Variant report

Variant	nsv481719
Chromosome Location	chrX:31470100-31807209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1079)
CpG islands
(count:123)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31655046-31655134	K562	blood:	n/a	n/a
2	ARID3A	chrX:31558422-31558741	K562	blood:	n/a	n/a
3	ARID3A	chrX:31562099-31562120	K562	blood:	n/a	n/a
4	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
5	ATF1	chrX:31608896-31609186	K562	blood:	n/a	n/a
6	ATF1	chrX:31581912-31582258	K562	blood:	n/a	n/a
7	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
8	ATF1	chrX:31573635-31574055	K562	blood:	n/a	n/a
9	ATF1	chrX:31561944-31562144	K562	blood:	n/a	n/a
10	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
11	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
12	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
13	ATF3	chrX:31581903-31582162	K562	blood:	n/a	n/a
14	BACH1	chrX:31628530-31628567	K562	blood:	n/a	n/a
15	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
16	BACH1	chrX:31517260-31517602	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chrX:31622862-31623383	GM12878	blood:	n/a	chrX:31623346-31623355
18	BATF	chrX:31622870-31623366	GM12878	blood:	n/a	chrX:31623346-31623355
19	BCL11A	chrX:31622897-31623396	GM12878	blood:	n/a	n/a
20	BCL11A	chrX:31622993-31623321	GM12878	blood:	n/a	n/a
21	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
22	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
23	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
24	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
25	BHLHE40	chrX:31622917-31623247	GM12878	blood:	n/a	n/a
26	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
27	BHLHE40	chrX:31582083-31582277	K562	blood:	n/a	n/a
28	BRCA1	chrX:31564152-31564544	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chrX:31573688-31573950	K562	blood:	n/a	n/a
31	CCNT2	chrX:31608833-31609110	K562	blood:	n/a	n/a
32	CEBPB	chrX:31498870-31499174	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chrX:31739555-31739659	Hela-S3	cervix:	n/a	chrX:31739596-31739607
34	CEBPB	chrX:31597405-31597744	IMR90	lung:	n/a	chrX:31597566-31597577 chrX:31597566-31597579 chrX:31597568-31597579
35	CEBPB	chrX:31577786-31577986	HepG2	liver:	n/a	chrX:31577816-31577827
36	CEBPB	chrX:31498839-31499206	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:31609555-31609778	HepG2	liver:	n/a	chrX:31609679-31609690
38	CEBPB	chrX:31569997-31570394	IMR90	lung:	n/a	n/a
39	CEBPB	chrX:31676300-31676599	IMR90	lung:	n/a	n/a
40	CEBPB	chrX:31720394-31720668	IMR90	lung:	n/a	n/a
41	CEBPB	chrX:31498840-31499200	HepG2	liver:	n/a	n/a
42	CEBPB	chrX:31609580-31609776	H1-hESC	embryonic stem cell:	n/a	chrX:31609679-31609690
43	CEBPB	chrX:31498832-31499204	K562	blood:	n/a	n/a
44	CEBPB	chrX:31570105-31570305	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
46	CEBPB	chrX:31609526-31609843	K562	blood:	n/a	chrX:31609679-31609690
47	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
48	CEBPB	chrX:31524549-31524822	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chrX:31498859-31499182	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chrX:31477547-31477852	IMR90	lung:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31526745-31526795	GM19239	blood:	n/a
2	chrX:31526745-31526795	GM19239	blood:	n/a
3	chrX:31526745-31526795	K562	blood:	n/a
4	chrX:31526531-31526581	NT2-D1	testis:	n/a
5	chrX:31526531-31526581	GM06990	blood:	n/a
6	chrX:31526531-31526581	HCF	heart:	n/a
7	chrX:31526531-31526581	HAEpiC	amniotic membrane:	n/a
8	chrX:31526745-31526795	HMEC	breast:	n/a
9	chrX:31526745-31526795	NHDF-neo	bronchial:	n/a
10	chrX:31526531-31526581	AoSMC	blood vessel:	n/a
11	chrX:31526531-31526581	HL-60	blood:	n/a
12	chrX:31526531-31526581	HRCEpiC	kidney:	n/a
13	chrX:31526745-31526795	NH-A	brain:	n/a
14	chrX:31526531-31526581	IMR90	lung:	fetal
15	chrX:31526745-31526795	NHBE	bronchial:	n/a
16	chrX:31526531-31526581	AG04450	lung:	fetal
17	chrX:31526531-31526581	HIPEpiC	eye:	n/a
18	chrX:31526531-31526581	PANC-1	pancreas:	n/a
19	chrX:31526745-31526795	HNPCEpiC	eye:	n/a
20	chrX:31526745-31526795	BE2_C	brain:	n/a
21	chrX:31526531-31526581	U87	brain:	n/a
22	chrX:31526531-31526581	K562	blood:	n/a
23	chrX:31526745-31526795	T-47D	breast:	n/a
24	chrX:31526745-31526795	MCF10A-Er-Src	breast:	n/a
25	chrX:31526745-31526795	A549	lung:	n/a
26	chrX:31526531-31526581	BJ	skin:	n/a
27	chrX:31526531-31526581	Hela-S3	cervix:	n/a
28	chrX:31526531-31526581	MCF10A-Er-Src	breast:	n/a
29	chrX:31526531-31526581	HepG2	liver:	n/a
30	chrX:31526745-31526795	HAEpiC	amniotic membrane:	n/a
31	chrX:31526531-31526581	PFSK-1	brain:	n/a
32	chrX:31526745-31526795	IMR90	lung:	fetal
33	chrX:31526531-31526581	ECC-1	luminal epithelium:	n/a
34	chrX:31526745-31526795	HCT-116	colon:	n/a
35	chrX:31526531-31526581	LNCaP	prostate:	n/a
36	chrX:31526745-31526795	ovcar-3	ovarian:	n/a
37	chrX:31526745-31526795	AG04449	skin:	fetal
38	chrX:31526745-31526795	HEK293	kidney:	embryo
39	chrX:31526531-31526581	GM12891	blood:	n/a
40	chrX:31526745-31526795	HRE	kidney:	n/a
41	chrX:31526531-31526581	HRE	kidney:	n/a
42	chrX:31526745-31526795	Hela-S3	cervix:	n/a
43	chrX:31526745-31526795	PFSK-1	brain:	n/a
44	chrX:31526531-31526581	NHDF-neo	bronchial:	n/a
45	chrX:31526745-31526795	GM12878	blood:	n/a
46	chrX:31526531-31526581	RPTEC	kidney:	n/a
47	chrX:31526745-31526795	Caco-2	colon:	n/a
48	chrX:31526745-31526795	RPTEC	kidney:	n/a
49	chrX:31526531-31526581	Jurkat	blood:	n/a
50	chrX:31526745-31526795	GM12892	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
2	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
3	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
4	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
5	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
6	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
7	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
8	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
9	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
10	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
11	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
12	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
13	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
14	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
15	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
16	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
17	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
18	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
19	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
20	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
21	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
22	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
23	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
24	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
25	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
26	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
27	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
28	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
29	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
30	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
31	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:

No data

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

Extended variants
information (count: 2870 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2870 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192299817	chrX:31474014-31474015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72310784	chrX:31474178-31474179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs57908791	chrX:31474199-31474200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111397152	chrX:31474291-31474292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184642661	chrX:31474298-31474299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111578237	chrX:31474427-31474428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs59818839	chrX:31474513-31474514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200710072	chrX:31477003-31477004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149971563	chrX:31477179-31477180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183124430	chrX:31477244-31477245	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185826226	chrX:31477273-31477274	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145193479	chrX:31477289-31477290	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111947260	chrX:31477299-31477300	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190543207	chrX:31477301-31477302	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12863500	chrX:31477302-31477303	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183192463	chrX:31477355-31477356	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143469797	chrX:31477501-31477502	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17340791	chrX:31477547-31477548	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs371746868	chrX:31477637-31477638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187854282	chrX:31477870-31477871	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193212815	chrX:31478032-31478033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183890528	chrX:31478077-31478078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113057442	chrX:31478185-31478186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs68165503	chrX:31478215-31478216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73450062	chrX:31478248-31478249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72625585	chrX:31478275-31478276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575625545	chrX:31479566-31479567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190011457	chrX:31479587-31479588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377668126	chrX:31479849-31479850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189385432	chrX:31479866-31479867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371268138	chrX:31480077-31480078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180966120	chrX:31480113-31480114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150650689	chrX:31480128-31480129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144071416	chrX:31481418-31481419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191501224	chrX:31481434-31481435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184079804	chrX:31481613-31481614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16989651	chrX:31481840-31481841	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs544615279	chrX:31482013-31482014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115246080	chrX:31482049-31482050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114716873	chrX:31482050-31482051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374032852	chrX:31482056-31482057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149096053	chrX:31482064-31482065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185593065	chrX:31482261-31482262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190566925	chrX:31482313-31482314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7064141	chrX:31482430-31482431	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs12689193	chrX:31482432-31482433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371186460	chrX:31482574-31482575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs16989652	chrX:31482629-31482630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141094238	chrX:31482667-31482668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180841834	chrX:31482710-31482711	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Disorders of sex development	22290220	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Gastric adenocarcinoma	19115996	CNVD
Duchenne-like muscular dystrophy	22470819	CNVD
Muscular dystrophy	22470819	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Duchenne and Becker muscular dystrophies	18663755	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31474000-31474600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chrX:31474000-31474600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chrX:31477000-31478400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chrX:31477200-31477600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chrX:31477200-31477600	Enhancers	NHEK	skin
6	chrX:31477200-31478000	Enhancers	Muscle Satellite Cultured Cells	--
7	chrX:31477200-31478000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chrX:31477200-31478000	Enhancers	Hela-S3	cervix
9	chrX:31477200-31478000	Enhancers	HSMM	muscle
10	chrX:31477600-31477800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chrX:31477800-31478000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chrX:31477800-31478400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chrX:31478000-31478400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chrX:31479400-31479600	Enhancers	NHEK	skin
15	chrX:31479800-31480200	Enhancers	HMEC	breast
16	chrX:31481200-31482800	Enhancers	Dnd41	blood
17	chrX:31482400-31483000	Enhancers	HUVEC	blood vessel
18	chrX:31482400-31483200	Enhancers	Fetal Lung	lung
19	chrX:31482600-31483200	Enhancers	Primary T cells from cord blood	blood
20	chrX:31482800-31483200	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chrX:31486800-31495400	Weak transcription	Stomach Smooth Muscle	stomach
22	chrX:31488200-31497800	Weak transcription	Psoas Muscle	Psoas
23	chrX:31488200-31498400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chrX:31489000-31489600	Active TSS	HepG2	liver
25	chrX:31493400-31506400	Weak transcription	HSMMtube	muscle
26	chrX:31493600-31496000	Weak transcription	Left Ventricle	heart
27	chrX:31494000-31496600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chrX:31494800-31495600	Enhancers	HUVEC	blood vessel
29	chrX:31497000-31497600	Enhancers	Brain Germinal Matrix	brain
30	chrX:31499000-31499200	Enhancers	HMEC	breast
31	chrX:31499200-31500000	Weak transcription	HMEC	breast
32	chrX:31500000-31500800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chrX:31500000-31500800	Enhancers	HMEC	breast
34	chrX:31500800-31501800	Weak transcription	HMEC	breast
35	chrX:31501400-31503000	Enhancers	Muscle Satellite Cultured Cells	--
36	chrX:31501600-31502800	Enhancers	HUVEC	blood vessel
37	chrX:31501800-31502200	Enhancers	HSMM	muscle
38	chrX:31501800-31503000	Enhancers	NHEK	skin
39	chrX:31501800-31503200	Enhancers	HMEC	breast
40	chrX:31502000-31502600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chrX:31502000-31503200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chrX:31503000-31504600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chrX:31504600-31504800	Enhancers	Muscle Satellite Cultured Cells	--
44	chrX:31506400-31507200	Enhancers	HSMMtube	muscle
45	chrX:31507200-31515600	Weak transcription	HSMMtube	muscle
46	chrX:31507400-31507600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chrX:31513000-31526000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chrX:31513400-31515800	Weak transcription	Liver	Liver
49	chrX:31514200-31516600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chrX:31514800-31515200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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