Variant report

Variant	nsv461851
Chromosome Location	chr1:71442626-71507541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:61)
Chromatin interactive
region (count:38)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
2	ARID3A	chr1:71460522-71460848	K562	blood:	n/a	n/a
3	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
4	ARID3A	chr1:71468699-71468724	K562	blood:	n/a	n/a
5	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
6	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
7	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
8	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
9	BHLHE40	chr1:71485053-71485253	K562	blood:	n/a	n/a
10	BHLHE40	chr1:71501191-71501340	K562	blood:	n/a	n/a
11	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
12	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
13	CEBPB	chr1:71504008-71504240	K562	blood:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
14	CEBPB	chr1:71503963-71504259	HepG2	liver:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
15	CEBPB	chr1:71467358-71467677	IMR90	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
16	CEBPB	chr1:71458240-71458524	HepG2	liver:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
17	CEBPB	chr1:71474287-71474494	K562	blood:	n/a	n/a
18	CEBPB	chr1:71503962-71504242	IMR90	lung:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
19	CEBPB	chr1:71458228-71458549	K562	blood:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
20	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
21	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
22	CEBPB	chr1:71485706-71485857	A549	lung:	n/a	chr1:71485756-71485767
23	CEBPB	chr1:71467360-71467695	K562	blood:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
24	CEBPB	chr1:71503735-71504291	K562	blood:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
25	CEBPB	chr1:71477204-71477504	K562	blood:	n/a	chr1:71477360-71477371
26	CEBPB	chr1:71444470-71444536	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:71485618-71485862	IMR90	lung:	n/a	chr1:71485756-71485767
28	CEBPB	chr1:71467353-71467636	A549	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
29	CEBPB	chr1:71469996-71470196	K562	blood:	n/a	chr1:71470127-71470140 chr1:71470129-71470140
30	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:71467389-71467679	H1-hESC	embryonic stem cell:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
32	CEBPB	chr1:71470760-71470839	HepG2	liver:	n/a	chr1:71470810-71470821
33	CTCF	chr1:71490249-71490387	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr1:71444360-71444510	HRE	kidney:	n/a	n/a
35	CTCF	chr1:71467834-71467882	GM13977	blood:	n/a	n/a
36	CTCF	chr1:71499046-71499086	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:71490248-71490384	GM10248	blood:	n/a	n/a
38	CTCF	chr1:71460680-71460830	K562	blood:	n/a	n/a
39	CTCF	chr1:71478740-71478890	GM12866	blood:	n/a	n/a
40	CTCF	chr1:71460614-71460768	K562	blood:	n/a	n/a
41	CTCF	chr1:71457285-71457353	GM20000	blood:	n/a	n/a
42	CTCF	chr1:71444300-71444450	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr1:71460527-71460872	K562	blood:	n/a	n/a
44	CTCF	chr1:71460149-71460221	Fibrobl	skin:	n/a	n/a
45	CUX1	chr1:71446571-71446754	K562	blood:	n/a	n/a
46	CUX1	chr1:71444716-71444781	GM12878	blood:	n/a	n/a
47	CUX1	chr1:71466475-71466477	GM12878	blood:	n/a	n/a
48	CUX1	chr1:71481194-71481342	K562	blood:	n/a	n/a
49	ELK1	chr1:71451684-71452008	K562	blood:	n/a	n/a
50	EP300	chr1:71484234-71487033	SK-N-SH	brain:	n/a	chr1:71486260-71486269 chr1:71484313-71484327 chr1:71484888-71484895 chr1:71485709-71485723

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71472738-71472788	HEK293	kidney:	embryo
2	chr1:71472738-71472788	GM12892	blood:	n/a
3	chr1:71472738-71472788	AG09319	gingival:	n/a
4	chr1:71472738-71472788	NHBE	bronchial:	n/a
5	chr1:71472738-71472788	GM19239	blood:	n/a
6	chr1:71472738-71472788	CMK	blood:	n/a
7	chr1:71472738-71472788	IMR90	lung:	fetal
8	chr1:71472738-71472788	MCF-7	breast:	n/a
9	chr1:71472738-71472788	HNPCEpiC	eye:	n/a
10	chr1:71472738-71472788	Caco-2	colon:	n/a
11	chr1:71472738-71472788	PANC-1	pancreas:	n/a
12	chr1:71472738-71472788	SKMC	muscle:	n/a
13	chr1:71472738-71472788	NB4	blood:	n/a
14	chr1:71472738-71472788	HRE	kidney:	n/a
15	chr1:71472738-71472788	HCT-116	colon:	n/a
16	chr1:71472738-71472788	ovcar-3	ovarian:	n/a
17	chr1:71472738-71472788	AG04449	skin:	fetal
18	chr1:71472738-71472788	HCPEpiC	choroid plexus:	n/a
19	chr1:71472738-71472788	RPTEC	kidney:	n/a
20	chr1:71472738-71472788	BE2_C	brain:	n/a
21	chr1:71472738-71472788	K562	blood:	n/a
22	chr1:71472738-71472788	HIPEpiC	eye:	n/a
23	chr1:71472738-71472788	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:71472738-71472788	HCM	heart:	n/a
25	chr1:71472738-71472788	Jurkat	blood:	n/a
26	chr1:71472738-71472788	PrEC	prostate:	n/a
27	chr1:71472738-71472788	HRCEpiC	kidney:	n/a
28	chr1:71472738-71472788	SK-N-SH	brain:	n/a
29	chr1:71472738-71472788	LNCaP	prostate:	n/a
30	chr1:71472738-71472788	H1-hESC	embryonic stem cell:	embryo
31	chr1:71472738-71472788	NH-A	brain:	n/a
32	chr1:71472738-71472788	GM06990	blood:	n/a
33	chr1:71472738-71472788	PFSK-1	brain:	n/a
34	chr1:71472738-71472788	ECC-1	luminal epithelium:	n/a
35	chr1:71472738-71472788	HEEpiC	esophagus:	n/a
36	chr1:71472738-71472788	NT2-D1	testis:	n/a
37	chr1:71472738-71472788	HL-60	blood:	n/a
38	chr1:71472738-71472788	SAEC	small airway:	n/a
39	chr1:71472738-71472788	HepG2	liver:	n/a
40	chr1:71472738-71472788	HAEpiC	amniotic membrane:	n/a
41	chr1:71472738-71472788	HUVEC	blood vessel:	n/a
42	chr1:71472738-71472788	SK-N-MC	brain:	n/a
43	chr1:71472738-71472788	HMEC	breast:	n/a
44	chr1:71472738-71472788	Hela-S3	cervix:	n/a
45	chr1:71472738-71472788	AG09309	skin:	n/a
46	chr1:71472738-71472788	A549	lung:	n/a
47	chr1:71472738-71472788	AG10803	skin:	n/a
48	chr1:71472738-71472788	HRPEpiC	eye:	n/a
49	chr1:71472738-71472788	GM12878	blood:	n/a
50	chr1:71472738-71472788	AoSMC	blood vessel:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71488605..71491550-chr1:71545533..71547496,2	K562	blood:
2	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
3	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
4	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
5	chr1:71032636..71034814-chr1:71507461..71509971,2	K562	blood:
6	chr1:71492429..71494900-chr1:71500523..71502933,2	K562	blood:
7	chr1:71470890..71473474-chr1:71500472..71503086,2	MCF-7	breast:
8	chr1:71497365..71498885-chr1:71507254..71510170,2	K562	blood:
9	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
10	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
11	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
12	chr1:71498308..71501736-chr1:71503473..71506751,3	K562	blood:
13	chr1:71499543..71503702-chr1:71511179..71513554,5	K562	blood:
14	chr1:71497365..71498885-chr1:71507254..71510170,2	K562	blood:
15	chr1:71493469..71495950-chr1:71496070..71500224,3	K562	blood:
16	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
17	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
18	chr1:71496393..71498256-chr1:71498283..71500475,2	K562	blood:
19	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
20	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
21	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
22	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
23	chr1:71493019..71494900-chr1:71500523..71502505,2	K562	blood:
24	chr1:71493019..71494900-chr1:71500523..71502505,2	K562	blood:
25	chr1:71128661..71130608-chr1:71489552..71491952,2	K562	blood:
26	chr1:71498308..71501736-chr1:71503473..71506751,3	K562	blood:
27	chr1:71492579..71496076-chr1:71511495..71513785,3	K562	blood:
28	chr1:71492429..71494900-chr1:71500523..71502933,2	K562	blood:
29	chr1:71493469..71495950-chr1:71496070..71500224,3	K562	blood:
30	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
31	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
32	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:
33	chr1:71496393..71498256-chr1:71498283..71500475,2	K562	blood:
34	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
35	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
36	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
37	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
38	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
2	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
3	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
4	lnc-CTH-13	chr1:71489270-71489329	NONHSAT003876
5	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
6	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
7	lnc-CTH-13	chr1:71489933-71490390	NONHSAT003876
8	lnc-CTH-14	chr1:71500505-71500572	l_71_chr1:71319635-71475982_testes

No data

Variant related genes	Relation type
ENSG00000269933	TF binding region
ENSG00000269933	CpG island
ENSG00000229956	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000269933	chromatin interactions
ENSG00000050628	chromatin interactions

Extended variants
information (count: 2407 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3819783	chr1:71442626-71442627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527279339	chr1:71442671-71442672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs484538	chr1:71442683-71442684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs112530395	chr1:71442712-71442713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs484675	chr1:71442737-71442738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189256040	chr1:71442744-71442745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180976172	chr1:71442766-71442767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373391527	chr1:71442790-71442791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377719027	chr1:71442804-71442805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538883725	chr1:71442809-71442810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558262262	chr1:71442871-71442872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145863992	chr1:71442897-71442898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369286571	chr1:71442898-71442899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540750932	chr1:71442902-71442903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549674124	chr1:71442940-71442941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs508513	chr1:71442971-71442972	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186161858	chr1:71443006-71443007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532064551	chr1:71443038-71443039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs873658	chr1:71443042-71443043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563240429	chr1:71443065-71443066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs3819787	chr1:71443066-71443067	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs3819788	chr1:71443083-71443084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565156512	chr1:71443103-71443104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367965516	chr1:71443104-71443105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs909847	chr1:71443127-71443128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs3819790	chr1:71443135-71443136	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs909848	chr1:71443150-71443151	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
28	rs371281196	chr1:71443205-71443206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549805071	chr1:71443254-71443255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569994867	chr1:71443259-71443260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538949645	chr1:71443260-71443261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552372555	chr1:71443332-71443333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574596741	chr1:71443333-71443334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534656483	chr1:71443355-71443356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534245095	chr1:71443374-71443375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs726764	chr1:71443399-71443400	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs371046288	chr1:71443431-71443432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573946538	chr1:71443470-71443471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190637387	chr1:71443493-71443494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138877437	chr1:71443514-71443515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181411511	chr1:71443567-71443568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552159991	chr1:71443607-71443608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185531008	chr1:71443654-71443655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562310649	chr1:71443692-71443693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190830926	chr1:71443717-71443718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183016442	chr1:71443722-71443723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188033953	chr1:71443732-71443733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529636105	chr1:71443790-71443791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531525275	chr1:71443820-71443821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563294489	chr1:71443844-71443845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71430200-71444200	Weak transcription	Adipose Nuclei	Adipose
2	chr1:71441600-71444800	Enhancers	Fetal Brain Male	brain
3	chr1:71443000-71443200	Enhancers	Gastric	stomach
4	chr1:71443000-71443600	Enhancers	Pancreas	Pancrea
5	chr1:71443200-71456800	Weak transcription	Gastric	stomach
6	chr1:71443600-71446000	Weak transcription	Pancreas	Pancrea
7	chr1:71444000-71444600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr1:71444000-71445600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:71444200-71444600	Enhancers	Fetal Heart	heart
10	chr1:71444200-71446200	Enhancers	Primary hematopoietic stem cells	blood
11	chr1:71444200-71446600	Enhancers	Adipose Nuclei	Adipose
12	chr1:71444200-71447000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:71444400-71444600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:71444400-71444800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:71444400-71445400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr1:71444600-71445200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr1:71444600-71446000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:71444600-71446600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr1:71444800-71445600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:71445000-71446200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:71445200-71445400	Enhancers	Colon Smooth Muscle	Colon
22	chr1:71445200-71446200	Enhancers	K562	blood
23	chr1:71445200-71464200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:71445600-71446200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:71446000-71446200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:71446000-71446200	Enhancers	Colon Smooth Muscle	Colon
27	chr1:71446000-71446600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr1:71446000-71446600	Enhancers	Pancreas	Pancrea
29	chr1:71446200-71450600	Weak transcription	K562	blood
30	chr1:71446600-71447200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:71446600-71449200	Weak transcription	Adipose Nuclei	Adipose
32	chr1:71446600-71456200	Weak transcription	Pancreas	Pancrea
33	chr1:71447400-71448200	Enhancers	Aorta	Aorta
34	chr1:71448200-71456800	Weak transcription	Aorta	Aorta
35	chr1:71449200-71449800	Enhancers	Adipose Nuclei	Adipose
36	chr1:71449800-71451400	Weak transcription	Adipose Nuclei	Adipose
37	chr1:71450600-71451600	Enhancers	NHDF-Ad	bronchial
38	chr1:71450600-71452200	Enhancers	K562	blood
39	chr1:71451400-71451800	Enhancers	Adipose Nuclei	Adipose
40	chr1:71456200-71457200	Enhancers	Pancreas	Pancrea
41	chr1:71456800-71458000	Enhancers	Gastric	stomach
42	chr1:71456800-71458400	Enhancers	Aorta	Aorta
43	chr1:71457000-71457400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:71458000-71459400	Weak transcription	Gastric	stomach
45	chr1:71459200-71459400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:71459200-71460000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:71459400-71459600	Enhancers	Gastric	stomach
48	chr1:71459600-71460400	Enhancers	Left Ventricle	heart
49	chr1:71459800-71461000	Enhancers	Fetal Heart	heart
50	chr1:71460600-71461200	Enhancers	K562	blood

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