Variant report

Variant	nsv601166
Chromosome Location	chr6:25084718-25165486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:1098)
Chromatin interactive
region (count:23)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 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	ATF1	chr6:25138444-25138722	K562	blood:	n/a	n/a
2	ATF2	chr6:25137739-25139485	GM12878	blood:	n/a	n/a
3	ATF2	chr6:25147259-25147841	GM12878	blood:	n/a	n/a
4	ATF2	chr6:25138138-25139054	GM12878	blood:	n/a	n/a
5	BATF	chr6:25138159-25138751	GM12878	blood:	n/a	n/a
6	BATF	chr6:25138903-25139261	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:25138247-25138752	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:25138131-25139253	GM12878	blood:	n/a	chr6:25139184-25139193
9	BCLAF1	chr6:25147298-25147929	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:25153388-25153590	K562	blood:	n/a	n/a
11	BHLHE40	chr6:25147488-25147755	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:25138008-25138134	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:25105254-25106364	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:25113502-25113596	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr6:25158038-25158380	K562	blood:	n/a	n/a
16	CBX3	chr6:25153290-25153675	K562	blood:	n/a	n/a
17	CBX3	chr6:25153138-25153755	K562	blood:	n/a	n/a
18	CBX3	chr6:25158090-25158421	K562	blood:	n/a	n/a
19	CEBPB	chr6:25151589-25151871	Hela-S3	cervix:	n/a	chr6:25151734-25151745
20	CEBPB	chr6:25151596-25151872	IMR90	lung:	n/a	chr6:25151734-25151745
21	CEBPB	chr6:25105274-25106365	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:25131226-25131432	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:25137797-25138153	A549	lung:	n/a	n/a
24	CEBPB	chr6:25112171-25113249	Hela-S3	cervix:	n/a	chr6:25112734-25112746 chr6:25112253-25112264
25	CEBPB	chr6:25096423-25096594	A549	lung:	n/a	chr6:25096572-25096583 chr6:25096425-25096442
26	CEBPB	chr6:25093588-25093661	HepG2	liver:	n/a	chr6:25093623-25093634
27	CEBPB	chr6:25130817-25131067	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:25137779-25139523	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr6:25151600-25151828	K562	blood:	n/a	chr6:25151734-25151745
30	CEBPB	chr6:25151589-25151834	HepG2	liver:	n/a	chr6:25151734-25151745
31	CEBPB	chr6:25137795-25138133	K562	blood:	n/a	n/a
32	CEBPB	chr6:25124599-25124718	HepG2	liver:	n/a	chr6:25124636-25124647 chr6:25124655-25124666
33	CEBPB	chr6:25137713-25139611	GM12878	blood:	n/a	n/a
34	CEBPB	chr6:25137782-25139143	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:25137793-25138137	HepG2	liver:	n/a	n/a
36	CHD1	chr6:25138115-25139561	GM12878	blood:	n/a	n/a
37	CHD1	chr6:25147481-25147774	GM12878	blood:	n/a	n/a
38	CHD2	chr6:25153388-25153462	K562	blood:	n/a	n/a
39	CHD2	chr6:25105415-25105664	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr6:25147409-25147799	GM12878	blood:	n/a	n/a
41	CHD2	chr6:25155552-25155714	GM12878	blood:	n/a	n/a
42	CHD2	chr6:25137341-25137374	GM12878	blood:	n/a	n/a
43	CTCF	chr6:25139920-25140070	NHEK	skin:	n/a	n/a
44	CTCF	chr6:25138540-25138690	HMF	breast:	n/a	n/a
45	CTCF	chr6:25153353-25153614	K562	blood:	n/a	n/a
46	CTCF	chr6:25137300-25137450	HCFaa	heart:	n/a	n/a
47	CTCF	chr6:25138505-25138674	ProgFib	skin:	n/a	n/a
48	CTCF	chr6:25153360-25153510	K562	blood:	n/a	n/a
49	CTCF	chr6:25138440-25138590	GM12872	blood:	n/a	n/a
50	CTCF	chr6:25138560-25138710	HCM	heart:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:25140063-25140113	HRPEpiC	eye:	n/a
2	chr6:25140377-25140427	RPTEC	kidney:	n/a
3	chr6:25153422-25153472	NHBE	bronchial:	n/a
4	chr6:25140377-25140427	GM06990	blood:	n/a
5	chr6:25140063-25140113	HCM	heart:	n/a
6	chr6:25153473-25153523	HRCEpiC	kidney:	n/a
7	chr6:25138416-25138466	HL-60	blood:	n/a
8	chr6:25140063-25140113	AG04450	lung:	fetal
9	chr6:25156302-25156352	NHBE	bronchial:	n/a
10	chr6:25137864-25137914	SK-N-SH	brain:	n/a
11	chr6:25137971-25138021	BE2_C	brain:	n/a
12	chr6:25137864-25137914	SK-N-SH_RA	brain:	n/a
13	chr6:25143214-25143264	Hela-S3	cervix:	n/a
14	chr6:25138416-25138466	GM12892	blood:	n/a
15	chr6:25153422-25153472	HMEC	breast:	n/a
16	chr6:25137971-25138021	AG04449	skin:	fetal
17	chr6:25138951-25139001	ECC-1	luminal epithelium:	n/a
18	chr6:25138169-25138219	SK-N-SH_RA	brain:	n/a
19	chr6:25138905-25138955	CMK	blood:	n/a
20	chr6:25156302-25156352	AoSMC	blood vessel:	n/a
21	chr6:25140377-25140427	AG04450	lung:	fetal
22	chr6:25143214-25143264	AoSMC	blood vessel:	n/a
23	chr6:25140063-25140113	GM12891	blood:	n/a
24	chr6:25138169-25138219	HL-60	blood:	n/a
25	chr6:25138416-25138466	H1-hESC	embryonic stem cell:	embryo
26	chr6:25140091-25140141	U87	brain:	n/a
27	chr6:25088999-25089049	MCF10A-Er-Src	breast:	n/a
28	chr6:25153422-25153472	BJ	skin:	n/a
29	chr6:25137971-25138021	HAEpiC	amniotic membrane:	n/a
30	chr6:25156302-25156352	SAEC	small airway:	n/a
31	chr6:25153422-25153472	IMR90	lung:	fetal
32	chr6:25140063-25140113	HRCEpiC	kidney:	n/a
33	chr6:25143214-25143264	K562	blood:	n/a
34	chr6:25138551-25138601	AG09309	skin:	n/a
35	chr6:25138416-25138466	NH-A	brain:	n/a
36	chr6:25140063-25140113	Caco-2	colon:	n/a
37	chr6:25140136-25140186	HEK293	kidney:	embryo
38	chr6:25140136-25140186	SK-N-MC	brain:	n/a
39	chr6:25138169-25138219	HCM	heart:	n/a
40	chr6:25153566-25153616	HRE	kidney:	n/a
41	chr6:25137864-25137914	SAEC	small airway:	n/a
42	chr6:25140136-25140186	LNCaP	prostate:	n/a
43	chr6:25143214-25143264	AG04450	lung:	fetal
44	chr6:25137864-25137914	HMEC	breast:	n/a
45	chr6:25140377-25140427	HRPEpiC	eye:	n/a
46	chr6:25088999-25089049	SK-N-SH_RA	brain:	n/a
47	chr6:25088999-25089049	BJ	skin:	n/a
48	chr6:25138905-25138955	Jurkat	blood:	n/a
49	chr6:25153473-25153523	HUVEC	blood vessel:	n/a
50	chr6:25140136-25140186	HRCEpiC	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:25138546..25140373-chr6:25141189..25143013,2	MCF-7	breast:
2	chr6:25110856..25114923-chr6:25121965..25124614,3	MCF-7	breast:
3	chr6:25151401..25154186-chr6:25154333..25156125,2	MCF-7	breast:
4	chr6:24719858..24721554-chr6:25106494..25110308,3	MCF-7	breast:
5	chr6:25085087..25087243-chr6:25089273..25091853,2	K562	blood:
6	chr6:25150825..25153623-chr6:25154043..25156150,2	K562	blood:
7	chr6:25104314..25106415-chr6:25107785..25110653,2	MCF-7	breast:
8	chr6:25110740..25112750-chr6:25114092..25116124,2	K562	blood:
9	chr6:25084985..25086769-chr6:25088550..25090244,2	MCF-7	breast:
10	chr6:25083346..25086259-chr6:25098635..25100927,2	MCF-7	breast:
11	chr6:25112288..25113816-chr6:25114376..25117367,2	MCF-7	breast:
12	chr6:25096659..25099596-chr6:25104363..25107003,2	MCF-7	breast:
13	chr6:25111673..25113955-chr6:25164740..25166276,2	MCF-7	breast:
14	chr6:25122897..25125650-chr6:25128706..25130794,2	MCF-7	breast:
15	chr6:25044748..25046790-chr6:25120372..25122694,2	K562	blood:
16	chr6:25111673..25113955-chr6:25164740..25166276,2	MCF-7	breast:
17	chr6:25154053..25159519-chr6:25164374..25167875,7	MCF-7	breast:
18	chr6:25122897..25125650-chr6:25128706..25130794,2	MCF-7	breast:
19	chr6:25085087..25087243-chr6:25089273..25091853,2	K562	blood:
20	chr3:48488059..48488869-chr6:25100447..25101140,2	Hela-S3	cervix:
21	chr6:25110856..25114923-chr6:25121965..25124614,3	MCF-7	breast:
22	chr6:25110740..25112750-chr6:25114092..25116124,2	K562	blood:
23	chr6:25112288..25113816-chr6:25114376..25117367,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM65B-5	chr6:25162207-25162252	NONHSAT108140
2	lnc-FAM65B-4	chr6:25123162-25123790	ucscGeneNc_uc010jpw_1
3	lnc-LRRC16A-6	chr6:25164526-25164871	NONHSAT108139
4	lnc-FAM65B-5	chr6:25161834-25162061	NONHSAT108140
5	lnc-FAM65B-4	chr6:25150058-25150377	ucscGeneNc_uc010jpw_1
6	lnc-LRRC16A-6	chr6:25150046-25150123	NONHSAT108139
7	lnc-FAM65B-3	chr6:25084708-25085013	NONHSAT108136
8	lnc-FAM65B-5	chr6:25165219-25165280	NONHSAT108140
9	lnc-FAM65B-4	chr6:25123965-25124042	ucscGeneNc_uc010jpw_1
10	lnc-LRRC16A-6	chr6:25163170-25163322	NONHSAT108139
11	lnc-FAM65B-5	chr6:25162663-25162756	NONHSAT108140

No data

Variant related genes	Relation type
ENSG00000219682	TF binding region
CMAHP	TF binding region
ENSG00000262400	TF binding region
ENSG00000219682	CpG island
CMAHP	CpG island
ENSG00000262400	CpG island
ENSG00000219682	chromatin interactions
ENSG00000262400	chromatin interactions
ENSG00000164053	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000168405	chromatin interactions
ENSG00000244380	chromatin interactions

Extended variants
information (count: 3306 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3306 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs303006	chr6:25084718-25084719	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116068888	chr6:25084798-25084799	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs375883997	chr6:25084822-25084823	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs6917740	chr6:25084840-25084841	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs115126560	chr6:25084850-25084851	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs6917980	chr6:25084858-25084859	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs146847474	chr6:25084866-25084867	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs4538700	chr6:25084942-25084943	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs6918166	chr6:25084969-25084970	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs6918168	chr6:25084972-25084973	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528445061	chr6:25084978-25084979	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs189577816	chr6:25084981-25084982	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs11282039	chr6:25085002-25085003	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs371744171	chr6:25085011-25085012	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs571905196	chr6:25085161-25085162	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147932498	chr6:25085173-25085174	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114201325	chr6:25085181-25085182	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141600563	chr6:25085191-25085192	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6918864	chr6:25085214-25085215	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147067940	chr6:25085219-25085220	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565649900	chr6:25085270-25085271	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191640200	chr6:25085284-25085285	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115925396	chr6:25085342-25085343	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77907637	chr6:25085345-25085346	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374900259	chr6:25085351-25085352	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3792983	chr6:25085354-25085355	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs73384199	chr6:25085415-25085416	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs373673392	chr6:25085421-25085422	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79547624	chr6:25085422-25085423	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570467809	chr6:25085423-25085424	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573843454	chr6:25085428-25085429	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184689161	chr6:25085452-25085453	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376680613	chr6:25085551-25085552	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189059370	chr6:25085552-25085553	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73729433	chr6:25085587-25085588	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs573302790	chr6:25085617-25085618	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73384200	chr6:25085745-25085746	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs114063419	chr6:25085753-25085754	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs563056125	chr6:25085775-25085776	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542583661	chr6:25085783-25085784	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540806265	chr6:25085841-25085842	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs370101958	chr6:25085842-25085843	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs557266091	chr6:25085868-25085869	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575744399	chr6:25085898-25085899	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182031920	chr6:25085961-25085962	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185618178	chr6:25086005-25086006	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs149146025	chr6:25086013-25086014	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530193361	chr6:25086025-25086026	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs73729435	chr6:25086046-25086047	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565767779	chr6:25086053-25086054	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25071200-25085200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr6:25071200-25085400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr6:25071400-25084800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:25071400-25085600	Weak transcription	Primary B cells from cord blood	blood
5	chr6:25077000-25086600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:25079400-25085200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr6:25079400-25093000	Weak transcription	Ovary	ovary
8	chr6:25079600-25086800	Weak transcription	Aorta	Aorta
9	chr6:25079800-25086800	Weak transcription	Spleen	Spleen
10	chr6:25080200-25085800	Strong transcription	Dnd41	blood
11	chr6:25080400-25085200	Strong transcription	Thymus	Thymus
12	chr6:25080400-25085400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr6:25080400-25098000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:25080600-25084800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:25080800-25085000	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:25080800-25085400	Strong transcription	Fetal Thymus	thymus
17	chr6:25081000-25086600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:25081200-25084800	Weak transcription	Primary T cells from cord blood	blood
19	chr6:25081200-25092000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr6:25081600-25088800	Weak transcription	Osteobl	bone
21	chr6:25082000-25085000	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr6:25082200-25094800	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:25082400-25085200	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr6:25082400-25085600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr6:25082600-25084800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr6:25082600-25085200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:25082600-25105200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:25082800-25086000	Weak transcription	GM12878-XiMat	blood
29	chr6:25083000-25086000	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr6:25083000-25086800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr6:25083200-25085800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr6:25083800-25084800	Flanking Active TSS	HepG2	liver
33	chr6:25083800-25085000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr6:25083800-25085000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:25083800-25089800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:25083800-25093200	Weak transcription	Colonic Mucosa	Colon
37	chr6:25084000-25084800	Enhancers	Fetal Intestine Large	intestine
38	chr6:25084000-25084800	Enhancers	Gastric	stomach
39	chr6:25084000-25084800	Enhancers	Stomach Mucosa	stomach
40	chr6:25084000-25085400	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr6:25084000-25085600	Strong transcription	Placenta	Placenta
42	chr6:25084000-25087600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:25084200-25087000	Enhancers	Liver	Liver
44	chr6:25084200-25089800	Weak transcription	Hela-S3	cervix
45	chr6:25084400-25085000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:25084400-25085000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr6:25084400-25085000	Enhancers	Fetal Intestine Small	intestine
48	chr6:25084400-25085000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
49	chr6:25084400-25085400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr6:25084600-25084800	Enhancers	H9 Cell Line	embryonic stem cell

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