Variant report

Variant	nsv1025144
Chromosome Location	chr7:80197286-80271841
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	chr7:80240786-80241747	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80263770-80264169	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:80218074-80218152	HepG2	liver:	n/a	n/a
4	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
5	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
6	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
7	BACH1	chr7:80217948-80218267	H1-hESC	embryonic stem cell:	n/a	chr7:80218106-80218120
8	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
9	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
10	BATF	chr7:80221037-80221261	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	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
14	BCL3	chr7:80241066-80241560	A549	lung:	n/a	n/a
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	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:80244154-80244821	HCT-116	colon:	n/a	n/a
20	CEBPB	chr7:80259785-80260226	MCF-7	breast:	n/a	chr7:80260003-80260014
21	CEBPB	chr7:80263803-80264151	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
22	CEBPB	chr7:80263777-80264203	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
23	CEBPB	chr7:80263632-80264325	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
24	CEBPB	chr7:80268439-80268641	A549	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
25	CEBPB	chr7:80213969-80214570	HCT-116	colon:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
26	CEBPB	chr7:80268417-80268679	IMR90	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
27	CEBPB	chr7:80259836-80260218	Hela-S3	cervix:	n/a	chr7:80260003-80260014
28	CEBPB	chr7:80214088-80214466	A549	lung:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
29	CEBPB	chr7:80210888-80211046	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
31	CEBPB	chr7:80214099-80214559	MCF-7	breast:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
32	CEBPB	chr7:80255387-80255390	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:80223484-80223782	IMR90	lung:	n/a	chr7:80223612-80223623
34	CEBPB	chr7:80241130-80241436	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:80223426-80223952	Hela-S3	cervix:	n/a	chr7:80223612-80223623
36	CEBPB	chr7:80214122-80214532	MCF-7	breast:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
37	CEBPB	chr7:80223485-80223864	A549	lung:	n/a	chr7:80223612-80223623
38	CEBPB	chr7:80262186-80262489	HepG2	liver:	n/a	chr7:80262334-80262345
39	CEBPB	chr7:80214073-80214485	Hela-S3	cervix:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
40	CEBPB	chr7:80263864-80264074	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
41	CEBPB	chr7:80214131-80214420	H1-hESC	embryonic stem cell:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
42	CEBPB	chr7:80214045-80214449	IMR90	lung:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
43	CEBPB	chr7:80204735-80204849	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:80263773-80264293	IMR90	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
45	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
46	CEBPB	chr7:80214038-80214445	HepG2	liver:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
47	CEBPB	chr7:80223156-80223784	A549	lung:	n/a	chr7:80223612-80223623
48	CEBPB	chr7:80263755-80264281	Hela-S3	cervix:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
49	CEBPB	chr7:80263820-80264077	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
50	CEBPB	chr7:80263826-80264127	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80266930-80266980	AG09319	gingival:	n/a
2	chr7:80230544-80230594	AG10803	skin:	n/a
3	chr7:80252533-80252583	HL-60	blood:	n/a
4	chr7:80267943-80267993	HRE	kidney:	n/a
5	chr7:80230544-80230594	SK-N-SH_RA	brain:	n/a
6	chr7:80267943-80267993	BE2_C	brain:	n/a
7	chr7:80231599-80231649	Caco-2	colon:	n/a
8	chr7:80236112-80236162	K562	blood:	n/a
9	chr7:80230544-80230594	HNPCEpiC	eye:	n/a
10	chr7:80230525-80230575	SK-N-SH_RA	brain:	n/a
11	chr7:80230062-80230112	Hepatocyte	liver:	n/a
12	chr7:80266930-80266980	HL-60	blood:	n/a
13	chr7:80244500-80244550	GM12878	blood:	n/a
14	chr7:80244500-80244550	ECC-1	luminal epithelium:	n/a
15	chr7:80231599-80231649	GM12892	blood:	n/a
16	chr7:80267619-80267669	GM12892	blood:	n/a
17	chr7:80230062-80230112	BE2_C	brain:	n/a
18	chr7:80244500-80244550	NHDF-neo	bronchial:	n/a
19	chr7:80266930-80266980	MCF-7	breast:	n/a
20	chr7:80236112-80236162	HCT-116	colon:	n/a
21	chr7:80252533-80252583	BE2_C	brain:	n/a
22	chr7:80244500-80244550	MCF10A-Er-Src	breast:	n/a
23	chr7:80230528-80230578	HIPEpiC	eye:	n/a
24	chr7:80267943-80267993	HEK293	kidney:	embryo
25	chr7:80252533-80252583	NHBE	bronchial:	n/a
26	chr7:80230062-80230112	AG10803	skin:	n/a
27	chr7:80231599-80231649	MCF10A-Er-Src	breast:	n/a
28	chr7:80230062-80230112	HIPEpiC	eye:	n/a
29	chr7:80230062-80230112	NB4	blood:	n/a
30	chr7:80252533-80252583	PrEC	prostate:	n/a
31	chr7:80231599-80231649	SK-N-SH_RA	brain:	n/a
32	chr7:80266930-80266980	HIPEpiC	eye:	n/a
33	chr7:80252533-80252583	HCPEpiC	choroid plexus:	n/a
34	chr7:80267619-80267669	AG09309	skin:	n/a
35	chr7:80266930-80266980	HRCEpiC	kidney:	n/a
36	chr7:80236112-80236162	MCF10A-Er-Src	breast:	n/a
37	chr7:80266930-80266980	HCM	heart:	n/a
38	chr7:80230525-80230575	NB4	blood:	n/a
39	chr7:80266930-80266980	Hepatocyte	liver:	n/a
40	chr7:80267619-80267669	RPTEC	kidney:	n/a
41	chr7:80231599-80231649	GM12878	blood:	n/a
42	chr7:80230528-80230578	HRE	kidney:	n/a
43	chr7:80230544-80230594	NT2-D1	testis:	n/a
44	chr7:80230544-80230594	LNCaP	prostate:	n/a
45	chr7:80230528-80230578	HepG2	liver:	n/a
46	chr7:80267619-80267669	ECC-1	luminal epithelium:	n/a
47	chr7:80266930-80266980	NT2-D1	testis:	n/a
48	chr7:80230544-80230594	NHDF-neo	bronchial:	n/a
49	chr7:80244500-80244550	HUVEC	blood vessel:	n/a
50	chr7:80266930-80266980	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:
2	chr7:80226468..80229283-chr7:80231335..80233921,2	K562	blood:
3	chr7:80215015..80216821-chr7:80218593..80220289,2	K562	blood:
4	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
5	chr7:80057560..80058347-chr7:80243745..80244716,2	MCF-7	breast:
6	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
7	chr7:80198036..80200312-chr7:80208194..80210191,2	MCF-7	breast:
8	chr7:80198036..80200312-chr7:80208194..80210191,2	MCF-7	breast:
9	chr7:80215015..80216821-chr7:80218593..80220289,2	K562	blood:
10	chr7:80230076..80232841-chr7:80236237..80238542,2	MCF-7	breast:
11	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746
2	lnc-GNAI1-4	chr7:80253211-80253506	NONHSAT121747
3	lnc-GNAI1-5	chr7:80231466-80231695	NONHSAT121745
4	lnc-GNAI1-5	chr7:80231541-80231695	NONHSAT121746
5	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747

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

Extended variants
information (count: 2746 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2746 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs819457	chr7:80197286-80197287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139289274	chr7:80197298-80197299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530683129	chr7:80197313-80197314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550876719	chr7:80197349-80197350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570021121	chr7:80197446-80197447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79220678	chr7:80197467-80197468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191036386	chr7:80197549-80197550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149400625	chr7:80197562-80197563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143514941	chr7:80197695-80197696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554827119	chr7:80197756-80197757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs819456	chr7:80197758-80197759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs183101813	chr7:80197826-80197827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187349229	chr7:80197840-80197841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557642072	chr7:80197847-80197848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76111026	chr7:80197874-80197875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545393164	chr7:80197958-80197959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79808480	chr7:80197965-80197966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368107320	chr7:80197966-80197967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552727619	chr7:80197973-80197974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199957228	chr7:80198001-80198002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201744348	chr7:80198004-80198005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199795524	chr7:80198005-80198006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572588925	chr7:80198015-80198016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541925284	chr7:80198034-80198035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561706918	chr7:80198041-80198042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531211589	chr7:80198048-80198049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530737837	chr7:80198056-80198057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371087347	chr7:80198116-80198117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192538919	chr7:80198132-80198133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564366251	chr7:80198133-80198134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185085611	chr7:80198138-80198139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12154593	chr7:80198174-80198175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200158651	chr7:80198227-80198228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533291244	chr7:80198259-80198260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188770871	chr7:80198268-80198269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566093381	chr7:80198287-80198288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528548164	chr7:80198300-80198301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548665593	chr7:80198302-80198303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541452244	chr7:80198321-80198322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568519932	chr7:80198332-80198333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537642756	chr7:80198333-80198334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs819455	chr7:80198342-80198343	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs564656137	chr7:80198386-80198387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570788915	chr7:80198462-80198463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192775455	chr7:80198525-80198526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533324995	chr7:80198527-80198528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148001666	chr7:80198573-80198574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552517900	chr7:80198586-80198587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7778094	chr7:80198588-80198589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs541515842	chr7:80198615-80198616	Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80193800-80204000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:80200600-80200800	Enhancers	Right Atrium	heart
3	chr7:80201000-80210400	Weak transcription	Right Atrium	heart
4	chr7:80204000-80204200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:80204400-80204800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr7:80209000-80209200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr7:80209400-80212400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr7:80209400-80216800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr7:80209800-80210000	Enhancers	Fetal Heart	heart
10	chr7:80210000-80210200	Flanking Active TSS	Fetal Heart	heart
11	chr7:80210200-80210400	Enhancers	Fetal Heart	heart
12	chr7:80210200-80211000	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr7:80210400-80210600	Flanking Active TSS	Fetal Heart	heart
14	chr7:80210400-80210600	Enhancers	Right Atrium	heart
15	chr7:80210400-80211000	Enhancers	Left Ventricle	heart
16	chr7:80210400-80211000	Enhancers	Psoas Muscle	Psoas
17	chr7:80210400-80211200	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr7:80210600-80212000	Enhancers	Fetal Heart	heart
19	chr7:80210800-80211200	Enhancers	HMEC	breast
20	chr7:80210800-80211200	Enhancers	NHLF	lung
21	chr7:80211000-80212800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr7:80211000-80213200	Weak transcription	Psoas Muscle	Psoas
23	chr7:80211000-80223200	Weak transcription	Left Ventricle	heart
24	chr7:80211200-80212800	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:80211200-80213200	Weak transcription	HMEC	breast
26	chr7:80212000-80212400	Weak transcription	Fetal Heart	heart
27	chr7:80212400-80212600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr7:80212400-80214800	Enhancers	Fetal Heart	heart
29	chr7:80212600-80213600	Enhancers	Colon Smooth Muscle	Colon
30	chr7:80212600-80213800	Enhancers	Fetal Intestine Large	intestine
31	chr7:80212600-80226000	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:80212800-80213800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:80212800-80213800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:80212800-80214200	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr7:80212800-80214400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:80212800-80214400	Enhancers	Osteobl	bone
37	chr7:80212800-80214800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr7:80213000-80213200	Enhancers	Stomach Mucosa	stomach
39	chr7:80213000-80214400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:80213000-80215200	Enhancers	Fetal Intestine Small	intestine
41	chr7:80213200-80213600	Enhancers	Psoas Muscle	Psoas
42	chr7:80213200-80214200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:80213200-80214200	Weak transcription	Stomach Mucosa	stomach
44	chr7:80213200-80214400	Enhancers	NHEK	skin
45	chr7:80213200-80214600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:80213200-80214600	Enhancers	HMEC	breast
47	chr7:80213200-80215200	Enhancers	Adipose Nuclei	Adipose
48	chr7:80213600-80223600	Weak transcription	Psoas Muscle	Psoas
49	chr7:80213800-80214400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:80213800-80220600	Weak transcription	Fetal Intestine Large	intestine

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