Variant report

Variant	nsv933197
Chromosome Location	chr1:98003867-98039582
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	BATF	chr1:98003636-98003954	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:98029519-98029746	K562	blood:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
3	CEBPB	chr1:98029328-98029864	HepG2	liver:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
4	CEBPB	chr1:98039132-98039464	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:98032993-98033294	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:98010188-98010326	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:98039138-98039475	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:98029335-98029853	Hela-S3	cervix:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
9	CEBPB	chr1:98038143-98038477	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:98031433-98031738	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:98029340-98029867	A549	lung:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
12	CEBPB	chr1:98029511-98029813	H1-hESC	embryonic stem cell:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
13	CEBPB	chr1:98029324-98029866	IMR90	lung:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
14	CEBPB	chr1:98029529-98029805	MCF-7	breast:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
15	CEBPB	chr1:98039241-98039362	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:98016800-98016950	AG09319	gingival:	n/a	n/a
17	CTCF	chr1:98016660-98016810	HMEC	breast:	n/a	n/a
18	CTCF	chr1:98016847-98016938	LNCaP	prostate:	n/a	n/a
19	CTCF	chr1:98014687-98014737	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:98027480-98027630	AG09319	gingival:	n/a	n/a
21	CTCF	chr1:98016810-98016974	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:98016826-98016965	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr1:98016860-98017010	AG10803	skin:	n/a	n/a
24	CTCF	chr1:98016800-98016950	AG10803	skin:	n/a	n/a
25	CTCF	chr1:98027360-98027510	AG09319	gingival:	n/a	n/a
26	CTCF	chr1:98016860-98017010	HMEC	breast:	n/a	n/a
27	CTCF	chr1:98016720-98016870	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr1:98012894-98012963	GM20000	blood:	n/a	n/a
29	CTCF	chr1:98016820-98016970	AG09319	gingival:	n/a	n/a
30	CTCF	chr1:98016755-98017047	GM12878	blood:	n/a	n/a
31	E2F4	chr1:98013857-98013881	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr1:98003791-98004146	GM12878	blood:	n/a	n/a
33	EP300	chr1:98028783-98028833	K562	blood:	n/a	n/a
34	EP300	chr1:98020127-98020237	GM12878	blood:	n/a	n/a
35	FOS	chr1:98006415-98006447	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:98006314-98006513	MCF10A-Er-Src	breast:	n/a	n/a
37	GATA3	chr1:98038053-98038584	SK-N-SH	brain:	n/a	chr1:98038354-98038363 chr1:98038390-98038407
38	GATA3	chr1:98019141-98019152	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr1:98036283-98036392	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr1:98038202-98038427	SH-SY5Y	brain:	n/a	chr1:98038354-98038363 chr1:98038390-98038407
41	GATA3	chr1:98016764-98017148	SH-SY5Y	brain:	n/a	chr1:98017119-98017126 chr1:98017112-98017133 chr1:98017119-98017129 chr1:98017119-98017126 chr1:98017117-98017126 chr1:98017117-98017127 chr1:98017114-98017130 chr1:98017119-98017126
42	GATA3	chr1:98016566-98017197	SK-N-SH	brain:	n/a	chr1:98017119-98017126 chr1:98017112-98017133 chr1:98017119-98017129 chr1:98017119-98017126 chr1:98017117-98017126 chr1:98017117-98017127 chr1:98017114-98017130 chr1:98017119-98017126
43	GATA3	chr1:98004011-98004207	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr1:98016566-98017171	SK-N-SH	brain:	n/a	chr1:98017119-98017126 chr1:98017112-98017133 chr1:98017119-98017129 chr1:98017119-98017126 chr1:98017117-98017126 chr1:98017117-98017127 chr1:98017114-98017130 chr1:98017119-98017126
45	GATA3	chr1:98038084-98038610	SK-N-SH	brain:	n/a	chr1:98038354-98038363 chr1:98038390-98038407
46	JUN	chr1:98019627-98019824	K562	blood:	n/a	n/a
47	JUN	chr1:98030920-98031105	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUN	chr1:98006998-98007354	K562	blood:	n/a	n/a
49	MAFF	chr1:98012389-98012661	HepG2	liver:	n/a	chr1:98012503-98012521
50	MAFK	chr1:98012356-98012697	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98036695-98036745	NT2-D1	testis:	n/a
2	chr1:98036695-98036745	H1-hESC	embryonic stem cell:	embryo
3	chr1:98031839-98031889	AG10803	skin:	n/a
4	chr1:98031839-98031889	BE2_C	brain:	n/a
5	chr1:98036695-98036745	HMEC	breast:	n/a
6	chr1:98036695-98036745	MCF-7	breast:	n/a
7	chr1:98031839-98031889	H1-hESC	embryonic stem cell:	embryo
8	chr1:98036695-98036745	NHDF-neo	bronchial:	n/a
9	chr1:98036695-98036745	RPTEC	kidney:	n/a
10	chr1:98031839-98031889	HRE	kidney:	n/a
11	chr1:98031839-98031889	NB4	blood:	n/a
12	chr1:98031839-98031889	HRPEpiC	eye:	n/a
13	chr1:98031839-98031889	ProgFib	skin:	n/a
14	chr1:98031839-98031889	SK-N-SH	brain:	n/a
15	chr1:98036695-98036745	PFSK-1	brain:	n/a
16	chr1:98036695-98036745	SK-N-SH	brain:	n/a
17	chr1:98036695-98036745	SK-N-MC	brain:	n/a
18	chr1:98031839-98031889	NH-A	brain:	n/a
19	chr1:98036695-98036745	HEK293	kidney:	embryo
20	chr1:98031839-98031889	GM12892	blood:	n/a
21	chr1:98036695-98036745	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:98036695-98036745	HCT-116	colon:	n/a
23	chr1:98031839-98031889	Hela-S3	cervix:	n/a
24	chr1:98031839-98031889	HRCEpiC	kidney:	n/a
25	chr1:98036695-98036745	BJ	skin:	n/a
26	chr1:98031839-98031889	T-47D	breast:	n/a
27	chr1:98031839-98031889	Caco-2	colon:	n/a
28	chr1:98036695-98036745	HepG2	liver:	n/a
29	chr1:98031839-98031889	RPTEC	kidney:	n/a
30	chr1:98036695-98036745	HRPEpiC	eye:	n/a
31	chr1:98031839-98031889	GM06990	blood:	n/a
32	chr1:98031839-98031889	U87	brain:	n/a
33	chr1:98036695-98036745	HRE	kidney:	n/a
34	chr1:98031839-98031889	HCPEpiC	choroid plexus:	n/a
35	chr1:98036695-98036745	Jurkat	blood:	n/a
36	chr1:98036695-98036745	U87	brain:	n/a
37	chr1:98031839-98031889	HepG2	liver:	n/a
38	chr1:98031839-98031889	AG09319	gingival:	n/a
39	chr1:98031839-98031889	ovcar-3	ovarian:	n/a
40	chr1:98036695-98036745	AG04450	lung:	fetal
41	chr1:98036695-98036745	IMR90	lung:	fetal
42	chr1:98036695-98036745	HRCEpiC	kidney:	n/a
43	chr1:98036695-98036745	GM06990	blood:	n/a
44	chr1:98031839-98031889	PrEC	prostate:	n/a
45	chr1:98036695-98036745	HUVEC	blood vessel:	n/a
46	chr1:98036695-98036745	HIPEpiC	eye:	n/a
47	chr1:98031839-98031889	CMK	blood:	n/a
48	chr1:98036695-98036745	PrEC	prostate:	n/a
49	chr1:98031839-98031889	GM12878	blood:	n/a
50	chr1:98036695-98036745	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:98035531..98037801-chr1:98038552..98041185,2	K562	blood:
2	chr1:98035531..98037801-chr1:98038552..98041185,2	K562	blood:

Variant related genes	Relation type
SEC63P1	TF binding region
SEC63P1	CpG island

Extended variants
information (count: 1280 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558991385	chr1:98003888-98003889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143001872	chr1:98003892-98003893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4950041	chr1:98003908-98003909	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555119750	chr1:98003912-98003913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574623462	chr1:98003920-98003921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543499508	chr1:98003933-98003934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184972837	chr1:98003996-98003997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551820976	chr1:98004040-98004041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576828891	chr1:98004044-98004045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552321118	chr1:98004058-98004059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74550569	chr1:98004090-98004091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377148075	chr1:98004160-98004161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565047544	chr1:98004169-98004170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370840634	chr1:98004170-98004171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527553220	chr1:98004182-98004183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547304292	chr1:98004191-98004192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375071532	chr1:98004200-98004201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561047428	chr1:98004219-98004220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148274651	chr1:98004279-98004280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112814770	chr1:98004314-98004315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189771138	chr1:98004326-98004327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4950042	chr1:98004418-98004419	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538265958	chr1:98004436-98004437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552119079	chr1:98004438-98004439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs386633721	chr1:98004510-98004511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183865044	chr1:98004511-98004512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10875097	chr1:98004512-98004513	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188093145	chr1:98004515-98004516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181945022	chr1:98004576-98004577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376081290	chr1:98004585-98004586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145783847	chr1:98004669-98004670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557043931	chr1:98004696-98004697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566954850	chr1:98004714-98004715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3956688	chr1:98004718-98004719	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187343074	chr1:98004746-98004747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371556513	chr1:98004747-98004748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559677638	chr1:98004796-98004797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35589952	chr1:98004813-98004814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78071449	chr1:98004825-98004826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541308616	chr1:98004838-98004839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561113902	chr1:98004906-98004907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529918824	chr1:98004912-98004913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146988911	chr1:98005025-98005026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76105829	chr1:98005084-98005085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532208787	chr1:98005103-98005104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2811171	chr1:98005144-98005145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs190170884	chr1:98005150-98005151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528827225	chr1:98005160-98005161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34738275	chr1:98005162-98005163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138146426	chr1:98005258-98005259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Pancreatic cancer	17952125	CNVD
Cancer	20803296	CNVD
Colorectal cancer	20653680	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97872600-98014600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:97928600-98018200	Weak transcription	Ovary	ovary
3	chr1:97956400-98009400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:97963000-98009400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr1:97964600-98010400	Weak transcription	Dnd41	blood
6	chr1:97976600-98014600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:97976600-98054200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:97976800-98009400	Weak transcription	Primary B cells from cord blood	blood
9	chr1:97976800-98051400	Weak transcription	Left Ventricle	heart
10	chr1:97980000-98013400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:97986600-98014600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:97988200-98023000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:97990000-98013000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:97995800-98012000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr1:97996000-98037400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:97997000-98004400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr1:97997000-98009200	Weak transcription	HSMM	muscle
18	chr1:97998600-98063800	Weak transcription	Right Ventricle	heart
19	chr1:97998800-98012600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr1:97999000-98014600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:97999400-98064600	Weak transcription	Psoas Muscle	Psoas
22	chr1:97999400-98074000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:98000800-98007800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:98001200-98062400	Weak transcription	Fetal Lung	lung
25	chr1:98001800-98012200	Weak transcription	HUVEC	blood vessel
26	chr1:98002000-98004000	Strong transcription	Primary T cells from cord blood	blood
27	chr1:98002000-98054600	Weak transcription	Lung	lung
28	chr1:98002000-98069400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:98002800-98058800	Weak transcription	Gastric	stomach
30	chr1:98003600-98004200	Strong transcription	Liver	Liver
31	chr1:98003800-98004400	Strong transcription	Primary hematopoietic stem cells	blood
32	chr1:98003800-98022800	Weak transcription	Fetal Intestine Large	intestine
33	chr1:98004000-98009400	Weak transcription	Primary T cells from cord blood	blood
34	chr1:98004000-98014600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr1:98004200-98006000	Weak transcription	Liver	Liver
36	chr1:98004400-98006200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr1:98004400-98009400	Weak transcription	Primary hematopoietic stem cells	blood
38	chr1:98004400-98022200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr1:98004400-98058400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr1:98004800-98022800	Weak transcription	Fetal Intestine Small	intestine
41	chr1:98005000-98014600	Weak transcription	Adipose Nuclei	Adipose
42	chr1:98006000-98006600	Enhancers	Liver	Liver
43	chr1:98006000-98016200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr1:98006200-98006400	Enhancers	Pancreas	Pancrea
45	chr1:98006200-98007000	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr1:98006200-98014800	Weak transcription	Osteobl	bone
47	chr1:98006400-98040600	Weak transcription	Pancreas	Pancrea
48	chr1:98006600-98009400	Weak transcription	Liver	Liver
49	chr1:98006600-98012600	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr1:98007000-98008800	Weak transcription	Primary monocytes fromperipheralblood	blood

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