Variant report

Variant	nsv2032
Chromosome Location	chr1:98319851-98369285
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	CEBPB	chr1:98353754-98353891	A549	lung:	n/a	chr1:98353856-98353867
3	CEBPB	chr1:98353733-98353979	IMR90	lung:	n/a	chr1:98353856-98353867
4	CEBPB	chr1:98338769-98339043	HepG2	liver:	n/a	chr1:98338884-98338895
5	CEBPB	chr1:98353680-98353978	HepG2	liver:	n/a	chr1:98353856-98353867
6	CEBPB	chr1:98366545-98366914	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:98338761-98339040	IMR90	lung:	n/a	chr1:98338884-98338895
8	CTCF	chr1:98336279-98336382	HUVEC	blood vessel:	n/a	chr1:98336324-98336345
9	CTCF	chr1:98330320-98330470	BE2_C	brain:	n/a	n/a
10	CTCF	chr1:98336293-98336401	Hela-S3	cervix:	n/a	chr1:98336324-98336345
11	CTCF	chr1:98331831-98331880	GM20000	blood:	n/a	n/a
12	E2F4	chr1:98341578-98341837	MCF10A-Er-Src	breast:	n/a	chr1:98341578-98341587
13	E2F4	chr1:98350836-98350966	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr1:98366775-98367039	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr1:98368139-98368511	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr1:98331065-98331075	GM12878	blood:	n/a	n/a
17	FAM48A	chr1:98335345-98335411	GM12878	blood:	n/a	n/a
18	FOS	chr1:98366608-98366955	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:98359459-98359712	MCF10A-Er-Src	breast:	n/a	chr1:98359543-98359553
20	FOS	chr1:98359501-98359755	MCF10A-Er-Src	breast:	n/a	chr1:98359543-98359553
21	FOS	chr1:98341532-98341936	MCF10A-Er-Src	breast:	n/a	chr1:98341775-98341787 chr1:98341778-98341789
22	FOS	chr1:98366585-98367230	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:98358771-98358904	MCF10A-Er-Src	breast:	n/a	chr1:98358839-98358847 chr1:98358837-98358848 chr1:98358838-98358848 chr1:98358839-98358847 chr1:98358840-98358847
24	FOS	chr1:98366609-98366894	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:98359306-98359862	MCF10A-Er-Src	breast:	n/a	chr1:98359543-98359553
26	FOS	chr1:98364545-98364939	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:98341520-98342016	MCF10A-Er-Src	breast:	n/a	chr1:98341775-98341787 chr1:98341778-98341789
28	FOS	chr1:98369200-98369591	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:98359402-98359832	MCF10A-Er-Src	breast:	n/a	chr1:98359543-98359553
30	FOS	chr1:98334251-98334304	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:98341531-98341938	MCF10A-Er-Src	breast:	n/a	chr1:98341775-98341787 chr1:98341778-98341789
32	FOS	chr1:98328813-98328845	HUVEC	blood vessel:	n/a	n/a
33	FOS	chr1:98358711-98358895	MCF10A-Er-Src	breast:	n/a	chr1:98358839-98358847 chr1:98358837-98358848 chr1:98358838-98358848 chr1:98358839-98358847 chr1:98358840-98358847
34	FOS	chr1:98364567-98364964	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:98366558-98367297	HUVEC	blood vessel:	n/a	n/a
36	FOS	chr1:98366579-98367155	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:98364175-98364333	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:98367638-98368121	MCF10A-Er-Src	breast:	n/a	chr1:98367783-98367794 chr1:98367821-98367830
39	FOS	chr1:98367792-98368150	MCF10A-Er-Src	breast:	n/a	chr1:98367821-98367830
40	FOS	chr1:98341520-98341997	MCF10A-Er-Src	breast:	n/a	chr1:98341775-98341787 chr1:98341778-98341789
41	FOS	chr1:98364167-98365030	MCF10A-Er-Src	breast:	n/a	n/a
42	FOSL2	chr1:98359255-98359813	SK-N-SH	brain:	n/a	chr1:98359543-98359553
43	FOXA2	chr1:98327991-98328424	A549	lung:	n/a	chr1:98328125-98328137
44	GATA3	chr1:98357716-98357753	SH-SY5Y	brain:	n/a	chr1:98357731-98357752
45	GATA3	chr1:98361481-98362253	SK-N-SH	brain:	n/a	chr1:98361815-98361826 chr1:98361832-98361839
46	GATA3	chr1:98359186-98359878	SK-N-SH	brain:	n/a	chr1:98359492-98359499
47	GATA3	chr1:98367034-98367057	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr1:98361484-98362154	SK-N-SH	brain:	n/a	chr1:98361815-98361826 chr1:98361832-98361839
49	GATA3	chr1:98329840-98330387	SK-N-SH	brain:	n/a	chr1:98330119-98330135 chr1:98330067-98330078 chr1:98330119-98330135
50	GATA3	chr1:98349994-98350152	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	MCF-7	breast:	n/a
2	chr1:98336448-98336498	GM12878	blood:	n/a
3	chr1:98336448-98336498	SKMC	muscle:	n/a
4	chr1:98336448-98336498	HCM	heart:	n/a
5	chr1:98336448-98336498	HEK293	kidney:	embryo
6	chr1:98336448-98336498	PANC-1	pancreas:	n/a
7	chr1:98336448-98336498	PFSK-1	brain:	n/a
8	chr1:98336448-98336498	BJ	skin:	n/a
9	chr1:98336448-98336498	ProgFib	skin:	n/a
10	chr1:98336448-98336498	SAEC	small airway:	n/a
11	chr1:98336448-98336498	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:98336448-98336498	NH-A	brain:	n/a
13	chr1:98336448-98336498	HCT-116	colon:	n/a
14	chr1:98336448-98336498	AG10803	skin:	n/a
15	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a
16	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
17	chr1:98336448-98336498	Hela-S3	cervix:	n/a
18	chr1:98336448-98336498	NHBE	bronchial:	n/a
19	chr1:98336448-98336498	NT2-D1	testis:	n/a
20	chr1:98336448-98336498	MCF10A-Er-Src	breast:	n/a
21	chr1:98336448-98336498	AG04449	skin:	fetal
22	chr1:98336448-98336498	NB4	blood:	n/a
23	chr1:98336448-98336498	GM06990	blood:	n/a
24	chr1:98336448-98336498	LNCaP	prostate:	n/a
25	chr1:98336448-98336498	GM12891	blood:	n/a
26	chr1:98336448-98336498	HNPCEpiC	eye:	n/a
27	chr1:98336448-98336498	SK-N-SH	brain:	n/a
28	chr1:98336448-98336498	Hepatocyte	liver:	n/a
29	chr1:98336448-98336498	AG09309	skin:	n/a
30	chr1:98336448-98336498	Jurkat	blood:	n/a
31	chr1:98336448-98336498	HepG2	liver:	n/a
32	chr1:98336448-98336498	T-47D	breast:	n/a
33	chr1:98336448-98336498	BE2_C	brain:	n/a
34	chr1:98336448-98336498	HIPEpiC	eye:	n/a
35	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
36	chr1:98336448-98336498	CMK	blood:	n/a
37	chr1:98336448-98336498	Caco-2	colon:	n/a
38	chr1:98336448-98336498	SK-N-MC	brain:	n/a
39	chr1:98336448-98336498	GM19239	blood:	n/a
40	chr1:98336448-98336498	A549	lung:	n/a
41	chr1:98336448-98336498	HCPEpiC	choroid plexus:	n/a
42	chr1:98336448-98336498	HCF	heart:	n/a
43	chr1:98336448-98336498	IMR90	lung:	fetal
44	chr1:98336448-98336498	HRCEpiC	kidney:	n/a
45	chr1:98336448-98336498	PrEC	prostate:	n/a
46	chr1:98336448-98336498	NHDF-neo	bronchial:	n/a
47	chr1:98336448-98336498	RPTEC	kidney:	n/a
48	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
49	chr1:98336448-98336498	HUVEC	blood vessel:	n/a
50	chr1:98336448-98336498	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
2	chr1:98360000..98361724-chr1:98365980..98368297,2	K562	blood:
3	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
4	chr1:98360000..98361724-chr1:98365980..98368297,2	K562	blood:
5	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
6	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

Extended variants
information (count: 1602 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1602 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528242637	chr1:98319890-98319891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541667044	chr1:98319938-98319939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570232925	chr1:98319941-98319942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539174917	chr1:98319969-98319970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12093707	chr1:98320041-98320042	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549740917	chr1:98320051-98320052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373415892	chr1:98320071-98320072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555592046	chr1:98320102-98320103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182153296	chr1:98320299-98320300	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187177857	chr1:98320326-98320327	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575545079	chr1:98320365-98320366	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532414911	chr1:98320376-98320377	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35330951	chr1:98320397-98320398	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544300898	chr1:98320399-98320400	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4367807	chr1:98320408-98320409	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs117983815	chr1:98320428-98320429	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535180830	chr1:98320453-98320454	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4372296	chr1:98320492-98320493	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376207786	chr1:98320510-98320511	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537770744	chr1:98320513-98320514	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72979736	chr1:98320538-98320539	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558796766	chr1:98320547-98320548	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576879153	chr1:98320550-98320551	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577679427	chr1:98320586-98320587	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545483973	chr1:98320617-98320618	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552991668	chr1:98320643-98320644	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144745101	chr1:98320654-98320655	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542002754	chr1:98320667-98320668	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561571773	chr1:98320720-98320721	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138333483	chr1:98320725-98320726	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190578735	chr1:98320730-98320731	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs60132939	chr1:98320777-98320778	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544063928	chr1:98320788-98320789	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141869848	chr1:98320862-98320863	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111255323	chr1:98320865-98320866	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150615185	chr1:98320897-98320898	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs45522136	chr1:98320923-98320924	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559791040	chr1:98320931-98320932	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528625400	chr1:98320950-98320951	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528777038	chr1:98320998-98320999	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370746714	chr1:98321019-98321020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182757198	chr1:98321028-98321029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367963978	chr1:98321101-98321102	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537657831	chr1:98321110-98321111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575983276	chr1:98321129-98321130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542973596	chr1:98321144-98321145	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs187144868	chr1:98321149-98321150	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs190017860	chr1:98321151-98321152	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs539408594	chr1:98321168-98321169	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs552739505	chr1:98321176-98321177	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98303200-98351000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr1:98309400-98367200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:98311600-98320000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr1:98311600-98320200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:98311600-98320400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr1:98311600-98320600	Weak transcription	Right Ventricle	heart
7	chr1:98311600-98326600	Weak transcription	Gastric	stomach
8	chr1:98311600-98337800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:98311800-98320400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:98311800-98320400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:98311800-98320400	Weak transcription	Esophagus	oesophagus
12	chr1:98311800-98320400	Weak transcription	Left Ventricle	heart
13	chr1:98311800-98320400	Weak transcription	Lung	lung
14	chr1:98311800-98320400	Weak transcription	Pancreas	Pancrea
15	chr1:98311800-98320400	Weak transcription	Spleen	Spleen
16	chr1:98311800-98322000	Weak transcription	Aorta	Aorta
17	chr1:98311800-98322200	Weak transcription	Ovary	ovary
18	chr1:98311800-98322400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:98311800-98350400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:98312000-98320200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:98312000-98320200	Weak transcription	Thymus	Thymus
22	chr1:98312000-98322400	Weak transcription	Liver	Liver
23	chr1:98312000-98324000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:98312000-98324200	Weak transcription	Fetal Thymus	thymus
25	chr1:98312200-98320200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr1:98312200-98344400	Weak transcription	Fetal Intestine Small	intestine
27	chr1:98314000-98320400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:98315600-98321400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:98315600-98337200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr1:98315800-98320400	Weak transcription	Brain Substantia Nigra	brain
31	chr1:98315800-98320600	Weak transcription	Brain Angular Gyrus	brain
32	chr1:98315800-98323400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:98315800-98330000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr1:98315800-98330000	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:98315800-98330200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr1:98315800-98330200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:98315800-98332200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr1:98316000-98327800	Weak transcription	HMEC	breast
39	chr1:98316200-98320200	Weak transcription	Primary T cells from cord blood	blood
40	chr1:98316200-98320200	Weak transcription	Adipose Nuclei	Adipose
41	chr1:98316200-98327000	Weak transcription	Primary B cells from cord blood	blood
42	chr1:98316400-98320000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:98316400-98320000	Weak transcription	HSMM	muscle
44	chr1:98316400-98320600	Weak transcription	NH-A	brain
45	chr1:98316400-98322000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr1:98316400-98330000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:98316400-98330200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:98316400-98330200	Weak transcription	Osteobl	bone
49	chr1:98316400-98346400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:98316400-98348000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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