Variant report

Variant	nsv546873
Chromosome Location	chr1:98283854-98348885
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	chr1:98315544-98315841	HCT-116	colon:	n/a	chr1:98315683-98315694
9	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
10	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
11	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
12	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
13	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:98338761-98339040	IMR90	lung:	n/a	chr1:98338884-98338895
15	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
16	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
17	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
18	CEBPB	chr1:98299523-98299768	IMR90	lung:	n/a	chr1:98299621-98299632
19	CEBPB	chr1:98338769-98339043	HepG2	liver:	n/a	chr1:98338884-98338895
20	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
21	CEBPB	chr1:98288531-98288718	A549	lung:	n/a	n/a
22	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
23	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
24	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
25	CEBPB	chr1:98315476-98315890	IMR90	lung:	n/a	chr1:98315683-98315694
26	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
27	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221
28	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694
29	CHD2	chr1:98315502-98315865	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr1:98293520-98293730	GM12878	blood:	n/a	n/a
31	CREB1	chr1:98293481-98293885	GM12878	blood:	n/a	n/a
32	CREB1	chr1:98293440-98293909	GM12878	blood:	n/a	n/a
33	CTCF	chr1:98286160-98286310	AG10803	skin:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
34	CTCF	chr1:98286160-98286310	HRE	kidney:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
35	CTCF	chr1:98286120-98286270	GM12865	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
36	CTCF	chr1:98286051-98286327	A549	lung:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
37	CTCF	chr1:98286156-98286279	GM10266	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
38	CTCF	chr1:98286140-98286290	HEK293	kidney:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
39	CTCF	chr1:98286100-98286250	GM12870	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
40	CTCF	chr1:98286120-98286270	HVMF	connective:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
41	CTCF	chr1:98286140-98286290	HA-sp	spinal cord:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
42	CTCF	chr1:98286140-98286290	GM12872	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
43	CTCF	chr1:98286100-98286250	HUVEC	blood vessel:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
44	CTCF	chr1:98286120-98286270	HFF	foreskin:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
45	CTCF	chr1:98286000-98286150	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:98286000-98286150	NHLF	lung:	n/a	n/a
47	CTCF	chr1:98286160-98286310	HPAF	blood vessel:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
48	CTCF	chr1:98286120-98286270	GM12875	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
49	CTCF	chr1:98286029-98286358	MCF-7	breast:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
50	CTCF	chr1:98286100-98286250	GM12872	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	HUVEC	blood vessel:	n/a
2	chr1:98336448-98336498	LNCaP	prostate:	n/a
3	chr1:98336448-98336498	GM19239	blood:	n/a
4	chr1:98336448-98336498	GM12878	blood:	n/a
5	chr1:98336448-98336498	HCPEpiC	choroid plexus:	n/a
6	chr1:98336448-98336498	U87	brain:	n/a
7	chr1:98336448-98336498	HCF	heart:	n/a
8	chr1:98336448-98336498	SK-N-SH	brain:	n/a
9	chr1:98336448-98336498	AG09319	gingival:	n/a
10	chr1:98336448-98336498	HRPEpiC	eye:	n/a
11	chr1:98336448-98336498	NB4	blood:	n/a
12	chr1:98336448-98336498	A549	lung:	n/a
13	chr1:98336448-98336498	HepG2	liver:	n/a
14	chr1:98336448-98336498	BJ	skin:	n/a
15	chr1:98336448-98336498	HMEC	breast:	n/a
16	chr1:98336448-98336498	NT2-D1	testis:	n/a
17	chr1:98336448-98336498	PANC-1	pancreas:	n/a
18	chr1:98336448-98336498	MCF10A-Er-Src	breast:	n/a
19	chr1:98336448-98336498	BE2_C	brain:	n/a
20	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
21	chr1:98336448-98336498	PFSK-1	brain:	n/a
22	chr1:98336448-98336498	Hepatocyte	liver:	n/a
23	chr1:98336448-98336498	AG04449	skin:	fetal
24	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
25	chr1:98336448-98336498	H1-hESC	embryonic stem cell:	embryo
26	chr1:98336448-98336498	HEK293	kidney:	embryo
27	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a
28	chr1:98336448-98336498	ProgFib	skin:	n/a
29	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
30	chr1:98336448-98336498	T-47D	breast:	n/a
31	chr1:98336448-98336498	IMR90	lung:	fetal
32	chr1:98336448-98336498	CMK	blood:	n/a
33	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
34	chr1:98336448-98336498	K562	blood:	n/a
35	chr1:98336448-98336498	HRE	kidney:	n/a
36	chr1:98336448-98336498	HRCEpiC	kidney:	n/a
37	chr1:98336448-98336498	SAEC	small airway:	n/a
38	chr1:98336448-98336498	SK-N-SH_RA	brain:	n/a
39	chr1:98336448-98336498	GM12892	blood:	n/a
40	chr1:98336448-98336498	SK-N-MC	brain:	n/a
41	chr1:98336448-98336498	HIPEpiC	eye:	n/a
42	chr1:98336448-98336498	NHBE	bronchial:	n/a
43	chr1:98336448-98336498	PrEC	prostate:	n/a
44	chr1:98336448-98336498	RPTEC	kidney:	n/a
45	chr1:98336448-98336498	HCT-116	colon:	n/a
46	chr1:98336448-98336498	NH-A	brain:	n/a
47	chr1:98336448-98336498	GM12891	blood:	n/a
48	chr1:98336448-98336498	Jurkat	blood:	n/a
49	chr1:98336448-98336498	MCF-7	breast:	n/a
50	chr1:98336448-98336498	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
2	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:

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

Extended variants
information (count: 2183 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2183 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1931064	chr1:98283854-98283855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192208807	chr1:98283866-98283867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566465414	chr1:98283904-98283905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541750379	chr1:98283929-98283930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1931065	chr1:98283941-98283942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs574722168	chr1:98283956-98283957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1931066	chr1:98283965-98283966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149907936	chr1:98284011-98284012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76693219	chr1:98284070-98284071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374217511	chr1:98284091-98284092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143931442	chr1:98284177-98284178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559510477	chr1:98284194-98284195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139852326	chr1:98284212-98284213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548577502	chr1:98284283-98284284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184465815	chr1:98284318-98284319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553972960	chr1:98284345-98284346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565245712	chr1:98284346-98284347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111706499	chr1:98284429-98284430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188775167	chr1:98284437-98284438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570465271	chr1:98284485-98284486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181255037	chr1:98284486-98284487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372545106	chr1:98284497-98284498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553146548	chr1:98284516-98284517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548902086	chr1:98284575-98284576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566535875	chr1:98284618-98284619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114841092	chr1:98284640-98284641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555296674	chr1:98284646-98284647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4309016	chr1:98284693-98284694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184641463	chr1:98284733-98284734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77250873	chr1:98284736-98284737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189207249	chr1:98284760-98284761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576863985	chr1:98284791-98284792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545875274	chr1:98284875-98284876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559447458	chr1:98284883-98284884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573277949	chr1:98284896-98284897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542374047	chr1:98284921-98284922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1034215	chr1:98284940-98284941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs180676768	chr1:98284961-98284962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186360480	chr1:98284967-98284968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537677609	chr1:98284989-98284990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564062414	chr1:98285005-98285006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190763182	chr1:98285035-98285036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146662141	chr1:98285052-98285053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372422098	chr1:98285074-98285075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557150585	chr1:98285083-98285084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566535625	chr1:98285140-98285141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570574374	chr1:98285143-98285144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181652746	chr1:98285147-98285148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549123358	chr1:98285158-98285159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539551348	chr1:98285249-98285250	Weak 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:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98240400-98309800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:98242200-98291600	Weak transcription	Dnd41	blood
3	chr1:98248600-98310600	Weak transcription	Primary B cells from cord blood	blood
4	chr1:98255800-98310800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:98257200-98315200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:98257600-98310200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr1:98258000-98291400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:98258200-98293600	Weak transcription	Primary T cells from cord blood	blood
9	chr1:98258400-98285600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr1:98266600-98288200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr1:98270800-98293800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:98272800-98310200	Weak transcription	HSMM	muscle
13	chr1:98273000-98287800	Weak transcription	Adipose Nuclei	Adipose
14	chr1:98273000-98289800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:98273600-98297600	Weak transcription	Psoas Muscle	Psoas
16	chr1:98274800-98311200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:98275600-98308400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:98276400-98300200	Weak transcription	Liver	Liver
19	chr1:98279000-98293600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr1:98279000-98295200	Weak transcription	Left Ventricle	heart
21	chr1:98280200-98316000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:98280400-98297400	Weak transcription	NHDF-Ad	bronchial
23	chr1:98280400-98298000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:98281400-98288400	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:98286800-98294200	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr1:98287000-98297000	Weak transcription	Lung	lung
27	chr1:98287600-98309800	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr1:98288200-98288800	Enhancers	Fetal Brain Male	brain
29	chr1:98288200-98289400	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr1:98288400-98292600	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr1:98288800-98297400	Weak transcription	Fetal Brain Male	brain
32	chr1:98289000-98289800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:98289200-98290000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:98289200-98290400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:98289400-98289800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:98289400-98290200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr1:98289400-98290600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:98289400-98298800	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:98289600-98290400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr1:98289800-98290400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:98289800-98290800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:98289800-98293400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr1:98290000-98290400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:98290000-98290800	Enhancers	Aorta	Aorta
45	chr1:98290000-98293400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:98290200-98290600	Enhancers	Osteobl	bone
47	chr1:98290200-98294000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr1:98290400-98290600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:98290400-98290600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:98290400-98291600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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