Variant report

Variant	nsv888647
Chromosome Location	chr7:84866308-85091003
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	ARID3A	chr7:85046963-85047244	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:85055557-85056303	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:85044798-85045544	HepG2	liver:	n/a	n/a
4	ATF1	chr7:84946020-84946102	K562	blood:	n/a	n/a
5	BACH1	chr7:85077761-85077773	K562	blood:	n/a	n/a
6	BATF	chr7:84972886-84973042	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:84922251-84922904	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:85055776-85056346	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:84918375-84918822	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:85045189-85045320	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:85056041-85056112	HepG2	liver:	n/a	n/a
12	CCNT2	chr7:85016458-85016593	K562	blood:	n/a	n/a
13	CEBPB	chr7:85055704-85056676	HepG2	liver:	n/a	chr7:85056185-85056196
14	CEBPB	chr7:85066986-85067213	K562	blood:	n/a	chr7:85067120-85067131 chr7:85067122-85067133 chr7:85067120-85067133 chr7:85067122-85067131
15	CEBPB	chr7:84890091-84890158	Hela-S3	cervix:	n/a	chr7:84890123-84890136
16	CEBPB	chr7:85020950-85021150	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:85055686-85056382	HepG2	liver:	n/a	chr7:85056185-85056196
18	CEBPB	chr7:85087476-85087634	H1-hESC	embryonic stem cell:	n/a	chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087605 chr7:85087596-85087605 chr7:85087594-85087605 chr7:85087596-85087607 chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087607 chr7:85087594-85087607
19	CEBPB	chr7:84901231-84901542	HepG2	liver:	n/a	chr7:84901362-84901373 chr7:84901361-84901374 chr7:84901361-84901374
20	CEBPB	chr7:85018642-85018954	A549	lung:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
21	CEBPB	chr7:85045114-85045272	HepG2	liver:	n/a	chr7:85045124-85045136
22	CEBPB	chr7:85039810-85040110	HepG2	liver:	n/a	chr7:85039948-85039959
23	CEBPB	chr7:85018669-85018940	Hela-S3	cervix:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
24	CEBPB	chr7:85066956-85067250	HepG2	liver:	n/a	chr7:85067120-85067131 chr7:85067122-85067133 chr7:85067120-85067133 chr7:85067122-85067131
25	CEBPB	chr7:85056004-85056320	IMR90	lung:	n/a	chr7:85056185-85056196
26	CEBPB	chr7:84973611-84973755	HepG2	liver:	n/a	chr7:84973658-84973671 chr7:84973658-84973671 chr7:84973689-84973706 chr7:84973658-84973669 chr7:84973660-84973671
27	CEBPB	chr7:84889979-84890286	IMR90	lung:	n/a	chr7:84890123-84890136
28	CEBPB	chr7:85087413-85087769	IMR90	lung:	n/a	chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087605 chr7:85087596-85087605 chr7:85087594-85087605 chr7:85087596-85087607 chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087607 chr7:85087594-85087607
29	CEBPB	chr7:85018621-85018966	HepG2	liver:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
30	CEBPB	chr7:84950037-84950289	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:85067006-85067267	IMR90	lung:	n/a	chr7:85067120-85067131 chr7:85067122-85067133 chr7:85067120-85067133 chr7:85067122-85067131
32	CEBPB	chr7:84866952-84867340	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:85018698-85018881	K562	blood:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
34	CEBPB	chr7:85039804-85040047	A549	lung:	n/a	chr7:85039948-85039959
35	CEBPB	chr7:84985143-84985300	A549	lung:	n/a	n/a
36	CEBPB	chr7:85087471-85087748	HepG2	liver:	n/a	chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087605 chr7:85087596-85087605 chr7:85087594-85087605 chr7:85087596-85087607 chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087607 chr7:85087594-85087607
37	CEBPB	chr7:85018630-85018971	IMR90	lung:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
38	CEBPB	chr7:84901217-84901488	IMR90	lung:	n/a	chr7:84901362-84901373 chr7:84901361-84901374 chr7:84901361-84901374
39	CEBPB	chr7:85056069-85056256	HepG2	liver:	n/a	chr7:85056185-85056196
40	CEBPB	chr7:84899353-84899454	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:84890670-84891033	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:85018665-85018957	H1-hESC	embryonic stem cell:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
43	CEBPB	chr7:85066988-85067237	A549	lung:	n/a	chr7:85067120-85067131 chr7:85067122-85067133 chr7:85067120-85067133 chr7:85067122-85067131
44	CEBPB	chr7:84950063-84950279	A549	lung:	n/a	n/a
45	CEBPB	chr7:84879438-84879637	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:85045090-85045521	HepG2	liver:	n/a	chr7:85045338-85045355 chr7:85045124-85045136
47	CEBPB	chr7:85087499-85087717	A549	lung:	n/a	chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087605 chr7:85087596-85087605 chr7:85087594-85087605 chr7:85087596-85087607 chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087607 chr7:85087594-85087607
48	CHD1	chr7:84879439-84879633	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:85055687-85056104	HepG2	liver:	n/a	n/a
50	CHD2	chr7:84879438-84879639	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:85010774-85010824	GM06990	blood:	n/a
2	chr7:85010741-85010791	HIPEpiC	eye:	n/a
3	chr7:85010676-85010726	AoSMC	blood vessel:	n/a
4	chr7:85010741-85010791	ProgFib	skin:	n/a
5	chr7:84892267-84892317	ovcar-3	ovarian:	n/a
6	chr7:84904903-84904953	NB4	blood:	n/a
7	chr7:85010741-85010791	AG04450	lung:	fetal
8	chr7:84879326-84879376	SK-N-SH	brain:	n/a
9	chr7:84892267-84892317	HMEC	breast:	n/a
10	chr7:84879464-84879514	AG04450	lung:	fetal
11	chr7:84892267-84892317	AG10803	skin:	n/a
12	chr7:84964803-84964853	SK-N-SH	brain:	n/a
13	chr7:84904903-84904953	RPTEC	kidney:	n/a
14	chr7:84904903-84904953	T-47D	breast:	n/a
15	chr7:84964803-84964853	HL-60	blood:	n/a
16	chr7:84879326-84879376	ECC-1	luminal epithelium:	n/a
17	chr7:84879326-84879376	HNPCEpiC	eye:	n/a
18	chr7:85010676-85010726	SK-N-SH_RA	brain:	n/a
19	chr7:85010676-85010726	BJ	skin:	n/a
20	chr7:84904903-84904953	PANC-1	pancreas:	n/a
21	chr7:85010774-85010824	HRE	kidney:	n/a
22	chr7:84879464-84879514	SK-N-MC	brain:	n/a
23	chr7:84964803-84964853	NT2-D1	testis:	n/a
24	chr7:84904903-84904953	MCF10A-Er-Src	breast:	n/a
25	chr7:84879464-84879514	MCF10A-Er-Src	breast:	n/a
26	chr7:84904903-84904953	MCF-7	breast:	n/a
27	chr7:85010774-85010824	HCT-116	colon:	n/a
28	chr7:84892267-84892317	PFSK-1	brain:	n/a
29	chr7:84879464-84879514	Jurkat	blood:	n/a
30	chr7:84879326-84879376	NT2-D1	testis:	n/a
31	chr7:85010676-85010726	AG04449	skin:	fetal
32	chr7:84879464-84879514	PFSK-1	brain:	n/a
33	chr7:84879326-84879376	T-47D	breast:	n/a
34	chr7:84879326-84879376	LNCaP	prostate:	n/a
35	chr7:84904903-84904953	HUVEC	blood vessel:	n/a
36	chr7:85010676-85010726	CMK	blood:	n/a
37	chr7:85010774-85010824	Hela-S3	cervix:	n/a
38	chr7:84879464-84879514	H1-hESC	embryonic stem cell:	embryo
39	chr7:84879326-84879376	HRE	kidney:	n/a
40	chr7:84964803-84964853	AG09319	gingival:	n/a
41	chr7:84904903-84904953	SAEC	small airway:	n/a
42	chr7:84892267-84892317	NHBE	bronchial:	n/a
43	chr7:85010741-85010791	PrEC	prostate:	n/a
44	chr7:85010676-85010726	Hela-S3	cervix:	n/a
45	chr7:84964803-84964853	HCT-116	colon:	n/a
46	chr7:84964803-84964853	NHDF-neo	bronchial:	n/a
47	chr7:85010774-85010824	HAEpiC	amniotic membrane:	n/a
48	chr7:84964803-84964853	HEEpiC	esophagus:	n/a
49	chr7:84879326-84879376	HepG2	liver:	n/a
50	chr7:84904903-84904953	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:84973626..84975407-chr7:84976832..84979639,2	K562	blood:
2	chr7:84976573..84978423-chr7:84984780..84986370,2	K562	blood:
3	chr7:84922126..84922846-chr8:107469062..107469738,2	HCT-116	colon:
4	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
5	chr7:84973626..84975407-chr7:84976832..84979639,2	K562	blood:
6	chr7:84914222..84917543-chr7:84917652..84920035,3	K562	blood:
7	chr7:85056336..85059058-chr7:85072984..85075218,2	K562	blood:
8	chr7:85005716..85007479-chr7:85012871..85015681,2	K562	blood:
9	chr7:85005716..85007479-chr7:85012871..85015681,2	K562	blood:
10	chr7:84921780..84923883-chr7:84923986..84925555,2	MCF-7	breast:
11	chr7:84859657..84862402-chr7:84865275..84867622,2	MCF-7	breast:
12	chr7:85056336..85059058-chr7:85072984..85075218,2	K562	blood:
13	chr7:84921780..84923883-chr7:84923986..84925555,2	MCF-7	breast:
14	chr7:84914222..84917543-chr7:84917652..84920035,3	K562	blood:
15	chr7:84976573..84978423-chr7:84984780..84986370,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-1	chr7:85050438-85050574	XLOC_006160
2	lnc-GRM3-1	chr7:85079176-85079305	XLOC_006160

Variant related genes	Relation type
LINC00972	TF binding region
ENSG00000230614	TF binding region
LINC00972	CpG island
ENSG00000230614	CpG island

Extended variants
information (count: 3991 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3991 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2732736	chr7:84866308-84866309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184189571	chr7:84866363-84866364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569317063	chr7:84866384-84866385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2159578	chr7:84866397-84866398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554541725	chr7:84866406-84866407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573243383	chr7:84866576-84866577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534182859	chr7:84866618-84866619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559110106	chr7:84866627-84866628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577341535	chr7:84866634-84866635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545107157	chr7:84866644-84866645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57700640	chr7:84866652-84866653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570836200	chr7:84866660-84866661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575390270	chr7:84866671-84866672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187019677	chr7:84866673-84866674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2109504	chr7:84866699-84866700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573379340	chr7:84866720-84866721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528394995	chr7:84866725-84866726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546546848	chr7:84866755-84866756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148602285	chr7:84866763-84866764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376424212	chr7:84866769-84866770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550727363	chr7:84866784-84866785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542007994	chr7:84866800-84866801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142072260	chr7:84866822-84866823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536338431	chr7:84866850-84866851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191875869	chr7:84866853-84866854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151159267	chr7:84866961-84866962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534530790	chr7:84866989-84866990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140239181	chr7:84867020-84867021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7789503	chr7:84867046-84867047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs145108800	chr7:84867068-84867069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28828445	chr7:84867070-84867071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553132371	chr7:84867078-84867079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556705498	chr7:84867085-84867086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575419125	chr7:84867092-84867093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544647004	chr7:84867109-84867110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2109503	chr7:84867115-84867116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184855863	chr7:84867129-84867130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558163273	chr7:84867208-84867209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146857223	chr7:84867362-84867363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533309522	chr7:84867365-84867366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538296718	chr7:84867413-84867414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540520415	chr7:84867424-84867425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28869937	chr7:84867495-84867496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189322649	chr7:84867567-84867568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10277030	chr7:84867575-84867576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs180817491	chr7:84867578-84867579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530137359	chr7:84867588-84867589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548249309	chr7:84867610-84867611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539062545	chr7:84867648-84867649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73705911	chr7:84867662-84867663	Weak transcription	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84864400-84868400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:84866600-84866800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:84868400-84869200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:84871200-84872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:84871600-84873000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:84871600-84873600	Enhancers	Primary hematopoietic stem cells	blood
7	chr7:84871800-84872400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:84872200-84872800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:84872400-84872800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr7:84872400-84872800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:84872800-84873000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:84872800-84873400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:84873000-84879400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:84878600-84879400	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr7:84879200-84879400	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr7:84879200-84879600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
18	chr7:84879400-84879600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr7:84879400-84879600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:84879400-84879600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:84879400-84879600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
22	chr7:84879400-84879600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:84879400-84879600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
26	chr7:84879400-84879600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr7:84879400-84879600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
28	chr7:84879400-84879600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
29	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr7:84879400-84879600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:84879400-84879600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:84879400-84879600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr7:84879400-84879600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:84879400-84879600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr7:84879400-84879600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr7:84879400-84879600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:84879400-84879600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
39	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
40	chr7:84879400-84879600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
41	chr7:84879400-84879600	ZNF genes & repeats	Esophagus	oesophagus
42	chr7:84879400-84879600	Enhancers	Fetal Lung	lung
43	chr7:84879400-84879600	ZNF genes & repeats	Gastric	stomach
44	chr7:84879400-84879600	ZNF genes & repeats	Pancreas	Pancrea
45	chr7:84879400-84879600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
46	chr7:84879400-84879600	ZNF genes & repeats	Rectal Smooth Muscle	rectum
47	chr7:84879400-84879600	ZNF genes & repeats	Right Atrium	heart
48	chr7:84879400-84879600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
49	chr7:84879400-84879600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
50	chr7:84889000-84889200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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