Variant report

Variant	nsv1026688
Chromosome Location	chr7:80231657-80307236
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	chr7:80263770-80264169	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80288875-80289153	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:80240786-80241747	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:80284287-80284555	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:80272116-80272564	HepG2	liver:	n/a	n/a
6	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
7	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
8	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
9	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
10	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:80267588-80268026	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:80267684-80267984	GM12878	blood:	n/a	n/a
13	BCL3	chr7:80241066-80241560	A549	lung:	n/a	n/a
14	BCL3	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
15	BCLAF1	chr7:80267523-80268057	GM12878	blood:	n/a	chr7:80267573-80267582
16	BHLHE40	chr7:80267457-80267965	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:80241129-80241645	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:80302176-80302364	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:80288768-80289107	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:80263869-80264105	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
22	CEBPB	chr7:80262200-80262511	Hela-S3	cervix:	n/a	chr7:80262334-80262345
23	CEBPB	chr7:80272854-80273198	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr7:80259785-80260226	MCF-7	breast:	n/a	chr7:80260003-80260014
25	CEBPB	chr7:80263790-80264179	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
26	CEBPB	chr7:80241109-80241523	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:80252795-80253074	HepG2	liver:	n/a	chr7:80252895-80252908 chr7:80252895-80252906 chr7:80252913-80252926 chr7:80252897-80252908 chr7:80252915-80252926 chr7:80252895-80252908 chr7:80252915-80252926 chr7:80252913-80252926 chr7:80252913-80252924 chr7:80252895-80252908
28	CEBPB	chr7:80272144-80272538	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
29	CEBPB	chr7:80267337-80268157	GM12878	blood:	n/a	chr7:80267547-80267560 chr7:80267352-80267363 chr7:80267356-80267367
30	CEBPB	chr7:80262186-80262489	HepG2	liver:	n/a	chr7:80262334-80262345
31	CEBPB	chr7:80244329-80244720	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:80272158-80272462	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
33	CEBPB	chr7:80255387-80255390	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:80263632-80264325	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
35	CEBPB	chr7:80263757-80264252	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
36	CEBPB	chr7:80263803-80264151	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
37	CEBPB	chr7:80263864-80264074	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
38	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
39	CEBPB	chr7:80272790-80273832	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr7:80263826-80264127	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
41	CEBPB	chr7:80272148-80272537	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
42	CEBPB	chr7:80244154-80244821	HCT-116	colon:	n/a	n/a
43	CEBPB	chr7:80268410-80268678	K562	blood:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
44	CEBPB	chr7:80272188-80272426	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
45	CEBPB	chr7:80263676-80264299	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
46	CEBPB	chr7:80268417-80268679	IMR90	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
47	CEBPB	chr7:80268377-80268683	HepG2	liver:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
48	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
49	CEBPB	chr7:80263773-80264293	IMR90	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
50	CEBPB	chr7:80263785-80264123	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80274460-80274510	PrEC	prostate:	n/a
2	chr7:80274460-80274510	Caco-2	colon:	n/a
3	chr7:80274460-80274510	PrEC	prostate:	n/a
4	chr7:80274460-80274510	Caco-2	colon:	n/a
5	chr7:80267943-80267993	Hela-S3	cervix:	n/a
6	chr7:80267619-80267669	NB4	blood:	n/a
7	chr7:80244500-80244550	IMR90	lung:	fetal
8	chr7:80275870-80275920	SKMC	muscle:	n/a
9	chr7:80267943-80267993	HAEpiC	amniotic membrane:	n/a
10	chr7:80252533-80252583	HCF	heart:	n/a
11	chr7:80274460-80274510	HIPEpiC	eye:	n/a
12	chr7:80236112-80236162	CMK	blood:	n/a
13	chr7:80267619-80267669	HUVEC	blood vessel:	n/a
14	chr7:80252533-80252583	NT2-D1	testis:	n/a
15	chr7:80291832-80291882	PANC-1	pancreas:	n/a
16	chr7:80236112-80236162	HRCEpiC	kidney:	n/a
17	chr7:80305251-80305301	K562	blood:	n/a
18	chr7:80291794-80291844	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:80267943-80267993	AG04449	skin:	fetal
20	chr7:80305251-80305301	HMEC	breast:	n/a
21	chr7:80291794-80291844	IMR90	lung:	fetal
22	chr7:80274687-80274737	ProgFib	skin:	n/a
23	chr7:80252533-80252583	SKMC	muscle:	n/a
24	chr7:80244500-80244550	Hepatocyte	liver:	n/a
25	chr7:80267943-80267993	A549	lung:	n/a
26	chr7:80267943-80267993	MCF-7	breast:	n/a
27	chr7:80274460-80274510	NB4	blood:	n/a
28	chr7:80236112-80236162	PrEC	prostate:	n/a
29	chr7:80244500-80244550	H1-hESC	embryonic stem cell:	embryo
30	chr7:80274460-80274510	GM12891	blood:	n/a
31	chr7:80252533-80252583	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:80267619-80267669	CMK	blood:	n/a
33	chr7:80274460-80274510	HMEC	breast:	n/a
34	chr7:80236112-80236162	GM19239	blood:	n/a
35	chr7:80267619-80267669	HAEpiC	amniotic membrane:	n/a
36	chr7:80274460-80274510	HAEpiC	amniotic membrane:	n/a
37	chr7:80291794-80291844	GM12892	blood:	n/a
38	chr7:80244500-80244550	AG04449	skin:	fetal
39	chr7:80291832-80291882	NB4	blood:	n/a
40	chr7:80275870-80275920	HIPEpiC	eye:	n/a
41	chr7:80291794-80291844	HCT-116	colon:	n/a
42	chr7:80267619-80267669	HL-60	blood:	n/a
43	chr7:80236112-80236162	Hepatocyte	liver:	n/a
44	chr7:80244500-80244550	ovcar-3	ovarian:	n/a
45	chr7:80266930-80266980	HCT-116	colon:	n/a
46	chr7:80274687-80274737	HRCEpiC	kidney:	n/a
47	chr7:80275870-80275920	SK-N-SH	brain:	n/a
48	chr7:80236112-80236162	SAEC	small airway:	n/a
49	chr7:80305251-80305301	GM12878	blood:	n/a
50	chr7:80252533-80252583	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:
2	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:
3	chr7:80230076..80232841-chr7:80236237..80238542,2	MCF-7	breast:
4	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
5	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:
6	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
7	chr7:80288156..80289657-chr7:80291382..80293831,2	K562	blood:
8	chr7:80057560..80058347-chr7:80243745..80244716,2	MCF-7	breast:
9	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
10	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:
11	chr7:80290704..80291673-chr7:80310324..80310826,2	MCF-7	breast:
12	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
13	chr7:80291053..80291665-chr7:81099051..81099939,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-4	chr7:80253211-80253506	NONHSAT121747
2	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746
3	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
4	lnc-GNAI1-5	chr7:80231466-80231695	NONHSAT121745
5	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747
6	lnc-GNAI1-5	chr7:80231541-80231695	NONHSAT121746
7	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745
8	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
9	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746

No.	miRNA target gene	miRNA name	Chromosome Location
1	CD36	hsa-miR-26b-5p	chr7:80303497-80303519
2	CD36	hsa-miR-155-5p	chr7:80306787-80306809
3	CD36	hsa-miR-155-5p	chr7:80306164-80306186

Variant related genes	Relation type
ENSG00000229436	TF binding region
CD36	TF binding region
ENSG00000229436	CpG island
CD36	CpG island
ENSG00000135218	chromatin interactions
ENSG00000229436	chromatin interactions

Extended variants
information (count: 3135 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3135 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151218598	chr7:80231668-80231669	Active TSS Flanking Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs539733007	chr7:80231670-80231671	Active TSS Flanking Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs140329618	chr7:80231672-80231673	Active TSS Flanking Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs182279912	chr7:80231686-80231687	Active TSS Flanking Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs534758295	chr7:80231723-80231724	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1194181	chr7:80231793-80231794	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs144080688	chr7:80231802-80231803	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1194180	chr7:80231908-80231909	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs186475776	chr7:80231916-80231917	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534183828	chr7:80231926-80231927	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577088956	chr7:80231930-80231931	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546455084	chr7:80231936-80231937	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559840959	chr7:80231954-80231955	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190149122	chr7:80231962-80231963	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1880410	chr7:80232004-80232005	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs17154147	chr7:80232006-80232007	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs368312992	chr7:80232027-80232028	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs71555071	chr7:80232048-80232049	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112740176	chr7:80232077-80232078	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs371874652	chr7:80232134-80232135	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs145639607	chr7:80232190-80232191	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs554660714	chr7:80232201-80232202	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546873020	chr7:80232211-80232212	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138263194	chr7:80232263-80232264	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149135791	chr7:80232309-80232310	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556879417	chr7:80232449-80232450	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200086453	chr7:80232452-80232453	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs376488691	chr7:80232470-80232471	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs12531218	chr7:80232471-80232472	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183431854	chr7:80232505-80232506	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs537163891	chr7:80232528-80232529	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557068404	chr7:80232541-80232542	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs143411315	chr7:80232555-80232556	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs148369563	chr7:80232564-80232565	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs576848989	chr7:80232584-80232585	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs34345674	chr7:80232588-80232589	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs141530371	chr7:80232599-80232600	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs112229813	chr7:80232625-80232626	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs7784648	chr7:80232655-80232656	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs34620540	chr7:80232700-80232701	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs187972599	chr7:80232779-80232780	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs556906829	chr7:80232785-80232786	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561680797	chr7:80232789-80232790	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs35468175	chr7:80232850-80232851	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147499181	chr7:80232888-80232889	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs1194179	chr7:80232973-80232974	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs193182629	chr7:80233021-80233022	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533142741	chr7:80233024-80233025	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs140606317	chr7:80233031-80233032	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs200512431	chr7:80233032-80233033	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80227400-80238200	Weak transcription	Small Intestine	intestine
2	chr7:80230200-80234800	Weak transcription	Fetal Intestine Small	intestine
3	chr7:80230200-80237000	Weak transcription	Gastric	stomach
4	chr7:80231000-80231800	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:80231200-80232000	Enhancers	Fetal Heart	heart
6	chr7:80231200-80233400	Active TSS	Psoas Muscle	Psoas
7	chr7:80231200-80236400	Active TSS	Right Atrium	heart
8	chr7:80231400-80231800	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr7:80231400-80231800	Enhancers	Fetal Muscle Leg	muscle
10	chr7:80231400-80231800	Enhancers	NHLF	lung
11	chr7:80231400-80233600	Active TSS	Right Ventricle	heart
12	chr7:80231400-80235800	Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr7:80231600-80231800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:80231600-80231800	Enhancers	Fetal Lung	lung
15	chr7:80231600-80232000	Active TSS	Placenta	Placenta
16	chr7:80231600-80232800	Active TSS	Left Ventricle	heart
17	chr7:80231600-80233800	Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr7:80231800-80232200	Weak transcription	Fetal Lung	lung
19	chr7:80231800-80233800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:80231800-80234800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr7:80231800-80236600	Active TSS	Adipose Nuclei	Adipose
22	chr7:80231800-80240200	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:80232000-80236000	Weak transcription	Fetal Heart	heart
24	chr7:80232200-80232400	Enhancers	Fetal Lung	lung
25	chr7:80232400-80235800	Weak transcription	Fetal Lung	lung
26	chr7:80232800-80234600	Weak transcription	Left Ventricle	heart
27	chr7:80233400-80233600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr7:80233400-80234000	Enhancers	Fetal Intestine Large	intestine
29	chr7:80233400-80234000	Enhancers	Psoas Muscle	Psoas
30	chr7:80233600-80233800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:80233600-80236800	Weak transcription	Right Ventricle	heart
32	chr7:80233800-80234000	Enhancers	Duodenum Mucosa	Duodenum
33	chr7:80233800-80234000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
34	chr7:80233800-80234000	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr7:80233800-80234000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr7:80233800-80234600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:80234000-80235000	Weak transcription	Psoas Muscle	Psoas
38	chr7:80234000-80235600	Weak transcription	Fetal Intestine Large	intestine
39	chr7:80234000-80235800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr7:80234000-80236000	Weak transcription	Duodenum Mucosa	Duodenum
41	chr7:80234000-80236800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr7:80234600-80235800	Active TSS	Left Ventricle	heart
43	chr7:80234600-80240600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:80234800-80235000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr7:80234800-80241600	Enhancers	Fetal Intestine Small	intestine
46	chr7:80235000-80235400	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr7:80235000-80236200	Enhancers	Psoas Muscle	Psoas
48	chr7:80235400-80237600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr7:80235600-80236000	Weak transcription	Pancreas	Pancrea
50	chr7:80235600-80239600	Enhancers	Fetal Intestine Large	intestine

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