Variant report

Variant	nsv971195
Chromosome Location	chr7:80260254-80270989
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	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
3	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
4	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
5	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
6	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:80267684-80267984	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:80267588-80268026	GM12878	blood:	n/a	n/a
9	BCL3	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
10	BCLAF1	chr7:80267523-80268057	GM12878	blood:	n/a	chr7:80267573-80267582
11	BHLHE40	chr7:80267457-80267965	GM12878	blood:	n/a	n/a
12	BRCA1	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:80263676-80264299	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
14	CEBPB	chr7:80263820-80264077	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
15	CEBPB	chr7:80262186-80262489	HepG2	liver:	n/a	chr7:80262334-80262345
16	CEBPB	chr7:80263869-80264105	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
17	CEBPB	chr7:80263803-80264151	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
18	CEBPB	chr7:80263864-80264074	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
19	CEBPB	chr7:80263632-80264325	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
20	CEBPB	chr7:80263757-80264252	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
21	CEBPB	chr7:80268410-80268678	K562	blood:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
22	CEBPB	chr7:80263790-80264179	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
23	CEBPB	chr7:80262200-80262511	Hela-S3	cervix:	n/a	chr7:80262334-80262345
24	CEBPB	chr7:80263785-80264123	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
25	CEBPB	chr7:80263773-80264293	IMR90	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
26	CEBPB	chr7:80268439-80268641	A549	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
27	CEBPB	chr7:80263826-80264127	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
28	CEBPB	chr7:80263777-80264203	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
29	CEBPB	chr7:80263755-80264281	Hela-S3	cervix:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
30	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
31	CEBPB	chr7:80268377-80268683	HepG2	liver:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
32	CEBPB	chr7:80267337-80268157	GM12878	blood:	n/a	chr7:80267547-80267560 chr7:80267352-80267363 chr7:80267356-80267367
33	CEBPB	chr7:80268417-80268679	IMR90	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
34	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
35	CHD2	chr7:80267673-80268042	GM12878	blood:	n/a	chr7:80267904-80267914 chr7:80267907-80267917
36	CHD2	chr7:80263854-80264150	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr7:80267543-80268149	GM12878	blood:	n/a	n/a
38	CUX1	chr7:80267613-80268081	GM12878	blood:	n/a	n/a
39	E2F4	chr7:80260643-80260804	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr7:80263875-80264193	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr7:80270944-80271151	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr7:80267596-80268016	GM12878	blood:	n/a	n/a
43	EP300	chr7:80263762-80264310	Hela-S3	cervix:	n/a	chr7:80264206-80264216 chr7:80263977-80263991 chr7:80264175-80264184
44	EP300	chr7:80263748-80263882	K562	blood:	n/a	n/a
45	EP300	chr7:80268222-80268224	GM12878	blood:	n/a	n/a
46	EP300	chr7:80263764-80264220	HepG2	liver:	n/a	chr7:80264206-80264216 chr7:80263977-80263991 chr7:80264175-80264184
47	EP300	chr7:80263833-80264226	HepG2	liver:	n/a	chr7:80264206-80264216 chr7:80263977-80263991 chr7:80264175-80264184
48	EP300	chr7:80267633-80268009	GM12878	blood:	n/a	chr7:80267886-80267900
49	EP300	chr7:80263838-80264159	HepG2	liver:	n/a	chr7:80263977-80263991
50	EP300	chr7:80267477-80268066	GM12878	blood:	n/a	chr7:80267886-80267900

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80267943-80267993	GM12891	blood:	n/a
2	chr7:80266930-80266980	AG10803	skin:	n/a
3	chr7:80266930-80266980	LNCaP	prostate:	n/a
4	chr7:80267943-80267993	ProgFib	skin:	n/a
5	chr7:80266930-80266980	HMEC	breast:	n/a
6	chr7:80267943-80267993	A549	lung:	n/a
7	chr7:80267943-80267993	HCT-116	colon:	n/a
8	chr7:80266930-80266980	U87	brain:	n/a
9	chr7:80266930-80266980	BE2_C	brain:	n/a
10	chr7:80266930-80266980	HL-60	blood:	n/a
11	chr7:80267619-80267669	NB4	blood:	n/a
12	chr7:80267943-80267993	SK-N-SH	brain:	n/a
13	chr7:80267619-80267669	Jurkat	blood:	n/a
14	chr7:80266930-80266980	Jurkat	blood:	n/a
15	chr7:80267943-80267993	AG10803	skin:	n/a
16	chr7:80267943-80267993	HRPEpiC	eye:	n/a
17	chr7:80266930-80266980	SAEC	small airway:	n/a
18	chr7:80266930-80266980	AG09319	gingival:	n/a
19	chr7:80267619-80267669	GM12892	blood:	n/a
20	chr7:80267619-80267669	HCM	heart:	n/a
21	chr7:80267943-80267993	GM12878	blood:	n/a
22	chr7:80267619-80267669	SK-N-SH_RA	brain:	n/a
23	chr7:80267943-80267993	AoSMC	blood vessel:	n/a
24	chr7:80267619-80267669	PFSK-1	brain:	n/a
25	chr7:80266930-80266980	SKMC	muscle:	n/a
26	chr7:80266930-80266980	MCF10A-Er-Src	breast:	n/a
27	chr7:80267943-80267993	SK-N-MC	brain:	n/a
28	chr7:80266930-80266980	Hela-S3	cervix:	n/a
29	chr7:80266930-80266980	PFSK-1	brain:	n/a
30	chr7:80267943-80267993	NHDF-neo	bronchial:	n/a
31	chr7:80267943-80267993	MCF10A-Er-Src	breast:	n/a
32	chr7:80267619-80267669	HL-60	blood:	n/a
33	chr7:80267619-80267669	A549	lung:	n/a
34	chr7:80267619-80267669	HEK293	kidney:	embryo
35	chr7:80267943-80267993	HIPEpiC	eye:	n/a
36	chr7:80267943-80267993	IMR90	lung:	fetal
37	chr7:80267943-80267993	SK-N-SH_RA	brain:	n/a
38	chr7:80267619-80267669	LNCaP	prostate:	n/a
39	chr7:80266930-80266980	Caco-2	colon:	n/a
40	chr7:80266930-80266980	GM06990	blood:	n/a
41	chr7:80266930-80266980	GM19239	blood:	n/a
42	chr7:80267619-80267669	HRE	kidney:	n/a
43	chr7:80267943-80267993	PFSK-1	brain:	n/a
44	chr7:80266930-80266980	T-47D	breast:	n/a
45	chr7:80267619-80267669	CMK	blood:	n/a
46	chr7:80267619-80267669	K562	blood:	n/a
47	chr7:80266930-80266980	Hepatocyte	liver:	n/a
48	chr7:80266930-80266980	CMK	blood:	n/a
49	chr7:80267619-80267669	HCPEpiC	choroid plexus:	n/a
50	chr7:80267943-80267993	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:
2	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747
2	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746

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

Extended variants
information (count: 385 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543434282	chr7:80260362-80260363	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144921258	chr7:80260365-80260366	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532623894	chr7:80260370-80260371	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552430797	chr7:80260371-80260372	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187723601	chr7:80260374-80260375	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528680028	chr7:80260376-80260377	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368655384	chr7:80260383-80260384	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548858276	chr7:80260406-80260407	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568783042	chr7:80260446-80260447	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs371777409	chr7:80260448-80260449	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192299533	chr7:80260459-80260460	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184993062	chr7:80260474-80260475	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560440677	chr7:80260479-80260480	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371661586	chr7:80260481-80260482	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570396849	chr7:80260543-80260544	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149031385	chr7:80260580-80260581	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552798574	chr7:80260590-80260591	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566622143	chr7:80260600-80260601	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188482025	chr7:80260609-80260610	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs77968686	chr7:80260619-80260620	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575174047	chr7:80260644-80260645	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192159163	chr7:80260671-80260672	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78256291	chr7:80260854-80260855	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs367753239	chr7:80260871-80260872	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs397763283	chr7:80260884-80260885	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200121794	chr7:80260885-80260886	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189325806	chr7:80260912-80260913	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557314777	chr7:80260971-80260972	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147844944	chr7:80261051-80261052	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546230580	chr7:80261056-80261057	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559599345	chr7:80261064-80261065	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528113754	chr7:80261114-80261115	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528649825	chr7:80261124-80261125	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542462566	chr7:80261246-80261247	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141357948	chr7:80261296-80261297	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531212153	chr7:80261301-80261302	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536858631	chr7:80261338-80261339	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534082208	chr7:80261386-80261387	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182220422	chr7:80261518-80261519	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs548283813	chr7:80261528-80261529	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555787506	chr7:80261573-80261574	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs200544591	chr7:80261577-80261578	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs570383254	chr7:80261604-80261605	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs574089732	chr7:80261605-80261606	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532801699	chr7:80261628-80261629	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552008744	chr7:80261645-80261646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs187148679	chr7:80261720-80261721	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs146974876	chr7:80261746-80261747	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs535699397	chr7:80261750-80261751	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs555127101	chr7:80261876-80261877	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80255800-80261800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:80256400-80261600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr7:80257800-80260400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr7:80258000-80262800	Enhancers	Fetal Heart	heart
5	chr7:80258600-80264800	Weak transcription	Left Ventricle	heart
6	chr7:80259400-80260400	Enhancers	Small Intestine	intestine
7	chr7:80259400-80261600	Enhancers	Fetal Lung	lung
8	chr7:80259600-80262400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:80259600-80263400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:80259800-80260400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:80259800-80260400	Enhancers	Colon Smooth Muscle	Colon
12	chr7:80259800-80260600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:80259800-80260600	Enhancers	Osteobl	bone
14	chr7:80259800-80260800	Enhancers	Hela-S3	cervix
15	chr7:80259800-80260800	Enhancers	NHLF	lung
16	chr7:80260000-80260400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:80260000-80260400	Enhancers	Fetal Muscle Leg	muscle
18	chr7:80260000-80260400	Enhancers	Pancreas	Pancrea
19	chr7:80260000-80260400	Flanking Active TSS	Psoas Muscle	Psoas
20	chr7:80260000-80260400	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr7:80260000-80260400	Active TSS	Right Atrium	heart
22	chr7:80260000-80260400	Active TSS	Stomach Smooth Muscle	stomach
23	chr7:80260000-80260400	Flanking Active TSS	HepG2	liver
24	chr7:80260000-80260600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:80260000-80260600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:80260000-80260600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:80260000-80260600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:80260000-80260600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr7:80260000-80260600	Enhancers	Ovary	ovary
30	chr7:80260000-80260600	Enhancers	Right Ventricle	heart
31	chr7:80260000-80260600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr7:80260000-80260600	Enhancers	NHDF-Ad	bronchial
33	chr7:80260000-80260800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr7:80260000-80265600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr7:80260200-80260400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:80260200-80260400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:80260200-80260400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:80260200-80260600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:80260200-80260600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:80260200-80260600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr7:80260200-80260600	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr7:80260200-80260800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:80260200-80261800	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr7:80260200-80263400	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr7:80260200-80263400	Weak transcription	HMEC	breast
46	chr7:80260200-80263400	Weak transcription	NHEK	skin
47	chr7:80260200-80264400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:80260400-80260600	Enhancers	Rectal Smooth Muscle	rectum
49	chr7:80260400-80261000	Enhancers	HepG2	liver
50	chr7:80260400-80261200	Enhancers	Monocytes-CD14+_RO01746	blood

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