Variant report

Variant	nsv916917
Chromosome Location	chrX:65628203-65966658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1529)
CpG islands
(count:306)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:65951290-65951590	K562	blood:	n/a	n/a
2	ARID3A	chrX:65951349-65951572	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:65948594-65949132	K562	blood:	n/a	n/a
4	ATF1	chrX:65948586-65949187	K562	blood:	n/a	n/a
5	ATF2	chrX:65845358-65845783	GM12878	blood:	n/a	n/a
6	BATF	chrX:65858992-65859189	GM12878	blood:	n/a	chrX:65859077-65859087 chrX:65859076-65859087
7	BHLHE40	chrX:65963483-65963487	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:65858137-65858650	HepG2	liver:	n/a	n/a
9	BHLHE40	chrX:65949014-65949167	GM12878	blood:	n/a	n/a
10	BHLHE40	chrX:65951357-65951550	GM12878	blood:	n/a	n/a
11	BHLHE40	chrX:65858290-65858746	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:65628290-65628573	GM12878	blood:	n/a	n/a
13	BHLHE40	chrX:65948789-65949213	K562	blood:	n/a	n/a
14	BRCA1	chrX:65948601-65949144	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chrX:65948612-65949157	K562	blood:	n/a	n/a
16	CEBPB	chrX:65636462-65636724	K562	blood:	n/a	chrX:65636597-65636608
17	CEBPB	chrX:65905548-65905744	K562	blood:	n/a	chrX:65905636-65905647
18	CEBPB	chrX:65636442-65636753	HepG2	liver:	n/a	chrX:65636597-65636608
19	CEBPB	chrX:65709598-65709892	HepG2	liver:	n/a	chrX:65709750-65709761
20	CEBPB	chrX:65858925-65859280	A549	lung:	n/a	n/a
21	CEBPB	chrX:65948901-65949187	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:65948762-65949166	K562	blood:	n/a	n/a
23	CEBPB	chrX:65903973-65904229	HepG2	liver:	n/a	chrX:65904074-65904085 chrX:65904072-65904089
24	CEBPB	chrX:65808358-65808600	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:65897430-65897735	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:65855213-65855580	IMR90	lung:	n/a	n/a
27	CEBPB	chrX:65858749-65859261	HepG2	liver:	n/a	n/a
28	CEBPB	chrX:65744634-65744749	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:65858970-65859257	IMR90	lung:	n/a	n/a
30	CEBPB	chrX:65808392-65808578	A549	lung:	n/a	n/a
31	CEBPB	chrX:65842271-65842542	IMR90	lung:	n/a	n/a
32	CEBPB	chrX:65824836-65825136	HepG2	liver:	n/a	chrX:65824967-65824978
33	CEBPB	chrX:65743827-65743964	A549	lung:	n/a	n/a
34	CEBPB	chrX:65853337-65853731	IMR90	lung:	n/a	n/a
35	CEBPB	chrX:65636479-65636679	A549	lung:	n/a	chrX:65636597-65636608
36	CEBPB	chrX:65896305-65897200	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:65905478-65905769	HepG2	liver:	n/a	chrX:65905636-65905647
38	CEBPB	chrX:65964333-65964533	IMR90	lung:	n/a	n/a
39	CEBPB	chrX:65636424-65636739	IMR90	lung:	n/a	chrX:65636597-65636608
40	CEBPB	chrX:65905474-65905770	IMR90	lung:	n/a	chrX:65905636-65905647
41	CHD1	chrX:65858225-65858759	GM12878	blood:	n/a	n/a
42	CHD2	chrX:65859034-65859451	GM12878	blood:	n/a	n/a
43	CREB1	chrX:65948613-65949203	GM12878	blood:	n/a	n/a
44	CREB1	chrX:65948459-65949229	K562	blood:	n/a	n/a
45	CREB1	chrX:65948620-65949204	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chrX:65948577-65949100	A549	lung:	n/a	n/a
47	CREB1	chrX:65948606-65949020	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chrX:65948653-65949048	A549	lung:	n/a	n/a
49	CTCF	chrX:65822546-65822629	MCF-7	breast:	n/a	n/a
50	CTCF	chrX:65959849-65959971	GM20000	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:65835804-65835854	SAEC	small airway:	n/a
2	chrX:65835804-65835854	SAEC	small airway:	n/a
3	chrX:65818628-65818678	A549	lung:	n/a
4	chrX:65835804-65835854	AG04449	skin:	fetal
5	chrX:65835804-65835854	Hepatocyte	liver:	n/a
6	chrX:65835804-65835854	HMEC	breast:	n/a
7	chrX:65835992-65836042	AG10803	skin:	n/a
8	chrX:65818628-65818678	ECC-1	luminal epithelium:	n/a
9	chrX:65835804-65835854	HEK293	kidney:	embryo
10	chrX:65835804-65835854	ProgFib	skin:	n/a
11	chrX:65825449-65825499	H1-hESC	embryonic stem cell:	embryo
12	chrX:65836683-65836733	HepG2	liver:	n/a
13	chrX:65836683-65836733	LNCaP	prostate:	n/a
14	chrX:65818628-65818678	BJ	skin:	n/a
15	chrX:65835804-65835854	U87	brain:	n/a
16	chrX:65835992-65836042	SKMC	muscle:	n/a
17	chrX:65835992-65836042	HRE	kidney:	n/a
18	chrX:65836683-65836733	HRE	kidney:	n/a
19	chrX:65836683-65836733	BJ	skin:	n/a
20	chrX:65836683-65836733	ovcar-3	ovarian:	n/a
21	chrX:65835992-65836042	HUVEC	blood vessel:	n/a
22	chrX:65835804-65835854	K562	blood:	n/a
23	chrX:65818628-65818678	HRPEpiC	eye:	n/a
24	chrX:65835804-65835854	GM12892	blood:	n/a
25	chrX:65836683-65836733	Jurkat	blood:	n/a
26	chrX:65825449-65825499	HCM	heart:	n/a
27	chrX:65836683-65836733	NH-A	brain:	n/a
28	chrX:65835992-65836042	HNPCEpiC	eye:	n/a
29	chrX:65835804-65835854	MCF10A-Er-Src	breast:	n/a
30	chrX:65818628-65818678	HepG2	liver:	n/a
31	chrX:65818628-65818678	HCF	heart:	n/a
32	chrX:65835992-65836042	CMK	blood:	n/a
33	chrX:65825449-65825499	HRCEpiC	kidney:	n/a
34	chrX:65835804-65835854	HL-60	blood:	n/a
35	chrX:65825449-65825499	IMR90	lung:	fetal
36	chrX:65835804-65835854	BJ	skin:	n/a
37	chrX:65818628-65818678	SAEC	small airway:	n/a
38	chrX:65825449-65825499	NHDF-neo	bronchial:	n/a
39	chrX:65836683-65836733	AoSMC	blood vessel:	n/a
40	chrX:65835804-65835854	T-47D	breast:	n/a
41	chrX:65835992-65836042	HIPEpiC	eye:	n/a
42	chrX:65825449-65825499	U87	brain:	n/a
43	chrX:65835804-65835854	GM12891	blood:	n/a
44	chrX:65836683-65836733	PFSK-1	brain:	n/a
45	chrX:65835804-65835854	HCT-116	colon:	n/a
46	chrX:65835992-65836042	ProgFib	skin:	n/a
47	chrX:65818628-65818678	Hepatocyte	liver:	n/a
48	chrX:65825449-65825499	NT2-D1	testis:	n/a
49	chrX:65836683-65836733	AG04449	skin:	fetal
50	chrX:65835804-65835854	HAEpiC	amniotic membrane:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:65329020..65331623-chrX:65649142..65651331,2	K562	blood:
2	chrX:64801614..64802539-chrX:65948756..65949257,2	MCF-7	breast:
3	chrX:64801931..64802649-chrX:65627951..65628822,2	MCF-7	breast:
4	chrX:65852587..65855545-chrX:65857055..65858751,2	K562	blood:
5	chrX:65696857..65699812-chrX:65924534..65926662,2	MCF-7	breast:
6	chrX:65330062..65330591-chrX:65948300..65949050,3	MCF-7	breast:
7	chrX:65879551..65882090-chrX:65883298..65886042,2	K562	blood:
8	chrX:65696857..65699812-chrX:65924534..65926662,2	MCF-7	breast:
9	chrX:65421200..65421901-chrX:65948234..65949098,4	MCF-7	breast:
10	chrX:65420975..65421894-chrX:65948233..65949029,2	MCF-7	breast:
11	chrX:65668174..65671001-chrX:65671422..65673681,2	K562	blood:
12	chrX:65879551..65882090-chrX:65883298..65886042,2	K562	blood:
13	chrX:65628289..65628799-chrX:65948303..65948910,3	MCF-7	breast:
14	chrX:65852587..65855545-chrX:65857055..65858751,2	K562	blood:
15	chr1:16838565..16842080-chrX:65944520..65947520,4	K562	blood:
16	chrX:65420456..65421112-chrX:65948321..65948834,2	MCF-7	breast:
17	chrX:65628289..65628799-chrX:65948303..65948910,3	MCF-7	breast:
18	chr1:16839287..16842291-chrX:65944500..65946020,4	K562	blood:
19	chrX:65668174..65671001-chrX:65671422..65673681,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000226820	TF binding region
PKMP2	TF binding region
RNU6-394P	TF binding region
EDA2R	TF binding region
ENSG00000226820	CpG island
PKMP2	CpG island
RNU6-394P	CpG island
EDA2R	CpG island
ENSG00000206652	chromatin interactions
ENSG00000261135	chromatin interactions

Extended variants
information (count: 1137 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180745387	chrX:65652513-65652514	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200972340	chrX:65652562-65652563	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs185095916	chrX:65652564-65652565	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201649765	chrX:65652625-65652626	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs187866271	chrX:65653300-65653301	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs186685826	chrX:65656375-65656376	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190926342	chrX:65656433-65656434	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs7053735	chrX:65656452-65656453	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs149082964	chrX:65656472-65656473	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143109843	chrX:65656486-65656487	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs182924277	chrX:65656511-65656512	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs373907734	chrX:65656614-65656615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538479445	chrX:65656823-65656824	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs556835589	chrX:65656849-65656850	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs193258219	chrX:65656856-65656857	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185016658	chrX:65656885-65656886	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs56207749	chrX:65656906-65656907	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs4827476	chrX:65656981-65656982	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145574840	chrX:65657036-65657037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs386825576	chrX:65657056-65657057	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs375490625	chrX:65657057-65657058	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs554346054	chrX:65657108-65657109	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs187514728	chrX:65657183-65657184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs78390659	chrX:65657188-65657189	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs184095450	chrX:65657251-65657252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs376031819	chrX:65657259-65657260	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs572608415	chrX:65657322-65657323	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs145692690	chrX:65657356-65657357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs188605812	chrX:65657396-65657397	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs180761171	chrX:65657479-65657480	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs184484609	chrX:65657516-65657517	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs138241925	chrX:65657619-65657620	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs5965201	chrX:65657652-65657653	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs377160807	chrX:65657746-65657747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs144314157	chrX:65657871-65657872	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs4827479	chrX:65657889-65657890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs190219692	chrX:65657928-65657929	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373157781	chrX:65657975-65657976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs182551342	chrX:65657985-65657986	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs185803045	chrX:65666666-65666667	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs188314064	chrX:65666672-65666673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs193042493	chrX:65666693-65666694	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs185179988	chrX:65666750-65666751	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs144811303	chrX:65666847-65666848	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs199734713	chrX:65666940-65666941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs149310190	chrX:65666942-65666943	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs188732403	chrX:65712729-65712730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs181650545	chrX:65713439-65713440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561504679	chrX:65713483-65713484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7474216	chrX:65713506-65713507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Astrocytoma	22246337	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Craniofrontonasal syndrome	21572526	CNVD
Cerebellar hypoplasia	21569638	CNVD
Disorders of sex development	21048976	CNVD
Myxofibrosarcoma	16751306	CNVD
Cervical cancer	21062161	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Prostate cancer	21147910	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:65656800-65658000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chrX:65666600-65667000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
3	chrX:65724000-65724400	Enhancers	Placenta	Placenta
4	chrX:65773800-65774600	Enhancers	Dnd41	blood
5	chrX:65809800-65812200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chrX:65810200-65827400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chrX:65811000-65812800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chrX:65811200-65812800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chrX:65811200-65812800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chrX:65811200-65816400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chrX:65811200-65817000	Weak transcription	HSMM	muscle
12	chrX:65811400-65819400	Weak transcription	HMEC	breast
13	chrX:65811600-65815400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chrX:65811600-65816200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chrX:65811800-65815000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chrX:65811800-65817000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chrX:65811800-65817200	Weak transcription	Ovary	ovary
18	chrX:65811800-65821000	Weak transcription	NHDF-Ad	bronchial
19	chrX:65812000-65815000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chrX:65812000-65816200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chrX:65812200-65813200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chrX:65812200-65813600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chrX:65812800-65813200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chrX:65812800-65813800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
25	chrX:65812800-65814000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chrX:65812800-65823400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chrX:65812800-65825600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chrX:65813000-65814000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chrX:65813200-65813400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
30	chrX:65813200-65813400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
31	chrX:65813200-65813600	ZNF genes & repeats	NH-A	brain
32	chrX:65813200-65814000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chrX:65813200-65814000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chrX:65813400-65813800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chrX:65813400-65816400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chrX:65813400-65817200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chrX:65813600-65817200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chrX:65813600-65817800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chrX:65813600-65817800	Weak transcription	NH-A	brain
40	chrX:65813800-65814000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chrX:65813800-65814200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chrX:65813800-65814200	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chrX:65813800-65816200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chrX:65813800-65816200	Weak transcription	Aorta	Aorta
45	chrX:65813800-65817000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chrX:65814000-65815000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chrX:65814000-65816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chrX:65814000-65816400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chrX:65814000-65816600	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chrX:65814000-65817000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links