Variant report

Variant	esv1801843
Chromosome Location	chr6:110506109-110566328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:252)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:110530348-110530390	K562	blood:	n/a	n/a
2	ARID3A	chr6:110522771-110522987	K562	blood:	n/a	n/a
3	ARID3A	chr6:110561143-110561351	K562	blood:	n/a	n/a
4	ATF2	chr6:110526951-110527517	GM12878	blood:	n/a	n/a
5	BACH1	chr6:110528955-110529002	K562	blood:	n/a	n/a
6	BACH1	chr6:110529998-110530282	K562	blood:	n/a	chr6:110530104-110530118
7	BACH1	chr6:110560881-110561044	K562	blood:	n/a	n/a
8	BACH1	chr6:110518250-110518278	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:110530390-110530538	H1-hESC	embryonic stem cell:	n/a	chr6:110530521-110530535
10	BACH1	chr6:110518169-110518388	K562	blood:	n/a	n/a
11	BATF	chr6:110555248-110555485	GM12878	blood:	n/a	n/a
12	BATF	chr6:110555241-110555486	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:110555251-110555478	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:110507209-110507416	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:110532878-110533524	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr6:110521057-110521136	K562	blood:	n/a	n/a
17	CEBPB	chr6:110516865-110517226	A549	lung:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
18	CEBPB	chr6:110522734-110523035	K562	blood:	n/a	n/a
19	CEBPB	chr6:110516860-110517216	H1-hESC	embryonic stem cell:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
20	CEBPB	chr6:110516853-110517232	K562	blood:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
21	CEBPB	chr6:110532990-110533261	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:110542997-110543295	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:110516874-110517227	IMR90	lung:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
24	CEBPB	chr6:110516859-110517228	Hela-S3	cervix:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
25	CEBPB	chr6:110516912-110517200	ECC-1	luminal epithelium:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
26	CEBPB	chr6:110561164-110561417	K562	blood:	n/a	n/a
27	CEBPB	chr6:110532484-110533725	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:110533028-110533282	A549	lung:	n/a	n/a
29	CEBPB	chr6:110550841-110550973	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:110508204-110508301	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:110516887-110517173	ECC-1	luminal epithelium:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
32	CEBPB	chr6:110550809-110550933	K562	blood:	n/a	n/a
33	CEBPB	chr6:110516888-110517223	MCF-7	breast:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
34	CEBPB	chr6:110516879-110517226	HepG2	liver:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
35	CEBPB	chr6:110516829-110517197	A549	lung:	n/a	chr6:110517041-110517050 chr6:110517039-110517052 chr6:110517041-110517050 chr6:110517041-110517050 chr6:110517041-110517050
36	CEBPB	chr6:110532972-110533284	IMR90	lung:	n/a	n/a
37	CEBPD	chr6:110561050-110561562	K562	blood:	n/a	n/a
38	CEBPD	chr6:110561068-110561418	K562	blood:	n/a	n/a
39	CHD1	chr6:110507189-110507196	GM12878	blood:	n/a	n/a
40	CHD2	chr6:110560914-110560918	K562	blood:	n/a	n/a
41	CTCF	chr6:110517260-110517410	HMEC	breast:	n/a	n/a
42	CTCF	chr6:110517352-110517371	Medullo	brain:	n/a	n/a
43	CTCF	chr6:110538320-110538470	HAc	cerebellar:	n/a	n/a
44	CTCF	chr6:110538340-110538490	BJ	skin:	n/a	n/a
45	CTCF	chr6:110538440-110538590	AG10803	skin:	n/a	n/a
46	CTCF	chr6:110555359-110555437	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr6:110551670-110551735	Lung_OC	lung:	n/a	n/a
48	CTCF	chr6:110538480-110538630	HFF	foreskin:	n/a	n/a
49	CTCF	chr6:110538440-110538590	BJ	skin:	n/a	n/a
50	CTCF	chr6:110538320-110538470	HCPEpiC	choroid plexus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110552097-110552147	PFSK-1	brain:	n/a
2	chr6:110552097-110552147	AG09319	gingival:	n/a
3	chr6:110552097-110552147	HPAEpiC	pulmonary alveolar:	n/a
4	chr6:110552097-110552147	AG04449	skin:	fetal
5	chr6:110552097-110552147	T-47D	breast:	n/a
6	chr6:110552097-110552147	HEK293	kidney:	embryo
7	chr6:110552097-110552147	HRPEpiC	eye:	n/a
8	chr6:110552097-110552147	SKMC	muscle:	n/a
9	chr6:110552097-110552147	NT2-D1	testis:	n/a
10	chr6:110552097-110552147	HNPCEpiC	eye:	n/a
11	chr6:110552097-110552147	RPTEC	kidney:	n/a
12	chr6:110552097-110552147	SK-N-SH_RA	brain:	n/a
13	chr6:110552097-110552147	ProgFib	skin:	n/a
14	chr6:110552097-110552147	NHBE	bronchial:	n/a
15	chr6:110552097-110552147	NH-A	brain:	n/a
16	chr6:110552097-110552147	ovcar-3	ovarian:	n/a
17	chr6:110552097-110552147	HEEpiC	esophagus:	n/a
18	chr6:110552097-110552147	HRE	kidney:	n/a
19	chr6:110552097-110552147	HCM	heart:	n/a
20	chr6:110552097-110552147	HMEC	breast:	n/a
21	chr6:110552097-110552147	CMK	blood:	n/a
22	chr6:110552097-110552147	GM19239	blood:	n/a
23	chr6:110552097-110552147	HAEpiC	amniotic membrane:	n/a
24	chr6:110552097-110552147	HCPEpiC	choroid plexus:	n/a
25	chr6:110552097-110552147	PANC-1	pancreas:	n/a
26	chr6:110552097-110552147	HUVEC	blood vessel:	n/a
27	chr6:110552097-110552147	HL-60	blood:	n/a
28	chr6:110552097-110552147	AG04450	lung:	fetal
29	chr6:110552097-110552147	A549	lung:	n/a
30	chr6:110552097-110552147	SAEC	small airway:	n/a
31	chr6:110552097-110552147	NHDF-neo	bronchial:	n/a
32	chr6:110552097-110552147	Hepatocyte	liver:	n/a
33	chr6:110552097-110552147	BE2_C	brain:	n/a
34	chr6:110552097-110552147	LNCaP	prostate:	n/a
35	chr6:110552097-110552147	U87	brain:	n/a
36	chr6:110552097-110552147	SK-N-SH	brain:	n/a
37	chr6:110552097-110552147	Caco-2	colon:	n/a
38	chr6:110552097-110552147	AoSMC	blood vessel:	n/a
39	chr6:110552097-110552147	GM06990	blood:	n/a
40	chr6:110552097-110552147	GM12892	blood:	n/a
41	chr6:110552097-110552147	AG09309	skin:	n/a
42	chr6:110552097-110552147	BJ	skin:	n/a
43	chr6:110552097-110552147	MCF10A-Er-Src	breast:	n/a
44	chr6:110552097-110552147	Jurkat	blood:	n/a
45	chr6:110552097-110552147	ECC-1	luminal epithelium:	n/a
46	chr6:110552097-110552147	HCT-116	colon:	n/a
47	chr6:110552097-110552147	H1-hESC	embryonic stem cell:	embryo
48	chr6:110552097-110552147	PrEC	prostate:	n/a
49	chr6:110552097-110552147	K562	blood:	n/a
50	chr6:110552097-110552147	GM12878	blood:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110532696..110534924-chr6:110589578..110591934,2	K562	blood:
2	chr6:110499840..110501690-chr6:110520646..110522448,2	K562	blood:
3	chr6:110508464..110511221-chr6:110517530..110521627,4	K562	blood:
4	chr6:110511664..110513527-chr6:110524643..110526823,2	MCF-7	breast:
5	chr6:110500493..110502758-chr6:110507335..110510018,2	MCF-7	breast:
6	chr6:110500660..110503005-chr6:110505230..110508841,5	MCF-7	breast:
7	chr6:110530388..110533347-chr6:110533679..110536950,3	K562	blood:
8	chr6:110526245..110528126-chr6:110528743..110530781,2	K562	blood:
9	chr6:110500848..110506312-chr6:110514490..110518415,7	K562	blood:
10	chr6:110499664..110503910-chr6:110507183..110512081,7	K562	blood:
11	chr6:110503010..110505161-chr6:110508966..110510597,2	MCF-7	breast:
12	chr6:110522853..110524985-chr6:110532193..110534015,2	K562	blood:
13	chr6:110506447..110509996-chr6:110510060..110514287,5	K562	blood:
14	chr16:73103273..73105609-chr6:110532483..110534690,2	MCF-7	breast:
15	chr6:110522992..110525104-chr6:110527652..110529171,2	K562	blood:
16	chr6:110522853..110524985-chr6:110532193..110534015,2	K562	blood:
17	chr6:110521889..110524883-chr6:110552437..110554588,2	K562	blood:
18	chr6:110511080..110513805-chr6:110536717..110538803,2	K562	blood:
19	chr6:110514443..110518103-chr6:110520407..110523470,3	K562	blood:
20	chr6:110506447..110509996-chr6:110510060..110514287,5	K562	blood:
21	chr6:110525773..110528621-chr6:110547241..110549180,2	MCF-7	breast:
22	chr6:110525773..110528621-chr6:110547241..110549180,2	MCF-7	breast:
23	chr6:110499847..110502834-chr6:110509694..110511271,2	K562	blood:
24	chr6:110526245..110528126-chr6:110528743..110530781,2	K562	blood:
25	chr6:110500821..110504501-chr6:110516203..110518111,3	K562	blood:
26	chr6:110563724..110566253-chr6:110569811..110571861,3	K562	blood:
27	chr6:110511664..110513527-chr6:110524643..110526823,2	MCF-7	breast:
28	chr6:110501410..110504350-chr6:110509414..110512574,3	MCF-7	breast:
29	chr6:110528573..110531022-chr6:110531930..110534034,2	K562	blood:
30	chr6:110511080..110513805-chr6:110536717..110538803,2	K562	blood:
31	chr6:110504485..110506150-chr6:110519955..110521722,2	MCF-7	breast:
32	chr6:110501609..110503511-chr6:110521177..110523948,2	MCF-7	breast:
33	chr6:110528573..110531022-chr6:110531930..110534034,2	K562	blood:
34	chr6:110500660..110502175-chr6:110504680..110507002,2	MCF-7	breast:
35	chr6:110506402..110508834-chr6:110513795..110516786,2	K562	blood:
36	chr6:110550718..110552585-chr6:110556017..110558583,2	K562	blood:
37	chr6:110481649..110484031-chr6:110507011..110509592,2	K562	blood:
38	chr6:110550718..110552585-chr6:110556017..110558583,2	K562	blood:
39	chr6:110530388..110533347-chr6:110533679..110536950,3	K562	blood:
40	chr6:110506402..110508834-chr6:110513795..110516786,2	K562	blood:
41	chr6:110522992..110525104-chr6:110527652..110529171,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WASF1-1	chr6:110506697-110506731	NONHSAT114416
2	lnc-WASF1-1	chr6:110510755-110511131	NONHSAT114416
3	lnc-GPR6-1	chr6:110545499-110545632	ENSG00000244179.1
4	lnc-GPR6-1	chr6:110552655-110552835	ENSG00000244179.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDC40	hsa-miR-155-5p	chr6:110552894-110552917
2	CDC40	hsa-miR-155-5p	chr6:110553392-110553414

Variant related genes	Relation type
WASF1	TF binding region
CDC40	TF binding region
WASF1	CpG island
CDC40	CpG island
ENSG00000168438	chromatin interactions
ENSG00000112290	chromatin interactions

Extended variants
information (count: 2009 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2009 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36121596	chr6:110506109-110506110	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs148856368	chr6:110506112-110506113	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76375843	chr6:110506122-110506123	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
4	rs370654384	chr6:110506153-110506154	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541398904	chr6:110506158-110506159	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143532131	chr6:110506162-110506163	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569625302	chr6:110506198-110506199	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535352495	chr6:110506221-110506222	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548749005	chr6:110506230-110506231	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565648329	chr6:110506310-110506311	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534452991	chr6:110506318-110506319	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557847788	chr6:110506393-110506394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12660086	chr6:110506402-110506403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12660087	chr6:110506409-110506410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12660088	chr6:110506411-110506412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540040426	chr6:110506420-110506421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532953307	chr6:110506444-110506445	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556752786	chr6:110506452-110506453	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376483122	chr6:110506490-110506491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7740923	chr6:110506507-110506508	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7740924	chr6:110506508-110506509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555515273	chr6:110506597-110506598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572422260	chr6:110506600-110506601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541039931	chr6:110506613-110506614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112212375	chr6:110506649-110506650	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112809963	chr6:110506656-110506657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542009963	chr6:110506662-110506663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561055287	chr6:110506669-110506670	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs562219111	chr6:110506692-110506693	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201858189	chr6:110506725-110506726	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs12664697	chr6:110506739-110506740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs148036222	chr6:110506780-110506781	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549243701	chr6:110506782-110506783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141761934	chr6:110506801-110506802	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528107429	chr6:110506820-110506821	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77188290	chr6:110506847-110506848	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571372895	chr6:110506934-110506935	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537142599	chr6:110506936-110506937	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs556826272	chr6:110506948-110506949	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547791349	chr6:110506969-110506970	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570250029	chr6:110506991-110506992	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535642760	chr6:110507020-110507021	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs80266222	chr6:110507070-110507071	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
44	rs563109629	chr6:110507176-110507177	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530642381	chr6:110507197-110507198	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs371962667	chr6:110507220-110507221	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572604117	chr6:110507247-110507248	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188303558	chr6:110507253-110507254	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557858672	chr6:110507271-110507272	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533297302	chr6:110507467-110507468	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110502600-110515000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr6:110502600-110533200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:110502600-110536600	Weak transcription	Esophagus	oesophagus
4	chr6:110502800-110506400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:110502800-110508400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr6:110502800-110513800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:110502800-110533400	Weak transcription	HSMMtube	muscle
8	chr6:110503200-110506400	Enhancers	Adipose Nuclei	Adipose
9	chr6:110503200-110508600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:110503200-110511600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:110503200-110511800	Weak transcription	Right Ventricle	heart
12	chr6:110503200-110514800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:110503200-110515000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:110503200-110531400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:110503200-110533400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:110503400-110506400	Enhancers	Fetal Lung	lung
17	chr6:110503400-110506800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr6:110503400-110509000	Enhancers	Liver	Liver
19	chr6:110503400-110512000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr6:110503400-110515000	Weak transcription	Placenta	Placenta
21	chr6:110503400-110515000	Weak transcription	NH-A	brain
22	chr6:110503400-110530600	Weak transcription	Fetal Kidney	kidney
23	chr6:110503400-110536600	Weak transcription	Gastric	stomach
24	chr6:110503600-110514400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr6:110503600-110514400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:110503600-110514400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr6:110503600-110515200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr6:110503800-110506200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:110503800-110509800	Weak transcription	HSMM	muscle
30	chr6:110503800-110515400	Weak transcription	Fetal Intestine Large	intestine
31	chr6:110503800-110532800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr6:110503800-110533400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:110504200-110514400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:110504400-110506200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:110504400-110507000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:110504400-110507800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr6:110504400-110509600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:110504400-110514800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:110504400-110536600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:110504600-110507000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:110504600-110509600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:110504600-110513800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr6:110504600-110513800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr6:110504600-110514400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:110504600-110519400	Weak transcription	Fetal Intestine Small	intestine
46	chr6:110504600-110532400	Weak transcription	HMEC	breast
47	chr6:110504600-110536600	Weak transcription	Fetal Stomach	stomach
48	chr6:110504800-110506600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:110504800-110506800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:110504800-110507000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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