Variant report

Variant	esv2753481
Chromosome Location	chr1:62424207-62478878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:62433476-62433726	K562	blood:	n/a	n/a
2	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
4	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
5	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
6	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
7	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:62469339-62469469	A549	lung:	n/a	n/a
9	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
10	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
11	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
13	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
14	CEBPB	chr1:62432189-62432433	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr1:62448125-62448179	GM12878	blood:	n/a	n/a
16	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:62460265-62460346	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr1:62460140-62460290	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr1:62460196-62460323	HepG2	liver:	n/a	n/a
20	CTCF	chr1:62460140-62460290	HEK293	kidney:	n/a	n/a
21	CTCF	chr1:62460254-62460320	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:62426894-62426915	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr1:62460160-62460310	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr1:62460246-62460375	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:62460200-62460325	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:62460160-62460310	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:62460285-62460321	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr1:62460261-62460364	NHEK	skin:	n/a	n/a
30	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
31	CTCF	chr1:62460241-62460334	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:62460238-62460309	Medullo	brain:	n/a	n/a
33	CTCF	chr1:62460120-62460270	HMEC	breast:	n/a	n/a
34	CUX1	chr1:62433241-62433259	K562	blood:	n/a	n/a
35	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
36	E2F4	chr1:62451286-62451329	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
39	EP300	chr1:62477467-62478460	SK-N-SH	brain:	n/a	chr1:62478411-62478425 chr1:62478140-62478154
40	EP300	chr1:62432611-62432792	K562	blood:	n/a	n/a
41	EP300	chr1:62433430-62433743	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
42	EP300	chr1:62477703-62478208	SK-N-SH_RA	brain:	n/a	chr1:62478140-62478154
43	EP300	chr1:62433418-62433730	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
44	EP300	chr1:62460888-62460973	K562	blood:	n/a	chr1:62460919-62460929
45	ESR1	chr1:62432573-62432749	T-47D	breast:	n/a	n/a
46	ESR1	chr1:62432481-62432805	T-47D	breast:	n/a	n/a
47	FOS	chr1:62458894-62459527	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:62457147-62457168	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	AG04450	lung:	fetal
2	chr1:62445916-62445966	A549	lung:	n/a
3	chr1:62445916-62445966	LNCaP	prostate:	n/a
4	chr1:62445916-62445966	Jurkat	blood:	n/a
5	chr1:62445916-62445966	HNPCEpiC	eye:	n/a
6	chr1:62445916-62445966	GM19239	blood:	n/a
7	chr1:62445916-62445966	ProgFib	skin:	n/a
8	chr1:62445916-62445966	HCPEpiC	choroid plexus:	n/a
9	chr1:62445916-62445966	PFSK-1	brain:	n/a
10	chr1:62445916-62445966	HIPEpiC	eye:	n/a
11	chr1:62445916-62445966	NHDF-neo	bronchial:	n/a
12	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
13	chr1:62445916-62445966	ovcar-3	ovarian:	n/a
14	chr1:62445916-62445966	IMR90	lung:	fetal
15	chr1:62445916-62445966	U87	brain:	n/a
16	chr1:62445916-62445966	T-47D	breast:	n/a
17	chr1:62445916-62445966	BJ	skin:	n/a
18	chr1:62445916-62445966	AG04449	skin:	fetal
19	chr1:62445916-62445966	NT2-D1	testis:	n/a
20	chr1:62445916-62445966	K562	blood:	n/a
21	chr1:62445916-62445966	HCF	heart:	n/a
22	chr1:62445916-62445966	HCT-116	colon:	n/a
23	chr1:62445916-62445966	ECC-1	luminal epithelium:	n/a
24	chr1:62445916-62445966	Hela-S3	cervix:	n/a
25	chr1:62445916-62445966	HUVEC	blood vessel:	n/a
26	chr1:62445916-62445966	GM12878	blood:	n/a
27	chr1:62445916-62445966	SKMC	muscle:	n/a
28	chr1:62445916-62445966	SAEC	small airway:	n/a
29	chr1:62445916-62445966	GM12892	blood:	n/a
30	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:62445916-62445966	HRPEpiC	eye:	n/a
32	chr1:62445916-62445966	MCF-7	breast:	n/a
33	chr1:62445916-62445966	HMEC	breast:	n/a
34	chr1:62445916-62445966	SK-N-SH_RA	brain:	n/a
35	chr1:62445916-62445966	HepG2	liver:	n/a
36	chr1:62445916-62445966	AG09309	skin:	n/a
37	chr1:62445916-62445966	SK-N-MC	brain:	n/a
38	chr1:62445916-62445966	Caco-2	colon:	n/a
39	chr1:62445916-62445966	PrEC	prostate:	n/a
40	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
41	chr1:62445916-62445966	NHBE	bronchial:	n/a
42	chr1:62445916-62445966	CMK	blood:	n/a
43	chr1:62445916-62445966	Hepatocyte	liver:	n/a
44	chr1:62445916-62445966	GM12891	blood:	n/a
45	chr1:62445916-62445966	NB4	blood:	n/a
46	chr1:62445916-62445966	PANC-1	pancreas:	n/a
47	chr1:62445916-62445966	HEEpiC	esophagus:	n/a
48	chr1:62445916-62445966	HCM	heart:	n/a
49	chr1:62445916-62445966	SK-N-SH	brain:	n/a
50	chr1:62445916-62445966	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
2	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
3	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
4	chr1:62477919..62478756-chr9:3062250..3062792,2	MCF-7	breast:

No data

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island

Extended variants
information (count: 2123 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2123 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2482882	chr1:62424207-62424208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544654614	chr1:62424250-62424251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112428430	chr1:62424254-62424255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533515641	chr1:62424352-62424353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558702853	chr1:62424385-62424386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140215024	chr1:62424392-62424393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560141820	chr1:62424405-62424406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150290342	chr1:62424407-62424408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546504585	chr1:62424436-62424437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371867364	chr1:62424535-62424536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs137885059	chr1:62424542-62424543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185050840	chr1:62424563-62424564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188940352	chr1:62424574-62424575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143454550	chr1:62424597-62424598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559840141	chr1:62424621-62424622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568847243	chr1:62424716-62424717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539572127	chr1:62424750-62424751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557767287	chr1:62424780-62424781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566498321	chr1:62424808-62424809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12748525	chr1:62424816-62424817	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs76416054	chr1:62424824-62424825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574132732	chr1:62424878-62424879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544478040	chr1:62424918-62424919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368040778	chr1:62424945-62424946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2482883	chr1:62424959-62424960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192248553	chr1:62424973-62424974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372137214	chr1:62425054-62425055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560080912	chr1:62425061-62425062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113868823	chr1:62425081-62425082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377016305	chr1:62425098-62425099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552078755	chr1:62425104-62425105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375170571	chr1:62425105-62425106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201283262	chr1:62425110-62425111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2482884	chr1:62425111-62425112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199768878	chr1:62425114-62425115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527687109	chr1:62425152-62425153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540089149	chr1:62425195-62425196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561830016	chr1:62425198-62425199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138595677	chr1:62425258-62425259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550483864	chr1:62425283-62425284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569058491	chr1:62425353-62425354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143948791	chr1:62425362-62425363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551520112	chr1:62425399-62425400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144345783	chr1:62425447-62425448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542446604	chr1:62425461-62425462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369320740	chr1:62425486-62425487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533776049	chr1:62425522-62425523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148736123	chr1:62425537-62425538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368888939	chr1:62425570-62425571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141456803	chr1:62425599-62425600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
3	chr1:62406600-62430200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
8	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
9	chr1:62409400-62429600	Weak transcription	Gastric	stomach
10	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:62410200-62425200	Weak transcription	Fetal Intestine Small	intestine
12	chr1:62416800-62426800	Weak transcription	HepG2	liver
13	chr1:62417800-62431600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:62418000-62428800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
17	chr1:62418600-62432400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:62418600-62432400	Weak transcription	NHEK	skin
19	chr1:62418800-62432800	Weak transcription	HMEC	breast
20	chr1:62419200-62424400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr1:62419600-62426800	Weak transcription	Right Atrium	heart
22	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
23	chr1:62420800-62429800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr1:62422800-62432600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:62423400-62431200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr1:62423400-62433600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:62423600-62433800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:62423800-62432800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:62424000-62432000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:62424200-62427200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:62424200-62436600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
33	chr1:62424400-62424800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:62424800-62438200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr1:62425000-62441400	Weak transcription	Stomach Mucosa	stomach
36	chr1:62425200-62426200	Strong transcription	Fetal Intestine Small	intestine
37	chr1:62426200-62428400	Weak transcription	Fetal Intestine Small	intestine
38	chr1:62426800-62427000	Enhancers	HepG2	liver
39	chr1:62427200-62432800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:62428400-62428600	Enhancers	Right Atrium	heart
41	chr1:62428400-62430600	Strong transcription	Fetal Intestine Small	intestine
42	chr1:62430200-62430600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:62430600-62435400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:62430600-62442200	Weak transcription	Fetal Intestine Small	intestine
45	chr1:62431200-62431400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:62431600-62432200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:62432000-62433400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:62432000-62435600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr1:62432200-62439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:62432400-62433600	Enhancers	NHEK	skin

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