Variant report

Variant	nsv516122
Chromosome Location	chr7:103274567-103291825
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	CBX3	chr7:103287263-103287578	K562	blood:	n/a	n/a
2	CBX3	chr7:103284757-103285106	K562	blood:	n/a	n/a
3	CBX3	chr7:103288516-103288973	K562	blood:	n/a	n/a
4	CBX3	chr7:103288018-103288455	K562	blood:	n/a	n/a
5	CBX3	chr7:103284768-103285082	K562	blood:	n/a	n/a
6	CEBPB	chr7:103277585-103277932	Hela-S3	cervix:	n/a	chr7:103277743-103277756
7	CEBPB	chr7:103277418-103278076	IMR90	lung:	n/a	chr7:103277743-103277756
8	CTCF	chr7:103279022-103279040	Lung_OC	lung:	n/a	n/a
9	CTCF	chr7:103286600-103286750	GM06990	blood:	n/a	n/a
10	EP300	chr7:103290419-103290518	Hela-S3	cervix:	n/a	n/a
11	EP300	chr7:103277409-103278555	SK-N-SH	brain:	n/a	chr7:103278403-103278412
12	EP300	chr7:103277473-103277873	Hela-S3	cervix:	n/a	n/a
13	FOS	chr7:103277579-103277789	MCF10A-Er-Src	breast:	n/a	chr7:103277677-103277689 chr7:103277636-103277647
14	FOS	chr7:103280426-103280849	HUVEC	blood vessel:	n/a	chr7:103280665-103280674 chr7:103280664-103280675
15	FOS	chr7:103278254-103278546	MCF10A-Er-Src	breast:	n/a	chr7:103278403-103278412 chr7:103278402-103278411 chr7:103278402-103278412 chr7:103278401-103278412 chr7:103278403-103278410
16	FOS	chr7:103277355-103277988	HUVEC	blood vessel:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277636-103277647 chr7:103277859-103277867
17	FOS	chr7:103277460-103277977	MCF10A-Er-Src	breast:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277636-103277647 chr7:103277859-103277867
18	FOS	chr7:103278190-103278904	HUVEC	blood vessel:	n/a	chr7:103278403-103278412 chr7:103278402-103278411 chr7:103278402-103278412 chr7:103278401-103278412 chr7:103278403-103278410
19	FOS	chr7:103280620-103280799	MCF10A-Er-Src	breast:	n/a	chr7:103280665-103280674 chr7:103280664-103280675
20	FOS	chr7:103278238-103278553	MCF10A-Er-Src	breast:	n/a	chr7:103278403-103278412 chr7:103278402-103278411 chr7:103278402-103278412 chr7:103278401-103278412 chr7:103278403-103278410
21	FOS	chr7:103278230-103278552	MCF10A-Er-Src	breast:	n/a	chr7:103278403-103278412 chr7:103278402-103278411 chr7:103278402-103278412 chr7:103278401-103278412 chr7:103278403-103278410
22	FOS	chr7:103277537-103277813	MCF10A-Er-Src	breast:	n/a	chr7:103277677-103277689 chr7:103277636-103277647
23	FOS	chr7:103277465-103277946	MCF10A-Er-Src	breast:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277636-103277647 chr7:103277859-103277867
24	FOSL2	chr7:103280402-103280966	SK-N-SH	brain:	n/a	chr7:103280665-103280674
25	FOSL2	chr7:103277416-103277883	SK-N-SH	brain:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277859-103277867
26	FOSL2	chr7:103277475-103277898	A549	lung:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277859-103277867
27	FOSL2	chr7:103278188-103278610	SK-N-SH	brain:	n/a	chr7:103278403-103278412 chr7:103278402-103278411 chr7:103278402-103278412 chr7:103278403-103278410
28	FOSL2	chr7:103280534-103280843	SK-N-SH	brain:	n/a	chr7:103280665-103280674
29	FOSL2	chr7:103277378-103278092	SK-N-SH	brain:	n/a	chr7:103277859-103277867 chr7:103277859-103277866 chr7:103277677-103277689 chr7:103277859-103277867
30	GATA2	chr7:103277391-103278900	HUVEC	blood vessel:	n/a	chr7:103278481-103278497 chr7:103277577-103277584 chr7:103278778-103278794
31	GATA2	chr7:103281858-103282400	HUVEC	blood vessel:	n/a	chr7:103282341-103282354 chr7:103282344-103282352
32	GATA2	chr7:103280481-103280800	HUVEC	blood vessel:	n/a	chr7:103280554-103280570
33	GATA3	chr7:103290741-103290917	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr7:103291370-103291541	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr7:103278061-103278699	SK-N-SH	brain:	n/a	chr7:103278481-103278497
36	GATA3	chr7:103277368-103278754	SK-N-SH	brain:	n/a	chr7:103278481-103278497 chr7:103277577-103277584
37	GATA3	chr7:103280403-103280865	SK-N-SH	brain:	n/a	chr7:103280554-103280570
38	GATA3	chr7:103280446-103280913	SK-N-SH	brain:	n/a	chr7:103280554-103280570
39	GATA3	chr7:103277344-103278029	SK-N-SH	brain:	n/a	chr7:103277577-103277584
40	JUND	chr7:103280372-103280826	SK-N-SH	brain:	n/a	chr7:103280665-103280674
41	JUND	chr7:103280475-103280956	SK-N-SH	brain:	n/a	chr7:103280665-103280674
42	JUND	chr7:103278364-103278374	K562	blood:	n/a	n/a
43	KAP1	chr7:103287727-103288863	K562	blood:	n/a	n/a
44	KAP1	chr7:103287051-103287509	K562	blood:	n/a	n/a
45	KAP1	chr7:103284620-103285905	K562	blood:	n/a	n/a
46	KAP1	chr7:103283434-103283609	K562	blood:	n/a	n/a
47	MAFF	chr7:103282743-103282839	K562	blood:	n/a	n/a
48	MAFF	chr7:103291451-103291673	HepG2	liver:	n/a	n/a
49	MAFK	chr7:103282673-103282964	HepG2	liver:	n/a	n/a
50	MAFK	chr7:103283528-103283794	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103279088-103279138	HL-60	blood:	n/a
2	chr7:103279088-103279138	HL-60	blood:	n/a
3	chr7:103279088-103279138	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:103279088-103279138	HMEC	breast:	n/a
5	chr7:103279088-103279138	AG10803	skin:	n/a
6	chr7:103279088-103279138	BE2_C	brain:	n/a
7	chr7:103279088-103279138	PrEC	prostate:	n/a
8	chr7:103279088-103279138	SK-N-SH	brain:	n/a
9	chr7:103279088-103279138	HEK293	kidney:	embryo
10	chr7:103279088-103279138	HEEpiC	esophagus:	n/a
11	chr7:103279088-103279138	HAEpiC	amniotic membrane:	n/a
12	chr7:103279088-103279138	NHDF-neo	bronchial:	n/a
13	chr7:103279088-103279138	Jurkat	blood:	n/a
14	chr7:103279088-103279138	SAEC	small airway:	n/a
15	chr7:103279088-103279138	Caco-2	colon:	n/a
16	chr7:103279088-103279138	SK-N-MC	brain:	n/a
17	chr7:103279088-103279138	HRE	kidney:	n/a
18	chr7:103279088-103279138	PANC-1	pancreas:	n/a
19	chr7:103279088-103279138	HCPEpiC	choroid plexus:	n/a
20	chr7:103279088-103279138	GM19239	blood:	n/a
21	chr7:103279088-103279138	PFSK-1	brain:	n/a
22	chr7:103279088-103279138	MCF-7	breast:	n/a
23	chr7:103279088-103279138	ProgFib	skin:	n/a
24	chr7:103279088-103279138	ovcar-3	ovarian:	n/a
25	chr7:103279088-103279138	GM12878	blood:	n/a
26	chr7:103279088-103279138	AG04450	lung:	fetal
27	chr7:103279088-103279138	NH-A	brain:	n/a
28	chr7:103279088-103279138	IMR90	lung:	fetal
29	chr7:103279088-103279138	GM06990	blood:	n/a
30	chr7:103279088-103279138	SKMC	muscle:	n/a
31	chr7:103279088-103279138	BJ	skin:	n/a
32	chr7:103279088-103279138	HIPEpiC	eye:	n/a
33	chr7:103279088-103279138	H1-hESC	embryonic stem cell:	embryo
34	chr7:103279088-103279138	GM12891	blood:	n/a
35	chr7:103279088-103279138	HNPCEpiC	eye:	n/a
36	chr7:103279088-103279138	LNCaP	prostate:	n/a
37	chr7:103279088-103279138	SK-N-SH_RA	brain:	n/a
38	chr7:103279088-103279138	AG09319	gingival:	n/a
39	chr7:103279088-103279138	T-47D	breast:	n/a
40	chr7:103279088-103279138	HCF	heart:	n/a
41	chr7:103279088-103279138	HRPEpiC	eye:	n/a
42	chr7:103279088-103279138	HRCEpiC	kidney:	n/a
43	chr7:103279088-103279138	NHBE	bronchial:	n/a
44	chr7:103279088-103279138	MCF10A-Er-Src	breast:	n/a
45	chr7:103279088-103279138	Hepatocyte	liver:	n/a
46	chr7:103279088-103279138	HUVEC	blood vessel:	n/a
47	chr7:103279088-103279138	U87	brain:	n/a
48	chr7:103279088-103279138	AG04449	skin:	fetal
49	chr7:103279088-103279138	HCM	heart:	n/a
50	chr7:103279088-103279138	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:103254361..103256762-chr7:103277435..103279324,2	K562	blood:
2	chr7:103287552..103290222-chr7:103293075..103295780,3	K562	blood:
3	chr7:103282215..103284239-chr7:103291796..103293845,2	K562	blood:
4	chr7:103253287..103254849-chr7:103287404..103290090,2	K562	blood:
5	chr7:103282215..103284239-chr7:103291796..103293845,2	K562	blood:
6	chr7:103274516..103276734-chr7:103323210..103324865,2	K562	blood:
7	chr7:103267673..103270485-chr7:103274294..103276158,2	K562	blood:
8	chr7:103290439..103294290-chr7:103295616..103299130,4	K562	blood:

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

Extended variants
information (count: 680 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3808024	chr7:103274567-103274568	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182001814	chr7:103274626-103274627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6961304	chr7:103274678-103274679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs578074954	chr7:103274721-103274722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142132748	chr7:103274747-103274748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147789486	chr7:103274806-103274807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371533609	chr7:103274811-103274812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs118027383	chr7:103274833-103274834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542955744	chr7:103274882-103274883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139481790	chr7:103274904-103274905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561750942	chr7:103274954-103274955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186677466	chr7:103274972-103274973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17153873	chr7:103275017-103275018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs113846543	chr7:103275106-103275107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564708299	chr7:103275114-103275115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181169418	chr7:103275175-103275176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560481921	chr7:103275316-103275317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113778229	chr7:103275317-103275318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186626301	chr7:103275318-103275319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566764400	chr7:103275337-103275338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144978741	chr7:103275345-103275346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112117551	chr7:103275374-103275375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573541587	chr7:103275398-103275399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147644000	chr7:103275419-103275420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190627371	chr7:103275434-103275435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373151833	chr7:103275439-103275440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182318876	chr7:103275453-103275454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377331396	chr7:103275478-103275479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571548258	chr7:103275479-103275480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539178687	chr7:103275480-103275481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78241049	chr7:103275481-103275482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185499603	chr7:103275494-103275495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112466990	chr7:103275529-103275530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554581904	chr7:103275534-103275535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576318528	chr7:103275557-103275558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150166577	chr7:103275558-103275559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34568163	chr7:103275590-103275591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369083281	chr7:103275597-103275598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191000887	chr7:103275598-103275599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558975190	chr7:103275625-103275626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527900793	chr7:103275664-103275665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549589155	chr7:103275745-103275746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183526228	chr7:103275762-103275763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs362646	chr7:103275803-103275804	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs188294086	chr7:103275826-103275827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144653976	chr7:103275891-103275892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3025968	chr7:103275903-103275904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199631495	chr7:103275919-103275920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553568199	chr7:103275936-103275937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs398124191	chr7:103275961-103275962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103271200-103275800	Weak transcription	HepG2	liver
2	chr7:103271200-103276800	Weak transcription	NHLF	lung
3	chr7:103271200-103277000	Weak transcription	NHDF-Ad	bronchial
4	chr7:103272400-103274800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:103273000-103276600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:103273000-103283600	Weak transcription	K562	blood
7	chr7:103273200-103276600	Weak transcription	HMEC	breast
8	chr7:103273800-103276800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:103273800-103276800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:103273800-103276800	Weak transcription	Osteobl	bone
11	chr7:103274200-103276800	Weak transcription	NH-A	brain
12	chr7:103274200-103277000	Weak transcription	HUVEC	blood vessel
13	chr7:103274400-103276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:103274400-103277000	Weak transcription	NHEK	skin
15	chr7:103274400-103277400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:103274800-103276800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:103275800-103277000	Strong transcription	HepG2	liver
18	chr7:103276600-103277200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:103276600-103278800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:103276600-103279200	Enhancers	HMEC	breast
21	chr7:103276800-103277200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:103276800-103277400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:103276800-103277800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:103276800-103279000	Enhancers	NH-A	brain
25	chr7:103276800-103279000	Enhancers	NHLF	lung
26	chr7:103276800-103279200	Enhancers	Osteobl	bone
27	chr7:103277000-103278800	Enhancers	NHEK	skin
28	chr7:103277000-103279000	Enhancers	Hela-S3	cervix
29	chr7:103277000-103279000	Enhancers	HUVEC	blood vessel
30	chr7:103277000-103281200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:103277000-103281200	Enhancers	NHDF-Ad	bronchial
32	chr7:103277000-103289200	Weak transcription	HepG2	liver
33	chr7:103277200-103277600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:103277200-103278600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:103277400-103277600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:103277400-103278000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:103277400-103278400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:103277400-103278800	Enhancers	HSMM	muscle
39	chr7:103277600-103279600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:103277600-103281400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:103277800-103278200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr7:103278200-103278600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr7:103278600-103278800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr7:103278600-103279600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:103278800-103280600	Weak transcription	NHEK	skin
46	chr7:103278800-103280800	Weak transcription	HSMM	muscle
47	chr7:103278800-103281400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr7:103278800-103300800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:103279000-103280000	Weak transcription	NHLF	lung
50	chr7:103279000-103280600	Weak transcription	NH-A	brain

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