Variant report

Variant	nsv870536
Chromosome Location	chr1:73647909-74031554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 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	chr1:73797614-73797628	K562	blood:	n/a	n/a
2	BACH1	chr1:73917243-73917304	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:73649075-73649509	GM12878	blood:	n/a	chr1:73649321-73649332 chr1:73649293-73649304 chr1:73649265-73649276
4	BHLHE40	chr1:73838380-73838391	GM12878	blood:	n/a	n/a
5	CCNT2	chr1:73979521-73979667	K562	blood:	n/a	n/a
6	CEBPB	chr1:73911498-73911785	HepG2	liver:	n/a	chr1:73911652-73911663
7	CEBPB	chr1:73940199-73940378	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:73979116-73979322	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:73760044-73760362	HepG2	liver:	n/a	chr1:73760197-73760208
10	CEBPB	chr1:73818752-73819041	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:73818773-73819066	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:74017984-74018203	HepG2	liver:	n/a	chr1:74018057-74018068
13	CEBPB	chr1:73813006-73813102	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:73832736-73833045	Hela-S3	cervix:	n/a	chr1:73832896-73832907
15	CEBPB	chr1:73832783-73833051	H1-hESC	embryonic stem cell:	n/a	chr1:73832896-73832907
16	CEBPB	chr1:73986843-73987368	HepG2	liver:	n/a	chr1:73986939-73986950
17	CEBPB	chr1:73964652-73964675	K562	blood:	n/a	n/a
18	CEBPB	chr1:73843049-73843211	HepG2	liver:	n/a	chr1:73843090-73843101
19	CEBPB	chr1:73822850-73823153	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:73817263-73817513	HepG2	liver:	n/a	chr1:73817398-73817409
21	CEBPB	chr1:73672624-73672710	K562	blood:	n/a	n/a
22	CEBPB	chr1:74018019-74018219	IMR90	lung:	n/a	chr1:74018057-74018068
23	CEBPB	chr1:73686066-73686343	HepG2	liver:	n/a	chr1:73686199-73686212 chr1:73686201-73686210 chr1:73686200-73686211 chr1:73686199-73686210
24	CEBPB	chr1:73832744-73833026	HepG2	liver:	n/a	chr1:73832896-73832907
25	CEBPB	chr1:73940174-73940505	HepG2	liver:	n/a	n/a
26	CHD2	chr1:73938557-73938777	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:73867590-73867746	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:73779486-73779511	Fibrobl	skin:	n/a	n/a
29	CTCF	chr1:73918280-73918430	HMEC	breast:	n/a	n/a
30	CTCF	chr1:73671428-73671504	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:73671275-73671578	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:73810740-73810801	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr1:73671474-73671519	Medullo	brain:	n/a	n/a
34	CTCF	chr1:73730377-73730445	GM13976	blood:	n/a	n/a
35	CTCF	chr1:73671380-73671530	Caco-2	colon:	n/a	n/a
36	CTCF	chr1:73918320-73918470	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr1:73938727-73938763	Gliobla	brain:	n/a	n/a
38	CTCF	chr1:73671360-73671510	GM12865	blood:	n/a	n/a
39	CTCF	chr1:73867397-73867714	GM12878	blood:	n/a	n/a
40	CTCF	chr1:73918120-73918270	AG04450	lung:	n/a	n/a
41	CTCF	chr1:73918350-73918426	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:73918320-73918470	RPTEC	kidney:	n/a	n/a
43	CTCF	chr1:73671460-73671610	GM12875	blood:	n/a	n/a
44	CTCF	chr1:73867460-73867610	HRE	kidney:	n/a	n/a
45	CTCF	chr1:73867470-73867607	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:73671400-73671550	HRE	kidney:	n/a	n/a
47	CTCF	chr1:74001815-74001905	GM13976	blood:	n/a	n/a
48	CTCF	chr1:73671401-73671580	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:73938681-73938764	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:73816690-73816792	LNCaP	prostate:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:73938555..73940544-chr1:73941674..73943593,2	K562	blood:
2	chr1:73719821..73721687-chr1:73728566..73730529,2	K562	blood:
3	chr1:73939906..73941913-chr1:73944204..73946364,2	K562	blood:
4	chr1:73719821..73721687-chr1:73728566..73730529,2	K562	blood:
5	chr1:73798827..73801805-chr6:86383227..86385872,2	K562	blood:
6	chr1:73939906..73941913-chr1:73944204..73946364,2	K562	blood:
7	chr1:73938555..73940544-chr1:73941674..73943593,2	K562	blood:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
2	lnc-FPGT-3	chr1:73771821-73771957	XLOC_000256
3	lnc-FPGT-8	chr1:73947639-73947696	NONHSAT003948
4	lnc-FPGT-3	chr1:73785151-73785323	XLOC_000256
5	lnc-FPGT-3	chr1:73813816-73813995	NONHSAT003934
6	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
7	lnc-FPGT-3	chr1:73772851-73773046	XLOC_000256
8	lnc-FPGT-3	chr1:73820755-73820934	NONHSAT003934
9	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
10	lnc-FPGT-3	chr1:73776535-73776673	NONHSAT003934
11	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
12	lnc-FPGT-3	chr1:73776536-73776673	ENSG00000233973
13	lnc-FPGT-3	chr1:73785151-73785323	XLOC_000256
14	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
15	lnc-LRRIQ3-1	chr1:73657287-73657538	NONHSAT003933
16	lnc-FPGT-3	chr1:73772899-73773046	XLOC_000256
17	lnc-FPGT-3	chr1:73771912-73771957	XLOC_000256
18	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
19	lnc-FPGT-3	chr1:73785150-73785344	NONHSAT003934
20	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
21	lnc-FPGT-3	chr1:73820756-73820934	XLOC_000256
22	lnc-FPGT-8	chr1:73947415-73947852	NONHSAT003947
23	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
24	lnc-FPGT-3	chr1:73771917-73771957	XLOC_000256
25	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
26	lnc-FPGT-3	chr1:73820756-73820918	XLOC_000256
27	lnc-FPGT-3	chr1:73813817-73813934	XLOC_000256
28	lnc-FPGT-3	chr1:73771922-73771957	XLOC_000256
29	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
30	lnc-FPGT-3	chr1:73813817-73813975	XLOC_000256
31	lnc-FPGT-3	chr1:73771853-73771957	ENSG00000233973
32	lnc-FPGT-3	chr1:73785151-73785344	XLOC_000256
33	lnc-FPGT-3	chr1:73771635-73771957	XLOC_000256
34	lnc-FPGT-3	chr1:73813817-73813995	XLOC_000256
35	lnc-FPGT-3	chr1:73771634-73771980	NONHSAT003934
36	lnc-FPGT-3	chr1:73772851-73773046	ENSG00000233973
37	lnc-FPGT-3	chr1:73772851-73773255	XLOC_000256
38	lnc-FPGT-8	chr1:73953224-73953485	NONHSAT003948
39	lnc-FPGT-3	chr1:73772850-73773255	NONHSAT003934
40	lnc-FPGT-8	chr1:73938022-73938114	NONHSAT003947
41	lnc-FPGT-3	chr1:73801129-73804559	XLOC_000256
42	lnc-FPGT-3	chr1:73776536-73776673	XLOC_000256
43	lnc-FPGT-3	chr1:73801129-73804560	ENSG00000233973
44	lnc-FPGT-3	chr1:73771853-73771957	XLOC_000256
45	lnc-FPGT-8	chr1:73873487-73873512	NONHSAT003947

No data

Variant related genes	Relation type
RN7SKP19	TF binding region
ENSG00000233973	TF binding region
CEP350	miRNA target sites
CERS2	miRNA target sites
CEP68	miRNA target sites

Extended variants
information (count: 1910 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4609384	chr1:73647909-73647910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187695603	chr1:73647912-73647913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539683174	chr1:73647962-73647963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553145637	chr1:73647984-73647985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs193105884	chr1:73647995-73647996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577920725	chr1:73648040-73648041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112189219	chr1:73648041-73648042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567754974	chr1:73648079-73648080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555804432	chr1:73648084-73648085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541920675	chr1:73648097-73648098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374528066	chr1:73648112-73648113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538364287	chr1:73648132-73648133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111685223	chr1:73648142-73648143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141163390	chr1:73648158-73648159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112388901	chr1:73648184-73648185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556364597	chr1:73648187-73648188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577996669	chr1:73648228-73648229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548755550	chr1:73648252-73648253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540462042	chr1:73648271-73648272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375449574	chr1:73648283-73648284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183561197	chr1:73648284-73648285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113121119	chr1:73648285-73648286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529051663	chr1:73648338-73648339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548824899	chr1:73648354-73648355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375321961	chr1:73648356-73648357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562555936	chr1:73648357-73648358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75390331	chr1:73648412-73648413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550949568	chr1:73648453-73648454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115600000	chr1:73648459-73648460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11210175	chr1:73648472-73648473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188293953	chr1:73648484-73648485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79430454	chr1:73648529-73648530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386632379	chr1:73648544-73648545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78289071	chr1:73648626-73648627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536000540	chr1:73648657-73648658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140581368	chr1:73648721-73648722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538241111	chr1:73648728-73648729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79633859	chr1:73648729-73648730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372736039	chr1:73648774-73648775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558162331	chr1:73648797-73648798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142504452	chr1:73648803-73648804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375909443	chr1:73648804-73648805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200654754	chr1:73648805-73648806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200868937	chr1:73648806-73648807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202139271	chr1:73648807-73648808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200433455	chr1:73648809-73648810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193189316	chr1:73648817-73648818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545158593	chr1:73648819-73648820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572332266	chr1:73648880-73648881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61352371	chr1:73648952-73648953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73642600-73651000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:73642800-73653600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:73651000-73651200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:73651200-73651400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:73651400-73652800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:73652800-73653400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:73653200-73653600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:73653200-73653600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:73653200-73653800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr1:73653400-73653800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:73653600-73653800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:73653800-73654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:73664600-73665400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:73671000-73671200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:73693600-73694000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:73693800-73694400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:73693800-73695200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:73745200-73745400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:73752800-73753000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:73766600-73766800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:73766800-73767000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:73772800-73773200	Enhancers	Liver	Liver
23	chr1:73776200-73777000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:73776400-73776800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr1:73776400-73776800	Enhancers	Ovary	ovary
26	chr1:73776400-73777000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:73776400-73777200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr1:73776600-73777000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:73776600-73777000	Enhancers	Fetal Heart	heart
30	chr1:73776600-73777200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:73776600-73777200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:73792800-73795200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:73799400-73800200	Enhancers	Liver	Liver
34	chr1:73799600-73800000	Active TSS	Duodenum Mucosa	Duodenum
35	chr1:73809800-73810200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:73823800-73824000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr1:73831800-73833000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr1:73847400-73849400	Enhancers	Fetal Intestine Small	intestine
39	chr1:73848000-73848800	Enhancers	Duodenum Mucosa	Duodenum
40	chr1:73848800-73849400	Active TSS	Duodenum Mucosa	Duodenum
41	chr1:73860600-73861000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr1:73871800-73872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:73871800-73872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:73876600-73876800	Enhancers	Fetal Heart	heart
45	chr1:73876800-73877200	Flanking Active TSS	Fetal Heart	heart
46	chr1:73877200-73878400	Enhancers	Fetal Heart	heart
47	chr1:73885200-73886200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:73885200-73886400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:73909600-73910000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:73909600-73910000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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