Variant report

Variant	nsv934122
Chromosome Location	chrX:31676055-32080062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:958)
CpG islands
(count:61)
Chromatin interactive
region (count:52)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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:32011739-32012041	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:31890048-31890539	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	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
10	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
11	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
12	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
13	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
14	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
15	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
16	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
17	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
18	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
19	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
20	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
21	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
22	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
23	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
24	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
25	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
26	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
27	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
28	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
29	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
30	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
31	CEBPB	chrX:31999833-32000139	A549	lung:	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:31999832-32000168	IMR90	lung:	n/a	n/a
34	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
35	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
36	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
37	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
38	CEBPB	chrX:32062152-32062464	HepG2	liver:	n/a	n/a
39	CEBPB	chrX:31949361-31949579	H1-hESC	embryonic stem cell:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
40	CEBPB	chrX:31999809-32000152	H1-hESC	embryonic stem cell:	n/a	n/a
41	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
42	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
43	CEBPB	chrX:31967146-31967428	IMR90	lung:	n/a	chrX:31967281-31967292
44	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
45	CEBPB	chrX:32035738-32036006	IMR90	lung:	n/a	chrX:32035895-32035904 chrX:32035894-32035905
46	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
47	CEBPB	chrX:32061769-32062022	A549	lung:	n/a	n/a
48	CEBPB	chrX:31688381-31688643	HepG2	liver:	n/a	chrX:31688510-31688521
49	CEBPB	chrX:31739488-31739744	HepG2	liver:	n/a	chrX:31739596-31739607
50	CEBPB	chrX:31773913-31774042	HepG2	liver:	n/a	chrX:31773955-31773966 chrX:31773957-31773968

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	HEK293	kidney:	embryo
2	chrX:31889692-31889742	SK-N-MC	brain:	n/a
3	chrX:31889692-31889742	SKMC	muscle:	n/a
4	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
5	chrX:31889692-31889742	AG10803	skin:	n/a
6	chrX:31889692-31889742	HMEC	breast:	n/a
7	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
8	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
9	chrX:31889692-31889742	CMK	blood:	n/a
10	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
11	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
12	chrX:31889692-31889742	Jurkat	blood:	n/a
13	chrX:31889692-31889742	SAEC	small airway:	n/a
14	chrX:31889692-31889742	NT2-D1	testis:	n/a
15	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
16	chrX:31889692-31889742	HepG2	liver:	n/a
17	chrX:31889692-31889742	AG04449	skin:	fetal
18	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
19	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
20	chrX:31889692-31889742	SK-N-SH	brain:	n/a
21	chrX:31889692-31889742	BJ	skin:	n/a
22	chrX:31889692-31889742	NHBE	bronchial:	n/a
23	chrX:31889692-31889742	HCM	heart:	n/a
24	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a
25	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
26	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
27	chrX:31889692-31889742	GM12878	blood:	n/a
28	chrX:31889692-31889742	U87	brain:	n/a
29	chrX:31889692-31889742	BE2_C	brain:	n/a
30	chrX:31889692-31889742	GM19239	blood:	n/a
31	chrX:31889692-31889742	PANC-1	pancreas:	n/a
32	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
33	chrX:31889692-31889742	MCF-7	breast:	n/a
34	chrX:31889692-31889742	K562	blood:	n/a
35	chrX:31889692-31889742	Hela-S3	cervix:	n/a
36	chrX:31889692-31889742	RPTEC	kidney:	n/a
37	chrX:31889692-31889742	HRPEpiC	eye:	n/a
38	chrX:31889692-31889742	HL-60	blood:	n/a
39	chrX:31889692-31889742	Hepatocyte	liver:	n/a
40	chrX:31889692-31889742	IMR90	lung:	fetal
41	chrX:31889692-31889742	HCT-116	colon:	n/a
42	chrX:31889692-31889742	NB4	blood:	n/a
43	chrX:31889692-31889742	LNCaP	prostate:	n/a
44	chrX:31889692-31889742	HCF	heart:	n/a
45	chrX:31889692-31889742	ProgFib	skin:	n/a
46	chrX:31889692-31889742	GM12891	blood:	n/a
47	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
48	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
49	chrX:31889692-31889742	PFSK-1	brain:	n/a
50	chrX:31889692-31889742	NH-A	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
2	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
3	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
4	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
5	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
6	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
7	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
8	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
9	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
10	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
11	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
12	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
13	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
14	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
15	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
16	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
17	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
18	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
19	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
20	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
21	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
22	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
23	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
24	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
25	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
26	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
27	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
28	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
29	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
30	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
31	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
32	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
33	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
34	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
35	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
36	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
37	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
38	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
39	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
40	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
41	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
42	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
43	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
44	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
45	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
46	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
47	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
48	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
49	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
50	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:

No data

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

Extended variants
information (count: 3350 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3350 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370672967	chrX:31676062-31676063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181262803	chrX:31676070-31676071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184949918	chrX:31676086-31676087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376417532	chrX:31676089-31676090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2270672	chrX:31676096-31676097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs72466580	chrX:31676100-31676101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367665628	chrX:31676101-31676102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139254609	chrX:31676123-31676124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371437381	chrX:31676134-31676135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144103124	chrX:31676146-31676147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374433647	chrX:31676172-31676173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200170279	chrX:31676211-31676212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs398124059	chrX:31676212-31676213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146020545	chrX:31676215-31676216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368521550	chrX:31676217-31676218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs398124058	chrX:31676240-31676241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554209852	chrX:31676288-31676289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376671949	chrX:31676305-31676306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371909357	chrX:31676306-31676307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112088944	chrX:31676340-31676341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189846032	chrX:31676713-31676714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144602977	chrX:31676888-31676889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368362562	chrX:31676893-31676894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371249643	chrX:31676962-31676963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572734498	chrX:31676982-31676983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181501168	chrX:31677005-31677006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186189021	chrX:31677169-31677170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113449335	chrX:31677174-31677175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570691334	chrX:31677215-31677216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73455974	chrX:31677283-31677284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73617095	chrX:31677284-31677285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs16989773	chrX:31677301-31677302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113654123	chrX:31677303-31677304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182038652	chrX:31677327-31677328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6631356	chrX:31677441-31677442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143401118	chrX:31677474-31677475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185280869	chrX:31677532-31677533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190973590	chrX:31677547-31677548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6631357	chrX:31677563-31677564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59260859	chrX:31677582-31677583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140634443	chrX:31677589-31677590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182863232	chrX:31677612-31677613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187822953	chrX:31677675-31677676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112945418	chrX:31677681-31677682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6631358	chrX:31677733-31677734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6631359	chrX:31677752-31677753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200053280	chrX:31677754-31677755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1299889	chrX:31677757-31677758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1298909	chrX:31677791-31677792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201083789	chrX:31677913-31677914	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:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31673000-31679600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chrX:31674400-31676200	Weak transcription	Hela-S3	cervix
3	chrX:31676200-31676400	Enhancers	Hela-S3	cervix
4	chrX:31678200-31679800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chrX:31678400-31679800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chrX:31679400-31680000	Enhancers	Fetal Heart	heart
7	chrX:31679600-31679800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chrX:31679600-31679800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chrX:31679800-31680000	Bivalent Enhancer	Fetal Brain Male	brain
10	chrX:31679800-31681000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chrX:31680800-31681400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chrX:31681000-31681400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chrX:31681400-31682800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chrX:31682200-31682600	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chrX:31682200-31683200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chrX:31682800-31683000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chrX:31682800-31683200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chrX:31688000-31689000	Enhancers	HUVEC	blood vessel
19	chrX:31689600-31690600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chrX:31690600-31692400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chrX:31692200-31693000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chrX:31692200-31693400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chrX:31692200-31693400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chrX:31692400-31693000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chrX:31698200-31698600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chrX:31720200-31720800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chrX:31720200-31720800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chrX:31724800-31726800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chrX:31725000-31725600	Enhancers	Fetal Heart	heart
30	chrX:31725200-31725800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chrX:31725200-31726200	Enhancers	Muscle Satellite Cultured Cells	--
32	chrX:31726000-31726600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chrX:31733800-31734400	ZNF genes & repeats	Liver	Liver
34	chrX:31734400-31754400	Weak transcription	Liver	Liver
35	chrX:31735400-31736400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chrX:31735400-31736600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chrX:31736400-31737400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chrX:31736600-31736800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chrX:31736600-31749800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chrX:31739000-31747000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chrX:31741600-31742200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chrX:31745200-31747000	Weak transcription	Stomach Smooth Muscle	stomach
43	chrX:31745200-31748600	Weak transcription	K562	blood
44	chrX:31745600-31745800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
45	chrX:31745800-31748200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chrX:31746200-31748400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chrX:31746200-31748800	Weak transcription	Aorta	Aorta
48	chrX:31747000-31747600	Strong transcription	Stomach Smooth Muscle	stomach
49	chrX:31747000-31747800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chrX:31747600-31749200	Weak transcription	Stomach Smooth Muscle	stomach

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