Variant report

Variant	nsv1022066
Chromosome Location	chr7:112630168-113122748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3521)
CpG islands
(count:1953)
Chromatin interactive
region (count:264)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3521 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

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

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112726774-112726824	RPTEC	kidney:	n/a
2	chr7:112726774-112726824	RPTEC	kidney:	n/a
3	chr7:113034122-113034172	A549	lung:	n/a
4	chr7:112758502-112758552	CMK	blood:	n/a
5	chr7:112724674-112724724	HRCEpiC	kidney:	n/a
6	chr7:113090002-113090052	GM12891	blood:	n/a
7	chr7:112726869-112726919	HCPEpiC	choroid plexus:	n/a
8	chr7:113034122-113034172	ECC-1	luminal epithelium:	n/a
9	chr7:112726774-112726824	AG04449	skin:	fetal
10	chr7:112724674-112724724	K562	blood:	n/a
11	chr7:112726089-112726139	AG10803	skin:	n/a
12	chr7:112739805-112739855	GM19239	blood:	n/a
13	chr7:112758903-112758953	Hepatocyte	liver:	n/a
14	chr7:113091000-113091050	HNPCEpiC	eye:	n/a
15	chr7:112726774-112726824	SAEC	small airway:	n/a
16	chr7:112758734-112758784	GM12878	blood:	n/a
17	chr7:112726549-112726599	U87	brain:	n/a
18	chr7:112725899-112725949	Hela-S3	cervix:	n/a
19	chr7:112838431-112838481	HCM	heart:	n/a
20	chr7:112726653-112726703	HRCEpiC	kidney:	n/a
21	chr7:112758800-112758850	AG10803	skin:	n/a
22	chr7:112727423-112727473	HCT-116	colon:	n/a
23	chr7:112727506-112727556	BE2_C	brain:	n/a
24	chr7:112726089-112726139	SK-N-SH_RA	brain:	n/a
25	chr7:112724674-112724724	HL-60	blood:	n/a
26	chr7:112758800-112758850	NHBE	bronchial:	n/a
27	chr7:112758903-112758953	U87	brain:	n/a
28	chr7:112758903-112758953	K562	blood:	n/a
29	chr7:112727423-112727473	BJ	skin:	n/a
30	chr7:113034122-113034172	AG04449	skin:	fetal
31	chr7:112758903-112758953	A549	lung:	n/a
32	chr7:112739805-112739855	HEEpiC	esophagus:	n/a
33	chr7:112758954-112759004	RPTEC	kidney:	n/a
34	chr7:112726774-112726824	NB4	blood:	n/a
35	chr7:112907863-112907913	CMK	blood:	n/a
36	chr7:112758800-112758850	HCT-116	colon:	n/a
37	chr7:112727506-112727556	NH-A	brain:	n/a
38	chr7:112726802-112726852	H1-hESC	embryonic stem cell:	embryo
39	chr7:112758748-112758798	Hepatocyte	liver:	n/a
40	chr7:112903509-112903559	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:112726774-112726824	AG10803	skin:	n/a
42	chr7:112758502-112758552	HCPEpiC	choroid plexus:	n/a
43	chr7:113011963-113012013	IMR90	lung:	fetal
44	chr7:112726538-112726588	NT2-D1	testis:	n/a
45	chr7:113011963-113012013	GM12892	blood:	n/a
46	chr7:112903509-112903559	HEK293	kidney:	embryo
47	chr7:112726396-112726446	HEK293	kidney:	embryo
48	chr7:112758800-112758850	SAEC	small airway:	n/a
49	chr7:112758744-112758794	HL-60	blood:	n/a
50	chr7:113091000-113091050	HCM	heart:	n/a

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:112914755..112918139-chr7:112919654..112923102,3	K562	blood:
2	chr7:112758684..112760391-chr7:112965987..112967563,2	K562	blood:
3	chr7:6616906..6617576-chr7:112758559..112759124,2	Hela-S3	cervix:
4	chr7:112887063..112887777-chr7:112921303..112922004,3	MCF-7	breast:
5	chr7:112799910..112800953-chr7:113061499..113062556,5	MCF-7	breast:
6	chr7:113053644..113055850-chr7:113060152..113062983,2	MCF-7	breast:
7	chr7:112811150..112812144-chr7:112920712..112921503,2	MCF-7	breast:
8	chr7:112695979..112699168-chr7:112699243..112702331,3	K562	blood:
9	chr7:113028637..113030163-chr7:113052999..113055912,2	K562	blood:
10	chr7:112800339..112803140-chr7:112813993..112816435,2	K562	blood:
11	chr7:112799910..112800953-chr7:113061499..113062556,5	MCF-7	breast:
12	chr7:112801750..112803685-chr7:112813306..112816042,2	K562	blood:
13	chr7:112734000..112735828-chr7:112736599..112739272,2	MCF-7	breast:
14	chr7:112771938..112776955-chr7:112779975..112785331,6	K562	blood:
15	chr7:112836739..112839262-chr7:112840349..112843254,3	K562	blood:
16	chr7:112761834..112764773-chr7:112768104..112770317,2	K562	blood:
17	chr7:112732414..112734626-chr7:112757774..112759351,2	K562	blood:
18	chr7:112766821..112770020-chr7:112775041..112777462,3	K562	blood:
19	chr7:112841354..112843011-chr7:112844071..112845692,2	K562	blood:
20	chr7:112737881..112740697-chr7:112741857..112745616,3	K562	blood:
21	chr17:79885731..79886495-chr7:112758134..112758664,2	Hela-S3	cervix:
22	chr7:112713707..112715518-chr7:112717712..112719924,2	K562	blood:
23	chr7:112815199..112817636-chr7:112823311..112824921,2	MCF-7	breast:
24	chr7:112703408..112705692-chr7:112716673..112719279,2	K562	blood:
25	chr7:112764896..112766469-chr7:112769155..112770793,2	K562	blood:
26	chr7:112654683..112655746-chr7:113061433..113062375,3	K562	blood:
27	chr7:112716768..112718529-chr7:112755627..112758248,2	K562	blood:
28	chr7:112741820..112743488-chr7:112746778..112749070,2	K562	blood:
29	chr7:112919908..112922049-chr7:112922331..112926205,3	MCF-7	breast:
30	chr7:113030617..113032266-chr7:113032276..113034462,2	K562	blood:
31	chr7:112769278..112771459-chr7:113340632..113343613,2	K562	blood:
32	chr7:112759649..112762090-chr7:112783076..112784947,2	K562	blood:
33	chr7:112878168..112880923-chr7:112882880..112884449,2	K562	blood:
34	chr7:112764216..112766097-chr7:112779643..112782310,2	K562	blood:
35	chr7:112854163..112856387-chr7:112856648..112858157,2	MCF-7	breast:
36	chr7:112811148..112812106-chr7:112921056..112921827,2	MCF-7	breast:
37	chr7:112703408..112705692-chr7:112716673..112719279,2	K562	blood:
38	chr7:112725765..112728466-chr7:112738917..112741049,2	K562	blood:
39	chr7:112934260..112936230-chr7:112936620..112938273,2	MCF-7	breast:
40	chr7:112849832..112851498-chr7:112857060..112858734,2	K562	blood:
41	chr7:112682248..112683838-chr7:112894672..112896979,2	K562	blood:
42	chr7:112788647..112791637-chr7:112793429..112795616,2	K562	blood:
43	chr7:112723034..112725310-chr7:112753782..112755599,2	MCF-7	breast:
44	chr7:112654983..112656027-chr7:113061405..113062486,9	MCF-7	breast:
45	chr7:112760083..112762482-chr7:112787454..112790230,2	MCF-7	breast:
46	chr7:112759714..112761754-chr7:112774243..112776920,2	K562	blood:
47	chr7:112739468..112741215-chr7:112753236..112756208,2	K562	blood:
48	chr7:112764896..112766469-chr7:112769155..112770793,2	K562	blood:
49	chr7:112764216..112766097-chr7:112779643..112782310,2	K562	blood:
50	chr7:112628593..112630399-chr7:112648519..112650654,2	K562	blood:

(count:20 , 50 per page) page: 1

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

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
ENSG00000164603	chromatin interactions
ENSG00000236294	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000214194	chromatin interactions
ENSG00000265688	chromatin interactions
ENSG00000270997	chromatin interactions
ENSG00000225457	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000164604	chromatin interactions

Extended variants
information (count: 10182 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:10182 , 50 per page) page: 1 2 3 4 5 6 7 ... 204

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554016923	chr7:112630169-112630170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564960110	chr7:112630223-112630224	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs115471924	chr7:112630233-112630234	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550304279	chr7:112630254-112630255	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs562460963	chr7:112630259-112630260	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs529959014	chr7:112630273-112630274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs528115593	chr7:112630305-112630306	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs1349290	chr7:112630326-112630327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs186885121	chr7:112630397-112630398	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs533721788	chr7:112630414-112630415	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552292579	chr7:112630418-112630419	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs369326510	chr7:112630432-112630433	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs375078523	chr7:112630478-112630479	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs372727899	chr7:112630545-112630546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs192086598	chr7:112630599-112630600	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs538289144	chr7:112630611-112630612	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs74547583	chr7:112630676-112630677	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs556355322	chr7:112630717-112630718	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs181854021	chr7:112630727-112630728	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs59327203	chr7:112630737-112630738	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535796006	chr7:112630768-112630769	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs554485312	chr7:112630785-112630786	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs10252298	chr7:112630788-112630789	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs71561782	chr7:112630803-112630804	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs11984301	chr7:112630858-112630859	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs565022635	chr7:112631092-112631093	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576871608	chr7:112631151-112631152	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530006766	chr7:112631161-112631162	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs185246932	chr7:112631241-112631242	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs562363150	chr7:112631254-112631255	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs189714322	chr7:112631362-112631363	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182066937	chr7:112631431-112631432	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548111978	chr7:112631552-112631553	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs560006148	chr7:112631568-112631569	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527529072	chr7:112631589-112631590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116599352	chr7:112631608-112631609	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570586263	chr7:112631626-112631627	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs371447871	chr7:112631631-112631632	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs1569277	chr7:112631636-112631637	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs540712106	chr7:112631650-112631651	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550219936	chr7:112631662-112631663	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs188034667	chr7:112631664-112631665	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs535836171	chr7:112631705-112631706	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs1569276	chr7:112631713-112631714	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs565492271	chr7:112631722-112631723	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs74832356	chr7:112631759-112631760	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs540094217	chr7:112631775-112631776	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558396972	chr7:112631794-112631795	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs529956096	chr7:112631802-112631803	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs145750916	chr7:112631825-112631826	Weak transcription Active TSS	n/a	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:1727 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112594200-112630400	Weak transcription	Left Ventricle	heart
2	chr7:112625000-112631200	Enhancers	Fetal Heart	heart
3	chr7:112626800-112630400	Weak transcription	NHEK	skin
4	chr7:112626800-112631400	Enhancers	NH-A	brain
5	chr7:112627200-112631400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:112627400-112631600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:112627800-112630200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr7:112627800-112630400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:112627800-112635200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:112628000-112635200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:112628600-112634800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:112628600-112635200	Weak transcription	NHLF	lung
13	chr7:112628800-112634800	Weak transcription	HSMMtube	muscle
14	chr7:112629000-112630400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:112629000-112630400	Enhancers	Stomach Mucosa	stomach
16	chr7:112629600-112630600	Enhancers	HSMM	muscle
17	chr7:112629600-112631000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:112629600-112631200	Enhancers	HMEC	breast
19	chr7:112629800-112630200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:112629800-112631200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:112629800-112631400	Enhancers	Osteobl	bone
22	chr7:112629800-112634200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:112630000-112630200	Enhancers	Right Ventricle	heart
24	chr7:112630000-112630400	Weak transcription	NHDF-Ad	bronchial
25	chr7:112630200-112630600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:112630200-112630600	Flanking Active TSS	Right Ventricle	heart
27	chr7:112630200-112631000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:112630200-112631200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:112630400-112630800	Flanking Active TSS	Left Ventricle	heart
30	chr7:112630400-112631000	Enhancers	NHDF-Ad	bronchial
31	chr7:112630400-112631200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:112630400-112631200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr7:112630400-112631200	Enhancers	NHEK	skin
34	chr7:112630600-112634600	Weak transcription	HSMM	muscle
35	chr7:112630600-112635800	Active TSS	Right Ventricle	heart
36	chr7:112630800-112631000	Enhancers	Left Ventricle	heart
37	chr7:112631000-112632000	Weak transcription	Left Ventricle	heart
38	chr7:112631000-112634800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:112631000-112634800	Weak transcription	NHDF-Ad	bronchial
40	chr7:112631200-112631600	Weak transcription	Fetal Heart	heart
41	chr7:112631200-112634400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:112631200-112634400	Weak transcription	HMEC	breast
43	chr7:112631200-112634800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:112631200-112634800	Weak transcription	NHEK	skin
45	chr7:112631200-112635200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:112631200-112635200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr7:112631400-112634200	Weak transcription	Osteobl	bone
48	chr7:112631400-112634400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:112631400-112634600	Weak transcription	NH-A	brain
50	chr7:112631600-112631800	Enhancers	Fetal Heart	heart

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