Variant report

Variant	nsv470244
Chromosome Location	chr7:62012220-62838532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1940)
CpG islands
(count:2320)
Chromatin interactive
region (count:12)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:62071176-62071544	K562	blood:	n/a	n/a
2	ATF1	chr7:62039929-62040292	K562	blood:	n/a	n/a
3	ATF1	chr7:62330338-62330635	K562	blood:	n/a	n/a
4	ATF1	chr7:62021634-62022009	K562	blood:	n/a	n/a
5	ATF1	chr7:62546931-62547029	K562	blood:	n/a	n/a
6	ATF3	chr7:62021724-62021964	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:62019347-62019720	K562	blood:	n/a	n/a
8	BACH1	chr7:62435606-62435658	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:62031748-62032429	K562	blood:	n/a	n/a
10	BACH1	chr7:62601389-62601434	K562	blood:	n/a	n/a
11	BATF	chr7:62020109-62020357	GM12878	blood:	n/a	n/a
12	BATF	chr7:62021626-62022168	GM12878	blood:	n/a	n/a
13	BATF	chr7:62031502-62031772	GM12878	blood:	n/a	n/a
14	BATF	chr7:62021723-62022000	GM12878	blood:	n/a	n/a
15	BATF	chr7:62015078-62015365	GM12878	blood:	n/a	n/a
16	BATF	chr7:62016951-62017373	GM12878	blood:	n/a	n/a
17	BATF	chr7:62022676-62022882	GM12878	blood:	n/a	n/a
18	BATF	chr7:62031446-62031758	GM12878	blood:	n/a	n/a
19	BATF	chr7:62016953-62017229	GM12878	blood:	n/a	n/a
20	BATF	chr7:62565070-62565257	GM12878	blood:	n/a	chr7:62565199-62565210
21	BATF	chr7:62018400-62018730	GM12878	blood:	n/a	n/a
22	BATF	chr7:62400667-62400824	GM12878	blood:	n/a	n/a
23	BATF	chr7:62018405-62018666	GM12878	blood:	n/a	n/a
24	BATF	chr7:62188677-62188824	GM12878	blood:	n/a	n/a
25	BATF	chr7:62015074-62015366	GM12878	blood:	n/a	n/a
26	BATF	chr7:62032839-62033167	GM12878	blood:	n/a	n/a
27	BATF	chr7:62015481-62015671	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:62031479-62031795	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:62032887-62033140	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:62016960-62017167	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:62021646-62021990	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:62021616-62022037	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:62016876-62017421	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:62032885-62033176	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:62188685-62188838	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:62025259-62025541	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:62018357-62018721	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:62031464-62031707	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:62021746-62021862	H1-hESC	embryonic stem cell:	n/a	n/a
40	BCL11A	chr7:62015113-62015357	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:62020100-62020367	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:62015018-62015671	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:62021734-62021885	H1-hESC	embryonic stem cell:	n/a	n/a
44	BHLHE40	chr7:62468805-62468905	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:62476052-62476283	K562	blood:	n/a	n/a
46	BHLHE40	chr7:62032928-62033195	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:62188666-62188877	HepG2	liver:	n/a	n/a
48	BHLHE40	chr7:62031491-62031663	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:62031747-62032429	K562	blood:	n/a	n/a
50	BHLHE40	chr7:62016939-62017266	HepG2	liver:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:62574925-62574975	AoSMC	blood vessel:	n/a
2	chr7:62809321-62809371	ProgFib	skin:	n/a
3	chr7:62574925-62574975	AoSMC	blood vessel:	n/a
4	chr7:62809321-62809371	ProgFib	skin:	n/a
5	chr7:62577907-62577957	HCF	heart:	n/a
6	chr7:62555691-62555741	GM06990	blood:	n/a
7	chr7:62528691-62528741	SK-N-SH	brain:	n/a
8	chr7:62541571-62541621	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:62574479-62574529	A549	lung:	n/a
10	chr7:62528610-62528660	PANC-1	pancreas:	n/a
11	chr7:62514736-62514786	HL-60	blood:	n/a
12	chr7:62574479-62574529	HMEC	breast:	n/a
13	chr7:62693631-62693681	Jurkat	blood:	n/a
14	chr7:62809321-62809371	NB4	blood:	n/a
15	chr7:62562718-62562768	AG09319	gingival:	n/a
16	chr7:62198343-62198393	MCF10A-Er-Src	breast:	n/a
17	chr7:62490514-62490564	HNPCEpiC	eye:	n/a
18	chr7:62574200-62574250	IMR90	lung:	fetal
19	chr7:62560487-62560537	U87	brain:	n/a
20	chr7:62574200-62574250	NHBE	bronchial:	n/a
21	chr7:62562718-62562768	HepG2	liver:	n/a
22	chr7:62554288-62554338	HMEC	breast:	n/a
23	chr7:62514673-62514723	HUVEC	blood vessel:	n/a
24	chr7:62809331-62809381	PFSK-1	brain:	n/a
25	chr7:62528852-62528902	PFSK-1	brain:	n/a
26	chr7:62510825-62510875	AG04450	lung:	fetal
27	chr7:62514736-62514786	BJ	skin:	n/a
28	chr7:62528610-62528660	RPTEC	kidney:	n/a
29	chr7:62809620-62809670	SK-N-SH_RA	brain:	n/a
30	chr7:62762850-62762900	K562	blood:	n/a
31	chr7:62514926-62514976	Hela-S3	cervix:	n/a
32	chr7:62562718-62562768	HNPCEpiC	eye:	n/a
33	chr7:62765320-62765370	ECC-1	luminal epithelium:	n/a
34	chr7:62693631-62693681	NHBE	bronchial:	n/a
35	chr7:62693610-62693660	NHDF-neo	bronchial:	n/a
36	chr7:62191825-62191875	LNCaP	prostate:	n/a
37	chr7:62528241-62528291	MCF10A-Er-Src	breast:	n/a
38	chr7:62528241-62528291	PrEC	prostate:	n/a
39	chr7:62809331-62809381	GM06990	blood:	n/a
40	chr7:62528241-62528291	MCF-7	breast:	n/a
41	chr7:62809620-62809670	BE2_C	brain:	n/a
42	chr7:62809620-62809670	GM06990	blood:	n/a
43	chr7:62510825-62510875	HRE	kidney:	n/a
44	chr7:62809321-62809371	H1-hESC	embryonic stem cell:	embryo
45	chr7:62762850-62762900	PANC-1	pancreas:	n/a
46	chr7:62809373-62809423	SAEC	small airway:	n/a
47	chr7:62555691-62555741	H1-hESC	embryonic stem cell:	embryo
48	chr7:62514673-62514723	LNCaP	prostate:	n/a
49	chr7:62531318-62531368	NB4	blood:	n/a
50	chr7:62514736-62514786	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:62284727..62285228-chr9:30620902..30621883,2	MCF-7	breast:
2	chr17:41380312..41382165-chr7:62191292..62192792,2	K562	blood:
3	chr17:41398894..41400557-chr7:62191292..62192792,2	K562	blood:
4	chr5:178209012..178209534-chr7:62475815..62476717,2	MCF-7	breast:
5	chr1:121484723..121485367-chr7:62026258..62026778,2	MCF-7	breast:
6	chr17:41380367..41382313-chr7:62191292..62192792,2	MCF-7	breast:
7	chr17:41399589..41402142-chr7:62189772..62191292,2	K562	blood:
8	chr7:62475749..62476533-chr7:100925981..100926817,2	MCF-7	breast:
9	chr7:62093615..62095373-chr7:62122563..62125212,2	K562	blood:
10	chr7:61552820..61553340-chr7:62284727..62285248,3	MCF-7	breast:
11	chr7:62093615..62095373-chr7:62122563..62125212,2	K562	blood:
12	chr17:22017005..22017989-chr7:62476147..62476710,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006455.1-2	chr7:62815523-62815687	ENSG00000229301
2	lnc-AC006455.1-8	chr7:62669597-62669710	NONHSAT120895
3	lnc-ZNF680-8	chr7:62814625-62814704	ENSG00000226587.1
4	lnc-AC006455.1-2	chr7:62819441-62819684	ENSG00000229301
5	lnc-ZNF680-11	chr7:62441009-62441326	XLOC_006462
6	lnc-AC006455.1-2	chr7:62838321-62838411	NONHSAT120910
7	lnc-ZNF680-42	chr7:62764328-62764366	NONHSAT120900
8	lnc-ZNF680-8	chr7:62787052-62787278	ENSG00000226587.1
9	lnc-AC006455.1-2	chr7:62837707-62838611	NONHSAT120909
10	lnc-ZNF680-42	chr7:62758642-62758770	NONHSAT120900
11	lnc-AC006455.1-7	chr7:62723443-62723834	NONHSAT120898
12	lnc-AC006455.1-11	chr7:62517831-62517952	NONHSAT120889
13	lnc-AC006455.1-2	chr7:62814411-62814743	NONHSAT120906
14	lnc-AC006455.1-2	chr7:62814835-62814953	ENSG00000229301
15	lnc-ZNF680-42	chr7:62758071-62758166	NONHSAT120900
16	lnc-ZNF680-44	chr7:62547448-62548639	NONHSAT120891
17	lnc-ZNF680-42	chr7:62764328-62764434	NONHSAT120899
18	lnc-ZNF680-42	chr7:62751896-62753204	NONHSAT120900
19	lnc-ZNF680-10	chr7:62514734-62514809	XLOC_006463
20	lnc-ZNF680-42	chr7:62758644-62758770	NONHSAT120899
21	lnc-ZNF680-11	chr7:62452942-62453054	XLOC_006462
22	lnc-AC006455.1-2	chr7:62838106-62838187	NONHSAT120910
23	lnc-ZNF680-41	chr7:62827805-62828534	NONHSAT120908
24	lnc-ZNF680-8	chr7:62806338-62806547	ENSG00000226587.1
25	lnc-AC006455.1-6	chr7:62803089-62803578	NONHSAT120902
26	lnc-ZNF680-42	chr7:62751670-62753201	NONHSAT120899
27	lnc-AC006455.1-11	chr7:62520310-62520462	NONHSAT120889
28	lnc-AC006455.1-8	chr7:62672054-62672200	NONHSAT120895
29	lnc-ZNF680-10	chr7:62505205-62505547	XLOC_006463

No data

Variant related genes	Relation type
ENSG00000234312	TF binding region
ENSG00000199231	TF binding region
ENSG00000231523	TF binding region
ENSG00000244550	TF binding region
ENSG00000236638	TF binding region
ZNF90P3	TF binding region
ENSG00000265865	TF binding region
VN1R32P	TF binding region
ENSG00000230000	TF binding region
ENSG00000227148	TF binding region
ENSG00000226587	TF binding region
ZNF733P	TF binding region
ENSG00000227545	TF binding region
ENSG00000229301	TF binding region
PHKG1P1	TF binding region
ENSG00000227923	TF binding region
ENSG00000227298	TF binding region
SEPT7P4	TF binding region
ENSG00000232165	TF binding region
ENSG00000237572	TF binding region
RNU6-417P	TF binding region
VN1R31P	TF binding region
ENSG00000233454	TF binding region
ENSG00000234312	CpG island
ENSG00000199231	CpG island
ENSG00000231523	CpG island
ENSG00000244550	CpG island
ENSG00000236638	CpG island
ZNF90P3	CpG island
ENSG00000265865	CpG island
VN1R32P	CpG island
ENSG00000230000	CpG island
ENSG00000227148	CpG island
ENSG00000226587	CpG island
ZNF733P	CpG island
ENSG00000227545	CpG island
ENSG00000229301	CpG island
PHKG1P1	CpG island
ENSG00000227923	CpG island
ENSG00000227298	CpG island
SEPT7P4	CpG island
ENSG00000232165	CpG island
ENSG00000237572	CpG island
RNU6-417P	CpG island
VN1R31P	CpG island
ENSG00000233454	CpG island
ENSG00000236383	chromatin interactions

Extended variants
information (count: 29900 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:29900 , 50 per page) page: 1 2 3 4 5 6 7 ... 598

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7811078	chr7:62012221-62012222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190345616	chr7:62012230-62012231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533416555	chr7:62012232-62012233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533274249	chr7:62012238-62012239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551328175	chr7:62012243-62012244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182425449	chr7:62012253-62012254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186545386	chr7:62012265-62012266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201226742	chr7:62012274-62012275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112409407	chr7:62012278-62012279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201820840	chr7:62012287-62012288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555625975	chr7:62012298-62012299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191965793	chr7:62012301-62012302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534767884	chr7:62012303-62012304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142071582	chr7:62012307-62012308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150709360	chr7:62012327-62012328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200048294	chr7:62012328-62012329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545106274	chr7:62012334-62012335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4311556	chr7:62012341-62012342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575311352	chr7:62012351-62012352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542300890	chr7:62012353-62012354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111860310	chr7:62012373-62012374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562368647	chr7:62012396-62012397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202117774	chr7:62012423-62012424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200385217	chr7:62012435-62012436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529565905	chr7:62012439-62012440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541586869	chr7:62012444-62012445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559713558	chr7:62012445-62012446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533383685	chr7:62012450-62012451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551440311	chr7:62012453-62012454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569855056	chr7:62012454-62012455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530772728	chr7:62012470-62012471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113621916	chr7:62012480-62012481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549110478	chr7:62012481-62012482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200927252	chr7:62012483-62012484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9690376	chr7:62012492-62012493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs553263896	chr7:62012493-62012494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571442990	chr7:62012500-62012501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200231588	chr7:62012508-62012509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181653141	chr7:62012515-62012516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201409489	chr7:62012522-62012523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557085642	chr7:62012524-62012525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575423105	chr7:62012538-62012539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536200288	chr7:62012554-62012555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185381311	chr7:62012566-62012567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199726926	chr7:62012568-62012569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190297913	chr7:62012569-62012570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200478679	chr7:62012575-62012576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201401124	chr7:62012599-62012600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572423773	chr7:62012614-62012615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559648660	chr7:62012646-62012647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Bipolar disorder	19214233	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Schizophrenia	23813976	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:62006600-62015200	Weak transcription	K562	blood
2	chr7:62006800-62015000	Weak transcription	NH-A	brain
3	chr7:62008400-62017000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:62010000-62014400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:62010000-62014400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr7:62010000-62014400	Weak transcription	HUVEC	blood vessel
7	chr7:62010000-62015000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:62014400-62015400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
9	chr7:62014400-62015600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
10	chr7:62014400-62029800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:62014600-62015200	Active TSS	Aorta	Aorta
12	chr7:62014600-62025200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
13	chr7:62014600-62027600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr7:62014800-62015400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:62014800-62015600	ZNF genes & repeats	HUVEC	blood vessel
16	chr7:62014800-62017600	ZNF genes & repeats	HepG2	liver
17	chr7:62014800-62026800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr7:62014800-62026800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
19	chr7:62015000-62015400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:62015000-62015400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
21	chr7:62015000-62015600	ZNF genes & repeats	Liver	Liver
22	chr7:62015000-62015600	Active TSS	NH-A	brain
23	chr7:62015200-62015400	ZNF genes & repeats	Fetal Heart	heart
24	chr7:62015200-62015600	ZNF genes & repeats	K562	blood
25	chr7:62015200-62016800	Weak transcription	Aorta	Aorta
26	chr7:62015400-62015600	ZNF genes & repeats	Osteobl	bone
27	chr7:62015400-62017000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:62015600-62017000	Weak transcription	HUVEC	blood vessel
29	chr7:62015600-62017000	Weak transcription	NH-A	brain
30	chr7:62015600-62017800	Weak transcription	Osteobl	bone
31	chr7:62015600-62021600	Weak transcription	K562	blood
32	chr7:62016800-62017400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
33	chr7:62016800-62017400	Active TSS	Aorta	Aorta
34	chr7:62016800-62017400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
35	chr7:62017000-62017200	ZNF genes & repeats	Colon Smooth Muscle	Colon
36	chr7:62017000-62017400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:62017000-62017400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
38	chr7:62017000-62017400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
39	chr7:62017000-62017400	ZNF genes & repeats	Brain Angular Gyrus	brain
40	chr7:62017000-62017400	ZNF genes & repeats	Brain Substantia Nigra	brain
41	chr7:62017000-62017400	Active TSS	Right Atrium	heart
42	chr7:62017000-62017400	ZNF genes & repeats	HSMMtube	muscle
43	chr7:62017000-62017400	ZNF genes & repeats	NH-A	brain
44	chr7:62017000-62017600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:62017000-62017600	ZNF genes & repeats	HUVEC	blood vessel
46	chr7:62017200-62017400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
47	chr7:62017200-62021600	Weak transcription	Colon Smooth Muscle	Colon
48	chr7:62017400-62017800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:62017400-62019000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr7:62017400-62020000	Weak transcription	Brain Substantia Nigra	brain

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