Variant report

Variant	nsv831040
Chromosome Location	chr7:78623195-78831998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:678)
CpG islands
(count:62)
Chromatin interactive
region (count:12)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:78707803-78707913	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:78762229-78762644	HepG2	liver:	n/a	n/a
3	ATF2	chr7:78811739-78812017	GM12878	blood:	n/a	n/a
4	BACH1	chr7:78681414-78681594	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:78829434-78829686	GM12878	blood:	n/a	chr7:78829545-78829556
6	BATF	chr7:78786666-78786840	GM12878	blood:	n/a	chr7:78786772-78786783
7	BCL3	chr7:78638128-78638397	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:78760331-78760351	K562	blood:	n/a	n/a
9	CEBPB	chr7:78742365-78742521	A549	lung:	n/a	n/a
10	CEBPB	chr7:78675382-78675700	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:78675426-78675675	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:78685304-78685681	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr7:78720984-78721279	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:78709067-78709249	HepG2	liver:	n/a	chr7:78709184-78709195 chr7:78709159-78709170 chr7:78709160-78709171
15	CEBPB	chr7:78779117-78779451	IMR90	lung:	n/a	chr7:78779254-78779267 chr7:78779255-78779266
16	CEBPB	chr7:78749308-78749532	HepG2	liver:	n/a	chr7:78749420-78749431
17	CEBPB	chr7:78795795-78796005	HepG2	liver:	n/a	chr7:78795855-78795866
18	CEBPB	chr7:78779268-78779306	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:78760964-78760975	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:78693550-78693854	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:78795739-78796011	A549	lung:	n/a	chr7:78795855-78795866
22	CEBPB	chr7:78742297-78742596	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:78795756-78796013	IMR90	lung:	n/a	chr7:78795855-78795866
24	CEBPB	chr7:78762121-78762404	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:78675401-78675634	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr7:78749262-78749574	IMR90	lung:	n/a	chr7:78749420-78749431
27	CEBPB	chr7:78720957-78721319	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:78828383-78829263	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:78660521-78660831	IMR90	lung:	n/a	chr7:78660683-78660694
30	CEBPB	chr7:78829526-78830144	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:78660536-78660843	HepG2	liver:	n/a	chr7:78660683-78660694
32	CEBPB	chr7:78701651-78701829	HepG2	liver:	n/a	chr7:78701714-78701725 chr7:78701691-78701703
33	CHD1	chr7:78806206-78806356	GM12878	blood:	n/a	n/a
34	CTCF	chr7:78692700-78692850	GM12866	blood:	n/a	chr7:78692808-78692817
35	CTCF	chr7:78806023-78806750	A549	lung:	n/a	n/a
36	CTCF	chr7:78806380-78806530	K562	blood:	n/a	n/a
37	CTCF	chr7:78806267-78806473	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:78692760-78692910	HFF	foreskin:	n/a	chr7:78692808-78692817
39	CTCF	chr7:78692620-78692770	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:78806280-78806430	GM12871	blood:	n/a	n/a
41	CTCF	chr7:78692880-78693030	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:78692700-78692850	GM12865	blood:	n/a	chr7:78692808-78692817
43	CTCF	chr7:78806240-78806390	GM12865	blood:	n/a	n/a
44	CTCF	chr7:78806300-78806450	HAc	cerebellar:	n/a	n/a
45	CTCF	chr7:78806295-78806447	A549	lung:	n/a	n/a
46	CTCF	chr7:78806260-78806410	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr7:78648577-78648640	GM13977	blood:	n/a	n/a
48	CTCF	chr7:78806320-78806470	GM12872	blood:	n/a	n/a
49	CTCF	chr7:78692740-78692890	NB4	blood:	n/a	chr7:78692808-78692817
50	CTCF	chr7:78806101-78806566	MCF-7	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78659337-78659387	CMK	blood:	n/a
2	chr7:78659337-78659387	CMK	blood:	n/a
3	chr7:78659337-78659387	HEEpiC	esophagus:	n/a
4	chr7:78659337-78659387	AG10803	skin:	n/a
5	chr7:78659337-78659387	HEK293	kidney:	embryo
6	chr7:78659337-78659387	Jurkat	blood:	n/a
7	chr7:78659337-78659387	HRPEpiC	eye:	n/a
8	chr7:78659337-78659387	ECC-1	luminal epithelium:	n/a
9	chr7:78659337-78659387	HCF	heart:	n/a
10	chr7:78659337-78659387	SKMC	muscle:	n/a
11	chr7:78659337-78659387	HCM	heart:	n/a
12	chr7:78659337-78659387	NHBE	bronchial:	n/a
13	chr7:78659337-78659387	HL-60	blood:	n/a
14	chr7:78659337-78659387	Caco-2	colon:	n/a
15	chr7:78659337-78659387	NH-A	brain:	n/a
16	chr7:78659337-78659387	NB4	blood:	n/a
17	chr7:78659337-78659387	MCF10A-Er-Src	breast:	n/a
18	chr7:78659337-78659387	Hepatocyte	liver:	n/a
19	chr7:78659337-78659387	SAEC	small airway:	n/a
20	chr7:78659337-78659387	GM19239	blood:	n/a
21	chr7:78659337-78659387	GM06990	blood:	n/a
22	chr7:78659337-78659387	HCT-116	colon:	n/a
23	chr7:78659337-78659387	BE2_C	brain:	n/a
24	chr7:78659337-78659387	AG09319	gingival:	n/a
25	chr7:78659337-78659387	IMR90	lung:	fetal
26	chr7:78659337-78659387	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:78659337-78659387	SK-N-MC	brain:	n/a
28	chr7:78659337-78659387	A549	lung:	n/a
29	chr7:78659337-78659387	AG04449	skin:	fetal
30	chr7:78659337-78659387	HRE	kidney:	n/a
31	chr7:78659337-78659387	AG04450	lung:	fetal
32	chr7:78659337-78659387	PANC-1	pancreas:	n/a
33	chr7:78659337-78659387	Hela-S3	cervix:	n/a
34	chr7:78659337-78659387	HIPEpiC	eye:	n/a
35	chr7:78659337-78659387	GM12878	blood:	n/a
36	chr7:78659337-78659387	GM12892	blood:	n/a
37	chr7:78659337-78659387	SK-N-SH	brain:	n/a
38	chr7:78659337-78659387	HCPEpiC	choroid plexus:	n/a
39	chr7:78659337-78659387	SK-N-SH_RA	brain:	n/a
40	chr7:78659337-78659387	H1-hESC	embryonic stem cell:	embryo
41	chr7:78659337-78659387	RPTEC	kidney:	n/a
42	chr7:78659337-78659387	HAEpiC	amniotic membrane:	n/a
43	chr7:78659337-78659387	BJ	skin:	n/a
44	chr7:78659337-78659387	NHDF-neo	bronchial:	n/a
45	chr7:78659337-78659387	T-47D	breast:	n/a
46	chr7:78659337-78659387	HNPCEpiC	eye:	n/a
47	chr7:78659337-78659387	PrEC	prostate:	n/a
48	chr7:78659337-78659387	U87	brain:	n/a
49	chr7:78659337-78659387	NT2-D1	testis:	n/a
50	chr7:78659337-78659387	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:78776964..78780681-chr7:78782955..78785203,3	K562	blood:
2	chr7:78749811..78752141-chr7:78766151..78767665,2	MCF-7	breast:
3	chr7:78654781..78656773-chr7:78658469..78660779,2	K562	blood:
4	chr7:78749811..78752141-chr7:78766151..78767665,2	MCF-7	breast:
5	chr7:78656805..78659401-chr7:78662080..78664588,2	K562	blood:
6	chr7:78677390..78680466-chr7:78680728..78684116,3	K562	blood:
7	chr7:78677390..78680466-chr7:78680728..78684116,3	K562	blood:
8	chr7:78680321..78683272-chr7:78686502..78688648,2	MCF-7	breast:
9	chr7:78776964..78780681-chr7:78782955..78785203,3	K562	blood:
10	chr7:78218746..78219372-chr7:78805948..78806448,2	MCF-7	breast:
11	chr7:78680321..78683272-chr7:78686502..78688648,2	MCF-7	breast:
12	chr7:78656805..78659401-chr7:78662080..78664588,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHTF2-3	chr7:78638304-78638440	ENSG00000226978.1
2	lnc-PHTF2-3	chr7:78641400-78641593	ENSG00000226978.1
3	lnc-TMEM60-2	chr7:78629521-78629614	ENSG00000235751.3
4	lnc-PHTF2-3	chr7:78640243-78640387	ENSG00000226978.1
5	lnc-GNAI1-8	chr7:78754055-78755066	NONHSAT121697
6	lnc-GNAT3-8	chr7:78802389-78804340	NONHSAT121698

No data

Variant related genes	Relation type
MAGI2-AS2	TF binding region
RNU6-337P	TF binding region
MAGI2-IT1	TF binding region
ENSG00000229110	TF binding region
MAGI2-AS2	CpG island
RNU6-337P	CpG island
MAGI2-IT1	CpG island
ENSG00000229110	CpG island
ENSG00000212545	chromatin interactions

Extended variants
information (count: 5269 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5269 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577154511	chr7:78623261-78623262	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs545919020	chr7:78623270-78623271	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs186750159	chr7:78623276-78623277	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs191616091	chr7:78623306-78623307	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540793153	chr7:78623309-78623310	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140189270	chr7:78623317-78623318	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529874313	chr7:78623327-78623328	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs550031731	chr7:78623364-78623365	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184133741	chr7:78623374-78623375	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs143770458	chr7:78623420-78623421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145801841	chr7:78623421-78623422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs727652	chr7:78623437-78623438	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs534725357	chr7:78623459-78623460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556404701	chr7:78623502-78623503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555175288	chr7:78623590-78623591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113510497	chr7:78623601-78623602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537281818	chr7:78623614-78623615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188925759	chr7:78623630-78623631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs193158553	chr7:78623638-78623639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554556932	chr7:78623652-78623653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148568990	chr7:78623654-78623655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539779582	chr7:78623763-78623764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142558442	chr7:78623802-78623803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150970265	chr7:78623803-78623804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185407594	chr7:78623814-78623815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561879203	chr7:78623838-78623839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190704536	chr7:78623909-78623910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371614436	chr7:78623937-78623938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375340519	chr7:78623942-78623943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543296721	chr7:78623950-78623951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543708118	chr7:78623953-78623954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563549154	chr7:78623962-78623963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532316973	chr7:78623998-78623999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552170774	chr7:78624061-78624062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141916063	chr7:78624087-78624088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10485922	chr7:78624119-78624120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs180770357	chr7:78624123-78624124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568103902	chr7:78624143-78624144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371272998	chr7:78624148-78624149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145779769	chr7:78624153-78624154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372649725	chr7:78624164-78624165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375091564	chr7:78624181-78624182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147841873	chr7:78624194-78624195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141464345	chr7:78624213-78624214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577684588	chr7:78624247-78624248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544655835	chr7:78624295-78624296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376655501	chr7:78624327-78624328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553278625	chr7:78624335-78624336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150384491	chr7:78624342-78624343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535496154	chr7:78624393-78624394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Williams-beuren syndrome	16826523	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78614000-78632400	Weak transcription	Aorta	Aorta
2	chr7:78622800-78623400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:78622800-78623600	Enhancers	Brain Anterior Caudate	brain
4	chr7:78622800-78623600	Enhancers	Fetal Kidney	kidney
5	chr7:78622800-78624000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:78622800-78624000	Enhancers	Brain Substantia Nigra	brain
7	chr7:78623000-78624000	Enhancers	Brain Hippocampus Middle	brain
8	chr7:78623200-78624000	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr7:78623400-78623800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:78623400-78623800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:78623800-78628800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:78624000-78637600	Weak transcription	Brain Substantia Nigra	brain
13	chr7:78628800-78629000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:78629000-78629600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:78632400-78632600	ZNF genes & repeats	Aorta	Aorta
16	chr7:78632600-78648800	Weak transcription	Aorta	Aorta
17	chr7:78635800-78636000	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:78636000-78638000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:78637400-78638000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:78637600-78639000	Enhancers	Brain Hippocampus Middle	brain
21	chr7:78637600-78639200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr7:78637600-78639200	Enhancers	Brain Substantia Nigra	brain
23	chr7:78637600-78639400	Enhancers	Brain Angular Gyrus	brain
24	chr7:78637800-78638400	Enhancers	Brain Anterior Caudate	brain
25	chr7:78638000-78638400	Enhancers	Brain Cingulate Gyrus	brain
26	chr7:78645400-78645800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr7:78645400-78645800	Enhancers	Brain Cingulate Gyrus	brain
28	chr7:78645600-78646400	ZNF genes & repeats	Pancreas	Pancrea
29	chr7:78645800-78646000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:78645800-78646400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:78645800-78646600	Enhancers	Lung	lung
32	chr7:78645800-78646800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:78646200-78646600	Enhancers	Brain Angular Gyrus	brain
34	chr7:78646800-78650200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:78648800-78649200	ZNF genes & repeats	Aorta	Aorta
36	chr7:78650200-78650600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:78665400-78667000	Enhancers	Fetal Lung	lung
38	chr7:78665400-78667400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:78665800-78666400	Enhancers	Colon Smooth Muscle	Colon
40	chr7:78666600-78667000	Enhancers	Brain Angular Gyrus	brain
41	chr7:78677200-78677600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr7:78677400-78677800	Enhancers	Fetal Kidney	kidney
43	chr7:78677600-78679400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr7:78677800-78683800	Weak transcription	Fetal Kidney	kidney
45	chr7:78678600-78679000	Enhancers	Brain Germinal Matrix	brain
46	chr7:78679000-78679400	Weak transcription	Brain Germinal Matrix	brain
47	chr7:78679400-78679800	Enhancers	Brain Angular Gyrus	brain
48	chr7:78679400-78679800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr7:78679400-78680200	Enhancers	Brain Anterior Caudate	brain
50	chr7:78679400-78680200	Enhancers	Brain Germinal Matrix	brain

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