Variant report

Variant	nsv889096
Chromosome Location	chr7:118438184-118709754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:736)
CpG islands
(count:244)
Chromatin interactive
region (count:48)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:118609507-118609553	K562	blood:	n/a	n/a
2	ATF1	chr7:118549154-118549158	K562	blood:	n/a	n/a
3	ATF1	chr7:118605996-118606086	K562	blood:	n/a	n/a
4	ATF1	chr7:118508221-118508255	K562	blood:	n/a	n/a
5	ATF2	chr7:118476959-118477384	GM12878	blood:	n/a	n/a
6	ATF2	chr7:118476847-118477462	GM12878	blood:	n/a	n/a
7	BACH1	chr7:118542700-118543032	K562	blood:	n/a	n/a
8	BACH1	chr7:118542669-118543065	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:118476943-118477307	GM12878	blood:	n/a	n/a
10	BATF	chr7:118476894-118477341	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:118476987-118477362	GM12878	blood:	n/a	n/a
12	BCL3	chr7:118542569-118542969	GM12878	blood:	n/a	n/a
13	BCL3	chr7:118650678-118650912	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:118476904-118477400	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:118640025-118640296	GM12878	blood:	n/a	n/a
16	CEBPB	chr7:118646259-118646292	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:118512700-118513064	HepG2	liver:	n/a	chr7:118512885-118512896
18	CEBPB	chr7:118501446-118501656	K562	blood:	n/a	chr7:118501549-118501560
19	CEBPB	chr7:118548218-118548557	A549	lung:	n/a	chr7:118548398-118548409
20	CEBPB	chr7:118576878-118576970	HepG2	liver:	n/a	chr7:118576956-118576967
21	CEBPB	chr7:118635615-118635937	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:118512732-118512976	H1-hESC	embryonic stem cell:	n/a	chr7:118512885-118512896
23	CEBPB	chr7:118640929-118641155	A549	lung:	n/a	chr7:118641131-118641144
24	CEBPB	chr7:118512590-118513112	HCT-116	colon:	n/a	chr7:118512885-118512896
25	CEBPB	chr7:118548314-118548527	MCF-7	breast:	n/a	chr7:118548398-118548409
26	CEBPB	chr7:118512022-118513063	Hela-S3	cervix:	n/a	chr7:118512885-118512896
27	CEBPB	chr7:118512730-118512944	K562	blood:	n/a	chr7:118512885-118512896
28	CEBPB	chr7:118512077-118512295	K562	blood:	n/a	n/a
29	CEBPB	chr7:118635617-118635965	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:118548218-118548566	HepG2	liver:	n/a	chr7:118548398-118548409
31	CEBPB	chr7:118568797-118568997	K562	blood:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
32	CEBPB	chr7:118512830-118512967	HepG2	liver:	n/a	chr7:118512885-118512896
33	CEBPB	chr7:118572135-118572418	A549	lung:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
34	CEBPB	chr7:118597665-118597936	HepG2	liver:	n/a	chr7:118597811-118597822
35	CEBPB	chr7:118512684-118513033	MCF-7	breast:	n/a	chr7:118512885-118512896
36	CEBPB	chr7:118635637-118635889	A549	lung:	n/a	n/a
37	CEBPB	chr7:118552168-118552368	HepG2	liver:	n/a	chr7:118552250-118552261
38	CEBPB	chr7:118453739-118453939	K562	blood:	n/a	chr7:118453791-118453804 chr7:118453791-118453804
39	CEBPB	chr7:118568724-118569020	HepG2	liver:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
40	CEBPB	chr7:118640833-118641182	HepG2	liver:	n/a	chr7:118641131-118641144
41	CEBPB	chr7:118512540-118513101	HCT-116	colon:	n/a	chr7:118512885-118512896
42	CEBPB	chr7:118501387-118501708	HepG2	liver:	n/a	chr7:118501549-118501560
43	CEBPB	chr7:118664287-118664601	A549	lung:	n/a	n/a
44	CEBPB	chr7:118485953-118486161	K562	blood:	n/a	n/a
45	CEBPB	chr7:118501362-118501704	A549	lung:	n/a	chr7:118501549-118501560
46	CEBPB	chr7:118568719-118569041	IMR90	lung:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
47	CEBPB	chr7:118572185-118572434	H1-hESC	embryonic stem cell:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
48	CEBPB	chr7:118548225-118548596	H1-hESC	embryonic stem cell:	n/a	chr7:118548398-118548409
49	CEBPB	chr7:118453692-118453891	H1-hESC	embryonic stem cell:	n/a	chr7:118453791-118453804 chr7:118453791-118453804
50	CEBPB	chr7:118631545-118631767	HepG2	liver:	n/a	chr7:118631682-118631693

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:118572128-118572178	NB4	blood:	n/a
2	chr7:118572128-118572178	BE2_C	brain:	n/a
3	chr7:118572128-118572178	K562	blood:	n/a
4	chr7:118498806-118498856	HCPEpiC	choroid plexus:	n/a
5	chr7:118498965-118499015	Hela-S3	cervix:	n/a
6	chr7:118572128-118572178	HEK293	kidney:	embryo
7	chr7:118498965-118499015	AG04449	skin:	fetal
8	chr7:118498806-118498856	SK-N-SH	brain:	n/a
9	chr7:118572128-118572178	Hela-S3	cervix:	n/a
10	chr7:118498931-118498981	AG09319	gingival:	n/a
11	chr7:118572128-118572178	U87	brain:	n/a
12	chr7:118498806-118498856	HUVEC	blood vessel:	n/a
13	chr7:118498965-118499015	AoSMC	blood vessel:	n/a
14	chr7:118572128-118572178	AoSMC	blood vessel:	n/a
15	chr7:118498806-118498856	PrEC	prostate:	n/a
16	chr7:118498965-118499015	HRCEpiC	kidney:	n/a
17	chr7:118572128-118572178	NT2-D1	testis:	n/a
18	chr7:118498931-118498981	H1-hESC	embryonic stem cell:	embryo
19	chr7:118498965-118499015	GM06990	blood:	n/a
20	chr7:118498965-118499015	GM12891	blood:	n/a
21	chr7:118498965-118499015	PANC-1	pancreas:	n/a
22	chr7:118498965-118499015	BE2_C	brain:	n/a
23	chr7:118498965-118499015	Caco-2	colon:	n/a
24	chr7:118572128-118572178	HAEpiC	amniotic membrane:	n/a
25	chr7:118498965-118499015	HRE	kidney:	n/a
26	chr7:118498931-118498981	GM12891	blood:	n/a
27	chr7:118498931-118498981	HCF	heart:	n/a
28	chr7:118498806-118498856	AoSMC	blood vessel:	n/a
29	chr7:118572128-118572178	SKMC	muscle:	n/a
30	chr7:118498931-118498981	ECC-1	luminal epithelium:	n/a
31	chr7:118498806-118498856	HMEC	breast:	n/a
32	chr7:118498806-118498856	PANC-1	pancreas:	n/a
33	chr7:118572128-118572178	PrEC	prostate:	n/a
34	chr7:118572128-118572178	HIPEpiC	eye:	n/a
35	chr7:118572128-118572178	HCF	heart:	n/a
36	chr7:118498931-118498981	HepG2	liver:	n/a
37	chr7:118498931-118498981	RPTEC	kidney:	n/a
38	chr7:118498965-118499015	GM19239	blood:	n/a
39	chr7:118498931-118498981	T-47D	breast:	n/a
40	chr7:118572128-118572178	T-47D	breast:	n/a
41	chr7:118498931-118498981	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:118498965-118499015	Jurkat	blood:	n/a
43	chr7:118572128-118572178	GM12878	blood:	n/a
44	chr7:118498806-118498856	AG09319	gingival:	n/a
45	chr7:118498965-118499015	RPTEC	kidney:	n/a
46	chr7:118498931-118498981	MCF10A-Er-Src	breast:	n/a
47	chr7:118498965-118499015	GM12892	blood:	n/a
48	chr7:118572128-118572178	Jurkat	blood:	n/a
49	chr7:118498931-118498981	MCF-7	breast:	n/a
50	chr7:118572128-118572178	PANC-1	pancreas:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:118637455..118640247-chr7:118654338..118656624,3	K562	blood:
2	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
3	chr7:118635764..118637617-chr7:118641365..118644121,2	MCF-7	breast:
4	chr7:118448241..118450701-chr7:118452751..118455343,2	K562	blood:
5	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
6	chr7:118629006..118631002-chr7:118732998..118734533,2	K562	blood:
7	chr7:118383910..118385815-chr7:118436694..118438479,2	MCF-7	breast:
8	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:
9	chr7:118541712..118543750-chr7:118545681..118548097,2	K562	blood:
10	chr7:118510382..118510908-chr7:118815972..118816682,2	MCF-7	breast:
11	chr7:118519830..118521416-chr7:118526135..118527775,2	MCF-7	breast:
12	chr7:118476181..118478052-chr7:118487208..118490190,2	K562	blood:
13	chr7:118492020..118493688-chr7:118503141..118506054,2	K562	blood:
14	chr7:118503790..118506549-chr7:118510715..118512350,2	K562	blood:
15	chr7:118492020..118493688-chr7:118503141..118506054,2	K562	blood:
16	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
17	chr7:118637455..118640247-chr7:118654338..118656624,3	K562	blood:
18	chr7:118519135..118521104-chr7:118523180..118525034,2	K562	blood:
19	chr7:118476181..118478052-chr7:118487208..118490190,2	K562	blood:
20	chr7:118637455..118639784-chr7:118654717..118656624,2	K562	blood:
21	chr7:118558392..118559287-chr7:118815693..118816489,5	MCF-7	breast:
22	chr7:118558904..118559746-chr7:118816086..118816731,2	MCF-7	breast:
23	chr7:118635764..118637617-chr7:118641365..118644121,2	MCF-7	breast:
24	chr7:118637455..118639784-chr7:118654717..118656624,2	K562	blood:
25	chr7:118552988..118554537-chr7:118554629..118557088,2	MCF-7	breast:
26	chr7:118503790..118506549-chr7:118510715..118512350,2	K562	blood:
27	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
28	chr7:118448241..118450701-chr7:118452751..118455343,2	K562	blood:
29	chr3:27629054..27629554-chr7:118565092..118565730,2	MCF-7	breast:
30	chr7:118512499..118514711-chr7:118517595..118519435,2	MCF-7	breast:
31	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
32	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
33	chr7:118558340..118559254-chr7:118837696..118838683,4	MCF-7	breast:
34	chr7:118541712..118543750-chr7:118545681..118548097,2	K562	blood:
35	chr7:118445682..118447696-chr7:118455521..118457653,2	K562	blood:
36	chr7:118611978..118614798-chr7:118654699..118657373,2	K562	blood:
37	chr7:118512499..118514711-chr7:118517595..118519435,2	MCF-7	breast:
38	chr7:118457044..118459465-chr7:118462059..118464961,2	MCF-7	breast:
39	chr7:118519135..118521104-chr7:118522932..118525034,3	K562	blood:
40	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:
41	chr7:118611978..118614798-chr7:118654699..118657373,2	K562	blood:
42	chr7:118519135..118521104-chr7:118522932..118525034,3	K562	blood:
43	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
44	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
45	chr7:118552988..118554537-chr7:118554629..118557088,2	MCF-7	breast:
46	chr7:118445682..118447696-chr7:118455521..118457653,2	K562	blood:
47	chr7:118519135..118521104-chr7:118523180..118525034,2	K562	blood:
48	chr7:118457044..118459465-chr7:118462059..118464961,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-6	chr7:118590440-118591313	NONHSAT122979
2	lnc-CTTNBP2-5	chr7:118520499-118521342	NONHSAT122978
3	lnc-CTTNBP2-5	chr7:118520157-118520298	NONHSAT122978

No data

Variant related genes	Relation type
ENSG00000229982	TF binding region
ENSG00000230520	TF binding region
ENSG00000229982	CpG island
ENSG00000230520	CpG island
ENSG00000229982	chromatin interactions

Extended variants
information (count: 3331 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3331 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2204779	chr7:118438184-118438185	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77272746	chr7:118438214-118438215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552885654	chr7:118438227-118438228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572079867	chr7:118438229-118438230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114068595	chr7:118438273-118438274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191136883	chr7:118438300-118438301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116441093	chr7:118438318-118438319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2222815	chr7:118438331-118438332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182227096	chr7:118438369-118438370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73484219	chr7:118438479-118438480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534996302	chr7:118438502-118438503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186833789	chr7:118438514-118438515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191661444	chr7:118438597-118438598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141223469	chr7:118438603-118438604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13309745	chr7:118438624-118438625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10231061	chr7:118438660-118438661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185041442	chr7:118438673-118438674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531820473	chr7:118438685-118438686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548309285	chr7:118438711-118438712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543975790	chr7:118438715-118438716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532451189	chr7:118438719-118438720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6974190	chr7:118438729-118438730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs370859486	chr7:118438753-118438754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150240895	chr7:118438763-118438764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531858093	chr7:118438773-118438774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145795544	chr7:118438845-118438846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189923457	chr7:118438878-118438879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534463153	chr7:118438898-118438899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551953962	chr7:118438978-118438979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376962983	chr7:118438981-118438982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534109624	chr7:118439017-118439018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11979469	chr7:118439055-118439056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547815000	chr7:118439068-118439069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115347247	chr7:118439079-118439080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193182292	chr7:118439090-118439091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558602531	chr7:118439100-118439101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574958594	chr7:118439160-118439161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537568783	chr7:118439188-118439189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554304762	chr7:118439201-118439202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185444223	chr7:118439215-118439216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540520543	chr7:118439217-118439218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372262227	chr7:118439267-118439268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71567379	chr7:118439313-118439314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114382155	chr7:118439383-118439384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114957037	chr7:118439404-118439405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545843668	chr7:118439413-118439414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35883217	chr7:118439431-118439432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7810935	chr7:118439434-118439435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2699774	chr7:118439436-118439437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs189528721	chr7:118439479-118439480	Weak transcription	n/a	n/a	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
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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	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
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118437400-118438200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:118438200-118441400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:118439200-118439400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:118441400-118442400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:118447200-118451200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:118451200-118452400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:118452400-118456000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:118453400-118453800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:118456000-118458200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:118468800-118469200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:118484600-118485400	Enhancers	HMEC	breast
12	chr7:118484600-118485400	Enhancers	NHEK	skin
13	chr7:118484800-118486200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr7:118485000-118485400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:118486200-118486600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr7:118486600-118487200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:118493000-118493400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:118493400-118495200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:118495200-118495800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:118495400-118495800	Enhancers	Fetal Kidney	kidney
21	chr7:118495400-118495800	Enhancers	Fetal Lung	lung
22	chr7:118495800-118498400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:118495800-118501000	Weak transcription	Fetal Lung	lung
24	chr7:118496400-118497000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:118496400-118497000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:118496600-118497000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:118496800-118497000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:118497000-118498600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:118497200-118498600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr7:118498600-118499000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:118498600-118499200	Active TSS	Esophagus	oesophagus
32	chr7:118498600-118499400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr7:118501000-118502000	Enhancers	Fetal Lung	lung
34	chr7:118501600-118504400	Enhancers	Fetal Stomach	stomach
35	chr7:118505200-118506400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:118506400-118507600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:118507600-118508400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:118508200-118508400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:118508200-118509400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:118508200-118509400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:118508400-118509000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:118508400-118509200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr7:118508400-118509600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:118508400-118512800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr7:118508600-118509400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:118508600-118510400	Enhancers	Dnd41	blood
47	chr7:118509000-118509400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:118509200-118509400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr7:118509200-118509800	Enhancers	Fetal Lung	lung
50	chr7:118509200-118512600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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