Variant report

Variant	nsv533221
Chromosome Location	chrX:5970948-6352423
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	BACH1	chrX:6229269-6229469	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chrX:6143762-6143781	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:6243610-6243868	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chrX:6102924-6103158	GM12878	blood:	n/a	n/a
5	BCL11A	chrX:6102943-6103270	GM12878	blood:	n/a	chrX:6103065-6103074
6	BCL3	chrX:6021848-6022126	GM12878	blood:	n/a	n/a
7	BCL3	chrX:6021893-6022120	GM12878	blood:	n/a	n/a
8	CCNT2	chrX:6312899-6313115	K562	blood:	n/a	n/a
9	CEBPB	chrX:6232280-6232583	IMR90	lung:	n/a	chrX:6232438-6232449
10	CEBPB	chrX:6196312-6196512	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chrX:6294030-6294216	A549	lung:	n/a	n/a
12	CEBPB	chrX:6027488-6027796	IMR90	lung:	n/a	chrX:6027623-6027636
13	CEBPB	chrX:6138401-6138691	A549	lung:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
14	CEBPB	chrX:6196213-6196522	A549	lung:	n/a	n/a
15	CEBPB	chrX:6138377-6138688	HepG2	liver:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
16	CEBPB	chrX:6232394-6232537	HepG2	liver:	n/a	chrX:6232438-6232449
17	CEBPB	chrX:6128357-6128557	HepG2	liver:	n/a	chrX:6128465-6128476
18	CEBPB	chrX:6177455-6177729	IMR90	lung:	n/a	n/a
19	CEBPB	chrX:6196285-6196484	HepG2	liver:	n/a	n/a
20	CEBPB	chrX:6146621-6146954	H1-hESC	embryonic stem cell:	n/a	chrX:6146721-6146734
21	CEBPB	chrX:6088585-6088643	A549	lung:	n/a	n/a
22	CEBPB	chrX:6108447-6108656	HepG2	liver:	n/a	chrX:6108474-6108487 chrX:6108611-6108622
23	CEBPB	chrX:6177506-6177590	K562	blood:	n/a	n/a
24	CEBPB	chrX:6196250-6196493	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:6090505-6090705	HepG2	liver:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
26	CEBPB	chrX:6090544-6090693	A549	lung:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
27	CEBPB	chrX:6295507-6295722	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chrX:6128365-6128540	H1-hESC	embryonic stem cell:	n/a	chrX:6128465-6128476
29	CEBPB	chrX:6124249-6124452	HepG2	liver:	n/a	n/a
30	CEBPB	chrX:6138341-6138695	IMR90	lung:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
31	CHD1	chrX:6146143-6146272	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chrX:6143495-6144129	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chrX:6145610-6145849	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chrX:6145172-6145237	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chrX:6217947-6218079	GM12878	blood:	n/a	n/a
36	CHD2	chrX:6103011-6103142	GM12878	blood:	n/a	n/a
37	CHD2	chrX:6146792-6147044	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chrX:6143836-6144261	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chrX:6291664-6291747	K562	blood:	n/a	n/a
40	CTBP2	chrX:6144019-6144865	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chrX:6143900-6144050	GM12869	blood:	n/a	chrX:6143992-6144010
42	CTCF	chrX:6210761-6210833	MCF-7	breast:	n/a	n/a
43	CTCF	chrX:6281400-6281550	NHEK	skin:	n/a	n/a
44	CTCF	chrX:6144356-6144358	GM19239	blood:	n/a	n/a
45	CTCF	chrX:6167785-6167834	LNCaP	prostate:	n/a	n/a
46	CTCF	chrX:6289440-6289590	HEK293	kidney:	n/a	n/a
47	CTCF	chrX:6205725-6205802	Medullo	brain:	n/a	n/a
48	CTCF	chrX:6100066-6100075	GM10266	blood:	n/a	n/a
49	CTCF	chrX:6210740-6210890	GM12878	blood:	n/a	n/a
50	CTCF	chrX:6069057-6069082	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:6144121-6144171	HCPEpiC	choroid plexus:	n/a
2	chrX:6147159-6147209	GM12891	blood:	n/a
3	chrX:6145771-6145821	BJ	skin:	n/a
4	chrX:6146760-6146810	NH-A	brain:	n/a
5	chrX:6145771-6145821	HCM	heart:	n/a
6	chrX:6145730-6145780	T-47D	breast:	n/a
7	chrX:6146900-6146950	NB4	blood:	n/a
8	chrX:6146760-6146810	AG04449	skin:	fetal
9	chrX:6145771-6145821	CMK	blood:	n/a
10	chrX:6146608-6146658	AG04449	skin:	fetal
11	chrX:6146780-6146830	BE2_C	brain:	n/a
12	chrX:6147299-6147349	NB4	blood:	n/a
13	chrX:6147113-6147163	HepG2	liver:	n/a
14	chrX:6147113-6147163	HCT-116	colon:	n/a
15	chrX:6145096-6145146	GM06990	blood:	n/a
16	chrX:6146608-6146658	AG10803	skin:	n/a
17	chrX:6146780-6146830	ProgFib	skin:	n/a
18	chrX:6146900-6146950	NHBE	bronchial:	n/a
19	chrX:6146608-6146658	Hela-S3	cervix:	n/a
20	chrX:6055110-6055160	SAEC	small airway:	n/a
21	chrX:6145730-6145780	K562	blood:	n/a
22	chrX:6147299-6147349	GM12891	blood:	n/a
23	chrX:6147159-6147209	GM12878	blood:	n/a
24	chrX:6145771-6145821	HRCEpiC	kidney:	n/a
25	chrX:6146900-6146950	SK-N-SH	brain:	n/a
26	chrX:6146780-6146830	HRPEpiC	eye:	n/a
27	chrX:6145346-6145396	HRPEpiC	eye:	n/a
28	chrX:6145096-6145146	HCM	heart:	n/a
29	chrX:6147159-6147209	SK-N-MC	brain:	n/a
30	chrX:6145346-6145396	AoSMC	blood vessel:	n/a
31	chrX:6144121-6144171	NHDF-neo	bronchial:	n/a
32	chrX:6145557-6145607	BE2_C	brain:	n/a
33	chrX:6145557-6145607	ECC-1	luminal epithelium:	n/a
34	chrX:6146760-6146810	RPTEC	kidney:	n/a
35	chrX:6146760-6146810	HEK293	kidney:	embryo
36	chrX:6146608-6146658	HL-60	blood:	n/a
37	chrX:6145346-6145396	K562	blood:	n/a
38	chrX:6145096-6145146	A549	lung:	n/a
39	chrX:6145346-6145396	SK-N-SH_RA	brain:	n/a
40	chrX:6055110-6055160	ovcar-3	ovarian:	n/a
41	chrX:6145346-6145396	HCM	heart:	n/a
42	chrX:6144121-6144171	AG09319	gingival:	n/a
43	chrX:6055110-6055160	MCF10A-Er-Src	breast:	n/a
44	chrX:6147299-6147349	AG04450	lung:	fetal
45	chrX:6147159-6147209	RPTEC	kidney:	n/a
46	chrX:6145730-6145780	PANC-1	pancreas:	n/a
47	chrX:6147299-6147349	HUVEC	blood vessel:	n/a
48	chrX:6147113-6147163	BE2_C	brain:	n/a
49	chrX:6146900-6146950	HPAEpiC	pulmonary alveolar:	n/a
50	chrX:6146780-6146830	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:
2	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:
3	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:
4	chrX:5939484..5940010-chrX:6281086..6281665,2	MCF-7	breast:
5	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:
6	chr7:87849338..87850062-chrX:6327052..6327572,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STS-5	chrX:6194587-6194683	NONHSAT136166
2	lnc-STS-5	chrX:6193676-6193984	NONHSAT136166

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4770	chrX:6301948-6301965	MIMAT0019924

Variant related genes	Relation type
ENSG00000237730	TF binding region
ENSG00000225962	TF binding region
NLGN4X	TF binding region
MIR4770	TF binding region
ENSG00000229818	TF binding region
ENSG00000252291	TF binding region
ENSG00000237730	CpG island
ENSG00000225962	CpG island
NLGN4X	CpG island
MIR4770	CpG island
ENSG00000229818	CpG island
ENSG00000252291	CpG island
ENSG00000075142	chromatin interactions

Extended variants
information (count: 4418 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4418 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185712933	chrX:5971209-5971210	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373964500	chrX:5971230-5971231	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28503790	chrX:5971277-5971278	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113583699	chrX:5971301-5971302	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190470855	chrX:5971399-5971400	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183855969	chrX:5971465-5971466	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368942329	chrX:5971504-5971505	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142469766	chrX:5971508-5971509	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187903793	chrX:5971536-5971537	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151239441	chrX:5971615-5971616	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372638017	chrX:5971684-5971685	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576844060	chrX:5971772-5971773	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192974474	chrX:5971833-5971834	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6654810	chrX:5971862-5971863	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545510693	chrX:5971880-5971881	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372386897	chrX:5971971-5971972	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149997499	chrX:5972096-5972097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6654811	chrX:5972157-5972158	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72219346	chrX:5972262-5972263	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367921669	chrX:5972263-5972264	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111751265	chrX:5972358-5972359	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1882411	chrX:5972382-5972383	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575279738	chrX:5972450-5972451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182409284	chrX:5972723-5972724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372318290	chrX:5972750-5972751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377017324	chrX:5972753-5972754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368318561	chrX:5972761-5972762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61498160	chrX:5972819-5972820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369078983	chrX:5972869-5972870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186869452	chrX:5972890-5972891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192351699	chrX:5972940-5972941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5915630	chrX:5973034-5973035	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs12556740	chrX:5973048-5973049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184945332	chrX:5973145-5973146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189618312	chrX:5973231-5973232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143191751	chrX:5973264-5973265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192895424	chrX:5973292-5973293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376692209	chrX:5973312-5973313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148182428	chrX:5973338-5973339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111500805	chrX:5973377-5973378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12558750	chrX:5973392-5973393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs137957665	chrX:5973407-5973408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185396851	chrX:5973454-5973455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189434489	chrX:5973466-5973467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76922005	chrX:5973543-5973544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375509003	chrX:5973552-5973553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181481688	chrX:5973567-5973568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184125466	chrX:5973602-5973603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56156400	chrX:5973687-5973688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112648219	chrX:5973690-5973691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
short stature	22470819	CNVD
turner syndrome	20877625	CNVD
Kallmann Syndrome 1	22470819	CNVD
Oro-facial digital syndrome	19023858	CNVD
Oro-facial digital syndrome	21572526	CNVD
Aicardi syndrome	21572526	CNVD
Vermis hypoplasia	21569638	CNVD
Opitz syndrome	21569638	CNVD
Opitz syndrome	21572526	CNVD
Oro-facial digital syndrome	21569638	CNVD
Abnormal corpus callosum	21572526	CNVD
T-cell lymphomas	19863542	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Seminomas	18059402	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Mental retardation	17406619	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21785460	CNVD
XY gonadal dysgenesis	20685758	CNVD
Breast cancer	21364760	CNVD
Mental retardation	20486941	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20643418	CNVD
Autism	23710042	CNVD
Schizophrenia	23710042	CNVD
Abnormal phenotypes	21355048	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Microphthalmia	21572526	CNVD
Steroid sulfatase deficiency	21549014	CNVD
Attention deficit hyperactivity disorder	21355048	CNVD
Ichthyosis	21355048	CNVD
Mental retardation	21355048	CNVD
Immune disease	21076436	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5956200-5971200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chrX:5959600-5976400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chrX:5960000-6006200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chrX:5960200-5976000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chrX:5968000-5988800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chrX:5968400-5980400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chrX:5969800-5971200	Enhancers	HMEC	breast
8	chrX:5970000-5971200	Enhancers	HSMM	muscle
9	chrX:5970200-5971000	Enhancers	Brain Inferior Temporal Lobe	brain
10	chrX:5970200-5971000	Enhancers	Fetal Brain Female	brain
11	chrX:5970200-5971400	Enhancers	Brain Germinal Matrix	brain
12	chrX:5970200-5976400	Strong transcription	Dnd41	blood
13	chrX:5970400-5972000	Enhancers	Fetal Brain Male	brain
14	chrX:5970400-5972400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chrX:5970600-5971000	Enhancers	H1 Cell Line	embryonic stem cell
16	chrX:5970800-5971600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chrX:5971000-5971200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
18	chrX:5971000-5971200	Flanking Active TSS	Fetal Brain Female	brain
19	chrX:5971000-5971400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chrX:5971000-5971600	Active TSS	Brain Hippocampus Middle	brain
21	chrX:5971200-5971400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chrX:5971200-5971400	Active TSS	Brain Inferior Temporal Lobe	brain
23	chrX:5971200-5971400	Active TSS	Fetal Brain Female	brain
24	chrX:5971200-5971600	Active TSS	Brain Angular Gyrus	brain
25	chrX:5971200-5971600	Active TSS	Brain Cingulate Gyrus	brain
26	chrX:5971400-5971600	Enhancers	H1 Cell Line	embryonic stem cell
27	chrX:5971400-5971600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chrX:5971400-5971600	Flanking Active TSS	Fetal Brain Female	brain
29	chrX:5971400-5973000	Weak transcription	Fetal Thymus	thymus
30	chrX:5971600-5971800	Enhancers	Brain Angular Gyrus	brain
31	chrX:5971600-5971800	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chrX:5971600-5971800	Active TSS	Fetal Brain Female	brain
33	chrX:5971600-5972000	Enhancers	Brain Cingulate Gyrus	brain
34	chrX:5971600-5974200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chrX:5972400-5974600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chrX:5973000-5973600	Strong transcription	Fetal Thymus	thymus
37	chrX:5973600-6021000	Weak transcription	Fetal Thymus	thymus
38	chrX:5976400-5979600	Weak transcription	Dnd41	blood
39	chrX:5979600-5980800	Strong transcription	Dnd41	blood
40	chrX:5980400-5980600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
41	chrX:5980400-5982000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chrX:5980800-5982200	Weak transcription	Dnd41	blood
43	chrX:5982200-6008800	Strong transcription	Dnd41	blood
44	chrX:5983400-5983600	Enhancers	Fetal Brain Female	brain
45	chrX:5983600-5985200	Weak transcription	Fetal Brain Female	brain
46	chrX:5984200-5984600	Enhancers	Ovary	ovary
47	chrX:5984600-5993200	Weak transcription	Ovary	ovary
48	chrX:5985200-5985600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chrX:5985200-5986000	Enhancers	Fetal Brain Female	brain
50	chrX:5985200-5987000	Enhancers	HMEC	breast

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