Variant report

Variant	nsv871630
Chromosome Location	chr1:74578318-74709362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:628)
CpG islands
(count:917)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:628 , 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	BACH1	chr1:74579087-74579383	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr1:74663532-74664137	GM12878	blood:	n/a	chr1:74663930-74663943
7	BHLHE40	chr1:74665269-74665611	K562	blood:	n/a	n/a
8	BHLHE40	chr1:74663528-74664410	K562	blood:	n/a	n/a
9	BHLHE40	chr1:74663682-74664506	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:74665274-74665305	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:74663561-74664177	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr1:74663478-74664282	K562	blood:	n/a	n/a
13	CCNT2	chr1:74663575-74664088	K562	blood:	n/a	n/a
14	CEBPB	chr1:74624760-74625022	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:74646220-74646528	A549	lung:	n/a	chr1:74646354-74646365
16	CEBPB	chr1:74646171-74646567	HepG2	liver:	n/a	chr1:74646354-74646365
17	CEBPB	chr1:74612576-74612806	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:74664885-74665549	K562	blood:	n/a	n/a
19	CEBPB	chr1:74646172-74646569	IMR90	lung:	n/a	chr1:74646354-74646365
20	CEBPB	chr1:74612627-74612820	K562	blood:	n/a	n/a
21	CEBPB	chr1:74666607-74666817	HepG2	liver:	n/a	chr1:74666714-74666723 chr1:74666712-74666723
22	CEBPB	chr1:74646215-74646535	Hela-S3	cervix:	n/a	chr1:74646354-74646365
23	CEBPB	chr1:74584352-74584643	H1-hESC	embryonic stem cell:	n/a	chr1:74584485-74584496
24	CEBPB	chr1:74662337-74662650	K562	blood:	n/a	n/a
25	CEBPB	chr1:74612578-74612853	A549	lung:	n/a	n/a
26	CEBPB	chr1:74612578-74612900	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:74584371-74584659	IMR90	lung:	n/a	chr1:74584485-74584496
28	CEBPB	chr1:74607706-74608010	Hela-S3	cervix:	n/a	chr1:74607858-74607869
29	CEBPB	chr1:74646254-74646475	HepG2	liver:	n/a	chr1:74646354-74646365
30	CEBPB	chr1:74607787-74607950	K562	blood:	n/a	chr1:74607858-74607869
31	CEBPB	chr1:74607706-74607960	A549	lung:	n/a	chr1:74607858-74607869
32	CEBPB	chr1:74584311-74584580	HepG2	liver:	n/a	chr1:74584485-74584496
33	CEBPB	chr1:74627195-74627555	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:74607672-74608043	IMR90	lung:	n/a	chr1:74607858-74607869
35	CEBPB	chr1:74607713-74607984	H1-hESC	embryonic stem cell:	n/a	chr1:74607858-74607869
36	CEBPB	chr1:74663659-74664198	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:74607709-74607977	HepG2	liver:	n/a	chr1:74607858-74607869
38	CHD1	chr1:74663275-74664217	GM12878	blood:	n/a	n/a
39	CHD2	chr1:74663569-74664035	K562	blood:	n/a	n/a
40	CHD2	chr1:74663618-74664320	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr1:74663425-74664193	HepG2	liver:	n/a	n/a
42	CHD2	chr1:74663539-74664019	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr1:74663505-74664326	GM12878	blood:	n/a	n/a
44	CREB1	chr1:74663621-74664261	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr1:74663658-74664211	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr1:74663463-74664255	HepG2	liver:	n/a	n/a
47	CREB1	chr1:74663648-74664117	A549	lung:	n/a	n/a
48	CTCF	chr1:74663857-74663881	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr1:74663860-74664010	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr1:74663960-74664110	AG04449	skin:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74664132-74664182	LNCaP	prostate:	n/a
2	chr1:74620779-74620829	HEEpiC	esophagus:	n/a
3	chr1:74664132-74664182	LNCaP	prostate:	n/a
4	chr1:74620779-74620829	HEEpiC	esophagus:	n/a
5	chr1:74664132-74664182	K562	blood:	n/a
6	chr1:74665362-74665412	GM06990	blood:	n/a
7	chr1:74663297-74663347	PANC-1	pancreas:	n/a
8	chr1:74663680-74663730	HCF	heart:	n/a
9	chr1:74663636-74663686	ECC-1	luminal epithelium:	n/a
10	chr1:74663899-74663949	SKMC	muscle:	n/a
11	chr1:74663636-74663686	SK-N-SH	brain:	n/a
12	chr1:74663750-74663800	SK-N-MC	brain:	n/a
13	chr1:74664160-74664210	HRE	kidney:	n/a
14	chr1:74663899-74663949	HCF	heart:	n/a
15	chr1:74664061-74664111	ovcar-3	ovarian:	n/a
16	chr1:74663927-74663977	ECC-1	luminal epithelium:	n/a
17	chr1:74664160-74664210	CMK	blood:	n/a
18	chr1:74663921-74663971	CMK	blood:	n/a
19	chr1:74663921-74663971	A549	lung:	n/a
20	chr1:74664132-74664182	PANC-1	pancreas:	n/a
21	chr1:74666471-74666521	HUVEC	blood vessel:	n/a
22	chr1:74666471-74666521	SK-N-SH_RA	brain:	n/a
23	chr1:74620779-74620829	HCM	heart:	n/a
24	chr1:74663899-74663949	NHDF-neo	bronchial:	n/a
25	chr1:74663827-74663877	HRPEpiC	eye:	n/a
26	chr1:74663921-74663971	HRE	kidney:	n/a
27	chr1:74666471-74666521	U87	brain:	n/a
28	chr1:74620779-74620829	HUVEC	blood vessel:	n/a
29	chr1:74663750-74663800	AG04450	lung:	fetal
30	chr1:74663750-74663800	K562	blood:	n/a
31	chr1:74663680-74663730	BJ	skin:	n/a
32	chr1:74663297-74663347	GM12892	blood:	n/a
33	chr1:74664061-74664111	PFSK-1	brain:	n/a
34	chr1:74664160-74664210	NB4	blood:	n/a
35	chr1:74620779-74620829	NH-A	brain:	n/a
36	chr1:74663636-74663686	NHBE	bronchial:	n/a
37	chr1:74663750-74663800	CMK	blood:	n/a
38	chr1:74664160-74664210	AoSMC	blood vessel:	n/a
39	chr1:74663297-74663347	Jurkat	blood:	n/a
40	chr1:74665362-74665412	SK-N-MC	brain:	n/a
41	chr1:74663636-74663686	HEK293	kidney:	embryo
42	chr1:74664132-74664182	CMK	blood:	n/a
43	chr1:74664061-74664111	HAEpiC	amniotic membrane:	n/a
44	chr1:74663680-74663730	AG04449	skin:	fetal
45	chr1:74664160-74664210	HIPEpiC	eye:	n/a
46	chr1:74664061-74664111	HCF	heart:	n/a
47	chr1:74663827-74663877	BE2_C	brain:	n/a
48	chr1:74664132-74664182	NHBE	bronchial:	n/a
49	chr1:74620779-74620829	CMK	blood:	n/a
50	chr1:74663680-74663730	SKMC	muscle:	n/a

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

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

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

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

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
ENSG00000188483	chromatin interactions
ENSG00000259030	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000162620	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000254685	chromatin interactions
ENSG00000153790	chromatin interactions

Extended variants
information (count: 2603 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2603 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535391834	chr1:74581003-74581004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184659819	chr1:74581011-74581012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76582038	chr1:74581014-74581015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565603391	chr1:74581154-74581155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11210417	chr1:74581159-74581160	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs557645653	chr1:74581206-74581207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575977249	chr1:74581240-74581241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17524893	chr1:74581311-74581312	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs555202707	chr1:74581313-74581314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573702699	chr1:74581328-74581329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541040347	chr1:74581365-74581366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559815623	chr1:74581399-74581400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578023974	chr1:74581413-74581414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571606033	chr1:74581434-74581435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545614088	chr1:74581459-74581460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563860017	chr1:74581553-74581554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375074651	chr1:74581625-74581626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531083387	chr1:74581661-74581662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549700849	chr1:74581672-74581673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561534516	chr1:74581687-74581688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371856872	chr1:74581788-74581789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375026643	chr1:74581789-74581790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368780392	chr1:74581790-74581791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528910611	chr1:74581809-74581810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538930398	chr1:74581820-74581821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189746860	chr1:74581825-74581826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17094880	chr1:74581826-74581827	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs192792604	chr1:74581891-74581892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553756941	chr1:74582058-74582059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs56758210	chr1:74582094-74582095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528454099	chr1:74582112-74582113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35614962	chr1:74582182-74582183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113697917	chr1:74582242-74582243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184431743	chr1:74582264-74582265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551594074	chr1:74582360-74582361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569524992	chr1:74582410-74582411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs55793584	chr1:74582439-74582440	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs555265878	chr1:74582476-74582477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573567111	chr1:74582517-74582518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535056078	chr1:74582532-74582533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543070109	chr1:74603819-74603820	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs187333356	chr1:74603834-74603835	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs199949341	chr1:74603847-74603848	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs201676750	chr1:74603848-74603849	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs199833919	chr1:74603849-74603850	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs554809184	chr1:74603850-74603851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs79003618	chr1:74603851-74603852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs398049368	chr1:74603859-74603860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs376725991	chr1:74603860-74603861	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs369611752	chr1:74603862-74603863	Active TSS	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:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74581000-74582200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr1:74581800-74582600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:74603800-74604600	Active TSS	Adipose Nuclei	Adipose
4	chr1:74610600-74611000	Enhancers	Brain Substantia Nigra	brain
5	chr1:74610800-74611200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:74610800-74611200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:74610800-74611200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:74610800-74611200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:74610800-74611200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:74610800-74611200	Enhancers	Brain Anterior Caudate	brain
11	chr1:74610800-74611400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:74617000-74617600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:74617200-74617600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:74617200-74617600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:74622800-74623200	Enhancers	Adipose Nuclei	Adipose
16	chr1:74624200-74624800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:74624200-74624800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:74624800-74626000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:74624800-74626800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:74625600-74626000	Enhancers	Fetal Heart	heart
21	chr1:74625800-74626600	Enhancers	HMEC	breast
22	chr1:74626800-74627800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:74639800-74640200	Enhancers	HepG2	liver
24	chr1:74646000-74646800	Enhancers	Liver	Liver
25	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:74659800-74660400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:74660400-74663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:74660600-74660800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr1:74660600-74660800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr1:74660600-74660800	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr1:74660800-74663200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr1:74661000-74663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr1:74661600-74662800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:74662200-74663000	Enhancers	Dnd41	blood
36	chr1:74662400-74662800	Active TSS	GM12878-XiMat	blood
37	chr1:74662400-74662800	Enhancers	K562	blood
38	chr1:74662600-74663000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr1:74662800-74663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr1:74662800-74663200	Flanking Active TSS	GM12878-XiMat	blood
41	chr1:74662800-74663400	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr1:74662800-74665800	Active TSS	K562	blood
43	chr1:74663000-74663200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:74663000-74663200	Enhancers	Primary B cells from cord blood	blood
45	chr1:74663000-74663200	Enhancers	Primary B cells from peripheral blood	blood
46	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells	blood
47	chr1:74663000-74663200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr1:74663000-74663200	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:74663000-74663200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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