Variant report

Variant	nsv1024942
Chromosome Location	chr7:57586049-58019983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2243)
CpG islands
(count:2932)
Chromatin interactive
region (count:4)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2243 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:58010298-58010461	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:57698544-57698607	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:57994141-57994509	HepG2	liver:	n/a	n/a
4	ATF1	chr7:57994002-57994510	K562	blood:	n/a	n/a
5	ATF1	chr7:57960924-57961116	K562	blood:	n/a	n/a
6	ATF1	chr7:57981808-57982008	K562	blood:	n/a	n/a
7	ATF1	chr7:57995641-57996010	K562	blood:	n/a	n/a
8	BACH1	chr7:58012973-58012998	K562	blood:	n/a	n/a
9	BACH1	chr7:57995639-57996394	K562	blood:	n/a	n/a
10	BACH1	chr7:57973523-57973897	K562	blood:	n/a	n/a
11	BACH1	chr7:57625009-57625034	K562	blood:	n/a	n/a
12	BACH1	chr7:58012803-58012998	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:57953074-57953078	K562	blood:	n/a	n/a
14	BACH1	chr7:57708717-57708917	K562	blood:	n/a	n/a
15	BACH1	chr7:57965177-57965554	K562	blood:	n/a	n/a
16	BATF	chr7:57994095-57994356	GM12878	blood:	n/a	n/a
17	BATF	chr7:57970948-57971464	GM12878	blood:	n/a	n/a
18	BATF	chr7:57956471-57956682	GM12878	blood:	n/a	n/a
19	BATF	chr7:57984879-57985099	GM12878	blood:	n/a	n/a
20	BATF	chr7:57953748-57954008	GM12878	blood:	n/a	n/a
21	BATF	chr7:57940500-57940831	GM12878	blood:	n/a	n/a
22	BATF	chr7:57940526-57940743	GM12878	blood:	n/a	n/a
23	BATF	chr7:57667672-57667890	GM12878	blood:	n/a	n/a
24	BATF	chr7:58014454-58014600	GM12878	blood:	n/a	n/a
25	BATF	chr7:57650647-57650907	GM12878	blood:	n/a	n/a
26	BATF	chr7:57978026-57978220	GM12878	blood:	n/a	n/a
27	BATF	chr7:57635362-57635498	GM12878	blood:	n/a	n/a
28	BATF	chr7:58006674-58006965	GM12878	blood:	n/a	n/a
29	BATF	chr7:58008446-58008790	GM12878	blood:	n/a	n/a
30	BATF	chr7:58009212-58009591	GM12878	blood:	n/a	n/a
31	BATF	chr7:57924008-57924207	GM12878	blood:	n/a	chr7:57924188-57924197
32	BATF	chr7:58009224-58009514	GM12878	blood:	n/a	n/a
33	BATF	chr7:58014452-58014715	GM12878	blood:	n/a	n/a
34	BATF	chr7:57999505-57999877	GM12878	blood:	n/a	n/a
35	BATF	chr7:57667657-57667934	GM12878	blood:	n/a	n/a
36	BATF	chr7:57961728-57962181	GM12878	blood:	n/a	n/a
37	BATF	chr7:57957699-57958079	GM12878	blood:	n/a	n/a
38	BATF	chr7:58013747-58014011	GM12878	blood:	n/a	n/a
39	BATF	chr7:57984864-57985086	GM12878	blood:	n/a	n/a
40	BATF	chr7:57992052-57992285	GM12878	blood:	n/a	n/a
41	BATF	chr7:57999368-57999788	GM12878	blood:	n/a	n/a
42	BATF	chr7:58007790-58008139	GM12878	blood:	n/a	n/a
43	BATF	chr7:57994669-57994997	GM12878	blood:	n/a	n/a
44	BATF	chr7:57994043-57994353	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:57999330-57999887	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:57766889-57767133	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:57940500-57940743	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:57957712-57958049	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:57981694-57982016	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:57983903-57984076	GM12878	blood:	n/a	n/a

(count:2932 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:57830004-57830054	PFSK-1	brain:	n/a
2	chr7:57830625-57830675	AG04449	skin:	fetal
3	chr7:57927793-57927843	HRE	kidney:	n/a
4	chr7:57713841-57713891	NT2-D1	testis:	n/a
5	chr7:57830004-57830054	PFSK-1	brain:	n/a
6	chr7:57830625-57830675	AG04449	skin:	fetal
7	chr7:57927793-57927843	HRE	kidney:	n/a
8	chr7:57713841-57713891	NT2-D1	testis:	n/a
9	chr7:57711465-57711515	Hela-S3	cervix:	n/a
10	chr7:57710252-57710302	SAEC	small airway:	n/a
11	chr7:57927793-57927843	HCPEpiC	choroid plexus:	n/a
12	chr7:57830625-57830675	GM19239	blood:	n/a
13	chr7:57895070-57895120	Caco-2	colon:	n/a
14	chr7:57831919-57831969	PANC-1	pancreas:	n/a
15	chr7:57639252-57639302	IMR90	lung:	fetal
16	chr7:57928998-57929048	HL-60	blood:	n/a
17	chr7:57835813-57835863	LNCaP	prostate:	n/a
18	chr7:57707202-57707252	ovcar-3	ovarian:	n/a
19	chr7:57710136-57710186	MCF-7	breast:	n/a
20	chr7:57698643-57698693	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:57714385-57714435	GM12878	blood:	n/a
22	chr7:57830004-57830054	NT2-D1	testis:	n/a
23	chr7:57881130-57881180	PrEC	prostate:	n/a
24	chr7:57835813-57835863	AG04449	skin:	fetal
25	chr7:57928306-57928356	AG04449	skin:	fetal
26	chr7:57705701-57705751	GM12878	blood:	n/a
27	chr7:57830004-57830054	CMK	blood:	n/a
28	chr7:57832834-57832884	CMK	blood:	n/a
29	chr7:57712819-57712869	NH-A	brain:	n/a
30	chr7:57832834-57832884	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:57880009-57880059	GM12892	blood:	n/a
32	chr7:57878945-57878995	PrEC	prostate:	n/a
33	chr7:57881130-57881180	NH-A	brain:	n/a
34	chr7:57715349-57715399	HCM	heart:	n/a
35	chr7:57705701-57705751	HCF	heart:	n/a
36	chr7:57710136-57710186	HCT-116	colon:	n/a
37	chr7:57930428-57930478	HNPCEpiC	eye:	n/a
38	chr7:57836342-57836392	HL-60	blood:	n/a
39	chr7:57707202-57707252	AG10803	skin:	n/a
40	chr7:57639360-57639410	HCPEpiC	choroid plexus:	n/a
41	chr7:57830004-57830054	SAEC	small airway:	n/a
42	chr7:57830004-57830054	H1-hESC	embryonic stem cell:	embryo
43	chr7:57714270-57714320	CMK	blood:	n/a
44	chr7:57711394-57711444	Hepatocyte	liver:	n/a
45	chr7:57878893-57878943	SK-N-SH_RA	brain:	n/a
46	chr7:57878777-57878827	HCT-116	colon:	n/a
47	chr7:57830625-57830675	GM12892	blood:	n/a
48	chr7:57715349-57715399	ECC-1	luminal epithelium:	n/a
49	chr7:57830625-57830675	BE2_C	brain:	n/a
50	chr7:57928306-57928356	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:21513323..21515345-chr7:57633825..57635715,2	K562	blood:
2	chr4:33836938..33837728-chr7:57607899..57608399,2	K562	blood:
3	chr20:26130778..26134198-chr7:57619861..57623955,5	K562	blood:
4	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF479-8	chr7:57689787-57689961	NONHSAT120850
2	lnc-ZNF479-8	chr7:57704747-57704895	NONHSAT120850
3	lnc-ZNF479-8	chr7:57688185-57688268	NONHSAT120847
4	lnc-ZNF479-14	chr7:57877307-57877718	NONHSAT120873
5	lnc-ZNF479-8	chr7:57696817-57696916	NONHSAT120850
6	lnc-ZNF716-7	chr7:57710227-57710560	NONHSAT120861
7	lnc-ZNF479-8	chr7:57696818-57696916	NONHSAT120847
8	lnc-ZNF479-8	chr7:57701610-57701660	NONHSAT120847
9	lnc-ZNF479-11	chr7:57830325-57830652	NONHSAT120868
10	lnc-ZNF479-8	chr7:57703900-57703975	NONHSAT120850
11	lnc-ZNF716-24	chr7:57888037-57888136	NONHSAT120882
12	lnc-ZNF479-8	chr7:57689759-57689961	NONHSAT120848
13	lnc-ZNF479-8	chr7:57703364-57703554	NONHSAT120850
14	lnc-ZNF479-16	chr7:57882150-57882506	NONHSAT120880
15	lnc-ZNF479-8	chr7:57696817-57696917	NONHSAT120848
16	lnc-ZNF716-21	chr7:57830672-57830879	NONHSAT120869
17	lnc-ZNF479-8	chr7:57689759-57689983	NONHSAT120847
18	lnc-ZNF479-8	chr7:57688668-57688812	NONHSAT120848
19	lnc-ZNF716-24	chr7:57894964-57895190	NONHSAT120882
20	lnc-ZNF716-24	chr7:57896673-57896752	NONHSAT120882
21	lnc-ZNF479-15	chr7:57879738-57880116	NONHSAT120878

No data

Variant related genes	Relation type
ENSG00000224653	TF binding region
ENSG00000227015	TF binding region
ENSG00000224484	TF binding region
ENSG00000231484	TF binding region
ENSG00000230271	TF binding region
ENSG00000231232	TF binding region
ENSG00000237236	TF binding region
ENSG00000270749	TF binding region
ENSG00000233962	TF binding region
ENSG00000237639	TF binding region
ENSG00000236907	TF binding region
ENSG00000232161	TF binding region
ENSG00000234085	TF binding region
ENSG00000250923	TF binding region
ENSG00000271696	TF binding region
ENSG00000243981	TF binding region
ENSG00000236261	TF binding region
ENSG00000250618	TF binding region
NCOR1P3	TF binding region
ENSG00000229627	TF binding region
ENSG00000230796	TF binding region
ENSG00000223836	TF binding region
ENSG00000224653	CpG island
ENSG00000227015	CpG island
ENSG00000224484	CpG island
ENSG00000231484	CpG island
ENSG00000230271	CpG island
ENSG00000231232	CpG island
ENSG00000237236	CpG island
ENSG00000270749	CpG island
ENSG00000233962	CpG island
ENSG00000237639	CpG island
ENSG00000236907	CpG island
ENSG00000232161	CpG island
ENSG00000234085	CpG island
ENSG00000250923	CpG island
ENSG00000271696	CpG island
ENSG00000243981	CpG island
ENSG00000236261	CpG island
ENSG00000250618	CpG island
NCOR1P3	CpG island
ENSG00000229627	CpG island
ENSG00000230796	CpG island
ENSG00000223836	CpG island

Extended variants
information (count: 16140 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:16140 , 50 per page) page: 1 2 3 4 5 6 7 ... 323

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57787861	chr7:57599272-57599273	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568533635	chr7:57599278-57599279	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs529418303	chr7:57599295-57599296	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547768425	chr7:57599353-57599354	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs539912128	chr7:57599362-57599363	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs371936945	chr7:57599363-57599364	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs558201914	chr7:57599364-57599365	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371828730	chr7:57599380-57599381	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs537212931	chr7:57599392-57599393	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs4870671	chr7:57599393-57599394	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573352428	chr7:57599394-57599395	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs540772699	chr7:57599452-57599453	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374829373	chr7:57599458-57599459	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs552922267	chr7:57599463-57599464	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs577598094	chr7:57599497-57599498	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369257043	chr7:57599499-57599500	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs563411057	chr7:57599503-57599504	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530851905	chr7:57599504-57599505	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542806388	chr7:57599523-57599524	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10215238	chr7:57599562-57599563	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529403863	chr7:57599573-57599574	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs547952154	chr7:57599578-57599579	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs4870672	chr7:57599610-57599611	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs566050074	chr7:57599633-57599634	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs533200673	chr7:57599643-57599644	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs181118895	chr7:57599654-57599655	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570212283	chr7:57599659-57599660	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs537350341	chr7:57599667-57599668	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs10215025	chr7:57599689-57599690	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs185227960	chr7:57599709-57599710	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs143439111	chr7:57599715-57599716	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534395700	chr7:57599718-57599719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs190129992	chr7:57599732-57599733	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577686638	chr7:57599735-57599736	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs544647557	chr7:57599755-57599756	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556928068	chr7:57599766-57599767	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575565185	chr7:57599772-57599773	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs542990838	chr7:57599773-57599774	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs561055596	chr7:57599774-57599775	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528329524	chr7:57599778-57599779	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370394824	chr7:57599782-57599783	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs533476271	chr7:57599799-57599800	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs551437652	chr7:57599804-57599805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562380109	chr7:57599807-57599808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137962184	chr7:57599808-57599809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199937928	chr7:57599809-57599810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139179834	chr7:57599813-57599814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563748728	chr7:57599822-57599823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531098572	chr7:57599833-57599834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549299726	chr7:57599837-57599838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:57599200-57599800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr7:57599800-57600800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:57600800-57601200	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr7:57607000-57607800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr7:57609200-57610400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr7:57609600-57610000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr7:57612400-57613200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr7:57612400-57613400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr7:57612800-57613200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr7:57613000-57613200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:57624200-57625000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:57639200-57641400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:57656400-57657200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:57695600-57695800	Enhancers	Spleen	Spleen
15	chr7:57696400-57696600	ZNF genes & repeats	Fetal Kidney	kidney
16	chr7:57697800-57698800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr7:57697800-57698800	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr7:57697800-57699000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
19	chr7:57697800-57699400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr7:57698000-57698600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:57698000-57698800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:57698000-57698800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:57698000-57698800	ZNF genes & repeats	Esophagus	oesophagus
24	chr7:57698000-57698800	ZNF genes & repeats	Gastric	stomach
25	chr7:57698000-57698800	ZNF genes & repeats	Pancreas	Pancrea
26	chr7:57698000-57699400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
27	chr7:57698200-57698800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:57698400-57698800	ZNF genes & repeats	Fetal Stomach	stomach
29	chr7:57698400-57699000	ZNF genes & repeats	Brain Anterior Caudate	brain
30	chr7:57698600-57698800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
31	chr7:57698800-57701200	Weak transcription	Gastric	stomach
32	chr7:57698800-57701200	Weak transcription	Pancreas	Pancrea
33	chr7:57699000-57701400	Weak transcription	Brain Anterior Caudate	brain
34	chr7:57701200-57701600	Active TSS	Primary T cells from cord blood	blood
35	chr7:57701200-57701800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr7:57701200-57701800	ZNF genes & repeats	Fetal Brain Male	brain
37	chr7:57701200-57701800	ZNF genes & repeats	Gastric	stomach
38	chr7:57701200-57701800	ZNF genes & repeats	Pancreas	Pancrea
39	chr7:57701200-57704000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
40	chr7:57701400-57701600	ZNF genes & repeats	Fetal Heart	heart
41	chr7:57701400-57701800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:57701400-57701800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr7:57701400-57701800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:57701400-57701800	ZNF genes & repeats	Brain Anterior Caudate	brain
45	chr7:57701400-57701800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
46	chr7:57701400-57702000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:57701600-57701800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
48	chr7:57701600-57701800	ZNF genes & repeats	Colonic Mucosa	Colon
49	chr7:57701800-57703000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:57703000-57703800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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