Variant report

Variant	nsv831098
Chromosome Location	chr7:112936711-113090844
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	ATF1	chr7:112946391-112946665	K562	blood:	n/a	n/a
2	ATF1	chr7:113011968-113011971	K562	blood:	n/a	n/a
3	ATF1	chr7:112989582-112989666	K562	blood:	n/a	n/a
4	BCLAF1	chr7:113061693-113062163	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:112957742-112957966	K562	blood:	n/a	chr7:112957843-112957864 chr7:112957849-112957858 chr7:112957849-112957858 chr7:112957848-112957857 chr7:112957847-112957860 chr7:112957850-112957859
6	BHLHE40	chr7:113061606-113062157	K562	blood:	n/a	chr7:113061662-113061675 chr7:113061931-113061947
7	BHLHE40	chr7:112942154-112942280	K562	blood:	n/a	n/a
8	BHLHE40	chr7:112971718-112971776	K562	blood:	n/a	n/a
9	BRCA1	chr7:113035535-113035595	HepG2	liver:	n/a	n/a
10	CBX3	chr7:113061624-113062128	K562	blood:	n/a	n/a
11	CEBPB	chr7:113015119-113015397	K562	blood:	n/a	n/a
12	CEBPB	chr7:112946416-112946690	K562	blood:	n/a	n/a
13	CEBPB	chr7:112975641-112975770	A549	lung:	n/a	chr7:112975743-112975754
14	CEBPB	chr7:112975731-112975761	IMR90	lung:	n/a	chr7:112975743-112975754
15	CEBPB	chr7:112979132-112979407	K562	blood:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
16	CEBPB	chr7:113056258-113056371	K562	blood:	n/a	n/a
17	CEBPB	chr7:112997353-112997549	K562	blood:	n/a	chr7:112997485-112997496
18	CEBPB	chr7:113034880-113035251	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:113017407-113017460	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:112979078-112979370	HepG2	liver:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
21	CEBPB	chr7:113033846-113034160	HepG2	liver:	n/a	chr7:113033966-113033977 chr7:113034007-113034018 chr7:113033964-113033977
22	CEBPB	chr7:112979137-112979342	MCF-7	breast:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
23	CEBPB	chr7:112975635-112975796	HepG2	liver:	n/a	chr7:112975743-112975754
24	CEBPB	chr7:112997394-112997628	HepG2	liver:	n/a	chr7:112997485-112997496
25	CEBPB	chr7:112979104-112979378	IMR90	lung:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
26	CEBPB	chr7:112979171-112979371	A549	lung:	n/a	chr7:112979224-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979226-112979235 chr7:112979225-112979236 chr7:112979224-112979237 chr7:112979226-112979235
27	CEBPB	chr7:113084552-113084769	HepG2	liver:	n/a	chr7:113084695-113084706
28	CEBPD	chr7:112946369-112946800	K562	blood:	n/a	n/a
29	CHD1	chr7:113044042-113044205	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr7:112971573-112971821	K562	blood:	n/a	n/a
31	CHD2	chr7:112971477-112971766	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:113055640-113055790	HBMEC	blood vessel:	n/a	chr7:113055718-113055731
33	CTCF	chr7:113061900-113062050	Caco-2	colon:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
34	CTCF	chr7:113055580-113055730	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr7:113037018-113037021	Gliobla	brain:	n/a	n/a
36	CTCF	chr7:113071600-113071750	HCT-116	colon:	n/a	n/a
37	CTCF	chr7:113044360-113044510	GM12865	blood:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
38	CTCF	chr7:113061860-113062010	AG09309	skin:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
39	CTCF	chr7:113044331-113044577	HepG2	liver:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
40	CTCF	chr7:113061880-113062030	NB4	blood:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
41	CTCF	chr7:113044303-113044616	K562	blood:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
42	CTCF	chr7:113061860-113062010	GM12872	blood:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
43	CTCF	chr7:113061815-113062106	Fibrobl	skin:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
44	CTCF	chr7:113061900-113062050	HRE	kidney:	n/a	chr7:113061970-113061988 chr7:113061972-113061985 chr7:113061965-113061986 chr7:113061935-113061948 chr7:113061933-113061951 chr7:113061940-113061948
45	CTCF	chr7:113055660-113055810	HPAF	blood vessel:	n/a	chr7:113055718-113055731
46	CTCF	chr7:113055660-113055810	HEK293	kidney:	n/a	chr7:113055718-113055731
47	CTCF	chr7:113071480-113071498	GM13977	blood:	n/a	n/a
48	CTCF	chr7:113044380-113044530	HRPEpiC	eye:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
49	CTCF	chr7:113044420-113044570	NHEK	skin:	n/a	chr7:113044475-113044493 chr7:113044480-113044490 chr7:113044478-113044491 chr7:113044477-113044498 chr7:113044476-113044492 chr7:113044478-113044487
50	CTCF	chr7:113044520-113044670	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:113034122-113034172	HEK293	kidney:	embryo
2	chr7:113034122-113034172	HEK293	kidney:	embryo
3	chr7:113034122-113034172	HL-60	blood:	n/a
4	chr7:113090002-113090052	MCF-7	breast:	n/a
5	chr7:113090002-113090052	MCF10A-Er-Src	breast:	n/a
6	chr7:113034122-113034172	SKMC	muscle:	n/a
7	chr7:113034122-113034172	SAEC	small airway:	n/a
8	chr7:113011963-113012013	RPTEC	kidney:	n/a
9	chr7:113034122-113034172	CMK	blood:	n/a
10	chr7:113011963-113012013	BJ	skin:	n/a
11	chr7:113090002-113090052	SKMC	muscle:	n/a
12	chr7:113034122-113034172	K562	blood:	n/a
13	chr7:113090002-113090052	ovcar-3	ovarian:	n/a
14	chr7:113090002-113090052	SK-N-SH_RA	brain:	n/a
15	chr7:113090002-113090052	HRE	kidney:	n/a
16	chr7:113034122-113034172	HCPEpiC	choroid plexus:	n/a
17	chr7:113011963-113012013	SKMC	muscle:	n/a
18	chr7:113090002-113090052	H1-hESC	embryonic stem cell:	embryo
19	chr7:113090002-113090052	HNPCEpiC	eye:	n/a
20	chr7:113034122-113034172	HCF	heart:	n/a
21	chr7:113034122-113034172	ECC-1	luminal epithelium:	n/a
22	chr7:113090002-113090052	ECC-1	luminal epithelium:	n/a
23	chr7:113090002-113090052	HepG2	liver:	n/a
24	chr7:113011963-113012013	SAEC	small airway:	n/a
25	chr7:113090002-113090052	HCT-116	colon:	n/a
26	chr7:113090002-113090052	SK-N-MC	brain:	n/a
27	chr7:113011963-113012013	HUVEC	blood vessel:	n/a
28	chr7:113034122-113034172	HepG2	liver:	n/a
29	chr7:113090002-113090052	PrEC	prostate:	n/a
30	chr7:113090002-113090052	HCM	heart:	n/a
31	chr7:113011963-113012013	HCF	heart:	n/a
32	chr7:113034122-113034172	GM12878	blood:	n/a
33	chr7:113034122-113034172	HRPEpiC	eye:	n/a
34	chr7:113090002-113090052	NT2-D1	testis:	n/a
35	chr7:113090002-113090052	BE2_C	brain:	n/a
36	chr7:113034122-113034172	HUVEC	blood vessel:	n/a
37	chr7:113034122-113034172	MCF10A-Er-Src	breast:	n/a
38	chr7:113090002-113090052	HCPEpiC	choroid plexus:	n/a
39	chr7:113034122-113034172	PANC-1	pancreas:	n/a
40	chr7:113034122-113034172	SK-N-MC	brain:	n/a
41	chr7:113011963-113012013	SK-N-MC	brain:	n/a
42	chr7:113090002-113090052	HIPEpiC	eye:	n/a
43	chr7:113011963-113012013	HL-60	blood:	n/a
44	chr7:113090002-113090052	Hepatocyte	liver:	n/a
45	chr7:113011963-113012013	NB4	blood:	n/a
46	chr7:113011963-113012013	HCM	heart:	n/a
47	chr7:113011963-113012013	HRPEpiC	eye:	n/a
48	chr7:113034122-113034172	U87	brain:	n/a
49	chr7:113011963-113012013	H1-hESC	embryonic stem cell:	embryo
50	chr7:113090002-113090052	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:112190294..112191180-chr7:113061506..113062330,4	MCF-7	breast:
2	chr7:112940051..112941689-chr7:112965313..112967695,2	K562	blood:
3	chr7:113042011..113045853-chr7:113047811..113051782,4	MCF-7	breast:
4	chr7:112799588..112800619-chr7:113061470..113062718,9	MCF-7	breast:
5	chr7:112950198..112952565-chr7:112958215..112960663,2	MCF-7	breast:
6	chr7:112578058..112580210-chr7:113025445..113027597,2	K562	blood:
7	chr7:112758684..112760391-chr7:112965987..112967563,2	K562	blood:
8	chr7:112655287..112655802-chr7:113061468..113062197,2	MCF-7	breast:
9	chr7:99433750..99434429-chr7:113008535..113009149,2	MCF-7	breast:
10	chr7:113001622..113003808-chr7:113017179..113018966,2	MCF-7	breast:
11	chr7:112950198..112952565-chr7:112958215..112960663,2	MCF-7	breast:
12	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
13	chr7:112654683..112655746-chr7:113061433..113062375,3	K562	blood:
14	chr7:112509091..112509840-chr7:113061486..113062019,3	MCF-7	breast:
15	chr7:113026289..113028138-chr7:113029115..113030912,2	K562	blood:
16	chr7:112949710..112952424-chr7:112954209..112957100,2	K562	blood:
17	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
18	chr7:112965647..112967560-chr7:112969669..112971397,2	K562	blood:
19	chr7:112799464..112800464-chr7:113061264..113062480,6	K562	blood:
20	chr7:112799910..112800953-chr7:113061499..113062556,5	MCF-7	breast:
21	chr7:113026289..113028138-chr7:113029115..113030912,2	K562	blood:
22	chr7:112953049..112955491-chr7:112958920..112960893,2	K562	blood:
23	chr7:112953049..112955491-chr7:112958920..112960893,2	K562	blood:
24	chr7:113044046..113044910-chr7:113338368..113338996,4	K562	blood:
25	chr7:112986796..112990552-chr7:112993911..112996520,3	MCF-7	breast:
26	chr7:113042011..113045853-chr7:113047811..113051782,4	MCF-7	breast:
27	chr7:112955793..112957716-chr7:112966619..112968256,2	K562	blood:
28	chr7:113033970..113036356-chr7:113044345..113046971,2	K562	blood:
29	chr7:112934260..112936230-chr7:112936620..112938273,2	MCF-7	breast:
30	chr7:113044065..113044754-chr7:113061519..113062155,3	MCF-7	breast:
31	chr7:112654983..112656027-chr7:113061405..113062486,9	MCF-7	breast:
32	chr7:113042048..113044438-chr7:113046056..113047809,2	K562	blood:
33	chr7:113011064..113013655-chr7:113032102..113033697,2	K562	blood:
34	chr7:112089237..112091482-chr7:112936057..112938859,2	MCF-7	breast:
35	chr7:113011064..113013655-chr7:113032102..113033697,2	K562	blood:
36	chr7:113061755..113062447-chrX:111985736..111986257,5	MCF-7	breast:
37	chr7:112949710..112952424-chr7:112954209..112957100,2	K562	blood:
38	chr7:113044065..113044754-chr7:113061519..113062155,3	MCF-7	breast:
39	chr7:113086419..113088488-chr7:113090237..113092945,2	K562	blood:
40	chr7:113001622..113003808-chr7:113017179..113018966,2	MCF-7	breast:
41	chr7:113028637..113030163-chr7:113052999..113055912,2	K562	blood:
42	chr7:112955793..112957716-chr7:112966619..112968256,2	K562	blood:
43	chr7:112986796..112990552-chr7:112993911..112996520,3	MCF-7	breast:
44	chr7:113061631..113062403-chr7:113350437..113351122,2	MCF-7	breast:
45	chr7:112757111..112758761-chr7:112957701..112959232,2	K562	blood:
46	chr7:113042048..113044438-chr7:113046056..113047809,2	K562	blood:
47	chr7:112965647..112967560-chr7:112969669..112971397,2	K562	blood:
48	chr7:112190261..112191145-chr7:113061834..113062368,2	K562	blood:
49	chr7:113053644..113055850-chr7:113060152..113062983,2	MCF-7	breast:
50	chr7:112940051..112941689-chr7:112965313..112967695,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073348.1-5	chr7:113055744-113056377	NONHSAT122817

Variant related genes	Relation type
ENSG00000270997	TF binding region
ENSG00000236294	TF binding region
ENSG00000270997	CpG island
ENSG00000236294	CpG island
ENSG00000164603	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000236294	chromatin interactions
ENSG00000270997	chromatin interactions
ENSG00000214194	chromatin interactions

Extended variants
information (count: 2979 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2979 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77965725	chr7:112936732-112936733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148622864	chr7:112936733-112936734	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs397754454	chr7:112936736-112936737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564049023	chr7:112936747-112936748	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575545636	chr7:112936757-112936758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543072149	chr7:112936777-112936778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574654487	chr7:112936853-112936854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542027669	chr7:112936916-112936917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556902626	chr7:112936986-112936987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182136938	chr7:112937020-112937021	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528558385	chr7:112937041-112937042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185343822	chr7:112937045-112937046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377445419	chr7:112937068-112937069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533196002	chr7:112937073-112937074	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551384520	chr7:112937080-112937081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575489311	chr7:112937087-112937088	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76493474	chr7:112937089-112937090	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs113432640	chr7:112937101-112937102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566945720	chr7:112937196-112937197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534370546	chr7:112937198-112937199	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553043066	chr7:112937219-112937220	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190836954	chr7:112937233-112937234	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539266403	chr7:112937261-112937262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184027686	chr7:112937269-112937270	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188936427	chr7:112937281-112937282	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561070430	chr7:112937301-112937302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs193078288	chr7:112937309-112937310	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545817136	chr7:112937324-112937325	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543356770	chr7:112937334-112937335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530189060	chr7:112937352-112937353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554971145	chr7:112937361-112937362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573275598	chr7:112937444-112937445	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540688141	chr7:112937506-112937507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146032836	chr7:112937533-112937534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138837978	chr7:112937551-112937552	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75504387	chr7:112937571-112937572	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565240798	chr7:112937589-112937590	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532373158	chr7:112937627-112937628	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558962269	chr7:112937651-112937652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs563353180	chr7:112937663-112937664	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541097861	chr7:112937688-112937689	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs76771555	chr7:112937695-112937696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560834694	chr7:112937735-112937736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559435314	chr7:112937745-112937746	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530162102	chr7:112937747-112937748	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34094070	chr7:112937767-112937768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1723476	chr7:112937797-112937798	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546373063	chr7:112937906-112937907	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548760407	chr7:112937958-112937959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538840896	chr7:112937964-112937965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112946200-112946800	Active TSS	K562	blood
2	chr7:112946800-112947400	Weak transcription	K562	blood
3	chr7:112947400-112948200	Enhancers	K562	blood
4	chr7:112948400-112948800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:112951800-112952000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:112952000-112952400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:112952000-112952400	Enhancers	Adipose Nuclei	Adipose
8	chr7:112952000-112953200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:112952400-112952800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:112952400-112954800	Weak transcription	Adipose Nuclei	Adipose
11	chr7:112952800-112954200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:112953200-112954600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:112954200-112955000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:112954400-112955200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr7:112954400-112955400	Enhancers	Fetal Lung	lung
16	chr7:112954600-112955000	Enhancers	Colon Smooth Muscle	Colon
17	chr7:112954600-112955200	Enhancers	Fetal Heart	heart
18	chr7:112954600-112955600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:112954800-112955200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:112954800-112955200	Enhancers	Fetal Brain Female	brain
21	chr7:112954800-112955200	Enhancers	Fetal Stomach	stomach
22	chr7:112954800-112955400	Enhancers	Adipose Nuclei	Adipose
23	chr7:112961200-112961600	Enhancers	NH-A	brain
24	chr7:112961400-112961800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:112961600-112962000	Enhancers	Rectal Smooth Muscle	rectum
26	chr7:112961800-112962400	Enhancers	K562	blood
27	chr7:112971200-112971400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:112971200-112971600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:112971200-112972000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:112971200-112972000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:112971200-112972000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:112971200-112972000	Enhancers	K562	blood
33	chr7:112971400-112971600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr7:112971400-112971800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:112971400-112971800	Enhancers	Right Ventricle	heart
36	chr7:112971400-112972000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:112971400-112972000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr7:112971400-112972000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:112971400-112972000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:112971400-112972000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:112971400-112972000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:112971400-112972000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:112971400-112972000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:112971400-112972200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:112971400-112972200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:112983200-112986200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:112983400-112983800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr7:112985600-112986000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:112999200-112999800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr7:113006400-113007000	Enhancers	Fetal Brain Male	brain

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