Variant report

Variant	nsv981512
Chromosome Location	chr7:66223352-66249901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:66244727-66245492	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:66247477-66248389	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:66241522-66242348	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:66237921-66238346	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:66230660-66230662	K562	blood:	n/a	n/a
6	ATF2	chr7:66223893-66224290	GM12878	blood:	n/a	n/a
7	ATF2	chr7:66223838-66224383	GM12878	blood:	n/a	n/a
8	BATF	chr7:66223906-66224290	GM12878	blood:	n/a	n/a
9	BATF	chr7:66223909-66224311	GM12878	blood:	n/a	n/a
10	BCLAF1	chr7:66223853-66224306	GM12878	blood:	n/a	n/a
11	BCLAF1	chr7:66234029-66234357	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:66248990-66249225	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:66234430-66234501	K562	blood:	n/a	n/a
14	BHLHE40	chr7:66241867-66242098	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:66241952-66242048	K562	blood:	n/a	n/a
16	BHLHE40	chr7:66241799-66242223	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:66248071-66248120	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:66242236-66242378	K562	blood:	n/a	chr7:66242317-66242328
19	CEBPB	chr7:66232512-66232718	K562	blood:	n/a	n/a
20	CEBPB	chr7:66234971-66235171	Hela-S3	cervix:	n/a	chr7:66235135-66235146
21	CEBPB	chr7:66242212-66242422	IMR90	lung:	n/a	chr7:66242317-66242328
22	CEBPB	chr7:66242146-66242483	HepG2	liver:	n/a	chr7:66242317-66242328
23	CEBPB	chr7:66244930-66245248	IMR90	lung:	n/a	chr7:66245058-66245070
24	CEBPB	chr7:66234959-66235502	IMR90	lung:	n/a	chr7:66235135-66235146
25	CEBPB	chr7:66247781-66248138	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:66247851-66248128	K562	blood:	n/a	n/a
27	CEBPB	chr7:66247818-66248093	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:66247891-66247984	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:66223908-66224485	GM12878	blood:	n/a	n/a
30	CEBPB	chr7:66223991-66224242	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:66247776-66248145	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:66223981-66224319	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:66235015-66235296	HepG2	liver:	n/a	chr7:66235135-66235146
34	CREB1	chr7:66223778-66224449	GM12878	blood:	n/a	n/a
35	CREB1	chr7:66223889-66224409	GM12878	blood:	n/a	n/a
36	CTCF	chr7:66241440-66241590	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr7:66241780-66241930	HCT-116	colon:	n/a	n/a
38	CTCF	chr7:66241460-66241610	AG04449	skin:	n/a	n/a
39	CTCF	chr7:66241480-66241630	HAc	cerebellar:	n/a	n/a
40	CTCF	chr7:66241460-66241610	GM12875	blood:	n/a	n/a
41	CTCF	chr7:66234780-66234930	HVMF	connective:	n/a	n/a
42	CTCF	chr7:66241480-66241630	GM12873	blood:	n/a	n/a
43	CTCF	chr7:66238128-66238511	A549	lung:	n/a	n/a
44	CTCF	chr7:66247960-66248110	AG04450	lung:	n/a	n/a
45	CTCF	chr7:66241540-66241690	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr7:66241540-66241690	HMF	breast:	n/a	n/a
47	CTCF	chr7:66234940-66235090	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr7:66241460-66241610	HEK293	kidney:	n/a	n/a
49	CTCF	chr7:66243060-66243116	GM10266	blood:	n/a	n/a
50	CTCF	chr7:66241445-66241472	Pancreas_OC	pancreas:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66237581-66237631	ovcar-3	ovarian:	n/a
2	chr7:66237581-66237631	U87	brain:	n/a
3	chr7:66237581-66237631	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:66237581-66237631	MCF-7	breast:	n/a
5	chr7:66237581-66237631	AG04450	lung:	fetal
6	chr7:66237581-66237631	T-47D	breast:	n/a
7	chr7:66237581-66237631	Caco-2	colon:	n/a
8	chr7:66237581-66237631	GM06990	blood:	n/a
9	chr7:66237581-66237631	HRCEpiC	kidney:	n/a
10	chr7:66237581-66237631	NH-A	brain:	n/a
11	chr7:66237581-66237631	HRPEpiC	eye:	n/a
12	chr7:66237581-66237631	SK-N-SH	brain:	n/a
13	chr7:66237581-66237631	RPTEC	kidney:	n/a
14	chr7:66237581-66237631	GM12892	blood:	n/a
15	chr7:66237581-66237631	SK-N-SH_RA	brain:	n/a
16	chr7:66237581-66237631	NB4	blood:	n/a
17	chr7:66237581-66237631	Hela-S3	cervix:	n/a
18	chr7:66237581-66237631	BJ	skin:	n/a
19	chr7:66237581-66237631	ECC-1	luminal epithelium:	n/a
20	chr7:66237581-66237631	HMEC	breast:	n/a
21	chr7:66237581-66237631	NT2-D1	testis:	n/a
22	chr7:66237581-66237631	NHBE	bronchial:	n/a
23	chr7:66237581-66237631	AG04449	skin:	fetal
24	chr7:66237581-66237631	BE2_C	brain:	n/a
25	chr7:66237581-66237631	CMK	blood:	n/a
26	chr7:66237581-66237631	HCPEpiC	choroid plexus:	n/a
27	chr7:66237581-66237631	PFSK-1	brain:	n/a
28	chr7:66237581-66237631	SK-N-MC	brain:	n/a
29	chr7:66237581-66237631	PANC-1	pancreas:	n/a
30	chr7:66237581-66237631	AG09309	skin:	n/a
31	chr7:66237581-66237631	HepG2	liver:	n/a
32	chr7:66237581-66237631	SKMC	muscle:	n/a
33	chr7:66237581-66237631	HNPCEpiC	eye:	n/a
34	chr7:66237581-66237631	SAEC	small airway:	n/a
35	chr7:66237581-66237631	AG10803	skin:	n/a
36	chr7:66237581-66237631	HCM	heart:	n/a
37	chr7:66237581-66237631	MCF10A-Er-Src	breast:	n/a
38	chr7:66237581-66237631	GM12878	blood:	n/a
39	chr7:66237581-66237631	HL-60	blood:	n/a
40	chr7:66237581-66237631	LNCaP	prostate:	n/a
41	chr7:66237581-66237631	K562	blood:	n/a
42	chr7:66237581-66237631	HEEpiC	esophagus:	n/a
43	chr7:66237581-66237631	HCF	heart:	n/a
44	chr7:66237581-66237631	NHDF-neo	bronchial:	n/a
45	chr7:66237581-66237631	IMR90	lung:	fetal
46	chr7:66237581-66237631	HRE	kidney:	n/a
47	chr7:66237581-66237631	PrEC	prostate:	n/a
48	chr7:66237581-66237631	HEK293	kidney:	embryo
49	chr7:66237581-66237631	AG09319	gingival:	n/a
50	chr7:66237581-66237631	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66228722..66231364-chr7:66237134..66239135,2	MCF-7	breast:
2	chr7:66228722..66231364-chr7:66237134..66239135,2	MCF-7	breast:
3	chr7:66232638..66234742-chr7:66239785..66241846,2	K562	blood:
4	chr7:66203830..66206564-chr7:66239736..66241863,2	K562	blood:
5	chr7:66222166..66224180-chr7:66308292..66309931,2	K562	blood:
6	chr7:66232638..66234742-chr7:66239785..66241846,2	K562	blood:
7	chr7:66233619..66236445-chr7:66238794..66241787,2	MCF-7	breast:
8	chr7:66233619..66236445-chr7:66238794..66241787,2	MCF-7	breast:
9	chr7:66204517..66207240-chr7:66227815..66230567,2	MCF-7	breast:
10	chr7:66220562..66222668-chr7:66223187..66225396,2	K562	blood:

No data

Variant related genes	Relation type
RABGEF1	TF binding region
RABGEF1	CpG island
ENSG00000272831	chromatin interactions
ENSG00000230583	chromatin interactions
ENSG00000154710	chromatin interactions
ENSG00000243335	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147190947	chr7:66223380-66223381	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs553555563	chr7:66223401-66223402	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs3800811	chr7:66223417-66223418	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs112867698	chr7:66223419-66223420	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189942192	chr7:66223425-66223426	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528595479	chr7:66223441-66223442	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs3800812	chr7:66223461-66223462	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs571855872	chr7:66223489-66223490	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537333294	chr7:66223509-66223510	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138744161	chr7:66223573-66223574	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs73139927	chr7:66223584-66223585	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs567247046	chr7:66223601-66223602	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536223756	chr7:66223650-66223651	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs113689161	chr7:66223675-66223676	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182112324	chr7:66223676-66223677	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs536020649	chr7:66223677-66223678	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7800620	chr7:66223688-66223689	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs189392421	chr7:66223690-66223691	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78119906	chr7:66223692-66223693	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs4380814	chr7:66223730-66223731	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575438418	chr7:66223775-66223776	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs180711303	chr7:66223854-66223855	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs185100685	chr7:66223901-66223902	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188340267	chr7:66223904-66223905	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377282757	chr7:66223911-66223912	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs574875545	chr7:66223916-66223917	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs117881067	chr7:66223948-66223949	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181242332	chr7:66223959-66223960	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144461361	chr7:66223972-66223973	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs148407181	chr7:66223977-66223978	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs528573192	chr7:66223982-66223983	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543871326	chr7:66224039-66224040	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs529550567	chr7:66224062-66224063	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145597413	chr7:66224078-66224079	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569636632	chr7:66224104-66224105	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186709515	chr7:66224155-66224156	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143955356	chr7:66224199-66224200	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551215944	chr7:66224200-66224201	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577382330	chr7:66224211-66224212	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567928447	chr7:66224234-66224235	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117271318	chr7:66224286-66224287	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546574835	chr7:66224298-66224299	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564887818	chr7:66224311-66224312	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566510779	chr7:66224371-66224372	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191496719	chr7:66224375-66224376	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558653894	chr7:66224408-66224409	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371128364	chr7:66224473-66224474	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183754804	chr7:66224476-66224477	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146455905	chr7:66224479-66224480	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186319421	chr7:66224480-66224481	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66206800-66223400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:66206800-66232600	Weak transcription	Primary T cells from cord blood	blood
3	chr7:66206800-66238800	Weak transcription	Aorta	Aorta
4	chr7:66207000-66227400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:66207000-66227400	Weak transcription	Fetal Stomach	stomach
6	chr7:66207000-66230600	Weak transcription	Fetal Intestine Large	intestine
7	chr7:66207000-66230600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr7:66207000-66234000	Weak transcription	Fetal Thymus	thymus
9	chr7:66207000-66238400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:66207000-66238400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr7:66207000-66255200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:66207200-66223400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr7:66207600-66223400	Weak transcription	K562	blood
14	chr7:66207600-66239800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:66207800-66225800	Weak transcription	Fetal Muscle Leg	muscle
16	chr7:66208000-66230600	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:66208000-66232400	Weak transcription	Thymus	Thymus
18	chr7:66208000-66236800	Weak transcription	Dnd41	blood
19	chr7:66208000-66238000	Weak transcription	A549	lung
20	chr7:66208000-66238600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:66208000-66238600	Weak transcription	Brain Germinal Matrix	brain
22	chr7:66208000-66240800	Weak transcription	HSMMtube	muscle
23	chr7:66208000-66241800	Weak transcription	Hela-S3	cervix
24	chr7:66209400-66239000	Weak transcription	HMEC	breast
25	chr7:66211000-66223400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:66211000-66228600	Weak transcription	Fetal Lung	lung
27	chr7:66212000-66236800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:66213200-66234400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:66213400-66230600	Weak transcription	NH-A	brain
30	chr7:66214000-66223400	Weak transcription	Small Intestine	intestine
31	chr7:66214200-66224000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:66214200-66224000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr7:66214200-66225800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr7:66214200-66234200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr7:66214400-66223400	Weak transcription	HSMM	muscle
36	chr7:66214400-66225000	Weak transcription	Ovary	ovary
37	chr7:66214400-66229600	Weak transcription	Brain Hippocampus Middle	brain
38	chr7:66214400-66234200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:66214400-66236600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:66214400-66239400	Weak transcription	Stomach Smooth Muscle	stomach
41	chr7:66214600-66223400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:66214600-66223800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:66214600-66224000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:66214600-66231000	Weak transcription	Left Ventricle	heart
45	chr7:66214600-66234000	Weak transcription	NHLF	lung
46	chr7:66214600-66234200	Weak transcription	Gastric	stomach
47	chr7:66215000-66230600	Weak transcription	Fetal Intestine Small	intestine
48	chr7:66215600-66234200	Weak transcription	Rectal Smooth Muscle	rectum
49	chr7:66215800-66234200	Weak transcription	NHEK	skin
50	chr7:66216600-66223400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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