Variant report

Variant	nsv540746
Chromosome Location	chr10:95384527-95449653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:183)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:95430867-95431043	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:95440152-95440733	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:95431713-95432196	HepG2	liver:	n/a	n/a
4	BHLHE40	chr10:95431897-95432071	HepG2	liver:	n/a	n/a
5	BRCA1	chr10:95413731-95413940	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr10:95426289-95426291	K562	blood:	n/a	n/a
7	CEBPB	chr10:95426177-95426366	HepG2	liver:	n/a	chr10:95426281-95426292 chr10:95426281-95426294 chr10:95426282-95426293
8	CEBPB	chr10:95427640-95427894	HepG2	liver:	n/a	chr10:95427745-95427756
9	CEBPZ	chr10:95437410-95437414	HepG2	liver:	n/a	n/a
10	CTCF	chr10:95440260-95440410	Caco-2	colon:	n/a	chr10:95440355-95440376
11	CTCF	chr10:95440240-95440390	HA-sp	spinal cord:	n/a	chr10:95440355-95440376
12	CTCF	chr10:95440260-95440410	HBMEC	blood vessel:	n/a	chr10:95440355-95440376
13	CTCF	chr10:95440280-95440430	GM12864	blood:	n/a	chr10:95440355-95440376
14	CTCF	chr10:95440300-95440450	AG10803	skin:	n/a	chr10:95440355-95440376
15	CTCF	chr10:95440180-95440330	HAc	cerebellar:	n/a	n/a
16	CTCF	chr10:95440262-95440421	MCF-7	breast:	n/a	chr10:95440355-95440376
17	CTCF	chr10:95440164-95440534	K562	blood:	n/a	chr10:95440355-95440376
18	CTCF	chr10:95440320-95440470	AoAF	blood vessel:	n/a	chr10:95440355-95440376
19	CTCF	chr10:95440300-95440450	NHEK	skin:	n/a	chr10:95440355-95440376
20	CTCF	chr10:95440307-95440439	Kidney_OC	kidney:	n/a	chr10:95440355-95440376
21	CTCF	chr10:95440240-95440390	GM12871	blood:	n/a	chr10:95440355-95440376
22	CTCF	chr10:95440270-95440447	Lung_OC	lung:	n/a	chr10:95440355-95440376
23	CTCF	chr10:95440590-95440619	Medullo	brain:	n/a	n/a
24	CTCF	chr10:95440291-95440370	Gliobla	brain:	n/a	n/a
25	CTCF	chr10:95440280-95440430	HPF	lung:	n/a	chr10:95440355-95440376
26	CTCF	chr10:95440280-95440430	AG09319	gingival:	n/a	chr10:95440355-95440376
27	CTCF	chr10:95440265-95440514	A549	lung:	n/a	chr10:95440355-95440376
28	CTCF	chr10:95440298-95440450	LNCaP	prostate:	n/a	chr10:95440355-95440376
29	CTCF	chr10:95440280-95440430	GM12872	blood:	n/a	chr10:95440355-95440376
30	CTCF	chr10:95440280-95440430	HRPEpiC	eye:	n/a	chr10:95440355-95440376
31	CTCF	chr10:95440260-95440410	MCF-7	breast:	n/a	chr10:95440355-95440376
32	CTCF	chr10:95440340-95440490	HVMF	connective:	n/a	chr10:95440355-95440376
33	CTCF	chr10:95440253-95440489	Pancreas_OC	pancreas:	n/a	chr10:95440355-95440376
34	CTCF	chr10:95440280-95440430	HepG2	liver:	n/a	chr10:95440355-95440376
35	CTCF	chr10:95440260-95440410	NHEK	skin:	n/a	chr10:95440355-95440376
36	CTCF	chr10:95440267-95440455	GM13977	blood:	n/a	chr10:95440355-95440376
37	CTCF	chr10:95440264-95440456	H1-hESC	embryonic stem cell:	n/a	chr10:95440355-95440376
38	CTCF	chr10:95440180-95440523	Medullo	brain:	n/a	chr10:95440355-95440376
39	CTCF	chr10:95440260-95440410	HA-sp	spinal cord:	n/a	chr10:95440355-95440376
40	CTCF	chr10:95440260-95440410	AG04450	lung:	n/a	chr10:95440355-95440376
41	CTCF	chr10:95440460-95440610	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr10:95440500-95440650	Caco-2	colon:	n/a	n/a
43	CTCF	chr10:95440220-95440370	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr10:95440241-95440478	GM12878	blood:	n/a	chr10:95440355-95440376
45	CTCF	chr10:95440300-95440450	AG04450	lung:	n/a	chr10:95440355-95440376
46	CTCF	chr10:95440173-95440547	GM12878	blood:	n/a	chr10:95440355-95440376
47	CTCF	chr10:95440039-95440651	HCT-116	colon:	n/a	chr10:95440355-95440376
48	CTCF	chr10:95440280-95440430	BJ	skin:	n/a	chr10:95440355-95440376
49	CTCF	chr10:95440320-95440470	AG10803	skin:	n/a	chr10:95440355-95440376
50	CTCF	chr10:95440420-95440570	HFF-Myc	foreskin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:95428731-95428781	NB4	blood:	n/a
2	chr10:95425262-95425312	Jurkat	blood:	n/a
3	chr10:95425262-95425312	GM12891	blood:	n/a
4	chr10:95425262-95425312	U87	brain:	n/a
5	chr10:95425262-95425312	GM12878	blood:	n/a
6	chr10:95425262-95425312	PrEC	prostate:	n/a
7	chr10:95428731-95428781	U87	brain:	n/a
8	chr10:95428731-95428781	SK-N-SH	brain:	n/a
9	chr10:95425262-95425312	NH-A	brain:	n/a
10	chr10:95428731-95428781	PrEC	prostate:	n/a
11	chr10:95389973-95390023	MCF10A-Er-Src	breast:	n/a
12	chr10:95425262-95425312	AG09309	skin:	n/a
13	chr10:95425262-95425312	Caco-2	colon:	n/a
14	chr10:95425262-95425312	BE2_C	brain:	n/a
15	chr10:95428731-95428781	Hela-S3	cervix:	n/a
16	chr10:95389973-95390023	HEEpiC	esophagus:	n/a
17	chr10:95425262-95425312	AG10803	skin:	n/a
18	chr10:95428731-95428781	GM19239	blood:	n/a
19	chr10:95425262-95425312	NB4	blood:	n/a
20	chr10:95389973-95390023	PANC-1	pancreas:	n/a
21	chr10:95428731-95428781	SKMC	muscle:	n/a
22	chr10:95425262-95425312	A549	lung:	n/a
23	chr10:95428731-95428781	IMR90	lung:	fetal
24	chr10:95389973-95390023	SK-N-SH	brain:	n/a
25	chr10:95428731-95428781	NHBE	bronchial:	n/a
26	chr10:95425262-95425312	Hela-S3	cervix:	n/a
27	chr10:95425262-95425312	HIPEpiC	eye:	n/a
28	chr10:95389973-95390023	BE2_C	brain:	n/a
29	chr10:95389973-95390023	IMR90	lung:	fetal
30	chr10:95389973-95390023	AG04449	skin:	fetal
31	chr10:95389973-95390023	NHDF-neo	bronchial:	n/a
32	chr10:95389973-95390023	HMEC	breast:	n/a
33	chr10:95389973-95390023	HCPEpiC	choroid plexus:	n/a
34	chr10:95389973-95390023	GM19239	blood:	n/a
35	chr10:95389973-95390023	NB4	blood:	n/a
36	chr10:95428731-95428781	BE2_C	brain:	n/a
37	chr10:95425262-95425312	NHDF-neo	bronchial:	n/a
38	chr10:95428731-95428781	NH-A	brain:	n/a
39	chr10:95389973-95390023	HL-60	blood:	n/a
40	chr10:95428731-95428781	GM06990	blood:	n/a
41	chr10:95389973-95390023	HAEpiC	amniotic membrane:	n/a
42	chr10:95425262-95425312	SKMC	muscle:	n/a
43	chr10:95425262-95425312	T-47D	breast:	n/a
44	chr10:95389973-95390023	CMK	blood:	n/a
45	chr10:95428731-95428781	HRPEpiC	eye:	n/a
46	chr10:95428731-95428781	HCM	heart:	n/a
47	chr10:95425262-95425312	ovcar-3	ovarian:	n/a
48	chr10:95428731-95428781	AG04450	lung:	fetal
49	chr10:95428731-95428781	BJ	skin:	n/a
50	chr10:95428731-95428781	HPAEpiC	pulmonary alveolar:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:95421490..95424125-chr10:95424853..95426569,2	K562	blood:
2	chr10:95314553..95315223-chr10:95440160..95440841,2	K562	blood:
3	chr10:95383780..95385964-chr10:95405920..95408715,2	K562	blood:
4	chr10:95366540..95368601-chr10:95416287..95418139,2	MCF-7	breast:
5	chr10:95314485..95315617-chr10:95439876..95440649,4	MCF-7	breast:
6	chr10:95429639..95431834-chr10:95437485..95439775,2	MCF-7	breast:
7	chr10:95314209..95315199-chr10:95439863..95440407,2	MCF-7	breast:
8	chr10:95388901..95391742-chr10:95395841..95398352,2	MCF-7	breast:
9	chr10:95301519..95302383-chr10:95439830..95440737,4	MCF-7	breast:
10	chr10:95383780..95385964-chr10:95405920..95408715,2	K562	blood:
11	chr10:95393089..95395645-chr10:95398110..95400657,2	MCF-7	breast:
12	chr10:95439071..95442072-chr10:95459371..95461736,3	MCF-7	breast:
13	chr10:95434915..95436614-chr10:95438819..95440992,2	MCF-7	breast:
14	chr10:95434759..95436484-chr10:95439444..95441223,2	K562	blood:
15	chr10:95393089..95395645-chr10:95398110..95400657,2	MCF-7	breast:
16	chr10:95414485..95416199-chr10:95419555..95422077,2	MCF-7	breast:
17	chr10:95377155..95379649-chr10:95382867..95384594,2	MCF-7	breast:
18	chr10:95431559..95432264-chr6:109330260..109330871,2	NB4	blood:
19	chr10:95429639..95431834-chr10:95437485..95439775,2	MCF-7	breast:
20	chr10:95344379..95346533-chr10:95422110..95424875,2	MCF-7	breast:
21	chr10:95419996..95421608-chr10:95427554..95429484,2	K562	blood:
22	chr10:95375109..95376987-chr10:95390239..95392066,2	MCF-7	breast:
23	chr10:95301224..95301948-chr10:95439951..95440459,2	MCF-7	breast:
24	chr10:95419996..95421608-chr10:95427554..95429484,2	K562	blood:
25	chr10:95388901..95391742-chr10:95395841..95398352,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBP4-2	chr10:95445003-95445220	NONHSAT015691
2	lnc-RBP4-2	chr10:95445010-95445116	NONHSAT015692
3	lnc-RBP4-2	chr10:95443812-95443855	NONHSAT015691
4	lnc-RBP4-2	chr10:95447161-95447698	NONHSAT015692

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C10orf4	hsa-miR-181a-5p	chr10:95428592-95428613

Variant related genes	Relation type
FRA10AC1	TF binding region
PDE6C	TF binding region
FRA10AC1	CpG island
PDE6C	CpG island
ENSG00000148690	chromatin interactions
ENSG00000095464	chromatin interactions
ENSG00000080546	chromatin interactions
ENSG00000221352	chromatin interactions

Extended variants
information (count: 1585 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183303271	chr10:95389011-95389012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs137978647	chr10:95389035-95389036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs714550	chr10:95389041-95389042	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556892228	chr10:95389044-95389045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141632582	chr10:95389045-95389046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145836229	chr10:95389047-95389048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs714549	chr10:95389083-95389084	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553298112	chr10:95389087-95389088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572510554	chr10:95389095-95389096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs714551	chr10:95389124-95389125	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373661949	chr10:95389136-95389137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115920237	chr10:95389158-95389159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574853551	chr10:95389181-95389182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552577227	chr10:95389203-95389204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71485914	chr10:95389249-95389250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1409334	chr10:95389251-95389252	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148155155	chr10:95389294-95389295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186176776	chr10:95389307-95389308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59194125	chr10:95389331-95389332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190843192	chr10:95389340-95389341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575263293	chr10:95389356-95389357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568013626	chr10:95389400-95389401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150184806	chr10:95389459-95389460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550601668	chr10:95389464-95389465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369961289	chr10:95389478-95389479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376214489	chr10:95389484-95389485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539632100	chr10:95389512-95389513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553334884	chr10:95389543-95389544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566797577	chr10:95389554-95389555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561097052	chr10:95389676-95389677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4919339	chr10:95389681-95389682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs74150296	chr10:95389687-95389688	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs685932	chr10:95389691-95389692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367847732	chr10:95389706-95389707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557417902	chr10:95389707-95389708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577058266	chr10:95389708-95389709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371342364	chr10:95389718-95389719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4917871	chr10:95389728-95389729	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573214912	chr10:95389742-95389743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138734412	chr10:95389751-95389752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143030823	chr10:95389752-95389753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527724819	chr10:95389757-95389758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183402320	chr10:95389765-95389766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4919340	chr10:95389781-95389782	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564152007	chr10:95389863-95389864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200866063	chr10:95389871-95389872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs386746639	chr10:95389874-95389875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186754909	chr10:95389875-95389876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10882288	chr10:95389876-95389877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10882289	chr10:95389907-95389908	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95389000-95391400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:95389600-95389800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr10:95389600-95390000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:95389600-95390000	Enhancers	Fetal Kidney	kidney
5	chr10:95389800-95391000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr10:95389800-95391400	Enhancers	Fetal Brain Female	brain
7	chr10:95390000-95391400	Enhancers	Fetal Brain Male	brain
8	chr10:95390000-95391400	Enhancers	Fetal Muscle Trunk	muscle
9	chr10:95390400-95390600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:95390400-95391000	Enhancers	Fetal Muscle Leg	muscle
11	chr10:95390400-95391200	Enhancers	Placenta	Placenta
12	chr10:95391000-95391400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:95394800-95395000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr10:95395000-95395400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:95397800-95398200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr10:95398800-95399000	Bivalent Enhancer	HepG2	liver
17	chr10:95410600-95412400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:95412200-95413200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr10:95412200-95429800	Weak transcription	Brain Substantia Nigra	brain
20	chr10:95412400-95413200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:95412400-95413200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr10:95412400-95413200	Enhancers	HMEC	breast
23	chr10:95412400-95413200	Enhancers	HSMM	muscle
24	chr10:95412600-95413000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:95412600-95413000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:95412600-95413000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr10:95412600-95413000	Enhancers	A549	lung
28	chr10:95412600-95413000	Enhancers	HUVEC	blood vessel
29	chr10:95412600-95413200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr10:95412600-95413200	Enhancers	Osteobl	bone
31	chr10:95412800-95413000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:95412800-95413000	Enhancers	HSMMtube	muscle
33	chr10:95412800-95413000	Enhancers	NH-A	brain
34	chr10:95412800-95413000	Enhancers	NHEK	skin
35	chr10:95412800-95413000	Enhancers	NHLF	lung
36	chr10:95412800-95413200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr10:95413000-95415600	Weak transcription	A549	lung
38	chr10:95413000-95419400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:95413000-95419600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:95413000-95425600	Weak transcription	HSMMtube	muscle
41	chr10:95413000-95425800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:95413000-95426600	Weak transcription	HUVEC	blood vessel
43	chr10:95413000-95427600	Weak transcription	NHEK	skin
44	chr10:95413000-95428600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:95413200-95415600	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr10:95413200-95419400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:95413200-95420800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:95413200-95422800	Weak transcription	HSMM	muscle
49	chr10:95413200-95425000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr10:95413200-95425600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links