Variant report

Variant	nsv527262
Chromosome Location	chrX:56758231-56774826
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	ATF3	chrX:56771415-56771798	HCT-116	colon:	n/a	n/a
2	ATF3	chrX:56771375-56771803	HCT-116	colon:	n/a	n/a
3	BCLAF1	chrX:56759936-56760248	GM12878	blood:	n/a	n/a
4	CBX3	chrX:56771416-56771790	HCT-116	colon:	n/a	n/a
5	CBX3	chrX:56771396-56771877	HCT-116	colon:	n/a	n/a
6	CEBPB	chrX:56759779-56760197	K562	blood:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
7	CEBPB	chrX:56759816-56760044	HepG2	liver:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
8	CEBPB	chrX:56759759-56760244	IMR90	lung:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
9	CEBPB	chrX:56771426-56771845	IMR90	lung:	n/a	chrX:56771654-56771665
10	CEBPB	chrX:56771437-56771826	A549	lung:	n/a	chrX:56771654-56771665
11	CEBPB	chrX:56771430-56771758	A549	lung:	n/a	chrX:56771654-56771665
12	CEBPB	chrX:56771343-56771883	A549	lung:	n/a	chrX:56771654-56771665
13	CEBPB	chrX:56771426-56771860	Hela-S3	cervix:	n/a	chrX:56771654-56771665
14	CEBPB	chrX:56759884-56760215	A549	lung:	n/a	chrX:56759886-56759899 chrX:56759888-56759897 chrX:56759888-56759899 chrX:56759886-56759897
15	CEBPB	chrX:56771481-56771800	HepG2	liver:	n/a	chrX:56771654-56771665
16	CEBPB	chrX:56771542-56771684	HepG2	liver:	n/a	chrX:56771654-56771665
17	CEBPB	chrX:56771342-56772000	HCT-116	colon:	n/a	chrX:56771654-56771665
18	CEBPB	chrX:56771345-56771821	HCT-116	colon:	n/a	chrX:56771654-56771665
19	CTCF	chrX:56759966-56760201	GM20000	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
20	CTCF	chrX:56760040-56760190	AG09319	gingival:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
21	CTCF	chrX:56760020-56760170	HRPEpiC	eye:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
22	CTCF	chrX:56759940-56760090	GM12868	blood:	n/a	chrX:56760083-56760090
23	CTCF	chrX:56759954-56760207	HepG2	liver:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
24	CTCF	chrX:56759940-56760252	GM12878	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
25	CTCF	chrX:56759993-56760148	SK-N-SH_RA	brain:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
26	CTCF	chrX:56759951-56760229	Kidney_OC	kidney:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
27	CTCF	chrX:56759980-56760130	GM12864	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
28	CTCF	chrX:56759998-56760109	MCF-7	breast:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
29	CTCF	chrX:56760000-56760150	GM12867	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
30	CTCF	chrX:56760060-56760210	HPAF	blood vessel:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
31	CTCF	chrX:56759935-56760193	LNCaP	prostate:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
32	CTCF	chrX:56760860-56761010	GM12873	blood:	n/a	n/a
33	CTCF	chrX:56759980-56760130	HFF-Myc	foreskin:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
34	CTCF	chrX:56759942-56760242	SK-N-SH_RA	brain:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
35	CTCF	chrX:56760040-56760190	AG10803	skin:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
36	CTCF	chrX:56759980-56760130	GM12874	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
37	CTCF	chrX:56759717-56760422	SK-N-SH	brain:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
38	CTCF	chrX:56759946-56760158	GM19240	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
39	CTCF	chrX:56762574-56762594	A549	lung:	n/a	n/a
40	CTCF	chrX:56760020-56760170	GM12873	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
41	CTCF	chrX:56759940-56760090	HCM	heart:	n/a	chrX:56760083-56760090
42	CTCF	chrX:56760080-56760230	GM12872	blood:	n/a	chrX:56760083-56760090
43	CTCF	chrX:56759947-56760134	GM12892	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
44	CTCF	chrX:56760020-56760170	HCM	heart:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
45	CTCF	chrX:56760020-56760170	HAc	cerebellar:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
46	CTCF	chrX:56760000-56760150	HL-60	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
47	CTCF	chrX:56760020-56760170	GM12872	blood:	n/a	chrX:56760083-56760090 chrX:56760071-56760092 chrX:56760076-56760094 chrX:56760077-56760093
48	CTCF	chrX:56760080-56760230	GM12871	blood:	n/a	chrX:56760083-56760090
49	CTCF	chrX:56771439-56771529	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chrX:56759724-56760455	A549	lung:	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:56764293-56764343	Jurkat	blood:	n/a
2	chrX:56764293-56764343	Jurkat	blood:	n/a
3	chrX:56764796-56764846	SAEC	small airway:	n/a
4	chrX:56764796-56764846	HUVEC	blood vessel:	n/a
5	chrX:56764796-56764846	AG09319	gingival:	n/a
6	chrX:56764796-56764846	AoSMC	blood vessel:	n/a
7	chrX:56764293-56764343	HEEpiC	esophagus:	n/a
8	chrX:56764293-56764343	RPTEC	kidney:	n/a
9	chrX:56764293-56764343	HRCEpiC	kidney:	n/a
10	chrX:56764796-56764846	Jurkat	blood:	n/a
11	chrX:56764293-56764343	K562	blood:	n/a
12	chrX:56764293-56764343	NB4	blood:	n/a
13	chrX:56764293-56764343	NHDF-neo	bronchial:	n/a
14	chrX:56764293-56764343	PFSK-1	brain:	n/a
15	chrX:56764796-56764846	HEK293	kidney:	embryo
16	chrX:56764293-56764343	HL-60	blood:	n/a
17	chrX:56764293-56764343	GM12891	blood:	n/a
18	chrX:56764293-56764343	NH-A	brain:	n/a
19	chrX:56764796-56764846	AG04449	skin:	fetal
20	chrX:56764796-56764846	PANC-1	pancreas:	n/a
21	chrX:56764796-56764846	MCF10A-Er-Src	breast:	n/a
22	chrX:56764293-56764343	SAEC	small airway:	n/a
23	chrX:56764293-56764343	HRE	kidney:	n/a
24	chrX:56764796-56764846	AG10803	skin:	n/a
25	chrX:56764293-56764343	AG09319	gingival:	n/a
26	chrX:56764796-56764846	IMR90	lung:	fetal
27	chrX:56764796-56764846	NB4	blood:	n/a
28	chrX:56764796-56764846	PFSK-1	brain:	n/a
29	chrX:56764796-56764846	Hela-S3	cervix:	n/a
30	chrX:56764293-56764343	GM06990	blood:	n/a
31	chrX:56764293-56764343	PrEC	prostate:	n/a
32	chrX:56764293-56764343	Caco-2	colon:	n/a
33	chrX:56764293-56764343	HUVEC	blood vessel:	n/a
34	chrX:56764796-56764846	AG04450	lung:	fetal
35	chrX:56764293-56764343	A549	lung:	n/a
36	chrX:56764293-56764343	H1-hESC	embryonic stem cell:	embryo
37	chrX:56764796-56764846	NH-A	brain:	n/a
38	chrX:56764796-56764846	PrEC	prostate:	n/a
39	chrX:56764796-56764846	NHBE	bronchial:	n/a
40	chrX:56764796-56764846	A549	lung:	n/a
41	chrX:56764796-56764846	HCM	heart:	n/a
42	chrX:56764796-56764846	RPTEC	kidney:	n/a
43	chrX:56764293-56764343	MCF-7	breast:	n/a
44	chrX:56764293-56764343	BJ	skin:	n/a
45	chrX:56764796-56764846	U87	brain:	n/a
46	chrX:56764796-56764846	NT2-D1	testis:	n/a
47	chrX:56764293-56764343	AG04449	skin:	fetal
48	chrX:56764796-56764846	K562	blood:	n/a
49	chrX:56764796-56764846	ProgFib	skin:	n/a
50	chrX:56764293-56764343	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:56755952..56758658-chrX:56787740..56790221,2	MCF-7	breast:
2	chrX:56754417..56757216-chrX:56757629..56759617,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBQLN2-6	chrX:56762139-56762989	NONHSAT137275
2	lnc-UBQLN2-5	chrX:56760584-56761001	NONHSAT137274
3	lnc-SPIN3-4	chrX:56763221-56764017	NR_002308
4	lnc-UBQLN2-7	chrX:56772443-56772747	ucscGeneNc_uc004dut_2
5	lnc-UBQLN2-4	chrX:56759851-56760504	NONHSAT137273

Variant related genes	Relation type
UQCRBP1	TF binding region
UQCRBP1	CpG island
ENSG00000204272	chromatin interactions

Extended variants
information (count: 201 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:201 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5914778	chrX:56758231-56758232	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192897343	chrX:56758323-56758324	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182761871	chrX:56758346-56758347	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187788120	chrX:56758494-56758495	Active TSS Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192647563	chrX:56758693-56758694	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184586149	chrX:56758973-56758974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189031975	chrX:56759096-56759097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191878184	chrX:56759110-56759111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547133313	chrX:56759328-56759329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs377456494	chrX:56759365-56759366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12690340	chrX:56759371-56759372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs201981508	chrX:56759406-56759407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs66887234	chrX:56759407-56759408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12839871	chrX:56759445-56759446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565776270	chrX:56759492-56759493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184909955	chrX:56759526-56759527	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189747271	chrX:56759655-56759656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181335954	chrX:56759796-56759797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199734319	chrX:56759833-56759834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs5913992	chrX:56760004-56760005	Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
21	rs34202128	chrX:56760031-56760032	Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
22	rs72621715	chrX:56760126-56760127	Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
23	rs140986251	chrX:56760275-56760276	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs189393496	chrX:56760425-56760426	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs28706907	chrX:56760558-56760559	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181967804	chrX:56760643-56760644	Strong transcription Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs138582999	chrX:56760817-56760818	Strong transcription Weak transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs186292422	chrX:56761142-56761143	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149260489	chrX:56761229-56761230	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6521511	chrX:56761346-56761347	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190675286	chrX:56761383-56761384	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147973317	chrX:56761647-56761648	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs141636305	chrX:56761847-56761848	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs376173340	chrX:56761899-56761900	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs559809280	chrX:56761901-56761902	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs2873172	chrX:56761922-56761923	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs141047689	chrX:56761968-56761969	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs551754346	chrX:56762122-56762123	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs181733252	chrX:56762203-56762204	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs186960580	chrX:56762240-56762241	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs191305437	chrX:56762248-56762249	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs532926762	chrX:56762253-56762254	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs59743966	chrX:56762395-56762396	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs183220521	chrX:56762477-56762478	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs187659002	chrX:56762518-56762519	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs60464842	chrX:56762634-56762635	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs6612629	chrX:56762778-56762779	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs189615442	chrX:56762786-56762787	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs371081074	chrX:56762946-56762947	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs183238167	chrX:56762962-56762963	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	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
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:56754800-56758600	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chrX:56755000-56758600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chrX:56755200-56758600	Active TSS	GM12878-XiMat	blood
4	chrX:56756000-56780000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chrX:56757000-56764600	Weak transcription	Pancreas	Pancrea
6	chrX:56757000-56764800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chrX:56757000-56765000	Weak transcription	Placenta	Placenta
8	chrX:56757000-56766800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chrX:56757200-56759800	Weak transcription	Osteobl	bone
10	chrX:56757200-56761000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chrX:56757200-56764800	Weak transcription	Liver	Liver
12	chrX:56757200-56764800	Weak transcription	Fetal Intestine Small	intestine
13	chrX:56757200-56764800	Weak transcription	Left Ventricle	heart
14	chrX:56757200-56765000	Weak transcription	Brain Angular Gyrus	brain
15	chrX:56757200-56765000	Weak transcription	HSMMtube	muscle
16	chrX:56757200-56766600	Weak transcription	Thymus	Thymus
17	chrX:56757200-56769200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chrX:56757200-56773800	Weak transcription	HSMM	muscle
19	chrX:56757200-56775600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chrX:56757200-56777600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chrX:56757400-56758400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chrX:56757400-56758600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chrX:56757400-56758600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chrX:56757400-56759400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chrX:56757400-56761200	Weak transcription	Duodenum Mucosa	Duodenum
26	chrX:56757400-56764800	Weak transcription	Brain Substantia Nigra	brain
27	chrX:56757400-56768000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chrX:56757400-56771600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chrX:56757400-56779400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chrX:56757400-56788000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chrX:56757400-56791200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chrX:56757400-56793200	Weak transcription	NH-A	brain
33	chrX:56757400-56793400	Weak transcription	Fetal Intestine Large	intestine
34	chrX:56757600-56758400	Enhancers	Brain Hippocampus Middle	brain
35	chrX:56757600-56758400	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chrX:56757600-56758400	Enhancers	HUVEC	blood vessel
37	chrX:56757600-56758800	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chrX:56757600-56759800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chrX:56757600-56760200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chrX:56757600-56760200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chrX:56757600-56762400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chrX:56757600-56762600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chrX:56757600-56763400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chrX:56757600-56764200	Weak transcription	Primary hematopoietic stem cells	blood
45	chrX:56757600-56764600	Weak transcription	HMEC	breast
46	chrX:56757600-56765000	Weak transcription	Brain Cingulate Gyrus	brain
47	chrX:56757600-56766600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chrX:56757600-56767600	Weak transcription	A549	lung
49	chrX:56757600-56767800	Weak transcription	Primary B cells from cord blood	blood
50	chrX:56757600-56779600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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