Variant report

Variant	nsv1110
Chromosome Location	chr1:62395723-62454435
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	chr1:62407480-62407847	HepG2	liver:	n/a	n/a
2	ATF2	chr1:62417577-62418091	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:62433476-62433726	K562	blood:	n/a	n/a
4	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
5	BACH1	chr1:62417538-62418004	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
8	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
10	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
11	CEBPB	chr1:62415035-62415226	K562	blood:	n/a	n/a
12	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
13	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
14	CEBPB	chr1:62418881-62419230	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
17	CEBPB	chr1:62432189-62432433	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
19	CEBPB	chr1:62418894-62419140	HepG2	liver:	n/a	n/a
20	CHD1	chr1:62416839-62416933	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr1:62417310-62417837	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:62417448-62418216	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:62448125-62448179	GM12878	blood:	n/a	n/a
25	CTCF	chr1:62416239-62416284	GM10248	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
26	CTCF	chr1:62416200-62416350	HMF	breast:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
27	CTCF	chr1:62416221-62416309	MCF-7	breast:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
28	CTCF	chr1:62416260-62416410	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr1:62416160-62416310	GM12868	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
30	CTCF	chr1:62415980-62416130	BJ	skin:	n/a	n/a
31	CTCF	chr1:62416162-62416324	GM13977	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
32	CTCF	chr1:62416100-62416250	K562	blood:	n/a	n/a
33	CTCF	chr1:62416200-62416350	GM12878	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
34	CTCF	chr1:62415658-62415694	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr1:62416160-62416310	HEEpiC	esophagus:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
36	CTCF	chr1:62416160-62416310	GM12864	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
37	CTCF	chr1:62415873-62416465	SK-N-SH	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
38	CTCF	chr1:62416180-62416330	NB4	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
39	CTCF	chr1:62416160-62416310	HL-60	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
40	CTCF	chr1:62416135-62416374	K562	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
41	CTCF	chr1:62396080-62396230	HCFaa	heart:	n/a	n/a
42	CTCF	chr1:62416160-62416310	GM12871	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
43	CTCF	chr1:62416086-62416443	K562	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
44	CTCF	chr1:62416166-62416346	HepG2	liver:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
45	CTCF	chr1:62416140-62416290	Caco-2	colon:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
46	CTCF	chr1:62416180-62416330	AG09309	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
47	CTCF	chr1:62416260-62416410	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:62416020-62416170	HFF	foreskin:	n/a	n/a
49	CTCF	chr1:62416140-62416290	SAEC	small airway:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
50	CTCF	chr1:62416101-62416363	SK-N-SH_RA	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	SK-N-SH	brain:	n/a
2	chr1:62445916-62445966	AG09309	skin:	n/a
3	chr1:62416593-62416643	GM12892	blood:	n/a
4	chr1:62416593-62416643	HCT-116	colon:	n/a
5	chr1:62445916-62445966	IMR90	lung:	fetal
6	chr1:62416593-62416643	AG09319	gingival:	n/a
7	chr1:62416593-62416643	NHBE	bronchial:	n/a
8	chr1:62445916-62445966	GM12878	blood:	n/a
9	chr1:62416593-62416643	SK-N-SH_RA	brain:	n/a
10	chr1:62416593-62416643	SAEC	small airway:	n/a
11	chr1:62416593-62416643	HIPEpiC	eye:	n/a
12	chr1:62416593-62416643	U87	brain:	n/a
13	chr1:62416593-62416643	ProgFib	skin:	n/a
14	chr1:62416593-62416643	HRPEpiC	eye:	n/a
15	chr1:62416593-62416643	NB4	blood:	n/a
16	chr1:62445916-62445966	MCF10A-Er-Src	breast:	n/a
17	chr1:62416593-62416643	PFSK-1	brain:	n/a
18	chr1:62416593-62416643	HCF	heart:	n/a
19	chr1:62416593-62416643	BE2_C	brain:	n/a
20	chr1:62416593-62416643	PrEC	prostate:	n/a
21	chr1:62445916-62445966	HCT-116	colon:	n/a
22	chr1:62416593-62416643	HMEC	breast:	n/a
23	chr1:62445916-62445966	ovcar-3	ovarian:	n/a
24	chr1:62445916-62445966	MCF-7	breast:	n/a
25	chr1:62445916-62445966	Jurkat	blood:	n/a
26	chr1:62416593-62416643	SK-N-MC	brain:	n/a
27	chr1:62416593-62416643	RPTEC	kidney:	n/a
28	chr1:62416593-62416643	Hepatocyte	liver:	n/a
29	chr1:62445916-62445966	AG09319	gingival:	n/a
30	chr1:62416593-62416643	AoSMC	blood vessel:	n/a
31	chr1:62445916-62445966	GM12891	blood:	n/a
32	chr1:62416593-62416643	AG10803	skin:	n/a
33	chr1:62416593-62416643	HEK293	kidney:	embryo
34	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
35	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
36	chr1:62445916-62445966	AG04450	lung:	fetal
37	chr1:62445916-62445966	SAEC	small airway:	n/a
38	chr1:62445916-62445966	HCM	heart:	n/a
39	chr1:62445916-62445966	HL-60	blood:	n/a
40	chr1:62416593-62416643	MCF10A-Er-Src	breast:	n/a
41	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
42	chr1:62416593-62416643	GM12878	blood:	n/a
43	chr1:62416593-62416643	ECC-1	luminal epithelium:	n/a
44	chr1:62416593-62416643	GM06990	blood:	n/a
45	chr1:62416593-62416643	SKMC	muscle:	n/a
46	chr1:62416593-62416643	LNCaP	prostate:	n/a
47	chr1:62445916-62445966	HEK293	kidney:	embryo
48	chr1:62416593-62416643	HEEpiC	esophagus:	n/a
49	chr1:62416593-62416643	AG09309	skin:	n/a
50	chr1:62445916-62445966	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
2	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
3	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
4	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
5	chr1:62417324..62419162-chr1:62419469..62421904,2	MCF-7	breast:

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island
ENSG00000132849	chromatin interactions

Extended variants
information (count: 2173 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2173 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546285179	chr1:62395734-62395735	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568112924	chr1:62395745-62395746	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528883989	chr1:62395766-62395767	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551227210	chr1:62395839-62395840	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569464404	chr1:62395847-62395848	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539980647	chr1:62395859-62395860	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182572216	chr1:62395894-62395895	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535218558	chr1:62395970-62395971	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186755423	chr1:62395978-62395979	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534275375	chr1:62396005-62396006	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191993519	chr1:62396054-62396055	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574056912	chr1:62396075-62396076	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544297801	chr1:62396120-62396121	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60382601	chr1:62396149-62396150	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575454304	chr1:62396169-62396170	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562996808	chr1:62396171-62396172	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371951461	chr1:62396194-62396195	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75948430	chr1:62396208-62396209	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs58785584	chr1:62396306-62396307	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs575079392	chr1:62396310-62396311	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151019002	chr1:62396358-62396359	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182621196	chr1:62396416-62396417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539918406	chr1:62396447-62396448	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185765832	chr1:62396483-62396484	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528846409	chr1:62396529-62396530	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370063440	chr1:62396575-62396576	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10889270	chr1:62396602-62396603	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569485584	chr1:62396622-62396623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533450982	chr1:62396638-62396639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552140225	chr1:62396647-62396648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374630816	chr1:62396666-62396667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567050680	chr1:62396684-62396685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147785248	chr1:62396741-62396742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74619786	chr1:62396780-62396781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532358909	chr1:62396781-62396782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567771731	chr1:62396788-62396789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75690407	chr1:62396823-62396824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556282481	chr1:62396829-62396830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578001807	chr1:62396836-62396837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572805848	chr1:62396874-62396875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545763678	chr1:62396885-62396886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12077526	chr1:62396904-62396905	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545647106	chr1:62396908-62396909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540053251	chr1:62396938-62396939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376316315	chr1:62396945-62396946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78742520	chr1:62397011-62397012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115238422	chr1:62397013-62397014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544338517	chr1:62397014-62397015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113624295	chr1:62397023-62397024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532974079	chr1:62397024-62397025	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62336000-62408600	Weak transcription	Pancreas	Pancrea
2	chr1:62340400-62399200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:62346200-62417600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:62350200-62397600	Weak transcription	Esophagus	oesophagus
5	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr1:62350800-62395800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:62350800-62397800	Weak transcription	Primary T cells from cord blood	blood
8	chr1:62350800-62417600	Weak transcription	Ovary	ovary
9	chr1:62353600-62396000	Weak transcription	Fetal Kidney	kidney
10	chr1:62353800-62408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:62361600-62408800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:62362000-62408600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:62372400-62408800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:62372400-62417600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:62374600-62410600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr1:62375200-62404600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr1:62376200-62417600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:62377200-62396600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr1:62380600-62408600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:62380800-62395800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:62380800-62410000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr1:62381000-62408200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:62381000-62416000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr1:62381200-62417400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr1:62381200-62418400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:62381600-62402800	Weak transcription	HepG2	liver
27	chr1:62383400-62408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:62384600-62403000	Weak transcription	Fetal Stomach	stomach
29	chr1:62384600-62408200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:62384600-62408800	Weak transcription	Fetal Intestine Large	intestine
31	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
32	chr1:62385400-62408400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:62385400-62408600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:62386000-62408600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:62386200-62397000	Weak transcription	Fetal Intestine Small	intestine
36	chr1:62388800-62397400	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr1:62389800-62396000	Weak transcription	NHEK	skin
38	chr1:62391800-62409000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:62392000-62408800	Weak transcription	Gastric	stomach
40	chr1:62392600-62408600	Weak transcription	Stomach Mucosa	stomach
41	chr1:62392600-62408800	Weak transcription	Left Ventricle	heart
42	chr1:62393200-62398200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:62393600-62396400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:62393800-62402800	Weak transcription	Hela-S3	cervix
45	chr1:62393800-62422400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr1:62394600-62395800	Strong transcription	Duodenum Mucosa	Duodenum
47	chr1:62394800-62396200	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr1:62394800-62397200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:62394800-62397600	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr1:62394800-62400400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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