chr19:35939422..35942094,2	MCF-7	breast:
20	chr10:4703699..4707665-chr10:4763385..4769263,9	MCF-7	breast:
21	chr10:4704371..4707713-chr10:4716720..4722125,6	MCF-7	breast:
22	chr10:4704243..4706913-chr10:4720436..4722129,2	MCF-7	breast:
23	chr10:4692495..4696289-chr10:4704356..4708036,4	MCF-7	breast:
24	chr10:4704812..4707104-chr10:4757845..4760690,2	MCF-7	breast:
25	chr10:4701957..4706155-chr10:4806561..4810168,4	MCF-7	breast:
26	chr10:4702582..4706500-chr10:4772852..4778695,11	MCF-7	breast:
27	chr10:4703462..4705241-chr10:4867377..4869732,2	MCF-7	breast:
28	chr10:4320010..4324018-chr10:4702839..4706546,5	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C2-4	chr10:4701645-4701872	ENSG00000231298
2	lnc-AKR1E2-1	chr10:4703891-4704611	ENSG00000225269
3	lnc-AKR1C2-9	chr10:4710241-4710262	l_243_NR_024475
4	lnc-AKR1E2-1	chr10:4702174-4702303	NR_015425
5	lnc-AKR1E2-1	chr10:4703891-4704606	NR_015425
6	lnc-AKR1E2-1	chr10:4703891-4704604	XLOC_008362
7	lnc-AKR1C2-4	chr10:4701645-4701872	XLOC_008703
8	lnc-AKR1C2-4	chr10:4701538-4701872	NONHSAT011101
9	lnc-AKR1E2-1	chr10:4702202-4702303	XLOC_008362
10	lnc-AKR1C2-4	chr10:4701645-4701872	ENSG00000231298.2
11	lnc-AKR1C2-4	chr10:4701645-4701872	XLOC_008703
12	lnc-AKR1E2-1	chr10:4703891-4704577	XLOC_008362
13	lnc-AKR1C2-4	chr10:4699793-4701526	NONHSAT011101
14	lnc-AKR1E2-1	chr10:4702174-4702303	ENSG00000225269
15	lnc-AKR1C2-4	chr10:4701645-4701872	NONHSAT011106
16	lnc-AKR1C2-9	chr10:4710241-4710324	NONHSAT011104
17	lnc-AKR1E2-1	chr10:4702174-4702303	XLOC_008362
18	lnc-AKR1C2-9	chr10:4710241-4710346	NONHSAT011102

No data

Variant related genes	Relation type
LINC00704	TF binding region
LINC00704	CpG island
ENSG00000067082	chromatin interactions
ENSG00000231298	chromatin interactions
ENSG00000230573	chromatin interactions
ENSG00000165568	chromatin interactions
ENSG00000126262	chromatin interactions
HMGA2	miRNA target sites

Extended variants
information (count: 407 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10508287	chr10:4700968-4700969	Weak transcription Enhancers Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567582369	chr10:4700974-4700975	Weak transcription Enhancers Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs184842887	chr10:4700975-4700976	Weak transcription Enhancers Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs547119905	chr10:4701047-4701048	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs189311104	chr10:4701069-4701070	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs545869353	chr10:4701072-4701073	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs191287804	chr10:4701152-4701153	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs535123166	chr10:4701198-4701199	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs572794231	chr10:4701203-4701204	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs368462029	chr10:4701211-4701212	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs11252645	chr10:4701226-4701227	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs566670256	chr10:4701283-4701284	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs561676783	chr10:4701285-4701286	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs529165748	chr10:4701294-4701295	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs142289384	chr10:4701339-4701340	Weak transcription Enhancers Active TSS Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs373585829	chr10:4701399-4701400	Weak transcription Enhancers Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs77625405	chr10:4701417-4701418	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs77400759	chr10:4701419-4701420	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs183482878	chr10:4701435-4701436	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs568842219	chr10:4701456-4701457	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs75936235	chr10:4701466-4701467	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs535682083	chr10:4701483-4701484	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs566897087	chr10:4701498-4701499	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs527798330	chr10:4701523-4701524	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs549276855	chr10:4701537-4701538	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs313494	chr10:4701546-4701547	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188633840	chr10:4701547-4701548	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs556474844	chr10:4701562-4701563	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs74872919	chr10:4701569-4701570	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs538909330	chr10:4701603-4701604	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs554347974	chr10:4701650-4701651	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs569028094	chr10:4701702-4701703	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs149460923	chr10:4701703-4701704	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs533092173	chr10:4701713-4701714	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs181517666	chr10:4701727-4701728	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs538156987	chr10:4701796-4701797	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs186293301	chr10:4701819-4701820	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs544499746	chr10:4701820-4701821	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs190401857	chr10:4701851-4701852	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs143855019	chr10:4701883-4701884	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368451030	chr10:4701979-4701980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148644374	chr10:4701990-4701991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546582984	chr10:4701992-4701993	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557427143	chr10:4701994-4701995	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544826764	chr10:4702015-4702016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560314286	chr10:4702040-4702041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540372563	chr10:4702080-4702081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181720519	chr10:4702094-4702095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144287768	chr10:4702095-4702096	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549095519	chr10:4702102-4702103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD
Glioma	20126413	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4680600-4703800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:4693000-4703000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr10:4693000-4703600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr10:4693000-4703600	Weak transcription	Right Atrium	heart
5	chr10:4693200-4702400	Weak transcription	Psoas Muscle	Psoas
6	chr10:4693200-4702400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr10:4693200-4703000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:4693200-4703000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr10:4693200-4703800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:4693200-4703800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr10:4693200-4703800	Weak transcription	Pancreas	Pancrea
12	chr10:4694600-4703800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr10:4694800-4701600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:4694800-4704200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:4696400-4705200	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr10:4697000-4701000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr10:4697800-4704600	Weak transcription	Osteobl	bone
18	chr10:4698000-4703000	Weak transcription	Fetal Muscle Leg	muscle
19	chr10:4698800-4701200	Enhancers	Fetal Brain Male	brain
20	chr10:4699000-4701400	Enhancers	A549	lung
21	chr10:4699000-4701400	Enhancers	HSMM	muscle
22	chr10:4699200-4701000	Weak transcription	Brain Angular Gyrus	brain
23	chr10:4699200-4703800	Weak transcription	Dnd41	blood
24	chr10:4699200-4704000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:4699400-4701400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr10:4699600-4701000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:4699600-4701800	Strong transcription	HUVEC	blood vessel
28	chr10:4699600-4702400	Weak transcription	Fetal Heart	heart
29	chr10:4699600-4702800	Weak transcription	Adipose Nuclei	Adipose
30	chr10:4699800-4701200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr10:4699800-4702000	Strong transcription	HMEC	breast
32	chr10:4699800-4704200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr10:4699800-4705200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:4700200-4702000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr10:4700400-4701200	Strong transcription	NHEK	skin
36	chr10:4700600-4701200	Enhancers	Brain Anterior Caudate	brain
37	chr10:4700600-4701200	Enhancers	Brain Substantia Nigra	brain
38	chr10:4700600-4701600	Enhancers	Liver	Liver
39	chr10:4700600-4702600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:4700600-4703800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr10:4700800-4701200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr10:4700800-4701400	Enhancers	Stomach Mucosa	stomach
43	chr10:4700800-4703600	Weak transcription	NHDF-Ad	bronchial
44	chr10:4700800-4705000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr10:4701000-4701200	Enhancers	Brain Cingulate Gyrus	brain
46	chr10:4701000-4701200	Enhancers	HepG2	liver
47	chr10:4701000-4701400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:4701000-4701400	Active TSS	Brain Angular Gyrus	brain
49	chr10:4701000-4701400	Active TSS	Brain Hippocampus Middle	brain
50	chr10:4701000-4701800	Weak transcription	NHLF	lung

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