Variant report

Variant	esv3379601
Chromosome Location	chr1:93249189-93251737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:733)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93250570-93250800	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:93251041-93251174	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:93250896-93251059	K562	blood:	n/a	n/a
4	ATF2	chr1:93250450-93251128	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:93249525-93249979	GM12878	blood:	n/a	n/a
6	ATF2	chr1:93250363-93251285	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:93249664-93250024	GM12878	blood:	n/a	n/a
8	BACH1	chr1:93250186-93251092	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr1:93249617-93250048	GM12878	blood:	n/a	n/a
10	BATF	chr1:93249658-93249946	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:93249657-93250023	GM12878	blood:	n/a	n/a
12	BCL3	chr1:93249631-93249981	GM12878	blood:	n/a	n/a
13	BCLAF1	chr1:93249566-93250079	GM12878	blood:	n/a	n/a
14	BCLAF1	chr1:93250790-93251322	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:93250593-93251309	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:93250331-93251283	K562	blood:	n/a	n/a
17	BHLHE40	chr1:93249990-93250097	K562	blood:	n/a	n/a
18	BRCA1	chr1:93250675-93251246	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:93250437-93251385	K562	blood:	n/a	n/a
20	CBX3	chr1:93250665-93251223	K562	blood:	n/a	n/a
21	CCNT2	chr1:93249970-93251125	K562	blood:	n/a	n/a
22	CEBPB	chr1:93251723-93251995	K562	blood:	n/a	chr1:93251922-93251933 chr1:93251922-93251933
23	CEBPB	chr1:93250167-93251250	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:93249273-93249325	K562	blood:	n/a	n/a
25	CEBPB	chr1:93250873-93251080	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:93249347-93249348	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:93249304-93249328	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:93249239-93249466	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:93249213-93249455	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:93249864-93249935	K562	blood:	n/a	n/a
31	CEBPB	chr1:93249706-93249983	GM12878	blood:	n/a	n/a
32	CEBPD	chr1:93250325-93251037	HepG2	liver:	n/a	n/a
33	CHD1	chr1:93250457-93250626	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr1:93249145-93251508	IMR90	lung:	n/a	n/a
35	CHD2	chr1:93250433-93251158	HepG2	liver:	n/a	n/a
36	CHD2	chr1:93250421-93251197	K562	blood:	n/a	n/a
37	CHD2	chr1:93249724-93251239	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr1:93250157-93251125	GM12878	blood:	n/a	n/a
39	CHD2	chr1:93250449-93251240	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:93249984-93250076	HepG2	liver:	n/a	n/a
41	CREB1	chr1:93250322-93251260	GM12878	blood:	n/a	n/a
42	CREB1	chr1:93250405-93251281	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr1:93250158-93251280	K562	blood:	n/a	n/a
44	CREB1	chr1:93250328-93251352	HepG2	liver:	n/a	n/a
45	CREB1	chr1:93250271-93251355	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr1:93250192-93251224	A549	lung:	n/a	n/a
47	CREB1	chr1:93250269-93250716	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr1:93250096-93251324	HepG2	liver:	n/a	n/a
49	CTCF	chr1:93250980-93251130	AG04449	skin:	n/a	n/a
50	CTCF	chr1:93250960-93251110	GM12867	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93250872-93250922	MCF-7	breast:	n/a
2	chr1:93250872-93250922	MCF-7	breast:	n/a
3	chr1:93250255-93250305	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:93250741-93250791	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:93250863-93250913	H1-hESC	embryonic stem cell:	embryo
6	chr1:93250590-93250640	GM19239	blood:	n/a
7	chr1:93249997-93250047	GM12891	blood:	n/a
8	chr1:93249656-93249706	HUVEC	blood vessel:	n/a
9	chr1:93249656-93249706	AG04450	lung:	fetal
10	chr1:93251203-93251253	IMR90	lung:	fetal
11	chr1:93251218-93251268	HRCEpiC	kidney:	n/a
12	chr1:93251044-93251094	HEK293	kidney:	embryo
13	chr1:93249997-93250047	AG04449	skin:	fetal
14	chr1:93249656-93249706	SK-N-SH	brain:	n/a
15	chr1:93251203-93251253	SKMC	muscle:	n/a
16	chr1:93249997-93250047	AG09319	gingival:	n/a
17	chr1:93250872-93250922	GM12892	blood:	n/a
18	chr1:93249656-93249706	NHBE	bronchial:	n/a
19	chr1:93251184-93251234	BJ	skin:	n/a
20	chr1:93250872-93250922	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:93249656-93249706	RPTEC	kidney:	n/a
22	chr1:93251203-93251253	GM12878	blood:	n/a
23	chr1:93251184-93251234	SK-N-SH	brain:	n/a
24	chr1:93250872-93250922	AG09309	skin:	n/a
25	chr1:93251218-93251268	HRPEpiC	eye:	n/a
26	chr1:93250590-93250640	AG09319	gingival:	n/a
27	chr1:93250741-93250791	HepG2	liver:	n/a
28	chr1:93251184-93251234	PANC-1	pancreas:	n/a
29	chr1:93250741-93250791	BJ	skin:	n/a
30	chr1:93250872-93250922	GM12878	blood:	n/a
31	chr1:93250590-93250640	BE2_C	brain:	n/a
32	chr1:93250741-93250791	HL-60	blood:	n/a
33	chr1:93250863-93250913	GM19239	blood:	n/a
34	chr1:93250863-93250913	Jurkat	blood:	n/a
35	chr1:93250255-93250305	GM12892	blood:	n/a
36	chr1:93249997-93250047	GM12878	blood:	n/a
37	chr1:93250255-93250305	ProgFib	skin:	n/a
38	chr1:93251203-93251253	A549	lung:	n/a
39	chr1:93250741-93250791	NH-A	brain:	n/a
40	chr1:93249656-93249706	AG10803	skin:	n/a
41	chr1:93249656-93249706	HMEC	breast:	n/a
42	chr1:93250863-93250913	PrEC	prostate:	n/a
43	chr1:93249656-93249706	ovcar-3	ovarian:	n/a
44	chr1:93249997-93250047	LNCaP	prostate:	n/a
45	chr1:93251218-93251268	HCM	heart:	n/a
46	chr1:93251203-93251253	HMEC	breast:	n/a
47	chr1:93251044-93251094	NT2-D1	testis:	n/a
48	chr1:93250255-93250305	ovcar-3	ovarian:	n/a
49	chr1:93250255-93250305	NHBE	bronchial:	n/a
50	chr1:93251044-93251094	AG04449	skin:	fetal

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93251519..93253551-chr1:93306747..93308884,2	K562	blood:
2	chr1:93250918..93254010-chr1:93306747..93309482,3	K562	blood:
3	chr1:93251020..93253744-chr1:93303793..93305482,2	K562	blood:
4	chr1:93250896..93252693-chr1:93297527..93299113,2	MCF-7	breast:
5	chr1:93251113..93254538-chr1:93261545..93264232,3	K562	blood:
6	chr1:93250962..93252670-chr1:93458393..93461376,2	K562	blood:
7	chr1:93250398..93251320-chr1:93297474..93298098,2	K562	blood:
8	chr1:93250412..93251179-chr19:10443660..10444173,2	NB4	blood:
9	chr1:93248724..93252766-chr1:93297083..93300077,5	MCF-7	breast:
10	chr1:93249360..93255989-chr1:93295958..93302033,8	K562	blood:
11	chr1:93250688..93252404-chr1:93256005..93257637,2	MCF-7	breast:
12	chr1:93219197..93221453-chr1:93249271..93251757,2	K562	blood:
13	chr1:93214671..93215199-chr1:93250016..93250945,2	K562	blood:
14	chr1:93213561..93216239-chr1:93249509..93251766,2	K562	blood:
15	chr1:93249660..93252667-chr1:93296431..93299077,5	K562	blood:
16	chr1:93249024..93254901-chr1:93255339..93260264,13	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM69A-2	chr1:93250393-93250663	NONHSAT004463

No data

Variant related genes	Relation type
EVI5	TF binding region
EVI5	CpG island
ENSG00000122406	chromatin interactions
ENSG00000067208	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000223896	chromatin interactions
ENSG00000234202	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543780322	chr1:93249195-93249196	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs565526689	chr1:93249253-93249254	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532410631	chr1:93249317-93249318	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs58484805	chr1:93249366-93249367	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs113467983	chr1:93249374-93249375	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs575202055	chr1:93249379-93249380	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs397980818	chr1:93249383-93249384	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs370488254	chr1:93249384-93249385	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs147703518	chr1:93249389-93249390	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs140585479	chr1:93249394-93249395	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs551200589	chr1:93249431-93249432	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs559778808	chr1:93249465-93249466	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs530243885	chr1:93249493-93249494	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs548683177	chr1:93249527-93249528	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs371230493	chr1:93249540-93249541	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs569764922	chr1:93249569-93249570	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs537225029	chr1:93249576-93249577	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs553969952	chr1:93249582-93249583	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs552193831	chr1:93249656-93249657	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs190881936	chr1:93249677-93249678	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs139490680	chr1:93249733-93249734	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs534596047	chr1:93249734-93249735	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs199946915	chr1:93249740-93249741	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs552597589	chr1:93249746-93249747	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs574073558	chr1:93249778-93249779	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs76427731	chr1:93249806-93249807	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs145519947	chr1:93249811-93249812	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs560457686	chr1:93249812-93249813	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs375692132	chr1:93249824-93249825	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs576564227	chr1:93249855-93249856	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs573927095	chr1:93249992-93249993	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs558874888	chr1:93250024-93250025	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs369848012	chr1:93250044-93250045	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs67117364	chr1:93250108-93250109	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs199936520	chr1:93250111-93250112	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs200857934	chr1:93250115-93250116	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs542799008	chr1:93250145-93250146	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs559817167	chr1:93250161-93250162	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs530078798	chr1:93250178-93250179	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs574022900	chr1:93250182-93250183	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs562486397	chr1:93250192-93250193	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs67055146	chr1:93250193-93250194	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs71586764	chr1:93250206-93250207	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs542366815	chr1:93250216-93250217	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs563759008	chr1:93250239-93250240	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs77895793	chr1:93250244-93250245	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs530629413	chr1:93250261-93250262	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs552391447	chr1:93250304-93250305	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs570552362	chr1:93250354-93250355	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs114068119	chr1:93250370-93250371	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93211800-93249200	Weak transcription	Fetal Stomach	stomach
2	chr1:93226000-93249200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:93234800-93249200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:93239600-93249400	Weak transcription	Ovary	ovary
5	chr1:93240600-93249400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr1:93240600-93249400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:93240800-93249600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:93241000-93249400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:93241000-93249400	Weak transcription	Brain Angular Gyrus	brain
10	chr1:93241200-93249400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:93243400-93249600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:93243600-93249200	Weak transcription	GM12878-XiMat	blood
13	chr1:93244600-93249400	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:93244800-93249800	Weak transcription	Esophagus	oesophagus
15	chr1:93245200-93249200	Weak transcription	NH-A	brain
16	chr1:93246000-93249600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:93246000-93249600	Weak transcription	Small Intestine	intestine
18	chr1:93246400-93249400	Weak transcription	Psoas Muscle	Psoas
19	chr1:93247200-93249200	Weak transcription	A549	lung
20	chr1:93247800-93249400	Enhancers	Brain Cingulate Gyrus	brain
21	chr1:93247800-93252000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:93248000-93249200	Enhancers	Adipose Nuclei	Adipose
23	chr1:93248000-93249200	Enhancers	Colonic Mucosa	Colon
24	chr1:93248000-93249200	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:93248000-93249200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:93248000-93249400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:93248000-93249600	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr1:93248000-93251800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:93248200-93249200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr1:93248200-93249200	Enhancers	Fetal Intestine Large	intestine
31	chr1:93248200-93249200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr1:93248200-93249200	Weak transcription	HMEC	breast
33	chr1:93248200-93249200	Weak transcription	Osteobl	bone
34	chr1:93248200-93249400	Enhancers	Primary B cells from cord blood	blood
35	chr1:93248200-93249600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr1:93248400-93249200	Enhancers	Brain Anterior Caudate	brain
37	chr1:93248400-93249200	Weak transcription	Colon Smooth Muscle	Colon
38	chr1:93248400-93249200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr1:93248400-93249200	Enhancers	Fetal Muscle Trunk	muscle
40	chr1:93248400-93249200	Enhancers	Fetal Muscle Leg	muscle
41	chr1:93248400-93249200	Enhancers	Placenta	Placenta
42	chr1:93248400-93249200	Enhancers	Pancreas	Pancrea
43	chr1:93248400-93249400	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr1:93248400-93249400	Enhancers	Primary hematopoietic stem cells	blood
45	chr1:93248400-93249400	Weak transcription	NHDF-Ad	bronchial
46	chr1:93248400-93249600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:93248400-93249600	Enhancers	Primary B cells from peripheral blood	blood
48	chr1:93248400-93249600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:93248400-93249800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr1:93248400-93251200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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