Variant report

Variant	nsv945914
Chromosome Location	chr1:76109781-76172388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:307)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76142701-76143423	K562	blood:	n/a	n/a
2	ARID3A	chr1:76138415-76138772	K562	blood:	n/a	n/a
3	ARID3A	chr1:76127609-76127665	K562	blood:	n/a	n/a
4	ARID3A	chr1:76143217-76143395	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:76156263-76156463	K562	blood:	n/a	n/a
6	ATF1	chr1:76156227-76156551	K562	blood:	n/a	n/a
7	ATF1	chr1:76139698-76139874	K562	blood:	n/a	n/a
8	ATF3	chr1:76138498-76138845	K562	blood:	n/a	n/a
9	BACH1	chr1:76137871-76139155	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:76138455-76138930	K562	blood:	n/a	n/a
11	BACH1	chr1:76137820-76137966	K562	blood:	n/a	n/a
12	BHLHE40	chr1:76137936-76138902	K562	blood:	n/a	n/a
13	BRCA1	chr1:76138437-76138629	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
15	CBX3	chr1:76138277-76138932	K562	blood:	n/a	n/a
16	CCNT2	chr1:76156253-76156492	K562	blood:	n/a	n/a
17	CCNT2	chr1:76159140-76159573	K562	blood:	n/a	chr1:76159162-76159171
18	CEBPB	chr1:76151060-76151260	HepG2	liver:	n/a	chr1:76151076-76151087
19	CEBPB	chr1:76123595-76123716	A549	lung:	n/a	chr1:76123673-76123684
20	CEBPB	chr1:76156353-76156661	K562	blood:	n/a	n/a
21	CEBPB	chr1:76151018-76151218	IMR90	lung:	n/a	chr1:76151076-76151087
22	CEBPB	chr1:76150919-76151183	A549	lung:	n/a	chr1:76151076-76151087
23	CEBPB	chr1:76150911-76151260	K562	blood:	n/a	chr1:76151076-76151087
24	CEBPB	chr1:76123509-76123812	HepG2	liver:	n/a	chr1:76123673-76123684
25	CHD2	chr1:76139304-76139502	K562	blood:	n/a	n/a
26	CHD2	chr1:76138353-76138771	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr1:76137806-76138079	HepG2	liver:	n/a	n/a
28	CHD2	chr1:76143852-76143884	K562	blood:	n/a	n/a
29	CHD2	chr1:76138563-76138824	K562	blood:	n/a	n/a
30	CHD2	chr1:76138594-76138636	HepG2	liver:	n/a	n/a
31	CHD2	chr1:76138617-76138632	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr1:76137933-76138735	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:76113742-76113774	GM13977	blood:	n/a	n/a
34	CTCF	chr1:76161820-76161970	AG10803	skin:	n/a	n/a
35	CTCF	chr1:76142099-76142132	LNCaP	prostate:	n/a	n/a
36	CTCF	chr1:76161787-76161987	GM12878	blood:	n/a	n/a
37	CTCF	chr1:76140155-76140193	GM10248	blood:	n/a	n/a
38	CTCF	chr1:76138694-76138705	K562	blood:	n/a	n/a
39	CTCF	chr1:76152916-76152964	GM13977	blood:	n/a	n/a
40	CTCF	chr1:76134070-76134132	ProgFib	skin:	n/a	n/a
41	CTCF	chr1:76135020-76135170	GM12873	blood:	n/a	n/a
42	CTCF	chr1:76161700-76161850	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:76163468-76163513	Gliobla	brain:	n/a	n/a
44	CTCF	chr1:76155845-76155867	LNCaP	prostate:	n/a	n/a
45	CUX1	chr1:76138515-76138794	K562	blood:	n/a	n/a
46	CUX1	chr1:76159002-76159636	K562	blood:	n/a	n/a
47	E2F4	chr1:76125930-76126131	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:76138629-76138854	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:76115139-76115315	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr1:76137686-76138176	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76138023-76138073	HRCEpiC	kidney:	n/a
2	chr1:76138023-76138073	Jurkat	blood:	n/a
3	chr1:76138023-76138073	SK-N-MC	brain:	n/a
4	chr1:76138023-76138073	BJ	skin:	n/a
5	chr1:76138023-76138073	GM19239	blood:	n/a
6	chr1:76138023-76138073	RPTEC	kidney:	n/a
7	chr1:76138023-76138073	SK-N-SH_RA	brain:	n/a
8	chr1:76138023-76138073	AG09309	skin:	n/a
9	chr1:76138023-76138073	AG10803	skin:	n/a
10	chr1:76138023-76138073	GM06990	blood:	n/a
11	chr1:76138023-76138073	HCF	heart:	n/a
12	chr1:76138023-76138073	HCT-116	colon:	n/a
13	chr1:76138023-76138073	CMK	blood:	n/a
14	chr1:76138023-76138073	HepG2	liver:	n/a
15	chr1:76138023-76138073	Caco-2	colon:	n/a
16	chr1:76138023-76138073	GM12891	blood:	n/a
17	chr1:76138023-76138073	PFSK-1	brain:	n/a
18	chr1:76138023-76138073	GM12878	blood:	n/a
19	chr1:76138023-76138073	SAEC	small airway:	n/a
20	chr1:76138023-76138073	NHBE	bronchial:	n/a
21	chr1:76138023-76138073	GM12892	blood:	n/a
22	chr1:76138023-76138073	PANC-1	pancreas:	n/a
23	chr1:76138023-76138073	SKMC	muscle:	n/a
24	chr1:76138023-76138073	HEK293	kidney:	embryo
25	chr1:76138023-76138073	HAEpiC	amniotic membrane:	n/a
26	chr1:76138023-76138073	HEEpiC	esophagus:	n/a
27	chr1:76138023-76138073	NH-A	brain:	n/a
28	chr1:76138023-76138073	A549	lung:	n/a
29	chr1:76138023-76138073	T-47D	breast:	n/a
30	chr1:76138023-76138073	MCF10A-Er-Src	breast:	n/a
31	chr1:76138023-76138073	ProgFib	skin:	n/a
32	chr1:76138023-76138073	MCF-7	breast:	n/a
33	chr1:76138023-76138073	LNCaP	prostate:	n/a
34	chr1:76138023-76138073	Hepatocyte	liver:	n/a
35	chr1:76138023-76138073	NHDF-neo	bronchial:	n/a
36	chr1:76138023-76138073	K562	blood:	n/a
37	chr1:76138023-76138073	HNPCEpiC	eye:	n/a
38	chr1:76138023-76138073	U87	brain:	n/a
39	chr1:76138023-76138073	HMEC	breast:	n/a
40	chr1:76138023-76138073	PrEC	prostate:	n/a
41	chr1:76138023-76138073	HCM	heart:	n/a
42	chr1:76138023-76138073	H1-hESC	embryonic stem cell:	embryo
43	chr1:76138023-76138073	IMR90	lung:	fetal
44	chr1:76138023-76138073	BE2_C	brain:	n/a
45	chr1:76138023-76138073	AoSMC	blood vessel:	n/a
46	chr1:76138023-76138073	HRPEpiC	eye:	n/a
47	chr1:76138023-76138073	AG04450	lung:	fetal
48	chr1:76138023-76138073	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:76138023-76138073	HL-60	blood:	n/a
50	chr1:76138023-76138073	NB4	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
2	chr1:76171478..76174682-chr1:76188816..76193676,7	K562	blood:
3	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
4	chr1:76135960..76138598-chr1:76257398..76259099,2	K562	blood:
5	chr1:76158085..76160004-chr1:76262153..76264534,2	K562	blood:
6	chr1:76152720..76155791-chr1:76253617..76257786,3	K562	blood:
7	chr1:76157193..76160004-chr1:76260955..76264534,3	K562	blood:
8	chr1:76171538..76176296-chr1:76182594..76187669,7	K562	blood:
9	chr1:76171242..76173918-chr1:76251777..76253452,2	MCF-7	breast:
10	chr1:76136512..76138761-chr1:76260290..76263855,4	K562	blood:
11	chr1:76138718..76140997-chr1:76142345..76144918,2	K562	blood:
12	chr1:76136446..76138259-chr1:76189741..76191373,2	K562	blood:
13	chr1:76156186..76158840-chr1:76189632..76191650,2	K562	blood:
14	chr1:76141089..76142781-chr1:76250261..76252071,2	K562	blood:
15	chr1:76160863..76164413-chr1:76188361..76190736,3	K562	blood:
16	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
17	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
18	chr1:76158932..76160525-chr1:76160690..76162510,2	K562	blood:
19	chr1:76168335..76170790-chr1:76173153..76175492,2	K562	blood:
20	chr1:76158932..76160525-chr1:76160690..76162510,2	K562	blood:
21	chr1:76138718..76140997-chr1:76142345..76144918,2	K562	blood:
22	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
23	chr1:76139328..76142229-chr1:76158809..76161190,2	K562	blood:
24	chr1:76171640..76173855-chr1:76188377..76192246,4	K562	blood:
25	chr1:76138876..76140835-chr1:76251753..76254513,3	K562	blood:
26	chr1:76154691..76156608-chr1:76251098..76253830,2	K562	blood:
27	chr1:76135232..76136937-chr1:76193196..76195615,2	K562	blood:
28	chr1:76157340..76160559-chr1:76189001..76191132,3	K562	blood:
29	chr1:76139328..76142229-chr1:76158809..76161190,2	K562	blood:
30	chr1:76140961..76144068-chr1:76250261..76252961,3	K562	blood:
31	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
32	chr1:76140670..76143009-chr1:76255806..76258053,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76143415-76143463	NONHSAT003985

No data

Variant related genes	Relation type
ENSG00000230863	TF binding region
ENSG00000230863	CpG island
ENSG00000117054	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000207241	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000206620	chromatin interactions

Extended variants
information (count: 1155 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555775612	chr1:76112645-76112646	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs116277704	chr1:76112656-76112657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs150578979	chr1:76112659-76112660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559433648	chr1:76112680-76112681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373781912	chr1:76112681-76112682	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs1621198	chr1:76112684-76112685	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371465220	chr1:76112701-76112702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs571923125	chr1:76112729-76112730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11576534	chr1:76112751-76112752	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534904341	chr1:76121014-76121015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs574083449	chr1:76121050-76121051	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs536700794	chr1:76121097-76121098	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs556734632	chr1:76121113-76121114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs553052940	chr1:76121135-76121136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs181314211	chr1:76121142-76121143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs376096954	chr1:76121204-76121205	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs11163904	chr1:76121208-76121209	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs556985975	chr1:76121222-76121223	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs562684850	chr1:76121261-76121262	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs575772201	chr1:76121272-76121273	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs185440966	chr1:76121281-76121282	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs12059588	chr1:76121290-76121291	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs445008	chr1:76121298-76121299	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142933529	chr1:76121321-76121322	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs565422863	chr1:76121324-76121325	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs189354269	chr1:76121346-76121347	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs381183	chr1:76121367-76121368	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577117695	chr1:76128465-76128466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528366874	chr1:76128486-76128487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187543020	chr1:76128586-76128587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145063389	chr1:76128624-76128625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192124596	chr1:76128666-76128667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571110408	chr1:76128766-76128767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538736885	chr1:76128782-76128783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541339123	chr1:76128860-76128861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569132788	chr1:76128910-76128911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540140887	chr1:76128925-76128926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369057562	chr1:76129072-76129073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554731871	chr1:76129141-76129142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546189934	chr1:76129152-76129153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558238687	chr1:76129180-76129181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112103351	chr1:76129193-76129194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12129523	chr1:76129223-76129224	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs814851	chr1:76129234-76129235	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs185133979	chr1:76129251-76129252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554753669	chr1:76129279-76129280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77775002	chr1:76129283-76129284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574969072	chr1:76129320-76129321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542886159	chr1:76129332-76129333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560923740	chr1:76129370-76129371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	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
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76109200-76109800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:76121000-76121400	ZNF genes & repeats	Aorta	Aorta
3	chr1:76128400-76129400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:76128800-76129200	Enhancers	HepG2	liver
5	chr1:76129200-76136400	Weak transcription	HepG2	liver
6	chr1:76131200-76137600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:76133800-76136600	Weak transcription	K562	blood
8	chr1:76136400-76138000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:76136400-76138000	Enhancers	HepG2	liver
10	chr1:76136400-76139000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:76136400-76139000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:76136600-76136800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:76136600-76137600	Enhancers	K562	blood
14	chr1:76136600-76139000	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:76136800-76137800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:76136800-76138800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:76136800-76139000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:76136800-76139200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:76137200-76139000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:76137600-76138800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:76137600-76138800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:76137600-76139000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr1:76137600-76139000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr1:76137600-76139400	Flanking Active TSS	K562	blood
25	chr1:76137800-76138600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:76137800-76138800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:76137800-76139000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:76137800-76139200	Enhancers	Hela-S3	cervix
29	chr1:76137800-76139400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:76137800-76139400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:76137800-76139400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:76137800-76139400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:76137800-76139800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:76138000-76138600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:76138000-76138800	Flanking Active TSS	HepG2	liver
36	chr1:76138000-76139000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr1:76138000-76139000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:76138000-76139200	Enhancers	HSMM	muscle
39	chr1:76138000-76139200	Enhancers	NHEK	skin
40	chr1:76138000-76139400	Enhancers	HMEC	breast
41	chr1:76138000-76139600	Enhancers	Placenta	Placenta
42	chr1:76138200-76138600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:76138200-76139000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:76138200-76139000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:76138200-76139000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr1:76138200-76139000	Enhancers	Esophagus	oesophagus
47	chr1:76138200-76139000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr1:76138200-76139000	Enhancers	Osteobl	bone
49	chr1:76138200-76139200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:76138200-76139200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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