Variant report

Variant	nsv886185
Chromosome Location	chr6:76320846-76498109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1384)
CpG islands
(count:549)
Chromatin interactive
region (count:170)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1384 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76333004-76333194	K562	blood:	n/a	n/a
2	ARID3A	chr6:76339500-76339892	K562	blood:	n/a	n/a
3	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76322881-76323353	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:76342477-76343204	K562	blood:	n/a	chr6:76342662-76342678
7	ARID3A	chr6:76331504-76331869	K562	blood:	n/a	n/a
8	ARID3A	chr6:76337921-76337975	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
10	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
11	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
13	ATF1	chr6:76342790-76343022	K562	blood:	n/a	n/a
14	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
15	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:76407134-76407232	K562	blood:	n/a	n/a
18	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
19	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
20	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
21	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
22	BCL11A	chr6:76453680-76454055	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:76463949-76464065	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:76463942-76463968	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:76452022-76452184	HepG2	liver:	n/a	chr6:76452041-76452057
27	BHLHE40	chr6:76397729-76398031	K562	blood:	n/a	n/a
28	BHLHE40	chr6:76485025-76485362	K562	blood:	n/a	n/a
29	BHLHE40	chr6:76458636-76459067	K562	blood:	n/a	chr6:76459001-76459017
30	BHLHE40	chr6:76458636-76459158	GM12878	blood:	n/a	chr6:76459001-76459017
31	BHLHE40	chr6:76486318-76486449	K562	blood:	n/a	n/a
32	BRCA1	chr6:76331729-76331799	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr6:76458481-76458684	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr6:76458548-76459230	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr6:76463601-76464204	HCT-116	colon:	n/a	n/a
36	CCNT2	chr6:76491068-76491258	K562	blood:	n/a	n/a
37	CCNT2	chr6:76458398-76459210	K562	blood:	n/a	n/a
38	CCNT2	chr6:76484983-76485301	K562	blood:	n/a	n/a
39	CCNT2	chr6:76342926-76343181	K562	blood:	n/a	n/a
40	CCNT2	chr6:76339667-76339842	K562	blood:	n/a	n/a
41	CEBPB	chr6:76322893-76323187	IMR90	lung:	n/a	chr6:76323018-76323029
42	CEBPB	chr6:76485110-76485470	K562	blood:	n/a	chr6:76485314-76485331 chr6:76485319-76485330 chr6:76485252-76485264 chr6:76485317-76485330
43	CEBPB	chr6:76400625-76401191	HCT-116	colon:	n/a	chr6:76400914-76400925
44	CEBPB	chr6:76400858-76401116	ECC-1	luminal epithelium:	n/a	chr6:76400914-76400925
45	CEBPB	chr6:76400838-76401046	H1-hESC	embryonic stem cell:	n/a	chr6:76400914-76400925
46	CEBPB	chr6:76396873-76397089	K562	blood:	n/a	n/a
47	CEBPB	chr6:76383017-76383259	HepG2	liver:	n/a	chr6:76383095-76383106
48	CEBPB	chr6:76383586-76384024	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:76465468-76465784	HepG2	liver:	n/a	chr6:76465644-76465657 chr6:76465645-76465656 chr6:76465646-76465655 chr6:76465644-76465657 chr6:76465644-76465657 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465646-76465655
50	CEBPB	chr6:76420511-76420824	IMR90	lung:	n/a	chr6:76420672-76420683

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76461321-76461371	AG04449	skin:	fetal
2	chr6:76459077-76459127	HRPEpiC	eye:	n/a
3	chr6:76461321-76461371	GM12891	blood:	n/a
4	chr6:76458005-76458055	PANC-1	pancreas:	n/a
5	chr6:76459077-76459127	AG04449	skin:	fetal
6	chr6:76330505-76330555	HEK293	kidney:	embryo
7	chr6:76459077-76459127	NH-A	brain:	n/a
8	chr6:76330505-76330555	AG10803	skin:	n/a
9	chr6:76330505-76330555	AG09309	skin:	n/a
10	chr6:76456187-76456237	PFSK-1	brain:	n/a
11	chr6:76458633-76458683	GM06990	blood:	n/a
12	chr6:76459077-76459127	RPTEC	kidney:	n/a
13	chr6:76341733-76341783	BE2_C	brain:	n/a
14	chr6:76456187-76456237	HCPEpiC	choroid plexus:	n/a
15	chr6:76456187-76456237	HRPEpiC	eye:	n/a
16	chr6:76458005-76458055	Jurkat	blood:	n/a
17	chr6:76458005-76458055	HUVEC	blood vessel:	n/a
18	chr6:76459077-76459127	CMK	blood:	n/a
19	chr6:76459511-76459561	ProgFib	skin:	n/a
20	chr6:76459511-76459561	HRCEpiC	kidney:	n/a
21	chr6:76461321-76461371	GM19239	blood:	n/a
22	chr6:76458005-76458055	ECC-1	luminal epithelium:	n/a
23	chr6:76458005-76458055	HRCEpiC	kidney:	n/a
24	chr6:76459077-76459127	AoSMC	blood vessel:	n/a
25	chr6:76458005-76458055	HEEpiC	esophagus:	n/a
26	chr6:76461321-76461371	HL-60	blood:	n/a
27	chr6:76330505-76330555	HL-60	blood:	n/a
28	chr6:76456187-76456237	HEEpiC	esophagus:	n/a
29	chr6:76459077-76459127	HCF	heart:	n/a
30	chr6:76330505-76330555	SK-N-MC	brain:	n/a
31	chr6:76425457-76425507	MCF10A-Er-Src	breast:	n/a
32	chr6:76458005-76458055	HL-60	blood:	n/a
33	chr6:76458633-76458683	Jurkat	blood:	n/a
34	chr6:76425457-76425507	HCPEpiC	choroid plexus:	n/a
35	chr6:76330505-76330555	ProgFib	skin:	n/a
36	chr6:76456187-76456237	K562	blood:	n/a
37	chr6:76461321-76461371	NT2-D1	testis:	n/a
38	chr6:76458005-76458055	MCF10A-Er-Src	breast:	n/a
39	chr6:76341733-76341783	AG09309	skin:	n/a
40	chr6:76330505-76330555	NH-A	brain:	n/a
41	chr6:76459511-76459561	IMR90	lung:	fetal
42	chr6:76459077-76459127	ECC-1	luminal epithelium:	n/a
43	chr6:76456187-76456237	HEK293	kidney:	embryo
44	chr6:76456187-76456237	GM12878	blood:	n/a
45	chr6:76459511-76459561	HL-60	blood:	n/a
46	chr6:76459077-76459127	HNPCEpiC	eye:	n/a
47	chr6:76330505-76330555	PFSK-1	brain:	n/a
48	chr6:76456187-76456237	HMEC	breast:	n/a
49	chr6:76458005-76458055	SK-N-MC	brain:	n/a
50	chr6:76458005-76458055	GM06990	blood:	n/a

(count:170 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:76359039..76361608-chr6:76376741..76379401,2	MCF-7	breast:
2	chr6:76325725..76327529-chr6:76327837..76330229,2	K562	blood:
3	chr6:76330148..76333811-chr6:76341672..76344273,3	K562	blood:
4	chr6:76309815..76313106-chr6:76322931..76328588,7	MCF-7	breast:
5	chr6:76461303..76463860-chr6:76468925..76471220,2	K562	blood:
6	chr6:76408144..76410485-chr6:76410972..76412755,2	MCF-7	breast:
7	chr6:76404187..76405990-chr6:76505413..76507332,2	MCF-7	breast:
8	chr6:76456956..76459058-chr6:76494657..76497303,3	MCF-7	breast:
9	chr6:76359039..76361608-chr6:76376741..76379401,2	MCF-7	breast:
10	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
11	chr6:76327323..76329622-chr6:76330394..76331981,2	K562	blood:
12	chr6:76371815..76374314-chr6:76380785..76382399,2	MCF-7	breast:
13	chr6:76386546..76388318-chr6:76399041..76401218,2	K562	blood:
14	chr6:76310717..76312305-chr6:76374454..76377244,2	K562	blood:
15	chr6:76463940..76466517-chr6:76472497..76474287,2	K562	blood:
16	chr6:76363284..76364897-chr6:76389536..76391998,2	MCF-7	breast:
17	chr6:76346868..76349503-chr6:76350758..76352426,2	MCF-7	breast:
18	chr6:76327800..76329805-chr6:76331383..76333611,2	K562	blood:
19	chr2:233562031..233562988-chr6:76458771..76459462,2	Hela-S3	cervix:
20	chr6:76348163..76350859-chr6:76356641..76358719,2	K562	blood:
21	chr6:76310119..76312323-chr6:76471979..76473614,2	MCF-7	breast:
22	chr6:76336673..76339246-chr6:76344928..76346520,2	MCF-7	breast:
23	chr6:76386546..76388318-chr6:76399041..76401218,2	K562	blood:
24	chr6:76450359..76452041-chr6:76457600..76459670,2	MCF-7	breast:
25	chr6:75992888..75995675-chr6:76335735..76338499,2	K562	blood:
26	chr6:76461153..76463947-chr6:76466842..76469998,3	MCF-7	breast:
27	chr6:76359388..76361142-chr6:76366344..76368393,2	K562	blood:
28	chr6:76431586..76433985-chr6:76438066..76440225,2	MCF-7	breast:
29	chr6:76472032..76473906-chr6:76480774..76483408,2	MCF-7	breast:
30	chr6:76316605..76319587-chr6:76326249..76328171,2	MCF-7	breast:
31	chr6:76402073..76403999-chr6:76420565..76422699,2	MCF-7	breast:
32	chr6:76348520..76350771-chr6:76351491..76354055,3	K562	blood:
33	chr6:76415966..76418474-chr6:76457642..76460557,4	MCF-7	breast:
34	chr6:76457754..76460582-chr6:76467683..76471676,6	MCF-7	breast:
35	chr6:76458851..76461588-chr6:76463826..76466127,2	K562	blood:
36	chr6:76458866..76461215-chr6:76472496..76475519,3	MCF-7	breast:
37	chr6:76330148..76333811-chr6:76341672..76344273,3	K562	blood:
38	chr6:76408144..76410485-chr6:76410972..76412755,2	MCF-7	breast:
39	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
40	chr6:76310839..76313480-chr6:76354672..76356986,2	MCF-7	breast:
41	chr6:76459866..76461619-chr6:76483545..76486040,2	K562	blood:
42	chr6:76423793..76426485-chr6:76434093..76435596,2	K562	blood:
43	chr6:76310925..76313590-chr6:76457201..76459634,2	K562	blood:
44	chr6:76369470..76371755-chr6:76372281..76373933,2	K562	blood:
45	chr6:76320866..76324674-chr6:76327767..76329913,3	MCF-7	breast:
46	chr6:76461303..76463860-chr6:76468925..76471220,2	K562	blood:
47	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
48	chr6:76406647..76409621-chr6:76410785..76413589,2	K562	blood:
49	chr6:76460418..76462531-chr6:76558690..76560910,2	MCF-7	breast:
50	chr6:76478606..76481168-chr6:76482628..76484653,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FILIP1-2	chr6:76320674-76321504	NONHSAT113622
2	lnc-MYO6-1	chr6:76359931-76362040	ENSG00000249080
3	lnc-MYO6-7	chr6:76343366-76343442	NONHSAT113624
4	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
5	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627
6	lnc-FILIP1-3	chr6:76364686-76365015	NONHSAT113628
7	lnc-MYO6-1	chr6:76362140-76362390	ENSG00000249080
8	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
9	lnc-MYO6-7	chr6:76344423-76344772	NONHSAT113624
10	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
11	lnc-MYO6-6	chr6:76357008-76357517	NONHSAT113627
12	lnc-FILIP1-2	chr6:76320906-76321661	NONHSAT113623

No data

Variant related genes	Relation type
RNU6-1016P	TF binding region
RN7SKP163	TF binding region
SENP6	TF binding region
MYO6	TF binding region
ENSG00000217488	TF binding region
RNU6-155P	TF binding region
RNU6-1016P	CpG island
RN7SKP163	CpG island
SENP6	CpG island
MYO6	CpG island
ENSG00000217488	CpG island
RNU6-155P	CpG island
ENSG00000196586	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000244265	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000252498	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000181788	chromatin interactions
KRAS	miRNA target sites
NR4A2	miRNA target sites

Extended variants
information (count: 6545 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:6545 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs646967	chr6:76320846-76320847	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551920622	chr6:76320861-76320862	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs149976547	chr6:76320906-76320907	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs9343312	chr6:76320932-76320933	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs113917815	chr6:76320974-76320975	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs558969707	chr6:76320980-76320981	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs191665072	chr6:76321021-76321022	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs544840225	chr6:76321099-76321100	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs563023615	chr6:76321134-76321135	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs529821560	chr6:76321247-76321248	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs375823933	chr6:76321252-76321253	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs634862	chr6:76321256-76321257	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs559271128	chr6:76321314-76321315	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs369296130	chr6:76321323-76321324	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs527278076	chr6:76321329-76321330	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs143805012	chr6:76321334-76321335	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs182078437	chr6:76321357-76321358	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs529236751	chr6:76321375-76321376	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs186383766	chr6:76321378-76321379	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs549342042	chr6:76321379-76321380	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs549575502	chr6:76321382-76321383	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs567904920	chr6:76321454-76321455	Weak transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs551501799	chr6:76321543-76321544	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs536395040	chr6:76321549-76321550	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs76690871	chr6:76321551-76321552	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs566890770	chr6:76321729-76321730	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs533955086	chr6:76321730-76321731	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs77148541	chr6:76321736-76321737	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs191188821	chr6:76321750-76321751	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544877005	chr6:76321786-76321787	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs370856277	chr6:76321881-76321882	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550658990	chr6:76321904-76321905	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556834494	chr6:76321906-76321907	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs115406167	chr6:76321945-76321946	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs541983079	chr6:76321976-76321977	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs146861958	chr6:76322022-76322023	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527354520	chr6:76322079-76322080	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182282743	chr6:76322080-76322081	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs75631474	chr6:76322094-76322095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186801277	chr6:76322104-76322105	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs368259401	chr6:76322107-76322108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs549661407	chr6:76322148-76322149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs191263113	chr6:76322152-76322153	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs183062945	chr6:76322247-76322248	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs188378412	chr6:76322251-76322252	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547533714	chr6:76322258-76322259	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs619920	chr6:76322300-76322301	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs7772914	chr6:76322313-76322314	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192872786	chr6:76322316-76322317	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs570812187	chr6:76322323-76322324	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Chronic lymphocytic leukemia	21546498	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4081 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76313800-76322200	Enhancers	Primary T helper naive cells from peripheral blood	blood
2	chr6:76313800-76322200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
3	chr6:76313800-76325400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:76313800-76331600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:76314000-76321800	Weak transcription	Fetal Intestine Large	intestine
6	chr6:76314000-76323400	Enhancers	Primary T cells from cord blood	blood
7	chr6:76314000-76324600	Weak transcription	Fetal Stomach	stomach
8	chr6:76314000-76325600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:76314000-76325800	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr6:76314000-76326000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:76314000-76343200	Weak transcription	Fetal Kidney	kidney
12	chr6:76314200-76321000	Weak transcription	Thymus	Thymus
13	chr6:76314200-76321800	Weak transcription	Fetal Thymus	thymus
14	chr6:76314200-76322000	Weak transcription	Placenta	Placenta
15	chr6:76314200-76322200	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:76314200-76324800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:76314200-76325200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr6:76314200-76325200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:76314200-76329000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:76314400-76321800	Weak transcription	Left Ventricle	heart
21	chr6:76314400-76323600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:76314400-76324600	Weak transcription	Esophagus	oesophagus
23	chr6:76314400-76327600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:76314400-76334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:76314400-76336800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:76314800-76321800	Weak transcription	Lung	lung
27	chr6:76314800-76321800	Weak transcription	Spleen	Spleen
28	chr6:76315000-76321600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr6:76315400-76322200	Weak transcription	Right Ventricle	heart
30	chr6:76316000-76323600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:76316400-76322800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr6:76316400-76326000	Enhancers	Colon Smooth Muscle	Colon
33	chr6:76316600-76321400	Genic enhancers	K562	blood
34	chr6:76316600-76321800	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr6:76316600-76324800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr6:76316800-76322600	Weak transcription	Fetal Intestine Small	intestine
37	chr6:76316800-76323400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:76317000-76321400	Weak transcription	Colonic Mucosa	Colon
39	chr6:76317000-76321800	Weak transcription	Pancreas	Pancrea
40	chr6:76317000-76323400	Enhancers	Adipose Nuclei	Adipose
41	chr6:76317200-76324000	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr6:76317400-76321400	Enhancers	Brain Anterior Caudate	brain
43	chr6:76317400-76322600	Enhancers	Brain Substantia Nigra	brain
44	chr6:76317600-76321600	Enhancers	Brain Hippocampus Middle	brain
45	chr6:76317600-76321800	Enhancers	Rectal Smooth Muscle	rectum
46	chr6:76317600-76323200	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:76317600-76327400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:76317800-76322400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:76318000-76324000	Enhancers	NHDF-Ad	bronchial
50	chr6:76318200-76321600	Enhancers	Brain Cingulate Gyrus	brain

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