Variant report

Variant	nsv481775
Chromosome Location	chrX:31726702-31970769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
3	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
5	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
6	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
7	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
8	ATF1	chrX:31854667-31854914	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	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
12	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
13	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
14	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
15	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
16	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
17	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
18	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
19	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
20	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
21	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
22	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
23	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
24	CEBPB	chrX:31778692-31778796	HepG2	liver:	n/a	n/a
25	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
26	CEBPB	chrX:31967146-31967428	IMR90	lung:	n/a	chrX:31967281-31967292
27	CEBPB	chrX:31739488-31739744	HepG2	liver:	n/a	chrX:31739596-31739607
28	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
29	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
30	CEBPB	chrX:31773913-31774042	HepG2	liver:	n/a	chrX:31773955-31773966 chrX:31773957-31773968
31	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
33	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
34	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
35	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
36	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
37	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
38	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
39	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
40	CEBPB	chrX:31967255-31967355	HepG2	liver:	n/a	chrX:31967281-31967292
41	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
42	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
43	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
44	CEBPB	chrX:31949328-31949638	K562	blood:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
45	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
46	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
47	CEBPB	chrX:31739458-31739663	IMR90	lung:	n/a	chrX:31739596-31739607
48	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
49	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
50	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	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	GM06990	blood:	n/a
2	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a
3	chrX:31889692-31889742	BJ	skin:	n/a
4	chrX:31889692-31889742	GM12892	blood:	n/a
5	chrX:31889692-31889742	LNCaP	prostate:	n/a
6	chrX:31889692-31889742	IMR90	lung:	fetal
7	chrX:31889692-31889742	SK-N-MC	brain:	n/a
8	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
9	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
10	chrX:31889692-31889742	NB4	blood:	n/a
11	chrX:31889692-31889742	AG09309	skin:	n/a
12	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
13	chrX:31889692-31889742	GM19239	blood:	n/a
14	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
15	chrX:31889692-31889742	HepG2	liver:	n/a
16	chrX:31889692-31889742	BE2_C	brain:	n/a
17	chrX:31889692-31889742	PrEC	prostate:	n/a
18	chrX:31889692-31889742	NHBE	bronchial:	n/a
19	chrX:31889692-31889742	AG04449	skin:	fetal
20	chrX:31889692-31889742	SK-N-SH	brain:	n/a
21	chrX:31889692-31889742	NH-A	brain:	n/a
22	chrX:31889692-31889742	RPTEC	kidney:	n/a
23	chrX:31889692-31889742	HMEC	breast:	n/a
24	chrX:31889692-31889742	GM12878	blood:	n/a
25	chrX:31889692-31889742	SAEC	small airway:	n/a
26	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
27	chrX:31889692-31889742	Hepatocyte	liver:	n/a
28	chrX:31889692-31889742	PFSK-1	brain:	n/a
29	chrX:31889692-31889742	GM12891	blood:	n/a
30	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
31	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
32	chrX:31889692-31889742	NT2-D1	testis:	n/a
33	chrX:31889692-31889742	ProgFib	skin:	n/a
34	chrX:31889692-31889742	HCT-116	colon:	n/a
35	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
36	chrX:31889692-31889742	Hela-S3	cervix:	n/a
37	chrX:31889692-31889742	CMK	blood:	n/a
38	chrX:31889692-31889742	HRPEpiC	eye:	n/a
39	chrX:31889692-31889742	T-47D	breast:	n/a
40	chrX:31889692-31889742	AG04450	lung:	fetal
41	chrX:31889692-31889742	AG09319	gingival:	n/a
42	chrX:31889692-31889742	U87	brain:	n/a
43	chrX:31889692-31889742	HRE	kidney:	n/a
44	chrX:31889692-31889742	K562	blood:	n/a
45	chrX:31889692-31889742	HCF	heart:	n/a
46	chrX:31889692-31889742	HIPEpiC	eye:	n/a
47	chrX:31889692-31889742	PANC-1	pancreas:	n/a
48	chrX:31889692-31889742	HCM	heart:	n/a
49	chrX:31889692-31889742	SKMC	muscle:	n/a
50	chrX:31889692-31889742	MCF-7	breast:	n/a

(count:43 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2637 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201116203	chrX:31726724-31726725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372035236	chrX:31726731-31726732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552043395	chrX:31726781-31726782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141821246	chrX:31726782-31726783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182911175	chrX:31733833-31733834	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs187641598	chrX:31733900-31733901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs568258702	chrX:31733968-31733969	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs5927036	chrX:31733995-31733996	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs145321805	chrX:31734175-31734176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs371482575	chrX:31734298-31734299	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs5927817	chrX:31734299-31734300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs28424590	chrX:31734433-31734434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28413145	chrX:31734464-31734465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28552538	chrX:31734473-31734474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199897264	chrX:31734696-31734697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147395224	chrX:31734742-31734743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535548330	chrX:31734767-31734768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2030005	chrX:31734778-31734779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187741533	chrX:31734803-31734804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192912753	chrX:31734850-31734851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200602355	chrX:31734865-31734866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79380877	chrX:31734870-31734871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3032283	chrX:31734871-31734872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201217458	chrX:31734872-31734873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34786293	chrX:31734943-31734944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72339097	chrX:31734944-31734945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3032284	chrX:31734970-31734971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12116317	chrX:31734973-31734974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568408993	chrX:31734974-31734975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2897019	chrX:31734975-31734976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199966083	chrX:31734977-31734978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201090939	chrX:31734989-31734990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7061865	chrX:31735258-31735259	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7061641	chrX:31735304-31735305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376527862	chrX:31735309-31735310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11421027	chrX:31735483-31735484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184571816	chrX:31735521-31735522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188722973	chrX:31735572-31735573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192025732	chrX:31735584-31735585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184611614	chrX:31735635-31735636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189372550	chrX:31735644-31735645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182244236	chrX:31735689-31735690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6628630	chrX:31735725-31735726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547936272	chrX:31735742-31735743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16989790	chrX:31735780-31735781	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17340888	chrX:31735805-31735806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186035308	chrX:31735994-31735995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189360513	chrX:31736106-31736107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6631375	chrX:31736139-31736140	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs137992950	chrX:31736344-31736345	Enhancers 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:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31724800-31726800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chrX:31733800-31734400	ZNF genes & repeats	Liver	Liver
3	chrX:31734400-31754400	Weak transcription	Liver	Liver
4	chrX:31735400-31736400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chrX:31735400-31736600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chrX:31736400-31737400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chrX:31736600-31736800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chrX:31736600-31749800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chrX:31739000-31747000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chrX:31741600-31742200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chrX:31745200-31747000	Weak transcription	Stomach Smooth Muscle	stomach
12	chrX:31745200-31748600	Weak transcription	K562	blood
13	chrX:31745600-31745800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
14	chrX:31745800-31748200	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chrX:31746200-31748400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chrX:31746200-31748800	Weak transcription	Aorta	Aorta
17	chrX:31747000-31747600	Strong transcription	Stomach Smooth Muscle	stomach
18	chrX:31747000-31747800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chrX:31747600-31749200	Weak transcription	Stomach Smooth Muscle	stomach
20	chrX:31747800-31749400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chrX:31749800-31750200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chrX:31754200-31754600	Enhancers	Hela-S3	cervix
23	chrX:31754400-31754600	Enhancers	Liver	Liver
24	chrX:31763200-31763400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chrX:31765000-31765400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chrX:31765200-31765800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chrX:31765400-31766400	Enhancers	Fetal Brain Male	brain
28	chrX:31765400-31767000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chrX:31765600-31766400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chrX:31765800-31766800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chrX:31766400-31770800	Weak transcription	Fetal Brain Male	brain
32	chrX:31766800-31770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chrX:31769400-31770400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chrX:31770200-31770800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chrX:31770200-31771000	Enhancers	Fetal Brain Female	brain
36	chrX:31770200-31771200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chrX:31770400-31771800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chrX:31770600-31771000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chrX:31770600-31771000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chrX:31770600-31771200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chrX:31770600-31771400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chrX:31770600-31772000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chrX:31770800-31771000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chrX:31770800-31771200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chrX:31770800-31771400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chrX:31770800-31771400	Enhancers	Fetal Brain Male	brain
47	chrX:31771400-31774200	Weak transcription	Fetal Brain Male	brain
48	chrX:31771800-31772200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chrX:31772200-31773000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chrX:31774200-31774400	Enhancers	Fetal Brain Male	brain

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