Variant report

Variant	nsv532935
Chromosome Location	chrX:138281469-138764448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1541)
CpG islands
(count:2443)
Chromatin interactive
region (count:59)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1541 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:138295023-138295971	K562	blood:	n/a	n/a
2	ARID3A	chrX:138287512-138287696	K562	blood:	n/a	n/a
3	ARID3A	chrX:138289663-138290110	K562	blood:	n/a	n/a
4	ATF1	chrX:138289392-138290348	K562	blood:	n/a	n/a
5	ATF1	chrX:138295368-138295921	K562	blood:	n/a	n/a
6	ATF2	chrX:138635945-138636320	GM12878	blood:	n/a	n/a
7	ATF2	chrX:138635839-138636421	GM12878	blood:	n/a	n/a
8	ATF3	chrX:138295470-138295866	K562	blood:	n/a	n/a
9	BACH1	chrX:138285444-138285520	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chrX:138635903-138636301	GM12878	blood:	n/a	n/a
11	BATF	chrX:138729786-138730024	GM12878	blood:	n/a	n/a
12	BATF	chrX:138729826-138730115	GM12878	blood:	n/a	n/a
13	BATF	chrX:138372480-138372835	GM12878	blood:	n/a	n/a
14	BATF	chrX:138635905-138636238	GM12878	blood:	n/a	n/a
15	BCL11A	chrX:138635988-138636192	GM12878	blood:	n/a	n/a
16	BCL11A	chrX:138307131-138307396	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chrX:138635980-138636326	GM12878	blood:	n/a	n/a
18	BCL3	chrX:138635969-138636245	GM12878	blood:	n/a	n/a
19	BHLHE40	chrX:138289810-138290157	K562	blood:	n/a	n/a
20	BHLHE40	chrX:138635984-138636294	GM12878	blood:	n/a	n/a
21	BHLHE40	chrX:138295463-138295916	K562	blood:	n/a	n/a
22	BHLHE40	chrX:138287156-138287846	K562	blood:	n/a	n/a
23	BHLHE40	chrX:138285845-138286260	K562	blood:	n/a	n/a
24	BHLHE40	chrX:138291601-138291855	K562	blood:	n/a	n/a
25	CBX3	chrX:138295237-138295989	K562	blood:	n/a	n/a
26	CBX3	chrX:138389778-138390005	K562	blood:	n/a	n/a
27	CBX3	chrX:138285971-138286300	K562	blood:	n/a	n/a
28	CBX3	chrX:138599842-138600120	K562	blood:	n/a	n/a
29	CBX3	chrX:138287013-138287401	K562	blood:	n/a	n/a
30	CBX3	chrX:138389776-138389984	K562	blood:	n/a	n/a
31	CCNT2	chrX:138286505-138286778	K562	blood:	n/a	n/a
32	CCNT2	chrX:138287009-138287448	K562	blood:	n/a	n/a
33	CCNT2	chrX:138295342-138295907	K562	blood:	n/a	n/a
34	CCNT2	chrX:138285810-138286281	K562	blood:	n/a	n/a
35	CEBPB	chrX:138350120-138350314	K562	blood:	n/a	n/a
36	CEBPB	chrX:138350111-138350345	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:138352307-138352507	A549	lung:	n/a	n/a
38	CEBPB	chrX:138700454-138700703	IMR90	lung:	n/a	n/a
39	CEBPB	chrX:138523978-138524255	IMR90	lung:	n/a	n/a
40	CEBPB	chrX:138470736-138470886	A549	lung:	n/a	n/a
41	CEBPB	chrX:138578687-138578998	IMR90	lung:	n/a	n/a
42	CEBPB	chrX:138548048-138548276	MCF-7	breast:	n/a	n/a
43	CEBPB	chrX:138460940-138461004	K562	blood:	n/a	n/a
44	CEBPB	chrX:138568805-138569090	HepG2	liver:	n/a	chrX:138568928-138568939
45	CEBPB	chrX:138487462-138487720	HepG2	liver:	n/a	chrX:138487552-138487563
46	CEBPB	chrX:138700503-138700710	K562	blood:	n/a	n/a
47	CEBPB	chrX:138630682-138630989	IMR90	lung:	n/a	chrX:138630802-138630815 chrX:138630802-138630815
48	CEBPB	chrX:138524043-138524221	K562	blood:	n/a	n/a
49	CEBPB	chrX:138293275-138293587	K562	blood:	n/a	chrX:138293567-138293580
50	CEBPB	chrX:138698838-138699213	IMR90	lung:	n/a	chrX:138698893-138698904

(count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:138724688-138724738	ProgFib	skin:	n/a
2	chrX:138664151-138664201	SAEC	small airway:	n/a
3	chrX:138664151-138664201	HIPEpiC	eye:	n/a
4	chrX:138724688-138724738	ProgFib	skin:	n/a
5	chrX:138664151-138664201	SAEC	small airway:	n/a
6	chrX:138664151-138664201	HIPEpiC	eye:	n/a
7	chrX:138285469-138285519	PFSK-1	brain:	n/a
8	chrX:138285828-138285878	K562	blood:	n/a
9	chrX:138726210-138726260	BJ	skin:	n/a
10	chrX:138286295-138286345	H1-hESC	embryonic stem cell:	embryo
11	chrX:138287613-138287663	HIPEpiC	eye:	n/a
12	chrX:138525808-138525858	AG04450	lung:	fetal
13	chrX:138285540-138285590	ovcar-3	ovarian:	n/a
14	chrX:138612616-138612666	HCT-116	colon:	n/a
15	chrX:138529221-138529271	GM06990	blood:	n/a
16	chrX:138664151-138664201	HL-60	blood:	n/a
17	chrX:138724737-138724787	HCM	heart:	n/a
18	chrX:138664151-138664201	PrEC	prostate:	n/a
19	chrX:138726210-138726260	A549	lung:	n/a
20	chrX:138287654-138287704	HCF	heart:	n/a
21	chrX:138285922-138285972	HEEpiC	esophagus:	n/a
22	chrX:138725077-138725127	ovcar-3	ovarian:	n/a
23	chrX:138285540-138285590	NH-A	brain:	n/a
24	chrX:138637710-138637760	NH-A	brain:	n/a
25	chrX:138530469-138530519	MCF-7	breast:	n/a
26	chrX:138285828-138285878	NH-A	brain:	n/a
27	chrX:138724688-138724738	LNCaP	prostate:	n/a
28	chrX:138285922-138285972	Hepatocyte	liver:	n/a
29	chrX:138287281-138287331	SK-N-SH_RA	brain:	n/a
30	chrX:138612736-138612786	ovcar-3	ovarian:	n/a
31	chrX:138664151-138664201	ProgFib	skin:	n/a
32	chrX:138291593-138291643	AG04450	lung:	fetal
33	chrX:138287529-138287579	ovcar-3	ovarian:	n/a
34	chrX:138612930-138612980	SK-N-MC	brain:	n/a
35	chrX:138287613-138287663	SK-N-MC	brain:	n/a
36	chrX:138529210-138529260	ovcar-3	ovarian:	n/a
37	chrX:138285393-138285443	RPTEC	kidney:	n/a
38	chrX:138287613-138287663	GM12892	blood:	n/a
39	chrX:138285393-138285443	HCT-116	colon:	n/a
40	chrX:138724688-138724738	NT2-D1	testis:	n/a
41	chrX:138287039-138287089	ovcar-3	ovarian:	n/a
42	chrX:138645497-138645547	Jurkat	blood:	n/a
43	chrX:138287613-138287663	HRCEpiC	kidney:	n/a
44	chrX:138291593-138291643	HRPEpiC	eye:	n/a
45	chrX:138530469-138530519	T-47D	breast:	n/a
46	chrX:138285540-138285590	NHDF-neo	bronchial:	n/a
47	chrX:138612930-138612980	HL-60	blood:	n/a
48	chrX:138287603-138287653	SK-N-SH	brain:	n/a
49	chrX:138285469-138285519	NHDF-neo	bronchial:	n/a
50	chrX:138282248-138282298	GM12891	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:138372023..138374491-chrX:138376845..138378767,2	K562	blood:
2	chrX:138283427..138286383-chrX:138318317..138320687,2	MCF-7	breast:
3	chrX:138306244..138308578-chrX:138311859..138314047,2	K562	blood:
4	chrX:138356047..138358814-chrX:138378314..138380829,2	K562	blood:
5	chrX:138446798..138450076-chrX:138451284..138453991,3	K562	blood:
6	chrX:138352078..138354558-chrX:138358074..138360822,2	K562	blood:
7	chrX:138284099..138286707-chrX:138374429..138376739,2	K562	blood:
8	chrX:138446798..138450076-chrX:138451284..138453991,3	K562	blood:
9	chrX:138275396..138277751-chrX:138300612..138302491,2	K562	blood:
10	chrX:138634060..138637033-chrX:138639674..138641583,2	K562	blood:
11	chrX:138287750..138289322-chrX:138289477..138291268,2	K562	blood:
12	chrX:138557281..138558203-chrX:138641564..138642155,3	MCF-7	breast:
13	chrX:137857909..137860601-chrX:138657318..138659293,2	K562	blood:
14	chrX:138282334..138284034-chrX:138350999..138353956,2	K562	blood:
15	chrX:138287750..138289322-chrX:138289477..138291268,2	K562	blood:
16	chrX:138439308..138442299-chrX:138451091..138453391,2	K562	blood:
17	chrX:138285958..138288510-chrX:138312890..138315621,2	MCF-7	breast:
18	chrX:138273663..138275580-chrX:138283129..138285298,2	K562	blood:
19	chrX:138292651..138294859-chrX:138296835..138298420,2	K562	blood:
20	chrX:138292255..138293899-chrX:138300358..138302432,2	K562	blood:
21	chrX:138560687..138562232-chrX:138567372..138569882,2	K562	blood:
22	chrX:138382162..138384388-chrX:138392358..138395096,2	K562	blood:
23	chrX:138292651..138294859-chrX:138296835..138298420,2	K562	blood:
24	chr20:47347091..47347859-chrX:138488421..138489145,2	MCF-7	breast:
25	chrX:138305410..138307857-chrX:138310310..138312252,2	MCF-7	breast:
26	chrX:138285411..138288031-chrX:138303226..138305707,3	K562	blood:
27	chr16:57126223..57126746-chrX:138285972..138286492,2	Hela-S3	cervix:
28	chrX:138634060..138637033-chrX:138639674..138641583,2	K562	blood:
29	chrX:138285215..138287696-chrX:138325143..138327379,2	MCF-7	breast:
30	chrX:138210555..138212279-chrX:138288161..138290124,2	MCF-7	breast:
31	chrX:138208455..138209376-chrX:138511849..138512725,3	MCF-7	breast:
32	chrX:138382162..138384388-chrX:138392358..138395096,2	K562	blood:
33	chrX:138208424..138209008-chrX:138641536..138642500,2	MCF-7	breast:
34	chrX:138396415..138398713-chrX:138400579..138402345,2	K562	blood:
35	chrX:138284334..138287436-chrX:138290637..138294293,4	MCF-7	breast:
36	chrX:138439308..138442299-chrX:138451091..138453391,2	K562	blood:
37	chrX:138687922..138690086-chrX:138692229..138695171,2	MCF-7	breast:
38	chrX:138293752..138295827-chrX:139014869..139017160,2	K562	blood:
39	chrX:138282334..138284034-chrX:138350999..138353956,2	K562	blood:
40	chrX:138560687..138562232-chrX:138567372..138569882,2	K562	blood:
41	chr2:88314358..88316144-chrX:138642872..138645193,2	MCF-7	breast:
42	chrX:137857443..137858431-chrX:138641744..138642437,4	MCF-7	breast:
43	chrX:138285411..138288031-chrX:138303226..138305707,3	K562	blood:
44	chrX:138272536..138275159-chrX:138281329..138282896,2	K562	blood:
45	chrX:138352078..138354558-chrX:138358074..138360822,2	K562	blood:
46	chrX:138306244..138308578-chrX:138311859..138314047,2	K562	blood:
47	chrX:138292255..138293899-chrX:138300358..138302432,2	K562	blood:
48	chrX:138284928..138287239-chrX:138302518..138304914,2	K562	blood:
49	chrX:138285405..138289309-chrX:138291346..138296622,6	MCF-7	breast:
50	chrX:138295717..138298370-chrX:138303162..138305381,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCF2-1	chrX:138651489-138651557	NONHSAT138777
2	lnc-SNURFL-3	chrX:138444199-138444541	NONHSAT138776
3	lnc-SNURFL-3	chrX:138444259-138444468	NONHSAT147754
4	lnc-MCF2-1	chrX:138651032-138651093	NONHSAT138777
5	lnc-ATP11C-1	chrX:138697040-138697109	NONHSAT138779
6	lnc-MCF2-3	chrX:138286222-138286433	NONHSAT138775
7	lnc-ATP11C-1	chrX:138692460-138692497	NONHSAT138779
8	lnc-ATP11C-1	chrX:138695375-138695422	NONHSAT138779
9	lnc-MCF2-3	chrX:138287084-138287153	NONHSAT138775
10	lnc-MCF2-1	chrX:138651277-138651427	NONHSAT138777
11	lnc-ATP11C-1	chrX:138689343-138689938	NONHSAT138779

No data

Variant related genes	Relation type
ENSG00000216114	TF binding region
FGF13	TF binding region
SNURFL	TF binding region
F9	TF binding region
MCF2	TF binding region
SRD5A1P1	TF binding region
ENSG00000216114	CpG island
FGF13	CpG island
SNURFL	CpG island
F9	CpG island
MCF2	CpG island
SRD5A1P1	CpG island
ENSG00000101977	chromatin interactions
ENSG00000101974	chromatin interactions
ENSG00000129682	chromatin interactions
ENSG00000140848	chromatin interactions
ENSG00000222724	chromatin interactions

Extended variants
information (count: 3020 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:3020 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185632370	chrX:138281469-138281470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201801721	chrX:138281471-138281472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201827656	chrX:138281474-138281475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530492617	chrX:138281493-138281494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144693222	chrX:138281738-138281739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183085685	chrX:138281857-138281858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34707195	chrX:138281903-138281904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200390599	chrX:138281931-138281932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148085888	chrX:138282002-138282003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528075559	chrX:138282067-138282068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185893521	chrX:138282258-138282259	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532452292	chrX:138282287-138282288	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569978267	chrX:138282321-138282322	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs67265560	chrX:138282349-138282350	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190814008	chrX:138282403-138282404	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184014680	chrX:138282425-138282426	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150682380	chrX:138282455-138282456	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112625042	chrX:138282529-138282530	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12008913	chrX:138282537-138282538	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188961356	chrX:138282632-138282633	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35086383	chrX:138282695-138282696	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375602678	chrX:138282998-138282999	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190438907	chrX:138283074-138283075	Bivalent Enhancer Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373839021	chrX:138283260-138283261	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143771858	chrX:138283280-138283281	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182767082	chrX:138283286-138283287	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377646320	chrX:138283299-138283300	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187454327	chrX:138283316-138283317	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111308972	chrX:138283509-138283510	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145974735	chrX:138283557-138283558	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12857787	chrX:138283570-138283571	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191497854	chrX:138283671-138283672	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76501795	chrX:138283800-138283801	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76767070	chrX:138283801-138283802	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184819232	chrX:138283938-138283939	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371847778	chrX:138283947-138283948	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368119617	chrX:138283968-138283969	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77256831	chrX:138283986-138283987	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs61334649	chrX:138284057-138284058	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs72289376	chrX:138284058-138284059	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs397954603	chrX:138284061-138284062	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139884757	chrX:138284070-138284071	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112103649	chrX:138284175-138284176	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187839495	chrX:138284203-138284204	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534833788	chrX:138284474-138284475	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192520137	chrX:138284492-138284493	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7066638	chrX:138284582-138284583	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369628701	chrX:138284592-138284593	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74816499	chrX:138284615-138284616	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375855142	chrX:138284694-138284695	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	17603634	CNVD
abnormal development	18461090	CNVD
Multiple myeloma	17550852	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Hereditary coagulopathy	21993689	CNVD
Cerebellar atrophy	21569638	CNVD
Fragile x	21569638	CNVD
Abnormal corpus callosum	21572526	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Haemophilia	22138850	CNVD
Hemophilia B	22138850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD
Congenital diaphragmatic hernia	21525063	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138274200-138282200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chrX:138277400-138285200	Weak transcription	Pancreas	Pancrea
3	chrX:138277600-138282400	Weak transcription	Stomach Mucosa	stomach
4	chrX:138277600-138284000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chrX:138277600-138285400	Weak transcription	Liver	Liver
6	chrX:138277600-138286000	Weak transcription	Right Atrium	heart
7	chrX:138277800-138282000	Weak transcription	K562	blood
8	chrX:138278000-138282400	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chrX:138278600-138281600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chrX:138278800-138281800	Weak transcription	Psoas Muscle	Psoas
11	chrX:138279000-138281600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chrX:138279000-138284800	Weak transcription	Gastric	stomach
13	chrX:138279400-138282400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chrX:138279600-138282000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chrX:138281400-138282000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chrX:138281600-138282800	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chrX:138281600-138283000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chrX:138281800-138282000	Enhancers	Esophagus	oesophagus
19	chrX:138281800-138282600	Enhancers	Psoas Muscle	Psoas
20	chrX:138282000-138283000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chrX:138282000-138283400	Enhancers	K562	blood
22	chrX:138282000-138284200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chrX:138282200-138283000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chrX:138282200-138283600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chrX:138282200-138283600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chrX:138282400-138282600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chrX:138282400-138282600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chrX:138282400-138282600	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chrX:138282400-138282800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chrX:138282400-138282800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chrX:138282400-138283000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
32	chrX:138282400-138283000	Bivalent Enhancer	Fetal Stomach	stomach
33	chrX:138282400-138283000	Enhancers	Stomach Mucosa	stomach
34	chrX:138282400-138283200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chrX:138282400-138283600	Enhancers	NH-A	brain
36	chrX:138282600-138282800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chrX:138282600-138282800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
38	chrX:138282600-138282800	Enhancers	Esophagus	oesophagus
39	chrX:138282600-138282800	Bivalent Enhancer	Fetal Lung	lung
40	chrX:138282600-138282800	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chrX:138282600-138283000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
42	chrX:138282600-138283200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
43	chrX:138282600-138284800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chrX:138282600-138284800	Weak transcription	Psoas Muscle	Psoas
45	chrX:138282800-138283200	Enhancers	HSMMtube	muscle
46	chrX:138282800-138283400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chrX:138282800-138284400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chrX:138282800-138285000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chrX:138282800-138285400	Weak transcription	Esophagus	oesophagus
50	chrX:138283000-138285000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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