Variant report

Variant	nsv531098
Chromosome Location	chrX:31462522-31824884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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:31558422-31558741	K562	blood:	n/a	n/a
3	ARID3A	chrX:31562099-31562120	K562	blood:	n/a	n/a
4	ARID3A	chrX:31655046-31655134	K562	blood:	n/a	n/a
5	ATF1	chrX:31573635-31574055	K562	blood:	n/a	n/a
6	ATF1	chrX:31608896-31609186	K562	blood:	n/a	n/a
7	ATF1	chrX:31625409-31625543	K562	blood:	n/a	n/a
8	ATF1	chrX:31581912-31582258	K562	blood:	n/a	n/a
9	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
10	ATF1	chrX:31561944-31562144	K562	blood:	n/a	n/a
11	ATF2	chrX:31622845-31623312	GM12878	blood:	n/a	n/a
12	ATF2	chrX:31622908-31623328	GM12878	blood:	n/a	n/a
13	ATF3	chrX:31581903-31582162	K562	blood:	n/a	n/a
14	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
15	BACH1	chrX:31628530-31628567	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:31766645-31766852	GM12878	blood:	n/a	n/a
23	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
24	BCL3	chrX:31766561-31766945	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:31609565-31609791	Hela-S3	cervix:	n/a	chrX:31609679-31609690
33	CEBPB	chrX:31609505-31609819	A549	lung:	n/a	chrX:31609679-31609690
34	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
35	CEBPB	chrX:31564204-31564621	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chrX:31577717-31577915	H1-hESC	embryonic stem cell:	n/a	chrX:31577816-31577827
37	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
38	CEBPB	chrX:31676300-31676599	IMR90	lung:	n/a	n/a
39	CEBPB	chrX:31573766-31573996	IMR90	lung:	n/a	chrX:31573965-31573977
40	CEBPB	chrX:31597405-31597744	IMR90	lung:	n/a	chrX:31597566-31597577 chrX:31597566-31597579 chrX:31597568-31597579
41	CEBPB	chrX:31570105-31570305	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chrX:31573689-31574029	Hela-S3	cervix:	n/a	chrX:31573965-31573977
43	CEBPB	chrX:31676339-31676606	K562	blood:	n/a	n/a
44	CEBPB	chrX:31627053-31627605	IMR90	lung:	n/a	chrX:31627336-31627353 chrX:31627337-31627350
45	CEBPB	chrX:31626911-31627652	Hela-S3	cervix:	n/a	chrX:31627336-31627353 chrX:31627337-31627350
46	CEBPB	chrX:31688381-31688643	HepG2	liver:	n/a	chrX:31688510-31688521
47	CEBPB	chrX:31558555-31558836	K562	blood:	n/a	n/a
48	CEBPB	chrX:31498832-31499204	K562	blood:	n/a	n/a
49	CEBPB	chrX:31597467-31597658	HepG2	liver:	n/a	chrX:31597566-31597577 chrX:31597566-31597579 chrX:31597568-31597579
50	CEBPB	chrX:31660505-31660807	IMR90	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31526531-31526581	HRE	kidney:	n/a
2	chrX:31526745-31526795	HRE	kidney:	n/a
3	chrX:31526531-31526581	IMR90	lung:	fetal
4	chrX:31526531-31526581	AG04449	skin:	fetal
5	chrX:31526531-31526581	NH-A	brain:	n/a
6	chrX:31526745-31526795	MCF10A-Er-Src	breast:	n/a
7	chrX:31526745-31526795	SAEC	small airway:	n/a
8	chrX:31526531-31526581	SAEC	small airway:	n/a
9	chrX:31526531-31526581	HCM	heart:	n/a
10	chrX:31526745-31526795	NHBE	bronchial:	n/a
11	chrX:31526745-31526795	PANC-1	pancreas:	n/a
12	chrX:31526745-31526795	IMR90	lung:	fetal
13	chrX:31526745-31526795	SK-N-SH_RA	brain:	n/a
14	chrX:31526531-31526581	ECC-1	luminal epithelium:	n/a
15	chrX:31526745-31526795	HAEpiC	amniotic membrane:	n/a
16	chrX:31526531-31526581	HRPEpiC	eye:	n/a
17	chrX:31526745-31526795	NHDF-neo	bronchial:	n/a
18	chrX:31526745-31526795	AG09319	gingival:	n/a
19	chrX:31526745-31526795	AG10803	skin:	n/a
20	chrX:31526745-31526795	BE2_C	brain:	n/a
21	chrX:31526531-31526581	HL-60	blood:	n/a
22	chrX:31526531-31526581	HEEpiC	esophagus:	n/a
23	chrX:31526531-31526581	HRCEpiC	kidney:	n/a
24	chrX:31526531-31526581	ovcar-3	ovarian:	n/a
25	chrX:31526745-31526795	CMK	blood:	n/a
26	chrX:31526531-31526581	AG10803	skin:	n/a
27	chrX:31526745-31526795	HCF	heart:	n/a
28	chrX:31526745-31526795	LNCaP	prostate:	n/a
29	chrX:31526531-31526581	HPAEpiC	pulmonary alveolar:	n/a
30	chrX:31526531-31526581	SK-N-SH_RA	brain:	n/a
31	chrX:31526531-31526581	HIPEpiC	eye:	n/a
32	chrX:31526531-31526581	GM12891	blood:	n/a
33	chrX:31526531-31526581	H1-hESC	embryonic stem cell:	embryo
34	chrX:31526531-31526581	SKMC	muscle:	n/a
35	chrX:31526531-31526581	HCT-116	colon:	n/a
36	chrX:31526531-31526581	HNPCEpiC	eye:	n/a
37	chrX:31526745-31526795	GM12892	blood:	n/a
38	chrX:31526531-31526581	HUVEC	blood vessel:	n/a
39	chrX:31526745-31526795	AG09309	skin:	n/a
40	chrX:31526745-31526795	GM19239	blood:	n/a
41	chrX:31526745-31526795	AG04450	lung:	fetal
42	chrX:31526531-31526581	NHDF-neo	bronchial:	n/a
43	chrX:31526745-31526795	Hela-S3	cervix:	n/a
44	chrX:31526531-31526581	LNCaP	prostate:	n/a
45	chrX:31526531-31526581	HAEpiC	amniotic membrane:	n/a
46	chrX:31526745-31526795	SK-N-SH	brain:	n/a
47	chrX:31526745-31526795	GM06990	blood:	n/a
48	chrX:31526531-31526581	Jurkat	blood:	n/a
49	chrX:31526745-31526795	HNPCEpiC	eye:	n/a
50	chrX:31526745-31526795	HMEC	breast:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
2	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
3	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
4	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
5	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
6	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
7	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
8	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
9	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
10	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
11	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
12	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
13	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
14	chrX:31589050..31591269-chrX:31593172..31595132,2	K562	blood:
15	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
16	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
17	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
18	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
19	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
20	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
21	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
22	chrX:31607664..31610419-chrX:31614245..31616179,2	K562	blood:
23	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
24	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
25	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:
26	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
27	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
28	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
29	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
30	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
31	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
32	chrX:31679912..31681425-chrX:31683220..31684967,2	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: 3205 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3205 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537476284	chrX:31462531-31462532	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72466565	chrX:31462532-31462533	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368098624	chrX:31462635-31462636	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143925896	chrX:31462650-31462651	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547060534	chrX:31462687-31462688	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148643665	chrX:31462699-31462700	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201691420	chrX:31462708-31462709	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs128625229	chrX:31462738-31462739	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs398124079	chrX:31462747-31462748	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370638647	chrX:31462769-31462770	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190253022	chrX:31462876-31462877	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181990572	chrX:31463009-31463010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112533799	chrX:31463032-31463033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs67957153	chrX:31463175-31463176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376813530	chrX:31463185-31463186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10126076	chrX:31463245-31463246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187470583	chrX:31463276-31463277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140573926	chrX:31463650-31463651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189119347	chrX:31463667-31463668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150425688	chrX:31463672-31463673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs66898423	chrX:31463694-31463695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142326049	chrX:31463708-31463709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1921965	chrX:31463871-31463872	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111917090	chrX:31463880-31463881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556015569	chrX:31463924-31463925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180981960	chrX:31464051-31464052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571703191	chrX:31464080-31464081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185702489	chrX:31464119-31464120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73617087	chrX:31464242-31464243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190417227	chrX:31464272-31464273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574299937	chrX:31464300-31464301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143626893	chrX:31464334-31464335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182702219	chrX:31464384-31464385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186537656	chrX:31464423-31464424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11316166	chrX:31464593-31464594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369578810	chrX:31464716-31464717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56134945	chrX:31464745-31464746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191961165	chrX:31464772-31464773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs60204649	chrX:31464819-31464820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs397951900	chrX:31464820-31464821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183696260	chrX:31464878-31464879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189190628	chrX:31464923-31464924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141752354	chrX:31464932-31464933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150528840	chrX:31465113-31465114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139873795	chrX:31465146-31465147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111242134	chrX:31465218-31465219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377491817	chrX:31465226-31465227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114786496	chrX:31465285-31465286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189623199	chrX:31465295-31465296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201350644	chrX:31465318-31465319	Weak transcription	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:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31461400-31467600	Weak transcription	Aorta	Aorta
2	chrX:31461800-31463000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chrX:31462000-31465200	Enhancers	Dnd41	blood
4	chrX:31462200-31463800	Weak transcription	Psoas Muscle	Psoas
5	chrX:31462200-31466200	Weak transcription	Liver	Liver
6	chrX:31463800-31464000	Enhancers	Psoas Muscle	Psoas
7	chrX:31465000-31465200	Enhancers	Ovary	ovary
8	chrX:31466200-31466400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chrX:31466200-31466400	Enhancers	Liver	Liver
10	chrX:31466200-31466600	Enhancers	HepG2	liver
11	chrX:31466400-31467200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chrX:31467200-31467800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chrX:31467200-31469000	Enhancers	Ovary	ovary
14	chrX:31467400-31467600	Enhancers	Rectal Smooth Muscle	rectum
15	chrX:31467600-31468000	Enhancers	Aorta	Aorta
16	chrX:31467600-31468600	Weak transcription	Rectal Smooth Muscle	rectum
17	chrX:31468000-31468200	Weak transcription	Aorta	Aorta
18	chrX:31468200-31468600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chrX:31468200-31468600	Enhancers	Aorta	Aorta
20	chrX:31468200-31468600	Enhancers	Brain Anterior Caudate	brain
21	chrX:31468200-31468600	Bivalent Enhancer	Fetal Lung	lung
22	chrX:31468600-31469000	Enhancers	Rectal Smooth Muscle	rectum
23	chrX:31468600-31469000	Enhancers	Stomach Smooth Muscle	stomach
24	chrX:31474000-31474600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chrX:31474000-31474600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chrX:31477000-31478400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chrX:31477200-31477600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chrX:31477200-31477600	Enhancers	NHEK	skin
29	chrX:31477200-31478000	Enhancers	Muscle Satellite Cultured Cells	--
30	chrX:31477200-31478000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chrX:31477200-31478000	Enhancers	Hela-S3	cervix
32	chrX:31477200-31478000	Enhancers	HSMM	muscle
33	chrX:31477600-31477800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chrX:31477800-31478000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chrX:31477800-31478400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chrX:31478000-31478400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chrX:31479400-31479600	Enhancers	NHEK	skin
38	chrX:31479800-31480200	Enhancers	HMEC	breast
39	chrX:31481200-31482800	Enhancers	Dnd41	blood
40	chrX:31482400-31483000	Enhancers	HUVEC	blood vessel
41	chrX:31482400-31483200	Enhancers	Fetal Lung	lung
42	chrX:31482600-31483200	Enhancers	Primary T cells from cord blood	blood
43	chrX:31482800-31483200	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chrX:31486800-31495400	Weak transcription	Stomach Smooth Muscle	stomach
45	chrX:31488200-31497800	Weak transcription	Psoas Muscle	Psoas
46	chrX:31488200-31498400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chrX:31489000-31489600	Active TSS	HepG2	liver
48	chrX:31493400-31506400	Weak transcription	HSMMtube	muscle
49	chrX:31493600-31496000	Weak transcription	Left Ventricle	heart
50	chrX:31494000-31496600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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