Variant report

Variant	esv34238
Chromosome Location	chr7:84279023-84591966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1978)
CpG islands
(count:489)
Chromatin interactive
region (count:171)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1978 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84302368-84302402	K562	blood:	n/a	n/a
2	ARID3A	chr7:84545421-84546020	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:84450135-84450579	K562	blood:	n/a	n/a
4	ARID3A	chr7:84532321-84532473	K562	blood:	n/a	n/a
5	ARID3A	chr7:84332343-84332393	K562	blood:	n/a	n/a
6	ARID3A	chr7:84580783-84580807	K562	blood:	n/a	n/a
7	ARID3A	chr7:84452501-84453151	K562	blood:	n/a	n/a
8	ARID3A	chr7:84305107-84305335	K562	blood:	n/a	n/a
9	ARID3A	chr7:84391734-84391764	K562	blood:	n/a	n/a
10	ARID3A	chr7:84466802-84467247	K562	blood:	n/a	n/a
11	ARID3A	chr7:84508916-84509895	K562	blood:	n/a	n/a
12	ARID3A	chr7:84453555-84454547	K562	blood:	n/a	n/a
13	ARID3A	chr7:84450814-84451621	K562	blood:	n/a	n/a
14	ARID3A	chr7:84577444-84577446	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:84445165-84445590	K562	blood:	n/a	n/a
16	ARID3A	chr7:84459071-84459723	K562	blood:	n/a	n/a
17	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
18	ARID3A	chr7:84497225-84497242	K562	blood:	n/a	n/a
19	ATF1	chr7:84453474-84453935	K562	blood:	n/a	n/a
20	ATF1	chr7:84449877-84450148	K562	blood:	n/a	n/a
21	ATF1	chr7:84363372-84363448	K562	blood:	n/a	n/a
22	ATF1	chr7:84305022-84305312	K562	blood:	n/a	n/a
23	ATF1	chr7:84477138-84477525	K562	blood:	n/a	n/a
24	ATF1	chr7:84323619-84323645	K562	blood:	n/a	n/a
25	ATF1	chr7:84542343-84542694	K562	blood:	n/a	n/a
26	ATF1	chr7:84466727-84467079	K562	blood:	n/a	n/a
27	ATF1	chr7:84358505-84358816	K562	blood:	n/a	n/a
28	ATF1	chr7:84452428-84452733	K562	blood:	n/a	n/a
29	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
30	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
31	ATF1	chr7:84509489-84510086	K562	blood:	n/a	n/a
32	ATF1	chr7:84450918-84451449	K562	blood:	n/a	n/a
33	ATF1	chr7:84331188-84331414	K562	blood:	n/a	n/a
34	ATF2	chr7:84542312-84542654	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr7:84539595-84539950	K562	blood:	n/a	n/a
36	ATF3	chr7:84509798-84510070	K562	blood:	n/a	n/a
37	ATF3	chr7:84331078-84331730	A549	lung:	n/a	n/a
38	BACH1	chr7:84561867-84561950	K562	blood:	n/a	n/a
39	BACH1	chr7:84314329-84314388	K562	blood:	n/a	n/a
40	BACH1	chr7:84372319-84372423	K562	blood:	n/a	n/a
41	BACH1	chr7:84453465-84453574	K562	blood:	n/a	n/a
42	BATF	chr7:84305143-84305369	GM12878	blood:	n/a	n/a
43	BATF	chr7:84529581-84529812	GM12878	blood:	n/a	n/a
44	BATF	chr7:84305070-84305360	GM12878	blood:	n/a	n/a
45	BCL3	chr7:84330997-84331738	A549	lung:	n/a	n/a
46	BHLHE40	chr7:84575928-84576179	K562	blood:	n/a	n/a
47	BHLHE40	chr7:84453219-84453705	K562	blood:	n/a	n/a
48	BHLHE40	chr7:84468227-84468262	K562	blood:	n/a	n/a
49	BHLHE40	chr7:84466755-84467086	K562	blood:	n/a	n/a
50	BHLHE40	chr7:84542391-84542516	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84494975-84495025	Caco-2	colon:	n/a
2	chr7:84494975-84495025	Caco-2	colon:	n/a
3	chr7:84494975-84495025	T-47D	breast:	n/a
4	chr7:84569518-84569568	HCM	heart:	n/a
5	chr7:84569243-84569293	HEEpiC	esophagus:	n/a
6	chr7:84569394-84569444	HUVEC	blood vessel:	n/a
7	chr7:84569518-84569568	HRE	kidney:	n/a
8	chr7:84494975-84495025	GM12892	blood:	n/a
9	chr7:84570538-84570588	ovcar-3	ovarian:	n/a
10	chr7:84569518-84569568	GM12892	blood:	n/a
11	chr7:84494975-84495025	GM06990	blood:	n/a
12	chr7:84330779-84330829	SKMC	muscle:	n/a
13	chr7:84569518-84569568	NT2-D1	testis:	n/a
14	chr7:84570538-84570588	HRCEpiC	kidney:	n/a
15	chr7:84569518-84569568	PrEC	prostate:	n/a
16	chr7:84330779-84330829	ECC-1	luminal epithelium:	n/a
17	chr7:84569518-84569568	HNPCEpiC	eye:	n/a
18	chr7:84569142-84569192	HEEpiC	esophagus:	n/a
19	chr7:84494975-84495025	HNPCEpiC	eye:	n/a
20	chr7:84494975-84495025	SAEC	small airway:	n/a
21	chr7:84569243-84569293	GM12892	blood:	n/a
22	chr7:84494975-84495025	HEEpiC	esophagus:	n/a
23	chr7:84569142-84569192	ovcar-3	ovarian:	n/a
24	chr7:84494975-84495025	Hepatocyte	liver:	n/a
25	chr7:84569243-84569293	Hepatocyte	liver:	n/a
26	chr7:84571827-84571877	H1-hESC	embryonic stem cell:	embryo
27	chr7:84569518-84569568	GM12878	blood:	n/a
28	chr7:84569518-84569568	H1-hESC	embryonic stem cell:	embryo
29	chr7:84494975-84495025	PFSK-1	brain:	n/a
30	chr7:84330779-84330829	MCF-7	breast:	n/a
31	chr7:84570538-84570588	NHDF-neo	bronchial:	n/a
32	chr7:84569518-84569568	Hela-S3	cervix:	n/a
33	chr7:84570538-84570588	HAEpiC	amniotic membrane:	n/a
34	chr7:84330779-84330829	HNPCEpiC	eye:	n/a
35	chr7:84571827-84571877	K562	blood:	n/a
36	chr7:84569518-84569568	AG10803	skin:	n/a
37	chr7:84569243-84569293	GM12878	blood:	n/a
38	chr7:84569243-84569293	SKMC	muscle:	n/a
39	chr7:84569243-84569293	MCF10A-Er-Src	breast:	n/a
40	chr7:84570538-84570588	GM19239	blood:	n/a
41	chr7:84494975-84495025	LNCaP	prostate:	n/a
42	chr7:84494975-84495025	AG10803	skin:	n/a
43	chr7:84569394-84569444	ProgFib	skin:	n/a
44	chr7:84569142-84569192	ECC-1	luminal epithelium:	n/a
45	chr7:84570538-84570588	ProgFib	skin:	n/a
46	chr7:84570538-84570588	NHBE	bronchial:	n/a
47	chr7:84571827-84571877	RPTEC	kidney:	n/a
48	chr7:84570538-84570588	SAEC	small airway:	n/a
49	chr7:84569394-84569444	BE2_C	brain:	n/a
50	chr7:84569518-84569568	PANC-1	pancreas:	n/a

(count:171 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
2	chr7:84364895..84368011-chr7:84369642..84373969,3	K562	blood:
3	chr7:84547551..84550481-chr7:84551151..84552773,2	K562	blood:
4	chr7:84567429..84570853-chr9:139619029..139623910,14	K562	blood:
5	chr7:84465310..84468926-chr7:84469765..84473361,5	K562	blood:
6	chr7:84375198..84377216-chr7:84380488..84382086,2	K562	blood:
7	chr7:84418939..84420597-chr7:84425654..84428000,2	K562	blood:
8	chr7:84453275..84455457-chr7:84508564..84511405,3	K562	blood:
9	chr7:84485903..84488713-chr7:84495287..84497033,2	K562	blood:
10	chr7:84491524..84493832-chr7:84496433..84498597,3	K562	blood:
11	chr7:84165149..84166023-chr7:84582151..84583096,5	MCF-7	breast:
12	chr7:84451703..84453306-chr7:84464208..84465822,2	K562	blood:
13	chr7:84434894..84436647-chr7:84442217..84444048,2	K562	blood:
14	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
15	chr7:84375198..84377216-chr7:84380488..84382086,2	K562	blood:
16	chr7:84442753..84444539-chr7:84451707..84453492,2	K562	blood:
17	chr7:84443133..84444638-chr7:84447039..84448903,2	MCF-7	breast:
18	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
19	chr7:84538449..84540115-chr7:84542353..84545055,2	K562	blood:
20	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
21	chr7:84569318..84570852-chr9:139620676..139624384,6	MCF-7	breast:
22	chr7:84437053..84440861-chr7:84448481..84451648,4	K562	blood:
23	chr7:84434894..84436647-chr7:84442217..84444048,2	K562	blood:
24	chr7:84542985..84545257-chr7:84546597..84549021,2	K562	blood:
25	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
26	chr7:84544371..84546770-chr7:84555059..84558105,3	K562	blood:
27	chr7:84393484..84395921-chr7:84399174..84401421,2	K562	blood:
28	chr7:84416565..84420321-chr7:84421212..84424088,3	K562	blood:
29	chr7:84500124..84502806-chr7:84508171..84509903,2	K562	blood:
30	chr7:84459040..84461064-chr7:84467075..84469112,2	K562	blood:
31	chr7:84358686..84359655-chr7:84369311..84369967,2	MCF-7	breast:
32	chr7:84440104..84442892-chr7:84507245..84509038,2	K562	blood:
33	chr7:84451703..84453306-chr7:84464208..84465822,2	K562	blood:
34	chr7:84344404..84346652-chr7:84371476..84374217,2	K562	blood:
35	chr7:84553263..84557308-chr7:84557996..84561050,4	K562	blood:
36	chr7:84361163..84363029-chr7:84368197..84369895,2	K562	blood:
37	chr7:84382986..84385389-chr7:84391049..84393499,2	K562	blood:
38	chr7:84358686..84359655-chr7:84369311..84369967,2	MCF-7	breast:
39	chr7:84567405..84570854-chr9:139616789..139624022,24	K562	blood:
40	chr7:84416565..84419447-chr7:84421178..84423441,2	K562	blood:
41	chr7:84529973..84531867-chr7:84533645..84535945,2	MCF-7	breast:
42	chr7:84455585..84459699-chr7:84461747..84465117,5	K562	blood:
43	chr7:84554524..84556792-chr7:84558035..84560018,2	K562	blood:
44	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
45	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
46	chr7:84533065..84535420-chr7:84561448..84563538,2	K562	blood:
47	chr7:84568824..84569852-chr9:139621874..139623038,21	HCT-116	colon:
48	chr7:84500124..84502806-chr7:84508171..84509903,2	K562	blood:
49	chr7:84344259..84346664-chr7:84348601..84350704,2	K562	blood:
50	chr7:84411277..84412944-chr7:84416634..84418827,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA3D-2	chr7:84477193-84477569	NONHSAT121793
2	lnc-GRM3-3	chr7:84505977-84506234	NONHSAT147587

No data

Variant related genes	Relation type
HMGN2P11	TF binding region
ENSG00000265050	TF binding region
ENSG00000235243	TF binding region
ENSG00000232019	TF binding region
HMGN2P11	CpG island
ENSG00000265050	CpG island
ENSG00000235243	CpG island
ENSG00000232019	CpG island
ENSG00000235243	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000232605	chromatin interactions

Extended variants
information (count: 10062 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:10062 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4385399	chr7:84279023-84279024	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562890565	chr7:84279076-84279077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530302463	chr7:84279079-84279080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78705693	chr7:84279104-84279105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185442097	chr7:84279114-84279115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534440356	chr7:84279116-84279117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187820665	chr7:84279124-84279125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192028788	chr7:84279170-84279171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145929958	chr7:84279297-84279298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10265431	chr7:84279338-84279339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35670995	chr7:84279393-84279394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs139800896	chr7:84279412-84279413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554490208	chr7:84279441-84279442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371101052	chr7:84279460-84279461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184441091	chr7:84279484-84279485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540337180	chr7:84279485-84279486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114488919	chr7:84279496-84279497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141168135	chr7:84279499-84279500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544237349	chr7:84279530-84279531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563177890	chr7:84279555-84279556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376212358	chr7:84279562-84279563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372082081	chr7:84279598-84279599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563276825	chr7:84279616-84279617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548161907	chr7:84279645-84279646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34967550	chr7:84279652-84279653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs150742455	chr7:84279673-84279674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188537389	chr7:84279685-84279686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs71558795	chr7:84279721-84279722	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs10281240	chr7:84279757-84279758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs538622671	chr7:84279767-84279768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550623953	chr7:84279789-84279790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112566288	chr7:84279793-84279794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565850022	chr7:84279794-84279795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114234218	chr7:84279800-84279801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536171999	chr7:84279801-84279802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146999158	chr7:84279809-84279810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554707740	chr7:84279821-84279822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73175465	chr7:84279849-84279850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533783445	chr7:84279862-84279863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558616641	chr7:84279871-84279872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554524865	chr7:84279904-84279905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576955776	chr7:84279908-84279909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181439943	chr7:84279913-84279914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562759875	chr7:84279920-84279921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575041477	chr7:84279930-84279931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542163876	chr7:84279931-84279932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560889987	chr7:84279966-84279967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139118464	chr7:84279987-84279988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117923632	chr7:84279992-84279993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184929089	chr7:84280011-84280012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84277600-84279600	Enhancers	NHLF	lung
2	chr7:84277800-84281000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:84278000-84281400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr7:84278000-84285000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:84278200-84281200	Weak transcription	Fetal Lung	lung
6	chr7:84278200-84281400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:84278400-84280000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr7:84278400-84280400	Enhancers	NHDF-Ad	bronchial
9	chr7:84278600-84283600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:84278800-84285000	Weak transcription	HSMM	muscle
11	chr7:84279000-84280800	Weak transcription	Osteobl	bone
12	chr7:84279000-84284600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:84279600-84281000	Weak transcription	NHLF	lung
14	chr7:84280000-84280800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr7:84280400-84280800	Weak transcription	NHDF-Ad	bronchial
16	chr7:84280800-84281000	Enhancers	Osteobl	bone
17	chr7:84280800-84281600	Enhancers	NHDF-Ad	bronchial
18	chr7:84281000-84281200	Enhancers	NHLF	lung
19	chr7:84281000-84281600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:84281200-84281800	Enhancers	Fetal Lung	lung
21	chr7:84281400-84281600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:84281400-84281800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:84281600-84285000	Weak transcription	NHDF-Ad	bronchial
24	chr7:84283600-84285400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:84284200-84298600	Weak transcription	K562	blood
26	chr7:84284600-84285600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:84285000-84285200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:84285000-84285200	Enhancers	HSMM	muscle
29	chr7:84285000-84285400	Enhancers	Adipose Nuclei	Adipose
30	chr7:84292200-84292800	Enhancers	Hela-S3	cervix
31	chr7:84292600-84292800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:84292600-84292800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:84292600-84292800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:84292600-84292800	Enhancers	Adipose Nuclei	Adipose
35	chr7:84292600-84292800	Enhancers	Colon Smooth Muscle	Colon
36	chr7:84292600-84292800	Enhancers	Fetal Lung	lung
37	chr7:84292600-84292800	Enhancers	Rectal Smooth Muscle	rectum
38	chr7:84292600-84292800	Flanking Active TSS	NHDF-Ad	bronchial
39	chr7:84292600-84292800	Flanking Active TSS	Osteobl	bone
40	chr7:84292800-84293000	Active TSS	Osteobl	bone
41	chr7:84292800-84293200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:84292800-84293200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:84292800-84293200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:84292800-84293200	Active TSS	Adipose Nuclei	Adipose
45	chr7:84292800-84293200	Active TSS	NHDF-Ad	bronchial
46	chr7:84292800-84293800	Weak transcription	Hela-S3	cervix
47	chr7:84292800-84294600	Weak transcription	Fetal Lung	lung
48	chr7:84292800-84297400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr7:84293000-84293200	Enhancers	Placenta Amnion	Placenta Amnion
50	chr7:84293000-84293200	Flanking Active TSS	Osteobl	bone

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