Variant report

Variant	nsv481881
Chromosome Location	chrX:32551766-32879933
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	BACH1	chrX:32695625-32695644	K562	blood:	n/a	n/a
3	BATF	chrX:32552060-32552305	GM12878	blood:	n/a	n/a
4	BATF	chrX:32552003-32552326	GM12878	blood:	n/a	n/a
5	BCL11A	chrX:32552025-32552248	GM12878	blood:	n/a	n/a
6	CEBPB	chrX:32843903-32844119	IMR90	lung:	n/a	n/a
7	CEBPB	chrX:32656576-32656845	IMR90	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
8	CEBPB	chrX:32866060-32866260	HepG2	liver:	n/a	chrX:32866223-32866234
9	CEBPB	chrX:32772797-32772997	A549	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906
10	CEBPB	chrX:32703017-32703217	IMR90	lung:	n/a	chrX:32703072-32703083
11	CEBPB	chrX:32556163-32556300	A549	lung:	n/a	n/a
12	CEBPB	chrX:32627620-32627925	IMR90	lung:	n/a	n/a
13	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
14	CEBPB	chrX:32656679-32656865	A549	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
15	CEBPB	chrX:32865997-32866399	Hela-S3	cervix:	n/a	chrX:32866223-32866234
16	CEBPB	chrX:32600924-32601258	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chrX:32766919-32767531	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chrX:32869772-32869902	A549	lung:	n/a	n/a
19	CEBPB	chrX:32831425-32831725	IMR90	lung:	n/a	n/a
20	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
21	CEBPB	chrX:32665303-32665641	HepG2	liver:	n/a	n/a
22	CEBPB	chrX:32702985-32703178	HepG2	liver:	n/a	chrX:32703072-32703083
23	CEBPB	chrX:32622293-32622487	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:32831465-32831687	HepG2	liver:	n/a	n/a
25	CTCF	chrX:32704458-32704480	GM10248	blood:	n/a	n/a
26	CTCF	chrX:32572944-32573021	A549	lung:	n/a	n/a
27	CTCF	chrX:32611147-32611187	ProgFib	skin:	n/a	n/a
28	CTCF	chrX:32610117-32610139	ProgFib	skin:	n/a	n/a
29	CTCF	chrX:32661868-32661958	IMR90	lung:	n/a	n/a
30	CTCF	chrX:32792641-32792723	LNCaP	prostate:	n/a	n/a
31	CTCF	chrX:32792685-32792697	NHEK	skin:	n/a	n/a
32	CTCF	chrX:32691400-32691550	HMEC	breast:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
33	CTCF	chrX:32757629-32757691	LNCaP	prostate:	n/a	n/a
34	CTCF	chrX:32691391-32691584	GM12878	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
35	CTCF	chrX:32830617-32830700	GM20000	blood:	n/a	n/a
36	CTCF	chrX:32691420-32691570	Caco-2	colon:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
37	CTCF	chrX:32671556-32671622	GM10248	blood:	n/a	n/a
38	CTCF	chrX:32671276-32671354	GM10248	blood:	n/a	n/a
39	CTCF	chrX:32691400-32691550	HRPEpiC	eye:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
40	CTCF	chrX:32649211-32649294	GM20000	blood:	n/a	n/a
41	CTCF	chrX:32792620-32792770	SAEC	small airway:	n/a	n/a
42	CTCF	chrX:32691400-32691550	BE2_C	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
43	CTCF	chrX:32691420-32691570	GM12874	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
44	CTCF	chrX:32794104-32794151	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chrX:32688940-32688989	LNCaP	prostate:	n/a	n/a
46	CTCF	chrX:32705680-32705830	GM12873	blood:	n/a	n/a
47	CTCF	chrX:32691360-32691510	HEK293	kidney:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
48	CTCF	chrX:32569225-32569300	GM10248	blood:	n/a	n/a
49	CTCF	chrX:32691340-32691490	HRE	kidney:	n/a	n/a
50	CTCF	chrX:32691420-32691570	GM12873	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:32830005-32830055	GM19239	blood:	n/a
2	chrX:32830005-32830055	PrEC	prostate:	n/a
3	chrX:32830005-32830055	GM12892	blood:	n/a
4	chrX:32830005-32830055	HRCEpiC	kidney:	n/a
5	chrX:32830005-32830055	HCT-116	colon:	n/a
6	chrX:32830005-32830055	HNPCEpiC	eye:	n/a
7	chrX:32830005-32830055	A549	lung:	n/a
8	chrX:32830005-32830055	PFSK-1	brain:	n/a
9	chrX:32830005-32830055	NT2-D1	testis:	n/a
10	chrX:32830005-32830055	K562	blood:	n/a
11	chrX:32830005-32830055	HUVEC	blood vessel:	n/a
12	chrX:32830005-32830055	SK-N-SH	brain:	n/a
13	chrX:32830005-32830055	Caco-2	colon:	n/a
14	chrX:32830005-32830055	HRE	kidney:	n/a
15	chrX:32830005-32830055	PANC-1	pancreas:	n/a
16	chrX:32830005-32830055	NHDF-neo	bronchial:	n/a
17	chrX:32830005-32830055	LNCaP	prostate:	n/a
18	chrX:32830005-32830055	SKMC	muscle:	n/a
19	chrX:32830005-32830055	HAEpiC	amniotic membrane:	n/a
20	chrX:32830005-32830055	AoSMC	blood vessel:	n/a
21	chrX:32830005-32830055	U87	brain:	n/a
22	chrX:32830005-32830055	CMK	blood:	n/a
23	chrX:32830005-32830055	HMEC	breast:	n/a
24	chrX:32830005-32830055	HPAEpiC	pulmonary alveolar:	n/a
25	chrX:32830005-32830055	ProgFib	skin:	n/a
26	chrX:32830005-32830055	HRPEpiC	eye:	n/a
27	chrX:32830005-32830055	RPTEC	kidney:	n/a
28	chrX:32830005-32830055	HL-60	blood:	n/a
29	chrX:32830005-32830055	NHBE	bronchial:	n/a
30	chrX:32830005-32830055	MCF-7	breast:	n/a
31	chrX:32830005-32830055	GM12878	blood:	n/a
32	chrX:32830005-32830055	H1-hESC	embryonic stem cell:	embryo
33	chrX:32830005-32830055	HCF	heart:	n/a
34	chrX:32830005-32830055	AG04449	skin:	fetal
35	chrX:32830005-32830055	HepG2	liver:	n/a
36	chrX:32830005-32830055	GM12891	blood:	n/a
37	chrX:32830005-32830055	Hepatocyte	liver:	n/a
38	chrX:32830005-32830055	AG10803	skin:	n/a
39	chrX:32830005-32830055	AG09319	gingival:	n/a
40	chrX:32830005-32830055	HCM	heart:	n/a
41	chrX:32830005-32830055	NH-A	brain:	n/a
42	chrX:32830005-32830055	HEEpiC	esophagus:	n/a
43	chrX:32830005-32830055	SAEC	small airway:	n/a
44	chrX:32830005-32830055	IMR90	lung:	fetal
45	chrX:32830005-32830055	Hela-S3	cervix:	n/a
46	chrX:32830005-32830055	T-47D	breast:	n/a
47	chrX:32830005-32830055	AG09309	skin:	n/a
48	chrX:32830005-32830055	ECC-1	luminal epithelium:	n/a
49	chrX:32830005-32830055	BJ	skin:	n/a
50	chrX:32830005-32830055	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
2	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:
3	chrX:32501789..32502365-chrX:32691222..32691959,2	MCF-7	breast:
4	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
5	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:
6	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:
7	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
8	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
9	chr17:2781701..2782584-chrX:32736765..32737525,2	MCF-7	breast:
10	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
11	chr1:185868339..185869318-chrX:32631259..32632008,2	MCF-7	breast:
12	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
13	chrX:32655856..32658575-chrX:32677287..32679370,2	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-3915	chrX:32601828-32601849	MIMAT0018189
hsa-miR-548f-3p	chrX:32659607-32659625	MIMAT0005895_4

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: 5811 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5811 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192436287	chrX:32551830-32551831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs80134045	chrX:32551843-32551844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149498734	chrX:32552001-32552002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548848827	chrX:32552021-32552022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183855635	chrX:32552106-32552107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188423230	chrX:32552110-32552111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144040063	chrX:32552117-32552118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17318147	chrX:32552118-32552119	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567081586	chrX:32552127-32552128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142133994	chrX:32552140-32552141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151138629	chrX:32552160-32552161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139122768	chrX:32552187-32552188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527858350	chrX:32552199-32552200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373522110	chrX:32552203-32552204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552512994	chrX:32552337-32552338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146867970	chrX:32552381-32552382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140718824	chrX:32552510-32552511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150455382	chrX:32552616-32552617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377306053	chrX:32552650-32552651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs228352	chrX:32552681-32552682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534800409	chrX:32552715-32552716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180785313	chrX:32552724-32552725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538344752	chrX:32552838-32552839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372776035	chrX:32552845-32552846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199781040	chrX:32552868-32552869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149161153	chrX:32552870-32552871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553000677	chrX:32552892-32552893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186528484	chrX:32553067-32553068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58295807	chrX:32553079-32553080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113896653	chrX:32553177-32553178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139166532	chrX:32553195-32553196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189685576	chrX:32553200-32553201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142965252	chrX:32553353-32553354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181731060	chrX:32553358-32553359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534725905	chrX:32553374-32553375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147039559	chrX:32553387-32553388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138159777	chrX:32553414-32553415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186852232	chrX:32553461-32553462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190950722	chrX:32553587-32553588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141811268	chrX:32553755-32553756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150559386	chrX:32553757-32553758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112006793	chrX:32553790-32553791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5927078	chrX:32553791-32553792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149265250	chrX:32553868-32553869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183397998	chrX:32553889-32553890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186163327	chrX:32553925-32553926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189887764	chrX:32553945-32553946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146204487	chrX:32553974-32553975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139214975	chrX:32553987-32553988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182787155	chrX:32554020-32554021	Weak transcription Enhancers	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32546800-32552000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chrX:32546800-32556000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chrX:32549400-32554000	Weak transcription	Fetal Intestine Small	intestine
4	chrX:32551200-32552600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chrX:32551400-32552800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chrX:32551600-32571800	Weak transcription	HSMMtube	muscle
7	chrX:32552000-32552400	Enhancers	H9 Cell Line	embryonic stem cell
8	chrX:32552000-32552800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chrX:32552400-32556000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chrX:32552600-32554400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chrX:32552800-32553800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chrX:32552800-32554600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chrX:32553800-32556600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chrX:32554000-32555800	Enhancers	Fetal Intestine Small	intestine
15	chrX:32554200-32555400	Enhancers	HepG2	liver
16	chrX:32554400-32554800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chrX:32554600-32555000	Enhancers	Fetal Kidney	kidney
18	chrX:32554600-32558200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chrX:32554800-32555400	Enhancers	Fetal Intestine Large	intestine
20	chrX:32554800-32555800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chrX:32555400-32555800	Enhancers	Stomach Mucosa	stomach
22	chrX:32555600-32558000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chrX:32555800-32556600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chrX:32556000-32556200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
25	chrX:32556000-32556200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chrX:32556200-32556600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chrX:32556600-32557000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chrX:32556600-32557000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chrX:32556600-32557600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chrX:32556600-32557600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chrX:32556600-32558200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chrX:32557000-32557200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chrX:32557000-32558200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chrX:32558200-32562800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chrX:32558200-32563000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chrX:32561600-32562000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chrX:32562600-32565000	Weak transcription	Psoas Muscle	Psoas
38	chrX:32562800-32563400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chrX:32563000-32563400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chrX:32563400-32563800	Enhancers	Fetal Heart	heart
41	chrX:32570000-32574000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
42	chrX:32571200-32572200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
43	chrX:32571600-32571800	Weak transcription	Ovary	ovary
44	chrX:32571800-32572200	ZNF genes & repeats	Ovary	ovary
45	chrX:32571800-32572200	ZNF genes & repeats	HSMMtube	muscle
46	chrX:32572200-32582000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chrX:32572200-32583400	Weak transcription	HSMMtube	muscle
48	chrX:32572200-32593400	Weak transcription	Ovary	ovary
49	chrX:32574600-32576400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chrX:32575800-32578600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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