Variant report

Variant	nsv981486
Chromosome Location	chr7:57602372-57731883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:1470)
Chromatin interactive
region (count:4)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:57698544-57698607	HepG2	liver:	n/a	n/a
2	BACH1	chr7:57625009-57625034	K562	blood:	n/a	n/a
3	BACH1	chr7:57708717-57708917	K562	blood:	n/a	n/a
4	BATF	chr7:57667672-57667890	GM12878	blood:	n/a	n/a
5	BATF	chr7:57635362-57635498	GM12878	blood:	n/a	n/a
6	BATF	chr7:57667657-57667934	GM12878	blood:	n/a	n/a
7	BATF	chr7:57650647-57650907	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:57635305-57635594	GM12878	blood:	n/a	n/a
9	BCL3	chr7:57608761-57609009	K562	blood:	n/a	n/a
10	BHLHE40	chr7:57708547-57708919	K562	blood:	n/a	n/a
11	BHLHE40	chr7:57710672-57710854	K562	blood:	n/a	n/a
12	BHLHE40	chr7:57713294-57713311	K562	blood:	n/a	n/a
13	BRCA1	chr7:57698528-57698644	HepG2	liver:	n/a	n/a
14	BRCA1	chr7:57651407-57651453	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:57626231-57626862	A549	lung:	n/a	chr7:57626695-57626706
16	CEBPB	chr7:57626204-57626872	IMR90	lung:	n/a	chr7:57626695-57626706
17	CEBPB	chr7:57612772-57613095	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:57612867-57613067	K562	blood:	n/a	n/a
19	CEBPB	chr7:57695840-57696024	A549	lung:	n/a	n/a
20	CEBPB	chr7:57626151-57626885	HepG2	liver:	n/a	chr7:57626695-57626706
21	CEBPB	chr7:57634292-57634596	IMR90	lung:	n/a	chr7:57634431-57634442 chr7:57634474-57634483 chr7:57634432-57634443 chr7:57634474-57634485 chr7:57634472-57634483
22	CEBPB	chr7:57659472-57659639	K562	blood:	n/a	n/a
23	CEBPB	chr7:57634309-57634600	HepG2	liver:	n/a	chr7:57634431-57634442 chr7:57634474-57634483 chr7:57634432-57634443 chr7:57634474-57634485 chr7:57634472-57634483
24	CEBPB	chr7:57710670-57710870	K562	blood:	n/a	n/a
25	CEBPB	chr7:57626529-57626874	K562	blood:	n/a	chr7:57626695-57626706
26	CEBPB	chr7:57708544-57708746	K562	blood:	n/a	n/a
27	CEBPB	chr7:57634314-57634595	A549	lung:	n/a	chr7:57634431-57634442 chr7:57634474-57634483 chr7:57634432-57634443 chr7:57634474-57634485 chr7:57634472-57634483
28	CEBPB	chr7:57729431-57729679	HepG2	liver:	n/a	chr7:57729582-57729593
29	CEBPB	chr7:57634333-57634591	K562	blood:	n/a	chr7:57634431-57634442 chr7:57634474-57634483 chr7:57634432-57634443 chr7:57634474-57634485 chr7:57634472-57634483
30	CHD2	chr7:57607407-57607910	K562	blood:	n/a	n/a
31	CHD2	chr7:57626203-57626699	K562	blood:	n/a	n/a
32	CHD2	chr7:57698601-57698644	HepG2	liver:	n/a	n/a
33	CHD2	chr7:57621489-57621677	K562	blood:	n/a	n/a
34	CHD2	chr7:57708603-57708917	K562	blood:	n/a	n/a
35	CHD2	chr7:57623182-57623237	K562	blood:	n/a	n/a
36	CHD2	chr7:57627096-57627154	K562	blood:	n/a	n/a
37	CHD2	chr7:57628321-57628627	K562	blood:	n/a	n/a
38	CTCF	chr7:57721801-57721856	GM13976	blood:	n/a	n/a
39	CTCF	chr7:57716068-57716335	K562	blood:	n/a	n/a
40	CTCF	chr7:57721795-57721862	LNCaP	prostate:	n/a	n/a
41	CTCF	chr7:57703880-57703942	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:57713331-57713346	K562	blood:	n/a	n/a
43	CTCF	chr7:57625285-57625324	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr7:57624598-57624642	A549	lung:	n/a	n/a
45	CTCF	chr7:57712149-57712164	GM10266	blood:	n/a	n/a
46	CTCF	chr7:57635540-57635545	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr7:57707457-57707520	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:57716100-57716339	K562	blood:	n/a	n/a
49	CTCF	chr7:57723654-57723683	LNCaP	prostate:	n/a	n/a
50	CTCF	chr7:57710833-57711038	K562	blood:	n/a	n/a

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:57707202-57707252	Hepatocyte	liver:	n/a
2	chr7:57712819-57712869	HCF	heart:	n/a
3	chr7:57711394-57711444	GM12892	blood:	n/a
4	chr7:57706707-57706757	HIPEpiC	eye:	n/a
5	chr7:57714756-57714806	HCT-116	colon:	n/a
6	chr7:57710136-57710186	PANC-1	pancreas:	n/a
7	chr7:57707202-57707252	Hepatocyte	liver:	n/a
8	chr7:57712819-57712869	HCF	heart:	n/a
9	chr7:57711394-57711444	GM12892	blood:	n/a
10	chr7:57706707-57706757	HIPEpiC	eye:	n/a
11	chr7:57714756-57714806	HCT-116	colon:	n/a
12	chr7:57710136-57710186	PANC-1	pancreas:	n/a
13	chr7:57688265-57688315	HMEC	breast:	n/a
14	chr7:57706707-57706757	ECC-1	luminal epithelium:	n/a
15	chr7:57688265-57688315	GM12891	blood:	n/a
16	chr7:57710136-57710186	HRPEpiC	eye:	n/a
17	chr7:57706707-57706757	NB4	blood:	n/a
18	chr7:57712819-57712869	AG10803	skin:	n/a
19	chr7:57715021-57715071	LNCaP	prostate:	n/a
20	chr7:57705910-57705960	NH-A	brain:	n/a
21	chr7:57710785-57710835	ECC-1	luminal epithelium:	n/a
22	chr7:57639360-57639410	SK-N-SH	brain:	n/a
23	chr7:57705701-57705751	HRCEpiC	kidney:	n/a
24	chr7:57639360-57639410	GM12891	blood:	n/a
25	chr7:57715021-57715071	GM12892	blood:	n/a
26	chr7:57706707-57706757	GM19239	blood:	n/a
27	chr7:57710252-57710302	ovcar-3	ovarian:	n/a
28	chr7:57639299-57639349	HRPEpiC	eye:	n/a
29	chr7:57639299-57639349	HRE	kidney:	n/a
30	chr7:57714756-57714806	T-47D	breast:	n/a
31	chr7:57714756-57714806	AG04450	lung:	fetal
32	chr7:57714270-57714320	AG04449	skin:	fetal
33	chr7:57710252-57710302	SK-N-MC	brain:	n/a
34	chr7:57714756-57714806	NT2-D1	testis:	n/a
35	chr7:57710252-57710302	HCPEpiC	choroid plexus:	n/a
36	chr7:57714385-57714435	GM12891	blood:	n/a
37	chr7:57712753-57712803	PANC-1	pancreas:	n/a
38	chr7:57714385-57714435	PANC-1	pancreas:	n/a
39	chr7:57710136-57710186	HAEpiC	amniotic membrane:	n/a
40	chr7:57714270-57714320	MCF10A-Er-Src	breast:	n/a
41	chr7:57713841-57713891	HCPEpiC	choroid plexus:	n/a
42	chr7:57711465-57711515	MCF10A-Er-Src	breast:	n/a
43	chr7:57714385-57714435	LNCaP	prostate:	n/a
44	chr7:57711394-57711444	GM12878	blood:	n/a
45	chr7:57705910-57705960	AG09319	gingival:	n/a
46	chr7:57710136-57710186	HL-60	blood:	n/a
47	chr7:57707202-57707252	BJ	skin:	n/a
48	chr7:57688265-57688315	SK-N-SH	brain:	n/a
49	chr7:57639360-57639410	HRPEpiC	eye:	n/a
50	chr7:57712753-57712803	SK-N-MC	brain:	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	chr20:26130778..26134198-chr7:57619861..57623955,5	K562	blood:
3	chr4:33836938..33837728-chr7:57607899..57608399,2	K562	blood:
4	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF479-8	chr7:57689759-57689983	NONHSAT120847
2	lnc-ZNF479-8	chr7:57688668-57688812	NONHSAT120848
3	lnc-ZNF479-8	chr7:57696818-57696916	NONHSAT120847
4	lnc-ZNF479-8	chr7:57703900-57703975	NONHSAT120850
5	lnc-ZNF479-8	chr7:57696817-57696916	NONHSAT120850
6	lnc-ZNF479-8	chr7:57704747-57704895	NONHSAT120850
7	lnc-ZNF479-8	chr7:57688185-57688268	NONHSAT120847
8	lnc-ZNF479-8	chr7:57701610-57701660	NONHSAT120847
9	lnc-ZNF479-8	chr7:57689759-57689961	NONHSAT120848
10	lnc-ZNF479-8	chr7:57696817-57696917	NONHSAT120848
11	lnc-ZNF479-8	chr7:57703364-57703554	NONHSAT120850
12	lnc-ZNF716-7	chr7:57710227-57710560	NONHSAT120861
13	lnc-ZNF479-8	chr7:57689787-57689961	NONHSAT120850

No data

Variant related genes	Relation type
ENSG00000270749	TF binding region
ENSG00000233962	TF binding region
ENSG00000237639	TF binding region
ENSG00000234085	TF binding region
ENSG00000243981	TF binding region
ENSG00000236261	TF binding region
NCOR1P3	TF binding region
ENSG00000229627	TF binding region
ENSG00000230796	TF binding region
ENSG00000270749	CpG island
ENSG00000233962	CpG island
ENSG00000237639	CpG island
ENSG00000234085	CpG island
ENSG00000243981	CpG island
ENSG00000236261	CpG island
NCOR1P3	CpG island
ENSG00000229627	CpG island
ENSG00000230796	CpG island

Extended variants
information (count: 2699 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2699 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527564180	chr7:57607000-57607001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552079565	chr7:57607002-57607003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77952556	chr7:57607013-57607014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34596597	chr7:57607015-57607016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139007676	chr7:57607025-57607026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78778977	chr7:57607067-57607068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115148090	chr7:57607100-57607101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570433357	chr7:57607101-57607102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571725794	chr7:57607112-57607113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138719621	chr7:57607114-57607115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150591868	chr7:57607116-57607117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143712805	chr7:57607118-57607119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141121652	chr7:57607119-57607120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372800385	chr7:57607121-57607122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75186479	chr7:57607123-57607124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73349785	chr7:57607158-57607159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537617406	chr7:57607162-57607163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73700444	chr7:57607183-57607184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79131912	chr7:57607202-57607203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200010019	chr7:57607208-57607209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75351867	chr7:57607209-57607210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144365209	chr7:57607223-57607224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs80009930	chr7:57607235-57607236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111254153	chr7:57607238-57607239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376474223	chr7:57607239-57607240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199518821	chr7:57607261-57607262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112718628	chr7:57607267-57607268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184845723	chr7:57607273-57607274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78556904	chr7:57607280-57607281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74948550	chr7:57607282-57607283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76043679	chr7:57607304-57607305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534485186	chr7:57607325-57607326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73349790	chr7:57607332-57607333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559267867	chr7:57607337-57607338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75799464	chr7:57607348-57607349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146364005	chr7:57607350-57607351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375892731	chr7:57607352-57607353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370803819	chr7:57607356-57607357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201619833	chr7:57607357-57607358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75037240	chr7:57607368-57607369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544768516	chr7:57607376-57607377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs202195888	chr7:57607382-57607383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563122032	chr7:57607400-57607401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79370426	chr7:57607413-57607414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574465239	chr7:57607417-57607418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541591583	chr7:57607426-57607427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9918637	chr7:57607429-57607430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148385056	chr7:57607440-57607441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560069792	chr7:57607448-57607449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9918638	chr7:57607460-57607461	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:57607000-57607800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr7:57609200-57610400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr7:57609600-57610000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr7:57612400-57613200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr7:57612400-57613400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr7:57612800-57613200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr7:57613000-57613200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:57624200-57625000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:57639200-57641400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:57656400-57657200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:57695600-57695800	Enhancers	Spleen	Spleen
12	chr7:57696400-57696600	ZNF genes & repeats	Fetal Kidney	kidney
13	chr7:57697800-57698800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr7:57697800-57698800	ZNF genes & repeats	Adipose Nuclei	Adipose
15	chr7:57697800-57699000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
16	chr7:57697800-57699400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr7:57698000-57698600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:57698000-57698800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:57698000-57698800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:57698000-57698800	ZNF genes & repeats	Esophagus	oesophagus
21	chr7:57698000-57698800	ZNF genes & repeats	Gastric	stomach
22	chr7:57698000-57698800	ZNF genes & repeats	Pancreas	Pancrea
23	chr7:57698000-57699400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
24	chr7:57698200-57698800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:57698400-57698800	ZNF genes & repeats	Fetal Stomach	stomach
26	chr7:57698400-57699000	ZNF genes & repeats	Brain Anterior Caudate	brain
27	chr7:57698600-57698800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
28	chr7:57698800-57701200	Weak transcription	Gastric	stomach
29	chr7:57698800-57701200	Weak transcription	Pancreas	Pancrea
30	chr7:57699000-57701400	Weak transcription	Brain Anterior Caudate	brain
31	chr7:57701200-57701600	Active TSS	Primary T cells from cord blood	blood
32	chr7:57701200-57701800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
33	chr7:57701200-57701800	ZNF genes & repeats	Fetal Brain Male	brain
34	chr7:57701200-57701800	ZNF genes & repeats	Gastric	stomach
35	chr7:57701200-57701800	ZNF genes & repeats	Pancreas	Pancrea
36	chr7:57701200-57704000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr7:57701400-57701600	ZNF genes & repeats	Fetal Heart	heart
38	chr7:57701400-57701800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:57701400-57701800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr7:57701400-57701800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:57701400-57701800	ZNF genes & repeats	Brain Anterior Caudate	brain
42	chr7:57701400-57701800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
43	chr7:57701400-57702000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:57701600-57701800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
45	chr7:57701600-57701800	ZNF genes & repeats	Colonic Mucosa	Colon
46	chr7:57701800-57703000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:57703000-57703800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:57705600-57707000	Active TSS	K562	blood
49	chr7:57705800-57710200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr7:57705800-57716600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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