Variant report

Variant	nsv481756
Chromosome Location	chrX:31785088-31928041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:62)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
3	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
5	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
6	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
7	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
8	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
9	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
10	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
11	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
12	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
13	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
14	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
15	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
16	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
17	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
18	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
19	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
20	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
21	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
23	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
24	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
25	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
27	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
28	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
29	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
30	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
32	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
33	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
34	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
35	CEBPD	chrX:31865879-31866246	K562	blood:	n/a	n/a
36	CEBPD	chrX:31890131-31890556	K562	blood:	n/a	n/a
37	CEBPD	chrX:31888350-31888723	K562	blood:	n/a	n/a
38	CEBPD	chrX:31890132-31890577	K562	blood:	n/a	n/a
39	CEBPD	chrX:31865787-31866260	K562	blood:	n/a	n/a
40	CHD2	chrX:31890070-31890404	K562	blood:	n/a	chrX:31890201-31890211
41	CREB1	chrX:31880714-31881288	K562	blood:	n/a	n/a
42	CREB1	chrX:31881331-31881799	K562	blood:	n/a	n/a
43	CTCF	chrX:31893448-31893484	LNCaP	prostate:	n/a	n/a
44	CTCF	chrX:31885277-31885356	LNCaP	prostate:	n/a	n/a
45	CTCF	chrX:31852823-31852921	Lung_OC	lung:	n/a	n/a
46	CTCF	chrX:31898855-31898933	LNCaP	prostate:	n/a	n/a
47	CTCF	chrX:31848509-31848524	GM10248	blood:	n/a	n/a
48	CTCF	chrX:31792218-31792298	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chrX:31848531-31848551	GM10248	blood:	n/a	n/a
50	CTCF	chrX:31810929-31810993	ProgFib	skin:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	SK-N-SH	brain:	n/a
2	chrX:31889692-31889742	SK-N-SH	brain:	n/a
3	chrX:31889692-31889742	GM12891	blood:	n/a
4	chrX:31889692-31889742	SAEC	small airway:	n/a
5	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
6	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
7	chrX:31889692-31889742	LNCaP	prostate:	n/a
8	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
9	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
10	chrX:31889692-31889742	T-47D	breast:	n/a
11	chrX:31889692-31889742	AG09309	skin:	n/a
12	chrX:31889692-31889742	NH-A	brain:	n/a
13	chrX:31889692-31889742	PANC-1	pancreas:	n/a
14	chrX:31889692-31889742	A549	lung:	n/a
15	chrX:31889692-31889742	GM06990	blood:	n/a
16	chrX:31889692-31889742	BE2_C	brain:	n/a
17	chrX:31889692-31889742	HRE	kidney:	n/a
18	chrX:31889692-31889742	AG10803	skin:	n/a
19	chrX:31889692-31889742	PrEC	prostate:	n/a
20	chrX:31889692-31889742	GM12878	blood:	n/a
21	chrX:31889692-31889742	PFSK-1	brain:	n/a
22	chrX:31889692-31889742	IMR90	lung:	fetal
23	chrX:31889692-31889742	Hela-S3	cervix:	n/a
24	chrX:31889692-31889742	SKMC	muscle:	n/a
25	chrX:31889692-31889742	HMEC	breast:	n/a
26	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
27	chrX:31889692-31889742	U87	brain:	n/a
28	chrX:31889692-31889742	SK-N-MC	brain:	n/a
29	chrX:31889692-31889742	Jurkat	blood:	n/a
30	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
31	chrX:31889692-31889742	Caco-2	colon:	n/a
32	chrX:31889692-31889742	GM12892	blood:	n/a
33	chrX:31889692-31889742	GM19239	blood:	n/a
34	chrX:31889692-31889742	Hepatocyte	liver:	n/a
35	chrX:31889692-31889742	HCT-116	colon:	n/a
36	chrX:31889692-31889742	HRPEpiC	eye:	n/a
37	chrX:31889692-31889742	K562	blood:	n/a
38	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
39	chrX:31889692-31889742	RPTEC	kidney:	n/a
40	chrX:31889692-31889742	ProgFib	skin:	n/a
41	chrX:31889692-31889742	AG09319	gingival:	n/a
42	chrX:31889692-31889742	NB4	blood:	n/a
43	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
44	chrX:31889692-31889742	NT2-D1	testis:	n/a
45	chrX:31889692-31889742	HL-60	blood:	n/a
46	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
47	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
48	chrX:31889692-31889742	AG04449	skin:	fetal
49	chrX:31889692-31889742	HEK293	kidney:	embryo
50	chrX:31889692-31889742	HCF	heart:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
2	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
3	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
4	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
5	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
6	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
7	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
8	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
9	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
10	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
11	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
12	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
13	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
14	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
15	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
16	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
17	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
18	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
19	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
20	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
21	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
22	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
23	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
24	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
25	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
26	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
27	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
28	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
29	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
30	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
31	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
32	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
33	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
34	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
35	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:

No data

Variant related genes	Relation type
DMD	TF binding region
DMD	CpG island
ENSG00000198947	chromatin interactions
ENSG00000047597	chromatin interactions

Extended variants
information (count: 1753 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1753 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191296995	chrX:31787435-31787436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs10521978	chrX:31787455-31787456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs10521979	chrX:31787619-31787620	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs73459901	chrX:31787749-31787750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191885089	chrX:31789007-31789008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34523466	chrX:31789296-31789297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184489798	chrX:31789528-31789529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs5972443	chrX:31789597-31789598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61503561	chrX:31789614-31789615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558195526	chrX:31789625-31789626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6631388	chrX:31789667-31789668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79320115	chrX:31789817-31789818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78032033	chrX:31789833-31789834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192161790	chrX:31789883-31789884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113328671	chrX:31789897-31789898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185523154	chrX:31789923-31789924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190447810	chrX:31789940-31789941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73461806	chrX:31789981-31789982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559599925	chrX:31790070-31790071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180768840	chrX:31790077-31790078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114613616	chrX:31790159-31790160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184489235	chrX:31790250-31790251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188512416	chrX:31790265-31790266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548397774	chrX:31790439-31790440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112092842	chrX:31790517-31790518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181356237	chrX:31790595-31790596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5927852	chrX:31790756-31790757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs5972444	chrX:31790852-31790853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185487855	chrX:31790934-31790935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73213854	chrX:31790976-31790977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190348076	chrX:31791297-31791298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113067271	chrX:31791347-31791348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148703702	chrX:31791413-31791414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181794772	chrX:31791579-31791580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199923172	chrX:31791862-31791863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4612538	chrX:31791863-31791864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187269999	chrX:31792017-31792018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72466585	chrX:31792064-31792065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs398124046	chrX:31792067-31792068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs398124047	chrX:31792070-31792071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112516305	chrX:31792098-31792099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142153424	chrX:31792143-31792144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147694734	chrX:31792147-31792148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142500746	chrX:31792165-31792166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs128626253	chrX:31792217-31792218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182761135	chrX:31792249-31792250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372593779	chrX:31792274-31792275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201919981	chrX:31792296-31792297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146817002	chrX:31792298-31792299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373230021	chrX:31792316-31792317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Cancer	16751803	CNVD
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian cancer	19835627	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Thyroid cancer	19087340	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17406619	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Gastric cancer	17229543	CNVD
Type 2 diabetes	21760887	CNVD
Cardiomyopathy	22138850	CNVD
Muscular dystrophy	21149563	CNVD
Skeletal myopathy	22138850	CNVD
Autism	21484199	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Duchenne-like muscular dystrophy	22138850	CNVD
Muscular dystrophy	22138850	CNVD
Disease	22090376	CNVD
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31787400-31787800	Enhancers	HSMMtube	muscle
2	chrX:31789000-31797400	Weak transcription	Liver	Liver
3	chrX:31797400-31797600	Enhancers	Liver	Liver
4	chrX:31809400-31838800	Weak transcription	Aorta	Aorta
5	chrX:31810800-31811400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chrX:31815400-31817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chrX:31816000-31816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chrX:31816400-31816800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chrX:31816600-31816800	Enhancers	HSMMtube	muscle
10	chrX:31816800-31825200	Weak transcription	HSMMtube	muscle
11	chrX:31823400-31826200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chrX:31824000-31827000	Enhancers	Liver	Liver
13	chrX:31825800-31827000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chrX:31825800-31827200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chrX:31826200-31826400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chrX:31826200-31826800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chrX:31826200-31826800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chrX:31826200-31827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chrX:31826200-31827000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chrX:31826400-31826800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chrX:31826600-31826800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chrX:31826800-31829600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chrX:31826800-31838800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chrX:31827000-31829200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chrX:31829200-31829400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chrX:31829200-31829600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chrX:31829400-31829600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chrX:31829600-31829800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chrX:31831600-31832200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chrX:31831600-31840200	Weak transcription	K562	blood
31	chrX:31832200-31834000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chrX:31835800-31836000	Enhancers	Ovary	ovary
33	chrX:31835800-31836200	Enhancers	Fetal Kidney	kidney
34	chrX:31836600-31838000	Enhancers	Fetal Lung	lung
35	chrX:31837200-31838000	Enhancers	Colon Smooth Muscle	Colon
36	chrX:31837600-31837800	Enhancers	Ovary	ovary
37	chrX:31837800-31840400	Weak transcription	Ovary	ovary
38	chrX:31838800-31839000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chrX:31838800-31839000	Enhancers	Aorta	Aorta
40	chrX:31839000-31839600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chrX:31839600-31839800	Enhancers	Fetal Brain Female	brain
42	chrX:31839600-31841600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chrX:31840000-31840600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chrX:31840000-31840800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chrX:31840200-31840600	Enhancers	Liver	Liver
46	chrX:31840200-31841600	Enhancers	K562	blood
47	chrX:31840400-31840800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chrX:31840400-31840800	Enhancers	Ovary	ovary
49	chrX:31840600-31841400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chrX:31841600-31856800	Weak transcription	K562	blood

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