Variant report

Variant	nsv993501
Chromosome Location	chr7:112625029-113125338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3603)
CpG islands
(count:1957)
Chromatin interactive
region (count:268)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:112740190-112740639	K562	blood:	n/a	n/a
2	ARID3A	chr7:112765831-112766053	K562	blood:	n/a	n/a
3	ARID3A	chr7:112903890-112904025	K562	blood:	n/a	n/a
4	ARID3A	chr7:112782280-112783198	K562	blood:	n/a	n/a
5	ARID3A	chr7:112727223-112728259	K562	blood:	n/a	n/a
6	ARID3A	chr7:112751837-112751866	K562	blood:	n/a	n/a
7	ARID3A	chr7:112724927-112725289	K562	blood:	n/a	n/a
8	ARID3A	chr7:113100171-113100369	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:112799920-112799963	K562	blood:	n/a	n/a
10	ARID3A	chr7:112721566-112721697	K562	blood:	n/a	n/a
11	ARID3A	chr7:112758448-112758962	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:112758083-112758932	K562	blood:	n/a	n/a
13	ATF1	chr7:112695650-112695833	K562	blood:	n/a	n/a
14	ATF1	chr7:112711587-112711816	K562	blood:	n/a	n/a
15	ATF1	chr7:112758385-112758989	K562	blood:	n/a	n/a
16	ATF1	chr7:112725919-112726283	K562	blood:	n/a	n/a
17	ATF1	chr7:112782341-112783153	K562	blood:	n/a	n/a
18	ATF1	chr7:112757504-112757709	K562	blood:	n/a	n/a
19	ATF1	chr7:113011968-113011971	K562	blood:	n/a	n/a
20	ATF1	chr7:112845598-112845838	K562	blood:	n/a	n/a
21	ATF1	chr7:112724379-112725078	K562	blood:	n/a	n/a
22	ATF1	chr7:112761243-112761443	K562	blood:	n/a	n/a
23	ATF1	chr7:112946391-112946665	K562	blood:	n/a	n/a
24	ATF1	chr7:112644827-112645228	K562	blood:	n/a	n/a
25	ATF1	chr7:112842586-112842605	K562	blood:	n/a	n/a
26	ATF1	chr7:112989582-112989666	K562	blood:	n/a	n/a
27	ATF1	chr7:112642741-112642792	K562	blood:	n/a	n/a
28	ATF1	chr7:112732912-112733232	K562	blood:	n/a	n/a
29	ATF1	chr7:112929247-112929556	K562	blood:	n/a	n/a
30	ATF1	chr7:112921615-112921625	K562	blood:	n/a	n/a
31	ATF1	chr7:112781184-112781280	K562	blood:	n/a	n/a
32	ATF1	chr7:112727241-112728091	K562	blood:	n/a	n/a
33	ATF2	chr7:112758357-112758936	GM12878	blood:	n/a	n/a
34	ATF3	chr7:112757306-112757768	K562	blood:	n/a	n/a
35	ATF3	chr7:112711624-112711766	K562	blood:	n/a	n/a
36	ATF3	chr7:112782820-112783360	K562	blood:	n/a	n/a
37	ATF3	chr7:112782231-112782744	K562	blood:	n/a	n/a
38	ATF3	chr7:112758479-112758831	K562	blood:	n/a	n/a
39	ATF3	chr7:112758551-112758720	GM12878	blood:	n/a	n/a
40	ATF3	chr7:112711542-112711857	K562	blood:	n/a	n/a
41	BACH1	chr7:112758215-112759089	K562	blood:	n/a	n/a
42	BACH1	chr7:112796528-112796607	K562	blood:	n/a	n/a
43	BACH1	chr7:112699090-112699105	K562	blood:	n/a	n/a
44	BACH1	chr7:112740136-112740140	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr7:112726678-112726937	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr7:112871958-112872067	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr7:112799638-112799698	K562	blood:	n/a	n/a
48	BACH1	chr7:112726746-112726772	K562	blood:	n/a	n/a
49	BACH1	chr7:112758317-112759015	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr7:112673397-112673415	K562	blood:	n/a	n/a

(count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112739805-112739855	U87	brain:	n/a
2	chr7:112725899-112725949	AG09309	skin:	n/a
3	chr7:112724674-112724724	H1-hESC	embryonic stem cell:	embryo
4	chr7:112907863-112907913	SK-N-SH	brain:	n/a
5	chr7:113090002-113090052	IMR90	lung:	fetal
6	chr7:112739805-112739855	U87	brain:	n/a
7	chr7:112725899-112725949	AG09309	skin:	n/a
8	chr7:112724674-112724724	H1-hESC	embryonic stem cell:	embryo
9	chr7:112907863-112907913	SK-N-SH	brain:	n/a
10	chr7:113090002-113090052	IMR90	lung:	fetal
11	chr7:112758748-112758798	NHDF-neo	bronchial:	n/a
12	chr7:112724674-112724724	PFSK-1	brain:	n/a
13	chr7:112907863-112907913	IMR90	lung:	fetal
14	chr7:112758748-112758798	AoSMC	blood vessel:	n/a
15	chr7:113090002-113090052	SK-N-SH	brain:	n/a
16	chr7:112758903-112758953	PFSK-1	brain:	n/a
17	chr7:112726547-112726597	Hela-S3	cervix:	n/a
18	chr7:112726538-112726588	NB4	blood:	n/a
19	chr7:112727914-112727964	GM19239	blood:	n/a
20	chr7:112726659-112726709	AG10803	skin:	n/a
21	chr7:112726774-112726824	AG04450	lung:	fetal
22	chr7:112907863-112907913	AG04449	skin:	fetal
23	chr7:113091000-113091050	HIPEpiC	eye:	n/a
24	chr7:112758800-112758850	ovcar-3	ovarian:	n/a
25	chr7:113090002-113090052	A549	lung:	n/a
26	chr7:112724674-112724724	HRCEpiC	kidney:	n/a
27	chr7:112726396-112726446	HepG2	liver:	n/a
28	chr7:112727914-112727964	HRPEpiC	eye:	n/a
29	chr7:112758744-112758794	SAEC	small airway:	n/a
30	chr7:112903509-112903559	H1-hESC	embryonic stem cell:	embryo
31	chr7:112720816-112720866	HNPCEpiC	eye:	n/a
32	chr7:112726869-112726919	NH-A	brain:	n/a
33	chr7:112726541-112726591	AG04450	lung:	fetal
34	chr7:113034122-113034172	A549	lung:	n/a
35	chr7:112758903-112758953	GM12891	blood:	n/a
36	chr7:112726802-112726852	AoSMC	blood vessel:	n/a
37	chr7:112726774-112726824	HCF	heart:	n/a
38	chr7:112727423-112727473	U87	brain:	n/a
39	chr7:113011963-113012013	NHBE	bronchial:	n/a
40	chr7:112724674-112724724	HCM	heart:	n/a
41	chr7:113091000-113091050	CMK	blood:	n/a
42	chr7:112903509-112903559	Hepatocyte	liver:	n/a
43	chr7:112726653-112726703	AG04450	lung:	fetal
44	chr7:113091000-113091050	GM19239	blood:	n/a
45	chr7:112726089-112726139	CMK	blood:	n/a
46	chr7:113090002-113090052	ovcar-3	ovarian:	n/a
47	chr7:112726869-112726919	T-47D	breast:	n/a
48	chr7:112758903-112758953	U87	brain:	n/a
49	chr7:113011963-113012013	PFSK-1	brain:	n/a
50	chr7:112726659-112726709	SK-N-MC	brain:	n/a

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:112815177..112817865-chr7:112886760..112888811,2	MCF-7	breast:
2	chr7:112758598..112760498-chr7:112761255..112766630,6	MCF-7	breast:
3	chr7:112902968..112904639-chr7:112919791..112922267,2	MCF-7	breast:
4	chr7:112682248..112683838-chr7:112894672..112896979,2	K562	blood:
5	chr7:112758675..112760298-chr7:112794842..112798647,3	K562	blood:
6	chr7:112714018..112716615-chr7:112717712..112719253,2	K562	blood:
7	chr7:112906005..112908006-chr7:112910862..112913062,2	K562	blood:
8	chr7:112738100..112740968-chr7:112754708..112756383,2	K562	blood:
9	chr7:112780258..112782167-chr7:112788988..112791512,2	K562	blood:
10	chr7:113044065..113044754-chr7:113061519..113062155,3	MCF-7	breast:
11	chr7:112190294..112191180-chr7:113061506..113062330,4	MCF-7	breast:
12	chr7:112756052..112760979-chr7:112769891..112772947,5	K562	blood:
13	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
14	chr7:112723161..112726364-chr7:112726656..112729737,3	K562	blood:
15	chr7:112703408..112705692-chr7:112716673..112719279,2	K562	blood:
16	chr7:112089330..112091829-chr7:112756736..112758677,2	K562	blood:
17	chr7:112190261..112191145-chr7:113061834..113062368,2	K562	blood:
18	chr7:112774778..112777011-chr7:112777152..112779575,2	K562	blood:
19	chr7:112759649..112762090-chr7:112783076..112784947,2	K562	blood:
20	chr7:113042048..113044438-chr7:113046056..113047809,2	K562	blood:
21	chr7:112845581..112848616-chr7:112850050..112854250,3	K562	blood:
22	chr7:112680260..112683174-chr7:112683232..112685538,2	MCF-7	breast:
23	chr7:112761834..112764773-chr7:112768104..112770317,2	K562	blood:
24	chr7:112934260..112936230-chr7:112936620..112938273,2	MCF-7	breast:
25	chr7:112713707..112715518-chr7:112717712..112719924,2	K562	blood:
26	chr7:112758299..112760850-chr7:113043245..113045081,2	K562	blood:
27	chr7:112950198..112952565-chr7:112958215..112960663,2	MCF-7	breast:
28	chr7:112934260..112936230-chr7:112936620..112938273,2	MCF-7	breast:
29	chr7:112815199..112817636-chr7:112823311..112824921,2	MCF-7	breast:
30	chr7:113061631..113062403-chr7:113350437..113351122,2	MCF-7	breast:
31	chr7:112797834..112800615-chr7:112802985..112805209,2	K562	blood:
32	chr7:112723034..112725310-chr7:112753782..112755599,2	MCF-7	breast:
33	chr7:112815199..112817636-chr7:112823311..112824921,2	MCF-7	breast:
34	chr7:112801750..112803685-chr7:112813306..112816042,2	K562	blood:
35	chr7:113042011..113045853-chr7:113047811..113051782,4	MCF-7	breast:
36	chr7:112655258..112655792-chr7:112749920..112750861,2	MCF-7	breast:
37	chr7:112768327..112770672-chr7:112770872..112773176,2	K562	blood:
38	chr7:112811148..112812106-chr7:112921056..112921827,2	MCF-7	breast:
39	chr7:112953049..112955491-chr7:112958920..112960893,2	K562	blood:
40	chr7:112654800..112655464-chr7:112754097..112754722,2	MCF-7	breast:
41	chr7:112761834..112764773-chr7:112768104..112770317,2	K562	blood:
42	chr7:112756695..112758581-chr7:112781055..112783118,2	K562	blood:
43	chr7:112764216..112766097-chr7:112779643..112782310,2	K562	blood:
44	chr7:113053644..113055850-chr7:113060152..113062983,2	MCF-7	breast:
45	chr7:112783216..112786523-chr7:112787566..112792352,4	K562	blood:
46	chr7:112764896..112766469-chr7:112769155..112770793,2	K562	blood:
47	chr7:112940051..112941689-chr7:112965313..112967695,2	K562	blood:
48	chr7:112845581..112848616-chr7:112850050..112854250,3	K562	blood:
49	chr7:112841907..112844246-chr7:112847503..112849248,2	K562	blood:
50	chr7:112654853..112656193-chr7:112753393..112754620,7	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf60-1	chr7:112635623-112635689	ENSG00000234520
2	lnc-AC073348.1-1	chr7:112740773-112740940	NONHSAT122814
3	lnc-AC073348.1-1	chr7:112785071-112785213	ENSG00000225457.1
4	lnc-C7orf60-1	chr7:112635623-112635698	NR_110162
5	lnc-C7orf60-1	chr7:112626591-112626719	NONHSAT122805
6	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122805
7	lnc-AC073348.1-1	chr7:112747810-112747854	NONHSAT122814
8	lnc-C7orf60-1	chr7:112635623-112635712	NONHSAT122810
9	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122803
10	lnc-AC073348.1-4	chr7:113109789-113110137	NONHSAT122818
11	lnc-AC073348.1-4	chr7:113117164-113124124	NONHSAT122818
12	lnc-C7orf60-1	chr7:112626594-112626719	NONHSAT122810
13	lnc-AC073348.1-1	chr7:112785721-112785830	ENSG00000225457.1
14	lnc-AC073348.1-1	chr7:112785718-112786095	ENSG00000225457.1
15	lnc-AC073348.1-1	chr7:112740718-112740940	ENSG00000225457.1
16	lnc-AC073348.1-1	chr7:112747810-112747859	ENSG00000225457.1
17	lnc-C7orf60-1	chr7:112635623-112635698	NONHSAT122806
18	lnc-C7orf60-1	chr7:112626591-112626719	ENSG00000234520
19	lnc-GPR85-1	chr7:112715179-112717236	NONHSAT122812
20	lnc-C7orf60-1	chr7:112635623-112635682	ENSG00000234520
21	lnc-AC073348.1-1	chr7:112785718-112785964	NONHSAT122814
22	lnc-C7orf60-1	chr7:112626591-112626719	NR_110162
23	lnc-AC073348.1-1	chr7:112786095-112786385	ENSG00000225457.1
24	lnc-AC073348.1-5	chr7:113055744-113056377	NONHSAT122817

No data

Variant related genes	Relation type
LINC00998	TF binding region
ENSG00000236294	TF binding region
ENSG00000270997	TF binding region
ENSG00000225457	TF binding region
GPR85	TF binding region
ENSG00000234520	TF binding region
LINC00998	CpG island
ENSG00000236294	CpG island
ENSG00000270997	CpG island
ENSG00000225457	CpG island
GPR85	CpG island
ENSG00000234520	CpG island
ENSG00000236294	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000164604	chromatin interactions
ENSG00000164603	chromatin interactions
ENSG00000225457	chromatin interactions
ENSG00000214194	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000270997	chromatin interactions
ENSG00000265688	chromatin interactions

Extended variants
information (count: 10457 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:10457 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147146234	chr7:112625052-112625053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561750397	chr7:112625062-112625063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529057922	chr7:112625071-112625072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76987215	chr7:112625105-112625106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138926729	chr7:112625114-112625115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12540378	chr7:112625211-112625212	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564850099	chr7:112625217-112625218	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73414800	chr7:112625223-112625224	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12533259	chr7:112625317-112625318	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532297643	chr7:112625457-112625458	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552013368	chr7:112625478-112625479	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386411031	chr7:112625479-112625480	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199617250	chr7:112625483-112625484	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75072688	chr7:112625494-112625495	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10687581	chr7:112625495-112625496	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537359715	chr7:112625500-112625501	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555996975	chr7:112625535-112625536	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565820185	chr7:112625538-112625539	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10282717	chr7:112625547-112625548	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535205655	chr7:112625571-112625572	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553492997	chr7:112625580-112625581	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571805042	chr7:112625617-112625618	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545448618	chr7:112625654-112625655	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551296412	chr7:112625655-112625656	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183683213	chr7:112625758-112625759	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10224427	chr7:112625799-112625800	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188785324	chr7:112625801-112625802	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs7797689	chr7:112625841-112625842	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs561999290	chr7:112625848-112625849	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs6466426	chr7:112625870-112625871	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs541213576	chr7:112625903-112625904	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559539855	chr7:112625980-112625981	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs149439826	chr7:112625984-112625985	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181248610	chr7:112626080-112626081	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570086427	chr7:112626086-112626087	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7798140	chr7:112626108-112626109	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186278090	chr7:112626134-112626135	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74801335	chr7:112626135-112626136	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567940166	chr7:112626186-112626187	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534953323	chr7:112626197-112626198	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144774020	chr7:112626202-112626203	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs77084183	chr7:112626226-112626227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs539164741	chr7:112626324-112626325	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs557406192	chr7:112626367-112626368	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs112838581	chr7:112626374-112626375	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537039410	chr7:112626394-112626395	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs547254511	chr7:112626413-112626414	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs552626082	chr7:112626549-112626550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541284292	chr7:112626553-112626554	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs142841960	chr7:112626655-112626656	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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	22037309	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112594200-112630400	Weak transcription	Left Ventricle	heart
2	chr7:112622400-112627800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr7:112622600-112625400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:112622600-112625600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:112622600-112625600	Weak transcription	HSMMtube	muscle
6	chr7:112622800-112625200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:112623200-112625600	Weak transcription	HSMM	muscle
8	chr7:112624000-112625800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr7:112624400-112625600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:112625000-112625600	Enhancers	Osteobl	bone
11	chr7:112625000-112626000	Weak transcription	Primary B cells from cord blood	blood
12	chr7:112625000-112626800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:112625000-112629000	Enhancers	HMEC	breast
14	chr7:112625000-112631200	Enhancers	Fetal Heart	heart
15	chr7:112625200-112625600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:112625200-112625600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:112625200-112626800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:112625200-112626800	Enhancers	NHEK	skin
19	chr7:112625400-112626200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:112625400-112626200	Active TSS	Colon Smooth Muscle	Colon
21	chr7:112625400-112626400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:112625400-112626400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:112625600-112625800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:112625600-112625800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:112625600-112625800	Active TSS	NH-A	brain
26	chr7:112625600-112625800	Active TSS	NHLF	lung
27	chr7:112625600-112626200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:112625600-112626200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:112625600-112626400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:112625600-112626400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:112625600-112626400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:112625600-112626400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:112625600-112626400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:112625600-112626400	Flanking Active TSS	Osteobl	bone
35	chr7:112625600-112626600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr7:112625600-112626600	Enhancers	Fetal Intestine Small	intestine
37	chr7:112625600-112626600	Enhancers	HSMMtube	muscle
38	chr7:112625600-112627400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr7:112625600-112627400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:112625600-112627800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:112625600-112627800	Enhancers	NHDF-Ad	bronchial
42	chr7:112625600-112628200	Enhancers	HSMM	muscle
43	chr7:112625800-112626000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:112625800-112626000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:112625800-112626200	Flanking Active TSS	NHLF	lung
46	chr7:112625800-112626600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:112625800-112626600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr7:112625800-112626800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:112625800-112626800	Enhancers	Primary B cells from peripheral blood	blood
50	chr7:112625800-112626800	Enhancers	Placenta	Placenta

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