Variant report

Variant	nsv1021902
Chromosome Location	chr7:118452600-118719244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:244)
Chromatin interactive
region (count:45)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 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	chr7:118605996-118606086	K562	blood:	n/a	n/a
2	ATF1	chr7:118609507-118609553	K562	blood:	n/a	n/a
3	ATF1	chr7:118549154-118549158	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	chr7:118650678-118650912	GM12878	blood:	n/a	n/a
13	BCL3	chr7:118542569-118542969	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	chr7:118686542-118686614	A549	lung:	n/a	n/a
17	CEBPB	chr7:118664287-118664601	A549	lung:	n/a	n/a
18	CEBPB	chr7:118706103-118706303	A549	lung:	n/a	n/a
19	CEBPB	chr7:118512077-118512295	K562	blood:	n/a	n/a
20	CEBPB	chr7:118501446-118501656	K562	blood:	n/a	chr7:118501549-118501560
21	CEBPB	chr7:118501387-118501708	HepG2	liver:	n/a	chr7:118501549-118501560
22	CEBPB	chr7:118713490-118713806	HepG2	liver:	n/a	chr7:118713628-118713641 chr7:118713591-118713604 chr7:118713668-118713679 chr7:118713628-118713639 chr7:118713630-118713641 chr7:118713591-118713603 chr7:118713668-118713681 chr7:118713628-118713641
23	CEBPB	chr7:118512022-118513063	Hela-S3	cervix:	n/a	chr7:118512885-118512896
24	CEBPB	chr7:118453692-118453891	H1-hESC	embryonic stem cell:	n/a	chr7:118453791-118453804 chr7:118453791-118453804
25	CEBPB	chr7:118485953-118486161	K562	blood:	n/a	n/a
26	CEBPB	chr7:118635615-118635937	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:118512700-118513064	HepG2	liver:	n/a	chr7:118512885-118512896
28	CEBPB	chr7:118548217-118548578	K562	blood:	n/a	chr7:118548398-118548409
29	CEBPB	chr7:118572120-118572404	HepG2	liver:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
30	CEBPB	chr7:118631545-118631767	HepG2	liver:	n/a	chr7:118631682-118631693
31	CEBPB	chr7:118501362-118501704	A549	lung:	n/a	chr7:118501549-118501560
32	CEBPB	chr7:118568724-118569020	HepG2	liver:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
33	CEBPB	chr7:118548218-118548566	HepG2	liver:	n/a	chr7:118548398-118548409
34	CEBPB	chr7:118548225-118548596	H1-hESC	embryonic stem cell:	n/a	chr7:118548398-118548409
35	CEBPB	chr7:118576878-118576970	HepG2	liver:	n/a	chr7:118576956-118576967
36	CEBPB	chr7:118501364-118501742	IMR90	lung:	n/a	chr7:118501549-118501560
37	CEBPB	chr7:118558763-118558904	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:118453739-118453939	K562	blood:	n/a	chr7:118453791-118453804 chr7:118453791-118453804
39	CEBPB	chr7:118572185-118572434	H1-hESC	embryonic stem cell:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
40	CEBPB	chr7:118512830-118512967	HepG2	liver:	n/a	chr7:118512885-118512896
41	CEBPB	chr7:118548258-118548571	IMR90	lung:	n/a	chr7:118548398-118548409
42	CEBPB	chr7:118512540-118513101	HCT-116	colon:	n/a	chr7:118512885-118512896
43	CEBPB	chr7:118512684-118513033	MCF-7	breast:	n/a	chr7:118512885-118512896
44	CEBPB	chr7:118568719-118569041	IMR90	lung:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
45	CEBPB	chr7:118512590-118513112	HCT-116	colon:	n/a	chr7:118512885-118512896
46	CEBPB	chr7:118572135-118572418	A549	lung:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
47	CEBPB	chr7:118597665-118597936	HepG2	liver:	n/a	chr7:118597811-118597822
48	CEBPB	chr7:118646259-118646292	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:118568797-118568997	K562	blood:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
50	CEBPB	chr7:118640929-118641155	A549	lung:	n/a	chr7:118641131-118641144

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:118498806-118498856	RPTEC	kidney:	n/a
2	chr7:118498931-118498981	HRPEpiC	eye:	n/a
3	chr7:118498806-118498856	LNCaP	prostate:	n/a
4	chr7:118498965-118499015	CMK	blood:	n/a
5	chr7:118498931-118498981	GM06990	blood:	n/a
6	chr7:118498806-118498856	HCT-116	colon:	n/a
7	chr7:118498806-118498856	BJ	skin:	n/a
8	chr7:118498931-118498981	SK-N-MC	brain:	n/a
9	chr7:118498931-118498981	PFSK-1	brain:	n/a
10	chr7:118498931-118498981	Hela-S3	cervix:	n/a
11	chr7:118498931-118498981	AoSMC	blood vessel:	n/a
12	chr7:118572128-118572178	HIPEpiC	eye:	n/a
13	chr7:118498931-118498981	HEK293	kidney:	embryo
14	chr7:118572128-118572178	AoSMC	blood vessel:	n/a
15	chr7:118498931-118498981	Caco-2	colon:	n/a
16	chr7:118498931-118498981	U87	brain:	n/a
17	chr7:118498931-118498981	AG04449	skin:	fetal
18	chr7:118572128-118572178	GM12891	blood:	n/a
19	chr7:118498965-118499015	GM12878	blood:	n/a
20	chr7:118498965-118499015	NH-A	brain:	n/a
21	chr7:118572128-118572178	Jurkat	blood:	n/a
22	chr7:118498931-118498981	GM12878	blood:	n/a
23	chr7:118498965-118499015	BE2_C	brain:	n/a
24	chr7:118498806-118498856	HEEpiC	esophagus:	n/a
25	chr7:118498806-118498856	HNPCEpiC	eye:	n/a
26	chr7:118498931-118498981	Hepatocyte	liver:	n/a
27	chr7:118572128-118572178	Hela-S3	cervix:	n/a
28	chr7:118572128-118572178	HEK293	kidney:	embryo
29	chr7:118498806-118498856	HAEpiC	amniotic membrane:	n/a
30	chr7:118498931-118498981	Jurkat	blood:	n/a
31	chr7:118498806-118498856	PFSK-1	brain:	n/a
32	chr7:118498931-118498981	HRE	kidney:	n/a
33	chr7:118498965-118499015	Caco-2	colon:	n/a
34	chr7:118498931-118498981	HepG2	liver:	n/a
35	chr7:118498965-118499015	LNCaP	prostate:	n/a
36	chr7:118498965-118499015	MCF-7	breast:	n/a
37	chr7:118498806-118498856	HEK293	kidney:	embryo
38	chr7:118498806-118498856	HL-60	blood:	n/a
39	chr7:118498806-118498856	AG10803	skin:	n/a
40	chr7:118498806-118498856	AG04449	skin:	fetal
41	chr7:118498931-118498981	H1-hESC	embryonic stem cell:	embryo
42	chr7:118498806-118498856	SKMC	muscle:	n/a
43	chr7:118498806-118498856	PANC-1	pancreas:	n/a
44	chr7:118498965-118499015	HCF	heart:	n/a
45	chr7:118572128-118572178	PrEC	prostate:	n/a
46	chr7:118572128-118572178	BE2_C	brain:	n/a
47	chr7:118498806-118498856	ECC-1	luminal epithelium:	n/a
48	chr7:118572128-118572178	NHDF-neo	bronchial:	n/a
49	chr7:118498931-118498981	NB4	blood:	n/a
50	chr7:118498965-118499015	A549	lung:	n/a

(count:45 , 50 per page) page: 1

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

(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: 3219 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3219 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142806868	chr7:118452645-118452646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574822032	chr7:118452739-118452740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144600208	chr7:118452797-118452798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560536880	chr7:118452819-118452820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2590585	chr7:118452826-118452827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs34112945	chr7:118452834-118452835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546374243	chr7:118452847-118452848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545104817	chr7:118452913-118452914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184056026	chr7:118452933-118452934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555091720	chr7:118452990-118452991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560703225	chr7:118453006-118453007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529673390	chr7:118453022-118453023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114168457	chr7:118453023-118453024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73217505	chr7:118453029-118453030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187799748	chr7:118453043-118453044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560129400	chr7:118453128-118453129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs118186185	chr7:118453245-118453246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566827709	chr7:118453267-118453268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115087224	chr7:118453295-118453296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375896208	chr7:118453305-118453306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148072979	chr7:118453316-118453317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537746737	chr7:118453320-118453321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192429838	chr7:118453418-118453419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116154151	chr7:118453419-118453420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73217506	chr7:118453420-118453421	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141403899	chr7:118453421-118453422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183878168	chr7:118453429-118453430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1881868	chr7:118453442-118453443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs150834189	chr7:118453448-118453449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377727022	chr7:118453481-118453482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373021774	chr7:118453520-118453521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139533797	chr7:118453548-118453549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188605785	chr7:118453567-118453568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73217508	chr7:118453578-118453579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs527997999	chr7:118453580-118453581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546139785	chr7:118453582-118453583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76809659	chr7:118453622-118453623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532067038	chr7:118453637-118453638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370445238	chr7:118453680-118453681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565332481	chr7:118453691-118453692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552295570	chr7:118453710-118453711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2699734	chr7:118453853-118453854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538011334	chr7:118453946-118453947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111687036	chr7:118453955-118453956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548106466	chr7:118453959-118453960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568316647	chr7:118454037-118454038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191918171	chr7:118454077-118454078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554201409	chr7:118454121-118454122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577359682	chr7:118454196-118454197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566997759	chr7:118454217-118454218	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:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118452400-118456000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:118453400-118453800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr7:118456000-118458200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:118468800-118469200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr7:118484600-118485400	Enhancers	HMEC	breast
6	chr7:118484600-118485400	Enhancers	NHEK	skin
7	chr7:118484800-118486200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:118485000-118485400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:118486200-118486600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr7:118486600-118487200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:118493000-118493400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:118493400-118495200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:118495200-118495800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:118495400-118495800	Enhancers	Fetal Kidney	kidney
15	chr7:118495400-118495800	Enhancers	Fetal Lung	lung
16	chr7:118495800-118498400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:118495800-118501000	Weak transcription	Fetal Lung	lung
18	chr7:118496400-118497000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:118496400-118497000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:118496600-118497000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:118496800-118497000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr7:118497000-118498600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:118497200-118498600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr7:118498600-118499000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:118498600-118499200	Active TSS	Esophagus	oesophagus
26	chr7:118498600-118499400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
27	chr7:118501000-118502000	Enhancers	Fetal Lung	lung
28	chr7:118501600-118504400	Enhancers	Fetal Stomach	stomach
29	chr7:118505200-118506400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:118506400-118507600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:118507600-118508400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:118508200-118508400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:118508200-118509400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:118508200-118509400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:118508400-118509000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:118508400-118509200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:118508400-118509600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:118508400-118512800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr7:118508600-118509400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:118508600-118510400	Enhancers	Dnd41	blood
41	chr7:118509000-118509400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:118509200-118509400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr7:118509200-118509800	Enhancers	Fetal Lung	lung
44	chr7:118509200-118512600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:118509400-118510200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr7:118509400-118510600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:118509400-118512600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr7:118509400-118512800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr7:118509600-118512600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr7:118510200-118510400	Enhancers	H1 Cell Line	embryonic stem cell

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