Variant report

Variant	nsv831008
Chromosome Location	chr7:56245775-56403107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:56396037-56396404	K562	blood:	n/a	n/a
2	ATF1	chr7:56392870-56393144	K562	blood:	n/a	n/a
3	ATF1	chr7:56317868-56318068	K562	blood:	n/a	n/a
4	BATF	chr7:56394887-56395134	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:56396053-56396246	K562	blood:	n/a	n/a
6	BRCA1	chr7:56291833-56291857	GM12878	blood:	n/a	n/a
7	BRCA1	chr7:56287789-56287892	GM12878	blood:	n/a	n/a
8	CEBPB	chr7:56354384-56354589	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:56264073-56264117	K562	blood:	n/a	n/a
10	CEBPB	chr7:56331752-56331815	HepG2	liver:	n/a	chr7:56331776-56331787
11	CEBPB	chr7:56331758-56331766	K562	blood:	n/a	n/a
12	CEBPB	chr7:56307103-56307194	A549	lung:	n/a	chr7:56307153-56307166 chr7:56307153-56307164
13	CEBPB	chr7:56264082-56264119	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:56361446-56361522	HepG2	liver:	n/a	chr7:56361484-56361495
15	CHD2	chr7:56246706-56246869	GM12878	blood:	n/a	n/a
16	CTCF	chr7:56381201-56381270	LNCaP	prostate:	n/a	n/a
17	CTCF	chr7:56394940-56395090	GM12868	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
18	CTCF	chr7:56394930-56395153	MCF-7	breast:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
19	CTCF	chr7:56394940-56395076	GM10266	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
20	CTCF	chr7:56381208-56381281	GM10266	blood:	n/a	n/a
21	CTCF	chr7:56394940-56395090	NB4	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
22	CTCF	chr7:56394880-56395030	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:56396200-56396277	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr7:56355239-56355277	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:56394935-56395147	Kidney_OC	kidney:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
26	CTCF	chr7:56396232-56396296	GM13976	blood:	n/a	n/a
27	CTCF	chr7:56396492-56396573	GM13976	blood:	n/a	n/a
28	CTCF	chr7:56394924-56395155	GM19240	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
29	CTCF	chr7:56395000-56395150	NHEK	skin:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
30	CTCF	chr7:56394940-56395090	GM12867	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
31	CTCF	chr7:56394850-56395124	A549	lung:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
32	CTCF	chr7:56394960-56395110	RPTEC	kidney:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
33	CTCF	chr7:56394920-56395070	GM12874	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
34	CTCF	chr7:56346360-56346510	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr7:56394929-56395140	ProgFib	skin:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
36	CTCF	chr7:56394940-56395090	GM12866	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
37	CTCF	chr7:56394920-56395070	Caco-2	colon:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
38	CTCF	chr7:56394943-56395153	LNCaP	prostate:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
39	CTCF	chr7:56394953-56395141	Fibrobl	skin:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
40	CTCF	chr7:56395020-56395170	GM12867	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
41	CTCF	chr7:56395760-56395910	GM06990	blood:	n/a	n/a
42	CTCF	chr7:56276782-56276832	GM10266	blood:	n/a	n/a
43	CTCF	chr7:56394960-56395110	HFF-Myc	foreskin:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
44	CTCF	chr7:56394839-56395120	K562	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
45	CTCF	chr7:56394920-56395070	HCFaa	heart:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
46	CTCF	chr7:56394920-56395070	GM12865	blood:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
47	CTCF	chr7:56398805-56398873	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:56355773-56355812	NHEK	skin:	n/a	n/a
49	CTCF	chr7:56394800-56395090	A549	lung:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052
50	CTCF	chr7:56395000-56395150	HepG2	liver:	n/a	chr7:56395038-56395054 chr7:56395037-56395055 chr7:56395042-56395052

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56246843-56246893	ECC-1	luminal epithelium:	n/a
2	chr7:56358512-56358562	LNCaP	prostate:	n/a
3	chr7:56297579-56297629	SK-N-SH	brain:	n/a
4	chr7:56246843-56246893	ECC-1	luminal epithelium:	n/a
5	chr7:56358512-56358562	LNCaP	prostate:	n/a
6	chr7:56297579-56297629	SK-N-SH	brain:	n/a
7	chr7:56297661-56297711	GM12892	blood:	n/a
8	chr7:56355681-56355731	Hepatocyte	liver:	n/a
9	chr7:56295392-56295442	SK-N-MC	brain:	n/a
10	chr7:56356698-56356748	AG10803	skin:	n/a
11	chr7:56362101-56362151	MCF10A-Er-Src	breast:	n/a
12	chr7:56297661-56297711	AG09319	gingival:	n/a
13	chr7:56362101-56362151	SAEC	small airway:	n/a
14	chr7:56297714-56297764	HUVEC	blood vessel:	n/a
15	chr7:56296973-56297023	ECC-1	luminal epithelium:	n/a
16	chr7:56362101-56362151	HNPCEpiC	eye:	n/a
17	chr7:56355681-56355731	GM06990	blood:	n/a
18	chr7:56297579-56297629	ProgFib	skin:	n/a
19	chr7:56358512-56358562	ovcar-3	ovarian:	n/a
20	chr7:56355681-56355731	H1-hESC	embryonic stem cell:	embryo
21	chr7:56301065-56301115	ovcar-3	ovarian:	n/a
22	chr7:56356698-56356748	H1-hESC	embryonic stem cell:	embryo
23	chr7:56354974-56355024	AoSMC	blood vessel:	n/a
24	chr7:56354974-56355024	HRE	kidney:	n/a
25	chr7:56352934-56352984	HIPEpiC	eye:	n/a
26	chr7:56362101-56362151	BJ	skin:	n/a
27	chr7:56297661-56297711	A549	lung:	n/a
28	chr7:56297661-56297711	HIPEpiC	eye:	n/a
29	chr7:56296570-56296620	GM19239	blood:	n/a
30	chr7:56297490-56297540	HEEpiC	esophagus:	n/a
31	chr7:56297579-56297629	HNPCEpiC	eye:	n/a
32	chr7:56246843-56246893	GM12878	blood:	n/a
33	chr7:56297714-56297764	NH-A	brain:	n/a
34	chr7:56357732-56357782	HIPEpiC	eye:	n/a
35	chr7:56301065-56301115	HCT-116	colon:	n/a
36	chr7:56296973-56297023	AoSMC	blood vessel:	n/a
37	chr7:56356698-56356748	Caco-2	colon:	n/a
38	chr7:56301065-56301115	HMEC	breast:	n/a
39	chr7:56295392-56295442	NT2-D1	testis:	n/a
40	chr7:56295392-56295442	Caco-2	colon:	n/a
41	chr7:56297490-56297540	GM12891	blood:	n/a
42	chr7:56295392-56295442	AG09309	skin:	n/a
43	chr7:56297579-56297629	GM12892	blood:	n/a
44	chr7:56296570-56296620	SK-N-MC	brain:	n/a
45	chr7:56358512-56358562	SK-N-MC	brain:	n/a
46	chr7:56296570-56296620	ProgFib	skin:	n/a
47	chr7:56356698-56356748	NT2-D1	testis:	n/a
48	chr7:56297661-56297711	SK-N-SH	brain:	n/a
49	chr7:56297714-56297764	NHDF-neo	bronchial:	n/a
50	chr7:56358512-56358562	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:56173625..56175741-chr7:56262885..56264422,2	MCF-7	breast:
2	chr7:56173528..56175860-chr7:56295526..56297795,2	K562	blood:
3	chr7:56171801..56173788-chr7:56307425..56310338,2	K562	blood:
4	chr7:56234975..56237932-chr7:56245748..56248480,2	MCF-7	breast:
5	chr7:56295830..56297823-chr7:56299936..56302375,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMF2-10	chr7:56355923-56357276	NONHSAT120740
2	lnc-SUMF2-10	chr7:56357589-56359118	NONHSAT120740
3	lnc-SUMF2-11	chr7:56390497-56390549	NONHSAT120741
4	lnc-SUMF2-11	chr7:56391008-56391294	NONHSAT120741

Variant related genes	Relation type
ENSG00000203462	TF binding region
CCNJP1	TF binding region
ENSG00000224155	TF binding region
ENSG00000223559	TF binding region
ENSG00000265887	TF binding region
ENSG00000203462	CpG island
CCNJP1	CpG island
ENSG00000224155	CpG island
ENSG00000223559	CpG island
ENSG00000265887	CpG island
ENSG00000227491	chromatin interactions
ENSG00000106153	chromatin interactions

Extended variants
information (count: 944 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11764929	chr7:56245781-56245782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181277783	chr7:56245789-56245790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547306731	chr7:56245792-56245793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544044255	chr7:56255477-56255478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180981655	chr7:56255498-56255499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7800889	chr7:56255502-56255503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560383065	chr7:56255516-56255517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7777451	chr7:56255522-56255523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557257230	chr7:56255527-56255528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141650223	chr7:56255568-56255569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542871813	chr7:56255616-56255617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560923418	chr7:56255640-56255641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528227681	chr7:56255661-56255662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539905274	chr7:56255671-56255672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6948587	chr7:56255691-56255692	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs531951157	chr7:56255750-56255751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527742086	chr7:56255768-56255769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569238859	chr7:56255778-56255779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530327087	chr7:56255793-56255794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548805554	chr7:56255798-56255799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566911021	chr7:56255808-56255809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368619581	chr7:56255811-56255812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534304240	chr7:56255818-56255819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377486276	chr7:56255925-56255926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs80264808	chr7:56255985-56255986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116040324	chr7:56259608-56259609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529049600	chr7:56259641-56259642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547258545	chr7:56259704-56259705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111712921	chr7:56259709-56259710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539532497	chr7:56259743-56259744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529891090	chr7:56259792-56259793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551406374	chr7:56259880-56259881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140971282	chr7:56259910-56259911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113961557	chr7:56259911-56259912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370427936	chr7:56259930-56259931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555994880	chr7:56259969-56259970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs698628	chr7:56259989-56259990	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs535252275	chr7:56259994-56259995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573031886	chr7:56259999-56260000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377100976	chr7:56262896-56262897	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532675353	chr7:56262923-56262924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550835149	chr7:56262968-56262969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142937773	chr7:56262981-56262982	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183735063	chr7:56263007-56263008	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369810612	chr7:56263037-56263038	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548742025	chr7:56263038-56263039	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566901325	chr7:56263065-56263066	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs698631	chr7:56263098-56263099	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs10252721	chr7:56263100-56263101	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188844776	chr7:56263112-56263113	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56243800-56245800	Weak transcription	Spleen	Spleen
2	chr7:56255400-56256000	Enhancers	Placenta	Placenta
3	chr7:56259600-56260000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr7:56263000-56264000	Enhancers	Placenta	Placenta
5	chr7:56264000-56264400	Weak transcription	Placenta	Placenta
6	chr7:56264400-56265000	Enhancers	Placenta	Placenta
7	chr7:56284800-56285200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr7:56286400-56286800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:56287600-56290600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:56294600-56295200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:56296400-56296800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:56296400-56296800	Enhancers	Gastric	stomach
13	chr7:56297200-56297400	Bivalent/Poised TSS	K562	blood
14	chr7:56297400-56297600	Active TSS	K562	blood
15	chr7:56297400-56297800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:56303200-56303400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:56323600-56324200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:56323800-56324600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr7:56323800-56324800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr7:56324400-56324800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr7:56324600-56325600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr7:56325600-56325800	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr7:56334000-56336600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:56336000-56336400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
25	chr7:56355000-56355200	Enhancers	Brain Anterior Caudate	brain
26	chr7:56355000-56355200	Enhancers	Brain Cingulate Gyrus	brain
27	chr7:56355000-56355800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:56355000-56355800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:56355000-56356000	Active TSS	Aorta	Aorta
30	chr7:56355000-56356000	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:56355000-56356000	Active TSS	Right Atrium	heart
32	chr7:56355000-56356000	Active TSS	Stomach Smooth Muscle	stomach
33	chr7:56355200-56355400	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr7:56355200-56355600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:56355200-56355600	Active TSS	Colon Smooth Muscle	Colon
36	chr7:56355200-56355600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr7:56355200-56355600	Active TSS	Fetal Stomach	stomach
38	chr7:56355200-56355600	Bivalent Enhancer	Left Ventricle	heart
39	chr7:56355200-56355800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:56355200-56355800	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr7:56355200-56355800	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr7:56355200-56355800	Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr7:56355200-56355800	Active TSS	Fetal Muscle Leg	muscle
44	chr7:56355200-56355800	Active TSS	Rectal Smooth Muscle	rectum
45	chr7:56355200-56355800	Active TSS	NHEK	skin
46	chr7:56355200-56356000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:56355200-56356000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:56355200-56356000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:56355200-56356000	Enhancers	Liver	Liver
50	chr7:56355200-56356000	Active TSS	Brain Angular Gyrus	brain

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