Variant report

Variant	nsv870824
Chromosome Location	chr1:75019390-75125581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr1:75118280-75118906	GM12878	blood:	n/a	n/a
3	ATF2	chr1:75118383-75118900	GM12878	blood:	n/a	n/a
4	BACH1	chr1:75047717-75047814	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:75118447-75118866	GM12878	blood:	n/a	n/a
6	BATF	chr1:75118560-75118835	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:75118462-75118823	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:75118485-75118784	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:75045035-75045562	GM12878	blood:	n/a	chr1:75045325-75045334
10	BCLAF1	chr1:75118415-75118901	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:75118413-75118508	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:75060173-75060284	HepG2	liver:	n/a	n/a
13	BHLHE40	chr1:75118336-75118929	GM12878	blood:	n/a	n/a
14	CEBPB	chr1:75044718-75044784	K562	blood:	n/a	n/a
15	CEBPB	chr1:75089025-75089235	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:75118243-75118621	MCF-7	breast:	n/a	n/a
17	CEBPB	chr1:75113332-75113595	IMR90	lung:	n/a	n/a
18	CHD2	chr1:75118490-75118793	GM12878	blood:	n/a	n/a
19	CTCF	chr1:75032920-75033070	AG10803	skin:	n/a	n/a
20	CTCF	chr1:75032900-75033050	AG10803	skin:	n/a	n/a
21	CTCF	chr1:75031160-75031310	GM12867	blood:	n/a	n/a
22	CTCF	chr1:75118531-75118605	GM19238	blood:	n/a	chr1:75118556-75118563
23	CTCF	chr1:75118320-75118470	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:75032953-75033130	IMR90	lung:	n/a	n/a
25	CTCF	chr1:75118530-75118556	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:75118460-75118610	RPTEC	kidney:	n/a	chr1:75118556-75118563
27	CTCF	chr1:75079712-75079785	GM12878	blood:	n/a	n/a
28	CTCF	chr1:75118500-75118650	GM12871	blood:	n/a	chr1:75118556-75118563
29	CTCF	chr1:75107048-75107083	Fibrobl	skin:	n/a	n/a
30	CTCF	chr1:75118520-75118670	HBMEC	blood vessel:	n/a	chr1:75118556-75118563
31	CTCF	chr1:75118522-75118598	MCF-7	breast:	n/a	chr1:75118556-75118563
32	CTCF	chr1:75064469-75064548	GM20000	blood:	n/a	n/a
33	CTCF	chr1:75118220-75118370	GM12873	blood:	n/a	n/a
34	CTCF	chr1:75090574-75090682	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr1:75118478-75118630	GM19239	blood:	n/a	chr1:75118556-75118563
36	CTCF	chr1:75075520-75075670	GM12868	blood:	n/a	n/a
37	CTCF	chr1:75067480-75067630	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:75033014-75033069	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:75118525-75118632	GM12892	blood:	n/a	chr1:75118556-75118563
40	CTCF	chr1:75079660-75079831	GM12878	blood:	n/a	n/a
41	CUX1	chr1:75118509-75118701	GM12878	blood:	n/a	n/a
42	E2F4	chr1:75098351-75098551	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr1:75106762-75106945	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr1:75045021-75045451	GM12878	blood:	n/a	chr1:75045162-75045173
45	EBF1	chr1:75118343-75118782	GM12878	blood:	n/a	n/a
46	EBF1	chr1:75045028-75045308	GM12878	blood:	n/a	chr1:75045162-75045173
47	EBF1	chr1:75118326-75118823	GM12878	blood:	n/a	n/a
48	EBF1	chr1:75118392-75118805	GM12878	blood:	n/a	n/a
49	ELF1	chr1:75118194-75118721	MCF-7	breast:	n/a	n/a
50	ELK1	chr1:75118488-75118628	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75100556-75100606	NB4	blood:	n/a
2	chr1:75043066-75043116	K562	blood:	n/a
3	chr1:75036016-75036066	RPTEC	kidney:	n/a
4	chr1:75036016-75036066	H1-hESC	embryonic stem cell:	embryo
5	chr1:75036016-75036066	NB4	blood:	n/a
6	chr1:75043066-75043116	HAEpiC	amniotic membrane:	n/a
7	chr1:75036016-75036066	HNPCEpiC	eye:	n/a
8	chr1:75100556-75100606	HCF	heart:	n/a
9	chr1:75036016-75036066	HL-60	blood:	n/a
10	chr1:75036016-75036066	HEEpiC	esophagus:	n/a
11	chr1:75036016-75036066	ECC-1	luminal epithelium:	n/a
12	chr1:75036016-75036066	Jurkat	blood:	n/a
13	chr1:75036016-75036066	BE2_C	brain:	n/a
14	chr1:75100556-75100606	GM12891	blood:	n/a
15	chr1:75043066-75043116	MCF10A-Er-Src	breast:	n/a
16	chr1:75036016-75036066	GM12892	blood:	n/a
17	chr1:75100556-75100606	MCF-7	breast:	n/a
18	chr1:75043066-75043116	GM19239	blood:	n/a
19	chr1:75043066-75043116	GM06990	blood:	n/a
20	chr1:75100556-75100606	SK-N-SH	brain:	n/a
21	chr1:75036016-75036066	Hepatocyte	liver:	n/a
22	chr1:75036016-75036066	AG09319	gingival:	n/a
23	chr1:75036016-75036066	MCF-7	breast:	n/a
24	chr1:75036016-75036066	BJ	skin:	n/a
25	chr1:75043066-75043116	HCT-116	colon:	n/a
26	chr1:75100556-75100606	ECC-1	luminal epithelium:	n/a
27	chr1:75100556-75100606	SK-N-SH_RA	brain:	n/a
28	chr1:75043066-75043116	PFSK-1	brain:	n/a
29	chr1:75100556-75100606	HAEpiC	amniotic membrane:	n/a
30	chr1:75100556-75100606	NHDF-neo	bronchial:	n/a
31	chr1:75100556-75100606	ProgFib	skin:	n/a
32	chr1:75043066-75043116	MCF-7	breast:	n/a
33	chr1:75100556-75100606	PFSK-1	brain:	n/a
34	chr1:75043066-75043116	PANC-1	pancreas:	n/a
35	chr1:75100556-75100606	PrEC	prostate:	n/a
36	chr1:75036016-75036066	AoSMC	blood vessel:	n/a
37	chr1:75043066-75043116	AG10803	skin:	n/a
38	chr1:75036016-75036066	HRCEpiC	kidney:	n/a
39	chr1:75043066-75043116	NB4	blood:	n/a
40	chr1:75043066-75043116	HEK293	kidney:	embryo
41	chr1:75036016-75036066	MCF10A-Er-Src	breast:	n/a
42	chr1:75036016-75036066	T-47D	breast:	n/a
43	chr1:75100556-75100606	HepG2	liver:	n/a
44	chr1:75100556-75100606	HIPEpiC	eye:	n/a
45	chr1:75036016-75036066	NT2-D1	testis:	n/a
46	chr1:75036016-75036066	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:75043066-75043116	SK-N-SH	brain:	n/a
48	chr1:75036016-75036066	A549	lung:	n/a
49	chr1:75043066-75043116	HCM	heart:	n/a
50	chr1:75043066-75043116	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:75117987..75118877-chr1:75155539..75156443,2	MCF-7	breast:
2	chr1:75100938..75103677-chr20:57465858..57468191,2	MCF-7	breast:
3	chr1:75110866..75112996-chr1:75116372..75118298,2	MCF-7	breast:
4	chr1:75036442..75039426-chr1:75040101..75042998,2	MCF-7	breast:
5	chr1:75117909..75120810-chr1:75128171..75131111,2	K562	blood:
6	chr1:75114474..75116619-chr1:75157243..75159501,2	MCF-7	breast:
7	chr1:75036442..75039426-chr1:75040101..75042998,2	MCF-7	breast:
8	chr1:75118268..75118957-chr1:75155576..75156140,2	MCF-7	breast:
9	chr1:75110866..75112996-chr1:75116372..75118298,2	MCF-7	breast:
10	chr1:75029648..75031890-chr1:75032751..75035408,2	K562	blood:
11	chr1:75029648..75031890-chr1:75032751..75035408,2	K562	blood:

(count:9 , 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	chr1:75055018-75055591	NONHSAT003967
4	lnc-FPGT-TNNI3K-1	chr1:75087080-75087373	NONHSAT003967
5	lnc-FPGT-TNNI3K-1	chr1:75080890-75080980	NONHSAT003967
6	lnc-FPGT-TNNI3K-1	chr1:75055419-75055591	ENSG00000234497.1
7	lnc-FPGT-TNNI3K-1	chr1:75087080-75087403	ENSG00000234497.1
8	lnc-FPGT-TNNI3K-1	chr1:75043114-75043193	NONHSAT003965
9	lnc-FPGT-TNNI3K-1	chr1:75087080-75091782	NONHSAT003965

No data

Variant related genes	Relation type
C1orf173	TF binding region
ENSG00000234497	TF binding region
C1orf173	CpG island
ENSG00000234497	CpG island
ENSG00000087460	chromatin interactions

Extended variants
information (count: 2792 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2792 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1838131	chr1:75019390-75019391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531831298	chr1:75019401-75019402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12074297	chr1:75019405-75019406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568549576	chr1:75019408-75019409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1443372	chr1:75019436-75019437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553771561	chr1:75019488-75019489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375922225	chr1:75019505-75019506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566010804	chr1:75019536-75019537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551586538	chr1:75019545-75019546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539774987	chr1:75019606-75019607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557919066	chr1:75019656-75019657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576604950	chr1:75019668-75019669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537653187	chr1:75019685-75019686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555953570	chr1:75019708-75019709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571880400	chr1:75019726-75019727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6666557	chr1:75019775-75019776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574499724	chr1:75019790-75019791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541827479	chr1:75019856-75019857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190053849	chr1:75019898-75019899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138623847	chr1:75019920-75019921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181625391	chr1:75019925-75019926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140123655	chr1:75019982-75019983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371546717	chr1:75020004-75020005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs59201609	chr1:75020068-75020069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138111501	chr1:75020128-75020129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149509989	chr1:75020134-75020135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562012077	chr1:75020135-75020136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529416073	chr1:75020156-75020157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547370930	chr1:75020167-75020168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565774462	chr1:75020180-75020181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61301514	chr1:75020260-75020261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551609332	chr1:75020291-75020292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145985546	chr1:75020292-75020293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138680605	chr1:75020295-75020296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555958199	chr1:75020306-75020307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574436794	chr1:75020326-75020327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184024219	chr1:75020329-75020330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551058564	chr1:75020344-75020345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535486972	chr1:75020395-75020396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142006402	chr1:75020444-75020445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564189442	chr1:75020452-75020453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576306393	chr1:75020472-75020473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375556803	chr1:75020479-75020480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200852498	chr1:75020491-75020492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543229409	chr1:75020503-75020504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114747493	chr1:75020529-75020530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188768278	chr1:75020568-75020569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569003862	chr1:75020579-75020580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180788280	chr1:75020681-75020682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561283805	chr1:75020717-75020718	Weak transcription	n/a	n/a	Overlapped CNVs	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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75019200-75034600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:75029800-75044800	Weak transcription	Brain Anterior Caudate	brain
3	chr1:75032200-75033000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:75032200-75033000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr1:75032600-75033000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr1:75033000-75036000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:75033000-75036400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:75036000-75037200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:75036200-75037800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:75036400-75037000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr1:75036400-75037000	Enhancers	Fetal Kidney	kidney
12	chr1:75036400-75037400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:75036600-75036800	Enhancers	Placenta	Placenta
14	chr1:75036600-75037000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:75036600-75037200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:75036600-75037200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:75036600-75037200	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr1:75036600-75037200	Enhancers	Fetal Brain Female	brain
19	chr1:75036600-75037200	Enhancers	Fetal Muscle Leg	muscle
20	chr1:75036600-75037200	Enhancers	Spleen	Spleen
21	chr1:75036600-75037400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr1:75036600-75037800	Enhancers	Brain Germinal Matrix	brain
23	chr1:75036600-75038000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:75036800-75037000	Enhancers	Liver	Liver
25	chr1:75036800-75037400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:75036800-75037400	Active TSS	Brain Substantia Nigra	brain
27	chr1:75036800-75037400	Enhancers	Fetal Muscle Trunk	muscle
28	chr1:75036800-75037400	Bivalent Enhancer	Placenta	Placenta
29	chr1:75036800-75037600	Enhancers	Adipose Nuclei	Adipose
30	chr1:75036800-75037800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:75037000-75037200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr1:75037000-75037600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:75037000-75038000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:75037200-75037800	Active TSS	Hela-S3	cervix
35	chr1:75037200-75038600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:75037400-75037600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr1:75037400-75037600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:75037400-75038400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
39	chr1:75038000-75038400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:75038000-75038600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:75038400-75039000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:75038600-75038800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:75038600-75038800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:75045000-75045400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:75045000-75045400	Enhancers	GM12878-XiMat	blood
46	chr1:75045400-75045600	Flanking Active TSS	GM12878-XiMat	blood
47	chr1:75049600-75050600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:75049800-75050400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:75049800-75050600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:75050600-75052000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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