Variant report

Variant	esv2762681
Chromosome Location	chr7:78958864-78982993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:78976025-78976341	GM12878	blood:	n/a	n/a
2	BCL3	chr7:78972497-78972744	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:78968559-78968876	IMR90	lung:	n/a	chr7:78968705-78968716
4	CEBPB	chr7:78968554-78968857	K562	blood:	n/a	chr7:78968705-78968716
5	CEBPB	chr7:78968526-78968882	HepG2	liver:	n/a	chr7:78968705-78968716
6	CEBPB	chr7:78964163-78964494	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:78961531-78961792	HepG2	liver:	n/a	chr7:78961647-78961656 chr7:78961645-78961658 chr7:78961647-78961656 chr7:78961647-78961656
8	CEBPB	chr7:78968570-78968844	A549	lung:	n/a	chr7:78968705-78968716
9	CTCF	chr7:78971386-78971396	LNCaP	prostate:	n/a	n/a
10	CTCF	chr7:78971313-78971422	SK-N-SH_RA	brain:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
11	CTCF	chr7:78969540-78969690	AG09319	gingival:	n/a	n/a
12	CTCF	chr7:78981440-78981590	HPF	lung:	n/a	n/a
13	CTCF	chr7:78971311-78971473	HepG2	liver:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
14	CTCF	chr7:78959605-78959617	GM20000	blood:	n/a	n/a
15	CTCF	chr7:78971460-78971610	BE2_C	brain:	n/a	n/a
16	CTCF	chr7:78971380-78971530	HMEC	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
17	CTCF	chr7:78971100-78971250	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr7:78971304-78971463	MCF-7	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
19	CTCF	chr7:78971278-78971461	HepG2	liver:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
20	CTCF	chr7:78971383-78971404	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr7:78971260-78971410	BE2_C	brain:	n/a	chr7:78971394-78971410
22	CTCF	chr7:78971020-78971170	BE2_C	brain:	n/a	n/a
23	CTCF	chr7:78971380-78971530	HFF	foreskin:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
24	CTCF	chr7:78971320-78971470	MCF-7	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
25	CTCF	chr7:78971340-78971490	HRE	kidney:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
26	CTCF	chr7:78971200-78971490	HVMF	connective:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
27	CTCF	chr7:78971260-78971410	SAEC	small airway:	n/a	chr7:78971394-78971410
28	CTCF	chr7:78971280-78971430	Caco-2	colon:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
29	CTCF	chr7:78970760-78970910	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr7:78971280-78971430	A549	lung:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
31	CTCF	chr7:78971362-78971440	A549	lung:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
32	CTCF	chr7:78971320-78971470	Caco-2	colon:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
33	CTCF	chr7:78971320-78971470	NHEK	skin:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
34	CTCF	chr7:78971300-78971450	MCF-7	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
35	CTCF	chr7:78971372-78971422	Hela-S3	cervix:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
36	CTCF	chr7:78971300-78971450	HRPEpiC	eye:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
37	CTCF	chr7:78971155-78971622	MCF-7	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
38	CTCF	chr7:78971020-78971170	SAEC	small airway:	n/a	n/a
39	CTCF	chr7:78971286-78971494	MCF-7	breast:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
40	CTCF	chr7:78971320-78971470	HepG2	liver:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
41	CTCF	chr7:78971340-78971490	BE2_C	brain:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
42	CTCF	chr7:78971238-78971458	A549	lung:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
43	CTCF	chr7:78971260-78971410	HA-sp	spinal cord:	n/a	chr7:78971394-78971410
44	CTCF	chr7:78971303-78971359	Gliobla	brain:	n/a	n/a
45	CTCF	chr7:78971280-78971430	HBMEC	blood vessel:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
46	CTCF	chr7:78971300-78971450	HCPEpiC	choroid plexus:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
47	CTCF	chr7:78971365-78971455	HUVEC	blood vessel:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
48	CTCF	chr7:78971320-78971470	HCPEpiC	choroid plexus:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
49	CTCF	chr7:78971280-78971430	RPTEC	kidney:	n/a	chr7:78971395-78971416 chr7:78971394-78971410
50	E2F4	chr7:78961504-78961721	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78982418-78982468	ProgFib	skin:	n/a
2	chr7:78982418-78982468	GM12878	blood:	n/a
3	chr7:78982418-78982468	K562	blood:	n/a
4	chr7:78982418-78982468	ECC-1	luminal epithelium:	n/a
5	chr7:78982418-78982468	SAEC	small airway:	n/a
6	chr7:78982418-78982468	PrEC	prostate:	n/a
7	chr7:78982418-78982468	AG10803	skin:	n/a
8	chr7:78982418-78982468	HCPEpiC	choroid plexus:	n/a
9	chr7:78982418-78982468	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:78982418-78982468	HNPCEpiC	eye:	n/a
11	chr7:78982418-78982468	AG04450	lung:	fetal
12	chr7:78982418-78982468	HL-60	blood:	n/a
13	chr7:78982418-78982468	AG09319	gingival:	n/a
14	chr7:78982418-78982468	HAEpiC	amniotic membrane:	n/a
15	chr7:78982418-78982468	GM12892	blood:	n/a
16	chr7:78982418-78982468	Jurkat	blood:	n/a
17	chr7:78982418-78982468	HIPEpiC	eye:	n/a
18	chr7:78982418-78982468	GM19239	blood:	n/a
19	chr7:78982418-78982468	U87	brain:	n/a
20	chr7:78982418-78982468	Hela-S3	cervix:	n/a
21	chr7:78982418-78982468	HUVEC	blood vessel:	n/a
22	chr7:78982418-78982468	BJ	skin:	n/a
23	chr7:78982418-78982468	HMEC	breast:	n/a
24	chr7:78982418-78982468	HRPEpiC	eye:	n/a
25	chr7:78982418-78982468	ovcar-3	ovarian:	n/a
26	chr7:78982418-78982468	Caco-2	colon:	n/a
27	chr7:78982418-78982468	PFSK-1	brain:	n/a
28	chr7:78982418-78982468	CMK	blood:	n/a
29	chr7:78982418-78982468	NB4	blood:	n/a
30	chr7:78982418-78982468	LNCaP	prostate:	n/a
31	chr7:78982418-78982468	NHBE	bronchial:	n/a
32	chr7:78982418-78982468	HCM	heart:	n/a
33	chr7:78982418-78982468	T-47D	breast:	n/a
34	chr7:78982418-78982468	PANC-1	pancreas:	n/a
35	chr7:78982418-78982468	SKMC	muscle:	n/a
36	chr7:78982418-78982468	HRCEpiC	kidney:	n/a
37	chr7:78982418-78982468	IMR90	lung:	fetal
38	chr7:78982418-78982468	RPTEC	kidney:	n/a
39	chr7:78982418-78982468	HCT-116	colon:	n/a
40	chr7:78982418-78982468	NH-A	brain:	n/a
41	chr7:78982418-78982468	AG09309	skin:	n/a
42	chr7:78982418-78982468	AG04449	skin:	fetal
43	chr7:78982418-78982468	GM06990	blood:	n/a
44	chr7:78982418-78982468	SK-N-SH	brain:	n/a
45	chr7:78982418-78982468	NT2-D1	testis:	n/a
46	chr7:78982418-78982468	HCF	heart:	n/a
47	chr7:78982418-78982468	A549	lung:	n/a
48	chr7:78982418-78982468	HRE	kidney:	n/a
49	chr7:78982418-78982468	HEK293	kidney:	embryo
50	chr7:78982418-78982468	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:78977361..78978896-chr7:79043903..79046403,2	K562	blood:
2	chr17:34140775..34141275-chr7:78979249..78979789,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-6	chr7:78982726-78983708	NONHSAT121700

Variant related genes	Relation type
ENSG00000222024	TF binding region
RNU6-530P	TF binding region
ENSG00000222024	CpG island
RNU6-530P	CpG island

Extended variants
information (count: 942 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7804010	chr7:78958864-78958865	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180912172	chr7:78958869-78958870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370644452	chr7:78958916-78958917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561775755	chr7:78958949-78958950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185672281	chr7:78958950-78958951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191617183	chr7:78958957-78958958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564383314	chr7:78958965-78958966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532337220	chr7:78958967-78958968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181642681	chr7:78958995-78958996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1881291	chr7:78959009-78959010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565994126	chr7:78959060-78959061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548065534	chr7:78959068-78959069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534948654	chr7:78959072-78959073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368141824	chr7:78959077-78959078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548478869	chr7:78959095-78959096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568107119	chr7:78959102-78959103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536605140	chr7:78959188-78959189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557024617	chr7:78959224-78959225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538150409	chr7:78959276-78959277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561450205	chr7:78959278-78959279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530071842	chr7:78959285-78959286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570425394	chr7:78959325-78959326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1881292	chr7:78959327-78959328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569768628	chr7:78959331-78959332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1881293	chr7:78959363-78959364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573080636	chr7:78959392-78959393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559373339	chr7:78959407-78959408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555631129	chr7:78959474-78959475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146866585	chr7:78959485-78959486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1881294	chr7:78959486-78959487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138778157	chr7:78959497-78959498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544172383	chr7:78959523-78959524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571980020	chr7:78959525-78959526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397832892	chr7:78959528-78959529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71531166	chr7:78959530-78959531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565865596	chr7:78959543-78959544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542378115	chr7:78959572-78959573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559612603	chr7:78959595-78959596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528290452	chr7:78959596-78959597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548516363	chr7:78959612-78959613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568318610	chr7:78959615-78959616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1881296	chr7:78959621-78959622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554836383	chr7:78959643-78959644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570412098	chr7:78959655-78959656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372301352	chr7:78959659-78959660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539187430	chr7:78959666-78959667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34024282	chr7:78959670-78959671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567201256	chr7:78959676-78959677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371471636	chr7:78959702-78959703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529756634	chr7:78959718-78959719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Williams-beuren syndrome	16826523	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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78958800-78959200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:78959200-78963400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:78961400-78962000	Enhancers	NHLF	lung
4	chr7:78961400-78962000	Enhancers	Osteobl	bone
5	chr7:78961600-78961800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:78961600-78962000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:78961600-78962200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:78961800-78969200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:78963400-78963600	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:78963400-78964200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:78963800-78966800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:78964200-78965800	Enhancers	Fetal Heart	heart
13	chr7:78964200-78966000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr7:78965800-78966200	Weak transcription	Fetal Heart	heart
15	chr7:78966000-78967000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:78966200-78967000	Enhancers	Brain Substantia Nigra	brain
17	chr7:78966200-78967200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr7:78966200-78967200	Enhancers	Fetal Heart	heart
19	chr7:78966400-78966800	Enhancers	Brain Hippocampus Middle	brain
20	chr7:78966600-78967000	Enhancers	Brain Angular Gyrus	brain
21	chr7:78966600-78967000	Enhancers	Brain Anterior Caudate	brain
22	chr7:78966600-78967600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:78966600-78967800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:78966800-78967000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:78966800-78967000	Enhancers	Brain Cingulate Gyrus	brain
26	chr7:78966800-78967000	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr7:78966800-78967200	Flanking Active TSS	Brain Hippocampus Middle	brain
28	chr7:78967000-78967200	Enhancers	Adipose Nuclei	Adipose
29	chr7:78967000-78967200	Enhancers	Brain Germinal Matrix	brain
30	chr7:78967000-78967400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:78967000-78967400	Active TSS	Brain Angular Gyrus	brain
32	chr7:78967000-78967400	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr7:78967000-78967400	Flanking Active TSS	Brain Cingulate Gyrus	brain
34	chr7:78967000-78967400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr7:78967000-78967400	Active TSS	Brain Substantia Nigra	brain
36	chr7:78967000-78967400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr7:78967000-78967600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr7:78967000-78967800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:78967200-78967400	Flanking Active TSS	Brain Germinal Matrix	brain
40	chr7:78967200-78967400	Enhancers	HSMMtube	muscle
41	chr7:78967200-78967600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr7:78967200-78967600	Active TSS	Adipose Nuclei	Adipose
43	chr7:78967200-78967600	Active TSS	Brain Hippocampus Middle	brain
44	chr7:78967400-78967600	Enhancers	Brain Cingulate Gyrus	brain
45	chr7:78967400-78967600	Active TSS	Brain Germinal Matrix	brain
46	chr7:78967400-78967600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:78967400-78967800	Enhancers	Brain Angular Gyrus	brain
48	chr7:78967400-78967800	Active TSS	Brain Anterior Caudate	brain
49	chr7:78967400-78967800	Enhancers	Brain Substantia Nigra	brain
50	chr7:78967400-78968200	Enhancers	Brain Inferior Temporal Lobe	brain

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