Variant report

Variant	nsv966896
Chromosome Location	chr7:140153046-140156664
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	ATF2	chr7:140155335-140155960	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:140155563-140155898	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:140154231-140154472	GM12878	blood:	n/a	n/a
4	BATF	chr7:140154110-140154526	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:140154177-140154470	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:140153856-140154218	K562	blood:	n/a	chr7:140154039-140154050
7	CEBPB	chr7:140153872-140154222	HepG2	liver:	n/a	chr7:140154039-140154050
8	CEBPB	chr7:140154021-140154212	H1-hESC	embryonic stem cell:	n/a	chr7:140154039-140154050
9	CEBPB	chr7:140156571-140156867	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:140153867-140154223	K562	blood:	n/a	chr7:140154039-140154050
11	CEBPB	chr7:140153886-140154221	IMR90	lung:	n/a	chr7:140154039-140154050
12	CEBPB	chr7:140153871-140154225	A549	lung:	n/a	chr7:140154039-140154050
13	CEBPB	chr7:140153857-140154218	Hela-S3	cervix:	n/a	chr7:140154039-140154050
14	CEBPB	chr7:140153915-140154091	K562	blood:	n/a	chr7:140154039-140154050
15	CHD2	chr7:140155503-140155895	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr7:140154238-140154279	GM10266	blood:	n/a	n/a
17	E2F6	chr7:140155654-140156016	H1-hESC	embryonic stem cell:	n/a	n/a
18	EBF1	chr7:140154095-140154319	GM12878	blood:	n/a	n/a
19	EGR1	chr7:140153462-140153663	K562	blood:	n/a	n/a
20	EP300	chr7:140154153-140154464	GM12878	blood:	n/a	n/a
21	FOXA1	chr7:140156606-140157039	HepG2	liver:	n/a	chr7:140156979-140156991 chr7:140156840-140156852 chr7:140156844-140156856
22	FOXA1	chr7:140156662-140156974	HepG2	liver:	n/a	chr7:140156840-140156852 chr7:140156844-140156856
23	FOXA1	chr7:140156632-140157029	HepG2	liver:	n/a	chr7:140156979-140156991 chr7:140156840-140156852 chr7:140156844-140156856
24	FOXA2	chr7:140156639-140156953	HepG2	liver:	n/a	chr7:140156840-140156852 chr7:140156844-140156856
25	FOXM1	chr7:140154089-140154589	GM12878	blood:	n/a	n/a
26	GTF2F1	chr7:140155559-140155752	H1-hESC	embryonic stem cell:	n/a	n/a
27	HDAC2	chr7:140155520-140155911	H1-hESC	embryonic stem cell:	n/a	n/a
28	JUND	chr7:140155322-140155965	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr7:140155490-140156065	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
30	MAX	chr7:140155513-140156021	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
31	MAX	chr7:140155534-140155992	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
32	MXI1	chr7:140155593-140156014	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr7:140155669-140156037	H1-hESC	embryonic stem cell:	n/a	chr7:140155807-140155814 chr7:140155806-140155816 chr7:140155806-140155815 chr7:140155805-140155816
34	NANOG	chr7:140155587-140155845	H1-hESC	embryonic stem cell:	n/a	n/a
35	NFATC1	chr7:140154302-140154831	GM12878	blood:	n/a	n/a
36	NFIC	chr7:140153988-140154598	GM12878	blood:	n/a	n/a
37	POLR2A	chr7:140154871-140156100	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr7:140154218-140154882	A549	lung:	n/a	n/a
39	POLR2A	chr7:140155678-140155915	K562	blood:	n/a	n/a
40	POLR2A	chr7:140155222-140155909	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr7:140153409-140154844	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:140155398-140155847	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr7:140154674-140155423	K562	blood:	n/a	n/a
44	POLR2A	chr7:140154309-140154418	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr7:140154388-140154813	K562	blood:	n/a	n/a
46	POLR2A	chr7:140154513-140154863	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:140155209-140155314	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr7:140156064-140156170	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr7:140153069-140153362	K562	blood:	n/a	n/a
50	POLR2A	chr7:140155390-140155402	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140156225-140156275	HAEpiC	amniotic membrane:	n/a
2	chr7:140153199-140153249	IMR90	lung:	fetal
3	chr7:140156225-140156275	HUVEC	blood vessel:	n/a
4	chr7:140156225-140156275	HCM	heart:	n/a
5	chr7:140154394-140154444	HRE	kidney:	n/a
6	chr7:140153199-140153249	LNCaP	prostate:	n/a
7	chr7:140153199-140153249	HepG2	liver:	n/a
8	chr7:140156225-140156275	BJ	skin:	n/a
9	chr7:140154394-140154444	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:140153199-140153249	K562	blood:	n/a
11	chr7:140153199-140153249	Jurkat	blood:	n/a
12	chr7:140154394-140154444	SKMC	muscle:	n/a
13	chr7:140153199-140153249	SK-N-SH_RA	brain:	n/a
14	chr7:140154394-140154444	H1-hESC	embryonic stem cell:	embryo
15	chr7:140153199-140153249	HEEpiC	esophagus:	n/a
16	chr7:140154394-140154444	NH-A	brain:	n/a
17	chr7:140156225-140156275	HL-60	blood:	n/a
18	chr7:140154394-140154444	HCF	heart:	n/a
19	chr7:140153199-140153249	HCF	heart:	n/a
20	chr7:140154394-140154444	HepG2	liver:	n/a
21	chr7:140154394-140154444	AoSMC	blood vessel:	n/a
22	chr7:140154394-140154444	MCF10A-Er-Src	breast:	n/a
23	chr7:140153199-140153249	RPTEC	kidney:	n/a
24	chr7:140154394-140154444	HCT-116	colon:	n/a
25	chr7:140153199-140153249	SK-N-MC	brain:	n/a
26	chr7:140154394-140154444	NHDF-neo	bronchial:	n/a
27	chr7:140156225-140156275	AG09309	skin:	n/a
28	chr7:140154394-140154444	A549	lung:	n/a
29	chr7:140154394-140154444	GM12892	blood:	n/a
30	chr7:140153199-140153249	CMK	blood:	n/a
31	chr7:140153199-140153249	AoSMC	blood vessel:	n/a
32	chr7:140153199-140153249	U87	brain:	n/a
33	chr7:140156225-140156275	HIPEpiC	eye:	n/a
34	chr7:140156225-140156275	HMEC	breast:	n/a
35	chr7:140154394-140154444	ProgFib	skin:	n/a
36	chr7:140154394-140154444	K562	blood:	n/a
37	chr7:140153199-140153249	SK-N-SH	brain:	n/a
38	chr7:140153199-140153249	HMEC	breast:	n/a
39	chr7:140156225-140156275	Jurkat	blood:	n/a
40	chr7:140154394-140154444	HIPEpiC	eye:	n/a
41	chr7:140153199-140153249	MCF-7	breast:	n/a
42	chr7:140156225-140156275	MCF-7	breast:	n/a
43	chr7:140154394-140154444	IMR90	lung:	fetal
44	chr7:140153199-140153249	HCPEpiC	choroid plexus:	n/a
45	chr7:140154394-140154444	AG04450	lung:	fetal
46	chr7:140153199-140153249	Caco-2	colon:	n/a
47	chr7:140156225-140156275	HCPEpiC	choroid plexus:	n/a
48	chr7:140156225-140156275	Hepatocyte	liver:	n/a
49	chr7:140156225-140156275	GM12878	blood:	n/a
50	chr7:140156225-140156275	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:140143508..140145426-chr7:140152981..140155575,2	K562	blood:
2	chr7:140152800..140155716-chr7:140177894..140179850,2	MCF-7	breast:
3	chr7:140155139..140157555-chr7:140177850..140179410,2	K562	blood:
4	chr7:140149903..140153274-chr7:140154077..140157814,3	MCF-7	breast:
5	chr7:140147176..140149855-chr7:140152753..140155201,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MKRN1	hsa-miR-375	chr7:140156047-140156068
2	MKRN1	hsa-miR-197-3p	chr7:140153584-140153605

Variant related genes	Relation type
MKRN1	TF binding region
MKRN1	CpG island
ENSG00000133606	chromatin interactions

Extended variants
information (count: 162 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:162 , 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	rs536834489	chr7:140153048-140153049	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs555172057	chr7:140153050-140153051	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573795558	chr7:140153080-140153081	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534834861	chr7:140153089-140153090	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553203504	chr7:140153123-140153124	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577938574	chr7:140153186-140153187	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189288235	chr7:140153192-140153193	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200061500	chr7:140153235-140153236	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563991525	chr7:140153265-140153266	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs17620927	chr7:140153311-140153312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575873701	chr7:140153320-140153321	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147568103	chr7:140153359-140153360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142013775	chr7:140153424-140153425	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs528705971	chr7:140153431-140153432	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs541080082	chr7:140153436-140153437	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192759214	chr7:140153482-140153483	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112549820	chr7:140153483-140153484	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551126552	chr7:140153512-140153513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569911355	chr7:140153570-140153571	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530764176	chr7:140153575-140153576	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538954705	chr7:140153636-140153637	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548760771	chr7:140153680-140153681	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567085312	chr7:140153705-140153706	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs60704749	chr7:140153707-140153708	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs397962072	chr7:140153713-140153714	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150116435	chr7:140153735-140153736	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529580769	chr7:140153810-140153811	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371344862	chr7:140153825-140153826	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138583092	chr7:140153828-140153829	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538999625	chr7:140153848-140153849	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557122633	chr7:140153893-140153894	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575997694	chr7:140153953-140153954	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551281749	chr7:140153981-140153982	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11556753	chr7:140153989-140153990	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148884557	chr7:140154000-140154001	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143595331	chr7:140154022-140154023	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188718944	chr7:140154058-140154059	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540486305	chr7:140154081-140154082	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76185706	chr7:140154148-140154149	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532914726	chr7:140154214-140154215	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372950794	chr7:140154233-140154234	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs544987703	chr7:140154236-140154237	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375609871	chr7:140154246-140154247	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34116813	chr7:140154257-140154258	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373438992	chr7:140154272-140154273	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181454094	chr7:140154283-140154284	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372477403	chr7:140154287-140154288	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201197588	chr7:140154302-140154303	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375734568	chr7:140154303-140154304	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548821157	chr7:140154307-140154308	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19826477	CNVD
Melanoma	19509136	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140126400-140176600	Weak transcription	Right Atrium	heart
2	chr7:140133200-140154200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:140135800-140156000	Weak transcription	NHEK	skin
4	chr7:140136600-140154600	Weak transcription	Fetal Brain Male	brain
5	chr7:140140800-140153800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:140142000-140154200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:140144000-140153200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr7:140144000-140153800	Weak transcription	HepG2	liver
9	chr7:140144000-140154200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:140144000-140154200	Weak transcription	A549	lung
11	chr7:140144000-140154400	Weak transcription	Pancreas	Pancrea
12	chr7:140144800-140153600	Weak transcription	Brain Germinal Matrix	brain
13	chr7:140146000-140153800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:140146400-140154400	Weak transcription	HMEC	breast
15	chr7:140146600-140153400	Weak transcription	Gastric	stomach
16	chr7:140146800-140153400	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:140146800-140154400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr7:140147400-140153600	Weak transcription	NH-A	brain
19	chr7:140147400-140153800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:140147600-140154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:140147800-140153600	Weak transcription	Fetal Lung	lung
22	chr7:140147800-140154000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr7:140148000-140153200	Weak transcription	Fetal Kidney	kidney
24	chr7:140148000-140153600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr7:140148200-140153600	Weak transcription	Brain Substantia Nigra	brain
26	chr7:140149600-140154200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:140149600-140155000	Weak transcription	Psoas Muscle	Psoas
28	chr7:140149800-140153200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr7:140149800-140153400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr7:140149800-140153400	Weak transcription	Lung	lung
31	chr7:140149800-140154200	Weak transcription	Right Ventricle	heart
32	chr7:140149800-140154600	Weak transcription	HSMMtube	muscle
33	chr7:140150200-140153600	Weak transcription	NHLF	lung
34	chr7:140150400-140153800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr7:140150800-140171800	Strong transcription	Fetal Thymus	thymus
36	chr7:140151000-140153200	Strong transcription	Aorta	Aorta
37	chr7:140151000-140154200	Weak transcription	HUVEC	blood vessel
38	chr7:140151000-140156200	Strong transcription	Fetal Brain Female	brain
39	chr7:140151000-140171600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:140151000-140171600	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr7:140151000-140173400	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr7:140151200-140154200	Weak transcription	Esophagus	oesophagus
43	chr7:140151200-140160600	Weak transcription	Stomach Mucosa	stomach
44	chr7:140151200-140161800	Strong transcription	Placenta	Placenta
45	chr7:140151200-140171600	Strong transcription	Adipose Nuclei	Adipose
46	chr7:140151200-140172200	Strong transcription	Fetal Stomach	stomach
47	chr7:140151400-140153200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr7:140151400-140153200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:140151400-140155400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:140151400-140156200	Strong transcription	Fetal Intestine Large	intestine

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