Variant report

Variant	esv3410436
Chromosome Location	chrX:55229677-55671986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2021)
CpG islands
(count:2630)
Chromatin interactive
region (count:26)
LncRNA
region (count:31)
Mature miRNA
region (count: 4)
miRNA target
sites (count:0)

(count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:55506933-55507364	K562	blood:	n/a	n/a
2	ATF1	chrX:55506954-55507404	K562	blood:	n/a	n/a
3	ATF1	chrX:55353407-55353649	K562	blood:	n/a	n/a
4	ATF3	chrX:55246617-55246796	K562	blood:	n/a	n/a
5	BACH1	chrX:55233024-55233326	K562	blood:	n/a	n/a
6	BACH1	chrX:55289555-55289666	K562	blood:	n/a	n/a
7	BACH1	chrX:55478411-55478700	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chrX:55516407-55516607	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chrX:55517421-55517768	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chrX:55667350-55667631	GM12878	blood:	n/a	n/a
11	BATF	chrX:55482384-55482629	GM12878	blood:	n/a	n/a
12	BATF	chrX:55543404-55543649	GM12878	blood:	n/a	n/a
13	BATF	chrX:55543419-55543629	GM12878	blood:	n/a	n/a
14	BATF	chrX:55534117-55534510	GM12878	blood:	n/a	n/a
15	BATF	chrX:55491525-55491918	GM12878	blood:	n/a	n/a
16	BATF	chrX:55490910-55491095	GM12878	blood:	n/a	n/a
17	BATF	chrX:55482404-55482614	GM12878	blood:	n/a	n/a
18	BATF	chrX:55534938-55535123	GM12878	blood:	n/a	n/a
19	BCL11A	chrX:55667330-55667582	GM12878	blood:	n/a	n/a
20	BCL11A	chrX:55667274-55667600	GM12878	blood:	n/a	n/a
21	BCL3	chrX:55360146-55360356	GM12878	blood:	n/a	n/a
22	BHLHE40	chrX:55246537-55246885	K562	blood:	n/a	n/a
23	BHLHE40	chrX:55667362-55667520	GM12878	blood:	n/a	n/a
24	BHLHE40	chrX:55515858-55516304	K562	blood:	n/a	n/a
25	BHLHE40	chrX:55515573-55516240	GM12878	blood:	n/a	n/a
26	BHLHE40	chrX:55478482-55478800	K562	blood:	n/a	n/a
27	BHLHE40	chrX:55507203-55507460	K562	blood:	n/a	n/a
28	BHLHE40	chrX:55369623-55369757	K562	blood:	n/a	n/a
29	BRCA1	chrX:55516007-55516048	GM12878	blood:	n/a	n/a
30	CBX3	chrX:55478345-55478660	K562	blood:	n/a	n/a
31	CBX3	chrX:55246247-55246955	K562	blood:	n/a	n/a
32	CBX3	chrX:55608910-55609158	K562	blood:	n/a	n/a
33	CCNT2	chrX:55514995-55516347	K562	blood:	n/a	chrX:55516326-55516335 chrX:55515661-55515670
34	CCNT2	chrX:55507150-55507397	K562	blood:	n/a	chrX:55507307-55507327
35	CEBPB	chrX:55506570-55506795	K562	blood:	n/a	n/a
36	CEBPB	chrX:55406772-55407008	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:55247162-55247484	K562	blood:	n/a	n/a
38	CEBPB	chrX:55507237-55507439	K562	blood:	n/a	n/a
39	CEBPB	chrX:55441143-55441278	A549	lung:	n/a	n/a
40	CEBPB	chrX:55262623-55262829	Hela-S3	cervix:	n/a	chrX:55262725-55262736
41	CEBPB	chrX:55412619-55412835	IMR90	lung:	n/a	n/a
42	CEBPB	chrX:55262592-55262871	HepG2	liver:	n/a	chrX:55262725-55262736
43	CEBPB	chrX:55262645-55262806	A549	lung:	n/a	chrX:55262725-55262736
44	CEBPB	chrX:55365982-55366294	HepG2	liver:	n/a	chrX:55366125-55366136
45	CEBPB	chrX:55284775-55284888	K562	blood:	n/a	n/a
46	CEBPB	chrX:55306935-55307135	K562	blood:	n/a	n/a
47	CEBPB	chrX:55472004-55472211	HepG2	liver:	n/a	chrX:55472028-55472039
48	CEBPB	chrX:55262559-55262803	IMR90	lung:	n/a	chrX:55262725-55262736
49	CEBPB	chrX:55365436-55365636	HepG2	liver:	n/a	chrX:55365525-55365536
50	CEBPB	chrX:55441069-55441359	IMR90	lung:	n/a	chrX:55441139-55441152 chrX:55441141-55441150

(count:2630 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:55478180-55478230	NB4	blood:	n/a
2	chrX:55649107-55649157	HCM	heart:	n/a
3	chrX:55290965-55291015	IMR90	lung:	fetal
4	chrX:55291317-55291367	RPTEC	kidney:	n/a
5	chrX:55479616-55479666	HNPCEpiC	eye:	n/a
6	chrX:55246977-55247027	IMR90	lung:	fetal
7	chrX:55478814-55478864	NH-A	brain:	n/a
8	chrX:55478180-55478230	NB4	blood:	n/a
9	chrX:55649107-55649157	HCM	heart:	n/a
10	chrX:55290965-55291015	IMR90	lung:	fetal
11	chrX:55291317-55291367	RPTEC	kidney:	n/a
12	chrX:55479616-55479666	HNPCEpiC	eye:	n/a
13	chrX:55246977-55247027	IMR90	lung:	fetal
14	chrX:55478814-55478864	NH-A	brain:	n/a
15	chrX:55478180-55478230	GM19239	blood:	n/a
16	chrX:55515614-55515664	HCM	heart:	n/a
17	chrX:55519357-55519407	GM12891	blood:	n/a
18	chrX:55515154-55515204	NH-A	brain:	n/a
19	chrX:55246455-55246505	HMEC	breast:	n/a
20	chrX:55516224-55516274	HNPCEpiC	eye:	n/a
21	chrX:55649107-55649157	IMR90	lung:	fetal
22	chrX:55651284-55651334	H1-hESC	embryonic stem cell:	embryo
23	chrX:55478539-55478589	LNCaP	prostate:	n/a
24	chrX:55291238-55291288	SK-N-SH_RA	brain:	n/a
25	chrX:55291382-55291432	SK-N-MC	brain:	n/a
26	chrX:55515952-55516002	SKMC	muscle:	n/a
27	chrX:55651284-55651334	T-47D	breast:	n/a
28	chrX:55290965-55291015	GM06990	blood:	n/a
29	chrX:55478814-55478864	SK-N-SH_RA	brain:	n/a
30	chrX:55649485-55649535	NT2-D1	testis:	n/a
31	chrX:55515653-55515703	SKMC	muscle:	n/a
32	chrX:55513079-55513129	MCF-7	breast:	n/a
33	chrX:55291238-55291288	IMR90	lung:	fetal
34	chrX:55479616-55479666	HAEpiC	amniotic membrane:	n/a
35	chrX:55649107-55649157	CMK	blood:	n/a
36	chrX:55478610-55478660	AG10803	skin:	n/a
37	chrX:55479202-55479252	ovcar-3	ovarian:	n/a
38	chrX:55246829-55246879	HRPEpiC	eye:	n/a
39	chrX:55249036-55249086	AoSMC	blood vessel:	n/a
40	chrX:55479357-55479407	CMK	blood:	n/a
41	chrX:55246758-55246808	SK-N-SH	brain:	n/a
42	chrX:55291238-55291288	NB4	blood:	n/a
43	chrX:55246829-55246879	AG09319	gingival:	n/a
44	chrX:55478610-55478660	SK-N-SH	brain:	n/a
45	chrX:55291544-55291594	AG04449	skin:	fetal
46	chrX:55479616-55479666	HRE	kidney:	n/a
47	chrX:55649485-55649535	HMEC	breast:	n/a
48	chrX:55246829-55246879	HMEC	breast:	n/a
49	chrX:55287213-55287263	HPAEpiC	pulmonary alveolar:	n/a
50	chrX:55649107-55649157	HepG2	liver:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:55478272..55480275-chrX:55742945..55745674,2	MCF-7	breast:
2	chrX:55244904..55248200-chrX:55250199..55253396,4	K562	blood:
3	chrX:55339432..55341262-chrX:55355594..55357140,2	K562	blood:
4	chrX:55507203..55510619-chrX:55512765..55519080,7	K562	blood:
5	chrX:55206255..55209119-chrX:55251306..55253131,2	K562	blood:
6	chrX:55477578..55479496-chrX:55512126..55514643,2	MCF-7	breast:
7	chrX:55621242..55623046-chrX:55624326..55626801,2	K562	blood:
8	chrX:55594022..55596169-chrX:55606010..55607784,2	K562	blood:
9	chrX:55226100..55228537-chrX:55229796..55231625,2	MCF-7	breast:
10	chrX:55594022..55596169-chrX:55606010..55607784,2	K562	blood:
11	chrX:55161366..55162313-chrX:55339201..55340117,3	MCF-7	breast:
12	chr3:145877632..145880246-chrX:55477813..55479806,2	MCF-7	breast:
13	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
14	chrX:55379431..55381921-chrX:55391030..55393821,2	K562	blood:
15	chrX:55339432..55341262-chrX:55355594..55357140,2	K562	blood:
16	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
17	chrX:55161388..55162489-chrX:55237435..55238247,4	MCF-7	breast:
18	chrX:55515441..55517417-chrX:55743446..55745792,2	MCF-7	breast:
19	chrX:55352524..55354094-chrX:55354666..55357445,2	MCF-7	breast:
20	chrX:55352524..55354094-chrX:55354666..55357445,2	MCF-7	breast:
21	chrX:55222394..55224552-chrX:55228694..55230550,2	MCF-7	breast:
22	chr4:129731682..129733884-chrX:55516164..55517683,2	K562	blood:
23	chrX:55161709..55162983-chrX:55369213..55369929,3	MCF-7	breast:
24	chrX:55379431..55381921-chrX:55391030..55393821,2	K562	blood:
25	chrX:55459913..55461518-chrX:55462425..55464666,2	K562	blood:
26	chrX:55459913..55461518-chrX:55462425..55464666,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRNR2L10-4	chrX:55290979-55291165	NR_033460
2	lnc-PAGE5-1	chrX:55308296-55308404	ENSG00000232765.2
3	lnc-USP51-4	chrX:55659464-55659589	NONHSAT137256
4	lnc-MTRNR2L10-4	chrX:55289684-55289792	NR_033460
5	lnc-USP51-1	chrX:55514448-55515421	NONHSAT137251
6	lnc-PAGE5-1	chrX:55307807-55307898	ENSG00000232765.2
7	lnc-PAGE5-1	chrX:55309153-55309278	NONHSAT137246
8	lnc-PAGE5-1	chrX:55315100-55315118	NONHSAT137246
9	lnc-USP51-2	chrX:55515669-55515798	NONHSAT137252
10	lnc-PAGE5-1	chrX:55308296-55308404	ENSG00000232765.3
11	lnc-PAGE5-1	chrX:55315102-55315178	NONHSAT137248
12	lnc-PAGE5-1	chrX:55309153-55309278	ENSG00000232765.2
13	lnc-PAGE5-1	chrX:55306272-55306323	NONHSAT137246
14	lnc-PAGE5-1	chrX:55306576-55306585	ENSG00000232765.2
15	lnc-MTRNR2L10-4	chrX:55290253-55290344	NR_033460
16	lnc-PAGE5-1	chrX:55309153-55309278	ENSG00000232765.3
17	lnc-USP51-1	chrX:55515603-55515641	NONHSAT137251
18	lnc-PAGE5-1	chrX:55307807-55307898	NONHSAT137246
19	lnc-PAGE5-1	chrX:55307809-55307898	NONHSAT137248
20	lnc-USP51-4	chrX:55661120-55661219	NONHSAT137256
21	lnc-PAGE5-1	chrX:55308296-55308404	NONHSAT137246
22	lnc-PAGE5-1	chrX:55315100-55315219	ENSG00000232765.2
23	lnc-USP51-2	chrX:55516209-55516513	NONHSAT137252
24	lnc-PAGE5-1	chrX:55315102-55315218	ENSG00000232765.3
25	lnc-PAGE5-1	chrX:55307804-55307898	ENSG00000232765.3
26	lnc-PAGE5-1	chrX:55309153-55309278	NONHSAT137248
27	lnc-PAGE5-1	chrX:55308296-55308404	NONHSAT137248
28	lnc-MTRNR2L10-4	chrX:55286967-55287092	NR_033460
29	lnc-MTRNR2L10-4	chrX:55284849-55284961	NR_033460
30	lnc-USP51-4	chrX:55662009-55662089	NONHSAT137256
31	lnc-USP51-3	chrX:55626096-55626539	NONHSAT137254

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4536-5p	chrX:55477994-55478014	MIMAT0019078_1
hsa-miR-4536-5p	chrX:55477929-55477949	MIMAT0019078
hsa-miR-4536-3p	chrX:55477995-55478015	MIMAT0020959
hsa-miR-4536-3p	chrX:55477928-55477948	MIMAT0020959_1

No data

Variant related genes	Relation type
ENSG00000232765	TF binding region
ENSG00000266328	TF binding region
USP51	TF binding region
PAGE5	TF binding region
ENSG00000200635	TF binding region
ENSG00000251617	TF binding region
PAGE3	TF binding region
ENSG00000235136	TF binding region
MAGEH1	TF binding region
ENSG00000229594	TF binding region
FOXR2	TF binding region
ENSG00000232765	CpG island
ENSG00000266328	CpG island
USP51	CpG island
PAGE5	CpG island
ENSG00000200635	CpG island
ENSG00000251617	CpG island
PAGE3	CpG island
ENSG00000235136	CpG island
MAGEH1	CpG island
ENSG00000229594	CpG island
FOXR2	CpG island
ENSG00000152952	chromatin interactions
ENSG00000238047	chromatin interactions
ENSG00000083750	chromatin interactions
ENSG00000158639	chromatin interactions
ENSG00000187601	chromatin interactions
ENSG00000235136	chromatin interactions
ENSG00000247746	chromatin interactions
ENSG00000266328	chromatin interactions
ENSG00000256045	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000231947	chromatin interactions

Extended variants
information (count: 1141 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1141 , 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	rs144754161	chrX:55229838-55229839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145691124	chrX:55229883-55229884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148513441	chrX:55229921-55229922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369145951	chrX:55229929-55229930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192470437	chrX:55230287-55230288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1927282	chrX:55230288-55230289	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs151224391	chrX:55230371-55230372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199977711	chrX:55230419-55230420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185796505	chrX:55230568-55230569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370020600	chrX:55230602-55230603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140448584	chrX:55230664-55230665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189970177	chrX:55230759-55230760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193193628	chrX:55230850-55230851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113599812	chrX:55230854-55230855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184591042	chrX:55230945-55230946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376980221	chrX:55230953-55230954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145449262	chrX:55231054-55231055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369671870	chrX:55231172-55231173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531307754	chrX:55231187-55231188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188561286	chrX:55231208-55231209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61635786	chrX:55231275-55231276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397961332	chrX:55231288-55231289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180742798	chrX:55231431-55231432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5914264	chrX:55231707-55231708	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1927283	chrX:55231757-55231758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1927284	chrX:55231827-55231828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550306573	chrX:55231993-55231994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188300432	chrX:55232034-55232035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1927285	chrX:55232054-55232055	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201774267	chrX:55232092-55232093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200103049	chrX:55232093-55232094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138367678	chrX:55232143-55232144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113568758	chrX:55232522-55232523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182018196	chrX:55232537-55232538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187670649	chrX:55232595-55232596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568548861	chrX:55232785-55232786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191411958	chrX:55233047-55233048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537079384	chrX:55233116-55233117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368563963	chrX:55233194-55233195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76479491	chrX:55233220-55233221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370353758	chrX:55233238-55233239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2094443	chrX:55233451-55233452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386825309	chrX:55233468-55233469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143465650	chrX:55233484-55233485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372827985	chrX:55233562-55233563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs137928545	chrX:55233591-55233592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs3049819	chrX:55233595-55233596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59497952	chrX:55233598-55233599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs56812594	chrX:55233601-55233602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181927282	chrX:55233768-55233769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Mental retardation	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55227400-55230400	Enhancers	Liver	Liver
2	chrX:55230200-55230400	Enhancers	Placenta Amnion	Placenta Amnion
3	chrX:55230400-55231400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chrX:55230400-55232400	Weak transcription	Liver	Liver
5	chrX:55231400-55232600	Enhancers	Placenta Amnion	Placenta Amnion
6	chrX:55232400-55233600	Enhancers	Liver	Liver
7	chrX:55233600-55236800	Weak transcription	Liver	Liver
8	chrX:55236800-55237000	Enhancers	Liver	Liver
9	chrX:55237000-55237400	Flanking Active TSS	Liver	Liver
10	chrX:55237200-55238000	Active TSS	Duodenum Mucosa	Duodenum
11	chrX:55237400-55238000	Active TSS	Liver	Liver
12	chrX:55237600-55238000	Active TSS	Hela-S3	cervix
13	chrX:55237600-55238000	Active TSS	HepG2	liver
14	chrX:55238000-55238400	Enhancers	Liver	Liver
15	chrX:55246200-55246400	Enhancers	K562	blood
16	chrX:55246400-55246800	Flanking Active TSS	K562	blood
17	chrX:55246800-55247800	Active TSS	K562	blood
18	chrX:55247800-55250000	Weak transcription	K562	blood
19	chrX:55282200-55282400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chrX:55290000-55292400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chrX:55307000-55307200	ZNF genes & repeats	NHEK	skin
22	chrX:55307200-55308400	Weak transcription	NHEK	skin
23	chrX:55308400-55308600	Enhancers	NHEK	skin
24	chrX:55339200-55340000	Enhancers	HMEC	breast
25	chrX:55349600-55350000	ZNF genes & repeats	Lung	lung
26	chrX:55353400-55354400	Enhancers	Rectal Mucosa Donor 31	rectum
27	chrX:55354800-55355200	Bivalent Enhancer	Adipose Nuclei	Adipose
28	chrX:55356600-55357400	Enhancers	Spleen	Spleen
29	chrX:55361000-55361400	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chrX:55361000-55361800	Enhancers	Primary T cells fromperipheralblood	blood
31	chrX:55361000-55361800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chrX:55361200-55362000	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chrX:55361800-55362000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chrX:55361800-55368200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chrX:55362000-55362800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chrX:55362000-55369200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chrX:55362800-55363000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chrX:55363000-55367000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chrX:55364400-55368200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chrX:55367000-55368200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chrX:55367000-55368400	Enhancers	NHEK	skin
42	chrX:55367200-55368400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chrX:55367400-55367800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chrX:55367600-55368200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chrX:55367600-55368400	Enhancers	Left Ventricle	heart
46	chrX:55367600-55369600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chrX:55368000-55368600	Enhancers	Fetal Intestine Small	intestine
48	chrX:55368000-55369200	Enhancers	Fetal Intestine Large	intestine
49	chrX:55368200-55368400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chrX:55368200-55368400	Enhancers	Primary T cells fromperipheralblood	blood

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