Variant report

Variant	nsv481754
Chromosome Location	chrX:31771988-31927012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:63)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
2	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
5	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
6	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
7	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
8	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
9	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
10	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
11	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
12	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
13	BHLHE40	chrX:31795023-31795206	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	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
17	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
18	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
19	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
20	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
21	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chrX:31778692-31778796	HepG2	liver:	n/a	n/a
23	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
24	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
25	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
26	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
27	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
28	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
30	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
31	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
32	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
33	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
34	CEBPB	chrX:31773913-31774042	HepG2	liver:	n/a	chrX:31773955-31773966 chrX:31773957-31773968
35	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
37	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
38	CEBPD	chrX:31888350-31888723	K562	blood:	n/a	n/a
39	CEBPD	chrX:31865879-31866246	K562	blood:	n/a	n/a
40	CEBPD	chrX:31890132-31890577	K562	blood:	n/a	n/a
41	CEBPD	chrX:31890131-31890556	K562	blood:	n/a	n/a
42	CEBPD	chrX:31865787-31866260	K562	blood:	n/a	n/a
43	CHD2	chrX:31890070-31890404	K562	blood:	n/a	chrX:31890201-31890211
44	CREB1	chrX:31881331-31881799	K562	blood:	n/a	n/a
45	CREB1	chrX:31880714-31881288	K562	blood:	n/a	n/a
46	CTCF	chrX:31842562-31842645	ProgFib	skin:	n/a	n/a
47	CTCF	chrX:31834014-31834048	GM10266	blood:	n/a	n/a
48	CTCF	chrX:31909536-31909601	GM10248	blood:	n/a	n/a
49	CTCF	chrX:31792218-31792298	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chrX:31844911-31844933	Medullo	brain:	n/a	n/a

(count:63 , 50 per page) page: 1 2

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

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
2	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
3	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
4	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
5	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
6	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
7	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
8	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
9	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
10	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
11	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
12	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
13	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
14	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
15	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
16	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
17	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
18	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
19	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
20	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
21	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
22	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
23	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
24	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
25	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
26	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
27	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
28	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
29	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
30	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
31	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
32	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
33	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
34	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
35	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
36	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
37	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
38	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:

No data

Variant related genes	Relation type
DMD	TF binding region
DMD	CpG island
ENSG00000106638	chromatin interactions
ENSG00000198947	chromatin interactions
ENSG00000047597	chromatin interactions

Extended variants
information (count: 1814 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1814 , 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	rs140522532	chrX:31771988-31771989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371510769	chrX:31771989-31771990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557191637	chrX:31772023-31772024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190850030	chrX:31772035-31772036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374121231	chrX:31772051-31772052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2646304	chrX:31772076-31772077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184085691	chrX:31772176-31772177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1353627	chrX:31772239-31772240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189066123	chrX:31772268-31772269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73210177	chrX:31772324-31772325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151008756	chrX:31772325-31772326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371505087	chrX:31772344-31772345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182943567	chrX:31772443-31772444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4433306	chrX:31772485-31772486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150135663	chrX:31772663-31772664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2738303	chrX:31772689-31772690	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs141199548	chrX:31772703-31772704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187086534	chrX:31772788-31772789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191897548	chrX:31772901-31772902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184503504	chrX:31772956-31772957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4829233	chrX:31773087-31773088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12834322	chrX:31773118-31773119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138055106	chrX:31773227-31773228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5927838	chrX:31773252-31773253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201324546	chrX:31773254-31773255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35366767	chrX:31773255-31773256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398101939	chrX:31773260-31773261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187681414	chrX:31773261-31773262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs5927839	chrX:31773328-31773329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192177045	chrX:31773413-31773414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185392431	chrX:31773493-31773494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190685091	chrX:31773505-31773506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180755308	chrX:31773573-31773574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184582586	chrX:31773838-31773839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143888908	chrX:31773952-31773953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188479950	chrX:31774109-31774110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376984783	chrX:31774131-31774132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201468940	chrX:31774151-31774152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2738302	chrX:31774154-31774155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73213848	chrX:31774155-31774156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2646305	chrX:31774258-31774259	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs113556416	chrX:31774280-31774281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201651220	chrX:31774438-31774439	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372115617	chrX:31774439-31774440	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72626003	chrX:31774440-31774441	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369009710	chrX:31774443-31774444	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530198919	chrX:31774528-31774529	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140132284	chrX:31774540-31774541	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201177196	chrX:31774581-31774582	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35139600	chrX:31774582-31774583	Bivalent Enhancer Enhancers	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:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31770600-31772000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chrX:31771400-31774200	Weak transcription	Fetal Brain Male	brain
3	chrX:31771800-31772200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chrX:31772200-31773000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chrX:31774200-31774400	Enhancers	Fetal Brain Male	brain
6	chrX:31774400-31774800	Bivalent Enhancer	Fetal Brain Male	brain
7	chrX:31774400-31774800	Enhancers	Fetal Heart	heart
8	chrX:31777800-31778400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chrX:31787400-31787800	Enhancers	HSMMtube	muscle
10	chrX:31789000-31797400	Weak transcription	Liver	Liver
11	chrX:31797400-31797600	Enhancers	Liver	Liver
12	chrX:31809400-31838800	Weak transcription	Aorta	Aorta
13	chrX:31810800-31811400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chrX:31815400-31817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chrX:31816000-31816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chrX:31816400-31816800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chrX:31816600-31816800	Enhancers	HSMMtube	muscle
18	chrX:31816800-31825200	Weak transcription	HSMMtube	muscle
19	chrX:31823400-31826200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chrX:31824000-31827000	Enhancers	Liver	Liver
21	chrX:31825800-31827000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chrX:31825800-31827200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chrX:31826200-31826400	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chrX:31826200-31826800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chrX:31826200-31826800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chrX:31826200-31827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chrX:31826200-31827000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chrX:31826400-31826800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chrX:31826600-31826800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
30	chrX:31826800-31829600	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chrX:31826800-31838800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chrX:31827000-31829200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chrX:31829200-31829400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chrX:31829200-31829600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chrX:31829400-31829600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chrX:31829600-31829800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chrX:31831600-31832200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chrX:31831600-31840200	Weak transcription	K562	blood
39	chrX:31832200-31834000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chrX:31835800-31836000	Enhancers	Ovary	ovary
41	chrX:31835800-31836200	Enhancers	Fetal Kidney	kidney
42	chrX:31836600-31838000	Enhancers	Fetal Lung	lung
43	chrX:31837200-31838000	Enhancers	Colon Smooth Muscle	Colon
44	chrX:31837600-31837800	Enhancers	Ovary	ovary
45	chrX:31837800-31840400	Weak transcription	Ovary	ovary
46	chrX:31838800-31839000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chrX:31838800-31839000	Enhancers	Aorta	Aorta
48	chrX:31839000-31839600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chrX:31839600-31839800	Enhancers	Fetal Brain Female	brain
50	chrX:31839600-31841600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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