Variant report

Variant	esv3648994
Chromosome Location	chrX:153829693-153919915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:488)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chrX:153884227-153884242	K562	blood:	n/a	n/a
2	BHLHE40	chrX:153906582-153906813	HepG2	liver:	n/a	n/a
3	BHLHE40	chrX:153906575-153906898	HepG2	liver:	n/a	n/a
4	CBX3	chrX:153852224-153852537	K562	blood:	n/a	n/a
5	CBX3	chrX:153842785-153843168	K562	blood:	n/a	n/a
6	CBX3	chrX:153871945-153872379	K562	blood:	n/a	n/a
7	CBX3	chrX:153852121-153852575	K562	blood:	n/a	n/a
8	CBX3	chrX:153842824-153843144	K562	blood:	n/a	n/a
9	CBX3	chrX:153849260-153849574	K562	blood:	n/a	n/a
10	CBX3	chrX:153841884-153842166	K562	blood:	n/a	n/a
11	CBX3	chrX:153890866-153891256	K562	blood:	n/a	n/a
12	CEBPB	chrX:153835689-153836059	HepG2	liver:	n/a	chrX:153835865-153835876
13	CEBPB	chrX:153835734-153836037	A549	lung:	n/a	chrX:153835865-153835876
14	CEBPB	chrX:153835730-153836066	MCF-7	breast:	n/a	chrX:153835865-153835876
15	CEBPB	chrX:153832522-153832702	A549	lung:	n/a	chrX:153832613-153832626
16	CEBPB	chrX:153832212-153832797	Hela-S3	cervix:	n/a	chrX:153832613-153832626
17	CEBPB	chrX:153834666-153834908	K562	blood:	n/a	n/a
18	CEBPB	chrX:153835755-153836020	Hela-S3	cervix:	n/a	chrX:153835865-153835876
19	CHD2	chrX:153832295-153832643	Hela-S3	cervix:	n/a	n/a
20	CTCF	chrX:153852487-153852515	LNCaP	prostate:	n/a	n/a
21	CTCF	chrX:153848161-153848247	GM10266	blood:	n/a	n/a
22	CTCF	chrX:153862113-153862215	GM10266	blood:	n/a	chrX:153862128-153862137 chrX:153862122-153862140
23	CTCF	chrX:153848489-153848544	GM10248	blood:	n/a	n/a
24	CTCF	chrX:153860022-153860089	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chrX:153863311-153863395	Medullo	brain:	n/a	n/a
26	CTCF	chrX:153863968-153864032	GM20000	blood:	n/a	n/a
27	CTCF	chrX:153842236-153842403	Gliobla	brain:	n/a	n/a
28	CTCF	chrX:153860850-153860913	LNCaP	prostate:	n/a	n/a
29	CTCF	chrX:153841951-153842152	MCF-7	breast:	n/a	n/a
30	CTCF	chrX:153864296-153864337	GM10248	blood:	n/a	n/a
31	CTCF	chrX:153849361-153849565	Kidney_OC	kidney:	n/a	chrX:153849462-153849478 chrX:153849466-153849474 chrX:153849463-153849484 chrX:153849461-153849479
32	CTCF	chrX:153857270-153857490	GM12892	blood:	n/a	chrX:153857409-153857427
33	CTCF	chrX:153845762-153845869	GM10266	blood:	n/a	n/a
34	CTCF	chrX:153862334-153862464	GM19239	blood:	n/a	n/a
35	CTCF	chrX:153864365-153864516	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chrX:153849243-153849618	LNCaP	prostate:	n/a	chrX:153849462-153849478 chrX:153849466-153849474 chrX:153849463-153849484 chrX:153849461-153849479
37	CTCF	chrX:153876241-153876257	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chrX:153867946-153867982	GM13976	blood:	n/a	n/a
39	CTCF	chrX:153849314-153849589	A549	lung:	n/a	chrX:153849462-153849478 chrX:153849466-153849474 chrX:153849463-153849484 chrX:153849461-153849479
40	CTCF	chrX:153841916-153842159	A549	lung:	n/a	n/a
41	CTCF	chrX:153841929-153842160	MCF-7	breast:	n/a	n/a
42	CTCF	chrX:153849358-153849584	Lung_OC	lung:	n/a	chrX:153849462-153849478 chrX:153849466-153849474 chrX:153849463-153849484 chrX:153849461-153849479
43	CTCF	chrX:153857310-153857553	GM20000	blood:	n/a	chrX:153857409-153857427
44	CTCF	chrX:153872831-153872928	GM10266	blood:	n/a	n/a
45	CTCF	chrX:153871156-153871223	GM20000	blood:	n/a	n/a
46	CTCF	chrX:153841944-153842173	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chrX:153842028-153842147	GM13976	blood:	n/a	n/a
48	CTCF	chrX:153862057-153862220	K562	blood:	n/a	chrX:153862128-153862137 chrX:153862122-153862140
49	CTCF	chrX:153849329-153849598	Pancreas_OC	pancreas:	n/a	chrX:153849462-153849478 chrX:153849466-153849474 chrX:153849463-153849484 chrX:153849461-153849479
50	CTCF	chrX:153857664-153857773	GM10248	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:153880742-153880792	BJ	skin:	n/a
2	chrX:153883245-153883295	AG04449	skin:	fetal
3	chrX:153906447-153906497	H1-hESC	embryonic stem cell:	embryo
4	chrX:153883245-153883295	Jurkat	blood:	n/a
5	chrX:153882028-153882078	HRPEpiC	eye:	n/a
6	chrX:153880742-153880792	HEK293	kidney:	embryo
7	chrX:153881541-153881591	GM19239	blood:	n/a
8	chrX:153880742-153880792	Hela-S3	cervix:	n/a
9	chrX:153882853-153882903	NHBE	bronchial:	n/a
10	chrX:153883245-153883295	HEEpiC	esophagus:	n/a
11	chrX:153883318-153883368	AG04450	lung:	fetal
12	chrX:153882028-153882078	HEK293	kidney:	embryo
13	chrX:153881541-153881591	PFSK-1	brain:	n/a
14	chrX:153882028-153882078	HUVEC	blood vessel:	n/a
15	chrX:153882028-153882078	Jurkat	blood:	n/a
16	chrX:153883318-153883368	AoSMC	blood vessel:	n/a
17	chrX:153880293-153880343	CMK	blood:	n/a
18	chrX:153882853-153882903	AG09309	skin:	n/a
19	chrX:153882028-153882078	GM12892	blood:	n/a
20	chrX:153906447-153906497	MCF-7	breast:	n/a
21	chrX:153882853-153882903	CMK	blood:	n/a
22	chrX:153883318-153883368	HCPEpiC	choroid plexus:	n/a
23	chrX:153882028-153882078	ProgFib	skin:	n/a
24	chrX:153906447-153906497	AG10803	skin:	n/a
25	chrX:153880742-153880792	HCM	heart:	n/a
26	chrX:153880742-153880792	Caco-2	colon:	n/a
27	chrX:153906447-153906497	HepG2	liver:	n/a
28	chrX:153883318-153883368	H1-hESC	embryonic stem cell:	embryo
29	chrX:153880293-153880343	NHDF-neo	bronchial:	n/a
30	chrX:153883245-153883295	GM12891	blood:	n/a
31	chrX:153883318-153883368	PrEC	prostate:	n/a
32	chrX:153882853-153882903	AG10803	skin:	n/a
33	chrX:153882028-153882078	IMR90	lung:	fetal
34	chrX:153882028-153882078	Hela-S3	cervix:	n/a
35	chrX:153880742-153880792	HCT-116	colon:	n/a
36	chrX:153880293-153880343	AG04450	lung:	fetal
37	chrX:153881541-153881591	GM12878	blood:	n/a
38	chrX:153883245-153883295	U87	brain:	n/a
39	chrX:153906447-153906497	HUVEC	blood vessel:	n/a
40	chrX:153882853-153882903	MCF10A-Er-Src	breast:	n/a
41	chrX:153882853-153882903	AoSMC	blood vessel:	n/a
42	chrX:153881541-153881591	CMK	blood:	n/a
43	chrX:153882028-153882078	HRE	kidney:	n/a
44	chrX:153883245-153883295	NHBE	bronchial:	n/a
45	chrX:153906447-153906497	PANC-1	pancreas:	n/a
46	chrX:153880293-153880343	Hela-S3	cervix:	n/a
47	chrX:153882028-153882078	PANC-1	pancreas:	n/a
48	chrX:153881541-153881591	HL-60	blood:	n/a
49	chrX:153883245-153883295	ProgFib	skin:	n/a
50	chrX:153880742-153880792	T-47D	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:153770673..153771411-chrX:153877763..153878515,2	MCF-7	breast:
2	chrX:153718876..153719771-chrX:153877675..153878348,2	MCF-7	breast:
3	chrX:153825422..153827737-chrX:153828218..153830991,2	K562	blood:
4	chrX:153877950..153878544-chrX:154216332..154217020,2	MCF-7	breast:
5	chrX:153826650..153830451-chrX:153834350..153838569,4	MCF-7	breast:
6	chrX:153826930..153829877-chrX:153833885..153836886,3	MCF-7	breast:
7	chrX:153774436..153776953-chrX:153831289..153833251,2	MCF-7	breast:
8	chrX:153900048..153901803-chrX:153902904..153904606,2	K562	blood:
9	chrX:153769556..153770370-chrX:153878017..153878518,2	MCF-7	breast:
10	chr8:102132680..102133483-chrX:153877983..153878973,2	MCF-7	breast:
11	chrX:153833912..153836898-chrX:153977644..153980565,2	K562	blood:
12	chrX:153903769..153907661-chrX:153908042..153910580,3	K562	blood:
13	X:153771683-153779571..X:153882988-153886134	GM12878	blood:
14	chrX:153877989..153878508-chrX:153926907..153927860,2	MCF-7	breast:
15	chrX:153826650..153830451-chrX:153834350..153838569,4	MCF-7	breast:
16	chrX:153882429..153884469-chrX:153886893..153889324,3	K562	blood:
17	chrX:153882429..153884469-chrX:153886893..153889324,3	K562	blood:
18	chrX:153602433..153603353-chrX:153878049..153878762,2	MCF-7	breast:
19	chrX:153769248..153770465-chrX:153877772..153878953,6	MCF-7	breast:
20	chrX:153647888..153648853-chrX:153877953..153878815,7	MCF-7	breast:
21	chrX:153647888..153648798-chrX:153877953..153878815,5	MCF-7	breast:
22	chrX:153824667..153827046-chrX:153830965..153832603,2	MCF-7	breast:
23	chrX:153900048..153901803-chrX:153902904..153904606,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTAG1A-3	chrX:153882820-153882916	NONHSAT139206
2	lnc-CTAG2-1	chrX:153908409-153908525	NONHSAT139207
3	lnc-CTAG1A-2	chrX:153881967-153882054	NONHSAT139205
4	lnc-CTAG1A-2	chrX:153883029-153883266	NONHSAT139205
5	lnc-CTAG1B-1	chrX:153860739-153861448	NR_027402
6	lnc-CTAG1A-3	chrX:153883365-153883599	NONHSAT139206
7	lnc-CTAG2-1	chrX:153906567-153906571	NONHSAT139207

No data

Variant related genes	Relation type
IKBKGP1	TF binding region
CTAG1B	TF binding region
CTAG2	TF binding region
GAB3	TF binding region
OR3B1P	TF binding region
ENSG00000226141	TF binding region
ATF4P1	TF binding region
ENSG00000232155	TF binding region
IKBKGP1	CpG island
CTAG1B	CpG island
CTAG2	CpG island
GAB3	CpG island
OR3B1P	CpG island
ENSG00000226141	CpG island
ATF4P1	CpG island
ENSG00000232155	CpG island
ENSG00000196924	chromatin interactions
ENSG00000160211	chromatin interactions
ENSG00000073009	chromatin interactions
ENSG00000160219	chromatin interactions
ENSG00000226141	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000102125	chromatin interactions
ENSG00000237619	chromatin interactions
ENSG00000232155	chromatin interactions

Extended variants
information (count: 615 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7879049	chrX:153829693-153829694	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139569170	chrX:153829893-153829894	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs149331933	chrX:153829962-153829963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372423097	chrX:153830097-153830098	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200706216	chrX:153830111-153830112	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147427606	chrX:153830121-153830122	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs112503673	chrX:153830128-153830129	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs139732065	chrX:153830137-153830138	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11797011	chrX:153830223-153830224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189289257	chrX:153830233-153830234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181025871	chrX:153830677-153830678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112133389	chrX:153830774-153830775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73575214	chrX:153830788-153830789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374095733	chrX:153831180-153831181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185004355	chrX:153831188-153831189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188690081	chrX:153831306-153831307	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373263116	chrX:153831321-153831322	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201658987	chrX:153831390-153831391	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376461121	chrX:153831448-153831449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181161184	chrX:153831480-153831481	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs186762870	chrX:153831520-153831521	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76064671	chrX:153831567-153831568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs191659776	chrX:153831730-153831731	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs5945211	chrX:153831748-153831749	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs183379324	chrX:153831855-153831856	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs73575216	chrX:153831905-153831906	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186576583	chrX:153831938-153831939	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs190947213	chrX:153832015-153832016	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs182418415	chrX:153832068-153832069	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs151097031	chrX:153832122-153832123	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs12689517	chrX:153832131-153832132	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs113051814	chrX:153832236-153832237	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs186656830	chrX:153832295-153832296	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs192746195	chrX:153832408-153832409	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183080784	chrX:153832425-153832426	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs188416761	chrX:153832546-153832547	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs150235918	chrX:153832687-153832688	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs370905641	chrX:153832694-153832695	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs34426290	chrX:153832727-153832728	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs193195537	chrX:153832760-153832761	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs185158376	chrX:153832831-153832832	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs374282670	chrX:153832921-153832922	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs377291799	chrX:153833089-153833090	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs189445785	chrX:153833141-153833142	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192441396	chrX:153833234-153833235	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370547695	chrX:153833297-153833298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs5986998	chrX:153833300-153833301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200412189	chrX:153833594-153833595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73575219	chrX:153833609-153833610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145249513	chrX:153833772-153833773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Neuroblastoma	18923191	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
lymphocytic leukemia	21291569	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 abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
abnormal development	18461090	CNVD
Multiple myeloma	17550852	CNVD
Premature ovarian failure	20952765	CNVD
Abnormal corpus callosum	21572526	CNVD
Breast cancer	21364760	CNVD
Astrocytoma	22246337	CNVD
Cerebellar atrophy	21569638	CNVD
periventricular nodular heterotopia	21572526	CNVD
Cerebellar hypoplasia	21569638	CNVD
Hoyeraal-Hreidarsson syndrome	21569638	CNVD
Oto-palato-digital type II	21569638	CNVD
incontinentia pigmenti anhidrotic ectodermal dysplasia with immunodeficiency	18350553	CNVD
Aqueductal stenosis	21572526	CNVD
Hirschsprung''s Disease	21712996	CNVD
Vermis hypoplasia	21569638	CNVD
X-linked hydrocephalus	21569638	CNVD
Rett syndrome	21569638	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Epilepsy	20970697	CNVD
Hemophilia A	17823971	CNVD
Rett syndrome	18923514	CNVD
Rett syndrome	22241247	CNVD
Intellectual disability	21984752	CNVD
Mental retardation	19951919	CNVD
Hypotonia	17088400	CNVD
Intellectual disability	22511893	CNVD
Mental retardation	17088400	CNVD
Mental retardation	21119712	CNVD
Neurodevelopmental disorder	19324899	CNVD
Recurrent Infections	17088400	CNVD
Rett syndrome	22283845	CNVD
Rett syndrome	21383316	CNVD
Cryptorchidism	21048976	CNVD
Disorders of sex development	21048976	CNVD
Cervical cancer	21062161	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Hemophilia A	18787571	CNVD
Hunters syndrom	18787571	CNVD
Prader-willi syndrome	20588305	CNVD
Mental retardation	19057379	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
abortions and stillbirths	19751515	CNVD
Hereditary coagulopathy	21993689	CNVD
Intellectual disability	23615299	CNVD
Mental retardation	17621639	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Heart failure	16880705	CNVD
Haemophilia	22138850	CNVD
Incontinentia Pigmenti	22121116	CNVD
Pancreatic cancer	17952125	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:153825400-153832000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chrX:153828000-153829800	Enhancers	HMEC	breast
3	chrX:153828000-153833000	Enhancers	HSMMtube	muscle
4	chrX:153828200-153829800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chrX:153828200-153831800	Weak transcription	Primary hematopoietic stem cells	blood
6	chrX:153828400-153829800	Enhancers	Muscle Satellite Cultured Cells	--
7	chrX:153828400-153830200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chrX:153828400-153830200	Flanking Active TSS	Hela-S3	cervix
9	chrX:153828400-153830200	Enhancers	NHDF-Ad	bronchial
10	chrX:153828400-153830200	Enhancers	NHEK	skin
11	chrX:153828400-153835000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chrX:153828600-153831000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chrX:153828600-153833400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chrX:153828800-153831600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chrX:153828800-153833200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chrX:153829000-153831800	Weak transcription	A549	lung
17	chrX:153829000-153832000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chrX:153829200-153831600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chrX:153829400-153829800	Enhancers	Osteobl	bone
20	chrX:153829400-153830000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chrX:153829400-153830200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chrX:153829400-153830400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chrX:153829400-153830600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chrX:153829400-153833000	Enhancers	HSMM	muscle
25	chrX:153829600-153831600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chrX:153829600-153831800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chrX:153829600-153832000	Weak transcription	NH-A	brain
28	chrX:153829800-153831200	Weak transcription	HMEC	breast
29	chrX:153829800-153831800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chrX:153829800-153832000	Weak transcription	Osteobl	bone
31	chrX:153829800-153836000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chrX:153830000-153830200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chrX:153830200-153831000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chrX:153830200-153831000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chrX:153830200-153831800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chrX:153830200-153832000	Weak transcription	NHDF-Ad	bronchial
37	chrX:153830200-153833200	Enhancers	Hela-S3	cervix
38	chrX:153830400-153830600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chrX:153830600-153831800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chrX:153831000-153831400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chrX:153831000-153833000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chrX:153831000-153833200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chrX:153831200-153833200	Enhancers	HMEC	breast
44	chrX:153831400-153831600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chrX:153831600-153832600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chrX:153831600-153833000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chrX:153831600-153833000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chrX:153831600-153833000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chrX:153831600-153833000	Enhancers	NHEK	skin
50	chrX:153831800-153832200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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