Variant report

Variant	nsv894721
Chromosome Location	chr10:771532-815149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:857)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:813001-813370	K562	blood:	n/a	n/a
2	BCL11A	chr10:811979-812582	GM12878	blood:	n/a	n/a
3	BCL3	chr10:812586-812912	GM12878	blood:	n/a	n/a
4	CBX3	chr10:806640-806884	K562	blood:	n/a	n/a
5	CEBPB	chr10:799626-799733	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:776542-776771	H1-hESC	embryonic stem cell:	n/a	chr10:776667-776678
7	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
8	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
9	CEBPB	chr10:799560-799705	K562	blood:	n/a	n/a
10	CEBPB	chr10:776514-776865	HepG2	liver:	n/a	chr10:776667-776678
11	CTCF	chr10:785654-785665	MCF-7	breast:	n/a	n/a
12	CTCF	chr10:773380-773530	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:785624-785630	MCF-7	breast:	n/a	n/a
14	CTCF	chr10:785780-785930	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:775240-775390	Caco-2	colon:	n/a	n/a
16	CTCF	chr10:798402-798426	GM10266	blood:	n/a	n/a
17	CTCF	chr10:775310-775349	Lung_OC	lung:	n/a	n/a
18	CTCF	chr10:804071-804155	K562	blood:	n/a	n/a
19	CTCF	chr10:806040-806190	GM12869	blood:	n/a	n/a
20	CTCF	chr10:805940-806090	GM12867	blood:	n/a	n/a
21	CTCF	chr10:788807-788881	Spleen_OC	spleen:	n/a	n/a
22	EP300	chr10:780354-780880	SK-N-SH	brain:	n/a	n/a
23	FOXA1	chr10:804560-804781	T-47D	breast:	n/a	n/a
24	FOXA1	chr10:792166-792474	HepG2	liver:	n/a	n/a
25	FOXA1	chr10:773011-773772	T-47D	breast:	n/a	n/a
26	FOXA1	chr10:773424-773698	T-47D	breast:	n/a	n/a
27	FOXA2	chr10:804073-804273	A549	lung:	n/a	n/a
28	FOXA2	chr10:792162-792455	A549	lung:	n/a	n/a
29	FOXA2	chr10:792068-792490	A549	lung:	n/a	n/a
30	GATA3	chr10:780322-780697	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr10:773038-773730	T-47D	breast:	n/a	n/a
32	GATA3	chr10:773027-773811	T-47D	breast:	n/a	n/a
33	GATA3	chr10:780123-780869	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr10:779968-780893	SK-N-SH	brain:	n/a	n/a
35	IRF4	chr10:772192-772527	GM12878	blood:	n/a	n/a
36	JUN	chr10:806696-806896	K562	blood:	n/a	n/a
37	KAP1	chr10:806581-807152	K562	blood:	n/a	n/a
38	KAP1	chr10:813652-814049	HEK293	kidney:	n/a	n/a
39	KAP1	chr10:791601-792092	HEK293	kidney:	n/a	n/a
40	MAFF	chr10:807985-808185	HepG2	liver:	n/a	chr10:808063-808081
41	MAFK	chr10:807917-808216	HepG2	liver:	n/a	chr10:808064-808079
42	MAFK	chr10:807978-808188	HepG2	liver:	n/a	chr10:808064-808079
43	MAX	chr10:785611-785809	NB4	blood:	n/a	chr10:785731-785741 chr10:785743-785753
44	MAX	chr10:772892-773582	MCF-7	breast:	n/a	chr10:773089-773096 chr10:773088-773099 chr10:773291-773307 chr10:773343-773353 chr10:773139-773155
45	MYC	chr10:805406-805787	MCF-7	breast:	n/a	n/a
46	MYC	chr10:805604-805654	MCF-7	breast:	n/a	n/a
47	MYC	chr10:805852-805992	MCF-7	breast:	n/a	n/a
48	MYC	chr10:779232-779263	MCF-7	breast:	n/a	n/a
49	MYC	chr10:785691-785703	MCF-7	breast:	n/a	n/a
50	MYC	chr10:805788-805801	MCF-7	breast:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:775353-775403	GM12891	blood:	n/a
2	chr10:782282-782332	HRCEpiC	kidney:	n/a
3	chr10:772969-773019	HRE	kidney:	n/a
4	chr10:775353-775403	GM12891	blood:	n/a
5	chr10:782282-782332	HRCEpiC	kidney:	n/a
6	chr10:772969-773019	HRE	kidney:	n/a
7	chr10:775353-775403	H1-hESC	embryonic stem cell:	embryo
8	chr10:772323-772373	NHBE	bronchial:	n/a
9	chr10:773141-773191	HIPEpiC	eye:	n/a
10	chr10:771624-771674	ProgFib	skin:	n/a
11	chr10:783312-783362	HL-60	blood:	n/a
12	chr10:778073-778123	NB4	blood:	n/a
13	chr10:775353-775403	T-47D	breast:	n/a
14	chr10:778073-778123	AoSMC	blood vessel:	n/a
15	chr10:772323-772373	SAEC	small airway:	n/a
16	chr10:778709-778759	GM19239	blood:	n/a
17	chr10:772600-772650	RPTEC	kidney:	n/a
18	chr10:778219-778269	T-47D	breast:	n/a
19	chr10:783591-783641	HepG2	liver:	n/a
20	chr10:778219-778269	SK-N-SH_RA	brain:	n/a
21	chr10:783591-783641	H1-hESC	embryonic stem cell:	embryo
22	chr10:772600-772650	ECC-1	luminal epithelium:	n/a
23	chr10:778709-778759	SK-N-SH	brain:	n/a
24	chr10:783312-783362	HMEC	breast:	n/a
25	chr10:773141-773191	AoSMC	blood vessel:	n/a
26	chr10:783312-783362	HUVEC	blood vessel:	n/a
27	chr10:772323-772373	GM12892	blood:	n/a
28	chr10:783312-783362	GM12878	blood:	n/a
29	chr10:778709-778759	Hela-S3	cervix:	n/a
30	chr10:778709-778759	HCF	heart:	n/a
31	chr10:778709-778759	SAEC	small airway:	n/a
32	chr10:778073-778123	BE2_C	brain:	n/a
33	chr10:783312-783362	GM12892	blood:	n/a
34	chr10:782282-782332	ECC-1	luminal epithelium:	n/a
35	chr10:775353-775403	K562	blood:	n/a
36	chr10:773101-773151	HRPEpiC	eye:	n/a
37	chr10:782282-782332	SKMC	muscle:	n/a
38	chr10:772600-772650	ovcar-3	ovarian:	n/a
39	chr10:773101-773151	GM19239	blood:	n/a
40	chr10:778123-778173	HRPEpiC	eye:	n/a
41	chr10:783591-783641	HCM	heart:	n/a
42	chr10:778073-778123	AG10803	skin:	n/a
43	chr10:778709-778759	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:778219-778269	AG10803	skin:	n/a
45	chr10:773101-773151	HCF	heart:	n/a
46	chr10:782282-782332	Hepatocyte	liver:	n/a
47	chr10:771624-771674	HL-60	blood:	n/a
48	chr10:773101-773151	SK-N-MC	brain:	n/a
49	chr10:772600-772650	NHBE	bronchial:	n/a
50	chr10:783312-783362	AG09319	gingival:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
2	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
3	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
4	chr10:733897..735933-chr10:814143..815828,2	MCF-7	breast:
5	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1827 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1827 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs877282	chr10:771532-771533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs79108828	chr10:771534-771535	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs877281	chr10:771557-771558	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs34448709	chr10:771579-771580	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs554932983	chr10:771596-771597	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs575101635	chr10:771598-771599	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs877280	chr10:771599-771600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189274788	chr10:771600-771601	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs577410884	chr10:771628-771629	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs116035267	chr10:771640-771641	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs562977999	chr10:771646-771647	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs147939717	chr10:771670-771671	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs373387335	chr10:771675-771676	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs561002780	chr10:771706-771707	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs562008737	chr10:771714-771715	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs530036493	chr10:771715-771716	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs114949244	chr10:771717-771718	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs114982977	chr10:771729-771730	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs115759234	chr10:771743-771744	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs114206089	chr10:771745-771746	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs10904549	chr10:771769-771770	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs115268875	chr10:771789-771790	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs377277579	chr10:771837-771838	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs554580954	chr10:771838-771839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs114277434	chr10:771842-771843	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140718191	chr10:771843-771844	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs34338917	chr10:771850-771851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs12782447	chr10:771870-771871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11253363	chr10:771891-771892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs546433763	chr10:771916-771917	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs556665102	chr10:771938-771939	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs386739768	chr10:771939-771940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185235860	chr10:771940-771941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs12763443	chr10:771941-771942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563653974	chr10:771948-771949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs529949173	chr10:771988-771989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs540565630	chr10:772027-772028	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114008532	chr10:772061-772062	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189718164	chr10:772072-772073	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11253364	chr10:772083-772084	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568630679	chr10:772084-772085	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367708120	chr10:772089-772090	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138449021	chr10:772105-772106	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534753656	chr10:772127-772128	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568096703	chr10:772128-772129	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12779159	chr10:772143-772144	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554542534	chr10:772170-772171	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571139854	chr10:772200-772201	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34652870	chr10:772218-772219	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs34912955	chr10:772222-772223	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
Breast cancer	21364760	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:764800-772000	Weak transcription	Right Atrium	heart
2	chr10:769000-771600	Weak transcription	Placenta	Placenta
3	chr10:770200-771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:770800-772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:771400-771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:771400-772200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:771400-772200	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr10:771400-772200	Enhancers	Fetal Muscle Trunk	muscle
9	chr10:771400-772200	Enhancers	Fetal Muscle Leg	muscle
10	chr10:771400-772200	Enhancers	Spleen	Spleen
11	chr10:771400-773000	Enhancers	Right Ventricle	heart
12	chr10:771600-771800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr10:771600-772000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr10:771600-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:771600-774800	Enhancers	Placenta	Placenta
16	chr10:771800-772200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:771800-772400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr10:772000-772200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr10:772000-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr10:772000-772200	Enhancers	Esophagus	oesophagus
21	chr10:772000-773400	Strong transcription	Right Atrium	heart
22	chr10:772200-772600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:772400-772800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr10:772600-773000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:772800-773200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr10:772800-773600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr10:773000-775200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:773400-775200	Weak transcription	Right Atrium	heart
29	chr10:774600-774800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr10:774600-774800	Enhancers	Right Ventricle	heart
31	chr10:774600-775400	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr10:774600-775600	Enhancers	Duodenum Mucosa	Duodenum
33	chr10:775200-775400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr10:775400-775600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
35	chr10:775400-776000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:775600-775800	Enhancers	Pancreas	Pancrea
37	chr10:775800-779400	Weak transcription	Pancreas	Pancrea
38	chr10:776000-779200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:778000-778200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:778600-779400	Enhancers	Placenta	Placenta
41	chr10:779200-779400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:779400-779600	Enhancers	Esophagus	oesophagus
43	chr10:779400-779600	Enhancers	Gastric	stomach
44	chr10:779400-779600	Enhancers	Pancreas	Pancrea
45	chr10:779400-785400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:779600-779800	Weak transcription	Pancreas	Pancrea
47	chr10:779600-785200	Weak transcription	Gastric	stomach
48	chr10:784000-790600	Weak transcription	Spleen	Spleen
49	chr10:785200-785600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr10:785200-785600	ZNF genes & repeats	Gastric	stomach

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