Variant report

Variant	nsv887893
Chromosome Location	chr7:27326739-27380936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:27380901-27380985	K562	blood:	n/a	n/a
2	BACH1	chr7:27379715-27379871	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:27379230-27379252	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:27356048-27356325	K562	blood:	n/a	chr7:27356206-27356217
5	CEBPB	chr7:27356062-27356334	IMR90	lung:	n/a	chr7:27356206-27356217
6	CEBPB	chr7:27356026-27356323	HepG2	liver:	n/a	chr7:27356206-27356217
7	CEBPB	chr7:27356068-27356324	Hela-S3	cervix:	n/a	chr7:27356206-27356217
8	CEBPB	chr7:27356049-27356306	A549	lung:	n/a	chr7:27356206-27356217
9	CEBPB	chr7:27356132-27356232	H1-hESC	embryonic stem cell:	n/a	chr7:27356206-27356217
10	CTCF	chr7:27369707-27369741	LNCaP	prostate:	n/a	n/a
11	CTCF	chr7:27369619-27369862	A549	lung:	n/a	n/a
12	CTCF	chr7:27369660-27369810	NHEK	skin:	n/a	n/a
13	CTCF	chr7:27342440-27342590	NB4	blood:	n/a	n/a
14	CTCF	chr7:27369660-27369810	HEK293	kidney:	n/a	n/a
15	CTCF	chr7:27369640-27369790	HMEC	breast:	n/a	n/a
16	CTCF	chr7:27369620-27369770	HCM	heart:	n/a	n/a
17	CTCF	chr7:27369660-27369810	NB4	blood:	n/a	n/a
18	CTCF	chr7:27369609-27369902	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:27373736-27373805	GM20000	blood:	n/a	n/a
20	CTCF	chr7:27369680-27369830	HMF	breast:	n/a	n/a
21	CTCF	chr7:27342460-27342610	GM12866	blood:	n/a	n/a
22	CTCF	chr7:27369700-27369850	A549	lung:	n/a	n/a
23	CTCF	chr7:27369660-27369810	SAEC	small airway:	n/a	n/a
24	CTCF	chr7:27342320-27342470	NHEK	skin:	n/a	n/a
25	CTCF	chr7:27369780-27369930	HepG2	liver:	n/a	n/a
26	CTCF	chr7:27368240-27368390	GM12864	blood:	n/a	n/a
27	CTCF	chr7:27353151-27353175	Fibrobl	skin:	n/a	n/a
28	CTCF	chr7:27369720-27369870	HFF	foreskin:	n/a	n/a
29	CTCF	chr7:27369600-27369750	BJ	skin:	n/a	n/a
30	CTCF	chr7:27369700-27369850	HCFaa	heart:	n/a	n/a
31	CTCF	chr7:27369700-27369850	HPF	lung:	n/a	n/a
32	CTCF	chr7:27369680-27369830	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr7:27369667-27369849	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:27369660-27369810	HPF	lung:	n/a	n/a
35	CTCF	chr7:27369660-27369810	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr7:27369620-27369770	HVMF	connective:	n/a	n/a
37	CTCF	chr7:27369699-27369812	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:27342340-27342490	HCFaa	heart:	n/a	n/a
39	CTCF	chr7:27342300-27342450	GM12872	blood:	n/a	n/a
40	CTCF	chr7:27369660-27369810	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr7:27369640-27369790	AG10803	skin:	n/a	n/a
42	CTCF	chr7:27342320-27342470	HepG2	liver:	n/a	n/a
43	CTCF	chr7:27369520-27369670	HCM	heart:	n/a	n/a
44	CTCF	chr7:27369680-27369830	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr7:27369620-27369770	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr7:27369680-27369830	AG09309	skin:	n/a	n/a
47	CTCF	chr7:27369600-27369750	HCT-116	colon:	n/a	n/a
48	CTCF	chr7:27369700-27369850	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr7:27369600-27369750	AG09309	skin:	n/a	n/a
50	CTCF	chr7:27369620-27369770	HRE	kidney:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27352954-27353004	U87	brain:	n/a
2	chr7:27352954-27353004	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:27338633-27338683	HEK293	kidney:	embryo
4	chr7:27338633-27338683	GM06990	blood:	n/a
5	chr7:27352954-27353004	PFSK-1	brain:	n/a
6	chr7:27338034-27338084	NHBE	bronchial:	n/a
7	chr7:27352954-27353004	GM19239	blood:	n/a
8	chr7:27352954-27353004	IMR90	lung:	fetal
9	chr7:27352954-27353004	NHBE	bronchial:	n/a
10	chr7:27338633-27338683	NHDF-neo	bronchial:	n/a
11	chr7:27338034-27338084	AG04450	lung:	fetal
12	chr7:27352954-27353004	HRE	kidney:	n/a
13	chr7:27338034-27338084	A549	lung:	n/a
14	chr7:27352954-27353004	T-47D	breast:	n/a
15	chr7:27338034-27338084	HMEC	breast:	n/a
16	chr7:27352954-27353004	SK-N-SH	brain:	n/a
17	chr7:27352954-27353004	HUVEC	blood vessel:	n/a
18	chr7:27338633-27338683	ProgFib	skin:	n/a
19	chr7:27338034-27338084	SK-N-SH	brain:	n/a
20	chr7:27338633-27338683	HNPCEpiC	eye:	n/a
21	chr7:27338034-27338084	MCF10A-Er-Src	breast:	n/a
22	chr7:27352954-27353004	Caco-2	colon:	n/a
23	chr7:27338633-27338683	AG09319	gingival:	n/a
24	chr7:27338034-27338084	SAEC	small airway:	n/a
25	chr7:27338034-27338084	PFSK-1	brain:	n/a
26	chr7:27352954-27353004	ovcar-3	ovarian:	n/a
27	chr7:27352954-27353004	HAEpiC	amniotic membrane:	n/a
28	chr7:27352954-27353004	HIPEpiC	eye:	n/a
29	chr7:27338034-27338084	K562	blood:	n/a
30	chr7:27338633-27338683	GM12892	blood:	n/a
31	chr7:27338633-27338683	K562	blood:	n/a
32	chr7:27352954-27353004	HCM	heart:	n/a
33	chr7:27338034-27338084	CMK	blood:	n/a
34	chr7:27352954-27353004	PrEC	prostate:	n/a
35	chr7:27338633-27338683	LNCaP	prostate:	n/a
36	chr7:27352954-27353004	RPTEC	kidney:	n/a
37	chr7:27338633-27338683	HIPEpiC	eye:	n/a
38	chr7:27338034-27338084	SK-N-SH_RA	brain:	n/a
39	chr7:27338633-27338683	HRE	kidney:	n/a
40	chr7:27338034-27338084	HAEpiC	amniotic membrane:	n/a
41	chr7:27338034-27338084	ProgFib	skin:	n/a
42	chr7:27352954-27353004	HRPEpiC	eye:	n/a
43	chr7:27338034-27338084	HUVEC	blood vessel:	n/a
44	chr7:27338034-27338084	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:27338633-27338683	NHBE	bronchial:	n/a
46	chr7:27352954-27353004	ECC-1	luminal epithelium:	n/a
47	chr7:27338034-27338084	GM06990	blood:	n/a
48	chr7:27338633-27338683	HCF	heart:	n/a
49	chr7:27338034-27338084	PrEC	prostate:	n/a
50	chr7:27338633-27338683	Hepatocyte	liver:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27349970..27352592-chr7:27352932..27355272,3	K562	blood:
2	7:27238414-27242313..7:27354053-27367655	Hela-S3	cervix:
3	7:27238414-27242313..7:27374130-27379429	K562	blood:
4	chr7:27362143..27365035-chr7:27372640..27375053,2	MCF-7	breast:
5	chr7:27276853..27279360-chr7:27341599..27343657,2	MCF-7	breast:
6	chr7:27249672..27250374-chr7:27369354..27370262,2	MCF-7	breast:
7	chr7:27373141..27375148-chr7:27379553..27381903,2	MCF-7	breast:
8	chr7:27315462..27318205-chr7:27377732..27379317,2	MCF-7	breast:
9	chr7:27316693..27318210-chr7:27338825..27341072,2	MCF-7	breast:
10	7:27238414-27242313..7:27339426-27339767	Hela-S3	cervix:
11	7:27238414-27242313..7:27379429-27382419	H1-hESC	embryonic stem cell:	embryo
12	chr7:27354696..27356208-chr7:27362416..27365005,2	MCF-7	breast:
13	chr7:27354696..27356208-chr7:27362416..27365005,2	MCF-7	breast:
14	chr7:27362143..27365035-chr7:27372640..27375053,2	MCF-7	breast:
15	chr7:27349970..27352592-chr7:27352932..27355272,3	K562	blood:
16	chr7:27353470..27355486-chr7:27620520..27622885,2	MCF-7	breast:
17	chr7:27373141..27375148-chr7:27379553..27381903,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-19	chr7:27367987-27368114	NONHSAT119729

No data

Variant related genes	Relation type
HNRNPA1P73	TF binding region
HNRNPA1P73	CpG island
ENSG00000106031	chromatin interactions
ENSG00000243766	chromatin interactions

Extended variants
information (count: 1494 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375017070	chr7:27335011-27335012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114829019	chr7:27335023-27335024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186678210	chr7:27335042-27335043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531404485	chr7:27335154-27335155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17502392	chr7:27335166-27335167	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs11564026	chr7:27335206-27335207	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558675875	chr7:27335239-27335240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553963149	chr7:27335271-27335272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199926300	chr7:27335360-27335361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs60624298	chr7:27335398-27335399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs59077573	chr7:27335400-27335401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181522870	chr7:27336811-27336812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17428464	chr7:27336812-27336813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs539217129	chr7:27336813-27336814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557624067	chr7:27336855-27336856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186342439	chr7:27336856-27336857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543365255	chr7:27336877-27336878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149677232	chr7:27336902-27336903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11564023	chr7:27336910-27336911	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs540711893	chr7:27336992-27336993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17502420	chr7:27336994-27336995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532912733	chr7:27337003-27337004	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs11769964	chr7:27337004-27337005	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563158025	chr7:27337017-27337018	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs561340211	chr7:27337038-27337039	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs11564022	chr7:27337046-27337047	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370882945	chr7:27337086-27337087	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs145864361	chr7:27337093-27337094	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs546708217	chr7:27337102-27337103	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs7777128	chr7:27337113-27337114	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs17473606	chr7:27337126-27337127	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs527306746	chr7:27337141-27337142	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs539154067	chr7:27337161-27337162	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs557563008	chr7:27337187-27337188	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs532839140	chr7:27337222-27337223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575913647	chr7:27337351-27337352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190407688	chr7:27337359-27337360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555236148	chr7:27337378-27337379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75551968	chr7:27337384-27337385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368439486	chr7:27339018-27339019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148650460	chr7:27339038-27339039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562884459	chr7:27339039-27339040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530181776	chr7:27339042-27339043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35264123	chr7:27339063-27339064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552944107	chr7:27339070-27339071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572426357	chr7:27339089-27339090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77128339	chr7:27339115-27339116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185915143	chr7:27339168-27339169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142049111	chr7:27339222-27339223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72593280	chr7:27339252-27339253	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27335000-27335400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:27335000-27335400	Enhancers	Pancreas	Pancrea
3	chr7:27335000-27335400	Enhancers	Stomach Mucosa	stomach
4	chr7:27335200-27335400	Enhancers	Fetal Kidney	kidney
5	chr7:27336800-27337400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:27337000-27337200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:27337000-27337200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:27337000-27337200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:27337000-27337400	Enhancers	Primary hematopoietic stem cells	blood
10	chr7:27337200-27337400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:27339000-27339200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr7:27339000-27339200	Enhancers	Brain Germinal Matrix	brain
13	chr7:27339200-27339800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:27339400-27340000	Enhancers	Fetal Brain Female	brain
15	chr7:27339600-27340400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:27339800-27340200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:27340000-27340200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:27340000-27340200	Enhancers	Brain Germinal Matrix	brain
19	chr7:27340000-27340400	Enhancers	HUVEC	blood vessel
20	chr7:27340000-27340400	Enhancers	Osteobl	bone
21	chr7:27340000-27340600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:27340000-27341400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr7:27340200-27341000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr7:27340200-27342200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:27340400-27342400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:27342000-27343000	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr7:27342200-27342800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:27342200-27342800	Enhancers	Psoas Muscle	Psoas
29	chr7:27342200-27343000	Enhancers	HMEC	breast
30	chr7:27342400-27342800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:27342400-27343000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr7:27342400-27343000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:27342400-27343000	Enhancers	NHEK	skin
34	chr7:27342600-27342800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:27342600-27343000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr7:27342800-27344600	Weak transcription	Psoas Muscle	Psoas
37	chr7:27343000-27344600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr7:27343000-27345000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr7:27344600-27344800	Enhancers	Psoas Muscle	Psoas
40	chr7:27344600-27346000	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr7:27344800-27345200	Weak transcription	Psoas Muscle	Psoas
42	chr7:27345000-27346400	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr7:27345200-27345800	Enhancers	Psoas Muscle	Psoas
44	chr7:27345400-27345600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:27345600-27346800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:27346800-27347200	Enhancers	Placenta Amnion	Placenta Amnion
47	chr7:27346800-27347600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:27347600-27352800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:27352200-27353400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr7:27352400-27353200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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