Variant report

Variant	nsv481819
Chromosome Location	chrX:31810179-32071653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:32011739-32012041	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
4	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
6	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
7	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
8	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
9	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
10	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
11	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
12	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
13	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
14	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
15	CBX3	chrX:31880787-31881579	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:31999832-32000168	IMR90	lung:	n/a	n/a
20	CEBPB	chrX:32061704-32062434	IMR90	lung:	n/a	n/a
21	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
22	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
23	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
24	CEBPB	chrX:31999833-32000139	A549	lung:	n/a	n/a
25	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
26	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
27	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chrX:31999809-32000152	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chrX:31967255-31967355	HepG2	liver:	n/a	chrX:31967281-31967292
30	CEBPB	chrX:31999879-32000086	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
32	CEBPB	chrX:31949303-31949614	HepG2	liver:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
33	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
34	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
35	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
36	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
37	CEBPB	chrX:31999045-31999149	HepG2	liver:	n/a	n/a
38	CEBPB	chrX:32061769-32062022	A549	lung:	n/a	n/a
39	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
40	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
41	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
42	CEBPB	chrX:31967146-31967428	IMR90	lung:	n/a	chrX:31967281-31967292
43	CEBPB	chrX:32035738-32036006	IMR90	lung:	n/a	chrX:32035895-32035904 chrX:32035894-32035905
44	CEBPB	chrX:31999817-32000171	K562	blood:	n/a	n/a
45	CEBPB	chrX:32062152-32062464	HepG2	liver:	n/a	n/a
46	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chrX:31949328-31949638	K562	blood:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
48	CEBPB	chrX:31949323-31949654	IMR90	lung:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
49	CEBPB	chrX:32035708-32035954	HepG2	liver:	n/a	chrX:32035895-32035904 chrX:32035894-32035905
50	CEBPB	chrX:31999819-32000155	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
2	chrX:31889692-31889742	SK-N-MC	brain:	n/a
3	chrX:31889692-31889742	BE2_C	brain:	n/a
4	chrX:31889692-31889742	IMR90	lung:	fetal
5	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
6	chrX:31889692-31889742	AG09309	skin:	n/a
7	chrX:31889692-31889742	HCT-116	colon:	n/a
8	chrX:31889692-31889742	SK-N-SH	brain:	n/a
9	chrX:31889692-31889742	CMK	blood:	n/a
10	chrX:31889692-31889742	SAEC	small airway:	n/a
11	chrX:31889692-31889742	Hepatocyte	liver:	n/a
12	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
13	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
14	chrX:31889692-31889742	Hela-S3	cervix:	n/a
15	chrX:31889692-31889742	HL-60	blood:	n/a
16	chrX:31889692-31889742	GM12891	blood:	n/a
17	chrX:31889692-31889742	GM06990	blood:	n/a
18	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
19	chrX:31889692-31889742	LNCaP	prostate:	n/a
20	chrX:31889692-31889742	PANC-1	pancreas:	n/a
21	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
22	chrX:31889692-31889742	GM12892	blood:	n/a
23	chrX:31889692-31889742	A549	lung:	n/a
24	chrX:31889692-31889742	AG09319	gingival:	n/a
25	chrX:31889692-31889742	BJ	skin:	n/a
26	chrX:31889692-31889742	U87	brain:	n/a
27	chrX:31889692-31889742	MCF-7	breast:	n/a
28	chrX:31889692-31889742	HRPEpiC	eye:	n/a
29	chrX:31889692-31889742	AG04450	lung:	fetal
30	chrX:31889692-31889742	NT2-D1	testis:	n/a
31	chrX:31889692-31889742	HMEC	breast:	n/a
32	chrX:31889692-31889742	ProgFib	skin:	n/a
33	chrX:31889692-31889742	NH-A	brain:	n/a
34	chrX:31889692-31889742	GM12878	blood:	n/a
35	chrX:31889692-31889742	HCF	heart:	n/a
36	chrX:31889692-31889742	HEK293	kidney:	embryo
37	chrX:31889692-31889742	Jurkat	blood:	n/a
38	chrX:31889692-31889742	Caco-2	colon:	n/a
39	chrX:31889692-31889742	K562	blood:	n/a
40	chrX:31889692-31889742	T-47D	breast:	n/a
41	chrX:31889692-31889742	SKMC	muscle:	n/a
42	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
43	chrX:31889692-31889742	AG10803	skin:	n/a
44	chrX:31889692-31889742	HIPEpiC	eye:	n/a
45	chrX:31889692-31889742	PFSK-1	brain:	n/a
46	chrX:31889692-31889742	HCM	heart:	n/a
47	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
48	chrX:31889692-31889742	HepG2	liver:	n/a
49	chrX:31889692-31889742	RPTEC	kidney:	n/a
50	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
2	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
3	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
4	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
5	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
6	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
7	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
8	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
9	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
10	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
11	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
12	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
13	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
14	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
15	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
16	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
17	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
18	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
19	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
20	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
21	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
22	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
23	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
24	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
25	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
26	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
27	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
28	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
29	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
30	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
31	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
32	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
33	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:

No data

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

Extended variants
information (count: 2437 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2437 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200157823	chrX:31810188-31810189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115009017	chrX:31810323-31810324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370299400	chrX:31810341-31810342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74443484	chrX:31810358-31810359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557866154	chrX:31810458-31810459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs5927042	chrX:31810540-31810541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs367728606	chrX:31810549-31810550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6628645	chrX:31810588-31810589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201205185	chrX:31810634-31810635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553357326	chrX:31810701-31810702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6631404	chrX:31810764-31810765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114597997	chrX:31810822-31810823	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141210203	chrX:31810864-31810865	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113025350	chrX:31810871-31810872	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112126104	chrX:31810932-31810933	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182207845	chrX:31810976-31810977	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6631405	chrX:31810977-31810978	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187213193	chrX:31810991-31810992	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140412853	chrX:31811008-31811009	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150341654	chrX:31811121-31811122	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199722056	chrX:31811127-31811128	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189709368	chrX:31811205-31811206	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182368845	chrX:31811259-31811260	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35053851	chrX:31811316-31811317	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35004454	chrX:31811439-31811440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138045059	chrX:31811481-31811482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185608795	chrX:31811492-31811493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6628646	chrX:31811505-31811506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs190375527	chrX:31811535-31811536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145879244	chrX:31811536-31811537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183377718	chrX:31811647-31811648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138763255	chrX:31811655-31811656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188835368	chrX:31811732-31811733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192914448	chrX:31811886-31811887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73213872	chrX:31811895-31811896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187824337	chrX:31811946-31811947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191177142	chrX:31812149-31812150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375600797	chrX:31812278-31812279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371468440	chrX:31812361-31812362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73461859	chrX:31812390-31812391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148556304	chrX:31812561-31812562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142695381	chrX:31812599-31812600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183728019	chrX:31812604-31812605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188489948	chrX:31812625-31812626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1458378	chrX:31812639-31812640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs5972446	chrX:31812699-31812700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372939825	chrX:31812718-31812719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192993537	chrX:31812733-31812734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540794617	chrX:31812837-31812838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373671829	chrX:31812849-31812850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Autism	20531469	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31809400-31838800	Weak transcription	Aorta	Aorta
2	chrX:31810800-31811400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chrX:31815400-31817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chrX:31816000-31816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chrX:31816400-31816800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chrX:31816600-31816800	Enhancers	HSMMtube	muscle
7	chrX:31816800-31825200	Weak transcription	HSMMtube	muscle
8	chrX:31823400-31826200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chrX:31824000-31827000	Enhancers	Liver	Liver
10	chrX:31825800-31827000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chrX:31825800-31827200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chrX:31826200-31826400	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chrX:31826200-31826800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chrX:31826200-31826800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chrX:31826200-31827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chrX:31826200-31827000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chrX:31826400-31826800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chrX:31826600-31826800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
19	chrX:31826800-31829600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chrX:31826800-31838800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chrX:31827000-31829200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chrX:31829200-31829400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chrX:31829200-31829600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chrX:31829400-31829600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chrX:31829600-31829800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chrX:31831600-31832200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chrX:31831600-31840200	Weak transcription	K562	blood
28	chrX:31832200-31834000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chrX:31835800-31836000	Enhancers	Ovary	ovary
30	chrX:31835800-31836200	Enhancers	Fetal Kidney	kidney
31	chrX:31836600-31838000	Enhancers	Fetal Lung	lung
32	chrX:31837200-31838000	Enhancers	Colon Smooth Muscle	Colon
33	chrX:31837600-31837800	Enhancers	Ovary	ovary
34	chrX:31837800-31840400	Weak transcription	Ovary	ovary
35	chrX:31838800-31839000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chrX:31838800-31839000	Enhancers	Aorta	Aorta
37	chrX:31839000-31839600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chrX:31839600-31839800	Enhancers	Fetal Brain Female	brain
39	chrX:31839600-31841600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chrX:31840000-31840600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chrX:31840000-31840800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chrX:31840200-31840600	Enhancers	Liver	Liver
43	chrX:31840200-31841600	Enhancers	K562	blood
44	chrX:31840400-31840800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chrX:31840400-31840800	Enhancers	Ovary	ovary
46	chrX:31840600-31841400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chrX:31841600-31856800	Weak transcription	K562	blood
48	chrX:31850200-31850600	Enhancers	HUVEC	blood vessel
49	chrX:31850200-31850800	Enhancers	Muscle Satellite Cultured Cells	--
50	chrX:31850200-31851000	Enhancers	HSMMtube	muscle

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