Variant report

Variant	nsv546953
Chromosome Location	chr1:104103057-104262061
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	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
3	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
4	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
5	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
10	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
12	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
13	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
15	CEBPB	chr1:104109313-104109613	A549	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
16	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
17	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
18	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
19	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
20	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
21	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
22	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
23	CEBPD	chr1:104163704-104163928	K562	blood:	n/a	n/a
24	CTCF	chr1:104209836-104209915	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr1:104230883-104230996	Medullo	brain:	n/a	n/a
26	CTCF	chr1:104130700-104130850	HEK293	kidney:	n/a	n/a
27	CTCF	chr1:104130820-104130970	BE2_C	brain:	n/a	n/a
28	CTCF	chr1:104227489-104227548	LNCaP	prostate:	n/a	n/a
29	CTCF	chr1:104193062-104193168	LNCaP	prostate:	n/a	n/a
30	CTCF	chr1:104205944-104206011	Medullo	brain:	n/a	n/a
31	CTCF	chr1:104130620-104130770	GM12872	blood:	n/a	n/a
32	CTCF	chr1:104163703-104163814	Gliobla	brain:	n/a	n/a
33	CTCF	chr1:104181385-104181428	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr1:104245983-104246104	GM13976	blood:	n/a	n/a
35	CTCF	chr1:104217890-104217971	LNCaP	prostate:	n/a	n/a
36	CTCF	chr1:104206422-104206450	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:104159439-104159464	ProgFib	skin:	n/a	n/a
38	CTCF	chr1:104127840-104127990	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:104238464-104238556	Lung_OC	lung:	n/a	n/a
40	CTCF	chr1:104248353-104248412	GM13976	blood:	n/a	n/a
41	CTCF	chr1:104250396-104250604	Lung_OC	lung:	n/a	n/a
42	CTCF	chr1:104186690-104186766	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:104258408-104258453	Lung_OC	lung:	n/a	n/a
44	CTCF	chr1:104149063-104149109	ProgFib	skin:	n/a	n/a
45	CTCF	chr1:104145192-104145310	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:104130700-104130850	NHEK	skin:	n/a	n/a
47	CTCF	chr1:104187456-104187510	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr1:104250422-104250534	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:104243355-104243439	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr1:104130620-104130770	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104160257-104160307	PFSK-1	brain:	n/a
2	chr1:104113061-104113111	K562	blood:	n/a
3	chr1:104113039-104113089	HIPEpiC	eye:	n/a
4	chr1:104112143-104112193	AG04449	skin:	fetal
5	chr1:104160257-104160307	SK-N-MC	brain:	n/a
6	chr1:104239696-104239746	HepG2	liver:	n/a
7	chr1:104239696-104239746	Caco-2	colon:	n/a
8	chr1:104113061-104113111	HCM	heart:	n/a
9	chr1:104111877-104111927	CMK	blood:	n/a
10	chr1:104113039-104113089	SAEC	small airway:	n/a
11	chr1:104112143-104112193	HCPEpiC	choroid plexus:	n/a
12	chr1:104160257-104160307	H1-hESC	embryonic stem cell:	embryo
13	chr1:104113061-104113111	GM12878	blood:	n/a
14	chr1:104113039-104113089	NB4	blood:	n/a
15	chr1:104113039-104113089	PrEC	prostate:	n/a
16	chr1:104160257-104160307	ProgFib	skin:	n/a
17	chr1:104113061-104113111	HEK293	kidney:	embryo
18	chr1:104160257-104160307	ECC-1	luminal epithelium:	n/a
19	chr1:104239696-104239746	HAEpiC	amniotic membrane:	n/a
20	chr1:104160257-104160307	SK-N-SH	brain:	n/a
21	chr1:104160257-104160307	HCM	heart:	n/a
22	chr1:104239696-104239746	HEEpiC	esophagus:	n/a
23	chr1:104113061-104113111	CMK	blood:	n/a
24	chr1:104160257-104160307	HCF	heart:	n/a
25	chr1:104111877-104111927	HRCEpiC	kidney:	n/a
26	chr1:104113039-104113089	HepG2	liver:	n/a
27	chr1:104160257-104160307	HEEpiC	esophagus:	n/a
28	chr1:104160257-104160307	HCT-116	colon:	n/a
29	chr1:104113039-104113089	AG09319	gingival:	n/a
30	chr1:104111877-104111927	HCF	heart:	n/a
31	chr1:104113061-104113111	HCT-116	colon:	n/a
32	chr1:104239696-104239746	HRE	kidney:	n/a
33	chr1:104111877-104111927	T-47D	breast:	n/a
34	chr1:104111877-104111927	AG10803	skin:	n/a
35	chr1:104160257-104160307	GM12891	blood:	n/a
36	chr1:104113061-104113111	HMEC	breast:	n/a
37	chr1:104160257-104160307	HepG2	liver:	n/a
38	chr1:104112143-104112193	BE2_C	brain:	n/a
39	chr1:104239696-104239746	AG04450	lung:	fetal
40	chr1:104111877-104111927	HCT-116	colon:	n/a
41	chr1:104113061-104113111	BE2_C	brain:	n/a
42	chr1:104113039-104113089	A549	lung:	n/a
43	chr1:104113039-104113089	HMEC	breast:	n/a
44	chr1:104160257-104160307	HUVEC	blood vessel:	n/a
45	chr1:104111877-104111927	H1-hESC	embryonic stem cell:	embryo
46	chr1:104112143-104112193	HIPEpiC	eye:	n/a
47	chr1:104111877-104111927	Hela-S3	cervix:	n/a
48	chr1:104160257-104160307	HAEpiC	amniotic membrane:	n/a
49	chr1:104112143-104112193	HCT-116	colon:	n/a
50	chr1:104111877-104111927	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
2	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:

Variant related genes	Relation type
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
ACTG1P4	TF binding region
AMYP1	TF binding region
AMY1A	TF binding region
AMY2B	TF binding region
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
ACTG1P4	CpG island
AMYP1	CpG island
AMY1A	CpG island
AMY2B	CpG island

Extended variants
information (count: 1452 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2050592	chr1:104103057-104103058	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147693988	chr1:104103062-104103063	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs34578057	chr1:104103085-104103086	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371820877	chr1:104103094-104103095	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs545403285	chr1:104103100-104103101	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs541194913	chr1:104103144-104103145	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199682189	chr1:104103148-104103149	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564175863	chr1:104103165-104103166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531646025	chr1:104103309-104103310	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577804126	chr1:104103410-104103411	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550138712	chr1:104103457-104103458	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs373416234	chr1:104103482-104103483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568257400	chr1:104103508-104103509	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs529127807	chr1:104103528-104103529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547143485	chr1:104103577-104103578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545078703	chr1:104103612-104103613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34357254	chr1:104103627-104103628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377437458	chr1:104103641-104103642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553215049	chr1:104103665-104103666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565790612	chr1:104103667-104103668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539016683	chr1:104103706-104103707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566060249	chr1:104103711-104103712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569355420	chr1:104103713-104103714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368565878	chr1:104103716-104103717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376303945	chr1:104103719-104103720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537347933	chr1:104103745-104103746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187078134	chr1:104103782-104103783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573877733	chr1:104103788-104103789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541239998	chr1:104103798-104103799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553160723	chr1:104103809-104103810	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372436294	chr1:104103830-104103831	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191253942	chr1:104103852-104103853	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545033554	chr1:104103891-104103892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs142428652	chr1:104103912-104103913	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12062800	chr1:104103951-104103952	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369613181	chr1:104103958-104103959	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs530807097	chr1:104103969-104103970	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561980221	chr1:104103984-104103985	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs573464945	chr1:104104014-104104015	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35902835	chr1:104104025-104104026	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182708984	chr1:104104063-104104064	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559145625	chr1:104104081-104104082	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533039554	chr1:104104090-104104091	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548974992	chr1:104104134-104104135	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187606932	chr1:104104179-104104180	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11184461	chr1:104104190-104104191	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs146027775	chr1:104104210-104104211	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs549228519	chr1:104104214-104104215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs138810710	chr1:104104236-104104237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs534845591	chr1:104104238-104104239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	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
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104083400-104103800	Weak transcription	Psoas Muscle	Psoas
2	chr1:104090400-104104400	Weak transcription	Brain Substantia Nigra	brain
3	chr1:104090600-104116600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:104090800-104114200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:104090800-104118200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:104091000-104104800	Weak transcription	Colon Smooth Muscle	Colon
7	chr1:104091000-104108000	Weak transcription	Pancreas	Pancrea
8	chr1:104091000-104111000	Weak transcription	Small Intestine	intestine
9	chr1:104091000-104124400	Weak transcription	Brain Angular Gyrus	brain
10	chr1:104091200-104112200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:104091600-104112800	Weak transcription	Esophagus	oesophagus
12	chr1:104091800-104104400	Weak transcription	HSMMtube	muscle
13	chr1:104091800-104112200	Weak transcription	Thymus	Thymus
14	chr1:104092000-104117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:104092200-104123400	Weak transcription	Brain Germinal Matrix	brain
16	chr1:104094200-104112000	Weak transcription	Brain Anterior Caudate	brain
17	chr1:104095000-104103400	Weak transcription	Fetal Intestine Large	intestine
18	chr1:104095000-104104000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:104095000-104104400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr1:104095000-104111400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:104095400-104104400	Weak transcription	Fetal Intestine Small	intestine
22	chr1:104095400-104104400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:104095400-104112200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:104095400-104112200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr1:104095400-104112200	Weak transcription	Aorta	Aorta
26	chr1:104095400-104112200	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:104095400-104112200	Weak transcription	Fetal Stomach	stomach
28	chr1:104095400-104112200	Weak transcription	Left Ventricle	heart
29	chr1:104095400-104112200	Weak transcription	Lung	lung
30	chr1:104095400-104112200	Weak transcription	Ovary	ovary
31	chr1:104095400-104112200	Weak transcription	Right Ventricle	heart
32	chr1:104095400-104114200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr1:104096000-104112200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr1:104096000-104113800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:104096200-104104400	Weak transcription	GM12878-XiMat	blood
36	chr1:104096800-104123400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:104097000-104111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr1:104097000-104112200	Weak transcription	Spleen	Spleen
39	chr1:104098600-104123400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:104098800-104103600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:104098800-104104800	Weak transcription	HSMM	muscle
42	chr1:104098800-104112200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr1:104098800-104112200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr1:104098800-104112200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr1:104098800-104118000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr1:104098800-104120000	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr1:104098800-104120000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr1:104099000-104103400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr1:104099000-104104400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:104099200-104104400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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