Variant report

Variant	nsv947289
Chromosome Location	chr1:93251307-93276080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:305)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93270211-93270691	K562	blood:	n/a	n/a
2	ARID3A	chr1:93270234-93270434	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:93252084-93252377	K562	blood:	n/a	n/a
4	ARID3A	chr1:93257035-93258372	K562	blood:	n/a	chr1:93257240-93257256
5	ATF1	chr1:93270289-93270734	K562	blood:	n/a	n/a
6	ATF3	chr1:93270367-93270815	K562	blood:	n/a	n/a
7	BACH1	chr1:93270491-93270638	K562	blood:	n/a	n/a
8	BACH1	chr1:93257674-93258210	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:93257817-93258182	K562	blood:	n/a	n/a
10	BCLAF1	chr1:93250790-93251322	GM12878	blood:	n/a	n/a
11	BDP1	chr1:93270334-93270864	Hela-S3	cervix:	n/a	n/a
12	BHLHE40	chr1:93270329-93270756	K562	blood:	n/a	n/a
13	BHLHE40	chr1:93257914-93258295	K562	blood:	n/a	n/a
14	BHLHE40	chr1:93256677-93257234	K562	blood:	n/a	n/a
15	BHLHE40	chr1:93250593-93251309	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:93270238-93270613	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr1:93257815-93258310	K562	blood:	n/a	n/a
18	CBX3	chr1:93270135-93270930	K562	blood:	n/a	n/a
19	CBX3	chr1:93271230-93271683	K562	blood:	n/a	n/a
20	CBX3	chr1:93270374-93270755	K562	blood:	n/a	n/a
21	CBX3	chr1:93250437-93251385	K562	blood:	n/a	n/a
22	CCNT2	chr1:93270486-93270715	K562	blood:	n/a	n/a
23	CEBPB	chr1:93257284-93257598	K562	blood:	n/a	n/a
24	CEBPB	chr1:93270298-93270739	K562	blood:	n/a	n/a
25	CEBPB	chr1:93257861-93258160	K562	blood:	n/a	n/a
26	CEBPB	chr1:93251723-93251995	K562	blood:	n/a	chr1:93251922-93251933 chr1:93251922-93251933
27	CEBPB	chr1:93257861-93258176	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:93274021-93274393	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:93270401-93270663	K562	blood:	n/a	n/a
30	CEBPB	chr1:93270317-93270720	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:93270354-93270704	IMR90	lung:	n/a	n/a
32	CEBPD	chr1:93270259-93270840	K562	blood:	n/a	n/a
33	CEBPD	chr1:93270201-93270826	K562	blood:	n/a	n/a
34	CHD1	chr1:93249145-93251508	IMR90	lung:	n/a	n/a
35	CHD1	chr1:93260500-93261186	IMR90	lung:	n/a	n/a
36	CHD2	chr1:93270421-93270586	K562	blood:	n/a	n/a
37	CHD2	chr1:93270718-93270719	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:93270364-93270691	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:93257927-93258270	K562	blood:	n/a	n/a
40	CREB1	chr1:93250271-93251355	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr1:93250096-93251324	HepG2	liver:	n/a	n/a
42	CREB1	chr1:93250328-93251352	HepG2	liver:	n/a	n/a
43	CTCF	chr1:93270573-93270619	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr1:93273771-93273806	ProgFib	skin:	n/a	n/a
45	CTCF	chr1:93270509-93270630	Lung_OC	lung:	n/a	n/a
46	CTCF	chr1:93260940-93261090	BJ	skin:	n/a	n/a
47	CTCF	chr1:93260940-93261090	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:93262042-93262062	GM10266	blood:	n/a	n/a
49	CTCF	chr1:93260840-93260990	AG10803	skin:	n/a	n/a
50	CTCF	chr1:93260880-93261030	AG04449	skin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93254890-93254940	BE2_C	brain:	n/a
2	chr1:93258288-93258338	HNPCEpiC	eye:	n/a
3	chr1:93258288-93258338	HEEpiC	esophagus:	n/a
4	chr1:93258288-93258338	U87	brain:	n/a
5	chr1:93254890-93254940	HRPEpiC	eye:	n/a
6	chr1:93254890-93254940	PANC-1	pancreas:	n/a
7	chr1:93258316-93258366	SKMC	muscle:	n/a
8	chr1:93258288-93258338	AG04449	skin:	fetal
9	chr1:93258908-93258958	LNCaP	prostate:	n/a
10	chr1:93258288-93258338	NH-A	brain:	n/a
11	chr1:93254890-93254940	HNPCEpiC	eye:	n/a
12	chr1:93258316-93258366	SAEC	small airway:	n/a
13	chr1:93258319-93258369	HEEpiC	esophagus:	n/a
14	chr1:93258316-93258366	RPTEC	kidney:	n/a
15	chr1:93258316-93258366	ECC-1	luminal epithelium:	n/a
16	chr1:93258319-93258369	SK-N-SH	brain:	n/a
17	chr1:93258908-93258958	HIPEpiC	eye:	n/a
18	chr1:93258316-93258366	AG09319	gingival:	n/a
19	chr1:93258316-93258366	HEK293	kidney:	embryo
20	chr1:93258316-93258366	PrEC	prostate:	n/a
21	chr1:93258908-93258958	SAEC	small airway:	n/a
22	chr1:93258288-93258338	H1-hESC	embryonic stem cell:	embryo
23	chr1:93258316-93258366	MCF-7	breast:	n/a
24	chr1:93258319-93258369	AG10803	skin:	n/a
25	chr1:93254890-93254940	NH-A	brain:	n/a
26	chr1:93258908-93258958	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:93258319-93258369	HEK293	kidney:	embryo
28	chr1:93258319-93258369	Jurkat	blood:	n/a
29	chr1:93258316-93258366	U87	brain:	n/a
30	chr1:93258288-93258338	LNCaP	prostate:	n/a
31	chr1:93258316-93258366	NH-A	brain:	n/a
32	chr1:93258319-93258369	SAEC	small airway:	n/a
33	chr1:93258316-93258366	HCM	heart:	n/a
34	chr1:93258288-93258338	CMK	blood:	n/a
35	chr1:93258288-93258338	Hepatocyte	liver:	n/a
36	chr1:93258288-93258338	SK-N-MC	brain:	n/a
37	chr1:93254890-93254940	Caco-2	colon:	n/a
38	chr1:93258288-93258338	HUVEC	blood vessel:	n/a
39	chr1:93254890-93254940	SKMC	muscle:	n/a
40	chr1:93258288-93258338	SK-N-SH	brain:	n/a
41	chr1:93258908-93258958	SK-N-SH	brain:	n/a
42	chr1:93258908-93258958	SK-N-MC	brain:	n/a
43	chr1:93258288-93258338	PFSK-1	brain:	n/a
44	chr1:93258319-93258369	Caco-2	colon:	n/a
45	chr1:93258908-93258958	PANC-1	pancreas:	n/a
46	chr1:93258319-93258369	PrEC	prostate:	n/a
47	chr1:93258288-93258338	HRPEpiC	eye:	n/a
48	chr1:93258319-93258369	GM12892	blood:	n/a
49	chr1:93258908-93258958	Hepatocyte	liver:	n/a
50	chr1:93254890-93254940	AG09319	gingival:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93260518..93262518-chr1:93265417..93267735,2	K562	blood:
2	chr1:93251519..93253551-chr1:93306747..93308884,2	K562	blood:
3	chr1:93268492..93270961-chr1:93296445..93298325,2	K562	blood:
4	chr1:93250918..93254010-chr1:93306747..93309482,3	K562	blood:
5	chr1:93256428..93259014-chr1:93269209..93271869,2	K562	blood:
6	chr1:93251113..93254538-chr1:93261545..93264232,3	K562	blood:
7	chr1:93253683..93256527-chr1:93296123..93298986,2	MCF-7	breast:
8	chr1:93249930..93252918-chr1:93264850..93266907,2	MCF-7	breast:
9	chr1:93260576..93262268-chr1:93262339..93263967,2	K562	blood:
10	chr1:93250688..93252404-chr1:93256005..93257637,2	MCF-7	breast:
11	chr1:93248724..93252766-chr1:93297083..93300077,5	MCF-7	breast:
12	chr1:93268938..93271046-chr1:93276676..93278269,2	K562	blood:
13	chr1:93260518..93262518-chr1:93265417..93267735,2	K562	blood:
14	chr1:93260576..93262268-chr1:93262339..93263967,2	K562	blood:
15	chr1:93251113..93254538-chr1:93261545..93264232,3	K562	blood:
16	chr1:93250962..93252670-chr1:93458393..93461376,2	K562	blood:
17	chr1:93251020..93253744-chr1:93303793..93305482,2	K562	blood:
18	chr1:93271712..93273787-chr1:93276299..93278239,2	K562	blood:
19	chr1:93249024..93254901-chr1:93255339..93260264,13	K562	blood:
20	chr1:93213561..93216239-chr1:93249509..93251766,2	K562	blood:
21	chr1:93249434..93252765-chr1:93275686..93278447,3	K562	blood:
22	chr1:93250896..93252693-chr1:93297527..93299113,2	MCF-7	breast:
23	chr1:93249024..93254901-chr1:93255339..93260264,13	K562	blood:
24	chr1:93249660..93252667-chr1:93296431..93299077,5	K562	blood:
25	chr1:93219197..93221453-chr1:93249271..93251757,2	K562	blood:
26	chr1:93250398..93251320-chr1:93297474..93298098,2	K562	blood:
27	chr1:93249360..93255989-chr1:93295958..93302033,8	K562	blood:
28	chr1:93250688..93252404-chr1:93256005..93257637,2	MCF-7	breast:
29	chr1:93256019..93258677-chr1:93296885..93300584,5	K562	blood:
30	chr1:93256221..93258760-chr1:93295783..93299962,5	K562	blood:

No data

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

Extended variants
information (count: 872 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572709376	chr1:93251338-93251339	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs187768517	chr1:93251358-93251359	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs36097156	chr1:93251364-93251365	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs34549064	chr1:93251411-93251412	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs55653993	chr1:93251444-93251445	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs536984579	chr1:93251447-93251448	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs56101107	chr1:93251468-93251469	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs55826362	chr1:93251470-93251471	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs374877080	chr1:93251482-93251483	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs75582964	chr1:93251483-93251484	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs36097015	chr1:93251494-93251495	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs539668486	chr1:93251578-93251579	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs529177390	chr1:93251609-93251610	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs527873800	chr1:93251646-93251647	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs80258046	chr1:93251647-93251648	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs397775975	chr1:93251658-93251659	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs199891806	chr1:93251659-93251660	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs192765878	chr1:93251682-93251683	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs114918011	chr1:93251718-93251719	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs145459322	chr1:93251747-93251748	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs148857041	chr1:93251748-93251749	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs199752470	chr1:93251791-93251792	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs397860427	chr1:93251793-93251794	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs79911111	chr1:93251795-93251796	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs74702780	chr1:93251796-93251797	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs33914637	chr1:93251810-93251811	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs78182894	chr1:93251826-93251827	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184824982	chr1:93251870-93251871	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs547265049	chr1:93251887-93251888	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs568650517	chr1:93251906-93251907	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs547741764	chr1:93251909-93251910	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs143488451	chr1:93252068-93252069	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs536181455	chr1:93252260-93252261	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs35405578	chr1:93252310-93252311	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs150645562	chr1:93252329-93252330	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs557338003	chr1:93252360-93252361	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs575617851	chr1:93252427-93252428	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs539409111	chr1:93252455-93252456	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs150947940	chr1:93252500-93252501	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs75902059	chr1:93252607-93252608	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs114387595	chr1:93252632-93252633	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs141031365	chr1:93252662-93252663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573717904	chr1:93252742-93252743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549944630	chr1:93252806-93252807	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555919769	chr1:93252828-93252829	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs74588782	chr1:93252855-93252856	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs538297315	chr1:93252858-93252859	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs532952676	chr1:93252892-93252893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557883088	chr1:93252918-93252919	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551438795	chr1:93252928-93252929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93247800-93252000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:93248000-93251800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:93248600-93251400	Active TSS	Right Ventricle	heart
4	chr1:93248600-93251600	Active TSS	NHLF	lung
5	chr1:93249000-93251400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:93249000-93251400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:93249000-93251400	Active TSS	Aorta	Aorta
8	chr1:93249000-93251600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:93249000-93251600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:93249000-93251600	Active TSS	Stomach Smooth Muscle	stomach
11	chr1:93249000-93251800	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr1:93249200-93251400	Active TSS	Colon Smooth Muscle	Colon
13	chr1:93249200-93251400	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr1:93249200-93251400	Active TSS	Fetal Kidney	kidney
15	chr1:93249200-93251400	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr1:93249200-93251400	Active TSS	Fetal Stomach	stomach
17	chr1:93249200-93251400	Active TSS	Left Ventricle	heart
18	chr1:93249200-93251400	Active TSS	Pancreas	Pancrea
19	chr1:93249200-93251400	Active TSS	A549	lung
20	chr1:93249200-93251400	Active TSS	NH-A	brain
21	chr1:93249200-93251600	Active TSS	Rectal Smooth Muscle	rectum
22	chr1:93249200-93251600	Active TSS	Osteobl	bone
23	chr1:93249400-93251400	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr1:93249400-93251400	Active TSS	Brain Substantia Nigra	brain
25	chr1:93249400-93251400	Active TSS	Fetal Lung	lung
26	chr1:93249400-93251400	Active TSS	Ovary	ovary
27	chr1:93249400-93251400	Active TSS	Psoas Muscle	Psoas
28	chr1:93249400-93251400	Active TSS	Stomach Mucosa	stomach
29	chr1:93249400-93251400	Active TSS	HSMMtube	muscle
30	chr1:93249400-93251400	Active TSS	NHDF-Ad	bronchial
31	chr1:93249400-93251600	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr1:93249600-93251400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:93249800-93251400	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr1:93249800-93251400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr1:93249800-93251400	Active TSS	Esophagus	oesophagus
36	chr1:93249800-93251600	Active TSS	Brain Anterior Caudate	brain
37	chr1:93250000-93251400	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr1:93250000-93251400	Active TSS	Liver	Liver
39	chr1:93250000-93251400	Active TSS	Brain Cingulate Gyrus	brain
40	chr1:93250000-93251400	Active TSS	Brain Germinal Matrix	brain
41	chr1:93250000-93251600	Active TSS	Brain Hippocampus Middle	brain
42	chr1:93250000-93251600	Active TSS	Colonic Mucosa	Colon
43	chr1:93250000-93251600	Active TSS	Duodenum Mucosa	Duodenum
44	chr1:93250000-93251600	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr1:93250000-93251600	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr1:93250200-93251400	Active TSS	Fetal Brain Female	brain
47	chr1:93250200-93256800	Weak transcription	Fetal Heart	heart
48	chr1:93250600-93251600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:93250800-93251400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr1:93250800-93251400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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