Variant report

Variant	nsv481760
Chromosome Location	chrX:31637622-31934461
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:61)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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:31825327-31825587	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
5	ARID3A	chrX:31655046-31655134	K562	blood:	n/a	n/a
6	ARID3A	chrX:31676512-31676712	HepG2	liver:	n/a	n/a
7	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
8	ATF1	chrX:31865924-31866215	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:31880836-31881481	K562	blood:	n/a	n/a
12	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
13	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
14	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
15	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
16	BCL3	chrX:31737905-31738230	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:31795023-31795206	K562	blood:	n/a	n/a
20	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
21	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
22	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
23	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
24	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
25	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
26	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
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:31778692-31778796	HepG2	liver:	n/a	n/a
30	CEBPB	chrX:31676300-31676599	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
32	CEBPB	chrX:31763086-31763279	A549	lung:	n/a	n/a
33	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
34	CEBPB	chrX:31739458-31739663	IMR90	lung:	n/a	chrX:31739596-31739607
35	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chrX:31880877-31881207	K562	blood:	n/a	n/a
37	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
38	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
39	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
40	CEBPB	chrX:31902677-31902924	A549	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
41	CEBPB	chrX:31902702-31902922	Hela-S3	cervix:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
42	CEBPB	chrX:31890153-31890439	K562	blood:	n/a	n/a
43	CEBPB	chrX:31676339-31676606	K562	blood:	n/a	n/a
44	CEBPB	chrX:31826634-31826676	K562	blood:	n/a	n/a
45	CEBPB	chrX:31688352-31688552	IMR90	lung:	n/a	chrX:31688510-31688521
46	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
47	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
48	CEBPB	chrX:31902680-31902999	HepG2	liver:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
49	CEBPB	chrX:31912424-31912651	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chrX:31739488-31739744	HepG2	liver:	n/a	chrX:31739596-31739607

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	SK-N-MC	brain:	n/a
2	chrX:31889692-31889742	HepG2	liver:	n/a
3	chrX:31889692-31889742	HL-60	blood:	n/a
4	chrX:31889692-31889742	HCF	heart:	n/a
5	chrX:31889692-31889742	PANC-1	pancreas:	n/a
6	chrX:31889692-31889742	AG09319	gingival:	n/a
7	chrX:31889692-31889742	PrEC	prostate:	n/a
8	chrX:31889692-31889742	SAEC	small airway:	n/a
9	chrX:31889692-31889742	BJ	skin:	n/a
10	chrX:31889692-31889742	Hela-S3	cervix:	n/a
11	chrX:31889692-31889742	T-47D	breast:	n/a
12	chrX:31889692-31889742	Caco-2	colon:	n/a
13	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
14	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
15	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
16	chrX:31889692-31889742	NB4	blood:	n/a
17	chrX:31889692-31889742	GM12878	blood:	n/a
18	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
19	chrX:31889692-31889742	GM06990	blood:	n/a
20	chrX:31889692-31889742	BE2_C	brain:	n/a
21	chrX:31889692-31889742	A549	lung:	n/a
22	chrX:31889692-31889742	U87	brain:	n/a
23	chrX:31889692-31889742	K562	blood:	n/a
24	chrX:31889692-31889742	Jurkat	blood:	n/a
25	chrX:31889692-31889742	Hepatocyte	liver:	n/a
26	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
27	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
28	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
29	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
30	chrX:31889692-31889742	NT2-D1	testis:	n/a
31	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
32	chrX:31889692-31889742	CMK	blood:	n/a
33	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
34	chrX:31889692-31889742	SK-N-SH_RA	brain:	n/a
35	chrX:31889692-31889742	HCM	heart:	n/a
36	chrX:31889692-31889742	HIPEpiC	eye:	n/a
37	chrX:31889692-31889742	SK-N-SH	brain:	n/a
38	chrX:31889692-31889742	AG04450	lung:	fetal
39	chrX:31889692-31889742	HRE	kidney:	n/a
40	chrX:31889692-31889742	HPAEpiC	pulmonary alveolar:	n/a
41	chrX:31889692-31889742	HMEC	breast:	n/a
42	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
43	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
44	chrX:31889692-31889742	GM12892	blood:	n/a
45	chrX:31889692-31889742	HRPEpiC	eye:	n/a
46	chrX:31889692-31889742	PFSK-1	brain:	n/a
47	chrX:31889692-31889742	HCT-116	colon:	n/a
48	chrX:31889692-31889742	IMR90	lung:	fetal
49	chrX:31889692-31889742	SKMC	muscle:	n/a
50	chrX:31889692-31889742	AG10803	skin:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
2	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
3	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
4	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
5	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
6	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
7	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
8	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
9	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
10	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
11	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
12	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
13	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
14	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
15	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
16	chr22:21979310..21981506-chrX:31657956..31659478,2	K562	blood:
17	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
18	chrX:30954183..30954687-chrX:31676252..31677226,2	MCF-7	breast:
19	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
20	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
21	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
22	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
23	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
24	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
25	chrX:31634777..31637402-chrX:31639574..31641177,2	K562	blood:
26	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
27	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
28	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
29	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
30	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
31	chrX:31056385..31057531-chrX:31676225..31677578,5	MCF-7	breast:
32	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
33	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
34	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
35	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
36	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
37	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
38	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
39	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
40	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
41	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
42	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
43	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
44	chr21:9824692..9827129-chrX:31658009..31660080,2	MCF-7	breast:
45	chrX:31640339..31643305-chrX:31652840..31655253,2	K562	blood:
46	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
47	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
48	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
49	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
50	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:

No data

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

Extended variants
information (count: 2765 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2765 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138831929	chrX:31644678-31644679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372908953	chrX:31644749-31644750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183241957	chrX:31644785-31644786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187827086	chrX:31644912-31644913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190126027	chrX:31644985-31644986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182793901	chrX:31645314-31645315	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs141831161	chrX:31645426-31645427	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187440299	chrX:31645522-31645523	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192398150	chrX:31645749-31645750	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369216772	chrX:31645764-31645765	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372600090	chrX:31645795-31645796	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375657730	chrX:31645849-31645850	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs398124062	chrX:31645921-31645922	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs144518527	chrX:31645931-31645932	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs398124061	chrX:31645938-31645939	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs398124060	chrX:31645942-31645943	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs1801189	chrX:31645952-31645953	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs369956942	chrX:31646015-31646016	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72466578	chrX:31646021-31646022	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377338692	chrX:31646028-31646029	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562866988	chrX:31646036-31646037	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367552049	chrX:31646046-31646047	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72466579	chrX:31646093-31646094	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185726509	chrX:31646157-31646158	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187861369	chrX:31646177-31646178	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192155480	chrX:31646237-31646238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184518060	chrX:31646280-31646281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199995916	chrX:31646385-31646386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188545802	chrX:31646398-31646399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376876362	chrX:31646405-31646406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181349776	chrX:31646408-31646409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77100549	chrX:31646481-31646482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80111621	chrX:31646613-31646614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375158942	chrX:31646629-31646630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577767666	chrX:31646658-31646659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374526584	chrX:31646753-31646754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs5972422	chrX:31646869-31646870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10524146	chrX:31647033-31647034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12853594	chrX:31647143-31647144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189206061	chrX:31647321-31647322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574767387	chrX:31647401-31647402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370690021	chrX:31647594-31647595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371734758	chrX:31647604-31647605	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs150574462	chrX:31647668-31647669	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs6631355	chrX:31647709-31647710	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs182354329	chrX:31647714-31647715	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs139509729	chrX:31647723-31647724	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs35130693	chrX:31647837-31647838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1039159	chrX:31647841-31647842	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374359688	chrX:31648030-31648031	Enhancers Weak transcription Bivalent Enhancer	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:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31644600-31645400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chrX:31645200-31646200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chrX:31645200-31646200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chrX:31645400-31645800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chrX:31645400-31646000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chrX:31645400-31646000	Enhancers	Muscle Satellite Cultured Cells	--
7	chrX:31645600-31646000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chrX:31645600-31646000	Active TSS	Duodenum Smooth Muscle	Duodenum
9	chrX:31645800-31646000	Enhancers	Colon Smooth Muscle	Colon
10	chrX:31645800-31646200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chrX:31645800-31646200	Active TSS	Brain Anterior Caudate	brain
12	chrX:31646000-31650000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chrX:31646200-31647400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chrX:31646200-31647600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chrX:31646200-31648200	Weak transcription	Brain Anterior Caudate	brain
16	chrX:31646400-31647800	Weak transcription	Colon Smooth Muscle	Colon
17	chrX:31646400-31648400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chrX:31646800-31647000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chrX:31647000-31648000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chrX:31647200-31647400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chrX:31647400-31647600	Enhancers	Stomach Smooth Muscle	stomach
22	chrX:31647400-31648000	Enhancers	Brain Angular Gyrus	brain
23	chrX:31647400-31648000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chrX:31647400-31648200	Enhancers	Duodenum Mucosa	Duodenum
25	chrX:31647400-31649400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chrX:31647400-31651600	Enhancers	Fetal Intestine Small	intestine
27	chrX:31647600-31647800	Bivalent Enhancer	Fetal Kidney	kidney
28	chrX:31647600-31648000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chrX:31647600-31649600	Enhancers	Fetal Brain Male	brain
30	chrX:31647600-31649800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chrX:31647800-31648000	Enhancers	Fetal Intestine Large	intestine
32	chrX:31647800-31648400	Enhancers	Colon Smooth Muscle	Colon
33	chrX:31648000-31648200	Enhancers	Rectal Mucosa Donor 29	rectum
34	chrX:31648000-31648400	Bivalent Enhancer	Fetal Kidney	kidney
35	chrX:31648000-31648400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chrX:31648000-31649000	Weak transcription	Brain Angular Gyrus	brain
37	chrX:31648000-31650200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chrX:31648200-31648400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chrX:31648200-31649000	Enhancers	Brain Anterior Caudate	brain
40	chrX:31648200-31649400	Weak transcription	Fetal Intestine Large	intestine
41	chrX:31648200-31650000	Weak transcription	Duodenum Mucosa	Duodenum
42	chrX:31648400-31648600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chrX:31648600-31649600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chrX:31649000-31649400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chrX:31649400-31649600	Enhancers	Brain Angular Gyrus	brain
46	chrX:31649400-31652400	Enhancers	Fetal Intestine Large	intestine
47	chrX:31649600-31649800	Enhancers	Rectal Mucosa Donor 29	rectum
48	chrX:31649600-31652000	Enhancers	Rectal Mucosa Donor 31	rectum
49	chrX:31650000-31650200	Enhancers	Duodenum Mucosa	Duodenum
50	chrX:31650000-31651400	Enhancers	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links