Variant report

Variant	nsv1034605
Chromosome Location	chr7:41096638-41222426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:672)
Chromatin interactive
region (count:30)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:41147669-41148097	GM12878	blood:	n/a	n/a
2	ATF2	chr7:41173721-41174155	GM12878	blood:	n/a	n/a
3	ATF2	chr7:41147667-41148133	GM12878	blood:	n/a	n/a
4	ATF2	chr7:41142788-41143331	GM12878	blood:	n/a	n/a
5	ATF2	chr7:41173709-41174313	GM12878	blood:	n/a	n/a
6	ATF2	chr7:41098966-41099395	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:41142815-41143480	GM12878	blood:	n/a	n/a
8	ATF2	chr7:41098936-41099494	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:41098880-41099504	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:41147343-41147350	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:41142837-41143136	GM12878	blood:	n/a	n/a
12	BATF	chr7:41142792-41143432	GM12878	blood:	n/a	n/a
13	BATF	chr7:41147728-41148048	GM12878	blood:	n/a	chr7:41147895-41147906
14	BATF	chr7:41137185-41137504	GM12878	blood:	n/a	n/a
15	BATF	chr7:41173845-41174227	GM12878	blood:	n/a	n/a
16	BATF	chr7:41173777-41174377	GM12878	blood:	n/a	n/a
17	BATF	chr7:41147621-41148149	GM12878	blood:	n/a	chr7:41147895-41147906
18	BATF	chr7:41177602-41177886	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:41173867-41174237	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:41098979-41099428	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr7:41142905-41143196	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:41147715-41148125	GM12878	blood:	n/a	chr7:41147935-41147944
23	BCL11A	chr7:41173858-41174170	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:41147679-41148140	GM12878	blood:	n/a	chr7:41147935-41147944
25	BCL3	chr7:41147671-41148127	GM12878	blood:	n/a	chr7:41147935-41147944
26	BCL3	chr7:41173755-41174225	GM12878	blood:	n/a	chr7:41173771-41173780
27	BCLAF1	chr7:41173664-41174244	GM12878	blood:	n/a	chr7:41173771-41173780
28	BHLHE40	chr7:41142932-41143231	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:41132940-41132969	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:41173384-41174184	GM12878	blood:	n/a	n/a
31	BRCA1	chr7:41147166-41147758	Hela-S3	cervix:	n/a	n/a
32	CCNT2	chr7:41189466-41189665	K562	blood:	n/a	n/a
33	CEBPB	chr7:41121801-41121926	IMR90	lung:	n/a	chr7:41121861-41121872 chr7:41121862-41121871
34	CEBPB	chr7:41153842-41154156	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:41173942-41174300	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:41121799-41121951	HepG2	liver:	n/a	chr7:41121861-41121872 chr7:41121862-41121871
37	CEBPB	chr7:41136309-41137457	IMR90	lung:	n/a	chr7:41136992-41137005
38	CEBPB	chr7:41149732-41150239	IMR90	lung:	n/a	chr7:41150054-41150066
39	CEBPB	chr7:41149870-41150229	A549	lung:	n/a	chr7:41150054-41150066
40	CEBPB	chr7:41147251-41147620	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:41149790-41150185	Hela-S3	cervix:	n/a	chr7:41150054-41150066
42	CEBPB	chr7:41098955-41099434	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:41149885-41150193	HepG2	liver:	n/a	chr7:41150054-41150066
44	CEBPB	chr7:41162343-41162624	Hela-S3	cervix:	n/a	chr7:41162517-41162530
45	CEBPB	chr7:41202389-41202400	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:41187983-41188564	MCF-7	breast:	n/a	chr7:41188123-41188135 chr7:41188221-41188238
47	CEBPB	chr7:41183607-41183677	IMR90	lung:	n/a	chr7:41183666-41183677
48	CEBPB	chr7:41104958-41105158	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:41187643-41188570	Hela-S3	cervix:	n/a	chr7:41188123-41188135 chr7:41188221-41188238
50	CEBPB	chr7:41098911-41099091	IMR90	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:41137309-41137359	A549	lung:	n/a
2	chr7:41137309-41137359	A549	lung:	n/a
3	chr7:41189021-41189071	HRCEpiC	kidney:	n/a
4	chr7:41189312-41189362	PANC-1	pancreas:	n/a
5	chr7:41099611-41099661	HCT-116	colon:	n/a
6	chr7:41189160-41189210	NB4	blood:	n/a
7	chr7:41148057-41148107	GM12891	blood:	n/a
8	chr7:41099611-41099661	T-47D	breast:	n/a
9	chr7:41148057-41148107	Caco-2	colon:	n/a
10	chr7:41099611-41099661	K562	blood:	n/a
11	chr7:41148057-41148107	MCF-7	breast:	n/a
12	chr7:41188092-41188142	HIPEpiC	eye:	n/a
13	chr7:41189160-41189210	HRE	kidney:	n/a
14	chr7:41188092-41188142	HCT-116	colon:	n/a
15	chr7:41189021-41189071	T-47D	breast:	n/a
16	chr7:41188092-41188142	HMEC	breast:	n/a
17	chr7:41189312-41189362	AG10803	skin:	n/a
18	chr7:41189038-41189088	IMR90	lung:	fetal
19	chr7:41189160-41189210	AG09319	gingival:	n/a
20	chr7:41170679-41170729	HMEC	breast:	n/a
21	chr7:41189312-41189362	PrEC	prostate:	n/a
22	chr7:41189021-41189071	SKMC	muscle:	n/a
23	chr7:41170679-41170729	SK-N-SH	brain:	n/a
24	chr7:41148057-41148107	NH-A	brain:	n/a
25	chr7:41137309-41137359	HAEpiC	amniotic membrane:	n/a
26	chr7:41189207-41189257	AG04449	skin:	fetal
27	chr7:41189021-41189071	NH-A	brain:	n/a
28	chr7:41174125-41174175	HCM	heart:	n/a
29	chr7:41174125-41174175	ProgFib	skin:	n/a
30	chr7:41137309-41137359	SK-N-MC	brain:	n/a
31	chr7:41137309-41137359	HEK293	kidney:	embryo
32	chr7:41137309-41137359	Jurkat	blood:	n/a
33	chr7:41189160-41189210	GM12891	blood:	n/a
34	chr7:41189021-41189071	ProgFib	skin:	n/a
35	chr7:41099611-41099661	SAEC	small airway:	n/a
36	chr7:41189312-41189362	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:41137309-41137359	H1-hESC	embryonic stem cell:	embryo
38	chr7:41137309-41137359	HRCEpiC	kidney:	n/a
39	chr7:41174125-41174175	GM12891	blood:	n/a
40	chr7:41174125-41174175	HCF	heart:	n/a
41	chr7:41189207-41189257	NHBE	bronchial:	n/a
42	chr7:41189021-41189071	HCT-116	colon:	n/a
43	chr7:41148057-41148107	HMEC	breast:	n/a
44	chr7:41170679-41170729	HIPEpiC	eye:	n/a
45	chr7:41189312-41189362	A549	lung:	n/a
46	chr7:41189207-41189257	AG04450	lung:	fetal
47	chr7:41189312-41189362	GM12891	blood:	n/a
48	chr7:41189021-41189071	GM06990	blood:	n/a
49	chr7:41189207-41189257	ovcar-3	ovarian:	n/a
50	chr7:41170679-41170729	GM19239	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:41103342..41106054-chr7:41112396..41114390,2	MCF-7	breast:
2	chr7:41218957..41220551-chr7:41225375..41228012,2	MCF-7	breast:
3	chr7:41191838..41193452-chr7:41197871..41200235,2	MCF-7	breast:
4	chr7:41196553..41198239-chr7:41199242..41201799,2	K562	blood:
5	chr7:41146553..41148320-chr7:41712206..41714771,2	MCF-7	breast:
6	chr7:41162891..41165369-chr7:41187985..41190735,2	MCF-7	breast:
7	chr7:41203420..41205145-chr7:41207158..41208668,2	MCF-7	breast:
8	chr7:41098763..41101210-chr7:41146647..41148149,2	MCF-7	breast:
9	chr7:41094208..41096030-chr7:41145732..41147304,2	MCF-7	breast:
10	chr7:41196553..41198239-chr7:41199242..41201799,2	K562	blood:
11	chr7:41082629..41084950-chr7:41094876..41097268,2	K562	blood:
12	chr7:41103342..41106054-chr7:41112396..41114390,2	MCF-7	breast:
13	chr7:41098763..41101210-chr7:41146647..41148149,2	MCF-7	breast:
14	chr7:41162698..41164993-chr7:41169262..41172086,2	MCF-7	breast:
15	chr7:41162698..41164993-chr7:41169262..41172086,2	MCF-7	breast:
16	chr7:41146681..41148489-chr7:41163349..41165376,2	MCF-7	breast:
17	chr7:41191838..41193452-chr7:41197871..41200235,2	MCF-7	breast:
18	chr7:41162891..41165369-chr7:41187985..41190735,2	MCF-7	breast:
19	chr7:41085265..41086925-chr7:41153421..41155023,2	MCF-7	breast:
20	chr7:41146681..41148489-chr7:41163349..41165376,2	MCF-7	breast:
21	chr7:41088384..41090384-chr7:41095246..41097625,2	MCF-7	breast:
22	chr7:41109428..41111588-chr7:41112880..41114571,2	MCF-7	breast:
23	chr7:41109428..41111588-chr7:41112880..41114571,2	MCF-7	breast:
24	chr7:41093416..41095310-chr7:41148067..41150545,2	MCF-7	breast:
25	chr7:41183525..41185543-chr7:41189175..41191996,2	K562	blood:
26	chr7:41183525..41185543-chr7:41189175..41191996,2	K562	blood:
27	chr7:41200450..41202683-chr7:41278426..41280923,2	MCF-7	breast:
28	chr7:41203420..41205145-chr7:41207158..41208668,2	MCF-7	breast:
29	chr7:41151620..41153539-chr7:41745016..41747984,2	MCF-7	breast:
30	chr7:41148550..41150535-chr7:41726571..41728919,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf10-1	chr7:41152042-41152161	XLOC_006059
2	lnc-C7orf10-1	chr7:41141202-41141457	XLOC_006059
3	lnc-C7orf10-1	chr7:41147457-41148212	XLOC_006059
4	lnc-C7orf10-1	chr7:41137093-41137235	XLOC_006059
5	lnc-C7orf10-1	chr7:41158565-41158881	XLOC_006059
6	lnc-C7orf10-1	chr7:41170270-41170447	XLOC_006059
7	lnc-C7orf10-1	chr7:41147457-41147521	XLOC_006059
8	lnc-C7orf10-1	chr7:41172822-41173105	XLOC_006059

No data

Variant related genes	Relation type
ENSG00000224017	TF binding region
ENSG00000224017	CpG island

Extended variants
information (count: 4587 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4587 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533155051	chr7:41096664-41096665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138828950	chr7:41096754-41096755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560292816	chr7:41096773-41096774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28483913	chr7:41096823-41096824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187996092	chr7:41096830-41096831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567833284	chr7:41096840-41096841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531298929	chr7:41096877-41096878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543043385	chr7:41096900-41096901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531972684	chr7:41096904-41096905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550192073	chr7:41096956-41096957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571949807	chr7:41096957-41096958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539059411	chr7:41096984-41096985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554348663	chr7:41097023-41097024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564921870	chr7:41097044-41097045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192835770	chr7:41097084-41097085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184140491	chr7:41097124-41097125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114368659	chr7:41097127-41097128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548144845	chr7:41097178-41097179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555063404	chr7:41097270-41097271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548769083	chr7:41097297-41097298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141939975	chr7:41097325-41097326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188470361	chr7:41097359-41097360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146405209	chr7:41097365-41097366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377567596	chr7:41097447-41097448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544987189	chr7:41097462-41097463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370090945	chr7:41097465-41097466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71538609	chr7:41097525-41097526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146856211	chr7:41097534-41097535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180793488	chr7:41097540-41097541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572496083	chr7:41097551-41097552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543122804	chr7:41097559-41097560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185062236	chr7:41097618-41097619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537591754	chr7:41097628-41097629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73319577	chr7:41097654-41097655	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115947936	chr7:41097709-41097710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550437629	chr7:41097773-41097774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139408147	chr7:41097831-41097832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150036428	chr7:41097850-41097851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144316028	chr7:41097901-41097902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558523525	chr7:41097912-41097913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73085509	chr7:41097944-41097945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548650982	chr7:41097996-41097997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374410787	chr7:41098005-41098006	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs570538914	chr7:41098096-41098097	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs148641775	chr7:41098098-41098099	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs75000198	chr7:41098263-41098264	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73319580	chr7:41098274-41098275	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs58334883	chr7:41098339-41098340	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs144273568	chr7:41098348-41098349	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117205835	chr7:41098404-41098405	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	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
Autism	22495311	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41088400-41099000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:41090200-41097000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:41091400-41097800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:41092200-41098800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:41095000-41100200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:41095200-41100000	Weak transcription	Aorta	Aorta
7	chr7:41095600-41100600	Weak transcription	HSMM	muscle
8	chr7:41096000-41097800	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:41097000-41097800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:41097400-41098200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:41097800-41098600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:41097800-41098800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:41098000-41098600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:41098000-41099000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr7:41098000-41099800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr7:41098200-41098400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:41098200-41098800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:41098200-41099800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:41098200-41100000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr7:41098200-41100200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr7:41098400-41098600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr7:41098400-41099200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr7:41098400-41099600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:41098400-41100400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:41098600-41099600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:41098600-41100000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:41098600-41100000	Enhancers	HMEC	breast
28	chr7:41098600-41104600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:41098800-41099400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:41098800-41099400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:41098800-41099400	Enhancers	NHEK	skin
32	chr7:41098800-41099600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:41098800-41099600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:41098800-41099600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:41099000-41099200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:41099000-41099200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:41099000-41099200	Enhancers	Fetal Muscle Leg	muscle
38	chr7:41099200-41104800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:41099400-41100400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:41099600-41099800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
41	chr7:41099600-41100000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr7:41099600-41104800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:41099800-41100200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:41099800-41100800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:41100000-41100600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:41100000-41101000	Strong transcription	Aorta	Aorta
47	chr7:41100000-41104600	Weak transcription	HMEC	breast
48	chr7:41100400-41100600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr7:41100400-41100800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:41100400-41101000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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