Variant report

Variant	nsv831041
Chromosome Location	chr7:78819499-78973222
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	ARID3A	chr7:78937579-78937886	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:78901378-78901750	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:78922900-78923304	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:78846821-78847639	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:78841102-78841331	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:78901558-78901758	K562	blood:	n/a	n/a
7	ATF3	chr7:78922855-78923475	A549	lung:	n/a	n/a
8	ATF3	chr7:78922705-78923470	A549	lung:	n/a	n/a
9	BACH1	chr7:78910738-78911098	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:78910752-78911100	K562	blood:	n/a	n/a
11	BACH1	chr7:78854500-78854508	K562	blood:	n/a	n/a
12	BATF	chr7:78829434-78829686	GM12878	blood:	n/a	chr7:78829545-78829556
13	BCL3	chr7:78922608-78923439	A549	lung:	n/a	n/a
14	BCL3	chr7:78912151-78913001	A549	lung:	n/a	n/a
15	BCL3	chr7:78972497-78972744	GM12878	blood:	n/a	n/a
16	BCL3	chr7:78922698-78923411	A549	lung:	n/a	n/a
17	BHLHE40	chr7:78923013-78923297	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:78927627-78927704	H1-hESC	embryonic stem cell:	n/a	n/a
19	CCNT2	chr7:78877079-78877222	K562	blood:	n/a	n/a
20	CEBPB	chr7:78911787-78912478	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr7:78968570-78968844	A549	lung:	n/a	chr7:78968705-78968716
22	CEBPB	chr7:78911803-78912177	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr7:78911354-78911841	A549	lung:	n/a	n/a
24	CEBPB	chr7:78841068-78841463	Hela-S3	cervix:	n/a	chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281
25	CEBPB	chr7:78865643-78865896	HepG2	liver:	n/a	chr7:78865743-78865754 chr7:78865741-78865752
26	CEBPB	chr7:78841049-78841387	HepG2	liver:	n/a	chr7:78841057-78841068 chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281
27	CEBPB	chr7:78911298-78911784	MCF-7	breast:	n/a	chr7:78911339-78911352
28	CEBPB	chr7:78968554-78968857	K562	blood:	n/a	chr7:78968705-78968716
29	CEBPB	chr7:78926057-78926126	A549	lung:	n/a	n/a
30	CEBPB	chr7:78838557-78838831	IMR90	lung:	n/a	chr7:78838703-78838714
31	CEBPB	chr7:78901567-78901631	A549	lung:	n/a	n/a
32	CEBPB	chr7:78829526-78830144	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:78968559-78968876	IMR90	lung:	n/a	chr7:78968705-78968716
34	CEBPB	chr7:78911356-78911743	A549	lung:	n/a	n/a
35	CEBPB	chr7:78841048-78841478	HepG2	liver:	n/a	chr7:78841057-78841068 chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281
36	CEBPB	chr7:78947055-78947217	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:78937515-78937900	HepG2	liver:	n/a	chr7:78937715-78937726
38	CEBPB	chr7:78911355-78911778	MCF-7	breast:	n/a	n/a
39	CEBPB	chr7:78937637-78937789	HepG2	liver:	n/a	chr7:78937715-78937726
40	CEBPB	chr7:78911393-78911718	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr7:78853481-78853796	A549	lung:	n/a	chr7:78853640-78853653 chr7:78853641-78853652 chr7:78853640-78853653
42	CEBPB	chr7:78961531-78961792	HepG2	liver:	n/a	chr7:78961647-78961656 chr7:78961645-78961658 chr7:78961647-78961656 chr7:78961647-78961656
43	CEBPB	chr7:78853504-78853727	HepG2	liver:	n/a	chr7:78853640-78853653 chr7:78853641-78853652 chr7:78853640-78853653
44	CEBPB	chr7:78923007-78923582	A549	lung:	n/a	n/a
45	CEBPB	chr7:78964163-78964494	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:78923038-78923587	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:78841085-78841453	IMR90	lung:	n/a	chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281
48	CEBPB	chr7:78911250-78911863	A549	lung:	n/a	chr7:78911339-78911352
49	CEBPB	chr7:78841076-78841404	HepG2	liver:	n/a	chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281
50	CEBPB	chr7:78841090-78841355	HepG2	liver:	n/a	chr7:78841270-78841281 chr7:78841268-78841281 chr7:78841268-78841279 chr7:78841268-78841281 chr7:78841265-78841282 chr7:78841270-78841281

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78948064-78948114	SK-N-SH	brain:	n/a
2	chr7:78870151-78870201	HepG2	liver:	n/a
3	chr7:78947094-78947144	ECC-1	luminal epithelium:	n/a
4	chr7:78948064-78948114	HCF	heart:	n/a
5	chr7:78947094-78947144	GM12892	blood:	n/a
6	chr7:78948064-78948114	HUVEC	blood vessel:	n/a
7	chr7:78947094-78947144	HUVEC	blood vessel:	n/a
8	chr7:78948064-78948114	MCF-7	breast:	n/a
9	chr7:78870151-78870201	AG09319	gingival:	n/a
10	chr7:78947094-78947144	HEK293	kidney:	embryo
11	chr7:78947094-78947144	HRCEpiC	kidney:	n/a
12	chr7:78948064-78948114	PANC-1	pancreas:	n/a
13	chr7:78947094-78947144	HRPEpiC	eye:	n/a
14	chr7:78948064-78948114	ProgFib	skin:	n/a
15	chr7:78870151-78870201	GM19239	blood:	n/a
16	chr7:78947094-78947144	PFSK-1	brain:	n/a
17	chr7:78947094-78947144	ProgFib	skin:	n/a
18	chr7:78948064-78948114	GM19239	blood:	n/a
19	chr7:78947094-78947144	GM12891	blood:	n/a
20	chr7:78870151-78870201	MCF10A-Er-Src	breast:	n/a
21	chr7:78947094-78947144	HCF	heart:	n/a
22	chr7:78948064-78948114	HEK293	kidney:	embryo
23	chr7:78870151-78870201	GM12878	blood:	n/a
24	chr7:78948064-78948114	NH-A	brain:	n/a
25	chr7:78870151-78870201	HCPEpiC	choroid plexus:	n/a
26	chr7:78948064-78948114	AoSMC	blood vessel:	n/a
27	chr7:78870151-78870201	SK-N-SH_RA	brain:	n/a
28	chr7:78870151-78870201	ECC-1	luminal epithelium:	n/a
29	chr7:78947094-78947144	GM06990	blood:	n/a
30	chr7:78948064-78948114	HCPEpiC	choroid plexus:	n/a
31	chr7:78947094-78947144	SK-N-SH	brain:	n/a
32	chr7:78947094-78947144	AG10803	skin:	n/a
33	chr7:78948064-78948114	IMR90	lung:	fetal
34	chr7:78948064-78948114	AG04449	skin:	fetal
35	chr7:78870151-78870201	U87	brain:	n/a
36	chr7:78870151-78870201	PFSK-1	brain:	n/a
37	chr7:78870151-78870201	MCF-7	breast:	n/a
38	chr7:78947094-78947144	AG09319	gingival:	n/a
39	chr7:78947094-78947144	CMK	blood:	n/a
40	chr7:78947094-78947144	ovcar-3	ovarian:	n/a
41	chr7:78948064-78948114	HRCEpiC	kidney:	n/a
42	chr7:78948064-78948114	AG04450	lung:	fetal
43	chr7:78870151-78870201	SAEC	small airway:	n/a
44	chr7:78948064-78948114	Caco-2	colon:	n/a
45	chr7:78948064-78948114	T-47D	breast:	n/a
46	chr7:78870151-78870201	ovcar-3	ovarian:	n/a
47	chr7:78948064-78948114	Jurkat	blood:	n/a
48	chr7:78948064-78948114	PrEC	prostate:	n/a
49	chr7:78947094-78947144	HIPEpiC	eye:	n/a
50	chr7:78948064-78948114	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:78901152..78901823-chr7:79676996..79677853,2	MCF-7	breast:
2	chr7:78936738..78938800-chr7:78940617..78942122,2	MCF-7	breast:
3	chr7:78900547..78903338-chr7:78905670..78907338,2	MCF-7	breast:
4	chr7:78900547..78903338-chr7:78905670..78907338,2	MCF-7	breast:
5	chr7:78926978..78927922-chr7:79676854..79677685,3	MCF-7	breast:
6	chr7:78901096..78902018-chr7:79648257..79649001,2	MCF-7	breast:
7	chr7:78936738..78938800-chr7:78940617..78942122,2	MCF-7	breast:
8	chr7:78949110..78950996-chr7:78951230..78952758,2	MCF-7	breast:
9	chr7:78927198..78927954-chr7:79647855..79648713,2	MCF-7	breast:
10	chr7:78927254..78927762-chr7:79370740..79371579,2	MCF-7	breast:
11	chr7:78949110..78950996-chr7:78951230..78952758,2	MCF-7	breast:
12	chr14:28170954..28172471-chr7:78954883..78956578,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-7	chr7:78922138-78922259	ucscGeneNc_uc010lea_1
2	lnc-GNAI1-7	chr7:78921244-78921496	ucscGeneNc_uc010lea_1
3	lnc-GNAI1-7	chr7:78926788-78930237	ucscGeneNc_uc010lea_1
4	lnc-GNAI1-7	chr7:78926099-78926251	ucscGeneNc_uc010lea_1

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

Extended variants
information (count: 4925 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4925 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556523568	chr7:78822201-78822202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4588789	chr7:78822234-78822235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576417347	chr7:78822245-78822246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545541796	chr7:78822305-78822306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150655028	chr7:78822327-78822328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577947230	chr7:78822373-78822374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181496452	chr7:78822417-78822418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370735038	chr7:78822470-78822471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540525565	chr7:78822514-78822515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560235456	chr7:78822553-78822554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376126336	chr7:78822588-78822589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548664186	chr7:78822593-78822594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140150709	chr7:78822613-78822614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184570240	chr7:78822625-78822626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551086549	chr7:78822765-78822766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571490179	chr7:78822876-78822877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368178119	chr7:78822893-78822894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112871342	chr7:78823002-78823003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377152633	chr7:78823046-78823047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548065263	chr7:78823051-78823052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567814683	chr7:78823063-78823064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536960480	chr7:78823088-78823089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556249948	chr7:78823142-78823143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17152044	chr7:78823143-78823144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs189288700	chr7:78823149-78823150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369382271	chr7:78823194-78823195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577910696	chr7:78823227-78823228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540384037	chr7:78823252-78823253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560281553	chr7:78823274-78823275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374334337	chr7:78823275-78823276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375098993	chr7:78823293-78823294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs118076177	chr7:78823295-78823296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573821807	chr7:78823413-78823414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112507161	chr7:78823420-78823421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112585573	chr7:78823455-78823456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79530103	chr7:78823474-78823475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185888647	chr7:78823522-78823523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143252442	chr7:78823538-78823539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527387208	chr7:78823591-78823592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547633733	chr7:78823632-78823633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567863237	chr7:78823704-78823705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189564865	chr7:78823705-78823706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550484964	chr7:78823712-78823713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570057684	chr7:78823734-78823735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112053369	chr7:78823757-78823758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146703025	chr7:78823901-78823902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566140513	chr7:78823971-78823972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577907345	chr7:78823996-78823997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535137172	chr7:78824006-78824007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139223051	chr7:78824071-78824072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78822200-78822800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:78822800-78823200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:78823200-78823400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:78823400-78823800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:78823400-78829000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:78823800-78824200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:78824200-78824800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:78829000-78829400	Enhancers	Osteobl	bone
9	chr7:78829000-78829600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:78829000-78829600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:78829000-78829800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:78829000-78831000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:78829000-78831000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr7:78829200-78829600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:78829200-78829800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr7:78829200-78829800	Enhancers	NHDF-Ad	bronchial
17	chr7:78830200-78830600	Enhancers	Brain Angular Gyrus	brain
18	chr7:78831000-78833400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:78833400-78833800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:78833400-78833800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:78833400-78833800	ZNF genes & repeats	Aorta	Aorta
22	chr7:78840800-78841400	Enhancers	Liver	Liver
23	chr7:78841000-78842400	Enhancers	HepG2	liver
24	chr7:78841400-78841600	Flanking Active TSS	Liver	Liver
25	chr7:78841600-78842200	Enhancers	Liver	Liver
26	chr7:78842200-78847000	Weak transcription	Liver	Liver
27	chr7:78842400-78845400	Weak transcription	HepG2	liver
28	chr7:78844600-78845000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:78845400-78846000	Enhancers	Lung	lung
30	chr7:78845400-78847000	Enhancers	HepG2	liver
31	chr7:78845800-78846200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:78845800-78846200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr7:78846000-78846200	Enhancers	Fetal Intestine Small	intestine
34	chr7:78846200-78847200	Weak transcription	Fetal Intestine Small	intestine
35	chr7:78846200-78856400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:78846600-78847400	Enhancers	HUVEC	blood vessel
37	chr7:78846800-78847400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr7:78847000-78847400	Enhancers	Liver	Liver
39	chr7:78847000-78847400	Flanking Active TSS	HepG2	liver
40	chr7:78847000-78847600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:78847200-78847600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:78847200-78848400	Enhancers	Fetal Intestine Small	intestine
43	chr7:78847400-78847800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr7:78847400-78847800	Active TSS	HepG2	liver
45	chr7:78847400-78848000	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr7:78847400-78850000	Weak transcription	Liver	Liver
47	chr7:78847600-78847800	Enhancers	Fetal Brain Male	brain
48	chr7:78847800-78848000	Flanking Active TSS	HepG2	liver
49	chr7:78847800-78848200	Weak transcription	Fetal Brain Male	brain
50	chr7:78847800-78850000	Weak transcription	Rectal Mucosa Donor 31	rectum

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