Variant report

Variant	nsv481814
Chromosome Location	chrX:31566314-32058570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1339)
CpG islands
(count:61)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:32011739-32012041	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
4	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
5	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:31655046-31655134	K562	blood:	n/a	n/a
7	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
8	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
9	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
10	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
11	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
12	ATF1	chrX:31573635-31574055	K562	blood:	n/a	n/a
13	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
14	ATF1	chrX:31581912-31582258	K562	blood:	n/a	n/a
15	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
16	ATF1	chrX:31608896-31609186	K562	blood:	n/a	n/a
17	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
18	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
19	ATF3	chrX:31581903-31582162	K562	blood:	n/a	n/a
20	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
21	BACH1	chrX:31628530-31628567	K562	blood:	n/a	n/a
22	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
23	BATF	chrX:31622862-31623383	GM12878	blood:	n/a	chrX:31623346-31623355
24	BATF	chrX:31622870-31623366	GM12878	blood:	n/a	chrX:31623346-31623355
25	BCL11A	chrX:31622993-31623321	GM12878	blood:	n/a	n/a
26	BCL11A	chrX:31622897-31623396	GM12878	blood:	n/a	n/a
27	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
28	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
29	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
30	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
31	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
32	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
33	BHLHE40	chrX:31622917-31623247	GM12878	blood:	n/a	n/a
34	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
35	BHLHE40	chrX:31582083-31582277	K562	blood:	n/a	n/a
36	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
37	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
38	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
39	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
40	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
41	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
42	CCNT2	chrX:31608833-31609110	K562	blood:	n/a	n/a
43	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
44	CCNT2	chrX:31573688-31573950	K562	blood:	n/a	n/a
45	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
46	CEBPB	chrX:31676300-31676599	IMR90	lung:	n/a	n/a
47	CEBPB	chrX:31773913-31774042	HepG2	liver:	n/a	chrX:31773955-31773966 chrX:31773957-31773968
48	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
49	CEBPB	chrX:31720394-31720668	IMR90	lung:	n/a	n/a
50	CEBPB	chrX:31880877-31881207	K562	blood:	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	BE2_C	brain:	n/a
2	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
3	chrX:31889692-31889742	MCF-7	breast:	n/a
4	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
5	chrX:31889692-31889742	NT2-D1	testis:	n/a
6	chrX:31889692-31889742	AG04449	skin:	fetal
7	chrX:31889692-31889742	HepG2	liver:	n/a
8	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
9	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
10	chrX:31889692-31889742	PrEC	prostate:	n/a
11	chrX:31889692-31889742	SKMC	muscle:	n/a
12	chrX:31889692-31889742	GM12891	blood:	n/a
13	chrX:31889692-31889742	Jurkat	blood:	n/a
14	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
15	chrX:31889692-31889742	SK-N-MC	brain:	n/a
16	chrX:31889692-31889742	RPTEC	kidney:	n/a
17	chrX:31889692-31889742	K562	blood:	n/a
18	chrX:31889692-31889742	HCT-116	colon:	n/a
19	chrX:31889692-31889742	A549	lung:	n/a
20	chrX:31889692-31889742	Hela-S3	cervix:	n/a
21	chrX:31889692-31889742	GM12878	blood:	n/a
22	chrX:31889692-31889742	HL-60	blood:	n/a
23	chrX:31889692-31889742	ProgFib	skin:	n/a
24	chrX:31889692-31889742	HRPEpiC	eye:	n/a
25	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
26	chrX:31889692-31889742	NB4	blood:	n/a
27	chrX:31889692-31889742	LNCaP	prostate:	n/a
28	chrX:31889692-31889742	Hepatocyte	liver:	n/a
29	chrX:31889692-31889742	BJ	skin:	n/a
30	chrX:31889692-31889742	CMK	blood:	n/a
31	chrX:31889692-31889742	HMEC	breast:	n/a
32	chrX:31889692-31889742	HRE	kidney:	n/a
33	chrX:31889692-31889742	SAEC	small airway:	n/a
34	chrX:31889692-31889742	AG04450	lung:	fetal
35	chrX:31889692-31889742	HEK293	kidney:	embryo
36	chrX:31889692-31889742	AG09309	skin:	n/a
37	chrX:31889692-31889742	NHBE	bronchial:	n/a
38	chrX:31889692-31889742	PFSK-1	brain:	n/a
39	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
40	chrX:31889692-31889742	NH-A	brain:	n/a
41	chrX:31889692-31889742	SK-N-SH	brain:	n/a
42	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
43	chrX:31889692-31889742	Caco-2	colon:	n/a
44	chrX:31889692-31889742	AG10803	skin:	n/a
45	chrX:31889692-31889742	HIPEpiC	eye:	n/a
46	chrX:31889692-31889742	T-47D	breast:	n/a
47	chrX:31889692-31889742	HCM	heart:	n/a
48	chrX:31889692-31889742	PANC-1	pancreas:	n/a
49	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
50	chrX:31889692-31889742	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
2	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
3	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
4	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
5	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
6	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
7	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
8	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
9	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
10	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
11	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
12	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
13	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
14	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
15	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
16	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
17	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
18	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
19	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
20	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
21	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
22	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
23	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
24	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
25	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
26	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
27	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
28	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
29	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
30	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
31	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
32	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
33	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
34	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
35	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
36	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
37	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
38	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
39	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
40	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
41	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
42	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
43	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
44	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
45	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
46	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
47	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
48	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
49	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
50	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:

No data

Variant related genes	Relation type
DMD	TF binding region
DMD	CpG island
ENSG00000264462	chromatin interactions
ENSG00000106638	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000047597	chromatin interactions
ENSG00000198947	chromatin interactions

Extended variants
information (count: 4003 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4003 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148293732	chrX:31566314-31566315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567773437	chrX:31566323-31566324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189149580	chrX:31566375-31566376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377085105	chrX:31566455-31566456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567401801	chrX:31566456-31566457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181045939	chrX:31566491-31566492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185998393	chrX:31566590-31566591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191243879	chrX:31566657-31566658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150367875	chrX:31566780-31566781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4495595	chrX:31566817-31566818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77223797	chrX:31566991-31566992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553730491	chrX:31567013-31567014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181350024	chrX:31567019-31567020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202044457	chrX:31567052-31567053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4240093	chrX:31567059-31567060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs5972407	chrX:31567060-31567061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143580983	chrX:31567155-31567156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9887172	chrX:31567249-31567250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183306706	chrX:31567388-31567389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78248217	chrX:31567443-31567444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77099792	chrX:31567444-31567445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73453973	chrX:31567623-31567624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs57260883	chrX:31567644-31567645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5927767	chrX:31567743-31567744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1344082	chrX:31567859-31567860	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1921958	chrX:31567877-31567878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189254595	chrX:31567888-31567889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111819438	chrX:31567942-31567943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200062527	chrX:31568036-31568037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190751896	chrX:31568038-31568039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62590901	chrX:31568255-31568256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150891413	chrX:31568267-31568268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139407302	chrX:31568473-31568474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs72625591	chrX:31568521-31568522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113605616	chrX:31568542-31568543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187662566	chrX:31568592-31568593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192840774	chrX:31568602-31568603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6631335	chrX:31568903-31568904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5972408	chrX:31569025-31569026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6628618	chrX:31569095-31569096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35588879	chrX:31569135-31569136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368673150	chrX:31569165-31569166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187294351	chrX:31569166-31569167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141365612	chrX:31569208-31569209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201088342	chrX:31569296-31569297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202051079	chrX:31569297-31569298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192283007	chrX:31569298-31569299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374796391	chrX:31569299-31569300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10659535	chrX:31569314-31569315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143669140	chrX:31569360-31569361	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:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31563200-31566600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chrX:31563800-31566400	Enhancers	HSMM	muscle
3	chrX:31563800-31566600	Enhancers	Osteobl	bone
4	chrX:31564600-31566400	Enhancers	Muscle Satellite Cultured Cells	--
5	chrX:31564600-31566400	Enhancers	HSMMtube	muscle
6	chrX:31565000-31570800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chrX:31565400-31566400	Enhancers	NH-A	brain
8	chrX:31566000-31566400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chrX:31566400-31566600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chrX:31566400-31573000	Weak transcription	HSMMtube	muscle
11	chrX:31566600-31570800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chrX:31567600-31568400	Enhancers	Brain Hippocampus Middle	brain
13	chrX:31568000-31568600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chrX:31570600-31571600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chrX:31570800-31571600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chrX:31570800-31571600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chrX:31570800-31571600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chrX:31573000-31574000	Enhancers	HSMMtube	muscle
19	chrX:31573600-31574000	Enhancers	Fetal Heart	heart
20	chrX:31573600-31574000	Enhancers	K562	blood
21	chrX:31574000-31578000	Weak transcription	HSMMtube	muscle
22	chrX:31574000-31583600	Weak transcription	Fetal Heart	heart
23	chrX:31578000-31578200	Enhancers	HSMMtube	muscle
24	chrX:31578200-31578400	Weak transcription	HSMMtube	muscle
25	chrX:31581800-31582600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chrX:31586200-31586600	Enhancers	Fetal Intestine Large	intestine
27	chrX:31589800-31591600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chrX:31590400-31591200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chrX:31590400-31591400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chrX:31590600-31591200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chrX:31598200-31599400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chrX:31598200-31599400	Enhancers	NHDF-Ad	bronchial
33	chrX:31598200-31599600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chrX:31598200-31599600	Enhancers	HMEC	breast
35	chrX:31598200-31599600	Enhancers	NHEK	skin
36	chrX:31598200-31599800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chrX:31598400-31598800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chrX:31598400-31599000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chrX:31598400-31599400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chrX:31598400-31599600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chrX:31598400-31599600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chrX:31598400-31599600	Enhancers	HSMM	muscle
43	chrX:31598400-31599600	Enhancers	NH-A	brain
44	chrX:31598400-31600000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chrX:31598600-31598800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chrX:31598600-31599600	Enhancers	HUVEC	blood vessel
47	chrX:31598600-31599600	Enhancers	Osteobl	bone
48	chrX:31598600-31599800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chrX:31598800-31599000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chrX:31598800-31599200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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