Variant report

Variant	nsv1045002
Chromosome Location	chr10:97214418-97250630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:305)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:97227169-97227433	K562	blood:	n/a	n/a
2	ARID3A	chr10:97235530-97236100	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:97245102-97245369	K562	blood:	n/a	chr10:97245227-97245243
4	ARID3A	chr10:97217011-97218253	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:97240610-97240832	HepG2	liver:	n/a	n/a
6	BACH1	chr10:97227105-97227454	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:97236953-97237254	GM12878	blood:	n/a	chr10:97237170-97237180
8	BATF	chr10:97236612-97236906	GM12878	blood:	n/a	chr10:97236743-97236754
9	BHLHE40	chr10:97240215-97240314	HepG2	liver:	n/a	n/a
10	BHLHE40	chr10:97227112-97227241	K562	blood:	n/a	n/a
11	BHLHE40	chr10:97239394-97240128	K562	blood:	n/a	n/a
12	CBX3	chr10:97227072-97227284	K562	blood:	n/a	n/a
13	CBX3	chr10:97226967-97227332	K562	blood:	n/a	n/a
14	CBX3	chr10:97226839-97227454	HCT-116	colon:	n/a	n/a
15	CCNT2	chr10:97227026-97227287	K562	blood:	n/a	chr10:97227195-97227204
16	CCNT2	chr10:97239906-97240068	K562	blood:	n/a	n/a
17	CEBPB	chr10:97232560-97232887	K562	blood:	n/a	chr10:97232738-97232749
18	CEBPB	chr10:97240402-97240448	K562	blood:	n/a	n/a
19	CEBPB	chr10:97231697-97231926	HepG2	liver:	n/a	chr10:97231880-97231891 chr10:97231848-97231860
20	CEBPB	chr10:97226983-97227332	HepG2	liver:	n/a	n/a
21	CEBPB	chr10:97234054-97234345	HepG2	liver:	n/a	chr10:97234112-97234123 chr10:97234185-97234196
22	CEBPB	chr10:97231747-97231748	K562	blood:	n/a	n/a
23	CEBPB	chr10:97226987-97227293	K562	blood:	n/a	n/a
24	CEBPB	chr10:97232642-97232828	K562	blood:	n/a	chr10:97232738-97232749
25	CEBPB	chr10:97240425-97240579	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:97226813-97227519	HCT-116	colon:	n/a	n/a
27	CEBPB	chr10:97226981-97227308	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr10:97233957-97234701	Hela-S3	cervix:	n/a	chr10:97234112-97234123 chr10:97234185-97234196
29	CEBPB	chr10:97226988-97227341	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:97234112-97234351	IMR90	lung:	n/a	chr10:97234112-97234123 chr10:97234185-97234196
31	CEBPB	chr10:97226978-97227375	MCF-7	breast:	n/a	n/a
32	CEBPB	chr10:97232622-97232891	K562	blood:	n/a	chr10:97232738-97232749
33	CEBPB	chr10:97234581-97234708	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr10:97217772-97218032	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:97226919-97227340	K562	blood:	n/a	n/a
36	CEBPB	chr10:97226974-97227304	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:97232639-97232827	HepG2	liver:	n/a	chr10:97232738-97232749
38	CHD2	chr10:97235725-97236084	HepG2	liver:	n/a	n/a
39	CHD2	chr10:97234537-97234700	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr10:97216500-97216650	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr10:97239820-97239970	AG10803	skin:	n/a	n/a
42	CTCF	chr10:97227100-97227250	Caco-2	colon:	n/a	n/a
43	CTCF	chr10:97239760-97239910	GM12874	blood:	n/a	n/a
44	CTCF	chr10:97227058-97227245	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr10:97235520-97235670	A549	lung:	n/a	n/a
46	CTCF	chr10:97216460-97216610	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr10:97227100-97227250	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr10:97216508-97216545	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr10:97227120-97227270	HCT-116	colon:	n/a	n/a
50	CTCF	chr10:97216420-97216570	RPTEC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:97242763-97242813	GM12892	blood:	n/a
2	chr10:97235787-97235837	HL-60	blood:	n/a
3	chr10:97242763-97242813	A549	lung:	n/a
4	chr10:97235787-97235837	HMEC	breast:	n/a
5	chr10:97219665-97219715	GM12892	blood:	n/a
6	chr10:97235787-97235837	SKMC	muscle:	n/a
7	chr10:97235787-97235837	ovcar-3	ovarian:	n/a
8	chr10:97242763-97242813	K562	blood:	n/a
9	chr10:97219665-97219715	T-47D	breast:	n/a
10	chr10:97229682-97229732	HEK293	kidney:	embryo
11	chr10:97243752-97243802	AG10803	skin:	n/a
12	chr10:97229682-97229732	Hela-S3	cervix:	n/a
13	chr10:97243752-97243802	HRPEpiC	eye:	n/a
14	chr10:97243752-97243802	PrEC	prostate:	n/a
15	chr10:97219665-97219715	NHDF-neo	bronchial:	n/a
16	chr10:97219665-97219715	GM12891	blood:	n/a
17	chr10:97219665-97219715	HRPEpiC	eye:	n/a
18	chr10:97235787-97235837	AG04450	lung:	fetal
19	chr10:97229682-97229732	BE2_C	brain:	n/a
20	chr10:97229682-97229732	AG09319	gingival:	n/a
21	chr10:97243752-97243802	BE2_C	brain:	n/a
22	chr10:97229682-97229732	HRPEpiC	eye:	n/a
23	chr10:97242763-97242813	HL-60	blood:	n/a
24	chr10:97235787-97235837	Jurkat	blood:	n/a
25	chr10:97229682-97229732	H1-hESC	embryonic stem cell:	embryo
26	chr10:97219665-97219715	RPTEC	kidney:	n/a
27	chr10:97243752-97243802	T-47D	breast:	n/a
28	chr10:97243752-97243802	GM06990	blood:	n/a
29	chr10:97219665-97219715	SK-N-SH_RA	brain:	n/a
30	chr10:97242763-97242813	HCT-116	colon:	n/a
31	chr10:97235787-97235837	HUVEC	blood vessel:	n/a
32	chr10:97219665-97219715	ovcar-3	ovarian:	n/a
33	chr10:97229682-97229732	GM19239	blood:	n/a
34	chr10:97229682-97229732	NHBE	bronchial:	n/a
35	chr10:97219665-97219715	Caco-2	colon:	n/a
36	chr10:97229682-97229732	SKMC	muscle:	n/a
37	chr10:97243752-97243802	Jurkat	blood:	n/a
38	chr10:97229682-97229732	PANC-1	pancreas:	n/a
39	chr10:97235787-97235837	NT2-D1	testis:	n/a
40	chr10:97229682-97229732	HIPEpiC	eye:	n/a
41	chr10:97235787-97235837	MCF10A-Er-Src	breast:	n/a
42	chr10:97242763-97242813	HRCEpiC	kidney:	n/a
43	chr10:97235787-97235837	GM12878	blood:	n/a
44	chr10:97235787-97235837	HRE	kidney:	n/a
45	chr10:97219665-97219715	GM19239	blood:	n/a
46	chr10:97242763-97242813	HRE	kidney:	n/a
47	chr10:97235787-97235837	AG09309	skin:	n/a
48	chr10:97229682-97229732	HL-60	blood:	n/a
49	chr10:97243752-97243802	IMR90	lung:	fetal
50	chr10:97243752-97243802	K562	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:97210894..97213718-chr10:97224956..97226923,2	K562	blood:
2	chr10:97249137..97252026-chr10:97257407..97259761,2	K562	blood:
3	chr10:97237607..97239480-chr10:97249428..97252400,2	K562	blood:
4	chr10:97208296..97210918-chr10:97214931..97216781,2	K562	blood:
5	chr10:97237607..97239480-chr10:97249428..97252400,2	K562	blood:
6	chr10:97220624..97225860-chr10:97227541..97231131,6	K562	blood:
7	chr10:97196672..97199755-chr10:97214969..97217951,3	K562	blood:
8	chr10:97234291..97235881-chr10:97262986..97265815,2	K562	blood:
9	chr10:97220624..97225860-chr10:97227541..97231131,6	K562	blood:
10	chr10:97230234..97233080-chr10:97234488..97236035,2	K562	blood:
11	chr10:97236296..97238318-chr10:97239863..97242448,2	MCF-7	breast:
12	chr10:97239375..97239913-chr10:97360587..97361534,2	MCF-7	breast:
13	chr10:97249016..97250688-chr10:97324094..97327075,2	MCF-7	breast:
14	chr10:97226590..97227155-chr10:97360952..97361496,2	K562	blood:
15	chr10:97230234..97233080-chr10:97234488..97236035,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SORBS1-1	chr10:97250494-97250877	NONHSAT015760

No data

Variant related genes	Relation type
SORBS1	TF binding region
SORBS1	CpG island
ENSG00000095637	chromatin interactions

Extended variants
information (count: 1299 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1299 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10450393	chr10:97214418-97214419	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146971392	chr10:97214419-97214420	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369692010	chr10:97214545-97214546	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564334600	chr10:97214636-97214637	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377009279	chr10:97214660-97214661	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577746970	chr10:97214665-97214666	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540563502	chr10:97214668-97214669	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560465443	chr10:97214672-97214673	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7069741	chr10:97214676-97214677	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs549010988	chr10:97214683-97214684	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147614281	chr10:97214699-97214700	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180672325	chr10:97214710-97214711	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550124241	chr10:97214728-97214729	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372637601	chr10:97214819-97214820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551171181	chr10:97214843-97214844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369011949	chr10:97214865-97214866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571063305	chr10:97214876-97214877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142312115	chr10:97214889-97214890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146125154	chr10:97214894-97214895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148201677	chr10:97214919-97214920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535715283	chr10:97214928-97214929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184849945	chr10:97214929-97214930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575528997	chr10:97214948-97214949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538370855	chr10:97214972-97214973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189743991	chr10:97214974-97214975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181205943	chr10:97214987-97214988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57630203	chr10:97215006-97215007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs560351676	chr10:97215039-97215040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565206410	chr10:97215071-97215072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141137129	chr10:97215087-97215088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562500099	chr10:97215183-97215184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11593619	chr10:97215219-97215220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35708647	chr10:97215231-97215232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369586237	chr10:97215235-97215236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186235492	chr10:97215254-97215255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150327171	chr10:97215315-97215316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75489408	chr10:97215344-97215345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377081882	chr10:97215351-97215352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373094193	chr10:97215359-97215360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60596642	chr10:97215367-97215368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190604696	chr10:97215375-97215376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535774775	chr10:97215384-97215385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549250814	chr10:97215401-97215402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80246562	chr10:97215402-97215403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537851030	chr10:97215416-97215417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558088101	chr10:97215432-97215433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571662164	chr10:97215458-97215459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568463513	chr10:97215472-97215473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534253462	chr10:97215510-97215511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2148892	chr10:97215511-97215512	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Prostate cancer	16573809	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1247 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97206000-97217000	Weak transcription	Gastric	stomach
2	chr10:97206000-97220000	Enhancers	Rectal Smooth Muscle	rectum
3	chr10:97206200-97219000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr10:97208000-97216000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr10:97208200-97216200	Weak transcription	Lung	lung
6	chr10:97208200-97219000	Weak transcription	Ovary	ovary
7	chr10:97208200-97219000	Weak transcription	HSMMtube	muscle
8	chr10:97208600-97216600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr10:97208800-97215800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr10:97208800-97215800	Weak transcription	Fetal Kidney	kidney
11	chr10:97209200-97215600	Weak transcription	Right Ventricle	heart
12	chr10:97209200-97219200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr10:97210000-97219400	Enhancers	Colon Smooth Muscle	Colon
14	chr10:97211200-97216600	Weak transcription	Brain Hippocampus Middle	brain
15	chr10:97211200-97217400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:97211400-97215400	Weak transcription	Fetal Brain Female	brain
17	chr10:97211400-97219000	Weak transcription	Brain Angular Gyrus	brain
18	chr10:97211400-97219000	Weak transcription	Brain Germinal Matrix	brain
19	chr10:97211600-97215800	Weak transcription	Fetal Intestine Large	intestine
20	chr10:97211600-97217000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr10:97211800-97215800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr10:97211800-97217000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr10:97211800-97219000	Weak transcription	Fetal Muscle Leg	muscle
24	chr10:97212000-97215600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr10:97212200-97215400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr10:97212200-97215800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:97212200-97215800	Weak transcription	Fetal Intestine Small	intestine
28	chr10:97212200-97215800	Weak transcription	Fetal Lung	lung
29	chr10:97212200-97215800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr10:97212200-97216000	Weak transcription	NHEK	skin
31	chr10:97212200-97216200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:97212200-97216200	Weak transcription	Fetal Stomach	stomach
33	chr10:97212200-97216600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr10:97212200-97219000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr10:97212400-97215800	Weak transcription	HMEC	breast
36	chr10:97212800-97215200	Weak transcription	Fetal Brain Male	brain
37	chr10:97212800-97216000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr10:97212800-97216200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:97212800-97217400	Weak transcription	Right Atrium	heart
40	chr10:97213000-97216200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr10:97213000-97217200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr10:97213200-97234200	Weak transcription	Colonic Mucosa	Colon
43	chr10:97213600-97214800	Genic enhancers	HepG2	liver
44	chr10:97213600-97219000	Weak transcription	Psoas Muscle	Psoas
45	chr10:97213800-97219800	Enhancers	Brain Anterior Caudate	brain
46	chr10:97213800-97219800	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr10:97214000-97215200	Enhancers	Aorta	Aorta
48	chr10:97214000-97215600	Weak transcription	Liver	Liver
49	chr10:97214000-97215800	Enhancers	Stomach Smooth Muscle	stomach
50	chr10:97214200-97215400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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