Variant report

Variant	nsv1032638
Chromosome Location	chr7:84550206-84603392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:367)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84577444-84577446	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:84580783-84580807	K562	blood:	n/a	n/a
3	BACH1	chr7:84561867-84561950	K562	blood:	n/a	n/a
4	BHLHE40	chr7:84575928-84576179	K562	blood:	n/a	n/a
5	BRCA1	chr7:84553857-84554108	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr7:84550539-84550822	A549	lung:	n/a	chr7:84550674-84550685
7	CEBPB	chr7:84580283-84580518	K562	blood:	n/a	n/a
8	CEBPB	chr7:84580265-84580465	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:84550542-84550842	HepG2	liver:	n/a	chr7:84550674-84550685
10	CEBPB	chr7:84575983-84576315	K562	blood:	n/a	chr7:84576158-84576171 chr7:84576158-84576169
11	CEBPB	chr7:84553663-84554313	Hela-S3	cervix:	n/a	chr7:84554243-84554256
12	CEBPB	chr7:84550529-84550857	IMR90	lung:	n/a	chr7:84550674-84550685
13	CEBPB	chr7:84570151-84570349	K562	blood:	n/a	n/a
14	CEBPB	chr7:84582313-84583027	Hela-S3	cervix:	n/a	chr7:84582772-84582785 chr7:84582414-84582425
15	CEBPB	chr7:84558928-84559109	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:84575948-84576287	K562	blood:	n/a	chr7:84576158-84576171 chr7:84576158-84576169
17	CEBPB	chr7:84550523-84550842	K562	blood:	n/a	chr7:84550674-84550685
18	CEBPD	chr7:84575806-84576352	K562	blood:	n/a	n/a
19	CEBPD	chr7:84575896-84576309	K562	blood:	n/a	n/a
20	CTCF	chr7:84558320-84558470	AoAF	blood vessel:	n/a	n/a
21	E2F4	chr7:84599724-84599847	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr7:84563481-84563537	GM12878	blood:	n/a	n/a
23	EP300	chr7:84573446-84573497	GM12878	blood:	n/a	n/a
24	EP300	chr7:84582366-84582978	Hela-S3	cervix:	n/a	n/a
25	EP300	chr7:84575927-84576205	K562	blood:	n/a	n/a
26	EP300	chr7:84554022-84554284	Hela-S3	cervix:	n/a	n/a
27	FOS	chr7:84550121-84550269	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:84580241-84580441	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr7:84580024-84580478	HUVEC	blood vessel:	n/a	n/a
30	FOS	chr7:84580232-84580500	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr7:84580207-84580505	MCF10A-Er-Src	breast:	n/a	n/a
32	FOXA1	chr7:84597640-84597951	T-47D	breast:	n/a	n/a
33	FOXA1	chr7:84597664-84597923	T-47D	breast:	n/a	n/a
34	GATA2	chr7:84575825-84576216	K562	blood:	n/a	chr7:84576101-84576111 chr7:84576117-84576130 chr7:84576096-84576117 chr7:84576103-84576110 chr7:84576100-84576112 chr7:84576101-84576110 chr7:84576092-84576109 chr7:84576128-84576139
35	GATA3	chr7:84551651-84552088	T-47D	breast:	n/a	n/a
36	GATA3	chr7:84567964-84568454	MCF-7	breast:	n/a	n/a
37	GATA3	chr7:84554070-84554680	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr7:84582307-84583050	MCF-7	breast:	n/a	n/a
39	GATA3	chr7:84551607-84552108	MCF-7	breast:	n/a	n/a
40	GATA3	chr7:84553804-84554341	MCF-7	breast:	n/a	chr7:84554030-84554040 chr7:84554035-84554045
41	GATA3	chr7:84591012-84591528	SK-N-SH	brain:	n/a	chr7:84591234-84591250 chr7:84591236-84591248
42	GATA3	chr7:84590995-84591590	SK-N-SH	brain:	n/a	chr7:84591234-84591250 chr7:84591236-84591248
43	GATA3	chr7:84551733-84552026	T-47D	breast:	n/a	n/a
44	HDAC2	chr7:84575954-84576092	K562	blood:	n/a	n/a
45	HEY1	chr7:84569312-84569512	K562	blood:	n/a	n/a
46	HEY1	chr7:84569145-84569542	K562	blood:	n/a	n/a
47	HEY1	chr7:84569328-84569647	HepG2	liver:	n/a	n/a
48	HEY1	chr7:84569374-84569558	HepG2	liver:	n/a	n/a
49	IRF1	chr7:84570104-84570308	K562	blood:	n/a	n/a
50	IRF1	chr7:84570169-84570305	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84569394-84569444	H1-hESC	embryonic stem cell:	embryo
2	chr7:84569394-84569444	H1-hESC	embryonic stem cell:	embryo
3	chr7:84570538-84570588	ovcar-3	ovarian:	n/a
4	chr7:84569518-84569568	SAEC	small airway:	n/a
5	chr7:84570538-84570588	HEK293	kidney:	embryo
6	chr7:84571827-84571877	AoSMC	blood vessel:	n/a
7	chr7:84569142-84569192	ProgFib	skin:	n/a
8	chr7:84569394-84569444	HL-60	blood:	n/a
9	chr7:84571827-84571877	CMK	blood:	n/a
10	chr7:84569518-84569568	AoSMC	blood vessel:	n/a
11	chr7:84569243-84569293	IMR90	lung:	fetal
12	chr7:84569142-84569192	GM12891	blood:	n/a
13	chr7:84570538-84570588	PFSK-1	brain:	n/a
14	chr7:84570538-84570588	HAEpiC	amniotic membrane:	n/a
15	chr7:84571827-84571877	HCM	heart:	n/a
16	chr7:84569142-84569192	Caco-2	colon:	n/a
17	chr7:84570538-84570588	AoSMC	blood vessel:	n/a
18	chr7:84570538-84570588	K562	blood:	n/a
19	chr7:84569394-84569444	GM12878	blood:	n/a
20	chr7:84569394-84569444	HCM	heart:	n/a
21	chr7:84569243-84569293	MCF-7	breast:	n/a
22	chr7:84570538-84570588	HIPEpiC	eye:	n/a
23	chr7:84569518-84569568	Jurkat	blood:	n/a
24	chr7:84569394-84569444	SK-N-SH	brain:	n/a
25	chr7:84569394-84569444	HCPEpiC	choroid plexus:	n/a
26	chr7:84570538-84570588	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:84571827-84571877	HCT-116	colon:	n/a
28	chr7:84569394-84569444	GM19239	blood:	n/a
29	chr7:84569243-84569293	SAEC	small airway:	n/a
30	chr7:84570538-84570588	HepG2	liver:	n/a
31	chr7:84570538-84570588	Hepatocyte	liver:	n/a
32	chr7:84569142-84569192	AG09309	skin:	n/a
33	chr7:84569142-84569192	HepG2	liver:	n/a
34	chr7:84570538-84570588	IMR90	lung:	fetal
35	chr7:84569394-84569444	SKMC	muscle:	n/a
36	chr7:84569142-84569192	Hela-S3	cervix:	n/a
37	chr7:84570538-84570588	SK-N-MC	brain:	n/a
38	chr7:84571827-84571877	HEEpiC	esophagus:	n/a
39	chr7:84569518-84569568	AG09309	skin:	n/a
40	chr7:84569518-84569568	NT2-D1	testis:	n/a
41	chr7:84569243-84569293	HNPCEpiC	eye:	n/a
42	chr7:84569243-84569293	CMK	blood:	n/a
43	chr7:84569518-84569568	GM12878	blood:	n/a
44	chr7:84569518-84569568	HRE	kidney:	n/a
45	chr7:84569243-84569293	HMEC	breast:	n/a
46	chr7:84571827-84571877	Hepatocyte	liver:	n/a
47	chr7:84569142-84569192	HRE	kidney:	n/a
48	chr7:84569518-84569568	U87	brain:	n/a
49	chr7:84569518-84569568	GM19239	blood:	n/a
50	chr7:84570538-84570588	SKMC	muscle:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:84587370..84589452-chr7:84590084..84592906,2	K562	blood:
2	chr7:84568824..84569852-chr9:139621874..139623038,21	HCT-116	colon:
3	chr7:84553263..84557308-chr7:84557996..84561050,4	K562	blood:
4	chr7:84547551..84549069-chr7:84551273..84552915,2	K562	blood:
5	chr7:84567429..84570853-chr9:139619029..139623910,14	K562	blood:
6	chr7:84533065..84535420-chr7:84561448..84563538,2	K562	blood:
7	chr7:84587370..84589452-chr7:84590084..84592906,2	K562	blood:
8	chr7:84579633..84582390-chr7:84598433..84600288,2	K562	blood:
9	chr7:84528164..84531131-chr7:84559401..84561148,2	K562	blood:
10	chr7:84544371..84546770-chr7:84555059..84558105,3	K562	blood:
11	chr7:84553263..84557308-chr7:84557996..84561050,4	K562	blood:
12	chr7:84579633..84582390-chr7:84598433..84600288,2	K562	blood:
13	chr7:84568918..84570842-chr9:139619990..139622918,5	MCF-7	breast:
14	chr7:84165149..84166023-chr7:84582151..84583096,5	MCF-7	breast:
15	chr7:84547551..84550481-chr7:84551151..84552773,2	K562	blood:
16	chr7:84567405..84570854-chr9:139616789..139624022,24	K562	blood:
17	chr7:84569140..84569977-chr9:139622087..139623308,10	Hela-S3	cervix:
18	chr7:84548735..84551374-chr7:84555159..84557939,2	K562	blood:
19	chr7:84569318..84570852-chr9:139620676..139624384,6	MCF-7	breast:
20	chr7:84569322..84569842-chr9:139622128..139622961,3	MCF-7	breast:
21	chr7:84547551..84550481-chr7:84551151..84552773,2	K562	blood:
22	chr7:84602502..84604355-chr7:84607200..84609135,2	K562	blood:
23	chr7:84554524..84556792-chr7:84558035..84560018,2	K562	blood:
24	chr7:84569339..84569844-chr9:139622178..139622773,3	MCF-7	breast:
25	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
26	chr7:84548735..84551374-chr7:84555159..84557939,2	K562	blood:
27	chr7:84554524..84556792-chr7:84558035..84560018,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000232019	TF binding region
ENSG00000232019	CpG island
ENSG00000233016	chromatin interactions

Extended variants
information (count: 1280 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116184037	chr7:84550210-84550211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557643778	chr7:84550216-84550217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369195861	chr7:84550217-84550218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372217495	chr7:84550238-84550239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555718961	chr7:84550245-84550246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116964988	chr7:84550265-84550266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561979627	chr7:84550279-84550280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574058270	chr7:84550303-84550304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541530367	chr7:84550321-84550322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138780130	chr7:84550353-84550354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368129655	chr7:84550356-84550357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183509322	chr7:84550360-84550361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527281818	chr7:84550398-84550399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552198574	chr7:84550432-84550433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115103309	chr7:84550502-84550503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545550830	chr7:84550510-84550511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188607412	chr7:84550527-84550528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373543415	chr7:84550593-84550594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149418482	chr7:84550596-84550597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1406339	chr7:84550612-84550613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562988157	chr7:84550624-84550625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566203225	chr7:84550633-84550634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1406340	chr7:84550635-84550636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs376140463	chr7:84550666-84550667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558157715	chr7:84550700-84550701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369469530	chr7:84550707-84550708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73179809	chr7:84550746-84550747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12669244	chr7:84550751-84550752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555661763	chr7:84550769-84550770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192984051	chr7:84550787-84550788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200951142	chr7:84550828-84550829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144865119	chr7:84550829-84550830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs202091921	chr7:84550836-84550837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146190669	chr7:84550838-84550839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144763001	chr7:84550869-84550870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201229438	chr7:84550884-84550885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs386359965	chr7:84550885-84550886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1534568	chr7:84550886-84550887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1534569	chr7:84550888-84550889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1534570	chr7:84550890-84550891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1534571	chr7:84550892-84550893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201566491	chr7:84550894-84550895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199689737	chr7:84550896-84550897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs398067048	chr7:84550905-84550906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs58780632	chr7:84550908-84550909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202060853	chr7:84550913-84550914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73711623	chr7:84550986-84550987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs572133658	chr7:84551032-84551033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542602431	chr7:84551034-84551035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184875674	chr7:84551049-84551050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84542800-84557000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:84543200-84550600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:84549400-84553200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:84549600-84551600	Weak transcription	Fetal Heart	heart
5	chr7:84551600-84553200	Enhancers	Fetal Heart	heart
6	chr7:84553600-84554200	Enhancers	Hela-S3	cervix
7	chr7:84553800-84554000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr7:84554000-84569200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:84554200-84556800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:84556600-84557200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:84556800-84557200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:84566000-84569200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:84567200-84568800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:84568000-84569200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:84568400-84571000	Weak transcription	Aorta	Aorta
16	chr7:84568800-84569200	Enhancers	Esophagus	oesophagus
17	chr7:84568800-84569400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:84568800-84569400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:84569000-84569400	Active TSS	HUVEC	blood vessel
20	chr7:84569200-84569600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:84569200-84569600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:84569200-84569600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:84569200-84569600	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr7:84569200-84569600	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr7:84569200-84569600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:84569200-84569600	Active TSS	Muscle Satellite Cultured Cells	--
27	chr7:84569200-84569600	Active TSS	Ovary	ovary
28	chr7:84569200-84569600	Active TSS	Psoas Muscle	Psoas
29	chr7:84569200-84569600	Active TSS	Hela-S3	cervix
30	chr7:84569400-84569600	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:84569400-84569600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:84569600-84569800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:84571000-84571400	Enhancers	Aorta	Aorta
34	chr7:84571400-84576400	Weak transcription	Aorta	Aorta
35	chr7:84576200-84576400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:84576200-84577200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:84576400-84577000	Enhancers	Aorta	Aorta
38	chr7:84576400-84577000	Enhancers	HSMM	muscle
39	chr7:84576400-84577000	Enhancers	HSMMtube	muscle
40	chr7:84576600-84577000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:84576600-84577800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:84576800-84577000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:84576800-84577000	Enhancers	NHEK	skin
44	chr7:84577000-84578000	Weak transcription	Aorta	Aorta
45	chr7:84577000-84578200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:84577000-84578400	Weak transcription	HSMM	muscle
47	chr7:84577000-84579200	Weak transcription	HSMMtube	muscle
48	chr7:84577800-84578200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:84577800-84578800	Enhancers	NHDF-Ad	bronchial
50	chr7:84578000-84578200	Enhancers	Aorta	Aorta

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