Variant report

Variant	nsv482619
Chromosome Location	chrX:55463837-55570914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1131)
CpG islands
(count:1347)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 4)
miRNA target
sites (count:0)

(count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	BACH1	chrX:55517421-55517768	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chrX:55516407-55516607	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:55478411-55478700	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chrX:55491525-55491918	GM12878	blood:	n/a	n/a
7	BATF	chrX:55534938-55535123	GM12878	blood:	n/a	n/a
8	BATF	chrX:55543419-55543629	GM12878	blood:	n/a	n/a
9	BATF	chrX:55482404-55482614	GM12878	blood:	n/a	n/a
10	BATF	chrX:55482384-55482629	GM12878	blood:	n/a	n/a
11	BATF	chrX:55490910-55491095	GM12878	blood:	n/a	n/a
12	BATF	chrX:55534117-55534510	GM12878	blood:	n/a	n/a
13	BATF	chrX:55543404-55543649	GM12878	blood:	n/a	n/a
14	BHLHE40	chrX:55515858-55516304	K562	blood:	n/a	n/a
15	BHLHE40	chrX:55507203-55507460	K562	blood:	n/a	n/a
16	BHLHE40	chrX:55515573-55516240	GM12878	blood:	n/a	n/a
17	BHLHE40	chrX:55478482-55478800	K562	blood:	n/a	n/a
18	BRCA1	chrX:55516007-55516048	GM12878	blood:	n/a	n/a
19	CBX3	chrX:55478345-55478660	K562	blood:	n/a	n/a
20	CCNT2	chrX:55514995-55516347	K562	blood:	n/a	chrX:55516326-55516335 chrX:55515661-55515670
21	CCNT2	chrX:55507150-55507397	K562	blood:	n/a	chrX:55507307-55507327
22	CEBPB	chrX:55514343-55514601	K562	blood:	n/a	n/a
23	CEBPB	chrX:55472004-55472211	HepG2	liver:	n/a	chrX:55472028-55472039
24	CEBPB	chrX:55472006-55472217	IMR90	lung:	n/a	chrX:55472028-55472039
25	CEBPB	chrX:55507237-55507439	K562	blood:	n/a	n/a
26	CEBPB	chrX:55506570-55506795	K562	blood:	n/a	n/a
27	CEBPD	chrX:55507118-55507575	K562	blood:	n/a	n/a
28	CEBPD	chrX:55507154-55507481	K562	blood:	n/a	n/a
29	CHD1	chrX:55515703-55516071	H1-hESC	embryonic stem cell:	n/a	chrX:55515715-55515722
30	CHD1	chrX:55515264-55515417	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chrX:55515733-55515968	GM12878	blood:	n/a	n/a
32	CHD2	chrX:55478389-55478765	HepG2	liver:	n/a	n/a
33	CHD2	chrX:55514838-55514950	K562	blood:	n/a	n/a
34	CHD2	chrX:55515357-55515805	H1-hESC	embryonic stem cell:	n/a	chrX:55515715-55515722
35	CHD2	chrX:55478405-55478743	K562	blood:	n/a	n/a
36	CHD2	chrX:55478454-55478665	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chrX:55515137-55516546	GM12878	blood:	n/a	chrX:55515715-55515722
38	CHD2	chrX:55517078-55517142	GM12878	blood:	n/a	n/a
39	CHD2	chrX:55515354-55515800	K562	blood:	n/a	chrX:55515715-55515722
40	CHD2	chrX:55478113-55478801	GM12878	blood:	n/a	n/a
41	CREB1	chrX:55516037-55516451	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chrX:55490512-55490834	GM19238	blood:	n/a	n/a
43	CTCF	chrX:55515657-55515807	MCF-7	breast:	n/a	n/a
44	CTCF	chrX:55515840-55515990	GM12872	blood:	n/a	n/a
45	CTCF	chrX:55515500-55515650	SAEC	small airway:	n/a	n/a
46	CTCF	chrX:55551060-55551210	SAEC	small airway:	n/a	chrX:55551115-55551133 chrX:55551110-55551131
47	CTCF	chrX:55492368-55492377	GM10248	blood:	n/a	n/a
48	CTCF	chrX:55515698-55515782	GM13977	blood:	n/a	n/a
49	CTCF	chrX:55515940-55516090	GM12864	blood:	n/a	n/a
50	CTCF	chrX:55515720-55515870	HBMEC	blood vessel:	n/a	n/a

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:55515720-55515770	AG09309	skin:	n/a
2	chrX:55515614-55515664	ovcar-3	ovarian:	n/a
3	chrX:55478814-55478864	Hela-S3	cervix:	n/a
4	chrX:55477154-55477204	NT2-D1	testis:	n/a
5	chrX:55516236-55516286	U87	brain:	n/a
6	chrX:55515720-55515770	AG09309	skin:	n/a
7	chrX:55515614-55515664	ovcar-3	ovarian:	n/a
8	chrX:55478814-55478864	Hela-S3	cervix:	n/a
9	chrX:55477154-55477204	NT2-D1	testis:	n/a
10	chrX:55516236-55516286	U87	brain:	n/a
11	chrX:55478329-55478379	GM19239	blood:	n/a
12	chrX:55515614-55515664	GM19239	blood:	n/a
13	chrX:55513504-55513554	Caco-2	colon:	n/a
14	chrX:55477154-55477204	AG09319	gingival:	n/a
15	chrX:55478539-55478589	MCF10A-Er-Src	breast:	n/a
16	chrX:55479357-55479407	GM06990	blood:	n/a
17	chrX:55479202-55479252	HCT-116	colon:	n/a
18	chrX:55516224-55516274	HRCEpiC	kidney:	n/a
19	chrX:55477154-55477204	LNCaP	prostate:	n/a
20	chrX:55515614-55515664	HPAEpiC	pulmonary alveolar:	n/a
21	chrX:55515315-55515365	HCPEpiC	choroid plexus:	n/a
22	chrX:55516224-55516274	GM06990	blood:	n/a
23	chrX:55515751-55515801	HL-60	blood:	n/a
24	chrX:55479202-55479252	IMR90	lung:	fetal
25	chrX:55515720-55515770	AG10803	skin:	n/a
26	chrX:55513504-55513554	PFSK-1	brain:	n/a
27	chrX:55515315-55515365	ECC-1	luminal epithelium:	n/a
28	chrX:55515751-55515801	HepG2	liver:	n/a
29	chrX:55478539-55478589	ECC-1	luminal epithelium:	n/a
30	chrX:55515315-55515365	GM19239	blood:	n/a
31	chrX:55478610-55478660	Caco-2	colon:	n/a
32	chrX:55516224-55516274	NB4	blood:	n/a
33	chrX:55515483-55515533	GM06990	blood:	n/a
34	chrX:55516224-55516274	ECC-1	luminal epithelium:	n/a
35	chrX:55478610-55478660	HepG2	liver:	n/a
36	chrX:55513079-55513129	HEEpiC	esophagus:	n/a
37	chrX:55515154-55515204	HUVEC	blood vessel:	n/a
38	chrX:55515483-55515533	GM19239	blood:	n/a
39	chrX:55479616-55479666	AG04449	skin:	fetal
40	chrX:55515614-55515664	T-47D	breast:	n/a
41	chrX:55478539-55478589	HCF	heart:	n/a
42	chrX:55515751-55515801	PFSK-1	brain:	n/a
43	chrX:55477154-55477204	IMR90	lung:	fetal
44	chrX:55515315-55515365	Hepatocyte	liver:	n/a
45	chrX:55515315-55515365	HUVEC	blood vessel:	n/a
46	chrX:55478610-55478660	HL-60	blood:	n/a
47	chrX:55515614-55515664	HRE	kidney:	n/a
48	chrX:55515483-55515533	SKMC	muscle:	n/a
49	chrX:55519357-55519407	CMK	blood:	n/a
50	chrX:55477154-55477204	SKMC	muscle:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:55477578..55479496-chrX:55512126..55514643,2	MCF-7	breast:
2	chrX:55459913..55461518-chrX:55462425..55464666,2	K562	blood:
3	chrX:55478272..55480275-chrX:55742945..55745674,2	MCF-7	breast:
4	chrX:55507203..55510619-chrX:55512765..55519080,7	K562	blood:
5	chr4:129731682..129733884-chrX:55516164..55517683,2	K562	blood:
6	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
7	chrX:55515441..55517417-chrX:55743446..55745792,2	MCF-7	breast:
8	chr3:145877632..145880246-chrX:55477813..55479806,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP51-1	chrX:55515603-55515641	NONHSAT137251
2	lnc-USP51-1	chrX:55514448-55515421	NONHSAT137251
3	lnc-USP51-2	chrX:55515669-55515798	NONHSAT137252
4	lnc-USP51-2	chrX:55516209-55516513	NONHSAT137252

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

No data

Variant related genes	Relation type
ENSG00000266328	TF binding region
USP51	TF binding region
MAGEH1	TF binding region
ENSG00000266328	CpG island
USP51	CpG island
MAGEH1	CpG island
ENSG00000187601	chromatin interactions
ENSG00000152952	chromatin interactions
ENSG00000247746	chromatin interactions
ENSG00000266328	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000083750	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181595533	chrX:55473692-55473693	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs186122260	chrX:55473737-55473738	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs150998954	chrX:55473799-55473800	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs537836411	chrX:55473843-55473844	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs140883503	chrX:55473953-55473954	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs150132340	chrX:55474071-55474072	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs12688603	chrX:55476377-55476378	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs192857845	chrX:55476397-55476398	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs375348486	chrX:55476424-55476425	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs184673426	chrX:55476434-55476435	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs60814518	chrX:55476664-55476665	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs57620007	chrX:55476740-55476741	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs528316272	chrX:55476850-55476851	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs149102180	chrX:55476881-55476882	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs144502506	chrX:55476923-55476924	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs189991919	chrX:55476930-55476931	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs368298434	chrX:55477044-55477045	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs34633855	chrX:55477112-55477113	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs372317717	chrX:55477175-55477176	Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
20	rs147858541	chrX:55477297-55477298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141332136	chrX:55477298-55477299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17250872	chrX:55477621-55477622	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs137970778	chrX:55477815-55477816	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs140779575	chrX:55477880-55477881	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs180831900	chrX:55477889-55477890	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs183967342	chrX:55477967-55477968	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189299760	chrX:55478026-55478027	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181962588	chrX:55478030-55478031	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546465763	chrX:55478069-55478070	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs367760667	chrX:55478152-55478153	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150080471	chrX:55478165-55478166	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185973851	chrX:55478199-55478200	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371499385	chrX:55478361-55478362	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs375259256	chrX:55478595-55478596	Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs191481220	chrX:55478744-55478745	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182118210	chrX:55478748-55478749	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200123910	chrX:55478793-55478794	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs367688659	chrX:55478797-55478798	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370434311	chrX:55478838-55478839	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148527152	chrX:55478869-55478870	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186314015	chrX:55478894-55478895	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142873199	chrX:55478897-55478898	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs147296374	chrX:55478960-55478961	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191607578	chrX:55479083-55479084	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182047410	chrX:55479115-55479116	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140966823	chrX:55479161-55479162	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375199093	chrX:55479173-55479174	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368079731	chrX:55479213-55479214	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199598585	chrX:55479232-55479233	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200891712	chrX:55479286-55479287	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	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
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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55476800-55477800	Enhancers	Fetal Muscle Leg	muscle
2	chrX:55476800-55478000	Enhancers	Liver	Liver
3	chrX:55477200-55477800	Enhancers	Fetal Intestine Small	intestine
4	chrX:55477200-55478000	Enhancers	Fetal Intestine Large	intestine
5	chrX:55477200-55478000	Enhancers	Fetal Stomach	stomach
6	chrX:55477400-55477600	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chrX:55477400-55477600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chrX:55477400-55477600	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chrX:55477400-55477600	Enhancers	Fetal Lung	lung
10	chrX:55477400-55477600	Enhancers	Dnd41	blood
11	chrX:55477400-55477800	Enhancers	Brain Anterior Caudate	brain
12	chrX:55477400-55477800	Enhancers	Brain Substantia Nigra	brain
13	chrX:55477400-55477800	Enhancers	Colon Smooth Muscle	Colon
14	chrX:55477400-55477800	Enhancers	Fetal Heart	heart
15	chrX:55477400-55477800	Enhancers	Fetal Kidney	kidney
16	chrX:55477400-55477800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chrX:55477400-55480000	Active TSS	Colonic Mucosa	Colon
18	chrX:55477600-55477800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chrX:55477600-55477800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chrX:55477600-55477800	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chrX:55477600-55477800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chrX:55477600-55477800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chrX:55477600-55477800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chrX:55477600-55477800	Active TSS	Brain Germinal Matrix	brain
25	chrX:55477600-55477800	Enhancers	Brain Hippocampus Middle	brain
26	chrX:55477600-55477800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chrX:55477600-55477800	Enhancers	Fetal Brain Male	brain
28	chrX:55477600-55477800	Enhancers	Rectal Smooth Muscle	rectum
29	chrX:55477600-55477800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chrX:55477600-55478000	Enhancers	Primary T cells fromperipheralblood	blood
31	chrX:55477600-55478000	Enhancers	Primary hematopoietic stem cells	blood
32	chrX:55477600-55478000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chrX:55477600-55478000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chrX:55477600-55478000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chrX:55477600-55478000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
36	chrX:55477600-55478000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chrX:55477600-55478000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chrX:55477600-55478000	Flanking Active TSS	Fetal Lung	lung
39	chrX:55477600-55478000	Enhancers	Lung	lung
40	chrX:55477600-55478000	Enhancers	Placenta Amnion	Placenta Amnion
41	chrX:55477600-55478200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chrX:55477600-55478200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chrX:55477600-55478200	Flanking Active TSS	Dnd41	blood
44	chrX:55477600-55480000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chrX:55477800-55478000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chrX:55477800-55478000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chrX:55477800-55478000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chrX:55477800-55478000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chrX:55477800-55478000	Enhancers	Primary B cells from peripheral blood	blood
50	chrX:55477800-55478000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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