Variant report

Variant	nsv461795
Chromosome Location	chr1:70475794-70551339
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70507413-70508355	K562	blood:	n/a	n/a
2	ARID3A	chr1:70516058-70516168	K562	blood:	n/a	n/a
3	ARID3A	chr1:70500148-70500446	K562	blood:	n/a	n/a
4	ATF1	chr1:70507065-70507752	K562	blood:	n/a	n/a
5	ATF1	chr1:70491630-70491777	K562	blood:	n/a	n/a
6	ATF1	chr1:70531620-70531733	K562	blood:	n/a	n/a
7	ATF1	chr1:70522460-70522734	K562	blood:	n/a	n/a
8	ATF1	chr1:70542996-70543014	K562	blood:	n/a	n/a
9	ATF1	chr1:70508023-70508451	K562	blood:	n/a	n/a
10	ATF3	chr1:70507425-70507826	K562	blood:	n/a	n/a
11	BACH1	chr1:70499988-70500046	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:70550258-70550499	K562	blood:	n/a	n/a
13	BACH1	chr1:70507441-70507755	K562	blood:	n/a	n/a
14	BACH1	chr1:70550207-70550511	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:70499196-70499403	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:70500094-70500465	K562	blood:	n/a	n/a
17	BHLHE40	chr1:70505111-70505270	K562	blood:	n/a	n/a
18	CCNT2	chr1:70508029-70508393	K562	blood:	n/a	n/a
19	CCNT2	chr1:70509626-70509826	K562	blood:	n/a	n/a
20	CCNT2	chr1:70500072-70500392	K562	blood:	n/a	n/a
21	CCNT2	chr1:70507380-70507801	K562	blood:	n/a	chr1:70507597-70507617
22	CEBPB	chr1:70542764-70543105	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:70478700-70478922	K562	blood:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
24	CEBPB	chr1:70545345-70545550	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:70492988-70493096	A549	lung:	n/a	n/a
26	CEBPB	chr1:70550813-70551667	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:70490029-70490288	HepG2	liver:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
28	CEBPB	chr1:70489995-70490313	H1-hESC	embryonic stem cell:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
29	CEBPB	chr1:70478660-70478961	HepG2	liver:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
30	CEBPB	chr1:70531843-70532108	HepG2	liver:	n/a	chr1:70531988-70531999
31	CEBPB	chr1:70478704-70478931	A549	lung:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
32	CEBPB	chr1:70542757-70543092	K562	blood:	n/a	n/a
33	CEBPB	chr1:70503670-70503981	K562	blood:	n/a	n/a
34	CEBPB	chr1:70490015-70490327	K562	blood:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
35	CEBPB	chr1:70503631-70503918	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:70478642-70478948	IMR90	lung:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
37	CEBPB	chr1:70489988-70490319	IMR90	lung:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
38	CEBPB	chr1:70490015-70490212	Hela-S3	cervix:	n/a	chr1:70490072-70490083 chr1:70490072-70490083
39	CEBPB	chr1:70506879-70508308	K562	blood:	n/a	n/a
40	CEBPB	chr1:70509519-70509858	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:70499985-70500315	K562	blood:	n/a	n/a
42	CEBPB	chr1:70507371-70507757	K562	blood:	n/a	n/a
43	CEBPB	chr1:70503731-70503934	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:70519194-70519468	K562	blood:	n/a	n/a
45	CEBPB	chr1:70506897-70508155	K562	blood:	n/a	n/a
46	CEBPD	chr1:70507324-70507868	K562	blood:	n/a	n/a
47	CHD2	chr1:70507795-70507995	K562	blood:	n/a	n/a
48	CTCF	chr1:70500200-70500350	BJ	skin:	n/a	n/a
49	CTCF	chr1:70500240-70500390	HMEC	breast:	n/a	n/a
50	CTCF	chr1:70500160-70500310	NHDF-neo	bronchial:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70509936-70509986	NH-A	brain:	n/a
2	chr1:70500419-70500469	K562	blood:	n/a
3	chr1:70501250-70501300	ECC-1	luminal epithelium:	n/a
4	chr1:70501250-70501300	HIPEpiC	eye:	n/a
5	chr1:70501250-70501300	ovcar-3	ovarian:	n/a
6	chr1:70509936-70509986	SK-N-SH	brain:	n/a
7	chr1:70509936-70509986	AG04449	skin:	fetal
8	chr1:70501250-70501300	Caco-2	colon:	n/a
9	chr1:70509936-70509986	GM06990	blood:	n/a
10	chr1:70509936-70509986	AoSMC	blood vessel:	n/a
11	chr1:70500419-70500469	NHBE	bronchial:	n/a
12	chr1:70509936-70509986	MCF-7	breast:	n/a
13	chr1:70501250-70501300	HL-60	blood:	n/a
14	chr1:70500419-70500469	Caco-2	colon:	n/a
15	chr1:70509936-70509986	AG09319	gingival:	n/a
16	chr1:70500419-70500469	Hela-S3	cervix:	n/a
17	chr1:70500419-70500469	HL-60	blood:	n/a
18	chr1:70501250-70501300	SK-N-SH_RA	brain:	n/a
19	chr1:70500419-70500469	AG04449	skin:	fetal
20	chr1:70501250-70501300	GM12892	blood:	n/a
21	chr1:70509936-70509986	K562	blood:	n/a
22	chr1:70500419-70500469	HCT-116	colon:	n/a
23	chr1:70509936-70509986	SK-N-SH_RA	brain:	n/a
24	chr1:70509936-70509986	NT2-D1	testis:	n/a
25	chr1:70500419-70500469	T-47D	breast:	n/a
26	chr1:70500419-70500469	HIPEpiC	eye:	n/a
27	chr1:70509936-70509986	LNCaP	prostate:	n/a
28	chr1:70509936-70509986	SK-N-MC	brain:	n/a
29	chr1:70509936-70509986	HCF	heart:	n/a
30	chr1:70501250-70501300	HRPEpiC	eye:	n/a
31	chr1:70500419-70500469	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:70501250-70501300	H1-hESC	embryonic stem cell:	embryo
33	chr1:70500419-70500469	HCPEpiC	choroid plexus:	n/a
34	chr1:70509936-70509986	HRE	kidney:	n/a
35	chr1:70501250-70501300	T-47D	breast:	n/a
36	chr1:70509936-70509986	HEEpiC	esophagus:	n/a
37	chr1:70509936-70509986	PrEC	prostate:	n/a
38	chr1:70501250-70501300	GM19239	blood:	n/a
39	chr1:70500419-70500469	LNCaP	prostate:	n/a
40	chr1:70509936-70509986	NHDF-neo	bronchial:	n/a
41	chr1:70500419-70500469	GM12878	blood:	n/a
42	chr1:70500419-70500469	HepG2	liver:	n/a
43	chr1:70501250-70501300	GM12891	blood:	n/a
44	chr1:70509936-70509986	ProgFib	skin:	n/a
45	chr1:70509936-70509986	HCT-116	colon:	n/a
46	chr1:70509936-70509986	GM12892	blood:	n/a
47	chr1:70501250-70501300	HRE	kidney:	n/a
48	chr1:70509936-70509986	MCF10A-Er-Src	breast:	n/a
49	chr1:70509936-70509986	U87	brain:	n/a
50	chr1:70509936-70509986	SKMC	muscle:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:70488967..70491122-chr1:70493902..70495892,2	K562	blood:
2	chr1:70522889..70525651-chr1:70527610..70529469,2	K562	blood:
3	chr1:70489437..70491215-chr1:70493568..70495892,3	K562	blood:
4	chr1:70531477..70533272-chr1:70537582..70540486,2	K562	blood:
5	chr1:70522889..70525651-chr1:70527610..70529469,2	K562	blood:
6	chr1:70506553..70508330-chr1:70513862..70516733,2	K562	blood:
7	chr1:70531477..70533272-chr1:70537582..70540486,2	K562	blood:
8	chr1:70478688..70481774-chr1:70484221..70487331,4	K562	blood:
9	chr1:70488967..70491122-chr1:70493902..70495892,2	K562	blood:
10	chr1:70499914..70500706-chr1:70608453..70608981,2	MCF-7	breast:
11	chr1:70506553..70508330-chr1:70513862..70516733,2	K562	blood:
12	chr1:70500723..70504696-chr1:70505322..70508157,4	K562	blood:
13	chr1:70478688..70481774-chr1:70484221..70487331,4	K562	blood:
14	chr1:70497178..70499324-chr1:70500642..70503385,2	K562	blood:
15	chr1:70497178..70499324-chr1:70500642..70503385,2	K562	blood:
16	chr1:70537552..70539411-chr1:70545771..70549953,3	K562	blood:
17	chr1:70489437..70491215-chr1:70493568..70495892,3	K562	blood:
18	chr1:70500217..70500734-chr1:70975931..70976504,2	K562	blood:
19	chr1:70495317..70498678-chr1:70499423..70502142,3	K562	blood:
20	chr1:70499352..70501847-chr1:70502427..70503999,2	K562	blood:
21	chr1:70504669..70508313-chr1:70509431..70511799,3	K562	blood:
22	chr1:70499830..70500350-chr1:70953253..70954208,2	K562	blood:
23	chr1:70537552..70539411-chr1:70545771..70549953,3	K562	blood:
24	chr1:70504669..70508313-chr1:70509431..70511799,3	K562	blood:
25	chr1:70512841..70514929-chr1:70517630..70519621,2	K562	blood:
26	chr1:70483697..70485490-chr1:70486525..70489030,2	K562	blood:
27	chr1:70499352..70501847-chr1:70502427..70503999,2	K562	blood:
28	chr1:70500723..70504696-chr1:70505322..70508157,4	K562	blood:
29	chr1:70512841..70514929-chr1:70517630..70519621,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC40-2	chr1:70479665-70479827	ENSG00000237919.1
2	lnc-SRSF11-1	chr1:70490889-70491259	expReg_chr1_10524_+
3	lnc-LRRC40-2	chr1:70486506-70487062	ENSG00000237919.1
4	lnc-LRRC40-2	chr1:70487945-70488081	ENSG00000237919.1
5	lnc-LRRC40-2	chr1:70487945-70488081	ENSG00000237919.1
6	lnc-LRRC40-2	chr1:70496815-70496905	ENSG00000237919.1
7	lnc-LRRC40-2	chr1:70486931-70487062	ENSG00000237919.1

No data

Variant related genes	Relation type
ENSG00000237919	TF binding region
ENSG00000237919	CpG island
ENSG00000237919	chromatin interactions

Extended variants
information (count: 2507 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565234490	chr1:70475794-70475795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539030990	chr1:70475795-70475796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148372076	chr1:70475859-70475860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188848352	chr1:70475914-70475915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550002447	chr1:70475945-70475946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570313095	chr1:70476038-70476039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181992965	chr1:70476043-70476044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185555794	chr1:70476090-70476091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141649782	chr1:70476156-70476157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534610916	chr1:70476163-70476164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150507904	chr1:70476174-70476175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139517040	chr1:70476182-70476183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543635582	chr1:70476199-70476200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189259363	chr1:70476210-70476211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72945209	chr1:70476215-70476216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113828294	chr1:70476243-70476244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200426713	chr1:70476255-70476256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577047313	chr1:70476329-70476330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545743301	chr1:70476392-70476393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559605491	chr1:70476420-70476421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143225875	chr1:70476421-70476422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368977883	chr1:70476431-70476432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561036257	chr1:70476435-70476436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556457919	chr1:70476472-70476473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180687457	chr1:70476480-70476481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550325205	chr1:70476500-70476501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550319715	chr1:70476534-70476535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570121184	chr1:70476536-70476537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575912760	chr1:70476552-70476553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552555884	chr1:70476565-70476566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566367083	chr1:70476566-70476567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146247364	chr1:70476586-70476587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75009863	chr1:70476609-70476610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568149558	chr1:70476627-70476628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537173298	chr1:70476663-70476664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35888449	chr1:70476670-70476671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12032200	chr1:70476739-70476740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576921409	chr1:70476798-70476799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545979561	chr1:70476846-70476847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12035905	chr1:70476915-70476916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs186391326	chr1:70476927-70476928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572842463	chr1:70476937-70476938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541011827	chr1:70476952-70476953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565863442	chr1:70476979-70476980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113454069	chr1:70477009-70477010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200838758	chr1:70477015-70477016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370024674	chr1:70477018-70477019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373225336	chr1:70477019-70477020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377404123	chr1:70477027-70477028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370506861	chr1:70477028-70477029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
small cell lung cancer	20016488	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
Esophageal cancer	21851588	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70450800-70481200	Weak transcription	Fetal Brain Female	brain
2	chr1:70464800-70509000	Weak transcription	Brain Angular Gyrus	brain
3	chr1:70475000-70475800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:70477800-70478200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:70478000-70503800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr1:70479400-70515600	Weak transcription	Fetal Brain Male	brain
7	chr1:70479800-70503800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr1:70481200-70481800	Strong transcription	Fetal Brain Female	brain
9	chr1:70481800-70488400	Weak transcription	Fetal Brain Female	brain
10	chr1:70483200-70483800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:70483400-70485200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:70485200-70488400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:70485200-70503800	Weak transcription	Brain Germinal Matrix	brain
14	chr1:70485600-70503800	Weak transcription	Brain Anterior Caudate	brain
15	chr1:70486800-70487200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:70486800-70487200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:70488000-70503200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:70488000-70503800	Weak transcription	Fetal Muscle Leg	muscle
19	chr1:70488400-70488600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:70488400-70489400	Strong transcription	Fetal Brain Female	brain
21	chr1:70488800-70489200	ZNF genes & repeats	Pancreas	Pancrea
22	chr1:70489200-70492800	Weak transcription	Pancreas	Pancrea
23	chr1:70489400-70501400	Weak transcription	Fetal Brain Female	brain
24	chr1:70492600-70492800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:70492800-70495800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:70495000-70495800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:70495000-70496800	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr1:70495800-70496000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:70495800-70496800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:70496800-70499800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr1:70499000-70499400	Enhancers	GM12878-XiMat	blood
32	chr1:70499200-70500600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:70499800-70500400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:70499800-70500400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr1:70499800-70500600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:70499800-70500800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:70500000-70500600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:70500000-70501200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:70500200-70500800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr1:70500200-70506200	Weak transcription	Brain Hippocampus Middle	brain
41	chr1:70500400-70500600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr1:70500600-70501000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:70500600-70503800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr1:70500600-70503800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr1:70500600-70503800	Weak transcription	Pancreas	Pancrea
46	chr1:70501000-70509400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr1:70501400-70505400	Strong transcription	Fetal Brain Female	brain
48	chr1:70503200-70503800	Weak transcription	Fetal Stomach	stomach
49	chr1:70503200-70504600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:70503200-70505000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain

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