Variant report

Variant	nsv885776
Chromosome Location	chr6:33817929-33846143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:33828949-33829307	GM12878	blood:	n/a	n/a
2	ATF3	chr6:33830350-33830631	K562	blood:	n/a	n/a
3	ATF3	chr6:33843565-33843838	K562	blood:	n/a	chr6:33843688-33843701
4	BACH1	chr6:33828919-33829357	H1-hESC	embryonic stem cell:	n/a	chr6:33829223-33829237
5	BACH1	chr6:33837763-33837958	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:33828947-33829270	K562	blood:	n/a	chr6:33829223-33829237
7	BACH1	chr6:33819854-33819887	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:33828921-33829267	GM12878	blood:	n/a	chr6:33829227-33829237 chr6:33829100-33829111
9	BCL3	chr6:33831724-33832214	GM12878	blood:	n/a	n/a
10	BCL3	chr6:33831744-33832243	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:33824426-33824800	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:33831701-33832111	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:33819725-33819905	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr6:33833899-33834252	K562	blood:	n/a	n/a
15	CBX3	chr6:33821554-33821785	K562	blood:	n/a	n/a
16	CEBPB	chr6:33830899-33831250	K562	blood:	n/a	chr6:33831075-33831088
17	CHD2	chr6:33819777-33819955	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr6:33839700-33839870	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr6:33819760-33819910	BE2_C	brain:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
20	CTCF	chr6:33819820-33819970	HAc	cerebellar:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
21	CTCF	chr6:33819760-33819910	GM12865	blood:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
22	CTCF	chr6:33819720-33819870	HCT-116	colon:	n/a	chr6:33819854-33819870
23	CTCF	chr6:33819780-33819930	AG10803	skin:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
24	CTCF	chr6:33819800-33819950	AG04449	skin:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
25	CTCF	chr6:33819714-33819991	MCF-7	breast:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
26	CTCF	chr6:33819769-33819950	HepG2	liver:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
27	CTCF	chr6:33819800-33819950	NHEK	skin:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
28	CTCF	chr6:33819626-33820041	HepG2	liver:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
29	CTCF	chr6:33819692-33819962	ECC-1	luminal epithelium:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
30	CTCF	chr6:33819770-33819938	GM10248	blood:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
31	CTCF	chr6:33819780-33819930	NHLF	lung:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
32	CTCF	chr6:33819800-33819950	SAEC	small airway:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
33	CTCF	chr6:33819740-33819890	HCM	heart:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
34	CTCF	chr6:33819725-33819969	ProgFib	skin:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
35	CTCF	chr6:33819780-33819930	HFF	foreskin:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
36	CTCF	chr6:33819780-33819930	AG04450	lung:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
37	CTCF	chr6:33819740-33819890	HRPEpiC	eye:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
38	CTCF	chr6:33819465-33820115	SK-N-SH	brain:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
39	CTCF	chr6:33838920-33839070	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr6:33819740-33819890	GM12868	blood:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
41	CTCF	chr6:33819765-33819935	LNCaP	prostate:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
42	CTCF	chr6:33819732-33819978	A549	lung:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
43	CTCF	chr6:33819780-33819930	AG09319	gingival:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
44	CTCF	chr6:33819711-33819997	H1-hESC	embryonic stem cell:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
45	CTCF	chr6:33819809-33819904	GM13976	blood:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
46	CTCF	chr6:33819597-33820063	MCF-7	breast:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
47	CTCF	chr6:33819757-33819964	Spleen_OC	spleen:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
48	CTCF	chr6:33819760-33819910	Hela-S3	cervix:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
49	CTCF	chr6:33819800-33819950	HVMF	connective:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876
50	CTCF	chr6:33819760-33819910	HPF	lung:	n/a	chr6:33819854-33819870 chr6:33819853-33819871 chr6:33819855-33819876

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33838308-33838358	HepG2	liver:	n/a
2	chr6:33819738-33819788	SAEC	small airway:	n/a
3	chr6:33819738-33819788	Jurkat	blood:	n/a
4	chr6:33838308-33838358	MCF-7	breast:	n/a
5	chr6:33838308-33838358	HUVEC	blood vessel:	n/a
6	chr6:33838308-33838358	ProgFib	skin:	n/a
7	chr6:33819738-33819788	NT2-D1	testis:	n/a
8	chr6:33819738-33819788	AG04449	skin:	fetal
9	chr6:33819738-33819788	SK-N-SH	brain:	n/a
10	chr6:33838308-33838358	NT2-D1	testis:	n/a
11	chr6:33838308-33838358	PFSK-1	brain:	n/a
12	chr6:33819738-33819788	PANC-1	pancreas:	n/a
13	chr6:33819738-33819788	CMK	blood:	n/a
14	chr6:33819738-33819788	HEEpiC	esophagus:	n/a
15	chr6:33838308-33838358	Caco-2	colon:	n/a
16	chr6:33819738-33819788	HMEC	breast:	n/a
17	chr6:33838308-33838358	IMR90	lung:	fetal
18	chr6:33819738-33819788	NHBE	bronchial:	n/a
19	chr6:33838308-33838358	PrEC	prostate:	n/a
20	chr6:33819738-33819788	GM06990	blood:	n/a
21	chr6:33838308-33838358	A549	lung:	n/a
22	chr6:33838308-33838358	AG10803	skin:	n/a
23	chr6:33819738-33819788	HepG2	liver:	n/a
24	chr6:33838308-33838358	HCPEpiC	choroid plexus:	n/a
25	chr6:33819738-33819788	Hepatocyte	liver:	n/a
26	chr6:33819738-33819788	HCF	heart:	n/a
27	chr6:33819738-33819788	HCPEpiC	choroid plexus:	n/a
28	chr6:33819738-33819788	SK-N-MC	brain:	n/a
29	chr6:33819738-33819788	AG09309	skin:	n/a
30	chr6:33819738-33819788	HRPEpiC	eye:	n/a
31	chr6:33819738-33819788	HL-60	blood:	n/a
32	chr6:33838308-33838358	SKMC	muscle:	n/a
33	chr6:33838308-33838358	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:33838308-33838358	HCT-116	colon:	n/a
35	chr6:33838308-33838358	SK-N-SH_RA	brain:	n/a
36	chr6:33838308-33838358	HRPEpiC	eye:	n/a
37	chr6:33819738-33819788	U87	brain:	n/a
38	chr6:33838308-33838358	HEEpiC	esophagus:	n/a
39	chr6:33838308-33838358	HCF	heart:	n/a
40	chr6:33819738-33819788	BJ	skin:	n/a
41	chr6:33838308-33838358	PANC-1	pancreas:	n/a
42	chr6:33838308-33838358	HMEC	breast:	n/a
43	chr6:33838308-33838358	Jurkat	blood:	n/a
44	chr6:33819738-33819788	AoSMC	blood vessel:	n/a
45	chr6:33838308-33838358	NHBE	bronchial:	n/a
46	chr6:33838308-33838358	AG09319	gingival:	n/a
47	chr6:33838308-33838358	GM12891	blood:	n/a
48	chr6:33838308-33838358	HRCEpiC	kidney:	n/a
49	chr6:33819738-33819788	NHDF-neo	bronchial:	n/a
50	chr6:33819738-33819788	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr6:33822070..33824859-chr6:33826063..33828962,3	K562	blood:
2	chr6:33819661..33820304-chr6:33935521..33936307,2	MCF-7	breast:
3	chr6:33815385..33820274-chr6:33821193..33824652,6	K562	blood:
4	chr6:33819522..33821091-chr6:33827275..33829014,2	K562	blood:
5	chr6:33748572..33751307-chr6:33828989..33830767,2	K562	blood:
6	chr6:33784923..33786692-chr6:33819953..33822581,2	K562	blood:
7	chr6:33819810..33820341-chr6:33995193..33995933,2	MCF-7	breast:
8	chr6:33827215..33829847-chr6:33845943..33848537,2	MCF-7	breast:
9	chr6:33834558..33836995-chr6:33837764..33839527,2	MCF-7	breast:
10	chr6:33837980..33839549-chr6:33845032..33847078,2	K562	blood:
11	chr6:33843627..33846530-chr6:33861836..33863752,2	K562	blood:
12	chr6:33837980..33839549-chr6:33845032..33847078,2	K562	blood:
13	chr6:33828653..33831388-chr6:33831678..33834637,3	K562	blood:
14	chr6:33817908..33819651-chr6:33841699..33844264,2	K562	blood:
15	chr6:33828985..33830562-chr6:33833456..33836165,2	MCF-7	breast:
16	chr6:33754413..33756841-chr6:33819959..33822850,2	MCF-7	breast:
17	chr6:33827215..33829847-chr6:33845943..33848537,2	MCF-7	breast:
18	chr6:33819382..33820118-chr6:34034290..34034944,2	MCF-7	breast:
19	chr6:33811878..33813846-chr6:33820796..33822819,2	K562	blood:
20	chr6:33804994..33807921-chr6:33844816..33847091,2	MCF-7	breast:
21	chr6:33839827..33842416-chr6:33843105..33844669,2	MCF-7	breast:
22	chr6:33828985..33830562-chr6:33833456..33836165,2	MCF-7	breast:
23	chr6:33829053..33831890-chr6:33860061..33862038,2	K562	blood:
24	chr6:33725421..33728114-chr6:33818801..33821160,2	MCF-7	breast:
25	chr6:33830042..33832096-chr6:33833170..33835454,2	MCF-7	breast:
26	chr6:33830042..33832096-chr6:33833170..33835454,2	MCF-7	breast:
27	chr6:33817908..33819651-chr6:33841699..33844264,2	K562	blood:
28	chr6:33764445..33767119-chr6:33821769..33823685,2	MCF-7	breast:
29	chr6:33819352..33820057-chr6:33935715..33936362,3	MCF-7	breast:
30	chr6:33819160..33821493-chr6:33955535..33958926,3	MCF-7	breast:
31	chr6:33840631..33842929-chr6:33851887..33853913,2	K562	blood:
32	chr6:33815385..33820274-chr6:33821193..33824652,6	K562	blood:
33	chr6:33829206..33831689-chr6:33838290..33840301,2	MCF-7	breast:
34	chr6:33812945..33816387-chr6:33817009..33820536,6	K562	blood:
35	chr6:33819522..33821091-chr6:33827275..33829014,2	K562	blood:
36	chr6:33829206..33831689-chr6:33838290..33840301,2	MCF-7	breast:
37	chr6:33832364..33832867-chr6:33864511..33865252,2	MCF-7	breast:
38	chr6:33834558..33836995-chr6:33837764..33839527,2	MCF-7	breast:
39	chr6:33828653..33831388-chr6:33831678..33834637,3	K562	blood:
40	chr6:28701062..28703950-chr6:33822430..33824102,2	MCF-7	breast:
41	chr6:33839827..33842416-chr6:33843105..33844669,2	MCF-7	breast:
42	chr6:33819423..33820326-chr6:33995229..33996032,2	K562	blood:
43	chr6:33822070..33824859-chr6:33826063..33828962,3	K562	blood:
44	chr6:33816600..33819400-chr6:33825889..33827498,2	MCF-7	breast:
45	chr6:33819439..33820478-chr6:33995355..33996344,6	MCF-7	breast:
46	chr6:33802445..33804788-chr6:33817259..33819823,2	K562	blood:
47	chr6:33816600..33819400-chr6:33825889..33827498,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITPR3-3	chr6:33842067-33842513	NONHSAT109066
2	lnc-ITPR3-3	chr6:33840939-33841053	NONHSAT109010
3	lnc-ITPR3-3	chr6:33840939-33841053	NONHSAT109011
4	lnc-ITPR3-3	chr6:33842087-33842402	NONHSAT109211
5	lnc-ITPR3-3	chr6:33824053-33824215	NONHSAT109011
6	lnc-MLN-3	chr6:33845092-33846024	NONHSAT109146
7	lnc-ITPR3-3	chr6:33845658-33847878	NONHSAT109010
8	lnc-ITPR3-3	chr6:33837821-33841053	NONHSAT109066
9	lnc-ITPR3-3	chr6:33842067-33842355	NONHSAT109011
10	lnc-MLN-3	chr6:33840231-33840679	NONHSAT109146
11	lnc-ITPR3-3	chr6:33841730-33841836	NONHSAT109066
12	lnc-ITPR3-3	chr6:33844694-33844901	NONHSAT109010
13	lnc-ITPR3-3	chr6:33841728-33841836	NONHSAT109212
14	lnc-ITPR3-3	chr6:33842067-33842402	NONHSAT109212
15	lnc-ITPR3-3	chr6:33824053-33824215	NONHSAT109010
16	lnc-ITPR3-3	chr6:33841730-33841836	NONHSAT109010
17	lnc-ITPR3-3	chr6:33841730-33841836	NONHSAT109011
18	lnc-ITPR3-3	chr6:33841728-33841836	NONHSAT109211
19	lnc-MLN-1	chr6:33835283-33835603	ENSG00000249346
20	lnc-ITPR3-3	chr6:33837638-33837800	NONHSAT109011
21	lnc-ITPR3-3	chr6:33837638-33837800	NONHSAT109010
22	lnc-MLN-3	chr6:33842038-33842520	NONHSAT109146
23	lnc-ITPR3-3	chr6:33835544-33835623	NONHSAT109010

Variant related genes	Relation type
ENSG00000271362	TF binding region
ENSG00000271362	CpG island
ENSG00000161904	chromatin interactions
ENSG00000249346	chromatin interactions
ENSG00000233183	chromatin interactions
CHORDC1	miRNA target sites

Extended variants
information (count: 1198 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4713693	chr6:33817929-33817930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance disease
2	rs534184275	chr6:33817930-33817931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185209105	chr6:33817970-33817971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4711356	chr6:33818001-33818002	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528433111	chr6:33818017-33818018	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188570052	chr6:33818048-33818049	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556303479	chr6:33818065-33818066	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577836371	chr6:33818067-33818068	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545300621	chr6:33818068-33818069	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560822698	chr6:33818094-33818095	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114548589	chr6:33818097-33818098	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542605310	chr6:33818115-33818116	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529112091	chr6:33818123-33818124	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372212522	chr6:33818130-33818131	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550343867	chr6:33818139-33818140	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372505422	chr6:33818158-33818159	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377034085	chr6:33818205-33818206	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193246265	chr6:33818234-33818235	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531394668	chr6:33818253-33818254	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139632731	chr6:33818254-33818255	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185394527	chr6:33818298-33818299	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189329638	chr6:33818312-33818313	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144193091	chr6:33818323-33818324	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565957725	chr6:33818342-33818343	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116997897	chr6:33818378-33818379	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376338269	chr6:33818437-33818438	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs369697794	chr6:33818438-33818439	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs555299151	chr6:33818449-33818450	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs539168984	chr6:33818452-33818453	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs117401464	chr6:33818455-33818456	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs374344350	chr6:33818458-33818459	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs145208710	chr6:33818460-33818461	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs556215856	chr6:33818498-33818499	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs577749594	chr6:33818525-33818526	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs376790233	chr6:33818526-33818527	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs545573333	chr6:33818527-33818528	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs71538220	chr6:33818571-33818572	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs71567409	chr6:33818573-33818574	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs559435305	chr6:33818581-33818582	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs551015029	chr6:33818587-33818588	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs368096963	chr6:33818588-33818589	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs572652191	chr6:33818590-33818591	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs113258004	chr6:33818594-33818595	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs542961535	chr6:33818647-33818648	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs149216810	chr6:33818658-33818659	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs531356179	chr6:33818678-33818679	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs543471621	chr6:33818685-33818686	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs180730690	chr6:33818689-33818690	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs183661661	chr6:33818725-33818726	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs141831014	chr6:33818726-33818727	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
abnormal development	18461090	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
Urothelial carcinoma	21177765	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33805400-33833400	Weak transcription	Right Atrium	heart
2	chr6:33806600-33818200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:33807200-33819400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:33808600-33818800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:33808600-33819400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:33809600-33823200	Weak transcription	Spleen	Spleen
7	chr6:33810800-33819200	Weak transcription	A549	lung
8	chr6:33811200-33818200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:33811800-33818600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:33811800-33819200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:33815400-33818000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:33816600-33818000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:33816600-33822200	Weak transcription	Pancreas	Pancrea
14	chr6:33817200-33818800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:33817400-33819400	Enhancers	Fetal Brain Male	brain
16	chr6:33817600-33818000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:33817600-33819600	Enhancers	Right Ventricle	heart
18	chr6:33818000-33818400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:33818000-33818400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:33818000-33819800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:33818000-33819800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr6:33818000-33820200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr6:33818000-33820400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:33818000-33820400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr6:33818000-33820400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:33818200-33818400	Enhancers	Fetal Lung	lung
27	chr6:33818200-33819600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr6:33818200-33820200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr6:33818200-33820400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:33818400-33819000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr6:33818400-33824800	Weak transcription	Fetal Lung	lung
32	chr6:33818600-33819000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr6:33818600-33819600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:33818800-33819000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:33818800-33819000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr6:33818800-33820000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr6:33818800-33821000	Enhancers	K562	blood
38	chr6:33819000-33819400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:33819200-33820200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr6:33819200-33820200	Enhancers	A549	lung
41	chr6:33819400-33819600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:33819400-33820200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr6:33819400-33820200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:33819400-33820200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:33819400-33820200	Bivalent Enhancer	Fetal Stomach	stomach
46	chr6:33819400-33820400	Enhancers	Placenta	Placenta
47	chr6:33819600-33820000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:33819600-33820000	Enhancers	Fetal Intestine Small	intestine
49	chr6:33819600-33823400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr6:33819800-33820200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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