Variant report

Variant	nsv981474
Chromosome Location	chr7:56127123-56131412
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	ARID3A	chr7:56129427-56130437	HepG2	liver:	n/a	chr7:56129829-56129845
2	ARID3A	chr7:56129765-56130529	K562	blood:	n/a	chr7:56129829-56129845
3	ARID3A	chr7:56130994-56132053	K562	blood:	n/a	n/a
4	ARID3A	chr7:56131056-56132588	HepG2	liver:	n/a	n/a
5	ATF1	chr7:56130095-56130477	K562	blood:	n/a	n/a
6	ATF2	chr7:56131373-56132300	GM12878	blood:	n/a	n/a
7	ATF3	chr7:56130047-56130417	K562	blood:	n/a	chr7:56130284-56130298
8	BACH1	chr7:56131357-56132042	K562	blood:	n/a	n/a
9	BATF	chr7:56130159-56130412	GM12878	blood:	n/a	chr7:56130286-56130297 chr7:56130287-56130297
10	BCL3	chr7:56131337-56132277	A549	lung:	n/a	chr7:56132176-56132189
11	BCL3	chr7:56131172-56132360	A549	lung:	n/a	chr7:56132176-56132189
12	BHLHE40	chr7:56131372-56132216	K562	blood:	n/a	n/a
13	BRCA1	chr7:56131402-56132199	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:56131178-56132251	K562	blood:	n/a	n/a
15	CCNT2	chr7:56130163-56130386	K562	blood:	n/a	n/a
16	CCNT2	chr7:56131370-56132325	K562	blood:	n/a	n/a
17	CEBPB	chr7:56131285-56132050	A549	lung:	n/a	chr7:56131652-56131663
18	CEBPB	chr7:56131363-56132051	K562	blood:	n/a	chr7:56131652-56131663
19	CEBPB	chr7:56131383-56131941	A549	lung:	n/a	chr7:56131652-56131663
20	CEBPB	chr7:56131410-56131983	MCF-7	breast:	n/a	chr7:56131652-56131663
21	CEBPB	chr7:56131238-56132263	Hela-S3	cervix:	n/a	chr7:56131652-56131663
22	CEBPB	chr7:56131388-56132111	GM12878	blood:	n/a	chr7:56131652-56131663
23	CEBPB	chr7:56131314-56132177	A549	lung:	n/a	chr7:56131652-56131663
24	CEBPB	chr7:56131394-56131921	MCF-7	breast:	n/a	chr7:56131652-56131663
25	CEBPB	chr7:56131305-56132038	K562	blood:	n/a	chr7:56131652-56131663
26	CEBPB	chr7:56131348-56132164	ECC-1	luminal epithelium:	n/a	chr7:56131652-56131663
27	CEBPB	chr7:56131409-56131747	HepG2	liver:	n/a	chr7:56131652-56131663
28	CEBPB	chr7:56131274-56131966	H1-hESC	embryonic stem cell:	n/a	chr7:56131652-56131663
29	CEBPB	chr7:56129952-56130570	IMR90	lung:	n/a	n/a
30	CEBPD	chr7:56131399-56132265	K562	blood:	n/a	chr7:56131651-56131662
31	CEBPD	chr7:56131410-56132318	K562	blood:	n/a	chr7:56131651-56131662
32	CHD1	chr7:56131347-56131854	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr7:56131356-56132309	K562	blood:	n/a	n/a
34	CHD2	chr7:56131310-56132412	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:56131356-56132285	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr7:56128189-56128274	GM10266	blood:	n/a	n/a
37	CTCF	chr7:56130223-56130533	K562	blood:	n/a	n/a
38	CUX1	chr7:56131355-56132574	K562	blood:	n/a	n/a
39	CUX1	chr7:56129888-56130675	K562	blood:	n/a	n/a
40	EGR1	chr7:56130200-56130441	K562	blood:	n/a	n/a
41	ELK1	chr7:56131270-56132072	K562	blood:	n/a	n/a
42	EP300	chr7:56129843-56130542	SK-N-SH	brain:	n/a	chr7:56130289-56130298 chr7:56130131-56130141 chr7:56130290-56130299
43	EP300	chr7:56129233-56129539	HepG2	liver:	n/a	n/a
44	EP300	chr7:56129845-56130707	K562	blood:	n/a	chr7:56130289-56130298 chr7:56130131-56130141 chr7:56130290-56130299
45	EP300	chr7:56129966-56130455	SK-N-SH_RA	brain:	n/a	chr7:56130289-56130298 chr7:56130131-56130141 chr7:56130290-56130299
46	EP300	chr7:56131259-56132148	HepG2	liver:	n/a	n/a
47	EP300	chr7:56130005-56130442	SK-N-SH_RA	brain:	n/a	chr7:56130289-56130298 chr7:56130131-56130141 chr7:56130290-56130299
48	EP300	chr7:56131376-56132290	K562	blood:	n/a	n/a
49	EP300	chr7:56131356-56131887	Hela-S3	cervix:	n/a	n/a
50	FOS	chr7:56130114-56130493	K562	blood:	n/a	chr7:56130289-56130299 chr7:56130288-56130300 chr7:56130290-56130299 chr7:56130291-56130298 chr7:56130288-56130299 chr7:56130290-56130298

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56128075-56128125	PFSK-1	brain:	n/a
2	chr7:56128075-56128125	HUVEC	blood vessel:	n/a
3	chr7:56128075-56128125	A549	lung:	n/a
4	chr7:56128075-56128125	HRPEpiC	eye:	n/a
5	chr7:56128075-56128125	IMR90	lung:	fetal
6	chr7:56128075-56128125	H1-hESC	embryonic stem cell:	embryo
7	chr7:56128075-56128125	AG04449	skin:	fetal
8	chr7:56128075-56128125	MCF10A-Er-Src	breast:	n/a
9	chr7:56128075-56128125	LNCaP	prostate:	n/a
10	chr7:56128075-56128125	GM19239	blood:	n/a
11	chr7:56128075-56128125	HCM	heart:	n/a
12	chr7:56128075-56128125	K562	blood:	n/a
13	chr7:56128075-56128125	Jurkat	blood:	n/a
14	chr7:56128075-56128125	HCPEpiC	choroid plexus:	n/a
15	chr7:56128075-56128125	GM12892	blood:	n/a
16	chr7:56128075-56128125	Hela-S3	cervix:	n/a
17	chr7:56128075-56128125	HEK293	kidney:	embryo
18	chr7:56128075-56128125	SKMC	muscle:	n/a
19	chr7:56128075-56128125	PANC-1	pancreas:	n/a
20	chr7:56128075-56128125	HCT-116	colon:	n/a
21	chr7:56128075-56128125	MCF-7	breast:	n/a
22	chr7:56128075-56128125	SAEC	small airway:	n/a
23	chr7:56128075-56128125	AG09319	gingival:	n/a
24	chr7:56128075-56128125	SK-N-SH	brain:	n/a
25	chr7:56128075-56128125	AoSMC	blood vessel:	n/a
26	chr7:56128075-56128125	BE2_C	brain:	n/a
27	chr7:56128075-56128125	HEEpiC	esophagus:	n/a
28	chr7:56128075-56128125	SK-N-SH_RA	brain:	n/a
29	chr7:56128075-56128125	NH-A	brain:	n/a
30	chr7:56128075-56128125	HMEC	breast:	n/a
31	chr7:56128075-56128125	HCF	heart:	n/a
32	chr7:56128075-56128125	AG10803	skin:	n/a
33	chr7:56128075-56128125	Hepatocyte	liver:	n/a
34	chr7:56128075-56128125	HIPEpiC	eye:	n/a
35	chr7:56128075-56128125	HepG2	liver:	n/a
36	chr7:56128075-56128125	SK-N-MC	brain:	n/a
37	chr7:56128075-56128125	HNPCEpiC	eye:	n/a
38	chr7:56128075-56128125	GM06990	blood:	n/a
39	chr7:56128075-56128125	GM12891	blood:	n/a
40	chr7:56128075-56128125	ProgFib	skin:	n/a
41	chr7:56128075-56128125	HL-60	blood:	n/a
42	chr7:56128075-56128125	U87	brain:	n/a
43	chr7:56128075-56128125	NT2-D1	testis:	n/a
44	chr7:56128075-56128125	HRCEpiC	kidney:	n/a
45	chr7:56128075-56128125	NB4	blood:	n/a
46	chr7:56128075-56128125	CMK	blood:	n/a
47	chr7:56128075-56128125	Caco-2	colon:	n/a
48	chr7:56128075-56128125	RPTEC	kidney:	n/a
49	chr7:56128075-56128125	T-47D	breast:	n/a
50	chr7:56128075-56128125	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:56124986..56128195-chr7:56129879..56132286,4	MCF-7	breast:
2	chr7:56131320..56133312-chr7:56141582..56144695,3	MCF-7	breast:
3	chr7:56130207..56133425-chr7:56142360..56145052,4	K562	blood:
4	chr7:56018165..56022272-chr7:56129856..56132253,4	K562	blood:
5	chr7:56124986..56128195-chr7:56129879..56132286,4	MCF-7	breast:
6	chr7:56031002..56032516-chr7:56130202..56131906,2	K562	blood:
7	chr7:56126631..56129395-chr7:56129953..56133299,4	MCF-7	breast:
8	chr7:56117123..56123487-chr7:56128716..56133468,11	MCF-7	breast:
9	chr7:56126631..56129395-chr7:56129953..56133299,4	MCF-7	breast:
10	chr7:56128361..56131760-chr7:56167519..56170434,3	K562	blood:
11	chr7:56018384..56020889-chr7:56129856..56132224,2	K562	blood:
12	chr7:56117578..56119708-chr7:56126304..56127920,2	MCF-7	breast:

Variant related genes	Relation type
SNORA15	TF binding region
CCT6A	TF binding region
SUMF2	TF binding region
SNORA15	CpG island
CCT6A	CpG island
SUMF2	CpG island
ENSG00000207168	chromatin interactions
ENSG00000206603	chromatin interactions
ENSG00000239789	chromatin interactions
ENSG00000129103	chromatin interactions
ENSG00000146729	chromatin interactions
ENSG00000238673	chromatin interactions
ENSG00000146733	chromatin interactions
ENSG00000146731	chromatin interactions

Extended variants
information (count: 192 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:192 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75705854	chr7:56127194-56127195	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs372119435	chr7:56127199-56127200	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs143081440	chr7:56127201-56127202	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs569200775	chr7:56127210-56127211	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs370725669	chr7:56127215-56127216	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs375756251	chr7:56127230-56127231	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs368245398	chr7:56127276-56127277	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs372800761	chr7:56127279-56127280	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs147515036	chr7:56127292-56127293	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs572890236	chr7:56127317-56127318	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs140044923	chr7:56127376-56127377	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs558629472	chr7:56127377-56127378	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs200832854	chr7:56127381-56127382	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs576730840	chr7:56127406-56127407	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs117697809	chr7:56127408-56127409	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs182670610	chr7:56127425-56127426	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs530363295	chr7:56127493-56127494	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs542012411	chr7:56127527-56127528	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs78567648	chr7:56127549-56127550	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs35171408	chr7:56127550-56127551	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs79776912	chr7:56127551-56127552	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs398004856	chr7:56127561-56127562	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs560571092	chr7:56127595-56127596	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs145667181	chr7:56127622-56127623	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs377037039	chr7:56127707-56127708	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs575994115	chr7:56127747-56127748	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs76288058	chr7:56127815-56127816	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs367877512	chr7:56127820-56127821	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs570944387	chr7:56127826-56127827	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs531713276	chr7:56127861-56127862	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs550230543	chr7:56127870-56127871	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs569164291	chr7:56127912-56127913	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs536595674	chr7:56127928-56127929	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs148413036	chr7:56127934-56127935	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs71015173	chr7:56127946-56127947	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs398004857	chr7:56127951-56127952	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs372118584	chr7:56127957-56127958	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs566507599	chr7:56128023-56128024	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs201280999	chr7:56128046-56128047	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs111336486	chr7:56128047-56128048	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs151087192	chr7:56128057-56128058	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs534008553	chr7:56128075-56128076	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs141113289	chr7:56128090-56128091	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs371562349	chr7:56128092-56128093	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs142501344	chr7:56128098-56128099	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs192970041	chr7:56128100-56128101	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs370756693	chr7:56128108-56128109	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs370258018	chr7:56128151-56128152	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs555783055	chr7:56128154-56128155	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs574791322	chr7:56128158-56128159	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 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
Lung adenocarcinoma	21935476	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56120200-56131200	Weak transcription	Aorta	Aorta
2	chr7:56120600-56131000	Strong transcription	Adipose Nuclei	Adipose
3	chr7:56120800-56127400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:56120800-56130000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr7:56120800-56130400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:56120800-56130800	Strong transcription	Brain Angular Gyrus	brain
7	chr7:56120800-56131200	Strong transcription	Fetal Thymus	thymus
8	chr7:56120800-56131400	Strong transcription	Fetal Muscle Leg	muscle
9	chr7:56120800-56131600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:56121000-56130000	Weak transcription	Stomach Mucosa	stomach
11	chr7:56121000-56130800	Strong transcription	Fetal Lung	lung
12	chr7:56121000-56131000	Strong transcription	Brain Anterior Caudate	brain
13	chr7:56121000-56131200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr7:56121000-56131200	Strong transcription	Brain Hippocampus Middle	brain
15	chr7:56121200-56128600	Strong transcription	HSMMtube	muscle
16	chr7:56121200-56129400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:56121200-56129400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:56121200-56129400	Strong transcription	Osteobl	bone
19	chr7:56121200-56130400	Strong transcription	Liver	Liver
20	chr7:56121200-56130600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr7:56121200-56130800	Strong transcription	Brain Cingulate Gyrus	brain
22	chr7:56121200-56130800	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr7:56121200-56131200	Strong transcription	Brain Germinal Matrix	brain
24	chr7:56121200-56131200	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr7:56121200-56131400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr7:56121200-56131400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr7:56121400-56128000	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr7:56121400-56128000	Strong transcription	HSMM	muscle
29	chr7:56121400-56128400	Strong transcription	NH-A	brain
30	chr7:56121400-56129000	Genic enhancers	HepG2	liver
31	chr7:56121400-56129400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:56121400-56129800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:56121400-56130600	Strong transcription	Primary B cells from peripheral blood	blood
34	chr7:56121400-56130800	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr7:56121400-56130800	Strong transcription	Fetal Muscle Trunk	muscle
36	chr7:56121400-56130800	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr7:56121400-56131000	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr7:56121400-56131000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:56121400-56131000	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr7:56121400-56131200	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr7:56121400-56131200	Strong transcription	Placenta	Placenta
42	chr7:56121400-56131200	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr7:56121400-56131200	Genic enhancers	Dnd41	blood
44	chr7:56121400-56131400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr7:56121400-56131400	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:56121600-56127400	Strong transcription	Fetal Intestine Large	intestine
47	chr7:56121600-56128800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:56121600-56129600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:56121600-56131000	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr7:56121600-56131000	Strong transcription	Stomach Smooth Muscle	stomach

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