Variant report

Variant	nsv871894
Chromosome Location	chr1:104049019-104140012
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	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
5	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
6	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
11	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
12	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
13	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
14	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
15	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
21	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
23	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
24	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
25	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
26	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
27	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
28	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
29	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
30	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
31	CEBPB	chr1:104071591-104071848	IMR90	lung:	n/a	chr1:104071695-104071706
32	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
34	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
35	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
36	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
37	CEBPB	chr1:104074143-104074222	HepG2	liver:	n/a	chr1:104074178-104074189
38	CEBPB	chr1:104069315-104069645	K562	blood:	n/a	chr1:104069437-104069448
39	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
40	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
41	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:104071533-104071833	HepG2	liver:	n/a	chr1:104071695-104071706
43	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
44	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
45	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
46	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
47	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
48	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
50	CHD1	chr1:104068464-104069301	GM12878	blood:	n/a	chr1:104068541-104068550

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104065263-104065313	AG09319	gingival:	n/a
2	chr1:104065263-104065313	AG09319	gingival:	n/a
3	chr1:104068118-104068168	LNCaP	prostate:	n/a
4	chr1:104097670-104097720	PFSK-1	brain:	n/a
5	chr1:104068118-104068168	HEEpiC	esophagus:	n/a
6	chr1:104068301-104068351	ProgFib	skin:	n/a
7	chr1:104068121-104068171	T-47D	breast:	n/a
8	chr1:104068603-104068653	MCF-7	breast:	n/a
9	chr1:104065263-104065313	HRCEpiC	kidney:	n/a
10	chr1:104068704-104068754	HUVEC	blood vessel:	n/a
11	chr1:104111877-104111927	GM12878	blood:	n/a
12	chr1:104068490-104068540	SK-N-SH_RA	brain:	n/a
13	chr1:104065263-104065313	BE2_C	brain:	n/a
14	chr1:104068419-104068469	HepG2	liver:	n/a
15	chr1:104068301-104068351	NB4	blood:	n/a
16	chr1:104068488-104068538	Hela-S3	cervix:	n/a
17	chr1:104068121-104068171	HEEpiC	esophagus:	n/a
18	chr1:104068664-104068714	GM12878	blood:	n/a
19	chr1:104113061-104113111	GM12891	blood:	n/a
20	chr1:104065263-104065313	AG10803	skin:	n/a
21	chr1:104068603-104068653	GM19239	blood:	n/a
22	chr1:104096517-104096567	CMK	blood:	n/a
23	chr1:104096621-104096671	HEEpiC	esophagus:	n/a
24	chr1:104113039-104113089	ProgFib	skin:	n/a
25	chr1:104096517-104096567	BJ	skin:	n/a
26	chr1:104113061-104113111	HRCEpiC	kidney:	n/a
27	chr1:104068118-104068168	PFSK-1	brain:	n/a
28	chr1:104068935-104068985	ECC-1	luminal epithelium:	n/a
29	chr1:104096517-104096567	GM12892	blood:	n/a
30	chr1:104068118-104068168	HRCEpiC	kidney:	n/a
31	chr1:104068419-104068469	PANC-1	pancreas:	n/a
32	chr1:104112143-104112193	HCM	heart:	n/a
33	chr1:104112143-104112193	HepG2	liver:	n/a
34	chr1:104068419-104068469	GM19239	blood:	n/a
35	chr1:104068419-104068469	HRE	kidney:	n/a
36	chr1:104096621-104096671	SAEC	small airway:	n/a
37	chr1:104068419-104068469	NB4	blood:	n/a
38	chr1:104068301-104068351	AG04450	lung:	fetal
39	chr1:104097670-104097720	GM12892	blood:	n/a
40	chr1:104068704-104068754	NB4	blood:	n/a
41	chr1:104112143-104112193	HAEpiC	amniotic membrane:	n/a
42	chr1:104111877-104111927	HCT-116	colon:	n/a
43	chr1:104068664-104068714	SK-N-SH	brain:	n/a
44	chr1:104113039-104113089	HEEpiC	esophagus:	n/a
45	chr1:104113039-104113089	IMR90	lung:	fetal
46	chr1:104096621-104096671	NT2-D1	testis:	n/a
47	chr1:104068567-104068617	HMEC	breast:	n/a
48	chr1:104113061-104113111	PFSK-1	brain:	n/a
49	chr1:104096517-104096567	HEEpiC	esophagus:	n/a
50	chr1:104068664-104068714	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
2	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
3	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
4	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
5	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
6	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
7	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
8	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
9	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
10	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
11	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
12	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
13	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
14	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
15	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
16	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
2	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
3	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
4	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
6	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
7	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
ACTG1P4	TF binding region
ENSG00000224613	TF binding region
RNPC3	TF binding region
RN7SKP285	TF binding region
AMY2B	TF binding region
ACTG1P4	CpG island
ENSG00000224613	CpG island
RNPC3	CpG island
RN7SKP285	CpG island
AMY2B	CpG island
ENSG00000185946	chromatin interactions
ENSG00000240038	chromatin interactions
ENSG00000224613	chromatin interactions
ENSG00000017797	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 3022 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:3022 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11807016	chr1:104049019-104049020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs193287816	chr1:104049063-104049064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547890817	chr1:104049154-104049155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559453832	chr1:104049191-104049192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565360626	chr1:104049235-104049236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533366324	chr1:104049299-104049300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532512306	chr1:104049331-104049332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374740311	chr1:104049354-104049355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570405439	chr1:104049359-104049360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531535171	chr1:104049387-104049388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544564272	chr1:104049448-104049449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34740197	chr1:104049459-104049460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549544772	chr1:104049467-104049468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567937604	chr1:104049506-104049507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149954806	chr1:104049574-104049575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199719448	chr1:104049597-104049598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553843672	chr1:104049600-104049601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111840045	chr1:104049618-104049619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547040386	chr1:104049668-104049669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185034132	chr1:104049672-104049673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562740458	chr1:104049692-104049693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144910906	chr1:104049742-104049743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188745944	chr1:104049855-104049856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576792027	chr1:104049936-104049937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544155510	chr1:104049940-104049941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371255074	chr1:104049952-104049953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537750719	chr1:104049997-104049998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375459468	chr1:104049998-104049999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7518121	chr1:104050033-104050034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs80016121	chr1:104050133-104050134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368566859	chr1:104050232-104050233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192530966	chr1:104050393-104050394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80139132	chr1:104050402-104050403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145730957	chr1:104050442-104050443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545371567	chr1:104050477-104050478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138733305	chr1:104050505-104050506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531478064	chr1:104050605-104050606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527865058	chr1:104050703-104050704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184204028	chr1:104050797-104050798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569711995	chr1:104050833-104050834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535593512	chr1:104050854-104050855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567876446	chr1:104050874-104050875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529091029	chr1:104050891-104050892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547320163	chr1:104050974-104050975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372235920	chr1:104051021-104051022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12564086	chr1:104051022-104051023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557763009	chr1:104051042-104051043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569688941	chr1:104051077-104051078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141182877	chr1:104051084-104051085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373787540	chr1:104051150-104051151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1550 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
2	chr1:104050000-104067400	Weak transcription	Left Ventricle	heart
3	chr1:104051800-104052400	Enhancers	HUVEC	blood vessel
4	chr1:104052000-104052600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr1:104052200-104052600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr1:104054400-104066200	Weak transcription	Psoas Muscle	Psoas
7	chr1:104054800-104062600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:104056200-104060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:104056400-104056600	Enhancers	HMEC	breast
10	chr1:104056400-104056800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:104056400-104057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:104056400-104059800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:104056600-104056800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:104056600-104056800	Enhancers	Osteobl	bone
15	chr1:104056800-104058400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:104056800-104058400	Weak transcription	Osteobl	bone
17	chr1:104057200-104058200	Weak transcription	HMEC	breast
18	chr1:104057600-104059000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:104057800-104058600	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr1:104058200-104060400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:104058200-104060400	Enhancers	NH-A	brain
22	chr1:104058200-104060600	Enhancers	HMEC	breast
23	chr1:104058400-104059800	Enhancers	Osteobl	bone
24	chr1:104058400-104060400	Enhancers	NHEK	skin
25	chr1:104058400-104060600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:104058400-104060600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:104058600-104059600	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr1:104058800-104060000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr1:104058800-104060600	Enhancers	HUVEC	blood vessel
30	chr1:104059000-104059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:104059200-104060400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:104059400-104060200	Enhancers	GM12878-XiMat	blood
33	chr1:104059600-104060000	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr1:104059800-104067400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:104059800-104067400	Weak transcription	Osteobl	bone
36	chr1:104060200-104060400	Enhancers	Fetal Heart	heart
37	chr1:104060200-104060400	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr1:104060200-104060400	Flanking Active TSS	GM12878-XiMat	blood
39	chr1:104060400-104060800	Active TSS	GM12878-XiMat	blood
40	chr1:104060400-104067400	Weak transcription	Fetal Heart	heart
41	chr1:104060600-104067200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:104060600-104067400	Weak transcription	HUVEC	blood vessel
43	chr1:104060800-104061000	Flanking Active TSS	GM12878-XiMat	blood
44	chr1:104061000-104067400	Weak transcription	GM12878-XiMat	blood
45	chr1:104062400-104067400	Weak transcription	Right Ventricle	heart
46	chr1:104062600-104062800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr1:104062800-104063600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:104063600-104064800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr1:104064000-104064200	Enhancers	Hela-S3	cervix
50	chr1:104064200-104067200	Weak transcription	Hela-S3	cervix

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