Variant report

Variant	nsv871050
Chromosome Location	chr1:98187755-98365310
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	ATF2	chr1:98256657-98257260	GM12878	blood:	n/a	n/a
2	BACH1	chr1:98330283-98330429	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:98256785-98257057	GM12878	blood:	n/a	n/a
4	BATF	chr1:98314987-98315181	GM12878	blood:	n/a	n/a
5	BCLAF1	chr1:98256717-98257173	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:98286119-98286347	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:98286097-98286281	HepG2	liver:	n/a	n/a
8	BHLHE40	chr1:98293557-98293863	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:98315427-98316172	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:98286063-98286327	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:98221656-98222027	IMR90	lung:	n/a	chr1:98221861-98221870
12	CEBPB	chr1:98208154-98208479	HepG2	liver:	n/a	chr1:98208316-98208327
13	CEBPB	chr1:98299523-98299768	IMR90	lung:	n/a	chr1:98299621-98299632
14	CEBPB	chr1:98211520-98211827	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:98252463-98252539	A549	lung:	n/a	n/a
16	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
17	CEBPB	chr1:98244025-98244225	A549	lung:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
18	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
19	CEBPB	chr1:98198657-98198872	IMR90	lung:	n/a	chr1:98198701-98198714
20	CEBPB	chr1:98208209-98208432	H1-hESC	embryonic stem cell:	n/a	chr1:98208316-98208327
21	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
22	CEBPB	chr1:98338761-98339040	IMR90	lung:	n/a	chr1:98338884-98338895
23	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
24	CEBPB	chr1:98228781-98228989	HepG2	liver:	n/a	chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228931-98228942 chr1:98228933-98228942 chr1:98228933-98228944
25	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
26	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
27	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
28	CEBPB	chr1:98353754-98353891	A549	lung:	n/a	chr1:98353856-98353867
29	CEBPB	chr1:98193010-98193283	A549	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
30	CEBPB	chr1:98243965-98244299	HepG2	liver:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
31	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
32	CEBPB	chr1:98353733-98353979	IMR90	lung:	n/a	chr1:98353856-98353867
33	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221
34	CEBPB	chr1:98208142-98208499	A549	lung:	n/a	chr1:98208316-98208327
35	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
36	CEBPB	chr1:98315544-98315841	HCT-116	colon:	n/a	chr1:98315683-98315694
37	CEBPB	chr1:98208214-98208462	Hela-S3	cervix:	n/a	chr1:98208316-98208327
38	CEBPB	chr1:98244033-98244278	K562	blood:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
39	CEBPB	chr1:98338769-98339043	HepG2	liver:	n/a	chr1:98338884-98338895
40	CEBPB	chr1:98236073-98236275	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:98243986-98244310	IMR90	lung:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
42	CEBPB	chr1:98288531-98288718	A549	lung:	n/a	n/a
43	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
44	CEBPB	chr1:98353680-98353978	HepG2	liver:	n/a	chr1:98353856-98353867
45	CEBPB	chr1:98208137-98208487	IMR90	lung:	n/a	chr1:98208316-98208327
46	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:98193045-98193294	HepG2	liver:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
48	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
49	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
50	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	HNPCEpiC	eye:	n/a
2	chr1:98336448-98336498	NB4	blood:	n/a
3	chr1:98336448-98336498	HCF	heart:	n/a
4	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
5	chr1:98336448-98336498	Hela-S3	cervix:	n/a
6	chr1:98336448-98336498	AG09319	gingival:	n/a
7	chr1:98336448-98336498	GM12892	blood:	n/a
8	chr1:98336448-98336498	SK-N-SH_RA	brain:	n/a
9	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
10	chr1:98336448-98336498	PFSK-1	brain:	n/a
11	chr1:98336448-98336498	K562	blood:	n/a
12	chr1:98336448-98336498	IMR90	lung:	fetal
13	chr1:98336448-98336498	NH-A	brain:	n/a
14	chr1:98336448-98336498	GM12878	blood:	n/a
15	chr1:98336448-98336498	HMEC	breast:	n/a
16	chr1:98336448-98336498	HUVEC	blood vessel:	n/a
17	chr1:98336448-98336498	HRCEpiC	kidney:	n/a
18	chr1:98336448-98336498	HEK293	kidney:	embryo
19	chr1:98336448-98336498	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:98336448-98336498	Jurkat	blood:	n/a
21	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
22	chr1:98336448-98336498	SAEC	small airway:	n/a
23	chr1:98336448-98336498	LNCaP	prostate:	n/a
24	chr1:98336448-98336498	AG09309	skin:	n/a
25	chr1:98336448-98336498	HCT-116	colon:	n/a
26	chr1:98336448-98336498	HL-60	blood:	n/a
27	chr1:98336448-98336498	AG04450	lung:	fetal
28	chr1:98336448-98336498	H1-hESC	embryonic stem cell:	embryo
29	chr1:98336448-98336498	NHDF-neo	bronchial:	n/a
30	chr1:98336448-98336498	GM19239	blood:	n/a
31	chr1:98336448-98336498	HIPEpiC	eye:	n/a
32	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
33	chr1:98336448-98336498	A549	lung:	n/a
34	chr1:98336448-98336498	T-47D	breast:	n/a
35	chr1:98336448-98336498	NT2-D1	testis:	n/a
36	chr1:98336448-98336498	CMK	blood:	n/a
37	chr1:98336448-98336498	RPTEC	kidney:	n/a
38	chr1:98336448-98336498	PrEC	prostate:	n/a
39	chr1:98336448-98336498	PANC-1	pancreas:	n/a
40	chr1:98336448-98336498	SK-N-MC	brain:	n/a
41	chr1:98336448-98336498	BJ	skin:	n/a
42	chr1:98336448-98336498	HCM	heart:	n/a
43	chr1:98336448-98336498	AG10803	skin:	n/a
44	chr1:98336448-98336498	HepG2	liver:	n/a
45	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a
46	chr1:98336448-98336498	NHBE	bronchial:	n/a
47	chr1:98336448-98336498	HRE	kidney:	n/a
48	chr1:98336448-98336498	SK-N-SH	brain:	n/a
49	chr1:98336448-98336498	HCPEpiC	choroid plexus:	n/a
50	chr1:98336448-98336498	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
2	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
3	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:
4	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
5	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
6	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
7	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
8	chr1:98232688..98235381-chr1:98240146..98242077,2	MCF-7	breast:
9	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
10	chr1:98228606..98230942-chr1:98231366..98234177,2	K562	blood:
11	chr1:98360000..98361724-chr1:98365980..98368297,2	K562	blood:
12	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
13	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
14	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
15	chr1:98228606..98230942-chr1:98231366..98234177,2	K562	blood:
16	chr1:98276910..98277431-chr11:65769065..65769690,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX7-2	chr1:98263024-98263607	NR_046591
2	lnc-LPPR5.1-4	chr1:98233060-98233679	l_97_chr1:98213107-98217461
3	lnc-SNX7-2	chr1:98262477-98262851	ENSG00000235777.1
4	lnc-SNX7-2	chr1:98263024-98263424	ENSG00000235777.1
5	lnc-SNX7-2	chr1:98262521-98262628	ENSG00000235777.1
6	lnc-LPPR5.1-4	chr1:98229394-98229587	l_97_chr1:98213107-98217461
7	lnc-SNX7-2	chr1:98262477-98262628	NR_046591
8	lnc-SNX7-2	chr1:98262771-98262851	NR_046591
9	lnc-SNX7-12	chr1:98240225-98240582	NONHSAT004719
10	lnc-LPPR5.1-4	chr1:98227401-98227713	l_97_chr1:98213107-98217461
11	lnc-SNX7-2	chr1:98262771-98262851	ENSG00000235777.1
12	lnc-SNX7-11	chr1:98321131-98322381	NONHSAT004723
13	lnc-SNX7-2	chr1:98263024-98263622	ENSG00000235777.1
14	lnc-LPPR5.1-4	chr1:98213403-98213506	l_97_chr1:98213107-98217461
15	lnc-LPPR5.1-4	chr1:98213108-98213244	l_97_chr1:98213107-98217461
16	lnc-LPPR5.1-4	chr1:98217399-98217461	l_97_chr1:98213107-98217461

Variant related genes	Relation type
ENSG00000270911	TF binding region
DPYD	TF binding region
ENSG00000230718	TF binding region
DPYD-AS2	TF binding region
ENSG00000270911	CpG island
DPYD	CpG island
ENSG00000230718	CpG island
DPYD-AS2	CpG island
ENSG00000175376	chromatin interactions
ENSG00000230718	chromatin interactions
ENSG00000175334	chromatin interactions
FXR1	miRNA target sites

Extended variants
information (count: 6157 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:6157 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4304627	chr1:98187755-98187756	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143355594	chr1:98187766-98187767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530004445	chr1:98187780-98187781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550144350	chr1:98187785-98187786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549176577	chr1:98187790-98187791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375917388	chr1:98187808-98187809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569225001	chr1:98187831-98187832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187322464	chr1:98187883-98187884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545125591	chr1:98187983-98187984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557945356	chr1:98187997-98187998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368726507	chr1:98188022-98188023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191808312	chr1:98188079-98188080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550356468	chr1:98188153-98188154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148346376	chr1:98188158-98188159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573943450	chr1:98188179-98188180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564502893	chr1:98188182-98188183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142774447	chr1:98188221-98188222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182995196	chr1:98188229-98188230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575596902	chr1:98188289-98188290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545010019	chr1:98188315-98188316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117712062	chr1:98188319-98188320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572091469	chr1:98188434-98188435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71657275	chr1:98188483-98188484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540806878	chr1:98188487-98188488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188034244	chr1:98188507-98188508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529916496	chr1:98188526-98188527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146957199	chr1:98188556-98188557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563597906	chr1:98188562-98188563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532478482	chr1:98188587-98188588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs67506694	chr1:98188650-98188651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192364675	chr1:98188651-98188652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551739745	chr1:98188747-98188748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571595752	chr1:98188797-98188798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534297398	chr1:98188849-98188850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547578882	chr1:98188878-98188879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567481657	chr1:98188906-98188907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536465223	chr1:98188908-98188909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34892116	chr1:98188922-98188923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79585971	chr1:98188969-98188970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556410507	chr1:98188972-98188973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12136249	chr1:98189004-98189005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551991935	chr1:98189005-98189006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138397078	chr1:98189024-98189025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184265599	chr1:98189034-98189035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367947436	chr1:98189037-98189038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77013890	chr1:98189083-98189084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571993323	chr1:98189120-98189121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72977737	chr1:98189207-98189208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs560973335	chr1:98189247-98189248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80056287	chr1:98189262-98189263	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:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98136200-98188800	Weak transcription	Left Ventricle	heart
2	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:98153400-98187800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:98176400-98188200	Weak transcription	Right Ventricle	heart
5	chr1:98177000-98188200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:98177200-98254600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:98179000-98188000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:98179000-98220800	Weak transcription	Psoas Muscle	Psoas
9	chr1:98181200-98188600	Weak transcription	Lung	lung
10	chr1:98181400-98204400	Weak transcription	Osteobl	bone
11	chr1:98181600-98188600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr1:98183600-98189600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:98183600-98279600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:98183800-98189200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:98184000-98188400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:98184200-98188600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr1:98184400-98188600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr1:98185600-98187800	Weak transcription	HMEC	breast
19	chr1:98186200-98220200	Weak transcription	Primary T cells from cord blood	blood
20	chr1:98186600-98188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:98186800-98188600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:98187000-98188400	Weak transcription	Adipose Nuclei	Adipose
23	chr1:98187000-98192800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr1:98187200-98187800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:98187200-98188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:98187200-98189000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr1:98187200-98189800	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr1:98187200-98189800	Weak transcription	Dnd41	blood
29	chr1:98187200-98190200	Weak transcription	HSMMtube	muscle
30	chr1:98187200-98203000	Weak transcription	Liver	Liver
31	chr1:98187200-98206000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr1:98187200-98207000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:98187200-98208400	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:98187200-98217200	Weak transcription	Primary B cells from cord blood	blood
35	chr1:98187200-98243400	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr1:98187400-98188800	Weak transcription	HSMM	muscle
37	chr1:98187400-98193000	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr1:98187400-98203800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr1:98188800-98189200	Strong transcription	HSMM	muscle
40	chr1:98189200-98189600	Weak transcription	HSMM	muscle
41	chr1:98189600-98189800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
42	chr1:98189600-98190200	ZNF genes & repeats	HSMM	muscle
43	chr1:98190200-98205000	Weak transcription	HSMM	muscle
44	chr1:98192800-98193600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:98193000-98193600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr1:98193000-98205600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:98193600-98202200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr1:98193600-98203600	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr1:98194200-98195000	Enhancers	Fetal Brain Male	brain
50	chr1:98198800-98224400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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