Variant report

Variant	nsv888517
Chromosome Location	chr7:79122018-79244452
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	chr7:79237396-79237695	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:79136530-79136804	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:79135879-79136195	HepG2	liver:	n/a	n/a
4	ATF1	chr7:79168827-79168925	K562	blood:	n/a	n/a
5	ATF1	chr7:79155465-79155511	K562	blood:	n/a	n/a
6	ATF3	chr7:79136418-79136929	A549	lung:	n/a	n/a
7	BCL3	chr7:79136419-79136964	A549	lung:	n/a	n/a
8	BCL3	chr7:79135674-79136308	A549	lung:	n/a	n/a
9	BCL3	chr7:79136354-79136969	A549	lung:	n/a	n/a
10	BCL3	chr7:79135704-79136201	A549	lung:	n/a	n/a
11	BHLHE40	chr7:79154489-79154768	HepG2	liver:	n/a	n/a
12	CCNT2	chr7:79229521-79229760	K562	blood:	n/a	n/a
13	CEBPB	chr7:79212204-79212474	HepG2	liver:	n/a	chr7:79212322-79212333
14	CEBPB	chr7:79238337-79238638	IMR90	lung:	n/a	chr7:79238501-79238512 chr7:79238503-79238512 chr7:79238502-79238513 chr7:79238501-79238514
15	CEBPB	chr7:79177973-79178548	A549	lung:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
16	CEBPB	chr7:79201511-79201650	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:79209272-79209522	HepG2	liver:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
18	CEBPB	chr7:79220570-79220924	HepG2	liver:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
19	CEBPB	chr7:79136335-79136839	A549	lung:	n/a	n/a
20	CEBPB	chr7:79238334-79238615	HepG2	liver:	n/a	chr7:79238501-79238512 chr7:79238503-79238512 chr7:79238502-79238513 chr7:79238501-79238514
21	CEBPB	chr7:79157659-79158257	HCT-116	colon:	n/a	n/a
22	CEBPB	chr7:79176485-79176822	A549	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
23	CEBPB	chr7:79177985-79178595	HepG2	liver:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
24	CEBPB	chr7:79152796-79153050	A549	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
25	CEBPB	chr7:79220574-79220912	Hela-S3	cervix:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
26	CEBPB	chr7:79152801-79153095	IMR90	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
27	CEBPB	chr7:79220593-79220881	A549	lung:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
28	CEBPB	chr7:79152819-79153052	Hela-S3	cervix:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
29	CEBPB	chr7:79159144-79159624	IMR90	lung:	n/a	chr7:79159560-79159573
30	CEBPB	chr7:79168045-79168264	A549	lung:	n/a	chr7:79168183-79168196 chr7:79168183-79168194 chr7:79168183-79168196
31	CEBPB	chr7:79176617-79176808	H1-hESC	embryonic stem cell:	n/a	chr7:79176648-79176659
32	CEBPB	chr7:79177969-79178309	Hela-S3	cervix:	n/a	chr7:79178066-79178077 chr7:79178142-79178153
33	CEBPB	chr7:79220585-79220896	ECC-1	luminal epithelium:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
34	CEBPB	chr7:79152850-79153090	HepG2	liver:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
35	CEBPB	chr7:79176480-79176829	IMR90	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
36	CEBPB	chr7:79212174-79212446	IMR90	lung:	n/a	chr7:79212322-79212333
37	CEBPB	chr7:79178069-79178269	H1-hESC	embryonic stem cell:	n/a	chr7:79178142-79178153
38	CEBPB	chr7:79228897-79229115	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:79135698-79136302	A549	lung:	n/a	n/a
40	CEBPB	chr7:79176477-79176825	HepG2	liver:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
41	CEBPB	chr7:79209289-79209502	IMR90	lung:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
42	CEBPB	chr7:79176528-79176817	K562	blood:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
43	CEBPB	chr7:79209298-79209544	A549	lung:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
44	CEBPB	chr7:79154457-79154741	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:79183216-79183696	A549	lung:	n/a	n/a
46	CEBPB	chr7:79124997-79125653	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:79161261-79161581	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:79220583-79220924	K562	blood:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
49	CEBPB	chr7:79183179-79183803	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:79142882-79143017	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79134707-79134757	AG09309	skin:	n/a
2	chr7:79134707-79134757	HMEC	breast:	n/a
3	chr7:79134707-79134757	HEEpiC	esophagus:	n/a
4	chr7:79134707-79134757	HNPCEpiC	eye:	n/a
5	chr7:79166927-79166977	GM12891	blood:	n/a
6	chr7:79134707-79134757	SAEC	small airway:	n/a
7	chr7:79166927-79166977	RPTEC	kidney:	n/a
8	chr7:79166927-79166977	BJ	skin:	n/a
9	chr7:79166927-79166977	PrEC	prostate:	n/a
10	chr7:79166927-79166977	HRCEpiC	kidney:	n/a
11	chr7:79166927-79166977	AoSMC	blood vessel:	n/a
12	chr7:79134707-79134757	HEK293	kidney:	embryo
13	chr7:79166927-79166977	Hela-S3	cervix:	n/a
14	chr7:79134707-79134757	PFSK-1	brain:	n/a
15	chr7:79166927-79166977	PFSK-1	brain:	n/a
16	chr7:79166927-79166977	T-47D	breast:	n/a
17	chr7:79166927-79166977	HCM	heart:	n/a
18	chr7:79166927-79166977	NB4	blood:	n/a
19	chr7:79134707-79134757	AoSMC	blood vessel:	n/a
20	chr7:79166927-79166977	H1-hESC	embryonic stem cell:	embryo
21	chr7:79166927-79166977	LNCaP	prostate:	n/a
22	chr7:79134707-79134757	MCF10A-Er-Src	breast:	n/a
23	chr7:79166927-79166977	BE2_C	brain:	n/a
24	chr7:79134707-79134757	IMR90	lung:	fetal
25	chr7:79166927-79166977	HL-60	blood:	n/a
26	chr7:79166927-79166977	NHBE	bronchial:	n/a
27	chr7:79166927-79166977	SK-N-SH	brain:	n/a
28	chr7:79166927-79166977	HEK293	kidney:	embryo
29	chr7:79134707-79134757	HCM	heart:	n/a
30	chr7:79166927-79166977	SK-N-MC	brain:	n/a
31	chr7:79134707-79134757	SK-N-SH	brain:	n/a
32	chr7:79134707-79134757	BJ	skin:	n/a
33	chr7:79166927-79166977	A549	lung:	n/a
34	chr7:79166927-79166977	Hepatocyte	liver:	n/a
35	chr7:79134707-79134757	AG04450	lung:	fetal
36	chr7:79134707-79134757	GM12891	blood:	n/a
37	chr7:79166927-79166977	AG04450	lung:	fetal
38	chr7:79166927-79166977	ProgFib	skin:	n/a
39	chr7:79166927-79166977	HCT-116	colon:	n/a
40	chr7:79134707-79134757	Jurkat	blood:	n/a
41	chr7:79166927-79166977	AG09309	skin:	n/a
42	chr7:79166927-79166977	ECC-1	luminal epithelium:	n/a
43	chr7:79134707-79134757	AG04449	skin:	fetal
44	chr7:79166927-79166977	HCF	heart:	n/a
45	chr7:79166927-79166977	AG10803	skin:	n/a
46	chr7:79134707-79134757	SKMC	muscle:	n/a
47	chr7:79134707-79134757	GM19239	blood:	n/a
48	chr7:79134707-79134757	HepG2	liver:	n/a
49	chr7:79134707-79134757	GM12892	blood:	n/a
50	chr7:79134707-79134757	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:79171467..79174385-chr7:79176496..79179081,2	K562	blood:
2	chr13:75245963..75246703-chr7:79210691..79211521,2	MCF-7	breast:
3	chr5:150846511..150848831-chr7:79188913..79190608,2	MCF-7	breast:
4	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAGI2-2	chr7:79173227-79174169	NONHSAT121727

Variant related genes	Relation type
ENSG00000226285	TF binding region
ENSG00000226285	CpG island
ENSG00000226285	chromatin interactions

Extended variants
information (count: 2976 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2976 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2079385	chr7:79122018-79122019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35921823	chr7:79122075-79122076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574135374	chr7:79122109-79122110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541082992	chr7:79122126-79122127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543009552	chr7:79122127-79122128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369416930	chr7:79122129-79122130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550397160	chr7:79122148-79122149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560369137	chr7:79122206-79122207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563079393	chr7:79122229-79122230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576546826	chr7:79122278-79122279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145341802	chr7:79122341-79122342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111713845	chr7:79122354-79122355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533101846	chr7:79122383-79122384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528647839	chr7:79122397-79122398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184037852	chr7:79122403-79122404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375002938	chr7:79122418-79122419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369269904	chr7:79122438-79122439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568736100	chr7:79122439-79122440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188008659	chr7:79122446-79122447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142355321	chr7:79122484-79122485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13221655	chr7:79122486-79122487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191371073	chr7:79122489-79122490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535486420	chr7:79122518-79122519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539568875	chr7:79122538-79122539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146885108	chr7:79122547-79122548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13235644	chr7:79122551-79122552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565745134	chr7:79122586-79122587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13235738	chr7:79122602-79122603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376042700	chr7:79122624-79122625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372463797	chr7:79122642-79122643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554488612	chr7:79122663-79122664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548826737	chr7:79122684-79122685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568604814	chr7:79122715-79122716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138950519	chr7:79122737-79122738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536913957	chr7:79122786-79122787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369816577	chr7:79122841-79122842	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556560971	chr7:79122842-79122843	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373163286	chr7:79122883-79122884	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572254714	chr7:79122902-79122903	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34192820	chr7:79122919-79122920	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368637162	chr7:79122926-79122927	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397821380	chr7:79122927-79122928	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201087560	chr7:79122928-79122929	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376630268	chr7:79122951-79122952	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373169536	chr7:79122961-79122962	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs137885855	chr7:79122963-79122964	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375739077	chr7:79122976-79122977	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200335665	chr7:79122978-79122979	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201713659	chr7:79122979-79122980	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376754642	chr7:79122984-79122985	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79119600-79124800	Weak transcription	NHDF-Ad	bronchial
2	chr7:79122800-79123200	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr7:79123000-79123200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:79123200-79124800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:79123400-79123600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:79123400-79123600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:79123400-79123600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:79123600-79124000	Enhancers	NH-A	brain
9	chr7:79123600-79124800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:79123600-79124800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:79123800-79124800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:79124000-79124400	Weak transcription	NH-A	brain
13	chr7:79124400-79125800	Enhancers	NH-A	brain
14	chr7:79124600-79125000	Enhancers	NHEK	skin
15	chr7:79124600-79125800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:79124800-79125200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:79124800-79125400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:79124800-79125400	Enhancers	NHLF	lung
19	chr7:79124800-79125600	Enhancers	HSMM	muscle
20	chr7:79124800-79125800	Enhancers	Osteobl	bone
21	chr7:79124800-79126000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:79124800-79126200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:79124800-79126200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:79124800-79126200	Enhancers	HMEC	breast
25	chr7:79124800-79126200	Enhancers	NHDF-Ad	bronchial
26	chr7:79125000-79125400	Enhancers	A549	lung
27	chr7:79125000-79125400	Flanking Active TSS	NHEK	skin
28	chr7:79125000-79125600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:79125000-79125800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:79125200-79125400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:79125400-79125600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:79125400-79126000	Weak transcription	NHLF	lung
33	chr7:79125400-79126200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:79125400-79126400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:79125400-79126400	Enhancers	NHEK	skin
36	chr7:79125600-79126200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:79125600-79126200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:79125800-79126000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:79126000-79126200	Enhancers	NHLF	lung
40	chr7:79126000-79126400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:79126200-79126400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:79126200-79126400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:79126400-79135800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:79133600-79133800	Enhancers	A549	lung
45	chr7:79133800-79134000	Flanking Active TSS	A549	lung
46	chr7:79133800-79134200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:79133800-79134600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:79133800-79134600	Enhancers	Placenta Amnion	Placenta Amnion
49	chr7:79133800-79134800	Enhancers	Ovary	ovary
50	chr7:79133800-79137600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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