Variant report

Variant	nsv1004014
Chromosome Location	chr1:79811049-80042309
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	ATF2	chr1:79937863-79938453	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79985055-79985451	GM12878	blood:	n/a	n/a
3	ATF2	chr1:79926354-79926962	GM12878	blood:	n/a	n/a
4	ATF2	chr1:79934334-79934820	GM12878	blood:	n/a	n/a
5	ATF2	chr1:79934329-79935130	GM12878	blood:	n/a	n/a
6	ATF2	chr1:79985113-79985414	GM12878	blood:	n/a	n/a
7	ATF2	chr1:79926267-79927116	GM12878	blood:	n/a	n/a
8	BATF	chr1:79926448-79926809	GM12878	blood:	n/a	n/a
9	BATF	chr1:79934433-79934808	GM12878	blood:	n/a	n/a
10	BATF	chr1:79923292-79923555	GM12878	blood:	n/a	n/a
11	BATF	chr1:79926443-79926789	GM12878	blood:	n/a	n/a
12	BATF	chr1:79923263-79923583	GM12878	blood:	n/a	n/a
13	BATF	chr1:79934470-79934763	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:79934429-79934778	GM12878	blood:	n/a	chr1:79934643-79934652 chr1:79934574-79934583
15	BCL11A	chr1:79938042-79938283	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:79926532-79926849	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:79926408-79926871	GM12878	blood:	n/a	n/a
18	BCL3	chr1:79934464-79934754	GM12878	blood:	n/a	chr1:79934643-79934652 chr1:79934574-79934583
19	BCLAF1	chr1:79934314-79934901	GM12878	blood:	n/a	chr1:79934643-79934652 chr1:79934574-79934583
20	BCLAF1	chr1:79926291-79927080	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:79937780-79938424	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:79923354-79923520	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:79934411-79934752	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:79937966-79938457	GM12878	blood:	n/a	n/a
25	CEBPB	chr1:79823903-79824108	A549	lung:	n/a	chr1:79823979-79823992
26	CEBPB	chr1:79940207-79940407	HepG2	liver:	n/a	chr1:79940312-79940323
27	CEBPB	chr1:79966863-79967171	K562	blood:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
28	CEBPB	chr1:80034012-80034595	MCF-7	breast:	n/a	chr1:80034307-80034318
29	CEBPB	chr1:79966887-79967286	A549	lung:	n/a	chr1:79967028-79967037 chr1:79967229-79967241 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
30	CEBPB	chr1:79818714-79819083	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:79966804-79967221	IMR90	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
32	CEBPB	chr1:79818744-79819030	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:79818713-79819070	A549	lung:	n/a	n/a
34	CEBPB	chr1:79966861-79967129	MCF-7	breast:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
35	CEBPB	chr1:79966859-79967219	A549	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
36	CEBPB	chr1:79952498-79952690	A549	lung:	n/a	n/a
37	CEBPB	chr1:79843977-79844294	A549	lung:	n/a	chr1:79844132-79844143 chr1:79844130-79844141
38	CEBPB	chr1:79966828-79967239	ECC-1	luminal epithelium:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
39	CEBPB	chr1:79966857-79967179	H1-hESC	embryonic stem cell:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
40	CEBPB	chr1:79923140-79923443	HepG2	liver:	n/a	chr1:79923272-79923283
41	CEBPB	chr1:79818740-79819166	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:80030851-80030965	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:79843997-79844295	IMR90	lung:	n/a	chr1:79844132-79844143 chr1:79844130-79844141
44	CEBPB	chr1:80034120-80034494	IMR90	lung:	n/a	chr1:80034307-80034318
45	CEBPB	chr1:80034129-80034419	HepG2	liver:	n/a	chr1:80034307-80034318
46	CEBPB	chr1:79818763-79819079	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr1:79966800-79967193	ECC-1	luminal epithelium:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
48	CEBPB	chr1:79823841-79824095	IMR90	lung:	n/a	chr1:79823979-79823992
49	CEBPB	chr1:79966805-79967217	HepG2	liver:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
50	CEBPB	chr1:79844065-79844303	H1-hESC	embryonic stem cell:	n/a	chr1:79844132-79844143 chr1:79844130-79844141

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79830414-79830464	GM12892	blood:	n/a
2	chr1:79830414-79830464	Jurkat	blood:	n/a
3	chr1:79830414-79830464	HIPEpiC	eye:	n/a
4	chr1:79943970-79944020	SK-N-MC	brain:	n/a
5	chr1:79943970-79944020	CMK	blood:	n/a
6	chr1:79961576-79961626	NH-A	brain:	n/a
7	chr1:79943970-79944020	NH-A	brain:	n/a
8	chr1:79830414-79830464	AG09319	gingival:	n/a
9	chr1:79830414-79830464	NHBE	bronchial:	n/a
10	chr1:79943970-79944020	AG09309	skin:	n/a
11	chr1:79961576-79961626	HNPCEpiC	eye:	n/a
12	chr1:79943970-79944020	PANC-1	pancreas:	n/a
13	chr1:79943970-79944020	HMEC	breast:	n/a
14	chr1:79830414-79830464	MCF-7	breast:	n/a
15	chr1:79830414-79830464	PrEC	prostate:	n/a
16	chr1:79830414-79830464	U87	brain:	n/a
17	chr1:79961576-79961626	HAEpiC	amniotic membrane:	n/a
18	chr1:79943970-79944020	HRPEpiC	eye:	n/a
19	chr1:79961576-79961626	GM12878	blood:	n/a
20	chr1:79961576-79961626	ProgFib	skin:	n/a
21	chr1:79961576-79961626	HUVEC	blood vessel:	n/a
22	chr1:79943970-79944020	RPTEC	kidney:	n/a
23	chr1:79961576-79961626	GM19239	blood:	n/a
24	chr1:79943970-79944020	IMR90	lung:	fetal
25	chr1:79961576-79961626	MCF-7	breast:	n/a
26	chr1:79943970-79944020	Hepatocyte	liver:	n/a
27	chr1:79961576-79961626	HCF	heart:	n/a
28	chr1:79830414-79830464	AG04449	skin:	fetal
29	chr1:79830414-79830464	SKMC	muscle:	n/a
30	chr1:79943970-79944020	HEEpiC	esophagus:	n/a
31	chr1:79943970-79944020	PrEC	prostate:	n/a
32	chr1:79830414-79830464	MCF10A-Er-Src	breast:	n/a
33	chr1:79830414-79830464	NB4	blood:	n/a
34	chr1:79961576-79961626	AG09309	skin:	n/a
35	chr1:79830414-79830464	HMEC	breast:	n/a
36	chr1:79961576-79961626	SK-N-SH	brain:	n/a
37	chr1:79961576-79961626	T-47D	breast:	n/a
38	chr1:79830414-79830464	SK-N-SH	brain:	n/a
39	chr1:79961576-79961626	BJ	skin:	n/a
40	chr1:79961576-79961626	HMEC	breast:	n/a
41	chr1:79830414-79830464	NT2-D1	testis:	n/a
42	chr1:79943970-79944020	NHDF-neo	bronchial:	n/a
43	chr1:79830414-79830464	ECC-1	luminal epithelium:	n/a
44	chr1:79943970-79944020	ECC-1	luminal epithelium:	n/a
45	chr1:79830414-79830464	HCM	heart:	n/a
46	chr1:79943970-79944020	AG09319	gingival:	n/a
47	chr1:79943970-79944020	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:79943970-79944020	GM06990	blood:	n/a
49	chr1:79961576-79961626	A549	lung:	n/a
50	chr1:79943970-79944020	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:78468665..78470165-chr1:80026349..80029039,2	K562	blood:
2	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
3	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:
4	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
5	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:
6	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
7	chr1:79860008..79862521-chr1:79862746..79865099,2	MCF-7	breast:
8	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
9	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
10	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
11	chr1:79860008..79862521-chr1:79862746..79865099,2	MCF-7	breast:
12	chr1:79266346..79267150-chr1:79858034..79858765,3	MCF-7	breast:
13	chr1:79962962..79963539-chr1:80683583..80684326,2	MCF-7	breast:
14	chr1:79901761..79904453-chr1:79988728..79990739,2	K562	blood:
15	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
16	chr1:79826260..79828689-chr6:111008268..111010656,2	MCF-7	breast:
17	chr1:79901761..79904453-chr1:79988728..79990739,2	K562	blood:
18	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-2	chr1:79871919-79871942	XLOC_000266
2	lnc-IFI44-2	chr1:79869657-79869841	XLOC_000266
3	lnc-IFI44-2	chr1:79842763-79842816	XLOC_000266
4	lnc-IFI44-2	chr1:79871919-79871942	XLOC_000266
5	lnc-ELTD1-10	chr1:79928312-79928481	NONHSAT004101
6	lnc-IFI44-2	chr1:79871919-79871942	XLOC_000266
7	lnc-IFI44-2	chr1:79869657-79869841	XLOC_000266
8	lnc-ELTD1-10	chr1:79959246-79959486	NONHSAT004101
9	lnc-ELTD1-9	chr1:79905724-79905888	NONHSAT004100
10	lnc-ELTD1-9	chr1:79908583-79908736	NONHSAT004100
11	lnc-IFI44-2	chr1:79868876-79868927	XLOC_000266
12	lnc-IFI44-2	chr1:79869657-79870246	XLOC_000266
13	lnc-IFI44-2	chr1:79869656-79870246	NONHSAT004088
14	lnc-IFI44-2	chr1:79869657-79869841	XLOC_000266

Variant related genes	Relation type
ADH5P2	TF binding region
ADH5P2	CpG island
MSN	miRNA target sites
SH3PXD2A	miRNA target sites
RELA	miRNA target sites
PHF17	miRNA target sites

Extended variants
information (count: 4162 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4162 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192197351	chr1:79818605-79818606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs35637486	chr1:79818610-79818611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377244484	chr1:79818632-79818633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149284101	chr1:79818633-79818634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529837638	chr1:79818645-79818646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547861522	chr1:79818649-79818650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373432986	chr1:79818681-79818682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559737764	chr1:79818708-79818709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72946510	chr1:79818719-79818720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557132206	chr1:79818739-79818740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79821383	chr1:79818745-79818746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546896916	chr1:79818772-79818773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377390825	chr1:79818830-79818831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2989849	chr1:79818896-79818897	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371114053	chr1:79818911-79818912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569234890	chr1:79818975-79818976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536776927	chr1:79819000-79819001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554977152	chr1:79819002-79819003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566889769	chr1:79819034-79819035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534041719	chr1:79819053-79819054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1331718	chr1:79819055-79819056	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577257460	chr1:79819069-79819070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544067511	chr1:79819131-79819132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556357844	chr1:79819183-79819184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144777231	chr1:79819190-79819191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148130790	chr1:79819211-79819212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183748373	chr1:79819291-79819292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559678622	chr1:79819341-79819342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539633148	chr1:79819395-79819396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141956813	chr1:79819448-79819449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545438239	chr1:79819452-79819453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188464410	chr1:79819470-79819471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191871083	chr1:79819489-79819490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184300648	chr1:79819519-79819520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372821896	chr1:79819568-79819569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550871052	chr1:79819577-79819578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569459385	chr1:79819584-79819585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189802622	chr1:79819585-79819586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548713108	chr1:79819597-79819598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566828000	chr1:79819604-79819605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534182521	chr1:79819615-79819616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558399689	chr1:79819630-79819631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572081248	chr1:79819707-79819708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540687506	chr1:79819712-79819713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147313251	chr1:79819725-79819726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570640421	chr1:79819726-79819727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538169656	chr1:79819847-79819848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556051507	chr1:79819911-79819912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574583845	chr1:79819946-79819947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141028408	chr1:79819964-79819965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79818600-79819000	Enhancers	GM12878-XiMat	blood
2	chr1:79818800-79819200	Enhancers	Adipose Nuclei	Adipose
3	chr1:79818800-79819600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:79818800-79821400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:79819200-79819400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:79819200-79819400	Enhancers	NHDF-Ad	bronchial
7	chr1:79819200-79819600	Enhancers	Osteobl	bone
8	chr1:79819600-79820600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:79819600-79820600	Weak transcription	NHDF-Ad	bronchial
10	chr1:79819600-79820600	Weak transcription	Osteobl	bone
11	chr1:79819600-79821000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:79820400-79821200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:79820400-79821200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:79820400-79821400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:79820400-79821600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:79820600-79821000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:79820600-79821000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr1:79820600-79821400	Enhancers	Fetal Stomach	stomach
19	chr1:79820600-79821400	Enhancers	NHDF-Ad	bronchial
20	chr1:79820600-79821400	Enhancers	Osteobl	bone
21	chr1:79820600-79821600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:79820600-79821600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:79821000-79821200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:79830000-79830200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:79830000-79831200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:79830200-79830800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:79830200-79831000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:79830200-79831200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:79830400-79831200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:79830400-79831200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:79830600-79831000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:79830600-79831200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:79830600-79831200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr1:79830800-79831000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:79830800-79831200	Enhancers	NHDF-Ad	bronchial
36	chr1:79831000-79834400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:79831200-79836800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:79832600-79833600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:79834400-79835400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:79835400-79839200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:79836800-79837200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:79837200-79839200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:79839000-79840600	Enhancers	Fetal Brain Male	brain
44	chr1:79839200-79839800	Enhancers	Adipose Nuclei	Adipose
45	chr1:79839200-79840400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:79839200-79840600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:79839200-79840800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:79839400-79839600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:79839400-79839800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:79839400-79840000	Enhancers	Cortex derived primary cultured neurospheres	brain

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