Variant report

Variant	nsv593696
Chromosome Location	chr4:10140551-10168849
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	ARID3A	chr4:10159442-10159716	K562	blood:	n/a	n/a
2	ATF1	chr4:10159418-10159720	K562	blood:	n/a	n/a
3	ATF2	chr4:10159321-10159751	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:10159305-10159743	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
6	ATF3	chr4:10159392-10159666	K562	blood:	n/a	chr4:10159502-10159515
7	BACH1	chr4:10166957-10167185	K562	blood:	n/a	n/a
8	BACH1	chr4:10166286-10166294	K562	blood:	n/a	n/a
9	BACH1	chr4:10159277-10159771	K562	blood:	n/a	n/a
10	BHLHE40	chr4:10159446-10159651	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:10164926-10165017	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:10163933-10164279	HepG2	liver:	n/a	n/a
13	BHLHE40	chr4:10159371-10160168	HepG2	liver:	n/a	chr4:10159971-10159980 chr4:10159965-10159986 chr4:10159971-10159980
14	BHLHE40	chr4:10159283-10159719	K562	blood:	n/a	n/a
15	BHLHE40	chr4:10142964-10143314	K562	blood:	n/a	n/a
16	CBX3	chr4:10161871-10162559	K562	blood:	n/a	n/a
17	CEBPB	chr4:10160205-10160400	HepG2	liver:	n/a	chr4:10160238-10160251
18	CEBPB	chr4:10163951-10164171	HepG2	liver:	n/a	chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164077-10164088 chr4:10164076-10164087 chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164078-10164087 chr4:10164078-10164087
19	CEBPB	chr4:10163943-10164279	HepG2	liver:	n/a	chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164077-10164088 chr4:10164076-10164087 chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164078-10164087 chr4:10164078-10164087
20	CEBPB	chr4:10164038-10164238	A549	lung:	n/a	chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164077-10164088 chr4:10164076-10164087 chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164078-10164087 chr4:10164078-10164087
21	CEBPB	chr4:10163904-10164275	HepG2	liver:	n/a	chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164077-10164088 chr4:10164076-10164087 chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164078-10164087 chr4:10164078-10164087
22	CEBPB	chr4:10166304-10166613	K562	blood:	n/a	chr4:10166484-10166495
23	CEBPB	chr4:10163990-10164230	K562	blood:	n/a	chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164077-10164088 chr4:10164076-10164087 chr4:10164076-10164089 chr4:10164078-10164087 chr4:10164078-10164087 chr4:10164078-10164087
24	CHD1	chr4:10159370-10160244	IMR90	lung:	n/a	n/a
25	CHD2	chr4:10143239-10143269	K562	blood:	n/a	n/a
26	CHD2	chr4:10159469-10159783	K562	blood:	n/a	n/a
27	CHD2	chr4:10142301-10142459	HepG2	liver:	n/a	n/a
28	CHD2	chr4:10161817-10161900	HepG2	liver:	n/a	n/a
29	CTCF	chr4:10162080-10162230	HFF	foreskin:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
30	CTCF	chr4:10161883-10162256	K562	blood:	n/a	chr4:10162084-10162105 chr4:10162082-10162100 chr4:10161946-10161959
31	CTCF	chr4:10159540-10159690	HBMEC	blood vessel:	n/a	chr4:10159567-10159588 chr4:10159566-10159582 chr4:10159568-10159577 chr4:10159568-10159581 chr4:10159565-10159583
32	CTCF	chr4:10166407-10166855	H1-hESC	embryonic stem cell:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
33	CTCF	chr4:10159500-10159650	NHDF-neo	bronchial:	n/a	chr4:10159567-10159588 chr4:10159566-10159582 chr4:10159568-10159577 chr4:10159568-10159581 chr4:10159565-10159583
34	CTCF	chr4:10161971-10162204	HUVEC	blood vessel:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
35	CTCF	chr4:10162020-10162170	SK-N-SH_RA	brain:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
36	CTCF	chr4:10159458-10159727	T-47D	breast:	n/a	chr4:10159567-10159588 chr4:10159566-10159582 chr4:10159568-10159577 chr4:10159568-10159581 chr4:10159565-10159583
37	CTCF	chr4:10166620-10166770	HVMF	connective:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
38	CTCF	chr4:10166580-10166730	AoAF	blood vessel:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
39	CTCF	chr4:10166600-10166750	MCF-7	breast:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
40	CTCF	chr4:10142620-10142770	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr4:10159460-10159610	GM12875	blood:	n/a	chr4:10159567-10159588 chr4:10159566-10159582 chr4:10159568-10159577 chr4:10159568-10159581 chr4:10159565-10159583
42	CTCF	chr4:10166572-10166748	H1-hESC	embryonic stem cell:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
43	CTCF	chr4:10166520-10166670	GM12872	blood:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
44	CTCF	chr4:10162056-10162130	GM19239	blood:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
45	CTCF	chr4:10162040-10162190	BJ	skin:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
46	CTCF	chr4:10166580-10166730	HBMEC	blood vessel:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
47	CTCF	chr4:10161959-10162174	T-47D	breast:	n/a	chr4:10162084-10162105 chr4:10162082-10162100
48	CTCF	chr4:10143160-10143310	SK-N-SH_RA	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
49	CTCF	chr4:10166519-10166833	LNCaP	prostate:	n/a	chr4:10166640-10166653 chr4:10166637-10166655
50	CTCF	chr4:10166580-10166730	GM12872	blood:	n/a	chr4:10166640-10166653 chr4:10166637-10166655

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10147330-10147380	AG09309	skin:	n/a
2	chr4:10147302-10147352	HepG2	liver:	n/a
3	chr4:10147100-10147150	Jurkat	blood:	n/a
4	chr4:10149849-10149899	CMK	blood:	n/a
5	chr4:10147038-10147088	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:10143053-10143103	BE2_C	brain:	n/a
7	chr4:10160060-10160110	AG09319	gingival:	n/a
8	chr4:10147302-10147352	HMEC	breast:	n/a
9	chr4:10147606-10147656	GM12878	blood:	n/a
10	chr4:10160060-10160110	Caco-2	colon:	n/a
11	chr4:10143053-10143103	AG04450	lung:	fetal
12	chr4:10160060-10160110	ECC-1	luminal epithelium:	n/a
13	chr4:10160060-10160110	RPTEC	kidney:	n/a
14	chr4:10149849-10149899	IMR90	lung:	fetal
15	chr4:10147100-10147150	HRE	kidney:	n/a
16	chr4:10147100-10147150	IMR90	lung:	fetal
17	chr4:10147330-10147380	RPTEC	kidney:	n/a
18	chr4:10147606-10147656	AG10803	skin:	n/a
19	chr4:10145483-10145533	RPTEC	kidney:	n/a
20	chr4:10147302-10147352	NB4	blood:	n/a
21	chr4:10147606-10147656	AG04449	skin:	fetal
22	chr4:10149849-10149899	SK-N-SH_RA	brain:	n/a
23	chr4:10145483-10145533	HCT-116	colon:	n/a
24	chr4:10143053-10143103	SKMC	muscle:	n/a
25	chr4:10147302-10147352	HRPEpiC	eye:	n/a
26	chr4:10147330-10147380	HEK293	kidney:	embryo
27	chr4:10145483-10145533	BE2_C	brain:	n/a
28	chr4:10147100-10147150	Caco-2	colon:	n/a
29	chr4:10147330-10147380	SK-N-SH	brain:	n/a
30	chr4:10145483-10145533	AG04450	lung:	fetal
31	chr4:10147302-10147352	HAEpiC	amniotic membrane:	n/a
32	chr4:10149849-10149899	HEEpiC	esophagus:	n/a
33	chr4:10147606-10147656	LNCaP	prostate:	n/a
34	chr4:10147330-10147380	PrEC	prostate:	n/a
35	chr4:10147302-10147352	PANC-1	pancreas:	n/a
36	chr4:10160060-10160110	NB4	blood:	n/a
37	chr4:10149849-10149899	HepG2	liver:	n/a
38	chr4:10160060-10160110	Hepatocyte	liver:	n/a
39	chr4:10147038-10147088	GM06990	blood:	n/a
40	chr4:10147302-10147352	AG10803	skin:	n/a
41	chr4:10147302-10147352	PFSK-1	brain:	n/a
42	chr4:10143053-10143103	SK-N-SH_RA	brain:	n/a
43	chr4:10147038-10147088	GM12878	blood:	n/a
44	chr4:10147100-10147150	AG04450	lung:	fetal
45	chr4:10147038-10147088	HCPEpiC	choroid plexus:	n/a
46	chr4:10147606-10147656	HepG2	liver:	n/a
47	chr4:10160060-10160110	HRE	kidney:	n/a
48	chr4:10149849-10149899	PANC-1	pancreas:	n/a
49	chr4:10147606-10147656	GM12892	blood:	n/a
50	chr4:10147038-10147088	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
2	chr4:10155458..10156959-chr4:10169942..10172746,2	K562	blood:
3	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
4	chr4:10166196..10167366-chr4:10404929..10406035,4	MCF-7	breast:
5	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
6	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
7	chr4:10159584..10164126-chr4:10173679..10176923,6	K562	blood:
8	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
9	chr4:10161449..10162536-chr4:10550736..10551916,8	MCF-7	breast:
10	chr4:10123771..10125496-chr4:10158100..10160475,2	K562	blood:
11	chr4:10118098..10119029-chr4:10159089..10159710,2	MCF-7	breast:
12	chr4:10166710..10169319-chr4:10326529..10330099,3	K562	blood:
13	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
14	chr4:10161526..10162602-chr4:10405096..10406350,5	K562	blood:
15	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
16	chr4:10156374..10159170-chr4:10457530..10459890,2	K562	blood:
17	chr4:10166236..10167092-chr4:10405236..10406016,3	MCF-7	breast:
18	chr4:10153604..10155530-chr4:10159159..10161032,2	K562	blood:
19	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
20	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:
21	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
22	chr4:10159016..10159805-chr4:10405257..10406163,3	MCF-7	breast:
23	chr4:10159145..10160030-chr4:10550948..10551977,4	MCF-7	breast:
24	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
25	chr4:10157043..10158718-chr4:10551029..10552565,2	K562	blood:
26	chr4:10161152..10162147-chr4:10556178..10556908,2	K562	blood:
27	chr4:10118185..10123341-chr4:10157230..10162785,8	K562	blood:
28	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
29	chr4:10162053..10164420-chr4:10458395..10460769,2	K562	blood:
30	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
31	chr4:10166113..10167122-chr4:10405126..10405888,4	K562	blood:
32	chr4:10118527..10121179-chr4:10164648..10167186,3	K562	blood:
33	chr4:10158010..10160333-chr4:10437817..10440737,2	K562	blood:
34	chr4:10143164..10147494-chr4:10150670..10153852,4	K562	blood:
35	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
36	chr4:10166189..10167113-chr4:10551000..10552086,3	MCF-7	breast:
37	chr4:10160663..10163901-chr4:10177399..10182680,5	K562	blood:
38	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
39	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
40	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
41	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
42	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
43	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
44	chr4:10166490..10167101-chr4:10539409..10540077,2	MCF-7	breast:
45	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
46	chr4:10117458..10122489-chr4:10158161..10162241,5	MCF-7	breast:
47	chr4:10117985..10121218-chr4:10149186..10152668,4	MCF-7	breast:
48	chr4:10117824..10124820-chr4:10157230..10164396,13	K562	blood:
49	chr4:10117694..10121179-chr4:10148695..10151564,3	MCF-7	breast:
50	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
2	lnc-WDR1-6	chr4:10168783-10169389	NONHSAT095487
3	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429
4	lnc-WDR1-4	chr4:10159007-10159491	NONHSAT095472

Variant related genes	Relation type
ENSG00000250393	TF binding region
ENSG00000250393	CpG island
ENSG00000178163	chromatin interactions
ENSG00000250393	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000251296	chromatin interactions

Extended variants
information (count: 2380 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10022911	chr4:10140551-10140552	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566687070	chr4:10140552-10140553	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs61033604	chr4:10140570-10140571	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548630636	chr4:10140577-10140578	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567003919	chr4:10140578-10140579	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs537874281	chr4:10140583-10140584	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs180793414	chr4:10140589-10140590	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs571557376	chr4:10140594-10140595	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538515941	chr4:10140614-10140615	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141375908	chr4:10140616-10140617	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572241894	chr4:10140622-10140623	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540746724	chr4:10140624-10140625	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs543926750	chr4:10140631-10140632	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555932810	chr4:10140642-10140643	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs574029332	chr4:10140643-10140644	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs562213098	chr4:10140645-10140646	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs187628833	chr4:10140646-10140647	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145166069	chr4:10140649-10140650	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533690903	chr4:10140651-10140652	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs545252737	chr4:10140673-10140674	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368046706	chr4:10140676-10140677	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs191941115	chr4:10140687-10140688	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549142454	chr4:10140694-10140695	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77665440	chr4:10140695-10140696	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531297211	chr4:10140704-10140705	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs10020804	chr4:10140724-10140725	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571110315	chr4:10140726-10140727	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs55806494	chr4:10140750-10140751	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs10020887	chr4:10140751-10140752	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182193890	chr4:10140755-10140756	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186549897	chr4:10140768-10140769	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200654232	chr4:10140778-10140779	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574121276	chr4:10140779-10140780	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537914273	chr4:10140780-10140781	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190142493	chr4:10140801-10140802	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577933606	chr4:10140809-10140810	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35077775	chr4:10140825-10140826	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs544983938	chr4:10140826-10140827	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs398063265	chr4:10140829-10140830	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs138970395	chr4:10140839-10140840	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542852057	chr4:10140840-10140841	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561283656	chr4:10140842-10140843	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75682209	chr4:10140850-10140851	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531438914	chr4:10140861-10140862	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182414589	chr4:10140875-10140876	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs60571028	chr4:10140894-10140895	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs58851167	chr4:10140895-10140896	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs114720840	chr4:10140907-10140908	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566026206	chr4:10140910-10140911	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536543304	chr4:10140919-10140920	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10142400-10142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:10142600-10142800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:10142600-10143000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:10142600-10143200	Enhancers	Fetal Thymus	thymus
5	chr4:10142800-10143000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr4:10142800-10143200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr4:10142800-10143200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:10142800-10143200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:10142800-10143200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:10142800-10143200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr4:10142800-10151800	Weak transcription	Spleen	Spleen
12	chr4:10143000-10143200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:10143000-10143200	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr4:10143000-10143200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:10143000-10143200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:10143200-10143600	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr4:10143200-10149800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:10146200-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:10146400-10146800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:10146400-10147600	Enhancers	Primary B cells from peripheral blood	blood
23	chr4:10146600-10147200	Bivalent Enhancer	Primary B cells from cord blood	blood
24	chr4:10149800-10150000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:10151000-10151200	Enhancers	Fetal Stomach	stomach
26	chr4:10151200-10164400	Weak transcription	Right Atrium	heart
27	chr4:10151400-10152400	Weak transcription	Fetal Stomach	stomach
28	chr4:10151800-10152000	Enhancers	Spleen	Spleen
29	chr4:10151800-10153000	Enhancers	Fetal Muscle Leg	muscle
30	chr4:10152000-10152200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr4:10152000-10153600	Enhancers	Primary B cells from cord blood	blood
32	chr4:10152200-10153800	Enhancers	Primary B cells from peripheral blood	blood
33	chr4:10152400-10152800	Enhancers	Fetal Stomach	stomach
34	chr4:10152600-10152800	Flanking Active TSS	GM12878-XiMat	blood
35	chr4:10152800-10153400	Enhancers	GM12878-XiMat	blood
36	chr4:10156800-10157000	Bivalent Enhancer	HSMMtube	muscle
37	chr4:10157600-10157800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr4:10157600-10160800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr4:10158000-10160800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr4:10158600-10160000	Enhancers	Thymus	Thymus
41	chr4:10158600-10165600	Enhancers	Fetal Thymus	thymus
42	chr4:10158800-10159800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:10158800-10161000	Enhancers	Fetal Stomach	stomach
44	chr4:10158800-10161200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr4:10159000-10160200	Enhancers	Brain Angular Gyrus	brain
46	chr4:10159000-10160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr4:10159000-10160800	Enhancers	Brain Hippocampus Middle	brain
48	chr4:10159000-10160800	Enhancers	Brain Substantia Nigra	brain
49	chr4:10159200-10159400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:10159200-10159400	Enhancers	Brain Inferior Temporal Lobe	brain

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