Variant report

Variant	nsv949481
Chromosome Location	chrX:5883977-6401143
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:5939545-5939724	HepG2	liver:	n/a	n/a
2	BACH1	chrX:5933538-5933757	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:5914130-5914334	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chrX:6229269-6229469	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:6243610-6243868	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:6143762-6143781	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chrX:6102924-6103158	GM12878	blood:	n/a	n/a
8	BATF	chrX:6384038-6384307	GM12878	blood:	n/a	chrX:6384168-6384179 chrX:6384169-6384179
9	BCL11A	chrX:6102943-6103270	GM12878	blood:	n/a	chrX:6103065-6103074
10	BCL3	chrX:6021893-6022120	GM12878	blood:	n/a	n/a
11	BCL3	chrX:5933456-5933812	GM12878	blood:	n/a	n/a
12	BCL3	chrX:6021848-6022126	GM12878	blood:	n/a	n/a
13	CCNT2	chrX:6312899-6313115	K562	blood:	n/a	n/a
14	CEBPB	chrX:6232280-6232583	IMR90	lung:	n/a	chrX:6232438-6232449
15	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
16	CEBPB	chrX:5940708-5941207	HepG2	liver:	n/a	chrX:5941068-5941079 chrX:5941067-5941080
17	CEBPB	chrX:6146621-6146954	H1-hESC	embryonic stem cell:	n/a	chrX:6146721-6146734
18	CEBPB	chrX:6090544-6090693	A549	lung:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
19	CEBPB	chrX:5961464-5961680	HepG2	liver:	n/a	chrX:5961510-5961521
20	CEBPB	chrX:5930411-5930766	IMR90	lung:	n/a	chrX:5930590-5930601
21	CEBPB	chrX:6124249-6124452	HepG2	liver:	n/a	n/a
22	CEBPB	chrX:5932685-5932910	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chrX:6128357-6128557	HepG2	liver:	n/a	chrX:6128465-6128476
24	CEBPB	chrX:6294030-6294216	A549	lung:	n/a	n/a
25	CEBPB	chrX:5930421-5930781	H1-hESC	embryonic stem cell:	n/a	chrX:5930590-5930601
26	CEBPB	chrX:5929097-5929277	HepG2	liver:	n/a	chrX:5929164-5929177 chrX:5929164-5929175
27	CEBPB	chrX:6177455-6177729	IMR90	lung:	n/a	n/a
28	CEBPB	chrX:6392183-6392377	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:5961398-5961625	IMR90	lung:	n/a	chrX:5961510-5961521
30	CEBPB	chrX:6088585-6088643	A549	lung:	n/a	n/a
31	CEBPB	chrX:5930410-5930763	HepG2	liver:	n/a	chrX:5930590-5930601
32	CEBPB	chrX:6090505-6090705	HepG2	liver:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
33	CEBPB	chrX:6128365-6128540	H1-hESC	embryonic stem cell:	n/a	chrX:6128465-6128476
34	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
35	CEBPB	chrX:6196312-6196512	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chrX:6232394-6232537	HepG2	liver:	n/a	chrX:6232438-6232449
37	CEBPB	chrX:6196250-6196493	IMR90	lung:	n/a	n/a
38	CEBPB	chrX:6196213-6196522	A549	lung:	n/a	n/a
39	CEBPB	chrX:6384648-6384957	IMR90	lung:	n/a	chrX:6384810-6384823
40	CEBPB	chrX:5930405-5930778	A549	lung:	n/a	chrX:5930590-5930601
41	CEBPB	chrX:6177506-6177590	K562	blood:	n/a	n/a
42	CEBPB	chrX:6027488-6027796	IMR90	lung:	n/a	chrX:6027623-6027636
43	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
44	CEBPB	chrX:6196285-6196484	HepG2	liver:	n/a	n/a
45	CEBPB	chrX:6108447-6108656	HepG2	liver:	n/a	chrX:6108474-6108487 chrX:6108611-6108622
46	CEBPB	chrX:6295507-6295722	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chrX:5930419-5930753	K562	blood:	n/a	chrX:5930590-5930601
48	CHD1	chrX:6145172-6145237	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chrX:6145610-6145849	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chrX:6143495-6144129	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:6144121-6144171	AoSMC	blood vessel:	n/a
2	chrX:6147299-6147349	U87	brain:	n/a
3	chrX:5961169-5961219	HEK293	kidney:	embryo
4	chrX:6145096-6145146	HCF	heart:	n/a
5	chrX:6145730-6145780	NB4	blood:	n/a
6	chrX:5961169-5961219	SKMC	muscle:	n/a
7	chrX:5961169-5961219	AG10803	skin:	n/a
8	chrX:6145771-6145821	HCM	heart:	n/a
9	chrX:6146809-6146859	HCM	heart:	n/a
10	chrX:6147299-6147349	HRE	kidney:	n/a
11	chrX:6145557-6145607	HRE	kidney:	n/a
12	chrX:5961169-5961219	H1-hESC	embryonic stem cell:	embryo
13	chrX:6145346-6145396	Hela-S3	cervix:	n/a
14	chrX:6145771-6145821	HNPCEpiC	eye:	n/a
15	chrX:6146809-6146859	RPTEC	kidney:	n/a
16	chrX:5961169-5961219	U87	brain:	n/a
17	chrX:6145346-6145396	GM19239	blood:	n/a
18	chrX:6147113-6147163	NHBE	bronchial:	n/a
19	chrX:6145557-6145607	Jurkat	blood:	n/a
20	chrX:6147113-6147163	HUVEC	blood vessel:	n/a
21	chrX:6144121-6144171	LNCaP	prostate:	n/a
22	chrX:6146656-6146706	NHDF-neo	bronchial:	n/a
23	chrX:6144633-6144683	NH-A	brain:	n/a
24	chrX:6145346-6145396	SK-N-SH	brain:	n/a
25	chrX:6145771-6145821	CMK	blood:	n/a
26	chrX:6145730-6145780	HPAEpiC	pulmonary alveolar:	n/a
27	chrX:6055110-6055160	HNPCEpiC	eye:	n/a
28	chrX:6145346-6145396	Caco-2	colon:	n/a
29	chrX:6144121-6144171	Jurkat	blood:	n/a
30	chrX:6145730-6145780	MCF-7	breast:	n/a
31	chrX:6146656-6146706	HNPCEpiC	eye:	n/a
32	chrX:6146608-6146658	ProgFib	skin:	n/a
33	chrX:5961169-5961219	ProgFib	skin:	n/a
34	chrX:6146809-6146859	NB4	blood:	n/a
35	chrX:6147113-6147163	HAEpiC	amniotic membrane:	n/a
36	chrX:6146900-6146950	SK-N-SH	brain:	n/a
37	chrX:6145346-6145396	AG09309	skin:	n/a
38	chrX:6145346-6145396	NH-A	brain:	n/a
39	chrX:6147159-6147209	Hepatocyte	liver:	n/a
40	chrX:6147299-6147349	NH-A	brain:	n/a
41	chrX:6146608-6146658	RPTEC	kidney:	n/a
42	chrX:6146900-6146950	NHBE	bronchial:	n/a
43	chrX:6145730-6145780	ProgFib	skin:	n/a
44	chrX:6147299-6147349	H1-hESC	embryonic stem cell:	embryo
45	chrX:6145346-6145396	PrEC	prostate:	n/a
46	chrX:6145771-6145821	HEEpiC	esophagus:	n/a
47	chrX:5961169-5961219	HCM	heart:	n/a
48	chrX:6145096-6145146	A549	lung:	n/a
49	chrX:6147113-6147163	HRE	kidney:	n/a
50	chrX:6145096-6145146	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:87849338..87850062-chrX:6327052..6327572,2	NB4	blood:
2	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:
3	chrX:5939484..5940010-chrX:6281086..6281665,2	MCF-7	breast:
4	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:
5	chrX:5939484..5940010-chrX:6281086..6281665,2	MCF-7	breast:
6	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:
7	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:
8	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:
9	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:

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

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

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

Extended variants
information (count: 6222 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6222 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5961389	chrX:5883977-5883978	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569879032	chrX:5884200-5884201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180826435	chrX:5884287-5884288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145967391	chrX:5884354-5884355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186276458	chrX:5884369-5884370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377547224	chrX:5884509-5884510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190303914	chrX:5884518-5884519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182035007	chrX:5884546-5884547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371064251	chrX:5884548-5884549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148220593	chrX:5884576-5884577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530692107	chrX:5884578-5884579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185955778	chrX:5884604-5884605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190718901	chrX:5884606-5884607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141498711	chrX:5884685-5884686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs5961902	chrX:5884755-5884756	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs182503798	chrX:5884790-5884791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35211998	chrX:5884817-5884818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57535542	chrX:5884818-5884819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186380288	chrX:5884866-5884867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139394035	chrX:5884961-5884962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376715392	chrX:5885037-5885038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72627591	chrX:5885154-5885155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147334921	chrX:5885224-5885225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140703426	chrX:5885273-5885274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191575078	chrX:5885278-5885279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182551644	chrX:5885404-5885405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187973934	chrX:5885554-5885555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144664726	chrX:5885588-5885589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75203620	chrX:5885630-5885631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141690702	chrX:5885631-5885632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72627593	chrX:5885693-5885694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35622086	chrX:5885715-5885716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs193066837	chrX:5885743-5885744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111343150	chrX:5885745-5885746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72627594	chrX:5885835-5885836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183367449	chrX:5885919-5885920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151201395	chrX:5886101-5886102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368353926	chrX:5886114-5886115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73442146	chrX:5886208-5886209	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187220228	chrX:5886234-5886235	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192144925	chrX:5886256-5886257	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs5961903	chrX:5886274-5886275	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138165114	chrX:5886398-5886399	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs5961904	chrX:5886428-5886429	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376156968	chrX:5886462-5886463	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373332262	chrX:5886479-5886480	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374541658	chrX:5886499-5886500	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs5961390	chrX:5886500-5886501	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199645820	chrX:5886501-5886502	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200658422	chrX:5886502-5886503	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5877400-5889800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chrX:5877800-5891200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chrX:5878400-5894400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chrX:5883600-5887000	Strong transcription	Dnd41	blood
5	chrX:5886200-5887000	Enhancers	H9 Cell Line	embryonic stem cell
6	chrX:5887000-5889200	Weak transcription	Dnd41	blood
7	chrX:5887000-5901000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chrX:5889200-5890200	Strong transcription	Dnd41	blood
9	chrX:5889200-5890400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chrX:5889200-5890400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chrX:5889200-5890400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chrX:5889400-5889800	Enhancers	Ovary	ovary
13	chrX:5889600-5890200	Enhancers	HSMM	muscle
14	chrX:5889800-5890000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chrX:5889800-5892000	Weak transcription	Ovary	ovary
16	chrX:5890000-5890400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chrX:5890000-5890600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chrX:5890000-5890600	Enhancers	NH-A	brain
19	chrX:5890200-5890400	Enhancers	HSMMtube	muscle
20	chrX:5890200-5892000	Weak transcription	Dnd41	blood
21	chrX:5890400-5891200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chrX:5890600-5891000	Weak transcription	NH-A	brain
23	chrX:5890600-5891600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chrX:5891000-5891400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chrX:5891000-5891400	Enhancers	NH-A	brain
26	chrX:5891200-5891600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chrX:5891200-5891600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chrX:5891400-5894800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chrX:5891600-5894400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chrX:5892000-5892200	Enhancers	Ovary	ovary
31	chrX:5892000-5893000	Strong transcription	Dnd41	blood
32	chrX:5892200-5894600	Weak transcription	Ovary	ovary
33	chrX:5892800-5893200	Enhancers	Brain Angular Gyrus	brain
34	chrX:5893000-5893200	Genic enhancers	Dnd41	blood
35	chrX:5893200-5895800	Weak transcription	Dnd41	blood
36	chrX:5894400-5894600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chrX:5894400-5894800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chrX:5894600-5895000	Active TSS	Ovary	ovary
39	chrX:5894800-5895000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chrX:5895800-5897600	Strong transcription	Dnd41	blood
41	chrX:5897600-5904800	Weak transcription	Dnd41	blood
42	chrX:5901000-5901200	Enhancers	H9 Cell Line	embryonic stem cell
43	chrX:5904800-5906600	Strong transcription	Dnd41	blood
44	chrX:5906600-5910800	Weak transcription	Dnd41	blood
45	chrX:5908400-5909600	Enhancers	Fetal Brain Male	brain
46	chrX:5908800-5909000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chrX:5908800-5909000	Enhancers	Fetal Brain Female	brain
48	chrX:5908800-5909200	Enhancers	H9 Cell Line	embryonic stem cell
49	chrX:5908800-5909200	Enhancers	Ovary	ovary
50	chrX:5908800-5910000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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