Variant report

Variant	nsv1017023
Chromosome Location	chr7:63891057-63937574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:428)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:63895222-63895430	K562	blood:	n/a	n/a
2	BACH1	chr7:63908265-63908542	K562	blood:	n/a	n/a
3	BACH1	chr7:63906115-63906206	K562	blood:	n/a	n/a
4	CBX3	chr7:63923957-63924388	K562	blood:	n/a	n/a
5	CEBPB	chr7:63899989-63900264	K562	blood:	n/a	n/a
6	CEBPB	chr7:63895134-63895460	K562	blood:	n/a	n/a
7	CEBPB	chr7:63924078-63924266	K562	blood:	n/a	n/a
8	CEBPB	chr7:63931329-63931627	HepG2	liver:	n/a	chr7:63931445-63931456 chr7:63931431-63931442
9	CEBPB	chr7:63900689-63900889	K562	blood:	n/a	chr7:63900720-63900731
10	CEBPB	chr7:63893214-63893408	K562	blood:	n/a	n/a
11	CEBPB	chr7:63893954-63894224	K562	blood:	n/a	n/a
12	CEBPB	chr7:63900653-63900841	HepG2	liver:	n/a	chr7:63900720-63900731
13	CEBPB	chr7:63923072-63923124	K562	blood:	n/a	n/a
14	CEBPB	chr7:63895212-63895422	K562	blood:	n/a	n/a
15	CEBPB	chr7:63895164-63895722	K562	blood:	n/a	chr7:63895504-63895517
16	CHD2	chr7:63923989-63924298	K562	blood:	n/a	n/a
17	CHD2	chr7:63924501-63924735	K562	blood:	n/a	n/a
18	CTCF	chr7:63911356-63911446	GM20000	blood:	n/a	n/a
19	CTCF	chr7:63895220-63895370	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:63920200-63920350	A549	lung:	n/a	n/a
21	CTCF	chr7:63895275-63895389	K562	blood:	n/a	n/a
22	CTCF	chr7:63905835-63905898	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr7:63893980-63894130	GM12866	blood:	n/a	n/a
24	CTCF	chr7:63895222-63895497	K562	blood:	n/a	n/a
25	CTCF	chr7:63924520-63924670	SK-N-SH_RA	brain:	n/a	chr7:63924561-63924582 chr7:63924559-63924577
26	CTCF	chr7:63895232-63895445	GM12878	blood:	n/a	n/a
27	CTCF	chr7:63895312-63895386	LNCaP	prostate:	n/a	n/a
28	CTCF	chr7:63924560-63924710	SK-N-SH_RA	brain:	n/a	chr7:63924561-63924582
29	CUX1	chr7:63922247-63922322	K562	blood:	n/a	n/a
30	E2F6	chr7:63923924-63924181	K562	blood:	n/a	n/a
31	E2F6	chr7:63923951-63924211	K562	blood:	n/a	n/a
32	EGR1	chr7:63893979-63894182	K562	blood:	n/a	n/a
33	EGR1	chr7:63924039-63924277	K562	blood:	n/a	n/a
34	EGR1	chr7:63894006-63894220	K562	blood:	n/a	chr7:63894194-63894204
35	EGR1	chr7:63924035-63924204	K562	blood:	n/a	n/a
36	ELF1	chr7:63923847-63924514	SK-N-SH	brain:	n/a	chr7:63924220-63924231 chr7:63924456-63924468 chr7:63924221-63924230
37	ELF1	chr7:63923909-63924440	K562	blood:	n/a	chr7:63924220-63924231 chr7:63924221-63924230
38	ELF1	chr7:63923943-63924396	GM12878	blood:	n/a	chr7:63924220-63924231 chr7:63924221-63924230
39	ELF1	chr7:63923979-63924481	SK-N-SH	brain:	n/a	chr7:63924220-63924231 chr7:63924456-63924468 chr7:63924221-63924230
40	ELF1	chr7:63923929-63924365	K562	blood:	n/a	chr7:63924220-63924231 chr7:63924221-63924230
41	EP300	chr7:63920176-63920373	GM12878	blood:	n/a	n/a
42	ESR1	chr7:63920238-63920503	T-47D	breast:	n/a	n/a
43	ESR1	chr7:63920218-63920664	T-47D	breast:	n/a	n/a
44	FOS	chr7:63924002-63924345	K562	blood:	n/a	n/a
45	FOXA1	chr7:63920262-63920494	T-47D	breast:	n/a	n/a
46	FOXA1	chr7:63920221-63920647	HepG2	liver:	n/a	n/a
47	GABPA	chr7:63923940-63924485	K562	blood:	n/a	n/a
48	GABPA	chr7:63924064-63924310	K562	blood:	n/a	n/a
49	GATA3	chr7:63919957-63920369	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr7:63926959-63927159	SH-SY5Y	brain:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:63924407-63924457	MCF-7	breast:	n/a
2	chr7:63924407-63924457	MCF-7	breast:	n/a
3	chr7:63924733-63924783	AG10803	skin:	n/a
4	chr7:63893881-63893931	PANC-1	pancreas:	n/a
5	chr7:63893895-63893945	HCM	heart:	n/a
6	chr7:63925298-63925348	H1-hESC	embryonic stem cell:	embryo
7	chr7:63924280-63924330	NHDF-neo	bronchial:	n/a
8	chr7:63894251-63894301	SAEC	small airway:	n/a
9	chr7:63925298-63925348	SK-N-MC	brain:	n/a
10	chr7:63924733-63924783	HCT-116	colon:	n/a
11	chr7:63893895-63893945	U87	brain:	n/a
12	chr7:63924733-63924783	Hepatocyte	liver:	n/a
13	chr7:63893881-63893931	T-47D	breast:	n/a
14	chr7:63924733-63924783	NHDF-neo	bronchial:	n/a
15	chr7:63894251-63894301	IMR90	lung:	fetal
16	chr7:63893881-63893931	ovcar-3	ovarian:	n/a
17	chr7:63893881-63893931	GM12892	blood:	n/a
18	chr7:63924407-63924457	AG09309	skin:	n/a
19	chr7:63893881-63893931	GM06990	blood:	n/a
20	chr7:63893895-63893945	T-47D	breast:	n/a
21	chr7:63893895-63893945	NHBE	bronchial:	n/a
22	chr7:63924280-63924330	RPTEC	kidney:	n/a
23	chr7:63893881-63893931	SAEC	small airway:	n/a
24	chr7:63893895-63893945	HRE	kidney:	n/a
25	chr7:63893895-63893945	HEEpiC	esophagus:	n/a
26	chr7:63893881-63893931	NH-A	brain:	n/a
27	chr7:63894251-63894301	HRPEpiC	eye:	n/a
28	chr7:63893881-63893931	HUVEC	blood vessel:	n/a
29	chr7:63924280-63924330	HMEC	breast:	n/a
30	chr7:63893895-63893945	HMEC	breast:	n/a
31	chr7:63924733-63924783	PFSK-1	brain:	n/a
32	chr7:63894251-63894301	ProgFib	skin:	n/a
33	chr7:63924733-63924783	SKMC	muscle:	n/a
34	chr7:63893881-63893931	AG09319	gingival:	n/a
35	chr7:63924280-63924330	PrEC	prostate:	n/a
36	chr7:63925298-63925348	MCF10A-Er-Src	breast:	n/a
37	chr7:63924280-63924330	HRE	kidney:	n/a
38	chr7:63893895-63893945	CMK	blood:	n/a
39	chr7:63893895-63893945	AG04449	skin:	fetal
40	chr7:63894251-63894301	HNPCEpiC	eye:	n/a
41	chr7:63925298-63925348	GM12878	blood:	n/a
42	chr7:63893881-63893931	HMEC	breast:	n/a
43	chr7:63924733-63924783	HCM	heart:	n/a
44	chr7:63925298-63925348	Caco-2	colon:	n/a
45	chr7:63893895-63893945	HNPCEpiC	eye:	n/a
46	chr7:63924733-63924783	GM12878	blood:	n/a
47	chr7:63925298-63925348	SKMC	muscle:	n/a
48	chr7:63924733-63924783	HCPEpiC	choroid plexus:	n/a
49	chr7:63893895-63893945	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:63893895-63893945	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:63901206..63903740-chr7:63907756..63910733,2	K562	blood:
2	chr7:63924988..63927243-chr7:63941510..63943605,2	K562	blood:
3	chr7:63924927..63926790-chr7:63928441..63929985,2	K562	blood:
4	chr7:63901206..63903740-chr7:63907756..63910733,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF680-13	chr7:63904180-63905120	NONHSAT121015

No data

Variant related genes	Relation type
ENSG00000228014	TF binding region
VN1R40P	TF binding region
YWHAEP1	TF binding region
ENSG00000228014	CpG island
VN1R40P	CpG island
YWHAEP1	CpG island
ENSG00000228014	chromatin interactions

Extended variants
information (count: 490 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552377491	chr7:63892107-63892108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113723789	chr7:63892151-63892152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs7776866	chr7:63892293-63892294	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs537967944	chr7:63892318-63892319	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs563113971	chr7:63892322-63892323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs75783705	chr7:63892326-63892327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs7800462	chr7:63892413-63892414	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs181412020	chr7:63892497-63892498	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375445607	chr7:63892528-63892529	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568567441	chr7:63893222-63893223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs191859644	chr7:63893252-63893253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs554112300	chr7:63893265-63893266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373073316	chr7:63893375-63893376	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs62461481	chr7:63893378-63893379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs533865356	chr7:63893399-63893400	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185700434	chr7:63893888-63893889	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs35027072	chr7:63893967-63893968	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550079350	chr7:63893974-63893975	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs578154513	chr7:63894012-63894013	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531342138	chr7:63894067-63894068	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547861170	chr7:63894082-63894083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs10258736	chr7:63894089-63894090	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs57810730	chr7:63894090-63894091	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7783150	chr7:63894098-63894099	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs570624949	chr7:63894123-63894124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539634657	chr7:63894149-63894150	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556117413	chr7:63894163-63894164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs535598497	chr7:63895095-63895096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575726160	chr7:63895114-63895115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201066112	chr7:63895115-63895116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528346442	chr7:63895146-63895147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78347641	chr7:63895178-63895179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181461480	chr7:63904180-63904181	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs551387121	chr7:63904196-63904197	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs10267973	chr7:63904201-63904202	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs537386943	chr7:63904251-63904252	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs186420934	chr7:63904269-63904270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs574163136	chr7:63904296-63904297	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs536823447	chr7:63904301-63904302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs13237578	chr7:63904302-63904303	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374938305	chr7:63904342-63904343	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs550447000	chr7:63904369-63904370	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs570523454	chr7:63904383-63904384	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs540753932	chr7:63904423-63904424	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs147055909	chr7:63904434-63904435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs189980175	chr7:63904460-63904461	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs6460156	chr7:63904466-63904467	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs563534298	chr7:63904497-63904498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs182142269	chr7:63904505-63904506	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs566789449	chr7:63904511-63904512	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:63895000-63895200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:63920200-63921000	Active TSS	Ovary	ovary
3	chr7:63921000-63921200	Enhancers	Ovary	ovary
4	chr7:63921200-63923800	Weak transcription	Ovary	ovary
5	chr7:63923400-63923800	Enhancers	K562	blood
6	chr7:63923800-63924000	Weak transcription	K562	blood
7	chr7:63923800-63924600	Active TSS	Primary B cells from cord blood	blood
8	chr7:63923800-63924600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
9	chr7:63923800-63924800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:63923800-63924800	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr7:63923800-63924800	Active TSS	Primary hematopoietic stem cells	blood
12	chr7:63923800-63924800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr7:63923800-63924800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:63923800-63924800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:63923800-63924800	Active TSS	Adipose Nuclei	Adipose
16	chr7:63923800-63924800	Active TSS	Brain Angular Gyrus	brain
17	chr7:63923800-63924800	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr7:63923800-63924800	Active TSS	Colon Smooth Muscle	Colon
19	chr7:63923800-63924800	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr7:63923800-63924800	Active TSS	Ovary	ovary
21	chr7:63923800-63924800	Active TSS	Right Atrium	heart
22	chr7:63923800-63924800	Active TSS	Right Ventricle	heart
23	chr7:63923800-63924800	Active TSS	Skeletal Muscle Male	skeletal muscle
24	chr7:63923800-63924800	Active TSS	Stomach Smooth Muscle	stomach
25	chr7:63923800-63925000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:63923800-63925000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:63924000-63924600	Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr7:63924000-63924600	Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr7:63924000-63924600	Bivalent/Poised TSS	Left Ventricle	heart
30	chr7:63924000-63924600	ZNF genes & repeats	Spleen	Spleen
31	chr7:63924000-63924800	Active TSS	Primary T cells from cord blood	blood
32	chr7:63924000-63924800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:63924000-63924800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:63924000-63924800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:63924000-63924800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:63924000-63924800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:63924000-63924800	Active TSS	Aorta	Aorta
38	chr7:63924000-63924800	Active TSS	Brain Anterior Caudate	brain
39	chr7:63924000-63924800	Active TSS	Brain Cingulate Gyrus	brain
40	chr7:63924000-63924800	ZNF genes & repeats	Brain Germinal Matrix	brain
41	chr7:63924000-63924800	Active TSS	Brain Hippocampus Middle	brain
42	chr7:63924000-63924800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:63924000-63924800	Active TSS	Brain Substantia Nigra	brain
44	chr7:63924000-63924800	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr7:63924000-63924800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
46	chr7:63924000-63924800	Active TSS	Fetal Kidney	kidney
47	chr7:63924000-63924800	ZNF genes & repeats	Gastric	stomach
48	chr7:63924000-63924800	ZNF genes & repeats	Lung	lung
49	chr7:63924000-63924800	ZNF genes & repeats	Pancreas	Pancrea
50	chr7:63924000-63924800	Active TSS	Placenta Amnion	Placenta Amnion

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