Variant report

Variant	esv1816562
Chromosome Location	chr1:120578662-120629915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1101)
CpG islands
(count:551)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:120594168-120594200	K562	blood:	n/a	n/a
2	ATF1	chr1:120604273-120604274	K562	blood:	n/a	n/a
3	BATF	chr1:120596954-120597150	GM12878	blood:	n/a	n/a
4	BATF	chr1:120601400-120601657	GM12878	blood:	n/a	n/a
5	BATF	chr1:120587372-120588174	GM12878	blood:	n/a	n/a
6	BATF	chr1:120611354-120611730	GM12878	blood:	n/a	n/a
7	BATF	chr1:120610859-120611051	GM12878	blood:	n/a	n/a
8	BATF	chr1:120608916-120609325	GM12878	blood:	n/a	n/a
9	BATF	chr1:120586095-120586463	GM12878	blood:	n/a	n/a
10	BATF	chr1:120623707-120624030	GM12878	blood:	n/a	n/a
11	BATF	chr1:120586664-120586958	GM12878	blood:	n/a	n/a
12	BATF	chr1:120586674-120586986	GM12878	blood:	n/a	n/a
13	BATF	chr1:120611088-120611280	GM12878	blood:	n/a	n/a
14	BATF	chr1:120607512-120607789	GM12878	blood:	n/a	chr1:120607521-120607530
15	BATF	chr1:120586089-120586477	GM12878	blood:	n/a	n/a
16	BATF	chr1:120608810-120609197	GM12878	blood:	n/a	n/a
17	BATF	chr1:120607492-120607681	GM12878	blood:	n/a	chr1:120607521-120607530
18	BATF	chr1:120611985-120612860	GM12878	blood:	n/a	chr1:120612243-120612251
19	BATF	chr1:120587338-120588241	GM12878	blood:	n/a	n/a
20	BATF	chr1:120589375-120589701	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:120609381-120609768	GM12878	blood:	n/a	chr1:120609456-120609465
22	BCL11A	chr1:120611434-120612789	GM12878	blood:	n/a	chr1:120611922-120611930 chr1:120611748-120611757 chr1:120611722-120611735 chr1:120612331-120612344 chr1:120612200-120612213 chr1:120612366-120612375 chr1:120612211-120612224 chr1:120611833-120611846 chr1:120612327-120612340 chr1:120612345-120612358
23	BCL11A	chr1:120586626-120587029	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:120589458-120589676	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:120602033-120602192	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr1:120587367-120588210	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:120612554-120612750	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:120612075-120612492	GM12878	blood:	n/a	chr1:120612331-120612344 chr1:120612200-120612213 chr1:120612366-120612375 chr1:120612211-120612224 chr1:120612327-120612340 chr1:120612345-120612358
29	BCL11A	chr1:120587370-120587848	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:120601519-120601693	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:120611089-120611634	GM12878	blood:	n/a	chr1:120611132-120611145
32	BCL11A	chr1:120602000-120602185	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr1:120609483-120609672	GM12878	blood:	n/a	n/a
34	BCL11A	chr1:120592394-120592624	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:120587885-120588175	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:120608870-120609348	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:120607513-120607814	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:120585798-120586515	GM12878	blood:	n/a	chr1:120586311-120586320
39	BCL11A	chr1:120612793-120613021	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:120611076-120611451	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:120612061-120612430	HepG2	liver:	n/a	chr1:120612210-120612226
42	BHLHE40	chr1:120613372-120613374	K562	blood:	n/a	n/a
43	BHLHE40	chr1:120612253-120612353	GM12878	blood:	n/a	n/a
44	BRCA1	chr1:120611172-120611268	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr1:120612017-120612854	K562	blood:	n/a	n/a
46	CEBPB	chr1:120604213-120604445	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:120593506-120593772	K562	blood:	n/a	n/a
48	CEBPB	chr1:120619486-120619844	IMR90	lung:	n/a	chr1:120619660-120619671
49	CEBPB	chr1:120617619-120617856	IMR90	lung:	n/a	chr1:120617743-120617754
50	CEBPB	chr1:120601946-120602302	IMR90	lung:	n/a	chr1:120602081-120602092

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120616221-120616271	LNCaP	prostate:	n/a
2	chr1:120612147-120612197	K562	blood:	n/a
3	chr1:120616221-120616271	LNCaP	prostate:	n/a
4	chr1:120612147-120612197	K562	blood:	n/a
5	chr1:120612404-120612454	SK-N-MC	brain:	n/a
6	chr1:120612147-120612197	HNPCEpiC	eye:	n/a
7	chr1:120612404-120612454	MCF10A-Er-Src	breast:	n/a
8	chr1:120612404-120612454	H1-hESC	embryonic stem cell:	embryo
9	chr1:120612147-120612197	BE2_C	brain:	n/a
10	chr1:120611593-120611643	AG09319	gingival:	n/a
11	chr1:120612147-120612197	HRE	kidney:	n/a
12	chr1:120611104-120611154	AoSMC	blood vessel:	n/a
13	chr1:120611593-120611643	Hepatocyte	liver:	n/a
14	chr1:120611593-120611643	HRCEpiC	kidney:	n/a
15	chr1:120611593-120611643	HIPEpiC	eye:	n/a
16	chr1:120611104-120611154	U87	brain:	n/a
17	chr1:120611104-120611154	NH-A	brain:	n/a
18	chr1:120611593-120611643	H1-hESC	embryonic stem cell:	embryo
19	chr1:120611104-120611154	Hepatocyte	liver:	n/a
20	chr1:120616221-120616271	BJ	skin:	n/a
21	chr1:120611593-120611643	LNCaP	prostate:	n/a
22	chr1:120612217-120612267	GM06990	blood:	n/a
23	chr1:120611593-120611643	NH-A	brain:	n/a
24	chr1:120613447-120613497	PANC-1	pancreas:	n/a
25	chr1:120612404-120612454	T-47D	breast:	n/a
26	chr1:120612217-120612267	BE2_C	brain:	n/a
27	chr1:120613447-120613497	AG04449	skin:	fetal
28	chr1:120611593-120611643	CMK	blood:	n/a
29	chr1:120611104-120611154	HRPEpiC	eye:	n/a
30	chr1:120612152-120612202	HCF	heart:	n/a
31	chr1:120612217-120612267	NHBE	bronchial:	n/a
32	chr1:120612217-120612267	HRE	kidney:	n/a
33	chr1:120612404-120612454	HEK293	kidney:	embryo
34	chr1:120611586-120611636	HCF	heart:	n/a
35	chr1:120611586-120611636	HUVEC	blood vessel:	n/a
36	chr1:120611593-120611643	HepG2	liver:	n/a
37	chr1:120616221-120616271	HCT-116	colon:	n/a
38	chr1:120612217-120612267	HL-60	blood:	n/a
39	chr1:120611104-120611154	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:120612152-120612202	GM12878	blood:	n/a
41	chr1:120611593-120611643	K562	blood:	n/a
42	chr1:120612404-120612454	HCF	heart:	n/a
43	chr1:120612404-120612454	NB4	blood:	n/a
44	chr1:120613447-120613497	Jurkat	blood:	n/a
45	chr1:120611586-120611636	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:120613447-120613497	A549	lung:	n/a
47	chr1:120612217-120612267	PFSK-1	brain:	n/a
48	chr1:120611104-120611154	HCM	heart:	n/a
49	chr1:120611593-120611643	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:120616221-120616271	U87	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120611941..120612674-chr1:145209107..145209637,6	MCF-7	breast:
2	chr1:120604407..120607124-chr1:149222293..149225022,2	MCF-7	breast:
3	chr1:120611803..120612535-chr1:145208972..145209627,6	MCF-7	breast:
4	chr1:120606120..120607638-chr1:145207438..145208952,2	MCF-7	breast:
5	chr1:120602747..120604407-chr1:145216153..145218112,2	MCF-7	breast:
6	chr1:120610124..120613523-chr1:145208226..145211226,7	MCF-7	breast:
7	chr1:120611958..120612515-chr1:145208972..145209639,2	NB4	blood:
8	chr1:120610094..120613669-chr1:145207447..145211087,11	MCF-7	breast:
9	chr1:120611825..120612753-chr1:145208933..145209629,3	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM72B-9	chr1:120619223-120619698	ENSG00000273406.1
2	lnc-NOTCH2-2	chr1:120617808-120619716	XLOC_000986
3	lnc-NOTCH2-2	chr1:120615908-120616134	XLOC_000986
4	lnc-FAM72B-4	chr1:120612586-120612625	XLOC_000373

No data

Variant related genes	Relation type
NOTCH2	TF binding region
ENSG00000273406	TF binding region
NOTCH2	CpG island
ENSG00000273406	CpG island
ENSG00000206737	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000213240	chromatin interactions

Extended variants
information (count: 1641 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1641 , 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	rs371557953	chr1:120578663-120578664	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10923940	chr1:120578664-120578665	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587682864	chr1:120578813-120578814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367591265	chr1:120578816-120578817	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201019079	chr1:120578820-120578821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587743765	chr1:120578857-120578858	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2603965	chr1:120579027-120579028	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188557788	chr1:120579063-120579064	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180716728	chr1:120579163-120579164	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587617040	chr1:120579212-120579213	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587698919	chr1:120579214-120579215	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587733387	chr1:120579233-120579234	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587626959	chr1:120579256-120579257	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71241148	chr1:120579281-120579282	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587666965	chr1:120579294-120579295	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2603964	chr1:120579361-120579362	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2794106	chr1:120579376-120579377	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587744293	chr1:120579382-120579383	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376650289	chr1:120579400-120579401	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587683529	chr1:120579417-120579418	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587762105	chr1:120579418-120579419	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587616134	chr1:120579419-120579420	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587694160	chr1:120579449-120579450	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587751175	chr1:120579457-120579458	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71241149	chr1:120579472-120579473	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587645366	chr1:120579485-120579486	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71241150	chr1:120579506-120579507	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587706829	chr1:120579508-120579509	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587762664	chr1:120579518-120579519	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1689981	chr1:120579525-120579526	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587743945	chr1:120579549-120579550	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587617263	chr1:120579550-120579551	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587699136	chr1:120579588-120579589	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587707563	chr1:120579625-120579626	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12042184	chr1:120579626-120579627	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs6674892	chr1:120579635-120579636	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs587612398	chr1:120579636-120579637	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs587661767	chr1:120579664-120579665	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs587727067	chr1:120579685-120579686	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs587624563	chr1:120579707-120579708	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587661244	chr1:120579721-120579722	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs587740821	chr1:120579748-120579749	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs587616461	chr1:120579759-120579760	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs200556823	chr1:120579760-120579761	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs371440284	chr1:120579796-120579797	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs150866684	chr1:120579797-120579798	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs587629797	chr1:120579798-120579799	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs587682974	chr1:120579857-120579858	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs201099920	chr1:120579884-120579885	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs587662471	chr1:120579935-120579936	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120548200-120579800	Weak transcription	Spleen	Spleen
2	chr1:120558800-120579400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:120559400-120579400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:120560000-120579400	Weak transcription	NH-A	brain
5	chr1:120564000-120579200	Weak transcription	NHLF	lung
6	chr1:120564000-120579400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:120564000-120579400	Weak transcription	Fetal Kidney	kidney
8	chr1:120564000-120610800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:120566800-120579200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:120567000-120580200	Weak transcription	Colonic Mucosa	Colon
11	chr1:120567200-120579200	Weak transcription	Colon Smooth Muscle	Colon
12	chr1:120567600-120604200	Weak transcription	Primary T cells from cord blood	blood
13	chr1:120567600-120608600	Weak transcription	Dnd41	blood
14	chr1:120568000-120579400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr1:120569400-120579400	Weak transcription	Fetal Stomach	stomach
16	chr1:120571000-120579000	Weak transcription	Osteobl	bone
17	chr1:120571000-120601600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:120571200-120595000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:120571600-120579200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:120573800-120579200	Weak transcription	NHDF-Ad	bronchial
21	chr1:120574200-120580200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:120574200-120589800	Weak transcription	Primary B cells from cord blood	blood
23	chr1:120574400-120579400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr1:120574400-120579400	Weak transcription	Fetal Intestine Large	intestine
25	chr1:120574400-120579400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:120574400-120586400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:120574400-120594000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:120574400-120594000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:120575200-120579400	Weak transcription	HMEC	breast
30	chr1:120575200-120588400	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr1:120575400-120579400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:120575400-120579400	Weak transcription	NHEK	skin
33	chr1:120575600-120579400	Weak transcription	Stomach Mucosa	stomach
34	chr1:120575600-120579400	Weak transcription	HSMM	muscle
35	chr1:120575600-120588400	Weak transcription	Aorta	Aorta
36	chr1:120575800-120579400	Weak transcription	HepG2	liver
37	chr1:120575800-120588400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:120575800-120589800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr1:120577400-120579200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:120577600-120579200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:120577800-120580000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr1:120577800-120580200	Enhancers	Fetal Heart	heart
43	chr1:120578000-120578800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:120578000-120578800	Enhancers	Adipose Nuclei	Adipose
45	chr1:120578200-120578800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr1:120578200-120578800	Enhancers	Liver	Liver
47	chr1:120578200-120579600	Strong transcription	Primary B cells from peripheral blood	blood
48	chr1:120578200-120579600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:120578200-120580200	Enhancers	HSMMtube	muscle
50	chr1:120578400-120578800	Enhancers	Right Atrium	heart

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