Variant report

Variant	nsv981324
Chromosome Location	chr6:34351435-34360764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:999)
CpG islands
(count:610)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34353646-34353947	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34356242-34356357	K562	blood:	n/a	n/a
3	ARID3A	chr6:34354166-34354831	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34360371-34360996	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:34354382-34354610	K562	blood:	n/a	n/a
6	ARID3A	chr6:34360494-34360822	K562	blood:	n/a	n/a
7	ARID3A	chr6:34358626-34359759	HepG2	liver:	n/a	n/a
8	ATF1	chr6:34358551-34359016	K562	blood:	n/a	n/a
9	ATF1	chr6:34360395-34360783	K562	blood:	n/a	chr6:34360428-34360442
10	ATF2	chr6:34360412-34360936	GM12878	blood:	n/a	chr6:34360428-34360442
11	ATF2	chr6:34360352-34360766	H1-hESC	embryonic stem cell:	n/a	chr6:34360428-34360442
12	ATF2	chr6:34360379-34360734	H1-hESC	embryonic stem cell:	n/a	chr6:34360428-34360442
13	ATF2	chr6:34359349-34359892	GM12878	blood:	n/a	n/a
14	ATF3	chr6:34360283-34360778	K562	blood:	n/a	chr6:34360430-34360443
15	BACH1	chr6:34360476-34360901	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:34360647-34360846	K562	blood:	n/a	n/a
17	BACH1	chr6:34359645-34359830	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:34360539-34360810	GM12878	blood:	n/a	n/a
19	BCL3	chr6:34360373-34360771	A549	lung:	n/a	n/a
20	BCL3	chr6:34359209-34359729	A549	lung:	n/a	n/a
21	BCLAF1	chr6:34359280-34360034	GM12878	blood:	n/a	chr6:34359751-34359764 chr6:34359956-34359969
22	BCLAF1	chr6:34360212-34361021	GM12878	blood:	n/a	chr6:34360278-34360291 chr6:34360288-34360297 chr6:34360288-34360301 chr6:34360274-34360283
23	BCLAF1	chr6:34360352-34361013	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:34359380-34359922	GM12878	blood:	n/a	chr6:34359751-34359764
25	BHLHE40	chr6:34359473-34360960	K562	blood:	n/a	chr6:34360277-34360293 chr6:34360451-34360467
26	BHLHE40	chr6:34359472-34359819	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:34359427-34360925	GM12878	blood:	n/a	chr6:34360277-34360293 chr6:34360451-34360467
28	BHLHE40	chr6:34360315-34360865	HepG2	liver:	n/a	chr6:34360451-34360467
29	BRCA1	chr6:34360471-34360771	GM12878	blood:	n/a	n/a
30	BRCA1	chr6:34360361-34360831	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr6:34358627-34359680	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr6:34360473-34360768	K562	blood:	n/a	n/a
33	CBX3	chr6:34360297-34360987	K562	blood:	n/a	n/a
34	CBX3	chr6:34359380-34359919	K562	blood:	n/a	n/a
35	CBX3	chr6:34356678-34357287	K562	blood:	n/a	n/a
36	CCNT2	chr6:34359535-34360908	K562	blood:	n/a	chr6:34360183-34360192
37	CEBPB	chr6:34353604-34353986	HepG2	liver:	n/a	chr6:34353793-34353804
38	CEBPB	chr6:34358744-34359303	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr6:34358865-34359089	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:34358887-34359062	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:34351049-34351810	IMR90	lung:	n/a	chr6:34351622-34351633
42	CEBPB	chr6:34353645-34353943	IMR90	lung:	n/a	chr6:34353793-34353804
43	CEBPB	chr6:34358793-34359064	K562	blood:	n/a	n/a
44	CEBPB	chr6:34358751-34359155	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:34353671-34353861	HepG2	liver:	n/a	chr6:34353793-34353804
46	CEBPB	chr6:34354464-34354628	K562	blood:	n/a	n/a
47	CEBPB	chr6:34353670-34353923	H1-hESC	embryonic stem cell:	n/a	chr6:34353793-34353804
48	CEBPB	chr6:34354255-34354741	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:34360403-34360991	GM12878	blood:	n/a	n/a
50	CEBPB	chr6:34358795-34359179	A549	lung:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34352082-34352132	T-47D	breast:	n/a
2	chr6:34356253-34356303	AG09319	gingival:	n/a
3	chr6:34360624-34360674	HCM	heart:	n/a
4	chr6:34360501-34360551	AG09319	gingival:	n/a
5	chr6:34360624-34360674	NHDF-neo	bronchial:	n/a
6	chr6:34360745-34360795	Caco-2	colon:	n/a
7	chr6:34360212-34360262	HCPEpiC	choroid plexus:	n/a
8	chr6:34360612-34360662	SAEC	small airway:	n/a
9	chr6:34360624-34360674	HIPEpiC	eye:	n/a
10	chr6:34359621-34359671	CMK	blood:	n/a
11	chr6:34360162-34360212	NHDF-neo	bronchial:	n/a
12	chr6:34352082-34352132	GM12878	blood:	n/a
13	chr6:34360745-34360795	BJ	skin:	n/a
14	chr6:34360612-34360662	BJ	skin:	n/a
15	chr6:34360162-34360212	Caco-2	colon:	n/a
16	chr6:34360162-34360212	RPTEC	kidney:	n/a
17	chr6:34360501-34360551	HRCEpiC	kidney:	n/a
18	chr6:34360612-34360662	GM06990	blood:	n/a
19	chr6:34360612-34360662	PANC-1	pancreas:	n/a
20	chr6:34359621-34359671	SK-N-SH_RA	brain:	n/a
21	chr6:34359621-34359671	ProgFib	skin:	n/a
22	chr6:34352082-34352132	NB4	blood:	n/a
23	chr6:34359501-34359551	AG09319	gingival:	n/a
24	chr6:34360162-34360212	HEK293	kidney:	embryo
25	chr6:34360162-34360212	SK-N-MC	brain:	n/a
26	chr6:34360745-34360795	GM12891	blood:	n/a
27	chr6:34359621-34359671	HIPEpiC	eye:	n/a
28	chr6:34360745-34360795	HNPCEpiC	eye:	n/a
29	chr6:34360162-34360212	HNPCEpiC	eye:	n/a
30	chr6:34360745-34360795	AG04449	skin:	fetal
31	chr6:34360501-34360551	GM12891	blood:	n/a
32	chr6:34356253-34356303	ECC-1	luminal epithelium:	n/a
33	chr6:34360162-34360212	BE2_C	brain:	n/a
34	chr6:34360212-34360262	BE2_C	brain:	n/a
35	chr6:34359501-34359551	HL-60	blood:	n/a
36	chr6:34352082-34352132	HCPEpiC	choroid plexus:	n/a
37	chr6:34359621-34359671	HUVEC	blood vessel:	n/a
38	chr6:34360212-34360262	PFSK-1	brain:	n/a
39	chr6:34360612-34360662	GM12892	blood:	n/a
40	chr6:34352082-34352132	BE2_C	brain:	n/a
41	chr6:34352082-34352132	HCF	heart:	n/a
42	chr6:34360612-34360662	HL-60	blood:	n/a
43	chr6:34360624-34360674	Jurkat	blood:	n/a
44	chr6:34360745-34360795	HEK293	kidney:	embryo
45	chr6:34360501-34360551	SK-N-SH	brain:	n/a
46	chr6:34360745-34360795	RPTEC	kidney:	n/a
47	chr6:34360624-34360674	SAEC	small airway:	n/a
48	chr6:34360212-34360262	SK-N-MC	brain:	n/a
49	chr6:34356253-34356303	SKMC	muscle:	n/a
50	chr6:34360612-34360662	IMR90	lung:	fetal

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34202422..34206409-chr6:34359682..34362061,4	MCF-7	breast:
2	chr6:34349500..34351699-chr6:34352826..34355839,3	K562	blood:
3	chr6:34202383..34217863-chr6:34357259..34364960,37	K562	blood:
4	chr6:34305135..34307781-chr6:34356782..34358757,2	MCF-7	breast:
5	chr6:34203144..34206658-chr6:34358641..34361602,5	MCF-7	breast:
6	chr6:34339964..34342823-chr6:34350298..34352076,2	K562	blood:
7	chr19:34662845..34663493-chr6:34359460..34360357,2	Hela-S3	cervix:
8	chr6:34346665..34350255-chr6:34350707..34354463,4	MCF-7	breast:
9	chr6:34214133..34219385-chr6:34356600..34362053,16	K562	blood:
10	chr6:34358377..34360251-chr6:34384641..34386602,2	MCF-7	breast:
11	chr6:34232571..34234778-chr6:34358274..34360439,2	K562	blood:
12	chr6:34358195..34361774-chr6:34391620..34393850,4	K562	blood:
13	chr6:34202852..34208935-chr6:34358420..34361531,11	K562	blood:
14	chr6:34357967..34362826-chr6:34390808..34395314,8	K562	blood:
15	chr6:34213633..34219276-chr6:34358105..34363296,16	MCF-7	breast:
16	chr6:34204870..34207622-chr6:34352958..34355269,2	K562	blood:
17	chr6:34353371..34356590-chr6:34358788..34361729,3	MCF-7	breast:
18	chr6:34216636..34217720-chr6:34359855..34360887,3	MCF-7	breast:
19	chr6:34358853..34362255-chr6:34392162..34395391,9	MCF-7	breast:
20	chr6:34216778..34218402-chr6:34353840..34355861,2	K562	blood:
21	chr6:34304154..34306840-chr6:34357586..34359775,2	MCF-7	breast:
22	chr6:34344409..34346828-chr6:34354344..34357154,2	K562	blood:
23	chr6:34341570..34343991-chr6:34351093..34353761,2	K562	blood:
24	chr6:34216509..34217580-chr6:34360199..34361678,8	K562	blood:
25	chr6:34355515..34358143-chr6:34358689..34360982,3	MCF-7	breast:
26	chr6:34180181..34181957-chr6:34360562..34363257,2	K562	blood:
27	chr6:34350156..34353339-chr6:34359370..34361777,7	MCF-7	breast:
28	chr6:34346965..34349809-chr6:34357029..34359430,2	MCF-7	breast:
29	chr6:34329241..34330151-chr6:34355752..34356539,2	K562	blood:
30	chr6:34216499..34217485-chr6:34360273..34361130,8	MCF-7	breast:
31	chr6:34215295..34220270-chr6:34358417..34361933,11	MCF-7	breast:
32	chr6:34336023..34338003-chr6:34357501..34359863,2	K562	blood:
33	chr6:34359786..34360581-chrX:107334340..107334971,2	Hela-S3	cervix:
34	chr6:34242678..34244532-chr6:34357227..34359923,2	MCF-7	breast:
35	chr6:34359614..34360461-chr9:130742747..130743592,2	HCT-116	colon:
36	chr6:34292790..34296171-chr6:34350622..34353853,3	K562	blood:
37	chr6:34343338..34346512-chr6:34355803..34358188,3	K562	blood:
38	chr6:34216778..34218697-chr6:34353840..34355736,2	K562	blood:
39	chr6:34349500..34351699-chr6:34352826..34355839,3	K562	blood:
40	chr6:34330571..34332725-chr6:34351916..34353996,2	K562	blood:
41	chr6:34355541..34358575-chr6:34361768..34363900,3	K562	blood:
42	chr1:171454646..171455442-chr6:34360140..34360662,2	HCT-116	colon:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACSIN1-1	chr6:34359628-34362546	l_3174_chr6:34355416-34362546_76bGuttman_hLF
2	lnc-PACSIN1-1	chr6:34360245-34362523	NONHSAT112134
3	lnc-RPS10-1	chr6:34355435-34357947	ucscGeneNc_uc003ojj_2
4	lnc-PACSIN1-1	chr6:34355417-34357076	l_3174_chr6:34355416-34362546_76bGuttman_hLF
5	lnc-PACSIN1-1	chr6:34355460-34360244	NONHSAT112133
6	lnc-NUDT3-2	chr6:34360305-34361774	ucscGeneNc_uc003ojk_1

No data

Variant related genes	Relation type
NUDT3	TF binding region
NUDT3	CpG island
ENSG00000117523	chromatin interactions
ENSG00000257103	chromatin interactions
ENSG00000101843	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000167106	chromatin interactions
ENSG00000101844	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000272325	chromatin interactions

Extended variants
information (count: 378 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542463954	chr6:34351450-34351451	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146340424	chr6:34351480-34351481	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530493478	chr6:34351499-34351500	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192036308	chr6:34351501-34351502	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147669856	chr6:34351503-34351504	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375760693	chr6:34351505-34351506	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200901554	chr6:34351506-34351507	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570540776	chr6:34351599-34351600	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560862710	chr6:34351609-34351610	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528329519	chr6:34351640-34351641	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116152166	chr6:34351652-34351653	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558010234	chr6:34351697-34351698	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375005731	chr6:34351723-34351724	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs3778077	chr6:34351767-34351768	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs534155154	chr6:34351823-34351824	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535394412	chr6:34351898-34351899	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs118002599	chr6:34352055-34352056	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569970118	chr6:34352078-34352079	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375580477	chr6:34352086-34352087	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187852873	chr6:34352098-34352099	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138287111	chr6:34352099-34352100	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576915136	chr6:34352116-34352117	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs116680338	chr6:34352159-34352160	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149565922	chr6:34352204-34352205	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112232358	chr6:34352280-34352281	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs76635412	chr6:34352365-34352366	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144202033	chr6:34352369-34352370	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192368927	chr6:34352391-34352392	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541800906	chr6:34352399-34352400	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34782152	chr6:34352426-34352427	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114564912	chr6:34352480-34352481	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545769316	chr6:34352503-34352504	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575172817	chr6:34352534-34352535	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528197251	chr6:34352582-34352583	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532360870	chr6:34352626-34352627	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546677017	chr6:34352636-34352637	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544294269	chr6:34352642-34352643	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564056748	chr6:34352649-34352650	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533136426	chr6:34352704-34352705	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183655791	chr6:34352723-34352724	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59104690	chr6:34352807-34352808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs55719137	chr6:34352822-34352823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186474276	chr6:34352837-34352838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192306639	chr6:34352863-34352864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569115412	chr6:34352864-34352865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372204147	chr6:34352878-34352879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548154732	chr6:34352891-34352892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547230008	chr6:34352894-34352895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552153241	chr6:34352912-34352913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529151885	chr6:34352939-34352940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34318200-34355800	Weak transcription	Brain Germinal Matrix	brain
2	chr6:34327000-34351600	Weak transcription	Ovary	ovary
3	chr6:34327800-34356400	Weak transcription	Hela-S3	cervix
4	chr6:34328600-34358000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:34331000-34358400	Weak transcription	Aorta	Aorta
6	chr6:34331200-34351600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr6:34331400-34353400	Weak transcription	Small Intestine	intestine
8	chr6:34331400-34353600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr6:34331600-34353600	Weak transcription	Fetal Intestine Large	intestine
10	chr6:34333600-34358000	Weak transcription	HMEC	breast
11	chr6:34335200-34354600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:34335600-34358800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:34337800-34359000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:34338000-34353600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr6:34338200-34351600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:34338200-34358600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:34338400-34353600	Weak transcription	Pancreas	Pancrea
18	chr6:34338400-34356600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr6:34338600-34351800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:34339200-34358000	Weak transcription	NHEK	skin
21	chr6:34339400-34358000	Weak transcription	HUVEC	blood vessel
22	chr6:34340400-34358000	Weak transcription	Fetal Thymus	thymus
23	chr6:34341000-34351800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr6:34342600-34355800	Weak transcription	Fetal Brain Female	brain
25	chr6:34342800-34353800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:34343000-34357600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr6:34343400-34356600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr6:34344000-34353800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:34344800-34351600	Weak transcription	Psoas Muscle	Psoas
30	chr6:34345200-34358600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr6:34346600-34351600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr6:34346600-34358400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:34346800-34353600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:34346800-34353600	Weak transcription	Spleen	Spleen
35	chr6:34346800-34353800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:34346800-34356400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr6:34347000-34351600	Weak transcription	Primary T cells from cord blood	blood
38	chr6:34347400-34351600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:34347800-34351800	Weak transcription	Fetal Intestine Small	intestine
40	chr6:34349000-34358800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:34349200-34355000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:34350200-34353800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:34350400-34352200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr6:34350400-34352600	Enhancers	Fetal Kidney	kidney
45	chr6:34350400-34352800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:34350400-34354200	Enhancers	Lung	lung
47	chr6:34350600-34359000	Weak transcription	Esophagus	oesophagus
48	chr6:34350800-34352400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:34350800-34352800	Enhancers	Osteobl	bone
50	chr6:34351000-34351800	Genic enhancers	Primary B cells from cord blood	blood

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