Variant report

Variant	esv2762616
Chromosome Location	chr6:132404708-132584324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1456)
CpG islands
(count:611)
Chromatin interactive
region (count:75)
LncRNA
region (count:92)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:132452907-132453166	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:132539273-132539587	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:132534456-132534636	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:132482500-132482836	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:132489365-132489419	HepG2	liver:	n/a	n/a
6	BATF	chr6:132406202-132406478	GM12878	blood:	n/a	n/a
7	BATF	chr6:132511679-132511874	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:132511684-132511928	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:132443955-132444371	HepG2	liver:	n/a	n/a
10	BRCA1	chr6:132411994-132412124	HepG2	liver:	n/a	n/a
11	CBX3	chr6:132530528-132530999	HCT-116	colon:	n/a	n/a
12	CBX3	chr6:132430920-132431283	K562	blood:	n/a	n/a
13	CBX3	chr6:132530418-132530968	HCT-116	colon:	n/a	n/a
14	CBX3	chr6:132431015-132431258	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:132430953-132431212	K562	blood:	n/a	n/a
16	CEBPB	chr6:132413154-132413421	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:132454087-132454475	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:132578444-132578943	HepG2	liver:	n/a	chr6:132578577-132578586 chr6:132578807-132578818 chr6:132578575-132578586
19	CEBPB	chr6:132513854-132514178	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:132534882-132535238	HepG2	liver:	n/a	chr6:132535048-132535059
21	CEBPB	chr6:132511166-132511341	A549	lung:	n/a	chr6:132511234-132511247 chr6:132511234-132511247 chr6:132511234-132511245 chr6:132511234-132511247
22	CEBPB	chr6:132511926-132512328	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:132549072-132549560	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:132513946-132514189	A549	lung:	n/a	n/a
25	CEBPB	chr6:132534908-132535245	A549	lung:	n/a	chr6:132535048-132535059
26	CEBPB	chr6:132544875-132545103	HepG2	liver:	n/a	chr6:132544924-132544935
27	CEBPB	chr6:132452600-132452611	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:132544799-132545028	IMR90	lung:	n/a	chr6:132544924-132544935
29	CEBPB	chr6:132405806-132406994	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:132452852-132453145	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:132513904-132514164	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:132535000-132535206	H1-hESC	embryonic stem cell:	n/a	chr6:132535048-132535059
33	CEBPB	chr6:132534921-132535146	K562	blood:	n/a	chr6:132535048-132535059
34	CEBPB	chr6:132523676-132524131	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:132482411-132482729	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:132525571-132525816	HepG2	liver:	n/a	chr6:132525700-132525711
37	CEBPB	chr6:132452910-132453180	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:132578464-132578966	IMR90	lung:	n/a	chr6:132578577-132578586 chr6:132578807-132578818 chr6:132578575-132578586
39	CEBPB	chr6:132534884-132535216	Hela-S3	cervix:	n/a	chr6:132535048-132535059
40	CEBPB	chr6:132430942-132431176	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:132511101-132511385	IMR90	lung:	n/a	chr6:132511234-132511247 chr6:132511234-132511247 chr6:132511234-132511245 chr6:132511234-132511247
42	CEBPB	chr6:132534869-132535277	IMR90	lung:	n/a	chr6:132535048-132535059
43	CEBPB	chr6:132578467-132578908	A549	lung:	n/a	chr6:132578577-132578586 chr6:132578807-132578818 chr6:132578575-132578586
44	CEBPB	chr6:132443786-132444378	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:132482353-132482751	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:132510025-132510520	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:132476794-132477081	IMR90	lung:	n/a	chr6:132476954-132476963 chr6:132476954-132476963
48	CEBPB	chr6:132434523-132434550	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:132452507-132453278	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:132476786-132477011	A549	lung:	n/a	chr6:132476954-132476963 chr6:132476954-132476963

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:132557557-132557607	CMK	blood:	n/a
2	chr6:132557557-132557607	CMK	blood:	n/a
3	chr6:132453778-132453828	T-47D	breast:	n/a
4	chr6:132455023-132455073	HCM	heart:	n/a
5	chr6:132531419-132531469	SK-N-MC	brain:	n/a
6	chr6:132557557-132557607	HepG2	liver:	n/a
7	chr6:132453670-132453720	HCF	heart:	n/a
8	chr6:132465076-132465126	BE2_C	brain:	n/a
9	chr6:132468790-132468840	Hepatocyte	liver:	n/a
10	chr6:132455023-132455073	MCF10A-Er-Src	breast:	n/a
11	chr6:132410188-132410238	BJ	skin:	n/a
12	chr6:132453778-132453828	ECC-1	luminal epithelium:	n/a
13	chr6:132453778-132453828	HNPCEpiC	eye:	n/a
14	chr6:132455023-132455073	NHBE	bronchial:	n/a
15	chr6:132465076-132465126	BJ	skin:	n/a
16	chr6:132468790-132468840	HEK293	kidney:	embryo
17	chr6:132557557-132557607	HL-60	blood:	n/a
18	chr6:132531419-132531469	A549	lung:	n/a
19	chr6:132453670-132453720	NB4	blood:	n/a
20	chr6:132468790-132468840	HCPEpiC	choroid plexus:	n/a
21	chr6:132465076-132465126	AG04449	skin:	fetal
22	chr6:132465076-132465126	HMEC	breast:	n/a
23	chr6:132580009-132580059	HCT-116	colon:	n/a
24	chr6:132468790-132468840	CMK	blood:	n/a
25	chr6:132580009-132580059	SK-N-MC	brain:	n/a
26	chr6:132531419-132531469	HEEpiC	esophagus:	n/a
27	chr6:132580009-132580059	ovcar-3	ovarian:	n/a
28	chr6:132568050-132568100	SK-N-SH	brain:	n/a
29	chr6:132557557-132557607	GM19239	blood:	n/a
30	chr6:132410188-132410238	AG09319	gingival:	n/a
31	chr6:132453670-132453720	RPTEC	kidney:	n/a
32	chr6:132568050-132568100	SAEC	small airway:	n/a
33	chr6:132580009-132580059	T-47D	breast:	n/a
34	chr6:132453670-132453720	NT2-D1	testis:	n/a
35	chr6:132410188-132410238	HCM	heart:	n/a
36	chr6:132580009-132580059	GM12892	blood:	n/a
37	chr6:132468790-132468840	PrEC	prostate:	n/a
38	chr6:132453778-132453828	HEEpiC	esophagus:	n/a
39	chr6:132465076-132465126	GM12892	blood:	n/a
40	chr6:132531419-132531469	SK-N-SH	brain:	n/a
41	chr6:132568050-132568100	IMR90	lung:	fetal
42	chr6:132410188-132410238	PANC-1	pancreas:	n/a
43	chr6:132410188-132410238	SK-N-SH	brain:	n/a
44	chr6:132455023-132455073	GM19239	blood:	n/a
45	chr6:132453670-132453720	NHDF-neo	bronchial:	n/a
46	chr6:132455023-132455073	SKMC	muscle:	n/a
47	chr6:132410188-132410238	SK-N-SH_RA	brain:	n/a
48	chr6:132453778-132453828	SK-N-SH_RA	brain:	n/a
49	chr6:132455023-132455073	IMR90	lung:	fetal
50	chr6:132568050-132568100	HIPEpiC	eye:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	6:132182612-132191683..6:132459405-132471553	GM12878	blood:
2	chr6:132236408..132236959-chr6:132579950..132580479,2	MCF-7	breast:
3	6:132176847-132180372..6:132483283-132485040	GM12878	blood:
4	chr6:132512891..132514685-chr6:132518793..132521767,2	MCF-7	breast:
5	6:132269655-132282174..6:132483283-132485040	GM12878	blood:
6	6:132269655-132282174..6:132542770-132543792	GM12878	blood:
7	chr6:132574260..132576242-chr6:132578431..132580676,2	K562	blood:
8	6:132269655-132282174..6:132550513-132556576	GM12878	blood:
9	6:132182612-132191683..6:132550513-132556576	GM12878	blood:
10	6:132176847-132180372..6:132564401-132574898	K562	blood:
11	chr6:132435293..132437623-chr6:132441893..132443467,2	MCF-7	breast:
12	6:132269655-132282174..6:132575568-132580912	GM12878	blood:
13	6:132182612-132191683..6:132575568-132580912	Hela-S3	cervix:
14	chr6:132244286..132245237-chr6:132580368..132580917,6	MCF-7	breast:
15	6:132182612-132191683..6:132506466-132514341	H1-hESC	embryonic stem cell:	embryo
16	6:132269655-132282174..6:132559814-132563625	H1-hESC	embryonic stem cell:	embryo
17	chr6:132512891..132514685-chr6:132518793..132521767,2	MCF-7	breast:
18	chr6:132245752..132246616-chr6:132580048..132580875,2	MCF-7	breast:
19	6:132459405-132471553..6:132646256-132647474	Hela-S3	cervix:
20	6:132269655-132282174..6:132422197-132424174	K562	blood:
21	6:132176847-132180372..6:132542770-132543792	Hela-S3	cervix:
22	6:132176847-132180372..6:132441471-132451441	K562	blood:
23	6:132182612-132191683..6:132441471-132451441	Hela-S3	cervix:
24	6:132269655-132282174..6:132438109-132441471	H1-hESC	embryonic stem cell:	embryo
25	6:132269655-132282174..6:132539300-132542380	GM12878	blood:
26	6:132182612-132191683..6:132539300-132542380	Hela-S3	cervix:
27	6:132269655-132282174..6:132480387-132483283	H1-hESC	embryonic stem cell:	embryo
28	6:132269655-132282174..6:132486779-132489747	H1-hESC	embryonic stem cell:	embryo
29	6:132269655-132282174..6:132530065-132532463	H1-hESC	embryonic stem cell:	embryo
30	6:132269655-132282174..6:132475528-132476977	H1-hESC	embryonic stem cell:	embryo
31	6:132182612-132191683..6:132483283-132485040	H1-hESC	embryonic stem cell:	embryo
32	chr6:132281702..132282383-chr6:132538997..132539850,2	MCF-7	breast:
33	6:132269655-132282174..6:132503283-132504311	GM12878	blood:
34	chr6:132246017..132246619-chr6:132482850..132483756,2	MCF-7	breast:
35	6:132269655-132282174..6:132547485-132550513	GM12878	blood:
36	chr6:132271480..132272371-chr6:132482420..132483016,2	MCF-7	breast:
37	6:132269655-132282174..6:132536758-132539300	GM12878	blood:
38	chr6:132549264..132551055-chr6:132553054..132555430,2	K562	blood:
39	6:132269655-132282174..6:132533382-132536758	H1-hESC	embryonic stem cell:	embryo
40	6:132176847-132180372..6:132550513-132556576	K562	blood:
41	6:132269655-132282174..6:132564401-132574898	GM12878	blood:
42	6:132269655-132282174..6:132416565-132417578	GM12878	blood:
43	6:132176847-132180372..6:132514341-132516787	GM12878	blood:
44	chr6:132271624..132272270-chr6:132482087..132482966,3	MCF-7	breast:
45	6:132269655-132282174..6:132402790-132406656	H1-hESC	embryonic stem cell:	embryo
46	6:132182612-132191683..6:132438109-132441471	GM12878	blood:
47	6:132269655-132282174..6:132459405-132471553	H1-hESC	embryonic stem cell:	embryo
48	6:132441471-132451441..6:132646256-132647474	K562	blood:
49	6:132269655-132282174..6:132424270-132433961	H1-hESC	embryonic stem cell:	embryo
50	chr6:132236129..132236633-chr6:132539268..132539863,2	MCF-7	breast:

(count:92 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENPP1-4	chr6:132455118-132455623	XLOC_005465
2	lnc-ENPP1-4	chr6:132490141-132490514	NONHSAT114951
3	lnc-ENPP1-7	chr6:132497105-132497316	NONHSAT114959
4	lnc-ENPP1-4	chr6:132453094-132453329	XLOC_005465
5	lnc-ENPP1-7	chr6:132517489-132517610	NONHSAT114961
6	lnc-ENPP1-3	chr6:132420071-132420366	XLOC_005464
7	lnc-ENPP1-4	chr6:132468925-132468984	XLOC_005465
8	lnc-ENPP1-4	chr6:132481907-132482058	XLOC_005465
9	lnc-ENPP1-7	chr6:132523597-132523747	NONHSAT114962
10	lnc-ENPP1-4	chr6:132475796-132475917	XLOC_005465
11	lnc-ENPP1-4	chr6:132475796-132475917	XLOC_005465
12	lnc-ENPP1-4	chr6:132475796-132475917	ENSG00000228495
13	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
14	lnc-ENPP1-4	chr6:132481904-132482054	NONHSAT114953
15	lnc-ENPP1-4	chr6:132468929-132468984	XLOC_005465
16	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
17	lnc-ENPP1-4	chr6:132467360-132467589	XLOC_005465
18	lnc-ENPP1-4	chr6:132490141-132490300	XLOC_005465
19	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
20	lnc-ENPP1-6	chr6:132453366-132453559	NONHSAT114950
21	lnc-ENPP1-4	chr6:132467360-132468196	XLOC_005465
22	lnc-ENPP1-7	chr6:132517489-132517610	ucscGeneNc_uc003qdd_2
23	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
24	lnc-ENPP1-4	chr6:132490141-132490514	ENSG00000228495
25	lnc-ENPP1-4	chr6:132490141-132490332	XLOC_005465
26	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
27	lnc-ENPP1-4	chr6:132455412-132455623	XLOC_005465
28	lnc-ENPP1-7	chr6:132496811-132497316	ucscGeneNc_uc003qdd_2
29	lnc-ENPP1-4	chr6:132475796-132475917	XLOC_005465
30	lnc-ENPP1-4	chr6:132485037-132486685	NONHSAT114953
31	lnc-ENPP1-4	chr6:132453298-132453329	XLOC_005465
32	lnc-ENPP1-4	chr6:132455582-132455623	XLOC_005465
33	lnc-ENPP1-4	chr6:132456580-132458073	XLOC_005465
34	lnc-ENPP1-7	chr6:132497244-132497316	NONHSAT114961
35	lnc-ENPP1-4	chr6:132455118-132455623	NONHSAT114953
36	lnc-ENPP1-6	chr6:132461764-132462059	NONHSAT114950
37	lnc-ENPP1-4	chr6:132485036-132485631	NONHSAT114957
38	lnc-ENPP1-4	chr6:132481907-132482058	XLOC_005465
39	lnc-ENPP1-4	chr6:132456803-132457146	NONHSAT114953
40	lnc-ENPP1-4	chr6:132453098-132453109	XLOC_005465
41	lnc-ENPP1-4	chr6:132455118-132455623	ENSG00000228495
42	lnc-ENPP1-3	chr6:132419818-132421535	NONHSAT114937
43	lnc-ENPP1-4	chr6:132453260-132453329	XLOC_005465
44	lnc-ENPP1-4	chr6:132481903-132482054	NONHSAT114957
45	lnc-ENPP1-7	chr6:132496811-132497316	NONHSAT114960
46	lnc-ENPP1-4	chr6:132467360-132468198	ENSG00000228495
47	lnc-ENPP1-4	chr6:132481904-132482054	XLOC_005465
48	lnc-ENPP1-4	chr6:132490141-132490501	XLOC_005465
49	lnc-ENPP1-4	chr6:132453298-132453329	XLOC_005465
50	lnc-ENPP1-4	chr6:132481907-132482058	XLOC_005465

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548aj-3p	chr6:132436339-132436359	MIMAT0018990

No data

Variant related genes	Relation type
MIR548AJ1	TF binding region
LINC01013	TF binding region
ENSG00000236166	TF binding region
MIR548AJ1	CpG island
LINC01013	CpG island
ENSG00000236166	CpG island
ENSG00000227220	chromatin interactions
ENSG00000079931	chromatin interactions
ENSG00000118523	chromatin interactions
ENSG00000265669	chromatin interactions
ENSG00000197594	chromatin interactions
COPG	miRNA target sites
XKRX	miRNA target sites
XIAP	miRNA target sites
SLA2	miRNA target sites
SEC23A	miRNA target sites
FOXP1	miRNA target sites
MAP1S	miRNA target sites
ANKRD52	miRNA target sites
FRS2	miRNA target sites
UBLCP1	miRNA target sites
HNRNPA1	miRNA target sites
RP1L1	miRNA target sites
FRMD8	miRNA target sites
FOXP4	miRNA target sites
ALMS1	miRNA target sites

Extended variants
information (count: 6838 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6838 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564807727	chr6:132404744-132404745	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs565467138	chr6:132404746-132404747	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368759659	chr6:132404769-132404770	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs4425614	chr6:132404881-132404882	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs550932702	chr6:132404902-132404903	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs114135594	chr6:132404911-132404912	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs373022401	chr6:132404926-132404927	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539933862	chr6:132404996-132404997	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540655264	chr6:132405026-132405027	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370087504	chr6:132405036-132405037	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs9321323	chr6:132405059-132405060	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs142788480	chr6:132405077-132405078	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs111259464	chr6:132405121-132405122	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533964608	chr6:132405130-132405131	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs552524541	chr6:132405185-132405186	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538744254	chr6:132405200-132405201	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs111366979	chr6:132405211-132405212	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs9388965	chr6:132405223-132405224	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs374325317	chr6:132405241-132405242	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs556448692	chr6:132405254-132405255	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371385805	chr6:132405258-132405259	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574691717	chr6:132405297-132405298	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs368259586	chr6:132405317-132405318	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs367941642	chr6:132405385-132405386	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs77281452	chr6:132405400-132405401	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138186934	chr6:132405425-132405426	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs12195132	chr6:132405428-132405429	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs532987766	chr6:132405439-132405440	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs545516241	chr6:132405520-132405521	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144674178	chr6:132405531-132405532	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs375835984	chr6:132405532-132405533	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs148520670	chr6:132405542-132405543	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs544508171	chr6:132405552-132405553	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs118068952	chr6:132405572-132405573	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142799334	chr6:132405573-132405574	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs150630693	chr6:132405577-132405578	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13213956	chr6:132405654-132405655	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75773252	chr6:132405791-132405792	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs527773420	chr6:132405797-132405798	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs143770555	chr6:132405817-132405818	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs146855560	chr6:132405878-132405879	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs566443616	chr6:132405920-132405921	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs200983973	chr6:132405949-132405950	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs10694779	chr6:132405950-132405951	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35775637	chr6:132405951-132405952	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs71030780	chr6:132405956-132405957	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs563375276	chr6:132405957-132405958	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs568331077	chr6:132405969-132405970	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs375604510	chr6:132406006-132406007	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535674237	chr6:132406027-132406028	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Autism	22495311	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
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	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
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1211 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132392000-132405000	Weak transcription	HMEC	breast
2	chr6:132392000-132405400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:132396000-132406200	Weak transcription	Aorta	Aorta
4	chr6:132402400-132405000	Weak transcription	NHLF	lung
5	chr6:132402400-132406400	Weak transcription	Ovary	ovary
6	chr6:132402600-132405000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:132403000-132406000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:132403400-132406200	Enhancers	HUVEC	blood vessel
9	chr6:132403400-132406400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr6:132403800-132406200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:132404000-132405000	Enhancers	HSMM	muscle
12	chr6:132404000-132405400	Weak transcription	NHDF-Ad	bronchial
13	chr6:132404000-132405800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:132404000-132406400	Enhancers	HSMMtube	muscle
15	chr6:132404000-132406400	Enhancers	Osteobl	bone
16	chr6:132404000-132410400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:132404200-132406200	Enhancers	Fetal Heart	heart
18	chr6:132404600-132406200	Enhancers	NH-A	brain
19	chr6:132404600-132407600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:132405000-132405200	Weak transcription	HSMM	muscle
21	chr6:132405000-132406200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:132405000-132406600	Enhancers	NHLF	lung
23	chr6:132405000-132407000	Enhancers	HMEC	breast
24	chr6:132405000-132407200	Enhancers	Placenta	Placenta
25	chr6:132405000-132407600	Enhancers	NHEK	skin
26	chr6:132405000-132408400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:132405200-132405400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:132405200-132406200	Enhancers	HSMM	muscle
29	chr6:132405200-132407200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:132405400-132405800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:132405400-132406000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:132405400-132406200	Enhancers	Colon Smooth Muscle	Colon
33	chr6:132405400-132406200	Enhancers	Stomach Smooth Muscle	stomach
34	chr6:132405400-132406200	Enhancers	GM12878-XiMat	blood
35	chr6:132405400-132406200	Enhancers	NHDF-Ad	bronchial
36	chr6:132405400-132406600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:132405400-132407200	Enhancers	Fetal Muscle Leg	muscle
38	chr6:132405400-132407200	Enhancers	Right Atrium	heart
39	chr6:132405400-132407600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:132405600-132405800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:132405800-132406400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:132405800-132406800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:132405800-132407000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:132405800-132409600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:132406000-132406200	Enhancers	HepG2	liver
46	chr6:132406000-132406400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:132406000-132406400	Enhancers	Brain Substantia Nigra	brain
48	chr6:132406000-132406800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:132406000-132407000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr6:132406000-132407600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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