Variant report

Variant	nsv871909
Chromosome Location	chr1:74594901-74703758
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:918)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:74663477-74664483	HepG2	liver:	n/a	chr1:74664007-74664022
2	ARID3A	chr1:74663686-74664378	K562	blood:	n/a	chr1:74664007-74664022
3	ATF2	chr1:74663457-74664203	GM12878	blood:	n/a	n/a
4	ATF2	chr1:74662907-74663375	GM12878	blood:	n/a	n/a
5	BCLAF1	chr1:74663532-74664137	GM12878	blood:	n/a	chr1:74663930-74663943
6	BHLHE40	chr1:74665269-74665611	K562	blood:	n/a	n/a
7	BHLHE40	chr1:74663682-74664506	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:74663528-74664410	K562	blood:	n/a	n/a
9	BHLHE40	chr1:74665274-74665305	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:74663561-74664177	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr1:74663478-74664282	K562	blood:	n/a	n/a
12	CCNT2	chr1:74663575-74664088	K562	blood:	n/a	n/a
13	CEBPB	chr1:74663659-74664198	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:74646172-74646569	IMR90	lung:	n/a	chr1:74646354-74646365
15	CEBPB	chr1:74646215-74646535	Hela-S3	cervix:	n/a	chr1:74646354-74646365
16	CEBPB	chr1:74666607-74666817	HepG2	liver:	n/a	chr1:74666714-74666723 chr1:74666712-74666723
17	CEBPB	chr1:74612576-74612806	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:74607672-74608043	IMR90	lung:	n/a	chr1:74607858-74607869
19	CEBPB	chr1:74607713-74607984	H1-hESC	embryonic stem cell:	n/a	chr1:74607858-74607869
20	CEBPB	chr1:74607787-74607950	K562	blood:	n/a	chr1:74607858-74607869
21	CEBPB	chr1:74607709-74607977	HepG2	liver:	n/a	chr1:74607858-74607869
22	CEBPB	chr1:74662337-74662650	K562	blood:	n/a	n/a
23	CEBPB	chr1:74612627-74612820	K562	blood:	n/a	n/a
24	CEBPB	chr1:74607706-74607960	A549	lung:	n/a	chr1:74607858-74607869
25	CEBPB	chr1:74612578-74612853	A549	lung:	n/a	n/a
26	CEBPB	chr1:74627195-74627555	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:74624760-74625022	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:74646171-74646567	HepG2	liver:	n/a	chr1:74646354-74646365
29	CEBPB	chr1:74646254-74646475	HepG2	liver:	n/a	chr1:74646354-74646365
30	CEBPB	chr1:74646220-74646528	A549	lung:	n/a	chr1:74646354-74646365
31	CEBPB	chr1:74664885-74665549	K562	blood:	n/a	n/a
32	CEBPB	chr1:74607706-74608010	Hela-S3	cervix:	n/a	chr1:74607858-74607869
33	CEBPB	chr1:74612578-74612900	IMR90	lung:	n/a	n/a
34	CHD1	chr1:74663275-74664217	GM12878	blood:	n/a	n/a
35	CHD2	chr1:74663425-74664193	HepG2	liver:	n/a	n/a
36	CHD2	chr1:74663569-74664035	K562	blood:	n/a	n/a
37	CHD2	chr1:74663618-74664320	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr1:74663539-74664019	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:74663505-74664326	GM12878	blood:	n/a	n/a
40	CREB1	chr1:74663648-74664117	A549	lung:	n/a	n/a
41	CREB1	chr1:74663658-74664211	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr1:74663463-74664255	HepG2	liver:	n/a	n/a
43	CREB1	chr1:74663621-74664261	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:74633892-74633964	GM10248	blood:	n/a	n/a
45	CTCF	chr1:74663865-74663949	Lung_OC	lung:	n/a	n/a
46	CTCF	chr1:74663902-74664051	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:74663963-74663970	GM12891	blood:	n/a	n/a
48	CTCF	chr1:74663960-74664110	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr1:74664020-74664170	HPF	lung:	n/a	n/a
50	CTCF	chr1:74663860-74664010	HCPEpiC	choroid plexus:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74666471-74666521	MCF-7	breast:	n/a
2	chr1:74664132-74664182	MCF10A-Er-Src	breast:	n/a
3	chr1:74663827-74663877	HRPEpiC	eye:	n/a
4	chr1:74666471-74666521	MCF-7	breast:	n/a
5	chr1:74664132-74664182	MCF10A-Er-Src	breast:	n/a
6	chr1:74663827-74663877	HRPEpiC	eye:	n/a
7	chr1:74663827-74663877	HEEpiC	esophagus:	n/a
8	chr1:74663899-74663949	H1-hESC	embryonic stem cell:	embryo
9	chr1:74663680-74663730	LNCaP	prostate:	n/a
10	chr1:74664132-74664182	SK-N-SH_RA	brain:	n/a
11	chr1:74664132-74664182	HCM	heart:	n/a
12	chr1:74663827-74663877	CMK	blood:	n/a
13	chr1:74663750-74663800	T-47D	breast:	n/a
14	chr1:74620779-74620829	HCT-116	colon:	n/a
15	chr1:74663927-74663977	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:74665362-74665412	HEK293	kidney:	embryo
17	chr1:74664061-74664111	ProgFib	skin:	n/a
18	chr1:74663927-74663977	HEEpiC	esophagus:	n/a
19	chr1:74666471-74666521	GM19239	blood:	n/a
20	chr1:74663899-74663949	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:74663583-74663633	RPTEC	kidney:	n/a
22	chr1:74663583-74663633	HMEC	breast:	n/a
23	chr1:74663921-74663971	CMK	blood:	n/a
24	chr1:74665362-74665412	HMEC	breast:	n/a
25	chr1:74663927-74663977	AG09309	skin:	n/a
26	chr1:74663750-74663800	HEK293	kidney:	embryo
27	chr1:74666471-74666521	Caco-2	colon:	n/a
28	chr1:74663297-74663347	U87	brain:	n/a
29	chr1:74620779-74620829	HCM	heart:	n/a
30	chr1:74663921-74663971	HCPEpiC	choroid plexus:	n/a
31	chr1:74663297-74663347	PrEC	prostate:	n/a
32	chr1:74663680-74663730	NH-A	brain:	n/a
33	chr1:74665362-74665412	SAEC	small airway:	n/a
34	chr1:74663899-74663949	HRE	kidney:	n/a
35	chr1:74663827-74663877	GM19239	blood:	n/a
36	chr1:74663921-74663971	GM12878	blood:	n/a
37	chr1:74663899-74663949	HCM	heart:	n/a
38	chr1:74663636-74663686	MCF10A-Er-Src	breast:	n/a
39	chr1:74665362-74665412	CMK	blood:	n/a
40	chr1:74664160-74664210	HepG2	liver:	n/a
41	chr1:74663927-74663977	GM12878	blood:	n/a
42	chr1:74663583-74663633	HCF	heart:	n/a
43	chr1:74666471-74666521	H1-hESC	embryonic stem cell:	embryo
44	chr1:74664160-74664210	HEK293	kidney:	embryo
45	chr1:74663899-74663949	PANC-1	pancreas:	n/a
46	chr1:74664160-74664210	AG04449	skin:	fetal
47	chr1:74663583-74663633	H1-hESC	embryonic stem cell:	embryo
48	chr1:74620779-74620829	HUVEC	blood vessel:	n/a
49	chr1:74620779-74620829	Jurkat	blood:	n/a
50	chr1:74666471-74666521	PFSK-1	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74663942..74664482-chr7:25219741..25220347,2	NB4	blood:
2	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
3	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
4	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
5	chr1:74662960..74663950-chr9:131940135..131940948,2	Hela-S3	cervix:
6	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
7	chr1:74656254..74659150-chr1:74661430..74664103,3	K562	blood:
8	chr1:74641537..74643099-chr1:74809509..74811733,2	K562	blood:
9	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
10	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
11	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
12	chr1:74613777..74616581-chr1:74619059..74620965,2	K562	blood:
13	chr1:74662396..74665247-chr1:74681410..74684026,2	K562	blood:
14	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
15	chr1:74649322..74651054-chr1:74653302..74655077,2	K562	blood:
16	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
17	chr1:74662984..74666783-chr1:74668983..74674031,7	K562	blood:
18	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
19	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
20	chr1:74662297..74664282-chr1:74667218..74669836,2	K562	blood:
21	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
22	chr1:74663449..74664076-chr20:1306022..1306565,2	Hela-S3	cervix:
23	chr1:74610872..74613542-chr1:74663622..74665411,2	K562	blood:
24	chr1:74646951..74649028-chr1:74654609..74657361,2	K562	blood:
25	chr1:74613777..74616581-chr1:74619059..74620965,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC53-2	chr1:74663680-74663831	NONHSAT003957
2	lnc-LRRC53-2	chr1:74648222-74648306	NONHSAT003956
3	lnc-LRRC53-2	chr1:74621347-74621550	NONHSAT003956
4	lnc-LRRC53-2	chr1:74645907-74649368	NONHSAT003957
5	lnc-LRRC53-2	chr1:74621417-74621533	NONHSAT003955

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FPGT	hsa-miR-335-5p	chr1:74672969-74672991

Variant related genes	Relation type
LRRIQ3	TF binding region
TNNI3K	TF binding region
FPGT-TNNI3K	TF binding region
FPGT	TF binding region
LRRIQ3	CpG island
TNNI3K	CpG island
FPGT-TNNI3K	CpG island
FPGT	CpG island
ENSG00000153790	chromatin interactions
ENSG00000254685	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000162620	chromatin interactions
ENSG00000259030	chromatin interactions

Extended variants
information (count: 2374 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543070109	chr1:74603819-74603820	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs187333356	chr1:74603834-74603835	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs199949341	chr1:74603847-74603848	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs201676750	chr1:74603848-74603849	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs199833919	chr1:74603849-74603850	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554809184	chr1:74603850-74603851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs79003618	chr1:74603851-74603852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs398049368	chr1:74603859-74603860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs376725991	chr1:74603860-74603861	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs369611752	chr1:74603862-74603863	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs373049859	chr1:74603868-74603869	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373924874	chr1:74603889-74603890	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs533861439	chr1:74603908-74603909	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577716205	chr1:74603935-74603936	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs78481204	chr1:74603988-74603989	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs577194394	chr1:74604004-74604005	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs141646530	chr1:74604009-74604010	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs556277039	chr1:74604010-74604011	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs367774163	chr1:74604016-74604017	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs574586771	chr1:74604018-74604019	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs147028140	chr1:74604050-74604051	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs560322427	chr1:74604054-74604055	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs527850323	chr1:74604111-74604112	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545107368	chr1:74604113-74604114	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546199913	chr1:74604167-74604168	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs12043976	chr1:74604188-74604189	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs111455873	chr1:74604214-74604215	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs532052320	chr1:74604311-74604312	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs192062856	chr1:74604315-74604316	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs78181577	chr1:74604337-74604338	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs572039966	chr1:74604338-74604339	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183677349	chr1:74604345-74604346	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs114953641	chr1:74604379-74604380	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs138313810	chr1:74604408-74604409	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs533969941	chr1:74604470-74604471	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs552220284	chr1:74604480-74604481	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs376439541	chr1:74604498-74604499	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368561056	chr1:74604551-74604552	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs570713989	chr1:74604568-74604569	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs538871058	chr1:74610604-74610605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1856789	chr1:74610686-74610687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs536501616	chr1:74610696-74610697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565493848	chr1:74610698-74610699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554681906	chr1:74610702-74610703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4557914	chr1:74610703-74610704	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540402204	chr1:74610704-74610705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182836170	chr1:74610711-74610712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113295604	chr1:74610723-74610724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532609782	chr1:74610775-74610776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544400994	chr1:74610780-74610781	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74603800-74604600	Active TSS	Adipose Nuclei	Adipose
2	chr1:74610600-74611000	Enhancers	Brain Substantia Nigra	brain
3	chr1:74610800-74611200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:74610800-74611200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:74610800-74611200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:74610800-74611200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:74610800-74611200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:74610800-74611200	Enhancers	Brain Anterior Caudate	brain
9	chr1:74610800-74611400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:74617000-74617600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:74617200-74617600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:74617200-74617600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr1:74622800-74623200	Enhancers	Adipose Nuclei	Adipose
14	chr1:74624200-74624800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:74624200-74624800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:74624800-74626000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:74624800-74626800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:74625600-74626000	Enhancers	Fetal Heart	heart
19	chr1:74625800-74626600	Enhancers	HMEC	breast
20	chr1:74626800-74627800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:74639800-74640200	Enhancers	HepG2	liver
22	chr1:74646000-74646800	Enhancers	Liver	Liver
23	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:74659800-74660400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:74660400-74663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:74660600-74660800	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr1:74660600-74660800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr1:74660600-74660800	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr1:74660800-74663200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr1:74661000-74663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr1:74661600-74662800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr1:74662200-74663000	Enhancers	Dnd41	blood
34	chr1:74662400-74662800	Active TSS	GM12878-XiMat	blood
35	chr1:74662400-74662800	Enhancers	K562	blood
36	chr1:74662600-74663000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr1:74662800-74663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:74662800-74663200	Flanking Active TSS	GM12878-XiMat	blood
39	chr1:74662800-74663400	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr1:74662800-74665800	Active TSS	K562	blood
41	chr1:74663000-74663200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:74663000-74663200	Enhancers	Primary B cells from cord blood	blood
43	chr1:74663000-74663200	Enhancers	Primary B cells from peripheral blood	blood
44	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells	blood
45	chr1:74663000-74663200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:74663000-74663200	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:74663000-74663200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:74663000-74663200	Enhancers	Adipose Nuclei	Adipose
50	chr1:74663000-74663200	Enhancers	Brain Hippocampus Middle	brain

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