Variant report

Variant	esv3362942
Chromosome Location	chrX:56719980-56761482
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:56752993-56753362	K562	blood:	n/a	n/a
2	BCLAF1	chrX:56759936-56760248	GM12878	blood:	n/a	n/a
3	BCLAF1	chrX:56753084-56753420	GM12878	blood:	n/a	n/a
4	BHLHE40	chrX:56755682-56755909	GM12878	blood:	n/a	n/a
5	BRCA1	chrX:56755547-56755866	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chrX:56755756-56755934	GM12878	blood:	n/a	n/a
7	CEBPB	chrX:56759884-56760215	A549	lung:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
8	CEBPB	chrX:56759816-56760044	HepG2	liver:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
9	CEBPB	chrX:56759779-56760197	K562	blood:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
10	CEBPB	chrX:56759759-56760244	IMR90	lung:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
11	CHD1	chrX:56755455-56756127	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chrX:56755707-56756560	GM12878	blood:	n/a	n/a
13	CHD2	chrX:56755474-56756049	Hela-S3	cervix:	n/a	n/a
14	CHD2	chrX:56738731-56738815	GM12878	blood:	n/a	n/a
15	CREB1	chrX:56755523-56755877	A549	lung:	n/a	n/a
16	CREB1	chrX:56755547-56755728	A549	lung:	n/a	n/a
17	CTCF	chrX:56753023-56753449	GM12878	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
18	CTCF	chrX:56753160-56753310	GM12875	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
19	CTCF	chrX:56759947-56760134	GM12892	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
20	CTCF	chrX:56760020-56760170	GM12875	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
21	CTCF	chrX:56753140-56753290	RPTEC	kidney:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
22	CTCF	chrX:56760020-56760170	HA-sp	spinal cord:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
23	CTCF	chrX:56760040-56760190	GM06990	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
24	CTCF	chrX:56759943-56760234	Gliobla	brain:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
25	CTCF	chrX:56760020-56760170	WERI-Rb-1	eye:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
26	CTCF	chrX:56760020-56760170	HAc	cerebellar:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
27	CTCF	chrX:56760009-56760197	GM10248	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
28	CTCF	chrX:56760040-56760190	K562	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
29	CTCF	chrX:56753160-56753310	GM12873	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
30	CTCF	chrX:56753100-56753250	GM12870	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
31	CTCF	chrX:56760000-56760150	BE2_C	brain:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
32	CTCF	chrX:56753009-56753388	T-47D	breast:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
33	CTCF	chrX:56760020-56760170	HPF	lung:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
34	CTCF	chrX:56753120-56753270	GM12867	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
35	CTCF	chrX:56760000-56760150	HL-60	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
36	CTCF	chrX:56760020-56760170	GM12870	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
37	CTCF	chrX:56759940-56760090	HCM	heart:	n/a	chrX:56760083-56760090
38	CTCF	chrX:56753080-56753230	HVMF	connective:	n/a	n/a
39	CTCF	chrX:56760000-56760150	GM12873	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
40	CTCF	chrX:56753140-56753290	GM12866	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
41	CTCF	chrX:56760020-56760170	GM12872	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
42	CTCF	chrX:56760060-56760210	GM12865	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
43	CTCF	chrX:56753106-56753352	GM13977	blood:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
44	CTCF	chrX:56759933-56760263	HUVEC	blood vessel:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
45	CTCF	chrX:56753140-56753290	HEK293	kidney:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
46	CTCF	chrX:56760020-56760170	AG04450	lung:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
47	CTCF	chrX:56760040-56760190	GM12871	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
48	CTCF	chrX:56759980-56760130	HFF-Myc	foreskin:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
49	CTCF	chrX:56753140-56753290	WI-38	lung:	n/a	chrX:56753225-56753238 chrX:56753218-56753239 chrX:56753223-56753241 chrX:56753224-56753240
50	CTCF	chrX:56760040-56760190	Hela-S3	cervix:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:56756686-56756736	BE2_C	brain:	n/a
2	chrX:56756686-56756736	ovcar-3	ovarian:	n/a
3	chrX:56756686-56756736	BE2_C	brain:	n/a
4	chrX:56756686-56756736	ovcar-3	ovarian:	n/a
5	chrX:56755717-56755767	AG09319	gingival:	n/a
6	chrX:56754534-56754584	PFSK-1	brain:	n/a
7	chrX:56755714-56755764	ECC-1	luminal epithelium:	n/a
8	chrX:56754534-56754584	HCPEpiC	choroid plexus:	n/a
9	chrX:56755714-56755764	NT2-D1	testis:	n/a
10	chrX:56755717-56755767	AoSMC	blood vessel:	n/a
11	chrX:56755714-56755764	SKMC	muscle:	n/a
12	chrX:56755717-56755767	SAEC	small airway:	n/a
13	chrX:56756686-56756736	SAEC	small airway:	n/a
14	chrX:56755717-56755767	HEK293	kidney:	embryo
15	chrX:56754534-56754584	HL-60	blood:	n/a
16	chrX:56755714-56755764	BE2_C	brain:	n/a
17	chrX:56755714-56755764	GM12878	blood:	n/a
18	chrX:56755717-56755767	Jurkat	blood:	n/a
19	chrX:56755714-56755764	HPAEpiC	pulmonary alveolar:	n/a
20	chrX:56754534-56754584	U87	brain:	n/a
21	chrX:56754534-56754584	GM06990	blood:	n/a
22	chrX:56755717-56755767	AG10803	skin:	n/a
23	chrX:56755717-56755767	AG04450	lung:	fetal
24	chrX:56755714-56755764	NHDF-neo	bronchial:	n/a
25	chrX:56755717-56755767	HCF	heart:	n/a
26	chrX:56754534-56754584	ECC-1	luminal epithelium:	n/a
27	chrX:56755717-56755767	ProgFib	skin:	n/a
28	chrX:56754534-56754584	HCM	heart:	n/a
29	chrX:56756686-56756736	HCF	heart:	n/a
30	chrX:56754534-56754584	A549	lung:	n/a
31	chrX:56756686-56756736	NB4	blood:	n/a
32	chrX:56756686-56756736	T-47D	breast:	n/a
33	chrX:56754534-56754584	HUVEC	blood vessel:	n/a
34	chrX:56754534-56754584	HPAEpiC	pulmonary alveolar:	n/a
35	chrX:56755714-56755764	Hela-S3	cervix:	n/a
36	chrX:56754534-56754584	NH-A	brain:	n/a
37	chrX:56754534-56754584	ovcar-3	ovarian:	n/a
38	chrX:56756686-56756736	AoSMC	blood vessel:	n/a
39	chrX:56754534-56754584	HRE	kidney:	n/a
40	chrX:56755717-56755767	MCF-7	breast:	n/a
41	chrX:56754534-56754584	AG10803	skin:	n/a
42	chrX:56755717-56755767	A549	lung:	n/a
43	chrX:56756686-56756736	GM19239	blood:	n/a
44	chrX:56755714-56755764	HUVEC	blood vessel:	n/a
45	chrX:56755714-56755764	U87	brain:	n/a
46	chrX:56755717-56755767	HAEpiC	amniotic membrane:	n/a
47	chrX:56756686-56756736	SKMC	muscle:	n/a
48	chrX:56754534-56754584	BE2_C	brain:	n/a
49	chrX:56755717-56755767	H1-hESC	embryonic stem cell:	embryo
50	chrX:56755717-56755767	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:56755952..56758658-chrX:56787740..56790221,2	MCF-7	breast:
2	chrX:56589521..56592004-chrX:56754888..56757482,3	MCF-7	breast:
3	chrX:56488558..56489404-chrX:56753028..56753703,4	MCF-7	breast:
4	chrX:56754417..56757216-chrX:56757629..56759617,2	MCF-7	breast:
5	chrX:56308361..56308892-chrX:56752872..56753378,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBQLN2-5	chrX:56760584-56761001	NONHSAT137274
2	lnc-UBQLN2-4	chrX:56759851-56760504	NONHSAT137273

Variant related genes	Relation type
ENSG00000204272	TF binding region
ENSG00000204272	CpG island
ENSG00000204272	chromatin interactions
ENSG00000188021	chromatin interactions

Extended variants
information (count: 126 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535217829	chrX:56722153-56722154	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs181307977	chrX:56722215-56722216	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs5914765	chrX:56722257-56722258	Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs141262878	chrX:56722281-56722282	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs80080174	chrX:56722377-56722378	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs145547041	chrX:56731002-56731003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186356480	chrX:56731003-56731004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373341418	chrX:56731080-56731081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs5960202	chrX:56731214-56731215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145082531	chrX:56731376-56731377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs61429868	chrX:56750969-56750970	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs150779923	chrX:56750974-56750975	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs191747138	chrX:56751000-56751001	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs368322159	chrX:56751007-56751008	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs183175370	chrX:56752705-56752706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs57180538	chrX:56752847-56752848	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs7876419	chrX:56752855-56752856	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78524489	chrX:56752921-56752922	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201972787	chrX:56753038-56753039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111760660	chrX:56753040-56753041	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs66764349	chrX:56753041-56753042	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs141724485	chrX:56753044-56753045	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs187505494	chrX:56753070-56753071	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs73626217	chrX:56753077-56753078	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs147906437	chrX:56753106-56753107	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs141537253	chrX:56753115-56753116	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs373284782	chrX:56753141-56753142	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs191866439	chrX:56753176-56753177	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs5914776	chrX:56753179-56753180	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182613399	chrX:56753188-56753189	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs572101456	chrX:56753275-56753276	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs73494903	chrX:56753293-56753294	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545967119	chrX:56753538-56753539	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs374974302	chrX:56753604-56753605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187957330	chrX:56753661-56753662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564171390	chrX:56753783-56753784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17277469	chrX:56753784-56753785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192151515	chrX:56753798-56753799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143605630	chrX:56753856-56753857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372677457	chrX:56753948-56753949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs5960785	chrX:56753997-56753998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185725042	chrX:56754109-56754110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190550014	chrX:56754138-56754139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142579642	chrX:56754139-56754140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565966598	chrX:56754186-56754187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144659575	chrX:56754271-56754272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192490851	chrX:56754375-56754376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184442527	chrX:56754377-56754378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188888870	chrX:56754406-56754407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181257236	chrX:56754566-56754567	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

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
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
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Alcoholism	21790672	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:56722000-56722400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chrX:56722000-56722400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chrX:56722000-56722400	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chrX:56731000-56731400	Enhancers	HepG2	liver
5	chrX:56752800-56755200	Enhancers	Liver	Liver
6	chrX:56753200-56753400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chrX:56753200-56753400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chrX:56753200-56753600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chrX:56753200-56754600	Enhancers	Dnd41	blood
10	chrX:56753400-56754400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chrX:56753400-56754800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chrX:56753600-56755000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chrX:56754000-56755200	Enhancers	Brain Hippocampus Middle	brain
14	chrX:56754400-56754600	Enhancers	Brain Substantia Nigra	brain
15	chrX:56754400-56755000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chrX:56754400-56755200	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chrX:56754600-56754800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chrX:56754600-56754800	Bivalent Enhancer	Fetal Brain Male	brain
19	chrX:56754600-56755000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chrX:56754600-56755000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chrX:56754600-56755400	Flanking Active TSS	Dnd41	blood
22	chrX:56754600-56755600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chrX:56754600-56757600	Active TSS	A549	lung
24	chrX:56754600-56757800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chrX:56754800-56755000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chrX:56754800-56755000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chrX:56754800-56755000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chrX:56754800-56755000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chrX:56754800-56755000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chrX:56754800-56755000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chrX:56754800-56755200	Enhancers	H1 Cell Line	embryonic stem cell
32	chrX:56754800-56755200	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chrX:56754800-56755200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chrX:56754800-56755200	Enhancers	Fetal Intestine Small	intestine
35	chrX:56754800-56755200	Bivalent Enhancer	Fetal Kidney	kidney
36	chrX:56754800-56755200	Enhancers	Hela-S3	cervix
37	chrX:56754800-56755600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chrX:56754800-56757200	Active TSS	Muscle Satellite Cultured Cells	--
39	chrX:56754800-56757200	Active TSS	Brain Angular Gyrus	brain
40	chrX:56754800-56757200	Active TSS	NHDF-Ad	bronchial
41	chrX:56754800-56757400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chrX:56754800-56757400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chrX:56754800-56757400	Active TSS	NH-A	brain
44	chrX:56754800-56757600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chrX:56754800-56757600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chrX:56754800-56758600	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chrX:56755000-56755200	Enhancers	Primary B cells from cord blood	blood
48	chrX:56755000-56755200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chrX:56755000-56755200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chrX:56755000-56755200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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