Variant report

Variant	esv3433491
Chromosome Location	chr7:65414034-65463477
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1492)
CpG islands
(count:2013)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1492 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65445966-65446151	K562	blood:	n/a	n/a
2	ARID3A	chr7:65447151-65447400	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:65447077-65447412	K562	blood:	n/a	n/a
4	ARID3A	chr7:65453282-65453411	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:65454435-65454695	HepG2	liver:	n/a	n/a
6	ATF1	chr7:65445769-65446159	K562	blood:	n/a	n/a
7	ATF1	chr7:65447060-65447460	K562	blood:	n/a	n/a
8	ATF1	chr7:65453324-65453356	K562	blood:	n/a	n/a
9	ATF2	chr7:65445705-65446301	GM12878	blood:	n/a	n/a
10	ATF2	chr7:65447034-65447435	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:65446932-65447474	GM12878	blood:	n/a	n/a
12	ATF2	chr7:65447033-65447445	GM12878	blood:	n/a	n/a
13	ATF2	chr7:65445713-65446255	GM12878	blood:	n/a	n/a
14	ATF2	chr7:65447052-65447518	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:65446985-65447520	HepG2	liver:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
16	ATF3	chr7:65447088-65447420	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
17	ATF3	chr7:65446981-65447472	A549	lung:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
18	ATF3	chr7:65447143-65447363	GM12878	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
19	ATF3	chr7:65447089-65447395	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
20	ATF3	chr7:65446956-65447515	H1-hESC	embryonic stem cell:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
21	ATF3	chr7:65447011-65447482	GM12878	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
22	ATF3	chr7:65447012-65447430	H1-hESC	embryonic stem cell:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
23	ATF3	chr7:65446983-65447646	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
24	ATF3	chr7:65447078-65447417	HepG2	liver:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
25	BACH1	chr7:65432845-65433050	H1-hESC	embryonic stem cell:	n/a	chr7:65432936-65432950
26	BCL11A	chr7:65445804-65446185	GM12878	blood:	n/a	n/a
27	BCL3	chr7:65446964-65447481	A549	lung:	n/a	n/a
28	BCLAF1	chr7:65446982-65447503	K562	blood:	n/a	n/a
29	BCLAF1	chr7:65446977-65447523	GM12878	blood:	n/a	n/a
30	BCLAF1	chr7:65445700-65446344	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:65445579-65446242	K562	blood:	n/a	n/a
32	BHLHE40	chr7:65446938-65447667	GM12878	blood:	n/a	chr7:65447320-65447336
33	BHLHE40	chr7:65446962-65447716	K562	blood:	n/a	chr7:65447320-65447336
34	BHLHE40	chr7:65445743-65446248	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:65453207-65453397	K562	blood:	n/a	n/a
36	BHLHE40	chr7:65447115-65447406	A549	lung:	n/a	chr7:65447320-65447336
37	BHLHE40	chr7:65447033-65447638	HepG2	liver:	n/a	chr7:65447320-65447336
38	BRCA1	chr7:65446949-65447471	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr7:65447058-65447393	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr7:65447178-65447689	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:65447137-65447387	HepG2	liver:	n/a	n/a
42	BRCA1	chr7:65449342-65449697	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr7:65447012-65447391	K562	blood:	n/a	n/a
44	CBX3	chr7:65446856-65447842	K562	blood:	n/a	n/a
45	CBX3	chr7:65445617-65446294	K562	blood:	n/a	n/a
46	CCNT2	chr7:65445729-65446235	K562	blood:	n/a	n/a
47	CCNT2	chr7:65446794-65447554	K562	blood:	n/a	chr7:65447317-65447326
48	CEBPB	chr7:65417089-65417503	K562	blood:	n/a	n/a
49	CEBPB	chr7:65417116-65417538	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:65454001-65454668	HepG2	liver:	n/a	chr7:65454484-65454495

(count:2013 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65447249-65447299	Caco-2	colon:	n/a
2	chr7:65447328-65447378	GM12878	blood:	n/a
3	chr7:65447418-65447468	HUVEC	blood vessel:	n/a
4	chr7:65420297-65420347	HL-60	blood:	n/a
5	chr7:65447451-65447501	LNCaP	prostate:	n/a
6	chr7:65444356-65444406	AoSMC	blood vessel:	n/a
7	chr7:65419190-65419240	PrEC	prostate:	n/a
8	chr7:65447565-65447615	AG04450	lung:	fetal
9	chr7:65420240-65420290	HCT-116	colon:	n/a
10	chr7:65419248-65419298	GM12892	blood:	n/a
11	chr7:65439512-65439562	Jurkat	blood:	n/a
12	chr7:65419194-65419244	AG04450	lung:	fetal
13	chr7:65447418-65447468	K562	blood:	n/a
14	chr7:65447418-65447468	HCM	heart:	n/a
15	chr7:65447138-65447188	HCM	heart:	n/a
16	chr7:65447242-65447292	BE2_C	brain:	n/a
17	chr7:65419194-65419244	HL-60	blood:	n/a
18	chr7:65447113-65447163	HMEC	breast:	n/a
19	chr7:65419185-65419235	AG09309	skin:	n/a
20	chr7:65445384-65445434	NHBE	bronchial:	n/a
21	chr7:65445384-65445434	ovcar-3	ovarian:	n/a
22	chr7:65447622-65447672	AG04450	lung:	fetal
23	chr7:65447332-65447382	NHDF-neo	bronchial:	n/a
24	chr7:65447489-65447539	GM12878	blood:	n/a
25	chr7:65447418-65447468	NHBE	bronchial:	n/a
26	chr7:65447249-65447299	K562	blood:	n/a
27	chr7:65420025-65420075	AoSMC	blood vessel:	n/a
28	chr7:65447384-65447434	Caco-2	colon:	n/a
29	chr7:65419231-65419281	PrEC	prostate:	n/a
30	chr7:65420240-65420290	LNCaP	prostate:	n/a
31	chr7:65447322-65447372	AG10803	skin:	n/a
32	chr7:65419194-65419244	A549	lung:	n/a
33	chr7:65420240-65420290	HEEpiC	esophagus:	n/a
34	chr7:65420297-65420347	HUVEC	blood vessel:	n/a
35	chr7:65447328-65447378	AG09309	skin:	n/a
36	chr7:65419190-65419240	LNCaP	prostate:	n/a
37	chr7:65447322-65447372	AG09309	skin:	n/a
38	chr7:65447384-65447434	AG09309	skin:	n/a
39	chr7:65419288-65419338	SK-N-SH	brain:	n/a
40	chr7:65447565-65447615	IMR90	lung:	fetal
41	chr7:65447622-65447672	PrEC	prostate:	n/a
42	chr7:65419231-65419281	GM12892	blood:	n/a
43	chr7:65420240-65420290	HIPEpiC	eye:	n/a
44	chr7:65449491-65449541	AG04450	lung:	fetal
45	chr7:65447418-65447468	NHDF-neo	bronchial:	n/a
46	chr7:65447332-65447382	ECC-1	luminal epithelium:	n/a
47	chr7:65419190-65419240	HepG2	liver:	n/a
48	chr7:65447451-65447501	HRCEpiC	kidney:	n/a
49	chr7:65444356-65444406	Jurkat	blood:	n/a
50	chr7:65419231-65419281	BE2_C	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
2	chr7:65418223..65420511-chr7:65422513..65424298,2	K562	blood:
3	chr7:65441240..65443607-chr7:65444690..65447035,2	MCF-7	breast:
4	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:
5	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
6	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
7	chr7:65421351..65423087-chr7:65426463..65428555,2	K562	blood:
8	chr7:65446738..65449065-chr7:65452732..65454803,2	K562	blood:
9	chr7:65421351..65423087-chr7:65426463..65428555,2	K562	blood:
10	chr7:65418223..65420511-chr7:65422513..65424298,2	K562	blood:
11	chr18:9614542..9615101-chr7:65425383..65426101,2	Hela-S3	cervix:
12	chr7:65419004..65421368-chr7:65431133..65432952,3	K562	blood:
13	chr7:65417227..65419058-chr7:65445876..65447532,2	MCF-7	breast:
14	chr7:65419413..65421834-chr7:65450885..65452622,2	K562	blood:
15	chr7:65430936..65433654-chr7:65438028..65439679,2	MCF-7	breast:
16	chr7:65419242..65420839-chr7:65426993..65428588,2	MCF-7	breast:
17	chr7:65338343..65340268-chr7:65414719..65416455,2	K562	blood:
18	chr7:65419413..65421834-chr7:65450885..65452622,2	K562	blood:
19	chr7:65426424..65431277-chr7:65442612..65445930,6	K562	blood:
20	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:
21	chr7:65439470..65441298-chr7:65540371..65542201,2	K562	blood:
22	chr7:65420692..65422750-chr7:65424011..65425945,2	MCF-7	breast:
23	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
24	chr7:65420692..65422750-chr7:65424011..65425945,2	MCF-7	breast:
25	chr7:65425587..65427267-chr7:65432943..65434454,2	K562	blood:
26	chr12:57039358..57039922-chr7:65446744..65447549,2	Hela-S3	cervix:
27	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:
28	chr7:65337107..65340268-chr7:65414236..65416219,3	K562	blood:
29	chr11:10829765..10830505-chr7:65446635..65447376,2	Hela-S3	cervix:
30	chr10:62042161..62042892-chr7:65418290..65419212,2	MCF-7	breast:
31	chr7:65445709..65448649-chr7:65579782..65581390,2	K562	blood:
32	chr7:65444977..65446741-chr7:65453126..65455205,2	K562	blood:
33	chr7:65416600..65418884-chr7:65442877..65445897,3	K562	blood:
34	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
35	chr7:65419242..65420839-chr7:65426993..65428588,2	MCF-7	breast:
36	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
37	chr7:65425587..65427267-chr7:65432943..65434454,2	K562	blood:

No data

Variant related genes	Relation type
GUSB	TF binding region
GUSB	CpG island
ENSG00000154845	chromatin interactions
ENSG00000196715	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000241258	chromatin interactions
ENSG00000126522	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000169919	chromatin interactions

Extended variants
information (count: 2004 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2004 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571515574	chr7:65414038-65414039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537457576	chr7:65414040-65414041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550061103	chr7:65414044-65414045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185991725	chr7:65414049-65414050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190549103	chr7:65414068-65414069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374633633	chr7:65414081-65414082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558678943	chr7:65414129-65414130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534385341	chr7:65414131-65414132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557854229	chr7:65414139-65414140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182778451	chr7:65414141-65414142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543021676	chr7:65414171-65414172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144461527	chr7:65414208-65414209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62470925	chr7:65414214-65414215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs187019733	chr7:65414265-65414266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559658081	chr7:65414298-65414299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377109952	chr7:65414378-65414379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528707761	chr7:65414390-65414391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191259311	chr7:65414404-65414405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28535370	chr7:65414421-65414422	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530919666	chr7:65414446-65414447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182725108	chr7:65414462-65414463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371640149	chr7:65414480-65414481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs71972777	chr7:65414481-65414482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs56928132	chr7:65414500-65414501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187851447	chr7:65414535-65414536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535782041	chr7:65414585-65414586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549313461	chr7:65414677-65414678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565708439	chr7:65414701-65414702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534818203	chr7:65414748-65414749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62470926	chr7:65414758-65414759	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs575110637	chr7:65414768-65414769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543636871	chr7:65414788-65414789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536644289	chr7:65414814-65414815	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112694050	chr7:65414823-65414824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs193135591	chr7:65414859-65414860	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556261999	chr7:65414901-65414902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556576814	chr7:65414949-65414950	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373913389	chr7:65414952-65414953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542887061	chr7:65414973-65414974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183447413	chr7:65415036-65415037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373722658	chr7:65415094-65415095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572078032	chr7:65415190-65415191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576051346	chr7:65415209-65415210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142503580	chr7:65415289-65415290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545624454	chr7:65415311-65415312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187788849	chr7:65415316-65415317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565232658	chr7:65415365-65415366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs35438895	chr7:65415366-65415367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531054825	chr7:65415370-65415371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12113646	chr7:65415382-65415383	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:78)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Chronic myeloid leukemia	18641042	CNVD

Chromatin state (count:1412 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65345200-65419000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:65368800-65418800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:65368800-65419000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:65373800-65424000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:65375000-65418800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:65375600-65419800	Weak transcription	HSMMtube	muscle
7	chr7:65379200-65419000	Weak transcription	Fetal Thymus	thymus
8	chr7:65381800-65420200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr7:65382000-65420600	Weak transcription	Primary B cells from cord blood	blood
10	chr7:65382800-65419800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr7:65383200-65419000	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr7:65383800-65419600	Weak transcription	GM12878-XiMat	blood
13	chr7:65389400-65423800	Weak transcription	Aorta	Aorta
14	chr7:65390400-65419000	Weak transcription	Thymus	Thymus
15	chr7:65390600-65423800	Weak transcription	Gastric	stomach
16	chr7:65392600-65418400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:65393200-65419600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:65393400-65419000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:65395600-65420400	Weak transcription	Esophagus	oesophagus
20	chr7:65395800-65420000	Weak transcription	Fetal Lung	lung
21	chr7:65396600-65418600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr7:65396800-65416800	Weak transcription	Hela-S3	cervix
23	chr7:65396800-65420000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:65397400-65419600	Weak transcription	Left Ventricle	heart
25	chr7:65399200-65425000	Weak transcription	Small Intestine	intestine
26	chr7:65399800-65419600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:65400200-65420200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:65400800-65420200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:65401000-65417200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:65401200-65420000	Weak transcription	HUVEC	blood vessel
31	chr7:65401200-65423800	Weak transcription	Spleen	Spleen
32	chr7:65401400-65425000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr7:65401800-65425000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:65402000-65420200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr7:65402000-65424800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:65402000-65425000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr7:65402200-65419000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr7:65402400-65419400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr7:65402800-65417800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr7:65403800-65419000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:65403800-65419600	Weak transcription	Osteobl	bone
42	chr7:65404000-65418800	Weak transcription	Fetal Muscle Leg	muscle
43	chr7:65404000-65420400	Weak transcription	HSMM	muscle
44	chr7:65404200-65417800	Weak transcription	Primary T cells from cord blood	blood
45	chr7:65404200-65418400	Weak transcription	K562	blood
46	chr7:65404200-65418800	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr7:65404400-65416800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:65404400-65419000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:65404400-65419000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr7:65404400-65419000	Weak transcription	Lung	lung

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