Variant report

Variant	nsv831049
Chromosome Location	chr7:84277599-84475710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1317)
CpG islands
(count:122)
Chromatin interactive
region (count:100)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84466802-84467247	K562	blood:	n/a	n/a
2	ARID3A	chr7:84305107-84305335	K562	blood:	n/a	n/a
3	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
4	ARID3A	chr7:84459071-84459723	K562	blood:	n/a	n/a
5	ARID3A	chr7:84453555-84454547	K562	blood:	n/a	n/a
6	ARID3A	chr7:84391734-84391764	K562	blood:	n/a	n/a
7	ARID3A	chr7:84450814-84451621	K562	blood:	n/a	n/a
8	ARID3A	chr7:84452501-84453151	K562	blood:	n/a	n/a
9	ARID3A	chr7:84450135-84450579	K562	blood:	n/a	n/a
10	ARID3A	chr7:84445165-84445590	K562	blood:	n/a	n/a
11	ARID3A	chr7:84302368-84302402	K562	blood:	n/a	n/a
12	ARID3A	chr7:84332343-84332393	K562	blood:	n/a	n/a
13	ATF1	chr7:84305022-84305312	K562	blood:	n/a	n/a
14	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
15	ATF1	chr7:84323619-84323645	K562	blood:	n/a	n/a
16	ATF1	chr7:84466727-84467079	K562	blood:	n/a	n/a
17	ATF1	chr7:84453474-84453935	K562	blood:	n/a	n/a
18	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
19	ATF1	chr7:84363372-84363448	K562	blood:	n/a	n/a
20	ATF1	chr7:84452428-84452733	K562	blood:	n/a	n/a
21	ATF1	chr7:84450918-84451449	K562	blood:	n/a	n/a
22	ATF1	chr7:84331188-84331414	K562	blood:	n/a	n/a
23	ATF1	chr7:84449877-84450148	K562	blood:	n/a	n/a
24	ATF1	chr7:84358505-84358816	K562	blood:	n/a	n/a
25	ATF3	chr7:84331078-84331730	A549	lung:	n/a	n/a
26	BACH1	chr7:84314329-84314388	K562	blood:	n/a	n/a
27	BACH1	chr7:84372319-84372423	K562	blood:	n/a	n/a
28	BACH1	chr7:84453465-84453574	K562	blood:	n/a	n/a
29	BATF	chr7:84305143-84305369	GM12878	blood:	n/a	n/a
30	BATF	chr7:84305070-84305360	GM12878	blood:	n/a	n/a
31	BCL3	chr7:84330997-84331738	A549	lung:	n/a	n/a
32	BHLHE40	chr7:84459146-84459346	K562	blood:	n/a	n/a
33	BHLHE40	chr7:84305313-84305318	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:84455695-84455712	K562	blood:	n/a	n/a
35	BHLHE40	chr7:84453219-84453705	K562	blood:	n/a	n/a
36	BHLHE40	chr7:84439571-84439754	K562	blood:	n/a	n/a
37	BHLHE40	chr7:84466755-84467086	K562	blood:	n/a	n/a
38	BHLHE40	chr7:84409852-84410441	K562	blood:	n/a	n/a
39	BHLHE40	chr7:84468227-84468262	K562	blood:	n/a	n/a
40	BRCA1	chr7:84397684-84397691	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:84302255-84302599	GM12878	blood:	n/a	n/a
42	BRCA1	chr7:84304850-84305429	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:84330839-84331723	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr7:84425833-84426255	K562	blood:	n/a	n/a
45	CBX3	chr7:84453522-84454089	K562	blood:	n/a	n/a
46	CBX3	chr7:84466714-84467202	K562	blood:	n/a	n/a
47	CBX3	chr7:84331137-84331706	HCT-116	colon:	n/a	n/a
48	CBX3	chr7:84330750-84331792	HCT-116	colon:	n/a	n/a
49	CCNT2	chr7:84305040-84305328	K562	blood:	n/a	n/a
50	CCNT2	chr7:84451125-84451468	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84330779-84330829	IMR90	lung:	fetal
2	chr7:84330779-84330829	AG04450	lung:	fetal
3	chr7:84330779-84330829	GM19239	blood:	n/a
4	chr7:84277775-84277825	K562	blood:	n/a
5	chr7:84277775-84277825	LNCaP	prostate:	n/a
6	chr7:84277775-84277825	BE2_C	brain:	n/a
7	chr7:84277775-84277825	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:84330779-84330829	HL-60	blood:	n/a
9	chr7:84277775-84277825	Hela-S3	cervix:	n/a
10	chr7:84330779-84330829	Hepatocyte	liver:	n/a
11	chr7:84277775-84277825	HCT-116	colon:	n/a
12	chr7:84277775-84277825	AG04450	lung:	fetal
13	chr7:84330779-84330829	HCPEpiC	choroid plexus:	n/a
14	chr7:84277775-84277825	NHDF-neo	bronchial:	n/a
15	chr7:84330779-84330829	LNCaP	prostate:	n/a
16	chr7:84330779-84330829	HMEC	breast:	n/a
17	chr7:84330779-84330829	Caco-2	colon:	n/a
18	chr7:84330779-84330829	GM12892	blood:	n/a
19	chr7:84330779-84330829	K562	blood:	n/a
20	chr7:84330779-84330829	PFSK-1	brain:	n/a
21	chr7:84330779-84330829	SAEC	small airway:	n/a
22	chr7:84330779-84330829	AG10803	skin:	n/a
23	chr7:84330779-84330829	HRCEpiC	kidney:	n/a
24	chr7:84330779-84330829	ECC-1	luminal epithelium:	n/a
25	chr7:84277775-84277825	GM06990	blood:	n/a
26	chr7:84330779-84330829	ProgFib	skin:	n/a
27	chr7:84277775-84277825	ovcar-3	ovarian:	n/a
28	chr7:84330779-84330829	HCT-116	colon:	n/a
29	chr7:84330779-84330829	MCF10A-Er-Src	breast:	n/a
30	chr7:84330779-84330829	U87	brain:	n/a
31	chr7:84330779-84330829	SK-N-SH_RA	brain:	n/a
32	chr7:84330779-84330829	HRE	kidney:	n/a
33	chr7:84277775-84277825	SK-N-SH	brain:	n/a
34	chr7:84277775-84277825	Caco-2	colon:	n/a
35	chr7:84330779-84330829	Hela-S3	cervix:	n/a
36	chr7:84277775-84277825	ProgFib	skin:	n/a
37	chr7:84330779-84330829	NHDF-neo	bronchial:	n/a
38	chr7:84277775-84277825	AG09309	skin:	n/a
39	chr7:84330779-84330829	PrEC	prostate:	n/a
40	chr7:84277775-84277825	HUVEC	blood vessel:	n/a
41	chr7:84330779-84330829	RPTEC	kidney:	n/a
42	chr7:84277775-84277825	T-47D	breast:	n/a
43	chr7:84277775-84277825	GM12878	blood:	n/a
44	chr7:84330779-84330829	Jurkat	blood:	n/a
45	chr7:84330779-84330829	PANC-1	pancreas:	n/a
46	chr7:84277775-84277825	RPTEC	kidney:	n/a
47	chr7:84277775-84277825	GM12892	blood:	n/a
48	chr7:84330779-84330829	AG04449	skin:	fetal
49	chr7:84277775-84277825	H1-hESC	embryonic stem cell:	embryo
50	chr7:84277775-84277825	U87	brain:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:84416565..84419447-chr7:84421178..84423441,2	K562	blood:
2	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
3	chr7:84450277..84452701-chr7:84455788..84457354,2	K562	blood:
4	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
5	chr7:84411277..84412944-chr7:84416634..84418827,2	K562	blood:
6	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
7	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
8	chr7:84426900..84429859-chr7:84431258..84433369,2	K562	blood:
9	chr7:84358686..84359655-chr7:84369311..84369967,2	MCF-7	breast:
10	chr7:84375198..84377216-chr7:84380488..84382086,2	K562	blood:
11	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
12	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
13	chr7:84453275..84455457-chr7:84508564..84511405,3	K562	blood:
14	chr7:84442753..84444539-chr7:84451707..84453492,2	K562	blood:
15	chr7:84438950..84442857-chr7:84443325..84445817,3	K562	blood:
16	chr7:84434894..84436647-chr7:84442217..84444048,2	K562	blood:
17	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
18	chr7:84436641..84439524-chr7:84444759..84447374,2	K562	blood:
19	chr7:84416565..84420321-chr7:84421212..84424088,3	K562	blood:
20	chr7:84465946..84467768-chr7:84474017..84476802,2	K562	blood:
21	chr7:84325930..84329136-chr7:84329688..84332999,3	K562	blood:
22	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
23	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
24	chr7:84471463..84475053-chr7:84476999..84480448,4	K562	blood:
25	chr7:84375198..84377216-chr7:84380488..84382086,2	K562	blood:
26	chr7:84418939..84420597-chr7:84425654..84428000,2	K562	blood:
27	chr7:84445226..84448615-chr7:84449710..84452993,3	K562	blood:
28	chr7:84361163..84363029-chr7:84368197..84369895,2	K562	blood:
29	chr7:84344404..84346652-chr7:84371476..84374217,2	K562	blood:
30	chr7:84451703..84453306-chr7:84464208..84465822,2	K562	blood:
31	chr7:84361163..84363029-chr7:84368197..84369895,2	K562	blood:
32	chr7:84451201..84454646-chr7:84455854..84458870,3	K562	blood:
33	chr7:84382986..84385389-chr7:84391049..84393499,2	K562	blood:
34	chr7:84420135..84422964-chr7:84508124..84511065,2	K562	blood:
35	chr7:84344259..84346664-chr7:84348601..84350704,2	K562	blood:
36	chr7:84411277..84412944-chr7:84416634..84418827,2	K562	blood:
37	chr7:84455585..84459699-chr7:84461747..84465117,5	K562	blood:
38	chr7:84445226..84448615-chr7:84449710..84452993,3	K562	blood:
39	chr7:84450277..84452701-chr7:84455788..84457354,2	K562	blood:
40	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
41	chr7:84465946..84467768-chr7:84474017..84476802,2	K562	blood:
42	chr7:84358686..84359655-chr7:84369311..84369967,2	MCF-7	breast:
43	chr7:84465310..84468926-chr7:84469765..84473361,5	K562	blood:
44	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
45	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
46	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
47	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
48	chr7:84369625..84373744-chr7:84376741..84380161,4	K562	blood:
49	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
50	chr7:84474585..84476459-chr7:84497349..84500162,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000265050	TF binding region
ENSG00000265050	CpG island
ENSG00000235243	chromatin interactions

Extended variants
information (count: 6528 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6528 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375700838	chr7:84277603-84277604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79981773	chr7:84277649-84277650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568005045	chr7:84277747-84277748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528372197	chr7:84277774-84277775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142400985	chr7:84277776-84277777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs60602920	chr7:84277780-84277781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533154582	chr7:84277796-84277797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551640848	chr7:84277862-84277863	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192260439	chr7:84277866-84277867	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs531050647	chr7:84277870-84277871	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183679945	chr7:84277873-84277874	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs537526923	chr7:84277929-84277930	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs113211251	chr7:84277939-84277940	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs537285287	chr7:84277951-84277952	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs186455809	chr7:84277961-84277962	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190534819	chr7:84277967-84277968	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528735331	chr7:84277973-84277974	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183145028	chr7:84277983-84277984	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576939407	chr7:84278015-84278016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187073535	chr7:84278042-84278043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557162427	chr7:84278060-84278061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150214003	chr7:84278109-84278110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537164616	chr7:84278117-84278118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539173444	chr7:84278121-84278122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555022572	chr7:84278158-84278159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6969331	chr7:84278163-84278164	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138842945	chr7:84278178-84278179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553291863	chr7:84278179-84278180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578024080	chr7:84278196-84278197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545200168	chr7:84278228-84278229	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs79210633	chr7:84278231-84278232	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs530987410	chr7:84278272-84278273	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs543112457	chr7:84278284-84278285	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561273917	chr7:84278290-84278291	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190425612	chr7:84278315-84278316	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs113067256	chr7:84278332-84278333	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs546712342	chr7:84278369-84278370	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs572876975	chr7:84278464-84278465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571588607	chr7:84278475-84278476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541840026	chr7:84278490-84278491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532687622	chr7:84278529-84278530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35589020	chr7:84278530-84278531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34890850	chr7:84278559-84278560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149295868	chr7:84278568-84278569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182787318	chr7:84278569-84278570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35754529	chr7:84278581-84278582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34656549	chr7:84278599-84278600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536701098	chr7:84278612-84278613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35676751	chr7:84278622-84278623	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143577169	chr7:84278623-84278624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84267200-84277800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:84275800-84277800	Enhancers	NHDF-Ad	bronchial
3	chr7:84276600-84278400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:84276600-84278400	Enhancers	HUVEC	blood vessel
5	chr7:84276600-84279000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:84276600-84279000	Enhancers	Osteobl	bone
7	chr7:84276800-84277800	Enhancers	A549	lung
8	chr7:84276800-84278000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:84276800-84278000	Enhancers	NH-A	brain
10	chr7:84276800-84278400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:84276800-84278600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:84276800-84278600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:84276800-84278800	Enhancers	HSMM	muscle
14	chr7:84277000-84277600	Enhancers	NHEK	skin
15	chr7:84277000-84277800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:84277000-84278200	Enhancers	Fetal Lung	lung
17	chr7:84277000-84278400	Enhancers	Fetal Brain Male	brain
18	chr7:84277000-84278600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:84277000-84278600	Enhancers	Fetal Stomach	stomach
20	chr7:84277200-84277600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr7:84277200-84277600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr7:84277200-84277600	Enhancers	HMEC	breast
23	chr7:84277200-84277600	Weak transcription	NHLF	lung
24	chr7:84277200-84277800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:84277200-84278200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:84277200-84278200	Enhancers	HSMMtube	muscle
27	chr7:84277400-84277600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr7:84277600-84278000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr7:84277600-84278000	Enhancers	Adipose Nuclei	Adipose
30	chr7:84277600-84278000	Enhancers	Fetal Brain Female	brain
31	chr7:84277600-84278200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:84277600-84278400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:84277600-84279600	Enhancers	NHLF	lung
34	chr7:84277800-84278000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:84277800-84278000	Flanking Active TSS	NHDF-Ad	bronchial
36	chr7:84277800-84278200	Enhancers	Fetal Muscle Leg	muscle
37	chr7:84277800-84279000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:84277800-84281000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:84278000-84278200	Enhancers	NHDF-Ad	bronchial
40	chr7:84278000-84281400	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr7:84278000-84285000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:84278200-84278400	Flanking Active TSS	NHDF-Ad	bronchial
43	chr7:84278200-84281200	Weak transcription	Fetal Lung	lung
44	chr7:84278200-84281400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:84278400-84280000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr7:84278400-84280400	Enhancers	NHDF-Ad	bronchial
47	chr7:84278600-84283600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:84278800-84285000	Weak transcription	HSMM	muscle
49	chr7:84279000-84280800	Weak transcription	Osteobl	bone
50	chr7:84279000-84284600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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