Variant report

Variant	nsv481891
Chromosome Location	chrX:32595387-33014181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:32719536-32719540	K562	blood:	n/a	n/a
2	ATF1	chrX:32999573-32999712	K562	blood:	n/a	n/a
3	BACH1	chrX:32695625-32695644	K562	blood:	n/a	n/a
4	BRCA1	chrX:32924311-32924335	GM12878	blood:	n/a	n/a
5	CEBPB	chrX:32772748-32773051	HepG2	liver:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906 chrX:32773000-32773017
6	CEBPB	chrX:32949269-32949597	IMR90	lung:	n/a	chrX:32949502-32949513 chrX:32949415-32949426 chrX:32949500-32949513 chrX:32949416-32949425
7	CEBPB	chrX:32831425-32831725	IMR90	lung:	n/a	n/a
8	CEBPB	chrX:32843903-32844119	IMR90	lung:	n/a	n/a
9	CEBPB	chrX:32656679-32656865	A549	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
10	CEBPB	chrX:32772797-32772997	A549	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906
11	CEBPB	chrX:32703017-32703217	IMR90	lung:	n/a	chrX:32703072-32703083
12	CEBPB	chrX:32656576-32656845	IMR90	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
13	CEBPB	chrX:32936731-32936967	A549	lung:	n/a	n/a
14	CEBPB	chrX:32622293-32622487	IMR90	lung:	n/a	n/a
15	CEBPB	chrX:32665303-32665641	HepG2	liver:	n/a	n/a
16	CEBPB	chrX:32899394-32899507	K562	blood:	n/a	chrX:32899493-32899506 chrX:32899408-32899420 chrX:32899495-32899504 chrX:32899495-32899504 chrX:32899495-32899504
17	CEBPB	chrX:32865997-32866399	Hela-S3	cervix:	n/a	chrX:32866223-32866234
18	CEBPB	chrX:32702985-32703178	HepG2	liver:	n/a	chrX:32703072-32703083
19	CEBPB	chrX:32866060-32866260	HepG2	liver:	n/a	chrX:32866223-32866234
20	CEBPB	chrX:32889591-32889922	IMR90	lung:	n/a	chrX:32889745-32889758
21	CEBPB	chrX:32949288-32949498	HepG2	liver:	n/a	chrX:32949415-32949426 chrX:32949416-32949425
22	CEBPB	chrX:32831465-32831687	HepG2	liver:	n/a	n/a
23	CEBPB	chrX:32936661-32936954	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:33006711-33006813	HepG2	liver:	n/a	chrX:33006751-33006764 chrX:33006751-33006762 chrX:33006753-33006764
25	CEBPB	chrX:32766919-32767531	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chrX:32886639-32886884	HepG2	liver:	n/a	chrX:32886759-32886770
27	CEBPB	chrX:32869772-32869902	A549	lung:	n/a	n/a
28	CEBPB	chrX:32895778-32896050	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chrX:32898887-32899628	IMR90	lung:	n/a	chrX:32899493-32899506 chrX:32899408-32899420 chrX:32899495-32899504 chrX:32899495-32899504 chrX:32899495-32899504
30	CEBPB	chrX:32772781-32773048	IMR90	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906 chrX:32773000-32773017
31	CEBPB	chrX:32627620-32627925	IMR90	lung:	n/a	n/a
32	CEBPB	chrX:32600924-32601258	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chrX:32889603-32889915	Hela-S3	cervix:	n/a	chrX:32889745-32889758
34	CHD2	chrX:32924317-32924414	K562	blood:	n/a	n/a
35	CTBP2	chrX:33005235-33005635	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chrX:32691412-32691579	LNCaP	prostate:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
37	CTCF	chrX:32691340-32691490	AG04450	lung:	n/a	n/a
38	CTCF	chrX:32691379-32691567	LNCaP	prostate:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
39	CTCF	chrX:32691440-32691590	SK-N-SH_RA	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
40	CTCF	chrX:32662874-32662882	GM10266	blood:	n/a	n/a
41	CTCF	chrX:32742715-32742791	GM20000	blood:	n/a	n/a
42	CTCF	chrX:32792620-32792770	BE2_C	brain:	n/a	n/a
43	CTCF	chrX:32940721-32940856	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chrX:32778746-32778761	GM10248	blood:	n/a	n/a
45	CTCF	chrX:32691340-32691490	AG09319	gingival:	n/a	n/a
46	CTCF	chrX:32691440-32691511	MCF-7	breast:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
47	CTCF	chrX:32691420-32691570	HPF	lung:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
48	CTCF	chrX:32674282-32674335	GM20000	blood:	n/a	n/a
49	CTCF	chrX:32691400-32691550	HRPEpiC	eye:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
50	CTCF	chrX:32860220-32860273	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:32886526-32886576	SK-N-SH	brain:	n/a
2	chrX:32886526-32886576	GM19239	blood:	n/a
3	chrX:32886461-32886511	PrEC	prostate:	n/a
4	chrX:32886526-32886576	GM12892	blood:	n/a
5	chrX:32886461-32886511	HPAEpiC	pulmonary alveolar:	n/a
6	chrX:32830005-32830055	PrEC	prostate:	n/a
7	chrX:32886461-32886511	HUVEC	blood vessel:	n/a
8	chrX:32830005-32830055	AG04450	lung:	fetal
9	chrX:32886461-32886511	Jurkat	blood:	n/a
10	chrX:32886526-32886576	HepG2	liver:	n/a
11	chrX:32886526-32886576	T-47D	breast:	n/a
12	chrX:32886526-32886576	NB4	blood:	n/a
13	chrX:32830005-32830055	Hela-S3	cervix:	n/a
14	chrX:32886461-32886511	GM12878	blood:	n/a
15	chrX:32886461-32886511	NT2-D1	testis:	n/a
16	chrX:32830005-32830055	Caco-2	colon:	n/a
17	chrX:32886526-32886576	PrEC	prostate:	n/a
18	chrX:32830005-32830055	GM12892	blood:	n/a
19	chrX:32886461-32886511	H1-hESC	embryonic stem cell:	embryo
20	chrX:32886526-32886576	HEEpiC	esophagus:	n/a
21	chrX:32830005-32830055	RPTEC	kidney:	n/a
22	chrX:32886461-32886511	NH-A	brain:	n/a
23	chrX:32886461-32886511	AoSMC	blood vessel:	n/a
24	chrX:32886526-32886576	Caco-2	colon:	n/a
25	chrX:32830005-32830055	SK-N-SH_RA	brain:	n/a
26	chrX:32830005-32830055	AG09319	gingival:	n/a
27	chrX:32886461-32886511	LNCaP	prostate:	n/a
28	chrX:32886461-32886511	AG10803	skin:	n/a
29	chrX:32830005-32830055	NHBE	bronchial:	n/a
30	chrX:32830005-32830055	SAEC	small airway:	n/a
31	chrX:32830005-32830055	HUVEC	blood vessel:	n/a
32	chrX:32886461-32886511	RPTEC	kidney:	n/a
33	chrX:32886461-32886511	Hepatocyte	liver:	n/a
34	chrX:32886526-32886576	MCF-7	breast:	n/a
35	chrX:32830005-32830055	GM06990	blood:	n/a
36	chrX:32830005-32830055	GM19239	blood:	n/a
37	chrX:32886526-32886576	AoSMC	blood vessel:	n/a
38	chrX:32830005-32830055	HepG2	liver:	n/a
39	chrX:32830005-32830055	PANC-1	pancreas:	n/a
40	chrX:32886526-32886576	NHBE	bronchial:	n/a
41	chrX:32886526-32886576	HAEpiC	amniotic membrane:	n/a
42	chrX:32886461-32886511	HRCEpiC	kidney:	n/a
43	chrX:32886526-32886576	HNPCEpiC	eye:	n/a
44	chrX:32886461-32886511	GM19239	blood:	n/a
45	chrX:32886461-32886511	SK-N-MC	brain:	n/a
46	chrX:32830005-32830055	HCT-116	colon:	n/a
47	chrX:32886526-32886576	HMEC	breast:	n/a
48	chrX:32886461-32886511	BE2_C	brain:	n/a
49	chrX:32886461-32886511	AG09309	skin:	n/a
50	chrX:32886461-32886511	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
2	chrX:32501789..32502365-chrX:32691222..32691959,2	MCF-7	breast:
3	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
4	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
5	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
6	chr7:145238372..145239192-chrX:32945954..32946528,2	MCF-7	breast:
7	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:
8	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
9	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
10	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
11	chrX:32978971..32981642-chrX:32988787..32991251,2	K562	blood:
12	chrX:32978971..32981642-chrX:32988787..32991251,2	K562	blood:
13	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:
14	chr1:185868339..185869318-chrX:32631259..32632008,2	MCF-7	breast:
15	chr17:2781701..2782584-chrX:32736765..32737525,2	MCF-7	breast:
16	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GK-5	chrX:32773057-32773106	ENSG00000236828.1
2	lnc-GK-5	chrX:32774275-32774517	ENSG00000236828.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chrX:32659607-32659625	MIMAT0005895_4
hsa-miR-3915	chrX:32601828-32601849	MIMAT0018189

Variant related genes	Relation type
MIR548F5	TF binding region
DMD	TF binding region
MIR3915	TF binding region
DMD-AS3	TF binding region
ENSG00000238969	TF binding region
MIR548F5	CpG island
DMD	CpG island
MIR3915	CpG island
DMD-AS3	CpG island
ENSG00000238969	CpG island

Extended variants
information (count: 7036 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7036 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56327621	chrX:32595443-32595444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11797535	chrX:32595459-32595460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73459785	chrX:32595478-32595479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181543983	chrX:32595527-32595528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540099237	chrX:32595550-32595551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146617571	chrX:32595578-32595579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372822345	chrX:32595587-32595588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564743318	chrX:32595642-32595643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184661170	chrX:32595655-32595656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541177411	chrX:32595667-32595668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532222887	chrX:32595679-32595680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376340899	chrX:32595742-32595743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12688970	chrX:32595773-32595774	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190425252	chrX:32595837-32595838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181703423	chrX:32595867-32595868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149159769	chrX:32595949-32595950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs5972601	chrX:32596014-32596015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186310244	chrX:32596049-32596050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12689018	chrX:32596098-32596099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148329103	chrX:32596190-32596191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190715606	chrX:32596353-32596354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369512027	chrX:32596364-32596365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180931533	chrX:32596493-32596494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs808568	chrX:32596517-32596518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185197454	chrX:32596581-32596582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190687827	chrX:32596616-32596617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147037330	chrX:32596736-32596737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552031431	chrX:32596794-32596795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183439407	chrX:32596821-32596822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187934574	chrX:32596839-32596840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138203016	chrX:32596874-32596875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570746287	chrX:32596888-32596889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16990471	chrX:32596965-32596966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs16990472	chrX:32597034-32597035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs3928369	chrX:32597112-32597113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs5928022	chrX:32597127-32597128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191912132	chrX:32597135-32597136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144472475	chrX:32597144-32597145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11393946	chrX:32597168-32597169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182864106	chrX:32597172-32597173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2107303	chrX:32597275-32597276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs142508215	chrX:32597422-32597423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145951154	chrX:32597423-32597424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187975241	chrX:32597477-32597478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192403781	chrX:32597598-32597599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377639354	chrX:32597658-32597659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184856635	chrX:32597698-32597699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370849850	chrX:32597749-32597750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139750609	chrX:32597767-32597768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144540857	chrX:32597865-32597866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Alcoholism	21790672	CNVD
Chronic granulomatous disease	22383943	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32579800-32618200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chrX:32584000-32661400	Weak transcription	HSMMtube	muscle
3	chrX:32594600-32595400	Enhancers	H9 Cell Line	embryonic stem cell
4	chrX:32594600-32596200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chrX:32595000-32595600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chrX:32595200-32595400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chrX:32600400-32601200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chrX:32600600-32600800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chrX:32600600-32601400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chrX:32600800-32601400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chrX:32600800-32601400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chrX:32600800-32601400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chrX:32600800-32601400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chrX:32600800-32601400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chrX:32601000-32611000	Weak transcription	Left Ventricle	heart
16	chrX:32604600-32612600	Weak transcription	Right Ventricle	heart
17	chrX:32606800-32609600	Weak transcription	Fetal Stomach	stomach
18	chrX:32607600-32609800	Weak transcription	Fetal Muscle Trunk	muscle
19	chrX:32607800-32609800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chrX:32608000-32609600	Weak transcription	Aorta	Aorta
21	chrX:32608800-32610000	Weak transcription	Stomach Smooth Muscle	stomach
22	chrX:32609600-32611200	ZNF genes & repeats	Fetal Stomach	stomach
23	chrX:32609600-32611400	Strong transcription	Aorta	Aorta
24	chrX:32609800-32611200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
25	chrX:32609800-32611400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chrX:32609800-32612000	Weak transcription	Colon Smooth Muscle	Colon
27	chrX:32610000-32611200	ZNF genes & repeats	Colonic Mucosa	Colon
28	chrX:32610000-32611400	Strong transcription	Stomach Smooth Muscle	stomach
29	chrX:32610200-32611200	ZNF genes & repeats	Fetal Muscle Leg	muscle
30	chrX:32610400-32611200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
31	chrX:32610600-32611000	ZNF genes & repeats	Adipose Nuclei	Adipose
32	chrX:32610800-32611200	ZNF genes & repeats	Gastric	stomach
33	chrX:32611000-32611200	Strong transcription	Left Ventricle	heart
34	chrX:32611200-32614000	Weak transcription	Left Ventricle	heart
35	chrX:32611400-32612600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chrX:32611400-32612800	Weak transcription	Aorta	Aorta
37	chrX:32611400-32613000	Weak transcription	Stomach Smooth Muscle	stomach
38	chrX:32612600-32614400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chrX:32615800-32616400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chrX:32616800-32617000	Enhancers	Brain Angular Gyrus	brain
41	chrX:32617000-32618000	Weak transcription	Brain Angular Gyrus	brain
42	chrX:32618200-32618400	Enhancers	Brain Angular Gyrus	brain
43	chrX:32618200-32618800	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chrX:32625200-32632000	Weak transcription	Psoas Muscle	Psoas
45	chrX:32627600-32627800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chrX:32627800-32628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chrX:32627800-32635400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chrX:32628000-32628200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chrX:32628200-32633000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chrX:32632000-32632200	Enhancers	Psoas Muscle	Psoas

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