Variant report

Variant	nsv888973
Chromosome Location	chr7:110509579-110699652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:790)
CpG islands
(count:367)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110668832-110669461	HepG2	liver:	n/a	chr7:110669031-110669047
2	ARID3A	chr7:110634723-110635192	K562	blood:	n/a	n/a
3	ARID3A	chr7:110665042-110665376	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:110666350-110666597	HepG2	liver:	n/a	n/a
5	ATF1	chr7:110634674-110635014	K562	blood:	n/a	n/a
6	ATF1	chr7:110594853-110594948	K562	blood:	n/a	n/a
7	ATF2	chr7:110559170-110559447	GM12878	blood:	n/a	n/a
8	ATF2	chr7:110669475-110670098	GM12878	blood:	n/a	n/a
9	ATF2	chr7:110669473-110669931	GM12878	blood:	n/a	n/a
10	ATF3	chr7:110634636-110635037	K562	blood:	n/a	n/a
11	ATF3	chr7:110629178-110629445	K562	blood:	n/a	n/a
12	BACH1	chr7:110584962-110585666	H1-hESC	embryonic stem cell:	n/a	chr7:110585569-110585583
13	BACH1	chr7:110566972-110567002	K562	blood:	n/a	n/a
14	BATF	chr7:110669545-110669924	GM12878	blood:	n/a	chr7:110669743-110669752
15	BATF	chr7:110554297-110554621	GM12878	blood:	n/a	n/a
16	BATF	chr7:110665136-110665403	GM12878	blood:	n/a	n/a
17	BATF	chr7:110653407-110653722	GM12878	blood:	n/a	n/a
18	BATF	chr7:110653358-110653749	GM12878	blood:	n/a	n/a
19	BATF	chr7:110559184-110559475	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
20	BATF	chr7:110559152-110559518	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
21	BCL11A	chr7:110559197-110559496	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:110559122-110559539	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:110669631-110669997	GM12878	blood:	n/a	chr7:110669736-110669745
24	BHLHE40	chr7:110634646-110634901	K562	blood:	n/a	n/a
25	BHLHE40	chr7:110669740-110670089	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:110559153-110559472	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:110653412-110653737	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:110665083-110665314	GM12878	blood:	n/a	n/a
29	BRCA1	chr7:110669958-110669964	HepG2	liver:	n/a	n/a
30	CBX3	chr7:110634597-110635044	K562	blood:	n/a	n/a
31	CCNT2	chr7:110511063-110511211	K562	blood:	n/a	n/a
32	CCNT2	chr7:110634682-110634982	K562	blood:	n/a	chr7:110634847-110634867
33	CEBPB	chr7:110562837-110563369	MCF-7	breast:	n/a	n/a
34	CEBPB	chr7:110685535-110685851	A549	lung:	n/a	chr7:110685682-110685693
35	CEBPB	chr7:110529337-110529519	A549	lung:	n/a	n/a
36	CEBPB	chr7:110681830-110681993	K562	blood:	n/a	chr7:110681877-110681890 chr7:110681878-110681889
37	CEBPB	chr7:110685542-110685831	HepG2	liver:	n/a	chr7:110685682-110685693
38	CEBPB	chr7:110605335-110605583	A549	lung:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
39	CEBPB	chr7:110652257-110652608	MCF-7	breast:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
40	CEBPB	chr7:110685552-110685868	Hela-S3	cervix:	n/a	chr7:110685682-110685693
41	CEBPB	chr7:110651925-110652603	Hela-S3	cervix:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
42	CEBPB	chr7:110654177-110654502	K562	blood:	n/a	n/a
43	CEBPB	chr7:110654357-110654423	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:110562920-110563368	A549	lung:	n/a	n/a
45	CEBPB	chr7:110685514-110685857	IMR90	lung:	n/a	chr7:110685682-110685693
46	CEBPB	chr7:110687741-110687923	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:110652324-110652446	K562	blood:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
48	CEBPB	chr7:110669122-110669519	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:110524438-110524770	IMR90	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
50	CEBPB	chr7:110605370-110605573	K562	blood:	n/a	chr7:110605435-110605448 chr7:110605435-110605446

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110693055-110693105	NT2-D1	testis:	n/a
2	chr7:110693055-110693105	NT2-D1	testis:	n/a
3	chr7:110693055-110693105	AG09309	skin:	n/a
4	chr7:110585140-110585190	MCF10A-Er-Src	breast:	n/a
5	chr7:110547138-110547188	SAEC	small airway:	n/a
6	chr7:110547138-110547188	HCT-116	colon:	n/a
7	chr7:110658544-110658594	ProgFib	skin:	n/a
8	chr7:110585140-110585190	NH-A	brain:	n/a
9	chr7:110658544-110658594	HNPCEpiC	eye:	n/a
10	chr7:110511335-110511385	SK-N-MC	brain:	n/a
11	chr7:110511335-110511385	NH-A	brain:	n/a
12	chr7:110658544-110658594	HCT-116	colon:	n/a
13	chr7:110693055-110693105	K562	blood:	n/a
14	chr7:110562986-110563036	K562	blood:	n/a
15	chr7:110562986-110563036	NHDF-neo	bronchial:	n/a
16	chr7:110562986-110563036	MCF-7	breast:	n/a
17	chr7:110585140-110585190	T-47D	breast:	n/a
18	chr7:110562986-110563036	LNCaP	prostate:	n/a
19	chr7:110585140-110585190	LNCaP	prostate:	n/a
20	chr7:110585140-110585190	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:110585140-110585190	NHBE	bronchial:	n/a
22	chr7:110693055-110693105	Jurkat	blood:	n/a
23	chr7:110562986-110563036	BE2_C	brain:	n/a
24	chr7:110547138-110547188	SKMC	muscle:	n/a
25	chr7:110511335-110511385	ProgFib	skin:	n/a
26	chr7:110562986-110563036	HCPEpiC	choroid plexus:	n/a
27	chr7:110585140-110585190	A549	lung:	n/a
28	chr7:110693055-110693105	NHDF-neo	bronchial:	n/a
29	chr7:110658544-110658594	LNCaP	prostate:	n/a
30	chr7:110547138-110547188	Caco-2	colon:	n/a
31	chr7:110511335-110511385	SAEC	small airway:	n/a
32	chr7:110562986-110563036	AoSMC	blood vessel:	n/a
33	chr7:110547138-110547188	Hepatocyte	liver:	n/a
34	chr7:110693055-110693105	HL-60	blood:	n/a
35	chr7:110562986-110563036	CMK	blood:	n/a
36	chr7:110511335-110511385	SK-N-SH	brain:	n/a
37	chr7:110562986-110563036	HepG2	liver:	n/a
38	chr7:110511335-110511385	AG04449	skin:	fetal
39	chr7:110693055-110693105	ECC-1	luminal epithelium:	n/a
40	chr7:110547138-110547188	PrEC	prostate:	n/a
41	chr7:110658544-110658594	HCPEpiC	choroid plexus:	n/a
42	chr7:110693055-110693105	SK-N-MC	brain:	n/a
43	chr7:110511335-110511385	IMR90	lung:	fetal
44	chr7:110658544-110658594	A549	lung:	n/a
45	chr7:110562986-110563036	Hela-S3	cervix:	n/a
46	chr7:110547138-110547188	HCPEpiC	choroid plexus:	n/a
47	chr7:110658544-110658594	PFSK-1	brain:	n/a
48	chr7:110511335-110511385	HCPEpiC	choroid plexus:	n/a
49	chr7:110562986-110563036	H1-hESC	embryonic stem cell:	embryo
50	chr7:110547138-110547188	BE2_C	brain:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:110641915..110646048-chr7:110658516..110661977,3	K562	blood:
2	chr7:110505153..110508497-chr7:110509523..110512758,4	K562	blood:
3	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
4	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
5	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
6	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
7	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
8	chr7:110679780..110681548-chr7:110685158..110686912,2	K562	blood:
9	chr7:110644466..110647207-chr7:110661227..110663752,2	MCF-7	breast:
10	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
11	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
12	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
13	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
14	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
15	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
16	chr1:244816363..244816913-chr7:110550021..110550823,2	MCF-7	breast:
17	chr7:110699046..110700709-chr7:110705786..110708655,2	K562	blood:
18	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
19	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
20	chr7:110667611..110669471-chr7:110672812..110675111,2	K562	blood:
21	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
22	chr7:110641915..110646048-chr7:110658516..110661977,3	K562	blood:
23	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
24	chr7:110644466..110647207-chr7:110661227..110663752,2	MCF-7	breast:
25	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
26	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
27	chr7:110650313..110653197-chr7:110655896..110658694,2	K562	blood:
28	chr7:110684762..110686902-chr7:110689607..110691796,2	K562	blood:
29	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
30	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
31	chr7:110642788..110644757-chr7:111200772..111203526,2	K562	blood:
32	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
33	chr7:110650313..110653197-chr7:110655896..110658694,2	K562	blood:
34	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
35	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
36	chr7:110635157..110638146-chr7:111201987..111204497,2	K562	blood:
37	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
38	chr7:110699046..110701763-chr7:110705311..110708989,4	K562	blood:
39	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
40	chr7:110685337..110687591-chr7:111322599..111325063,2	K562	blood:
41	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
42	chr7:110641707..110643850-chr7:110679248..110680877,2	K562	blood:
43	chr7:110679780..110681548-chr7:110685158..110686912,2	K562	blood:
44	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
45	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
46	chr7:110641707..110643850-chr7:110679248..110680877,2	K562	blood:
47	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
48	chr7:110506997..110509461-chr7:110511258..110513064,2	K562	blood:
49	chr7:110667611..110669471-chr7:110672812..110675111,2	K562	blood:
50	chr6:22768459..22769224-chr7:110535482..110536237,2	MCF-7	breast:

No data

Variant related genes	Relation type
IMMP2L	TF binding region
ENSG00000221279	TF binding region
IMMP2L	CpG island
ENSG00000221279	CpG island
ENSG00000184903	chromatin interactions
ENSG00000121644	chromatin interactions

Extended variants
information (count: 6285 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6285 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17158079	chr7:110509579-110509580	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535082160	chr7:110509645-110509646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551243555	chr7:110509649-110509650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564542721	chr7:110509658-110509659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372121323	chr7:110509678-110509679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546783778	chr7:110509730-110509731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566583694	chr7:110509758-110509759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6972694	chr7:110509774-110509775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs549009848	chr7:110509792-110509793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376071474	chr7:110509825-110509826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537782178	chr7:110509878-110509879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183279403	chr7:110509900-110509901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369373485	chr7:110509953-110509954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186850203	chr7:110509994-110509995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533948575	chr7:110510067-110510068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs28709655	chr7:110510104-110510105	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189691415	chr7:110510258-110510259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75368092	chr7:110510334-110510335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142726070	chr7:110510355-110510356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374215410	chr7:110510383-110510384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113119760	chr7:110510446-110510447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556232933	chr7:110510465-110510466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182694817	chr7:110510477-110510478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76086269	chr7:110510513-110510514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564757150	chr7:110510531-110510532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533369776	chr7:110510535-110510536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540861535	chr7:110510536-110510537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370612291	chr7:110510608-110510609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10234144	chr7:110510624-110510625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2396287	chr7:110510626-110510627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs571662742	chr7:110510636-110510637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549048760	chr7:110510649-110510650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4406344	chr7:110510653-110510654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187339870	chr7:110510680-110510681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192681030	chr7:110510714-110510715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372646590	chr7:110510735-110510736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs386716837	chr7:110510751-110510752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7809830	chr7:110510752-110510753	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs571559453	chr7:110510841-110510842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538640412	chr7:110510851-110510852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368966326	chr7:110510862-110510863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533843969	chr7:110510927-110510928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185436527	chr7:110510959-110510960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138053175	chr7:110510991-110510992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376133871	chr7:110510992-110510993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7810646	chr7:110511010-110511011	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs799624	chr7:110511038-110511039	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs544950945	chr7:110511098-110511099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558257065	chr7:110511103-110511104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578227683	chr7:110511108-110511109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Melanoma	17363583	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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110506000-110511000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:110506600-110511000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:110506600-110511200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr7:110506600-110512200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:110508000-110511200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:110508200-110511000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:110508400-110510800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:110508800-110512800	Weak transcription	Psoas Muscle	Psoas
9	chr7:110509400-110510200	Enhancers	Primary T cells from cord blood	blood
10	chr7:110510000-110513000	Enhancers	Fetal Thymus	thymus
11	chr7:110510200-110510600	Weak transcription	Primary T cells from cord blood	blood
12	chr7:110510200-110511600	Enhancers	Aorta	Aorta
13	chr7:110510600-110511200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:110510600-110511600	Enhancers	Dnd41	blood
15	chr7:110510600-110511800	Enhancers	Primary T cells from cord blood	blood
16	chr7:110510800-110511800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:110510800-110512600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:110510800-110512600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:110511000-110511800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:110511000-110512800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:110511000-110512800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:110511200-110511600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr7:110511200-110512200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:110511200-110512200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr7:110511200-110512600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:110511200-110512800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr7:110511400-110513000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:110511800-110512200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:110511800-110517200	Weak transcription	Primary T cells from cord blood	blood
30	chr7:110512200-110513000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:110512200-110513000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr7:110512600-110513000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:110512800-110513000	Enhancers	Psoas Muscle	Psoas
34	chr7:110514800-110515000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:110514800-110515000	Enhancers	Adipose Nuclei	Adipose
36	chr7:110515000-110522000	Weak transcription	Adipose Nuclei	Adipose
37	chr7:110515200-110515400	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr7:110515400-110515600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:110515400-110517200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:110515600-110517200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:110516400-110517600	Enhancers	Fetal Stomach	stomach
42	chr7:110516600-110517000	Enhancers	Fetal Lung	lung
43	chr7:110517000-110518200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:110517200-110517600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:110517200-110517600	Enhancers	Fetal Lung	lung
46	chr7:110517200-110517800	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr7:110517600-110521600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr7:110518200-110519400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:110519200-110519400	Enhancers	Spleen	Spleen
50	chr7:110519400-110522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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