Variant report

Variant	nsv871376
Chromosome Location	chr1:98274132-98365310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:98330283-98330429	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr1:98314987-98315181	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:98286119-98286347	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:98293557-98293863	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:98286097-98286281	HepG2	liver:	n/a	n/a
6	BRCA1	chr1:98315427-98316172	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:98286063-98286327	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694
9	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
10	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
11	CEBPB	chr1:98288531-98288718	A549	lung:	n/a	n/a
12	CEBPB	chr1:98353680-98353978	HepG2	liver:	n/a	chr1:98353856-98353867
13	CEBPB	chr1:98338769-98339043	HepG2	liver:	n/a	chr1:98338884-98338895
14	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
15	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
16	CEBPB	chr1:98353754-98353891	A549	lung:	n/a	chr1:98353856-98353867
17	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
18	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
19	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
20	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
21	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221
22	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
23	CEBPB	chr1:98338761-98339040	IMR90	lung:	n/a	chr1:98338884-98338895
24	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
25	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
26	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
27	CEBPB	chr1:98315544-98315841	HCT-116	colon:	n/a	chr1:98315683-98315694
28	CEBPB	chr1:98315476-98315890	IMR90	lung:	n/a	chr1:98315683-98315694
29	CEBPB	chr1:98353733-98353979	IMR90	lung:	n/a	chr1:98353856-98353867
30	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:98299523-98299768	IMR90	lung:	n/a	chr1:98299621-98299632
32	CHD2	chr1:98315502-98315865	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:98293520-98293730	GM12878	blood:	n/a	n/a
34	CREB1	chr1:98293440-98293909	GM12878	blood:	n/a	n/a
35	CREB1	chr1:98293481-98293885	GM12878	blood:	n/a	n/a
36	CTCF	chr1:98286120-98286270	HPF	lung:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
37	CTCF	chr1:98286077-98286315	MCF-7	breast:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
38	CTCF	chr1:98286120-98286270	HPAF	blood vessel:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
39	CTCF	chr1:98286153-98286307	GM13977	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
40	CTCF	chr1:98286120-98286270	HMF	breast:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
41	CTCF	chr1:98286120-98286270	GM06990	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
42	CTCF	chr1:98286120-98286270	AoAF	blood vessel:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
43	CTCF	chr1:98310820-98310970	GM12874	blood:	n/a	n/a
44	CTCF	chr1:98286120-98286270	AG09319	gingival:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
45	CTCF	chr1:98286120-98286270	HRPEpiC	eye:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
46	CTCF	chr1:98285980-98286130	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr1:98331831-98331880	GM20000	blood:	n/a	n/a
48	CTCF	chr1:98285934-98286407	HCT-116	colon:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
49	CTCF	chr1:98286093-98286245	SK-N-SH_RA	brain:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
50	CTCF	chr1:98286146-98286272	K562	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	LNCaP	prostate:	n/a
2	chr1:98336448-98336498	HCM	heart:	n/a
3	chr1:98336448-98336498	NHBE	bronchial:	n/a
4	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
5	chr1:98336448-98336498	NB4	blood:	n/a
6	chr1:98336448-98336498	HRE	kidney:	n/a
7	chr1:98336448-98336498	Hepatocyte	liver:	n/a
8	chr1:98336448-98336498	SAEC	small airway:	n/a
9	chr1:98336448-98336498	Caco-2	colon:	n/a
10	chr1:98336448-98336498	AG04449	skin:	fetal
11	chr1:98336448-98336498	HCPEpiC	choroid plexus:	n/a
12	chr1:98336448-98336498	PANC-1	pancreas:	n/a
13	chr1:98336448-98336498	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:98336448-98336498	RPTEC	kidney:	n/a
15	chr1:98336448-98336498	AG09309	skin:	n/a
16	chr1:98336448-98336498	AG10803	skin:	n/a
17	chr1:98336448-98336498	HRPEpiC	eye:	n/a
18	chr1:98336448-98336498	Jurkat	blood:	n/a
19	chr1:98336448-98336498	NHDF-neo	bronchial:	n/a
20	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
21	chr1:98336448-98336498	NT2-D1	testis:	n/a
22	chr1:98336448-98336498	NH-A	brain:	n/a
23	chr1:98336448-98336498	MCF-7	breast:	n/a
24	chr1:98336448-98336498	HepG2	liver:	n/a
25	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a
26	chr1:98336448-98336498	HRCEpiC	kidney:	n/a
27	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
28	chr1:98336448-98336498	HNPCEpiC	eye:	n/a
29	chr1:98336448-98336498	AG04450	lung:	fetal
30	chr1:98336448-98336498	BE2_C	brain:	n/a
31	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
32	chr1:98336448-98336498	SK-N-SH	brain:	n/a
33	chr1:98336448-98336498	AG09319	gingival:	n/a
34	chr1:98336448-98336498	GM06990	blood:	n/a
35	chr1:98336448-98336498	HMEC	breast:	n/a
36	chr1:98336448-98336498	GM12878	blood:	n/a
37	chr1:98336448-98336498	SK-N-SH_RA	brain:	n/a
38	chr1:98336448-98336498	Hela-S3	cervix:	n/a
39	chr1:98336448-98336498	CMK	blood:	n/a
40	chr1:98336448-98336498	A549	lung:	n/a
41	chr1:98336448-98336498	HIPEpiC	eye:	n/a
42	chr1:98336448-98336498	HCF	heart:	n/a
43	chr1:98336448-98336498	SKMC	muscle:	n/a
44	chr1:98336448-98336498	GM12891	blood:	n/a
45	chr1:98336448-98336498	IMR90	lung:	fetal
46	chr1:98336448-98336498	SK-N-MC	brain:	n/a
47	chr1:98336448-98336498	K562	blood:	n/a
48	chr1:98336448-98336498	HCT-116	colon:	n/a
49	chr1:98336448-98336498	PrEC	prostate:	n/a
50	chr1:98336448-98336498	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
2	chr1:98276910..98277431-chr11:65769065..65769690,2	Hela-S3	cervix:
3	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
4	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
5	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
6	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
7	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
8	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:
9	chr1:98360000..98361724-chr1:98365980..98368297,2	K562	blood:
10	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX7-11	chr1:98321131-98322381	NONHSAT004723

Variant related genes	Relation type
ENSG00000270911	TF binding region
ENSG00000270911	CpG island
ENSG00000175334	chromatin interactions
ENSG00000175376	chromatin interactions

Extended variants
information (count: 3080 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3080 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12568335	chr1:98274132-98274133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143614728	chr1:98274156-98274157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148068060	chr1:98274173-98274174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11165912	chr1:98274225-98274226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183292030	chr1:98274240-98274241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141779357	chr1:98274258-98274259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202021607	chr1:98274289-98274290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567788169	chr1:98274435-98274436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560685734	chr1:98274470-98274471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576772080	chr1:98274504-98274505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146012358	chr1:98274509-98274510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114332654	chr1:98274513-98274514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537023709	chr1:98274520-98274521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188388525	chr1:98274539-98274540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538877113	chr1:98274582-98274583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552232641	chr1:98274590-98274591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191588789	chr1:98274602-98274603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138669598	chr1:98274603-98274604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559192549	chr1:98274676-98274677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554285423	chr1:98274698-98274699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183791455	chr1:98274799-98274800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35151553	chr1:98274809-98274810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115166042	chr1:98274833-98274834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556678740	chr1:98274872-98274873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576564560	chr1:98274876-98274877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545681312	chr1:98274890-98274891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559030664	chr1:98274894-98274895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188113918	chr1:98274916-98274917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540655822	chr1:98274958-98274959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560573730	chr1:98274997-98274998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75422842	chr1:98275023-98275024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543152773	chr1:98275055-98275056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191119289	chr1:98275091-98275092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142858407	chr1:98275107-98275108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146080304	chr1:98275120-98275121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566008349	chr1:98275140-98275141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139701642	chr1:98275182-98275183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79425974	chr1:98275214-98275215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115539062	chr1:98275225-98275226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567674113	chr1:98275278-98275279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149357352	chr1:98275316-98275317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74108404	chr1:98275346-98275347	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs115298847	chr1:98275355-98275356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538899235	chr1:98275356-98275357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12742215	chr1:98275360-98275361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12746260	chr1:98275361-98275362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369093826	chr1:98275367-98275368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552207594	chr1:98275413-98275414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144668569	chr1:98275502-98275503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112523113	chr1:98275504-98275505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
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
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98183600-98279600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:98240400-98309800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr1:98242200-98291600	Weak transcription	Dnd41	blood
4	chr1:98248600-98310600	Weak transcription	Primary B cells from cord blood	blood
5	chr1:98255800-98310800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:98257200-98315200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr1:98257600-98310200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr1:98258000-98291400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:98258200-98293600	Weak transcription	Primary T cells from cord blood	blood
10	chr1:98258400-98285600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr1:98266600-98288200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:98266800-98274800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr1:98270800-98293800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:98272800-98279600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:98272800-98310200	Weak transcription	HSMM	muscle
16	chr1:98273000-98287800	Weak transcription	Adipose Nuclei	Adipose
17	chr1:98273000-98289800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:98273200-98276000	Weak transcription	Liver	Liver
19	chr1:98273600-98297600	Weak transcription	Psoas Muscle	Psoas
20	chr1:98274800-98277000	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr1:98274800-98311200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr1:98275600-98308400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr1:98276000-98276400	Strong transcription	Liver	Liver
24	chr1:98276400-98300200	Weak transcription	Liver	Liver
25	chr1:98277000-98279600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr1:98278800-98279800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr1:98279000-98293600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:98279000-98295200	Weak transcription	Left Ventricle	heart
29	chr1:98279400-98280000	Enhancers	HMEC	breast
30	chr1:98279400-98280400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:98279600-98280000	Enhancers	Osteobl	bone
32	chr1:98279600-98280200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:98279600-98280200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:98279600-98280200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr1:98279600-98280400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:98279600-98280400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:98279600-98280400	Enhancers	NHDF-Ad	bronchial
38	chr1:98279600-98280400	Enhancers	NHLF	lung
39	chr1:98279600-98281400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr1:98279800-98280000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr1:98279800-98280400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:98280200-98316000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:98280400-98297400	Weak transcription	NHDF-Ad	bronchial
44	chr1:98280400-98298000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr1:98281400-98288400	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr1:98286800-98294200	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr1:98287000-98297000	Weak transcription	Lung	lung
48	chr1:98287600-98309800	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr1:98288200-98288800	Enhancers	Fetal Brain Male	brain
50	chr1:98288200-98289400	Strong transcription	Primary monocytes fromperipheralblood	blood

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