Variant report

Variant	esv3329918
Chromosome Location	chr1:120607729-120626627
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	chr1:120611088-120611280	GM12878	blood:	n/a	n/a
2	BATF	chr1:120623707-120624030	GM12878	blood:	n/a	n/a
3	BATF	chr1:120610859-120611051	GM12878	blood:	n/a	n/a
4	BATF	chr1:120607512-120607789	GM12878	blood:	n/a	chr1:120607521-120607530
5	BATF	chr1:120611354-120611730	GM12878	blood:	n/a	n/a
6	BATF	chr1:120608916-120609325	GM12878	blood:	n/a	n/a
7	BATF	chr1:120608810-120609197	GM12878	blood:	n/a	n/a
8	BATF	chr1:120611985-120612860	GM12878	blood:	n/a	chr1:120612243-120612251
9	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
10	BCL11A	chr1:120612554-120612750	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:120609483-120609672	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:120608870-120609348	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:120611089-120611634	GM12878	blood:	n/a	chr1:120611132-120611145
14	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
15	BCL11A	chr1:120609381-120609768	GM12878	blood:	n/a	chr1:120609456-120609465
16	BCL11A	chr1:120612793-120613021	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:120607513-120607814	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:120613372-120613374	K562	blood:	n/a	n/a
19	BHLHE40	chr1:120612253-120612353	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:120612061-120612430	HepG2	liver:	n/a	chr1:120612210-120612226
21	BHLHE40	chr1:120611076-120611451	GM12878	blood:	n/a	n/a
22	BRCA1	chr1:120611172-120611268	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr1:120612017-120612854	K562	blood:	n/a	n/a
24	CEBPB	chr1:120619545-120619730	Hela-S3	cervix:	n/a	chr1:120619660-120619671
25	CEBPB	chr1:120617619-120617856	IMR90	lung:	n/a	chr1:120617743-120617754
26	CEBPB	chr1:120612085-120612439	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:120611070-120611293	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:120619491-120619746	HepG2	liver:	n/a	chr1:120619660-120619671
29	CEBPB	chr1:120612008-120613179	GM12878	blood:	n/a	n/a
30	CEBPB	chr1:120619540-120619850	K562	blood:	n/a	chr1:120619660-120619671
31	CEBPB	chr1:120619578-120619734	H1-hESC	embryonic stem cell:	n/a	chr1:120619660-120619671
32	CEBPB	chr1:120612210-120612508	GM12878	blood:	n/a	n/a
33	CEBPB	chr1:120619486-120619844	IMR90	lung:	n/a	chr1:120619660-120619671
34	CEBPD	chr1:120612146-120612492	K562	blood:	n/a	n/a
35	CHD1	chr1:120612161-120612168	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr1:120611498-120612373	IMR90	lung:	n/a	chr1:120612182-120612192
37	CHD2	chr1:120612091-120612461	Hela-S3	cervix:	n/a	chr1:120612182-120612192
38	CHD2	chr1:120612143-120612448	K562	blood:	n/a	chr1:120612182-120612192
39	CHD2	chr1:120612089-120612454	H1-hESC	embryonic stem cell:	n/a	chr1:120612182-120612192
40	CHD2	chr1:120611791-120612456	GM12878	blood:	n/a	chr1:120612182-120612192
41	CHD2	chr1:120611059-120611442	Hela-S3	cervix:	n/a	chr1:120611364-120611374
42	CHD2	chr1:120612088-120612444	HepG2	liver:	n/a	chr1:120612182-120612192
43	CTCF	chr1:120611220-120611370	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:120611900-120612050	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:120611402-120611551	MCF-7	breast:	n/a	chr1:120611465-120611475
46	CTCF	chr1:120611920-120612070	GM12866	blood:	n/a	n/a
47	CTCF	chr1:120611440-120611590	AG04449	skin:	n/a	chr1:120611465-120611475
48	CTCF	chr1:120611220-120611370	HCFaa	heart:	n/a	n/a
49	CTCF	chr1:120611240-120611390	BJ	skin:	n/a	n/a
50	CTCF	chr1:120612268-120612322	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120611593-120611643	Caco-2	colon:	n/a
2	chr1:120612404-120612454	HNPCEpiC	eye:	n/a
3	chr1:120611593-120611643	K562	blood:	n/a
4	chr1:120611104-120611154	BE2_C	brain:	n/a
5	chr1:120612404-120612454	HepG2	liver:	n/a
6	chr1:120612147-120612197	AG10803	skin:	n/a
7	chr1:120611586-120611636	GM12892	blood:	n/a
8	chr1:120612217-120612267	HCPEpiC	choroid plexus:	n/a
9	chr1:120612152-120612202	HCT-116	colon:	n/a
10	chr1:120612147-120612197	HCT-116	colon:	n/a
11	chr1:120612152-120612202	ProgFib	skin:	n/a
12	chr1:120616221-120616271	K562	blood:	n/a
13	chr1:120613447-120613497	A549	lung:	n/a
14	chr1:120613447-120613497	RPTEC	kidney:	n/a
15	chr1:120611586-120611636	H1-hESC	embryonic stem cell:	embryo
16	chr1:120612217-120612267	AG09309	skin:	n/a
17	chr1:120612217-120612267	MCF10A-Er-Src	breast:	n/a
18	chr1:120611586-120611636	NB4	blood:	n/a
19	chr1:120612147-120612197	CMK	blood:	n/a
20	chr1:120612404-120612454	SK-N-SH	brain:	n/a
21	chr1:120616221-120616271	ECC-1	luminal epithelium:	n/a
22	chr1:120611593-120611643	AG04449	skin:	fetal
23	chr1:120611104-120611154	NHDF-neo	bronchial:	n/a
24	chr1:120611104-120611154	A549	lung:	n/a
25	chr1:120616221-120616271	SK-N-MC	brain:	n/a
26	chr1:120612404-120612454	A549	lung:	n/a
27	chr1:120611593-120611643	AG09309	skin:	n/a
28	chr1:120612404-120612454	AG09309	skin:	n/a
29	chr1:120612404-120612454	SK-N-MC	brain:	n/a
30	chr1:120612217-120612267	AG04450	lung:	fetal
31	chr1:120613447-120613497	AG09319	gingival:	n/a
32	chr1:120616221-120616271	U87	brain:	n/a
33	chr1:120612217-120612267	Hepatocyte	liver:	n/a
34	chr1:120611104-120611154	T-47D	breast:	n/a
35	chr1:120612152-120612202	GM19239	blood:	n/a
36	chr1:120612404-120612454	T-47D	breast:	n/a
37	chr1:120616221-120616271	LNCaP	prostate:	n/a
38	chr1:120611593-120611643	PFSK-1	brain:	n/a
39	chr1:120612147-120612197	T-47D	breast:	n/a
40	chr1:120612404-120612454	AG10803	skin:	n/a
41	chr1:120612404-120612454	AG04450	lung:	fetal
42	chr1:120611586-120611636	AG09309	skin:	n/a
43	chr1:120611593-120611643	GM12891	blood:	n/a
44	chr1:120616221-120616271	Caco-2	colon:	n/a
45	chr1:120612404-120612454	HCF	heart:	n/a
46	chr1:120616221-120616271	AG09309	skin:	n/a
47	chr1:120611593-120611643	HCM	heart:	n/a
48	chr1:120616221-120616271	BJ	skin:	n/a
49	chr1:120612152-120612202	PANC-1	pancreas:	n/a
50	chr1:120612147-120612197	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120610124..120613523-chr1:145208226..145211226,7	MCF-7	breast:
2	chr1:120611803..120612535-chr1:145208972..145209627,6	MCF-7	breast:
3	chr1:120610094..120613669-chr1:145207447..145211087,11	MCF-7	breast:
4	chr1:120611958..120612515-chr1:145208972..145209639,2	NB4	blood:
5	chr1:120611825..120612753-chr1:145208933..145209629,3	Hela-S3	cervix:
6	chr1:120611941..120612674-chr1:145209107..145209637,6	MCF-7	breast:

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

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

Extended variants
information (count: 702 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2799240	chr1:120607772-120607773	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191817130	chr1:120607783-120607784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2604037	chr1:120607797-120607798	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs587620734	chr1:120607828-120607829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs587684204	chr1:120607847-120607848	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs587774648	chr1:120607878-120607879	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs183438958	chr1:120607911-120607912	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs112576043	chr1:120607924-120607925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs587713347	chr1:120607942-120607943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs587770726	chr1:120607962-120607963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs2604035	chr1:120608012-120608013	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs587648513	chr1:120608014-120608015	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs587701335	chr1:120608026-120608027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs61200250	chr1:120608075-120608076	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs374477449	chr1:120608084-120608085	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs587649508	chr1:120608085-120608086	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs587714443	chr1:120608105-120608106	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs587612865	chr1:120608124-120608125	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs200415550	chr1:120608159-120608160	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs587722631	chr1:120608160-120608161	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188893674	chr1:120608180-120608181	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs2799242	chr1:120608213-120608214	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs587677896	chr1:120608236-120608237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs587724180	chr1:120608260-120608261	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs587628128	chr1:120608262-120608263	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs587655767	chr1:120608263-120608264	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs587764480	chr1:120608279-120608280	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs2799243	chr1:120608323-120608324	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs587633561	chr1:120608329-120608330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587715145	chr1:120608377-120608378	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs587770970	chr1:120608379-120608380	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs111334782	chr1:120608422-120608423	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs2799244	chr1:120608429-120608430	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs12084158	chr1:120608444-120608445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs587754519	chr1:120608526-120608527	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587652761	chr1:120608556-120608557	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs587693657	chr1:120608583-120608584	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs201695557	chr1:120608636-120608637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs368683460	chr1:120608669-120608670	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs2799245	chr1:120608729-120608730	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587770698	chr1:120608734-120608735	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs2799246	chr1:120608744-120608745	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs4659278	chr1:120608772-120608773	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs587724733	chr1:120608778-120608779	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs149843135	chr1:120608796-120608797	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs368789464	chr1:120608810-120608811	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs587596212	chr1:120608834-120608835	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs587641499	chr1:120608840-120608841	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs587704556	chr1:120608918-120608919	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs587600565	chr1:120608958-120608959	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Aetanephric adenomas	20802469	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:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120564000-120610800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr1:120567600-120608600	Weak transcription	Dnd41	blood
3	chr1:120588600-120609600	Weak transcription	Aorta	Aorta
4	chr1:120588600-120610600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:120591000-120609600	Weak transcription	Fetal Brain Female	brain
6	chr1:120594400-120609800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:120595000-120610800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr1:120595200-120608800	Weak transcription	Fetal Lung	lung
9	chr1:120595200-120610600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:120595200-120610600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:120595200-120611000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:120597200-120608200	Weak transcription	Small Intestine	intestine
13	chr1:120597200-120608800	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:120597800-120610600	Weak transcription	Thymus	Thymus
15	chr1:120601200-120610800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr1:120602200-120608600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:120602200-120609200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:120602200-120609600	Weak transcription	HSMM	muscle
19	chr1:120602200-120610200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:120602200-120610600	Weak transcription	Brain Substantia Nigra	brain
21	chr1:120602200-120610800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:120602200-120610800	Weak transcription	Fetal Intestine Large	intestine
23	chr1:120602400-120608000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:120602400-120608400	Weak transcription	Brain Anterior Caudate	brain
25	chr1:120602400-120608800	Weak transcription	NHDF-Ad	bronchial
26	chr1:120602400-120609200	Weak transcription	NH-A	brain
27	chr1:120602400-120609600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr1:120602400-120610600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:120602400-120610800	Weak transcription	Right Ventricle	heart
30	chr1:120602400-120611000	Weak transcription	Esophagus	oesophagus
31	chr1:120602800-120609600	Weak transcription	NHLF	lung
32	chr1:120604400-120608000	Weak transcription	Adipose Nuclei	Adipose
33	chr1:120604400-120608200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:120604400-120608200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr1:120604400-120608400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr1:120604400-120608800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:120604400-120609200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr1:120604400-120609600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:120604400-120609600	Weak transcription	Liver	Liver
40	chr1:120604400-120610200	Weak transcription	Hela-S3	cervix
41	chr1:120604400-120610600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:120604400-120610600	Weak transcription	HUVEC	blood vessel
43	chr1:120604400-120610800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr1:120604400-120610800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:120604400-120610800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr1:120604400-120610800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:120604400-120610800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:120604400-120610800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr1:120604400-120610800	Weak transcription	A549	lung
50	chr1:120604600-120608600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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