Variant report

Variant	nsv871239
Chromosome Location	chr1:75057586-75125581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:310)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:310 , 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	chr1:75059841-75060174	HepG2	liver:	n/a	n/a
2	ATF2	chr1:75118383-75118900	GM12878	blood:	n/a	n/a
3	ATF2	chr1:75118280-75118906	GM12878	blood:	n/a	n/a
4	BATF	chr1:75118560-75118835	GM12878	blood:	n/a	n/a
5	BATF	chr1:75118447-75118866	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:75118485-75118784	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:75118462-75118823	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:75118415-75118901	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:75118336-75118929	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:75118413-75118508	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:75060173-75060284	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:75113332-75113595	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:75089025-75089235	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:75118243-75118621	MCF-7	breast:	n/a	n/a
15	CHD2	chr1:75118490-75118793	GM12878	blood:	n/a	n/a
16	CTCF	chr1:75118478-75118630	GM19239	blood:	n/a	chr1:75118556-75118563
17	CTCF	chr1:75067480-75067630	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr1:75118530-75118556	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:75107048-75107083	Fibrobl	skin:	n/a	n/a
20	CTCF	chr1:75118320-75118470	HAc	cerebellar:	n/a	n/a
21	CTCF	chr1:75118522-75118598	MCF-7	breast:	n/a	chr1:75118556-75118563
22	CTCF	chr1:75064469-75064548	GM20000	blood:	n/a	n/a
23	CTCF	chr1:75118460-75118610	RPTEC	kidney:	n/a	chr1:75118556-75118563
24	CTCF	chr1:75118525-75118632	GM12892	blood:	n/a	chr1:75118556-75118563
25	CTCF	chr1:75118520-75118670	HBMEC	blood vessel:	n/a	chr1:75118556-75118563
26	CTCF	chr1:75118531-75118605	GM19238	blood:	n/a	chr1:75118556-75118563
27	CTCF	chr1:75118500-75118650	GM12871	blood:	n/a	chr1:75118556-75118563
28	CTCF	chr1:75118220-75118370	GM12873	blood:	n/a	n/a
29	CTCF	chr1:75079660-75079831	GM12878	blood:	n/a	n/a
30	CTCF	chr1:75075520-75075670	GM12868	blood:	n/a	n/a
31	CTCF	chr1:75079712-75079785	GM12878	blood:	n/a	n/a
32	CTCF	chr1:75090574-75090682	Spleen_OC	spleen:	n/a	n/a
33	CUX1	chr1:75118509-75118701	GM12878	blood:	n/a	n/a
34	E2F4	chr1:75106762-75106945	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr1:75098351-75098551	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr1:75118392-75118805	GM12878	blood:	n/a	n/a
37	EBF1	chr1:75118326-75118823	GM12878	blood:	n/a	n/a
38	EBF1	chr1:75118343-75118782	GM12878	blood:	n/a	n/a
39	ELF1	chr1:75118194-75118721	MCF-7	breast:	n/a	n/a
40	ELK1	chr1:75118488-75118628	GM12878	blood:	n/a	n/a
41	EP300	chr1:75118326-75118923	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:75115973-75116852	SK-N-SH	brain:	n/a	n/a
43	EP300	chr1:75077602-75078029	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr1:75118455-75118779	GM12878	blood:	n/a	n/a
45	EP300	chr1:75118255-75119149	SK-N-SH	brain:	n/a	n/a
46	EP300	chr1:75075567-75075902	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr1:75118286-75119106	SK-N-SH	brain:	n/a	n/a
48	EP300	chr1:75118496-75118687	GM12878	blood:	n/a	n/a
49	EP300	chr1:75089458-75089763	SK-N-SH_RA	brain:	n/a	chr1:75089628-75089637
50	EP300	chr1:75100735-75101067	SK-N-SH_RA	brain:	n/a	chr1:75100837-75100846

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75100556-75100606	AG09309	skin:	n/a
2	chr1:75100556-75100606	RPTEC	kidney:	n/a
3	chr1:75100556-75100606	HEEpiC	esophagus:	n/a
4	chr1:75100556-75100606	GM12891	blood:	n/a
5	chr1:75100556-75100606	MCF10A-Er-Src	breast:	n/a
6	chr1:75100556-75100606	HUVEC	blood vessel:	n/a
7	chr1:75100556-75100606	Hela-S3	cervix:	n/a
8	chr1:75100556-75100606	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:75100556-75100606	AoSMC	blood vessel:	n/a
10	chr1:75100556-75100606	Caco-2	colon:	n/a
11	chr1:75100556-75100606	BE2_C	brain:	n/a
12	chr1:75100556-75100606	HRCEpiC	kidney:	n/a
13	chr1:75100556-75100606	GM06990	blood:	n/a
14	chr1:75100556-75100606	IMR90	lung:	fetal
15	chr1:75100556-75100606	PANC-1	pancreas:	n/a
16	chr1:75100556-75100606	PrEC	prostate:	n/a
17	chr1:75100556-75100606	Jurkat	blood:	n/a
18	chr1:75100556-75100606	HIPEpiC	eye:	n/a
19	chr1:75100556-75100606	HEK293	kidney:	embryo
20	chr1:75100556-75100606	GM12878	blood:	n/a
21	chr1:75100556-75100606	K562	blood:	n/a
22	chr1:75100556-75100606	NHDF-neo	bronchial:	n/a
23	chr1:75100556-75100606	HRPEpiC	eye:	n/a
24	chr1:75100556-75100606	HCF	heart:	n/a
25	chr1:75100556-75100606	MCF-7	breast:	n/a
26	chr1:75100556-75100606	NHBE	bronchial:	n/a
27	chr1:75100556-75100606	GM12892	blood:	n/a
28	chr1:75100556-75100606	AG04450	lung:	fetal
29	chr1:75100556-75100606	GM19239	blood:	n/a
30	chr1:75100556-75100606	HNPCEpiC	eye:	n/a
31	chr1:75100556-75100606	HepG2	liver:	n/a
32	chr1:75100556-75100606	AG09319	gingival:	n/a
33	chr1:75100556-75100606	CMK	blood:	n/a
34	chr1:75100556-75100606	NT2-D1	testis:	n/a
35	chr1:75100556-75100606	SAEC	small airway:	n/a
36	chr1:75100556-75100606	SK-N-MC	brain:	n/a
37	chr1:75100556-75100606	HRE	kidney:	n/a
38	chr1:75100556-75100606	HL-60	blood:	n/a
39	chr1:75100556-75100606	SKMC	muscle:	n/a
40	chr1:75100556-75100606	NB4	blood:	n/a
41	chr1:75100556-75100606	HCT-116	colon:	n/a
42	chr1:75100556-75100606	BJ	skin:	n/a
43	chr1:75100556-75100606	Hepatocyte	liver:	n/a
44	chr1:75100556-75100606	SK-N-SH	brain:	n/a
45	chr1:75100556-75100606	HCPEpiC	choroid plexus:	n/a
46	chr1:75100556-75100606	ECC-1	luminal epithelium:	n/a
47	chr1:75100556-75100606	A549	lung:	n/a
48	chr1:75100556-75100606	AG04449	skin:	fetal
49	chr1:75100556-75100606	ovcar-3	ovarian:	n/a
50	chr1:75100556-75100606	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:75110866..75112996-chr1:75116372..75118298,2	MCF-7	breast:
2	chr1:75114474..75116619-chr1:75157243..75159501,2	MCF-7	breast:
3	chr1:75117987..75118877-chr1:75155539..75156443,2	MCF-7	breast:
4	chr1:75118268..75118957-chr1:75155576..75156140,2	MCF-7	breast:
5	chr1:75100938..75103677-chr20:57465858..57468191,2	MCF-7	breast:
6	chr1:75117909..75120810-chr1:75128171..75131111,2	K562	blood:
7	chr1:75110866..75112996-chr1:75116372..75118298,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-TNNI3K-1	chr1:75080890-75080980	NONHSAT003965
2	lnc-FPGT-TNNI3K-1	chr1:75080890-75080980	ENSG00000234497.1
3	lnc-FPGT-TNNI3K-1	chr1:75080890-75080980	NONHSAT003967
4	lnc-FPGT-TNNI3K-1	chr1:75087080-75087403	ENSG00000234497.1
5	lnc-FPGT-TNNI3K-1	chr1:75087080-75087373	NONHSAT003967
6	lnc-FPGT-TNNI3K-1	chr1:75087080-75091782	NONHSAT003965

No data

Variant related genes	Relation type
C1orf173	TF binding region
C1orf173	CpG island
ENSG00000087460	chromatin interactions

Extended variants
information (count: 1249 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs696692	chr1:75057586-75057587	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543325871	chr1:75057600-75057601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191315408	chr1:75057604-75057605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558913331	chr1:75057611-75057612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182795355	chr1:75057627-75057628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547853619	chr1:75057651-75057652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559631299	chr1:75057678-75057679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552100318	chr1:75057689-75057690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148513354	chr1:75057713-75057714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113177143	chr1:75057762-75057763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186137899	chr1:75057792-75057793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374954763	chr1:75057831-75057832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570076027	chr1:75057887-75057888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537707255	chr1:75057975-75057976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189856811	chr1:75058004-75058005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75035060	chr1:75058032-75058033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183248133	chr1:75058130-75058131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560813184	chr1:75058257-75058258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573783814	chr1:75058258-75058259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75130029	chr1:75058277-75058278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539152734	chr1:75058312-75058313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141992659	chr1:75058320-75058321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368696467	chr1:75058331-75058332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187956345	chr1:75058352-75058353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190529433	chr1:75058359-75058360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374640424	chr1:75058387-75058388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573790441	chr1:75058411-75058412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540821550	chr1:75058431-75058432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559495972	chr1:75058469-75058470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202091575	chr1:75058478-75058479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533505816	chr1:75058524-75058525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551888691	chr1:75058531-75058532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201832687	chr1:75058542-75058543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75582451	chr1:75058611-75058612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140909378	chr1:75058618-75058619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs696693	chr1:75058625-75058626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570025474	chr1:75058633-75058634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117215961	chr1:75058652-75058653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183136524	chr1:75058653-75058654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546920935	chr1:75058681-75058682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12568388	chr1:75058729-75058730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539177092	chr1:75058781-75058782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144871598	chr1:75058787-75058788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9326117	chr1:75058821-75058822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs147930686	chr1:75058900-75058901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139493492	chr1:75058913-75058914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56225526	chr1:75058918-75058919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573898659	chr1:75058979-75058980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541308492	chr1:75058982-75058983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149697197	chr1:75059039-75059040	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75054000-75058200	Weak transcription	Liver	Liver
2	chr1:75057400-75059000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr1:75058200-75059400	Enhancers	Liver	Liver
4	chr1:75058800-75060200	Enhancers	Pancreas	Pancrea
5	chr1:75059400-75060600	Flanking Active TSS	Liver	Liver
6	chr1:75059400-75060600	Enhancers	HepG2	liver
7	chr1:75060600-75061400	Enhancers	Liver	Liver
8	chr1:75062400-75062800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:75062400-75062800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:75065400-75067200	Enhancers	Primary hematopoietic stem cells	blood
11	chr1:75065400-75067200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:75065400-75067200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:75074400-75074800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:75075000-75075600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:75076400-75076600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:75077200-75078000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr1:75083800-75084600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:75083800-75085400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:75084200-75085000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:75084400-75085000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:75084600-75085400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:75085400-75088000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:75088000-75088400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:75089400-75089800	Enhancers	Fetal Heart	heart
25	chr1:75094800-75095200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:75094800-75095400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:75094800-75095600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:75094800-75095600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:75095000-75095400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr1:75095000-75095400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:75095200-75095400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:75095400-75095800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:75095400-75102800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr1:75101200-75101600	Enhancers	GM12878-XiMat	blood
35	chr1:75102800-75103000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:75102800-75103200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr1:75102800-75103200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr1:75102800-75103200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:75102800-75103200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr1:75102800-75103200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr1:75102800-75103200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr1:75102800-75103400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:75102800-75103400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr1:75103000-75103600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:75103000-75103600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:75103000-75103800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:75103200-75104400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:75103400-75104400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr1:75103800-75104400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:75104200-75104600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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