Variant report

Variant	nsv6620
Chromosome Location	chr10:50197344-50224635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:212)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:212 , 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	BHLHE40	chr10:50217567-50218013	K562	blood:	n/a	n/a
2	BHLHE40	chr10:50209396-50209676	K562	blood:	n/a	n/a
3	CCNT2	chr10:50217061-50217152	K562	blood:	n/a	n/a
4	CEBPB	chr10:50197664-50197873	K562	blood:	n/a	chr10:50197774-50197785
5	CEBPB	chr10:50197650-50197808	HepG2	liver:	n/a	chr10:50197774-50197785
6	CEBPB	chr10:50209574-50209613	K562	blood:	n/a	n/a
7	CEBPB	chr10:50209205-50209272	K562	blood:	n/a	n/a
8	CTCF	chr10:50209460-50209610	RPTEC	kidney:	n/a	n/a
9	CTCF	chr10:50220802-50220906	H1-hESC	embryonic stem cell:	n/a	chr10:50220871-50220889
10	CTCF	chr10:50209440-50209590	HCM	heart:	n/a	n/a
11	CTCF	chr10:50209460-50209610	BE2_C	brain:	n/a	n/a
12	CTCF	chr10:50218906-50218922	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:50209488-50209610	Fibrobl	skin:	n/a	n/a
14	CTCF	chr10:50209346-50209676	K562	blood:	n/a	n/a
15	CTCF	chr10:50209411-50209669	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:50209440-50209590	AG09309	skin:	n/a	n/a
17	CTCF	chr10:50209228-50209852	A549	lung:	n/a	n/a
18	CTCF	chr10:50209441-50209655	Gliobla	brain:	n/a	n/a
19	CTCF	chr10:50220740-50220890	GM12872	blood:	n/a	chr10:50220871-50220889
20	CTCF	chr10:50209349-50209720	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr10:50220776-50220970	K562	blood:	n/a	chr10:50220871-50220889
22	CTCF	chr10:50220760-50220910	AG04449	skin:	n/a	chr10:50220871-50220889
23	CTCF	chr10:50209460-50209610	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr10:50220080-50220230	HEK293	kidney:	n/a	n/a
25	CTCF	chr10:50209505-50209590	GM19240	blood:	n/a	n/a
26	CTCF	chr10:50209520-50209670	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr10:50218894-50218947	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:50209520-50209670	HCT-116	colon:	n/a	n/a
29	CTCF	chr10:50209460-50209610	HepG2	liver:	n/a	n/a
30	CTCF	chr10:50211120-50211270	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr10:50210040-50210190	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr10:50220760-50220910	K562	blood:	n/a	chr10:50220871-50220889
33	CTCF	chr10:50220763-50220989	K562	blood:	n/a	chr10:50220871-50220889
34	CTCF	chr10:50209500-50209650	HepG2	liver:	n/a	n/a
35	CTCF	chr10:50209480-50209630	BJ	skin:	n/a	n/a
36	CTCF	chr10:50209359-50209807	HCT-116	colon:	n/a	n/a
37	CTCF	chr10:50209492-50209608	GM12892	blood:	n/a	n/a
38	CTCF	chr10:50209540-50209690	RPTEC	kidney:	n/a	n/a
39	CTCF	chr10:50209422-50209648	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:50209433-50209675	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:50209340-50209724	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr10:50209500-50209650	AG04449	skin:	n/a	n/a
43	CTCF	chr10:50220796-50220926	K562	blood:	n/a	chr10:50220871-50220889
44	CTCF	chr10:50217733-50217826	K562	blood:	n/a	chr10:50217780-50217798
45	CTCF	chr10:50209460-50209610	HVMF	connective:	n/a	n/a
46	CTCF	chr10:50209520-50209670	K562	blood:	n/a	n/a
47	CTCF	chr10:50220760-50220910	GM06990	blood:	n/a	chr10:50220871-50220889
48	CTCF	chr10:50209500-50209650	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr10:50218888-50218981	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:50209480-50209630	HCPEpiC	choroid plexus:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50221200-50221250	HCPEpiC	choroid plexus:	n/a
2	chr10:50224628-50224678	HCT-116	colon:	n/a
3	chr10:50224628-50224678	GM12892	blood:	n/a
4	chr10:50224628-50224678	GM19239	blood:	n/a
5	chr10:50224628-50224678	NHBE	bronchial:	n/a
6	chr10:50221200-50221250	RPTEC	kidney:	n/a
7	chr10:50221200-50221250	SK-N-SH_RA	brain:	n/a
8	chr10:50224628-50224678	NB4	blood:	n/a
9	chr10:50224628-50224678	ECC-1	luminal epithelium:	n/a
10	chr10:50224628-50224678	PFSK-1	brain:	n/a
11	chr10:50224628-50224678	NH-A	brain:	n/a
12	chr10:50224628-50224678	NT2-D1	testis:	n/a
13	chr10:50224628-50224678	AG09319	gingival:	n/a
14	chr10:50224628-50224678	A549	lung:	n/a
15	chr10:50221200-50221250	HAEpiC	amniotic membrane:	n/a
16	chr10:50224628-50224678	HMEC	breast:	n/a
17	chr10:50224628-50224678	HNPCEpiC	eye:	n/a
18	chr10:50221200-50221250	Hela-S3	cervix:	n/a
19	chr10:50224628-50224678	HCF	heart:	n/a
20	chr10:50224628-50224678	IMR90	lung:	fetal
21	chr10:50221200-50221250	BJ	skin:	n/a
22	chr10:50221200-50221250	CMK	blood:	n/a
23	chr10:50224628-50224678	HCPEpiC	choroid plexus:	n/a
24	chr10:50224628-50224678	ovcar-3	ovarian:	n/a
25	chr10:50221200-50221250	H1-hESC	embryonic stem cell:	embryo
26	chr10:50224628-50224678	BE2_C	brain:	n/a
27	chr10:50221200-50221250	AG09309	skin:	n/a
28	chr10:50221200-50221250	NB4	blood:	n/a
29	chr10:50224628-50224678	HIPEpiC	eye:	n/a
30	chr10:50221200-50221250	ECC-1	luminal epithelium:	n/a
31	chr10:50221200-50221250	GM06990	blood:	n/a
32	chr10:50224628-50224678	HL-60	blood:	n/a
33	chr10:50224628-50224678	RPTEC	kidney:	n/a
34	chr10:50221200-50221250	LNCaP	prostate:	n/a
35	chr10:50224628-50224678	AoSMC	blood vessel:	n/a
36	chr10:50221200-50221250	SK-N-SH	brain:	n/a
37	chr10:50221200-50221250	PANC-1	pancreas:	n/a
38	chr10:50221200-50221250	Caco-2	colon:	n/a
39	chr10:50221200-50221250	HepG2	liver:	n/a
40	chr10:50221200-50221250	AoSMC	blood vessel:	n/a
41	chr10:50221200-50221250	GM12891	blood:	n/a
42	chr10:50221200-50221250	IMR90	lung:	fetal
43	chr10:50221200-50221250	HCT-116	colon:	n/a
44	chr10:50221200-50221250	SKMC	muscle:	n/a
45	chr10:50221200-50221250	SK-N-MC	brain:	n/a
46	chr10:50221200-50221250	ovcar-3	ovarian:	n/a
47	chr10:50224628-50224678	HAEpiC	amniotic membrane:	n/a
48	chr10:50224628-50224678	Jurkat	blood:	n/a
49	chr10:50221200-50221250	HMEC	breast:	n/a
50	chr10:50221200-50221250	HRCEpiC	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:50194012..50196648-chr10:50208584..50210645,2	MCF-7	breast:
2	chr10:50208660..50210019-chr10:50369301..50370268,4	MCF-7	breast:
3	chr10:50217414..50220289-chr10:50222557..50225109,2	K562	blood:
4	chr10:50217414..50220289-chr10:50222557..50225109,2	K562	blood:
5	chr10:50192722..50194230-chr10:50195951..50198323,2	K562	blood:
6	chr10:50180497..50182804-chr10:50219120..50221241,2	K562	blood:
7	chr10:50209257..50210052-chr10:50272111..50272923,2	MCF-7	breast:
8	chr10:50209183..50209804-chr10:50372569..50373284,2	MCF-7	breast:
9	chr10:50208979..50209840-chr10:50369197..50369909,3	MCF-7	breast:
10	chr10:50219903..50222688-chr10:50236599..50239408,3	K562	blood:
11	chr10:50219935..50221949-chr10:50243957..50245901,2	K562	blood:
12	chr10:49899844..49902277-chr10:50218756..50220878,2	MCF-7	breast:
13	chr10:50221492..50223848-chr10:50223986..50225496,2	K562	blood:
14	chr10:50209070..50209954-chr10:50372326..50373284,5	MCF-7	breast:
15	chr10:50193213..50195144-chr10:50197588..50199974,2	K562	blood:
16	chr10:50221492..50223848-chr10:50223986..50225496,2	K562	blood:
17	chr10:50210429..50211061-chr10:50369700..50370308,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSTM4-2	chr10:50222412-50224993	NONHSAT013287
2	lnc-VSTM4-1	chr10:50200455-50201091	ENSG00000233665.4

No data

Variant related genes	Relation type
ENSG00000233665	TF binding region
MIR4294	TF binding region
ENSG00000233665	CpG island
MIR4294	CpG island
ENSG00000264800	chromatin interactions

Extended variants
information (count: 1158 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564359895	chr10:50197348-50197349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs531380502	chr10:50197388-50197389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7086917	chr10:50197435-50197436	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs537397204	chr10:50197452-50197453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs115156536	chr10:50197464-50197465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2249294	chr10:50197484-50197485	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148842268	chr10:50197511-50197512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368335145	chr10:50197512-50197513	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184850297	chr10:50197556-50197557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs533786735	chr10:50197562-50197563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189734682	chr10:50197582-50197583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527863910	chr10:50197595-50197596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577274180	chr10:50197604-50197605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552491162	chr10:50197657-50197658	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76927356	chr10:50197658-50197659	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs114041489	chr10:50197697-50197698	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143706914	chr10:50197765-50197766	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs73298996	chr10:50197768-50197769	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535552409	chr10:50197790-50197791	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs192649982	chr10:50197850-50197851	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140467566	chr10:50197869-50197870	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs183531547	chr10:50197923-50197924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs118104576	chr10:50197925-50197926	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149979475	chr10:50197953-50197954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2458671	chr10:50197994-50197995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528347042	chr10:50198068-50198069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188222424	chr10:50198105-50198106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371244663	chr10:50198123-50198124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115377399	chr10:50198183-50198184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528858795	chr10:50198208-50198209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114320827	chr10:50198260-50198261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559014480	chr10:50198267-50198268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145423211	chr10:50198290-50198291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114672684	chr10:50198294-50198295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs575587629	chr10:50198337-50198338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181760509	chr10:50198350-50198351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553927619	chr10:50198373-50198374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550172466	chr10:50198382-50198383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186276245	chr10:50198444-50198445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs58144692	chr10:50198482-50198483	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547954150	chr10:50198485-50198486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs74585160	chr10:50198498-50198499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539651585	chr10:50198537-50198538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541756871	chr10:50198538-50198539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573679451	chr10:50198559-50198560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188915321	chr10:50198574-50198575	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561345008	chr10:50198594-50198595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146895391	chr10:50198642-50198643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4838435	chr10:50198700-50198701	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116284832	chr10:50198766-50198767	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50189800-50201200	Weak transcription	Right Atrium	heart
2	chr10:50190400-50204600	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:50192400-50197600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr10:50196200-50198800	Weak transcription	Primary B cells from cord blood	blood
5	chr10:50197600-50198400	Enhancers	Brain Hippocampus Middle	brain
6	chr10:50197600-50198400	Enhancers	Brain Substantia Nigra	brain
7	chr10:50197800-50198400	Enhancers	Brain Cingulate Gyrus	brain
8	chr10:50198000-50198400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr10:50199600-50200200	Enhancers	Stomach Mucosa	stomach
10	chr10:50201200-50201600	Enhancers	Right Atrium	heart
11	chr10:50201400-50201800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:50204400-50205000	Enhancers	Fetal Intestine Large	intestine
13	chr10:50204400-50205200	Enhancers	Fetal Intestine Small	intestine
14	chr10:50205000-50206600	Weak transcription	Fetal Intestine Large	intestine
15	chr10:50205200-50206200	Weak transcription	Fetal Intestine Small	intestine
16	chr10:50206200-50210400	Enhancers	Duodenum Mucosa	Duodenum
17	chr10:50206200-50211200	Enhancers	Fetal Intestine Small	intestine
18	chr10:50206600-50211000	Enhancers	Fetal Intestine Large	intestine
19	chr10:50206800-50209800	Enhancers	Stomach Mucosa	stomach
20	chr10:50207800-50208200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:50208200-50208600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:50208200-50209600	Weak transcription	Gastric	stomach
23	chr10:50208600-50210200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr10:50208600-50210600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr10:50208600-50210800	Enhancers	Right Ventricle	heart
26	chr10:50208800-50209800	Enhancers	K562	blood
27	chr10:50209000-50209800	Enhancers	Fetal Stomach	stomach
28	chr10:50209000-50211000	Enhancers	Ovary	ovary
29	chr10:50209200-50209400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:50209200-50210000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr10:50209200-50210200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:50209200-50210200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr10:50209200-50210400	Enhancers	Fetal Heart	heart
34	chr10:50209200-50210400	Enhancers	Fetal Lung	lung
35	chr10:50209400-50210200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:50209400-50210600	Enhancers	Placenta	Placenta
37	chr10:50209600-50209800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr10:50209600-50209800	Enhancers	Gastric	stomach
39	chr10:50209600-50210800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr10:50209600-50210800	Enhancers	Spleen	Spleen
41	chr10:50209600-50211000	Enhancers	Left Ventricle	heart
42	chr10:50209800-50210200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:50209800-50210200	Bivalent Enhancer	Fetal Stomach	stomach
44	chr10:50209800-50210200	Enhancers	Right Atrium	heart
45	chr10:50209800-50210400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr10:50209800-50210800	Enhancers	Fetal Muscle Leg	muscle
47	chr10:50210000-50210200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:50210200-50210600	Weak transcription	Right Atrium	heart
49	chr10:50210200-50210800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr10:50210200-50215200	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links