Variant report

Variant	esv3363438
Chromosome Location	chr1:70655980-70675467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:637)
CpG islands
(count:1160)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70671150-70671813	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:70671280-70671917	K562	blood:	n/a	n/a
3	ARID3A	chr1:70670385-70670530	K562	blood:	n/a	n/a
4	ATF1	chr1:70670789-70671821	K562	blood:	n/a	chr1:70671371-70671385
5	ATF2	chr1:70670980-70671719	GM12878	blood:	n/a	chr1:70671371-70671385
6	ATF2	chr1:70671068-70671594	H1-hESC	embryonic stem cell:	n/a	chr1:70671371-70671385
7	ATF2	chr1:70671030-70671771	GM12878	blood:	n/a	chr1:70671371-70671385
8	ATF3	chr1:70671031-70671659	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:70671037-70671604	K562	blood:	n/a	n/a
10	ATF3	chr1:70671086-70671520	HepG2	liver:	n/a	n/a
11	ATF3	chr1:70671202-70671457	GM12878	blood:	n/a	n/a
12	ATF3	chr1:70671000-70671590	HepG2	liver:	n/a	n/a
13	ATF3	chr1:70671078-70671489	K562	blood:	n/a	n/a
14	ATF3	chr1:70671051-70671587	A549	lung:	n/a	n/a
15	ATF3	chr1:70671040-70671604	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr1:70671046-70671594	GM12878	blood:	n/a	n/a
17	ATF3	chr1:70671015-70671489	K562	blood:	n/a	n/a
18	BACH1	chr1:70668015-70668084	K562	blood:	n/a	n/a
19	BACH1	chr1:70671146-70671582	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr1:70668095-70668337	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:70671170-70671559	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:70671018-70671950	K562	blood:	n/a	n/a
23	BCLAF1	chr1:70670947-70671765	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:70670972-70671697	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:70670886-70671703	K562	blood:	n/a	n/a
26	BHLHE40	chr1:70670437-70670562	K562	blood:	n/a	n/a
27	BHLHE40	chr1:70671104-70671672	GM12878	blood:	n/a	n/a
28	BRCA1	chr1:70670744-70671986	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr1:70671064-70671524	GM12878	blood:	n/a	n/a
30	BRCA1	chr1:70671161-70671772	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr1:70671068-70671553	HepG2	liver:	n/a	n/a
32	CBX3	chr1:70671116-70671762	K562	blood:	n/a	n/a
33	CBX3	chr1:70670976-70671758	K562	blood:	n/a	n/a
34	CCNT2	chr1:70670964-70671809	K562	blood:	n/a	n/a
35	CEBPB	chr1:70670767-70671508	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:70671168-70671835	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:70671201-70671696	K562	blood:	n/a	n/a
38	CEBPB	chr1:70671124-70671689	K562	blood:	n/a	n/a
39	CEBPB	chr1:70670190-70670456	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:70671076-70671815	GM12878	blood:	n/a	n/a
41	CEBPB	chr1:70670723-70671814	Hela-S3	cervix:	n/a	n/a
42	CEBPD	chr1:70671020-70671433	HepG2	liver:	n/a	n/a
43	CHD1	chr1:70671809-70672116	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr1:70670907-70671690	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr1:70670989-70671550	K562	blood:	n/a	n/a
46	CHD2	chr1:70670949-70671678	HepG2	liver:	n/a	n/a
47	CHD2	chr1:70671097-70671817	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr1:70671009-70671580	GM12878	blood:	n/a	n/a
49	CREB1	chr1:70670794-70672002	K562	blood:	n/a	n/a
50	CREB1	chr1:70671065-70671596	A549	lung:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70671216-70671266	SK-N-SH	brain:	n/a
2	chr1:70671216-70671266	SK-N-SH	brain:	n/a
3	chr1:70671218-70671268	HL-60	blood:	n/a
4	chr1:70671119-70671169	AoSMC	blood vessel:	n/a
5	chr1:70671119-70671169	A549	lung:	n/a
6	chr1:70671364-70671414	GM12892	blood:	n/a
7	chr1:70671693-70671743	A549	lung:	n/a
8	chr1:70671186-70671236	GM12892	blood:	n/a
9	chr1:70669885-70669935	NB4	blood:	n/a
10	chr1:70675418-70675468	NH-A	brain:	n/a
11	chr1:70671218-70671268	PFSK-1	brain:	n/a
12	chr1:70671119-70671169	GM12891	blood:	n/a
13	chr1:70675418-70675468	HRE	kidney:	n/a
14	chr1:70671378-70671428	HCF	heart:	n/a
15	chr1:70669885-70669935	HUVEC	blood vessel:	n/a
16	chr1:70669885-70669935	Caco-2	colon:	n/a
17	chr1:70671645-70671695	HUVEC	blood vessel:	n/a
18	chr1:70671309-70671359	CMK	blood:	n/a
19	chr1:70671441-70671491	SKMC	muscle:	n/a
20	chr1:70671364-70671414	NHBE	bronchial:	n/a
21	chr1:70671693-70671743	Jurkat	blood:	n/a
22	chr1:70671146-70671196	Hela-S3	cervix:	n/a
23	chr1:70670919-70670969	GM06990	blood:	n/a
24	chr1:70671260-70671310	SKMC	muscle:	n/a
25	chr1:70669885-70669935	ECC-1	luminal epithelium:	n/a
26	chr1:70671216-70671266	HEK293	kidney:	embryo
27	chr1:70671645-70671695	HRE	kidney:	n/a
28	chr1:70671218-70671268	ProgFib	skin:	n/a
29	chr1:70670919-70670969	HRCEpiC	kidney:	n/a
30	chr1:70671645-70671695	SAEC	small airway:	n/a
31	chr1:70671260-70671310	T-47D	breast:	n/a
32	chr1:70671146-70671196	SAEC	small airway:	n/a
33	chr1:70671216-70671266	GM19239	blood:	n/a
34	chr1:70671762-70671812	GM12878	blood:	n/a
35	chr1:70671762-70671812	SK-N-SH	brain:	n/a
36	chr1:70671260-70671310	SK-N-SH_RA	brain:	n/a
37	chr1:70670919-70670969	HL-60	blood:	n/a
38	chr1:70671119-70671169	SAEC	small airway:	n/a
39	chr1:70670919-70670969	NT2-D1	testis:	n/a
40	chr1:70675418-70675468	GM12892	blood:	n/a
41	chr1:70671639-70671689	SKMC	muscle:	n/a
42	chr1:70671146-70671196	A549	lung:	n/a
43	chr1:70671200-70671250	SK-N-SH_RA	brain:	n/a
44	chr1:70671216-70671266	HCT-116	colon:	n/a
45	chr1:70669885-70669935	PrEC	prostate:	n/a
46	chr1:70671309-70671359	HAEpiC	amniotic membrane:	n/a
47	chr1:70671378-70671428	PANC-1	pancreas:	n/a
48	chr1:70671260-70671310	Hepatocyte	liver:	n/a
49	chr1:70671119-70671169	GM06990	blood:	n/a
50	chr1:70675418-70675468	SK-N-MC	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:70671247..70672785-chr1:70672964..70674754,3	K562	blood:
2	chr1:70670145..70673365-chr1:70675136..70679229,4	K562	blood:
3	chr1:70671207..70671772-chr16:30886017..30886837,2	HCT-116	colon:
4	chr1:70671444..70673368-chr1:70706387..70708615,2	K562	blood:
5	chr1:70661362..70665473-chr1:70669237..70671298,4	K562	blood:
6	chr1:70637171..70639889-chr1:70665455..70667033,2	K562	blood:
7	chr1:70669751..70673129-chr1:70685079..70688457,4	MCF-7	breast:
8	chr1:70667153..70674800-chr1:70681943..70693478,26	K562	blood:
9	chr1:70674826..70679166-chr1:70682889..70688598,11	K562	blood:
10	chr1:70674179..70677274-chr1:70677921..70681026,3	K562	blood:
11	chr1:70661362..70665473-chr1:70669237..70671298,4	K562	blood:
12	chr1:70671541..70672478-chr1:70876532..70877433,2	Hela-S3	cervix:
13	chr1:70671253..70671885-chr3:57582557..57583363,2	Hela-S3	cervix:
14	chr1:70652911..70655573-chr1:70665415..70667122,3	K562	blood:
15	chr1:70674646..70677124-chr1:70684729..70687341,2	MCF-7	breast:
16	chr1:70669434..70671203-chr1:70686815..70688649,2	MCF-7	breast:
17	chr1:70670191..70673421-chr1:70819814..70822311,3	K562	blood:
18	chr1:70668667..70673217-chr1:70684547..70688689,8	K562	blood:

No data

Variant related genes	Relation type
SRSF11	TF binding region
LRRC40	TF binding region
SRSF11	CpG island
LRRC40	CpG island
ENSG00000260083	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000066557	chromatin interactions
ENSG00000228988	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000265991	chromatin interactions
ENSG00000168374	chromatin interactions
ENSG00000197568	chromatin interactions

Extended variants
information (count: 677 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531897491	chr1:70655998-70655999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562662371	chr1:70656079-70656080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369555592	chr1:70656095-70656096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs118141904	chr1:70656107-70656108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571330965	chr1:70656135-70656136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573186288	chr1:70656139-70656140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190655884	chr1:70656164-70656165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149347538	chr1:70656185-70656186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374547940	chr1:70656191-70656192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61785271	chr1:70656195-70656196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9787191	chr1:70656206-70656207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563992475	chr1:70656219-70656220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547495193	chr1:70656233-70656234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182779161	chr1:70656254-70656255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367902004	chr1:70656259-70656260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188098844	chr1:70656317-70656318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144756742	chr1:70656346-70656347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529198692	chr1:70656349-70656350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111530730	chr1:70656358-70656359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59341874	chr1:70656379-70656380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112260807	chr1:70656462-70656463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371624386	chr1:70656482-70656483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191402759	chr1:70656503-70656504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142968308	chr1:70656654-70656655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570837546	chr1:70656670-70656671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539958512	chr1:70656730-70656731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546784149	chr1:70656762-70656763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566774390	chr1:70656777-70656778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79337999	chr1:70656818-70656819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535656691	chr1:70656874-70656875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555600622	chr1:70656908-70656909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575910399	chr1:70656924-70656925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146112635	chr1:70656950-70656951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183017584	chr1:70657011-70657012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577654718	chr1:70657091-70657092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562415782	chr1:70657109-70657110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34821575	chr1:70657185-70657186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs560292543	chr1:70657230-70657231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140194310	chr1:70657248-70657249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114216907	chr1:70657326-70657327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547949646	chr1:70657350-70657351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562611220	chr1:70657386-70657387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529461316	chr1:70657498-70657499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531659773	chr1:70657523-70657524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550685773	chr1:70657566-70657567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558861272	chr1:70657572-70657573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77766388	chr1:70657579-70657580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540983880	chr1:70657615-70657616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368035286	chr1:70657674-70657675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546645685	chr1:70657680-70657681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70606800-70661800	Weak transcription	Brain Hippocampus Middle	brain
2	chr1:70607000-70670200	Weak transcription	Psoas Muscle	Psoas
3	chr1:70607000-70670400	Weak transcription	Small Intestine	intestine
4	chr1:70609600-70661200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:70610000-70656600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:70610000-70667800	Weak transcription	HepG2	liver
7	chr1:70610600-70669600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr1:70611000-70666600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:70611200-70670400	Weak transcription	Pancreas	Pancrea
10	chr1:70612400-70669000	Weak transcription	HUVEC	blood vessel
11	chr1:70613400-70658400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:70613600-70657000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:70613600-70667800	Weak transcription	Brain Angular Gyrus	brain
14	chr1:70613800-70658000	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:70614400-70657800	Weak transcription	Fetal Kidney	kidney
16	chr1:70615000-70670000	Weak transcription	NH-A	brain
17	chr1:70615000-70670400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr1:70623000-70656600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:70623000-70661600	Weak transcription	K562	blood
20	chr1:70629800-70669600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:70632600-70656800	Weak transcription	NHLF	lung
22	chr1:70634000-70670400	Weak transcription	Lung	lung
23	chr1:70634200-70658000	Weak transcription	Brain Germinal Matrix	brain
24	chr1:70634400-70670200	Weak transcription	Fetal Stomach	stomach
25	chr1:70634600-70656800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:70635000-70670600	Weak transcription	Aorta	Aorta
27	chr1:70635400-70656200	Weak transcription	Fetal Heart	heart
28	chr1:70638600-70661400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr1:70639800-70670200	Weak transcription	Placenta	Placenta
30	chr1:70643600-70656600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:70643600-70668600	Weak transcription	Fetal Brain Female	brain
32	chr1:70644000-70656400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr1:70644000-70668600	Weak transcription	Ovary	ovary
34	chr1:70644200-70656600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:70644400-70669600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:70644800-70669800	Weak transcription	HSMM	muscle
37	chr1:70646200-70669200	Weak transcription	Fetal Intestine Small	intestine
38	chr1:70649600-70658200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:70649600-70668600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr1:70649600-70668600	Weak transcription	Left Ventricle	heart
41	chr1:70649600-70670400	Weak transcription	Fetal Muscle Leg	muscle
42	chr1:70649800-70670200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:70650000-70656400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:70650000-70670400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr1:70650200-70669800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:70650200-70670400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr1:70650400-70668200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:70650600-70669400	Weak transcription	Adipose Nuclei	Adipose
49	chr1:70650600-70669800	Weak transcription	Fetal Intestine Large	intestine
50	chr1:70650600-70670200	Weak transcription	Fetal Thymus	thymus

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