Variant report

Variant	nsv430120
Chromosome Location	chr10:747115-797509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:1345)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:758256-758463	HepG2	liver:	n/a	n/a
2	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
3	BHLHE40	chr10:769894-770344	K562	blood:	n/a	n/a
4	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
5	BHLHE40	chr10:764330-764448	K562	blood:	n/a	n/a
6	CBX3	chr10:769860-770105	K562	blood:	n/a	n/a
7	CEBPB	chr10:758111-758899	HepG2	liver:	n/a	chr10:758290-758301
8	CEBPB	chr10:758560-758911	A549	lung:	n/a	n/a
9	CEBPB	chr10:758593-758913	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr10:758593-758726	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
12	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
13	CEBPB	chr10:758153-758435	HepG2	liver:	n/a	chr10:758290-758301
14	CEBPB	chr10:758600-758822	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:758035-758475	MCF-7	breast:	n/a	chr10:758290-758301
16	CEBPB	chr10:758430-759010	A549	lung:	n/a	n/a
17	CEBPB	chr10:758494-758788	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:758111-758888	Hela-S3	cervix:	n/a	chr10:758290-758301
19	CEBPB	chr10:758238-758899	IMR90	lung:	n/a	chr10:758290-758301
20	CEBPB	chr10:758496-758932	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr10:758216-758902	A549	lung:	n/a	chr10:758290-758301
22	CEBPB	chr10:758051-759055	MCF-7	breast:	n/a	chr10:758290-758301
23	CEBPB	chr10:776542-776771	H1-hESC	embryonic stem cell:	n/a	chr10:776667-776678
24	CEBPB	chr10:758539-758922	MCF-7	breast:	n/a	n/a
25	CEBPB	chr10:776514-776865	HepG2	liver:	n/a	chr10:776667-776678
26	CEBPB	chr10:758039-758854	HepG2	liver:	n/a	chr10:758290-758301
27	CEBPB	chr10:758529-758903	K562	blood:	n/a	n/a
28	CEBPB	chr10:758054-758413	HepG2	liver:	n/a	chr10:758290-758301
29	CEBPD	chr10:758141-758412	HepG2	liver:	n/a	n/a
30	CHD2	chr10:764260-764276	K562	blood:	n/a	n/a
31	CHD2	chr10:758179-758233	HepG2	liver:	n/a	n/a
32	CREB1	chr10:757989-758546	HepG2	liver:	n/a	n/a
33	CTCF	chr10:766140-766290	GM12867	blood:	n/a	chr10:766151-766164 chr10:766227-766235
34	CTCF	chr10:785780-785930	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:773380-773530	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:764180-764330	HepG2	liver:	n/a	n/a
37	CTCF	chr10:767020-767170	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:775240-775390	Caco-2	colon:	n/a	n/a
39	CTCF	chr10:769672-769745	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr10:760840-760990	GM12869	blood:	n/a	n/a
41	CTCF	chr10:756920-757070	GM12869	blood:	n/a	n/a
42	CTCF	chr10:785654-785665	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:785624-785630	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:788807-788881	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr10:764240-764390	A549	lung:	n/a	n/a
46	CTCF	chr10:769512-769567	LNCaP	prostate:	n/a	n/a
47	CTCF	chr10:769293-769332	GM20000	blood:	n/a	n/a
48	CTCF	chr10:775310-775349	Lung_OC	lung:	n/a	n/a
49	E2F4	chr10:758258-758593	MCF10A-Er-Src	breast:	n/a	n/a
50	EGR1	chr10:769048-770116	GM12878	blood:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:773101-773151	HAEpiC	amniotic membrane:	n/a
2	chr10:782282-782332	NB4	blood:	n/a
3	chr10:773141-773191	SK-N-MC	brain:	n/a
4	chr10:773101-773151	HAEpiC	amniotic membrane:	n/a
5	chr10:782282-782332	NB4	blood:	n/a
6	chr10:773141-773191	SK-N-MC	brain:	n/a
7	chr10:783312-783362	HCT-116	colon:	n/a
8	chr10:773101-773151	SK-N-MC	brain:	n/a
9	chr10:766041-766091	NHDF-neo	bronchial:	n/a
10	chr10:768867-768917	BJ	skin:	n/a
11	chr10:778709-778759	AG09309	skin:	n/a
12	chr10:768867-768917	U87	brain:	n/a
13	chr10:772323-772373	LNCaP	prostate:	n/a
14	chr10:778123-778173	HRPEpiC	eye:	n/a
15	chr10:778073-778123	AG04450	lung:	fetal
16	chr10:772323-772373	SAEC	small airway:	n/a
17	chr10:766431-766481	Hepatocyte	liver:	n/a
18	chr10:771624-771674	PFSK-1	brain:	n/a
19	chr10:783312-783362	HEEpiC	esophagus:	n/a
20	chr10:783312-783362	NH-A	brain:	n/a
21	chr10:766501-766551	LNCaP	prostate:	n/a
22	chr10:766501-766551	PrEC	prostate:	n/a
23	chr10:775353-775403	HIPEpiC	eye:	n/a
24	chr10:768867-768917	T-47D	breast:	n/a
25	chr10:772600-772650	HCT-116	colon:	n/a
26	chr10:766294-766344	GM12878	blood:	n/a
27	chr10:766431-766481	ovcar-3	ovarian:	n/a
28	chr10:771624-771674	HAEpiC	amniotic membrane:	n/a
29	chr10:766041-766091	HAEpiC	amniotic membrane:	n/a
30	chr10:778123-778173	BJ	skin:	n/a
31	chr10:769945-769995	HRCEpiC	kidney:	n/a
32	chr10:766041-766091	GM12891	blood:	n/a
33	chr10:769945-769995	MCF10A-Er-Src	breast:	n/a
34	chr10:778709-778759	HCPEpiC	choroid plexus:	n/a
35	chr10:775353-775403	GM12878	blood:	n/a
36	chr10:783312-783362	AG04450	lung:	fetal
37	chr10:771624-771674	SK-N-SH	brain:	n/a
38	chr10:766294-766344	RPTEC	kidney:	n/a
39	chr10:775353-775403	GM12891	blood:	n/a
40	chr10:773101-773151	GM12891	blood:	n/a
41	chr10:768867-768917	Jurkat	blood:	n/a
42	chr10:766501-766551	H1-hESC	embryonic stem cell:	embryo
43	chr10:775353-775403	NHDF-neo	bronchial:	n/a
44	chr10:773101-773151	NB4	blood:	n/a
45	chr10:768541-768591	HCPEpiC	choroid plexus:	n/a
46	chr10:778219-778269	PrEC	prostate:	n/a
47	chr10:772323-772373	MCF-7	breast:	n/a
48	chr10:766041-766091	HL-60	blood:	n/a
49	chr10:778219-778269	ProgFib	skin:	n/a
50	chr10:778219-778269	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
2	chr10:731969..737087-chr10:747564..751327,5	MCF-7	breast:
3	chr10:734350..736432-chr10:761399..763324,2	MCF-7	breast:
4	chr10:734436..736142-chr10:751742..753613,2	MCF-7	breast:
5	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
6	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
7	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
8	chr10:739447..741646-chr10:745969..747507,2	MCF-7	breast:
9	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
10	chr10:734188..737067-chr10:751931..753657,2	MCF-7	breast:
11	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
12	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
13	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
14	chr10:750983..753337-chr10:755498..757369,2	MCF-7	breast:
15	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
16	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
17	chr10:750983..753337-chr10:755498..757369,2	MCF-7	breast:
18	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-6	chr10:779932-779973	NONHSAT010872
2	lnc-C10orf108-6	chr10:780517-780898	NONHSAT010872
3	lnc-C10orf108-4	chr10:790517-790898	XLOC_008335
4	lnc-C10orf108-4	chr10:789932-789973	XLOC_008335

No data

Variant related genes	Relation type
ENSG00000231601	TF binding region
ENSG00000231601	CpG island
ENSG00000231601	chromatin interactions
ENSG00000151240	chromatin interactions
SEC24A	miRNA target sites
SEC23IP	miRNA target sites

Extended variants
information (count: 2574 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2574 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2209625	chr10:747115-747116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184963308	chr10:747135-747136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76184903	chr10:747179-747180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562907848	chr10:747198-747199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575575402	chr10:747243-747244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544540227	chr10:747305-747306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561041493	chr10:747381-747382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112300934	chr10:747384-747385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73576313	chr10:747385-747386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559946240	chr10:747396-747397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189297555	chr10:747502-747503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77907478	chr10:747522-747523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181725145	chr10:747552-747553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568537014	chr10:747561-747562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148384521	chr10:747637-747638	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571666019	chr10:747642-747643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs140596810	chr10:747666-747667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568308232	chr10:747673-747674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150467745	chr10:747676-747677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554345881	chr10:747678-747679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61833035	chr10:747679-747680	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368264442	chr10:747733-747734	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1080048	chr10:747772-747773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117666254	chr10:747896-747897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536573278	chr10:747984-747985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576533870	chr10:748045-748046	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546428313	chr10:748055-748056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554942881	chr10:748056-748057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs117915768	chr10:748119-748120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574788638	chr10:748148-748149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540014593	chr10:748161-748162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560310661	chr10:748162-748163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532081835	chr10:748193-748194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561203110	chr10:748194-748195	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374283902	chr10:748210-748211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185264791	chr10:748354-748355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562131260	chr10:748358-748359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138272225	chr10:748369-748370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375355377	chr10:748385-748386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532216838	chr10:748388-748389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550711921	chr10:748390-748391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373312499	chr10:748397-748398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189749275	chr10:748400-748401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34842562	chr10:748432-748433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568366642	chr10:748480-748481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368774622	chr10:748481-748482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527994345	chr10:748490-748491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566666168	chr10:748491-748492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181235485	chr10:748512-748513	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376066120	chr10:748563-748564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	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
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
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:746600-747200	Weak transcription	Right Atrium	heart
2	chr10:746600-751600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:746600-758000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:751600-751800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:757800-759400	Enhancers	Placenta	Placenta
6	chr10:757800-759800	Enhancers	Fetal Intestine Small	intestine
7	chr10:758000-758800	Enhancers	Liver	Liver
8	chr10:758000-759200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:758000-759200	Enhancers	Hela-S3	cervix
10	chr10:758000-759400	Enhancers	Fetal Intestine Large	intestine
11	chr10:758000-759600	Enhancers	HepG2	liver
12	chr10:758200-759000	Enhancers	Small Intestine	intestine
13	chr10:758200-759200	Enhancers	Duodenum Mucosa	Duodenum
14	chr10:758600-759400	Enhancers	Stomach Mucosa	stomach
15	chr10:759400-760400	Weak transcription	Placenta	Placenta
16	chr10:760000-761400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
17	chr10:760400-761000	ZNF genes & repeats	Placenta	Placenta
18	chr10:760600-760800	ZNF genes & repeats	Gastric	stomach
19	chr10:760600-761000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:761000-768200	Weak transcription	Placenta	Placenta
21	chr10:761000-768400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:762800-763200	Enhancers	Fetal Heart	heart
23	chr10:764200-764400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr10:764200-764600	Bivalent Enhancer	HepG2	liver
25	chr10:764800-772000	Weak transcription	Right Atrium	heart
26	chr10:767800-768400	Weak transcription	Spleen	Spleen
27	chr10:768200-768600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:768200-769000	Enhancers	Placenta	Placenta
29	chr10:768400-768600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr10:768400-768600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr10:768400-768600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:768400-768600	Genic enhancers	Spleen	Spleen
33	chr10:768600-768800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:768600-770000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:768600-771400	Weak transcription	Spleen	Spleen
36	chr10:769000-771600	Weak transcription	Placenta	Placenta
37	chr10:770000-770200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr10:770000-770200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:770000-770400	Enhancers	Pancreas	Pancrea
40	chr10:770200-771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:770800-771000	Weak transcription	Esophagus	oesophagus
42	chr10:770800-772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:771400-771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:771400-772200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:771400-772200	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr10:771400-772200	Enhancers	Fetal Muscle Trunk	muscle
47	chr10:771400-772200	Enhancers	Fetal Muscle Leg	muscle
48	chr10:771400-772200	Enhancers	Spleen	Spleen
49	chr10:771400-773000	Enhancers	Right Ventricle	heart
50	chr10:771600-771800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links