Variant report

Variant	nsv998331
Chromosome Location	chr4:10124074-10152878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:549)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10125192-10125592	HepG2	liver:	n/a	n/a
2	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
3	BATF	chr4:10133064-10133309	GM12878	blood:	n/a	n/a
4	BATF	chr4:10133063-10133313	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:10132206-10132484	K562	blood:	n/a	chr4:10132332-10132353
6	BHLHE40	chr4:10142964-10143314	K562	blood:	n/a	n/a
7	BRCA1	chr4:10125143-10125377	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:10124238-10124604	HepG2	liver:	n/a	chr4:10124422-10124433
9	CEBPB	chr4:10124297-10124497	K562	blood:	n/a	chr4:10124422-10124433
10	CEBPB	chr4:10130839-10131364	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:10125157-10125545	HepG2	liver:	n/a	chr4:10125158-10125175 chr4:10125161-10125174
12	CHD2	chr4:10130972-10131141	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr4:10143239-10143269	K562	blood:	n/a	n/a
14	CHD2	chr4:10125158-10125559	HepG2	liver:	n/a	n/a
15	CHD2	chr4:10142301-10142459	HepG2	liver:	n/a	n/a
16	CTCF	chr4:10125346-10125363	HepG2	liver:	n/a	n/a
17	CTCF	chr4:10143040-10143190	NHEK	skin:	n/a	n/a
18	CTCF	chr4:10143100-10143250	HCM	heart:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
19	CTCF	chr4:10142900-10143050	GM12864	blood:	n/a	chr4:10142953-10142962
20	CTCF	chr4:10142680-10142830	GM12873	blood:	n/a	n/a
21	CTCF	chr4:10142640-10142790	HepG2	liver:	n/a	n/a
22	CTCF	chr4:10143100-10143250	HCFaa	heart:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
23	CTCF	chr4:10143240-10143390	K562	blood:	n/a	n/a
24	CTCF	chr4:10143160-10143310	GM12864	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
25	CTCF	chr4:10143200-10143350	GM12867	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
26	CTCF	chr4:10143140-10143290	NB4	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
27	CTCF	chr4:10143120-10143270	HFF-Myc	foreskin:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
28	CTCF	chr4:10146180-10146330	K562	blood:	n/a	n/a
29	CTCF	chr4:10146200-10146350	HEK293	kidney:	n/a	n/a
30	CTCF	chr4:10125140-10125290	HCM	heart:	n/a	n/a
31	CTCF	chr4:10143280-10143430	HCT-116	colon:	n/a	n/a
32	CTCF	chr4:10143140-10143290	GM12865	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
33	CTCF	chr4:10142620-10142770	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr4:10142700-10142850	BJ	skin:	n/a	n/a
35	CTCF	chr4:10143120-10143270	Hela-S3	cervix:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
36	CTCF	chr4:10143193-10143253	GM10266	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
37	CTCF	chr4:10142600-10142750	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr4:10125240-10125390	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr4:10146160-10146310	GM12864	blood:	n/a	n/a
40	CTCF	chr4:10146200-10146350	GM12872	blood:	n/a	n/a
41	CTCF	chr4:10125700-10125850	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr4:10143120-10143270	GM12872	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
43	CTCF	chr4:10142518-10143454	H1-hESC	embryonic stem cell:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
44	CTCF	chr4:10142808-10143435	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
45	CTCF	chr4:10142877-10143029	K562	blood:	n/a	chr4:10142953-10142962
46	CTCF	chr4:10142640-10142790	HEK293	kidney:	n/a	n/a
47	CTCF	chr4:10143160-10143310	BE2_C	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
48	CTCF	chr4:10143120-10143270	HRE	kidney:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
49	CTCF	chr4:10143120-10143270	GM06990	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
50	CTCF	chr4:10142815-10143400	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10149849-10149899	HIPEpiC	eye:	n/a
2	chr4:10147330-10147380	LNCaP	prostate:	n/a
3	chr4:10147038-10147088	BE2_C	brain:	n/a
4	chr4:10147100-10147150	NT2-D1	testis:	n/a
5	chr4:10143053-10143103	Hepatocyte	liver:	n/a
6	chr4:10147606-10147656	CMK	blood:	n/a
7	chr4:10147038-10147088	HEEpiC	esophagus:	n/a
8	chr4:10125330-10125380	BE2_C	brain:	n/a
9	chr4:10147302-10147352	T-47D	breast:	n/a
10	chr4:10147330-10147380	HEK293	kidney:	embryo
11	chr4:10147302-10147352	BE2_C	brain:	n/a
12	chr4:10145483-10145533	HCM	heart:	n/a
13	chr4:10149849-10149899	Caco-2	colon:	n/a
14	chr4:10147100-10147150	K562	blood:	n/a
15	chr4:10147038-10147088	HCF	heart:	n/a
16	chr4:10147302-10147352	AG04450	lung:	fetal
17	chr4:10125330-10125380	PANC-1	pancreas:	n/a
18	chr4:10125330-10125380	LNCaP	prostate:	n/a
19	chr4:10147302-10147352	HIPEpiC	eye:	n/a
20	chr4:10145483-10145533	CMK	blood:	n/a
21	chr4:10145483-10145533	AoSMC	blood vessel:	n/a
22	chr4:10147038-10147088	AG04449	skin:	fetal
23	chr4:10147330-10147380	GM06990	blood:	n/a
24	chr4:10147038-10147088	ovcar-3	ovarian:	n/a
25	chr4:10147330-10147380	BJ	skin:	n/a
26	chr4:10147330-10147380	K562	blood:	n/a
27	chr4:10125330-10125380	HCM	heart:	n/a
28	chr4:10125330-10125380	HEK293	kidney:	embryo
29	chr4:10147330-10147380	SK-N-SH_RA	brain:	n/a
30	chr4:10147330-10147380	HL-60	blood:	n/a
31	chr4:10149849-10149899	PANC-1	pancreas:	n/a
32	chr4:10147330-10147380	HepG2	liver:	n/a
33	chr4:10149849-10149899	MCF10A-Er-Src	breast:	n/a
34	chr4:10147038-10147088	PFSK-1	brain:	n/a
35	chr4:10147330-10147380	AG10803	skin:	n/a
36	chr4:10145483-10145533	SK-N-SH_RA	brain:	n/a
37	chr4:10147100-10147150	HRCEpiC	kidney:	n/a
38	chr4:10147100-10147150	AoSMC	blood vessel:	n/a
39	chr4:10143053-10143103	H1-hESC	embryonic stem cell:	embryo
40	chr4:10147100-10147150	GM06990	blood:	n/a
41	chr4:10147330-10147380	RPTEC	kidney:	n/a
42	chr4:10149849-10149899	HRPEpiC	eye:	n/a
43	chr4:10147302-10147352	MCF10A-Er-Src	breast:	n/a
44	chr4:10149849-10149899	HCF	heart:	n/a
45	chr4:10145483-10145533	AG04449	skin:	fetal
46	chr4:10145483-10145533	HCF	heart:	n/a
47	chr4:10145483-10145533	MCF-7	breast:	n/a
48	chr4:10147302-10147352	HCM	heart:	n/a
49	chr4:10147100-10147150	GM12892	blood:	n/a
50	chr4:10147038-10147088	GM19239	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10122708..10125358-chr4:10375421..10377082,2	K562	blood:
2	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:
3	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
4	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
5	chr4:10142468..10145387-chr4:10146611..10148310,2	MCF-7	breast:
6	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
7	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
8	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
9	chr4:10117528..10120943-chr4:10131939..10133897,4	MCF-7	breast:
10	chr4:10122860..10124582-chr4:10454402..10456296,2	K562	blood:
11	chr4:10143164..10147494-chr4:10150670..10153852,4	K562	blood:
12	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
13	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
14	chr4:10118110..10120453-chr4:10131867..10134092,3	MCF-7	breast:
15	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:
16	chr4:10123474..10124373-chr6:36856788..36857395,2	MCF-7	breast:
17	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
18	chr4:10124627..10126326-chr4:10129593..10131682,2	MCF-7	breast:
19	chr4:10147623..10149514-chr4:10156130..10157999,2	K562	blood:
20	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
21	chr4:10121162..10125014-chr4:10131852..10134322,3	MCF-7	breast:
22	chr4:10110208..10112839-chr4:10141638..10144449,2	MCF-7	breast:
23	chr4:10120679..10126916-chr4:10412453..10417013,7	K562	blood:
24	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
25	chr4:10117694..10121179-chr4:10148695..10151564,3	MCF-7	breast:
26	chr4:10117460..10124392-chr4:10456675..10465032,17	K562	blood:
27	chr4:10124627..10126326-chr4:10129593..10131682,2	MCF-7	breast:
28	chr4:10122680..10125562-chr4:10662021..10664504,2	K562	blood:
29	chr4:10123771..10125496-chr4:10158100..10160475,2	K562	blood:
30	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
31	chr4:10117985..10121218-chr4:10149186..10152668,4	MCF-7	breast:
32	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
33	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
34	chr4:10133192..10134746-chr4:10556529..10559334,2	K562	blood:
35	chr4:10120437..10124442-chr4:10402726..10405362,4	K562	blood:
36	chr4:10126622..10128433-chr4:10132503..10134257,2	MCF-7	breast:
37	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
38	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
39	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
40	chr4:10122589..10124935-chr4:10442923..10445169,2	K562	blood:
41	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
42	chr4:10121162..10125014-chr4:10131852..10134322,3	MCF-7	breast:
43	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
44	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
45	chr4:10137029..10138548-chr4:10444331..10446997,2	K562	blood:
46	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
47	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
48	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
49	chr4:10126622..10128433-chr4:10132503..10134257,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
2	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429

No data

Variant related genes	Relation type
ENSG00000250393	TF binding region
ENSG00000250393	CpG island
ENSG00000251296	chromatin interactions
ENSG00000250613	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000250393	chromatin interactions

Extended variants
information (count: 2555 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563456172	chr4:10124080-10124081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs375981234	chr4:10124093-10124094	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs147412426	chr4:10124096-10124097	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs558275287	chr4:10124108-10124109	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs59041810	chr4:10124123-10124124	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs397686970	chr4:10124124-10124125	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs552483764	chr4:10124149-10124150	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs116241415	chr4:10124151-10124152	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs528290519	chr4:10124155-10124156	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs560971096	chr4:10124161-10124162	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs566121599	chr4:10124165-10124166	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs113888816	chr4:10124168-10124169	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs377448537	chr4:10124170-10124171	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs554391654	chr4:10124171-10124172	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs576386237	chr4:10124173-10124174	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs149910890	chr4:10124174-10124175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs58390916	chr4:10124175-10124176	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs554917394	chr4:10124183-10124184	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs577805370	chr4:10124206-10124207	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs139752151	chr4:10124207-10124208	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs370027314	chr4:10124211-10124212	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs537778497	chr4:10124220-10124221	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs113884114	chr4:10124224-10124225	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs181678661	chr4:10124225-10124226	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs113496801	chr4:10124226-10124227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs186960742	chr4:10124232-10124233	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs367847800	chr4:10124236-10124237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs4697924	chr4:10124239-10124240	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375645158	chr4:10124240-10124241	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs541476779	chr4:10124246-10124247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs111297105	chr4:10124266-10124267	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs144868267	chr4:10124267-10124268	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs546163873	chr4:10124278-10124279	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs542988123	chr4:10124281-10124282	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs564360316	chr4:10124299-10124300	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs58358578	chr4:10124300-10124301	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191205406	chr4:10124308-10124309	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs531656032	chr4:10124310-10124311	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs368259847	chr4:10124320-10124321	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs75816308	chr4:10124324-10124325	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs4697925	chr4:10124330-10124331	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77564396	chr4:10124346-10124347	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs570080696	chr4:10124363-10124364	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs149035494	chr4:10124368-10124369	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs142081768	chr4:10124405-10124406	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs140381825	chr4:10124426-10124427	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs115552423	chr4:10124433-10124434	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534909952	chr4:10124444-10124445	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs181130991	chr4:10124446-10124447	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568184099	chr4:10124449-10124450	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 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:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10119400-10124600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:10119400-10124600	Weak transcription	Pancreas	Pancrea
3	chr4:10119400-10126200	Enhancers	Fetal Intestine Large	intestine
4	chr4:10119600-10124200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:10119600-10124600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:10119600-10124600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr4:10119600-10124600	Weak transcription	HSMM	muscle
8	chr4:10119600-10124800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:10119600-10125400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr4:10119600-10126000	Enhancers	Fetal Stomach	stomach
11	chr4:10119600-10126400	Enhancers	Fetal Intestine Small	intestine
12	chr4:10119800-10124800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:10119800-10124800	Weak transcription	Right Atrium	heart
14	chr4:10119800-10125000	Weak transcription	Hela-S3	cervix
15	chr4:10120000-10124200	Weak transcription	HUVEC	blood vessel
16	chr4:10120000-10124800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:10120000-10124800	Weak transcription	Brain Anterior Caudate	brain
18	chr4:10120000-10124800	Weak transcription	Esophagus	oesophagus
19	chr4:10120000-10125000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:10120000-10127200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:10120200-10124400	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr4:10120200-10124800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:10120200-10124800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr4:10120200-10124800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:10120200-10124800	Weak transcription	Adipose Nuclei	Adipose
26	chr4:10120200-10124800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr4:10120200-10125000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr4:10120200-10125000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:10120200-10125200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:10120200-10126800	Enhancers	Fetal Thymus	thymus
31	chr4:10120400-10124200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:10120400-10124600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:10120400-10125000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:10120400-10125000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr4:10120400-10125200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:10120400-10125200	Weak transcription	Brain Hippocampus Middle	brain
37	chr4:10120400-10125200	Weak transcription	Small Intestine	intestine
38	chr4:10120400-10125400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:10120400-10126200	Enhancers	Duodenum Mucosa	Duodenum
40	chr4:10120600-10124200	Weak transcription	Lung	lung
41	chr4:10120600-10124800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr4:10120600-10125200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr4:10120600-10125400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:10120600-10127400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr4:10120800-10124800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:10120800-10125000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr4:10120800-10125000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr4:10120800-10125200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr4:10120800-10125600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr4:10120800-10127400	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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