Variant report

Variant	nsv524155
Chromosome Location	chrX:55508099-55689174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:868)
CpG islands
(count:1040)
Chromatin interactive
region (count:10)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chrX:55674013-55674363	GM12878	blood:	n/a	n/a
2	BACH1	chrX:55517421-55517768	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:55516407-55516607	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chrX:55543419-55543629	GM12878	blood:	n/a	n/a
5	BATF	chrX:55543404-55543649	GM12878	blood:	n/a	n/a
6	BATF	chrX:55534938-55535123	GM12878	blood:	n/a	n/a
7	BATF	chrX:55667350-55667631	GM12878	blood:	n/a	n/a
8	BATF	chrX:55534117-55534510	GM12878	blood:	n/a	n/a
9	BCL11A	chrX:55667330-55667582	GM12878	blood:	n/a	n/a
10	BCL11A	chrX:55667274-55667600	GM12878	blood:	n/a	n/a
11	BCLAF1	chrX:55673940-55674272	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:55515858-55516304	K562	blood:	n/a	n/a
13	BHLHE40	chrX:55675087-55675088	GM12878	blood:	n/a	n/a
14	BHLHE40	chrX:55515573-55516240	GM12878	blood:	n/a	n/a
15	BHLHE40	chrX:55673944-55674223	GM12878	blood:	n/a	n/a
16	BHLHE40	chrX:55667362-55667520	GM12878	blood:	n/a	n/a
17	BRCA1	chrX:55682493-55682528	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chrX:55516007-55516048	GM12878	blood:	n/a	n/a
19	BRCA1	chrX:55674634-55674740	GM12878	blood:	n/a	n/a
20	CBX3	chrX:55608910-55609158	K562	blood:	n/a	n/a
21	CCNT2	chrX:55514995-55516347	K562	blood:	n/a	chrX:55516326-55516335 chrX:55515661-55515670
22	CEBPB	chrX:55514343-55514601	K562	blood:	n/a	n/a
23	CEBPB	chrX:55624875-55625043	HepG2	liver:	n/a	chrX:55624951-55624962
24	CEBPB	chrX:55624810-55625113	HepG2	liver:	n/a	chrX:55624951-55624962
25	CHD1	chrX:55515733-55515968	GM12878	blood:	n/a	n/a
26	CHD1	chrX:55515264-55515417	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chrX:55515703-55516071	H1-hESC	embryonic stem cell:	n/a	chrX:55515715-55515722
28	CHD2	chrX:55514838-55514950	K562	blood:	n/a	n/a
29	CHD2	chrX:55517078-55517142	GM12878	blood:	n/a	n/a
30	CHD2	chrX:55515354-55515800	K562	blood:	n/a	chrX:55515715-55515722
31	CHD2	chrX:55515137-55516546	GM12878	blood:	n/a	chrX:55515715-55515722
32	CHD2	chrX:55515357-55515805	H1-hESC	embryonic stem cell:	n/a	chrX:55515715-55515722
33	CREB1	chrX:55516037-55516451	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chrX:55592062-55592146	GM10248	blood:	n/a	n/a
35	CTCF	chrX:55533551-55533758	K562	blood:	n/a	chrX:55533725-55533746 chrX:55533649-55533657 chrX:55533639-55533660
36	CTCF	chrX:55550900-55551050	MCF-7	breast:	n/a	n/a
37	CTCF	chrX:55551060-55551210	SAEC	small airway:	n/a	chrX:55551115-55551133 chrX:55551110-55551131
38	CTCF	chrX:55551002-55551182	K562	blood:	n/a	chrX:55551115-55551133 chrX:55551110-55551131
39	CTCF	chrX:55515900-55516050	GM12872	blood:	n/a	n/a
40	CTCF	chrX:55535218-55535528	GM12891	blood:	n/a	n/a
41	CTCF	chrX:55550980-55551130	HMF	breast:	n/a	n/a
42	CTCF	chrX:55598587-55598670	LNCaP	prostate:	n/a	n/a
43	CTCF	chrX:55551000-55551150	AoAF	blood vessel:	n/a	chrX:55551115-55551133 chrX:55551110-55551131
44	CTCF	chrX:55515861-55516096	GM19238	blood:	n/a	n/a
45	CTCF	chrX:55515922-55516059	GM10248	blood:	n/a	n/a
46	CTCF	chrX:55535235-55535517	MCF-7	breast:	n/a	n/a
47	CTCF	chrX:55644047-55644140	GM10248	blood:	n/a	n/a
48	CTCF	chrX:55551040-55551190	AG04449	skin:	n/a	chrX:55551115-55551133 chrX:55551110-55551131
49	CTCF	chrX:55592052-55592053	GM10248	blood:	n/a	n/a
50	CTCF	chrX:55551049-55551283	GM12878	blood:	n/a	chrX:55551115-55551133 chrX:55551110-55551131

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:55515751-55515801	HCM	heart:	n/a
2	chrX:55651284-55651334	NH-A	brain:	n/a
3	chrX:55649107-55649157	AG09319	gingival:	n/a
4	chrX:55515751-55515801	HCM	heart:	n/a
5	chrX:55651284-55651334	NH-A	brain:	n/a
6	chrX:55649107-55649157	AG09319	gingival:	n/a
7	chrX:55515614-55515664	SK-N-MC	brain:	n/a
8	chrX:55513079-55513129	Hela-S3	cervix:	n/a
9	chrX:55515483-55515533	HNPCEpiC	eye:	n/a
10	chrX:55516236-55516286	SAEC	small airway:	n/a
11	chrX:55515751-55515801	AG09319	gingival:	n/a
12	chrX:55651284-55651334	HepG2	liver:	n/a
13	chrX:55515483-55515533	AoSMC	blood vessel:	n/a
14	chrX:55649107-55649157	HUVEC	blood vessel:	n/a
15	chrX:55515720-55515770	HRPEpiC	eye:	n/a
16	chrX:55515952-55516002	AoSMC	blood vessel:	n/a
17	chrX:55515952-55516002	IMR90	lung:	fetal
18	chrX:55516224-55516274	MCF-7	breast:	n/a
19	chrX:55650979-55651029	SKMC	muscle:	n/a
20	chrX:55515653-55515703	T-47D	breast:	n/a
21	chrX:55651284-55651334	HMEC	breast:	n/a
22	chrX:55515315-55515365	ProgFib	skin:	n/a
23	chrX:55513079-55513129	SK-N-MC	brain:	n/a
24	chrX:55513079-55513129	AG09319	gingival:	n/a
25	chrX:55515315-55515365	PrEC	prostate:	n/a
26	chrX:55515952-55516002	GM12891	blood:	n/a
27	chrX:55516236-55516286	HUVEC	blood vessel:	n/a
28	chrX:55516224-55516274	Jurkat	blood:	n/a
29	chrX:55515720-55515770	LNCaP	prostate:	n/a
30	chrX:55515720-55515770	ovcar-3	ovarian:	n/a
31	chrX:55651284-55651334	BJ	skin:	n/a
32	chrX:55513079-55513129	ovcar-3	ovarian:	n/a
33	chrX:55513079-55513129	GM06990	blood:	n/a
34	chrX:55513504-55513554	HepG2	liver:	n/a
35	chrX:55515315-55515365	HAEpiC	amniotic membrane:	n/a
36	chrX:55515483-55515533	U87	brain:	n/a
37	chrX:55649107-55649157	MCF-7	breast:	n/a
38	chrX:55516236-55516286	Hela-S3	cervix:	n/a
39	chrX:55519357-55519407	HCF	heart:	n/a
40	chrX:55513504-55513554	IMR90	lung:	fetal
41	chrX:55519357-55519407	AG10803	skin:	n/a
42	chrX:55515952-55516002	HUVEC	blood vessel:	n/a
43	chrX:55651284-55651334	HEK293	kidney:	embryo
44	chrX:55649485-55649535	HNPCEpiC	eye:	n/a
45	chrX:55515483-55515533	NB4	blood:	n/a
46	chrX:55515720-55515770	HCT-116	colon:	n/a
47	chrX:55513079-55513129	HRE	kidney:	n/a
48	chrX:55515720-55515770	HL-60	blood:	n/a
49	chrX:55515720-55515770	AG04450	lung:	fetal
50	chrX:55515653-55515703	Hela-S3	cervix:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:55594022..55596169-chrX:55606010..55607784,2	K562	blood:
2	chrX:55594022..55596169-chrX:55606010..55607784,2	K562	blood:
3	chrX:55507203..55510619-chrX:55512765..55519080,7	K562	blood:
4	chr4:129731682..129733884-chrX:55516164..55517683,2	K562	blood:
5	chrX:55621242..55623046-chrX:55624326..55626801,2	K562	blood:
6	chrX:55515441..55517417-chrX:55743446..55745792,2	MCF-7	breast:
7	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
8	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
9	chrX:55477578..55479496-chrX:55512126..55514643,2	MCF-7	breast:
10	chrX:52891716..52892347-chrX:55678736..55679597,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP51-5	chrX:55682789-55682874	NONHSAT137257
2	lnc-USP51-5	chrX:55683367-55683447	NONHSAT137257
3	lnc-USP51-1	chrX:55515603-55515641	NONHSAT137251
4	lnc-USP51-4	chrX:55661120-55661219	NONHSAT137256
5	lnc-USP51-4	chrX:55662009-55662089	NONHSAT137256
6	lnc-USP51-5	chrX:55682811-55682874	NONHSAT137258
7	lnc-USP51-2	chrX:55515669-55515798	NONHSAT137252
8	lnc-USP51-4	chrX:55659464-55659589	NONHSAT137256
9	lnc-USP51-2	chrX:55516209-55516513	NONHSAT137252
10	lnc-USP51-3	chrX:55626096-55626539	NONHSAT137254
11	lnc-USP51-5	chrX:55683367-55683398	NONHSAT137258
12	lnc-USP51-5	chrX:55681154-55681267	NONHSAT137258
13	lnc-USP51-5	chrX:55681142-55681267	NONHSAT137257
14	lnc-USP51-1	chrX:55514448-55515421	NONHSAT137251

No data

Variant related genes	Relation type
ENSG00000235136	TF binding region
USP51	TF binding region
ENSG00000169164	TF binding region
ENSG00000229594	TF binding region
ENSG00000200635	TF binding region
FOXR2	TF binding region
ENSG00000235136	CpG island
USP51	CpG island
ENSG00000169164	CpG island
ENSG00000229594	CpG island
ENSG00000200635	CpG island
FOXR2	CpG island
ENSG00000266328	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000083750	chromatin interactions
ENSG00000235136	chromatin interactions
ENSG00000187601	chromatin interactions
ENSG00000247746	chromatin interactions

Extended variants
information (count: 452 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3126254	chrX:55508099-55508100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376070845	chrX:55508101-55508102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190796418	chrX:55508103-55508104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143067680	chrX:55508295-55508296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181713103	chrX:55508332-55508333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs73491713	chrX:55508378-55508379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376143246	chrX:55508434-55508435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140229181	chrX:55508706-55508707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2499861	chrX:55508714-55508715	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs376957763	chrX:55509007-55509008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186977758	chrX:55509023-55509024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189403927	chrX:55509130-55509131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181254162	chrX:55509307-55509308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184973499	chrX:55509454-55509455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189631844	chrX:55509482-55509483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138453282	chrX:55509786-55509787	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370076980	chrX:55509864-55509865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373271244	chrX:55509882-55509883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs537051192	chrX:55509935-55509936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs28446189	chrX:55510024-55510025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377703452	chrX:55510080-55510081	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371010975	chrX:55510111-55510112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7891311	chrX:55510115-55510116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182320810	chrX:55510208-55510209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187159883	chrX:55510225-55510226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192510234	chrX:55510322-55510323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138882755	chrX:55510333-55510334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541364910	chrX:55510367-55510368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149412250	chrX:55510407-55510408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2473057	chrX:55510506-55510507	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376820889	chrX:55510542-55510543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148545059	chrX:55510594-55510595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2499862	chrX:55510918-55510919	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs183244718	chrX:55510939-55510940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73491718	chrX:55511053-55511054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188712683	chrX:55511216-55511217	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191675600	chrX:55511380-55511381	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182584769	chrX:55511450-55511451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367717112	chrX:55511873-55511874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200717691	chrX:55511937-55511938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371091444	chrX:55511949-55511950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201454373	chrX:55511951-55511952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191390012	chrX:55511983-55511984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375470699	chrX:55512234-55512235	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs3002630	chrX:55512314-55512315	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs183961461	chrX:55512423-55512424	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550324717	chrX:55512505-55512506	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190195375	chrX:55512598-55512599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs193261315	chrX:55512785-55512786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549855687	chrX:55513107-55513108	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
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
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
Thyroid cancer	19087340	CNVD
lymphocytic leukemia	21291569	CNVD
Cervical cancer	21062161	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	19835627	CNVD
Mental retardation	21735175	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55508000-55512800	Weak transcription	K562	blood
2	chrX:55510600-55511000	Enhancers	Brain Hippocampus Middle	brain
3	chrX:55511000-55513400	Weak transcription	Brain Hippocampus Middle	brain
4	chrX:55511200-55511400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
5	chrX:55511400-55513000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chrX:55511400-55513000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chrX:55511600-55513200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chrX:55511800-55513400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chrX:55512000-55513600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chrX:55512200-55514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chrX:55512200-55514600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chrX:55512600-55513600	Weak transcription	Dnd41	blood
13	chrX:55512600-55514600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chrX:55512800-55513400	Active TSS	Brain Angular Gyrus	brain
15	chrX:55512800-55514200	Enhancers	K562	blood
16	chrX:55512800-55514600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chrX:55512800-55514600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chrX:55512800-55515000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chrX:55513000-55513200	Bivalent Enhancer	Fetal Kidney	kidney
20	chrX:55513000-55513600	Enhancers	Brain Anterior Caudate	brain
21	chrX:55513000-55514000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chrX:55513000-55514200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chrX:55513000-55514200	Enhancers	Fetal Heart	heart
24	chrX:55513000-55514400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chrX:55513000-55514400	Enhancers	Brain Cingulate Gyrus	brain
26	chrX:55513000-55514600	Weak transcription	H1 Cell Line	embryonic stem cell
27	chrX:55513000-55514600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chrX:55513000-55514600	Weak transcription	Aorta	Aorta
29	chrX:55513000-55514600	Enhancers	Brain Inferior Temporal Lobe	brain
30	chrX:55513200-55513800	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chrX:55513200-55514400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chrX:55513200-55514600	Enhancers	Brain Substantia Nigra	brain
33	chrX:55513200-55514800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chrX:55513400-55514000	Flanking Active TSS	Brain Angular Gyrus	brain
35	chrX:55513400-55514000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chrX:55513400-55514400	Enhancers	Brain Hippocampus Middle	brain
37	chrX:55513400-55514600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chrX:55513400-55514600	Enhancers	Fetal Stomach	stomach
39	chrX:55513600-55513800	Enhancers	Primary T cells fromperipheralblood	blood
40	chrX:55513600-55513800	Enhancers	Muscle Satellite Cultured Cells	--
41	chrX:55513600-55513800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chrX:55513600-55513800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chrX:55513600-55513800	Enhancers	Brain Germinal Matrix	brain
44	chrX:55513600-55513800	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chrX:55513600-55513800	Enhancers	Pancreas	Pancrea
46	chrX:55513600-55514000	Flanking Active TSS	Brain Anterior Caudate	brain
47	chrX:55513600-55514000	Enhancers	Left Ventricle	heart
48	chrX:55513600-55514200	Genic enhancers	Dnd41	blood
49	chrX:55513600-55514400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chrX:55513600-55514400	Enhancers	Fetal Kidney	kidney

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