Variant report

Variant	nsv546415
Chromosome Location	chr1:62405873-62437872
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	chr1:62417538-62418004	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
6	CEBPB	chr1:62415035-62415226	K562	blood:	n/a	n/a
7	CEBPB	chr1:62432189-62432433	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:62418894-62419140	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:62418881-62419230	IMR90	lung:	n/a	n/a
10	CHD1	chr1:62417310-62417837	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr1:62416839-62416933	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr1:62417448-62418216	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:62416080-62416230	HCT-116	colon:	n/a	n/a
14	CTCF	chr1:62416120-62416270	GM12864	blood:	n/a	chr1:62416248-62416266 chr1:62416249-62416265
15	CTCF	chr1:62416158-62416377	LNCaP	prostate:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
16	CTCF	chr1:62416140-62416290	SAEC	small airway:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
17	CTCF	chr1:62416160-62416310	GM12871	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
18	CTCF	chr1:62416180-62416330	NHEK	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
19	CTCF	chr1:62416160-62416310	K562	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
20	CTCF	chr1:62416180-62416330	GM12865	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
21	CTCF	chr1:62416100-62416250	GM12872	blood:	n/a	n/a
22	CTCF	chr1:62416140-62416290	HPAF	blood vessel:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
23	CTCF	chr1:62416160-62416310	GM12868	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
24	CTCF	chr1:62416160-62416310	RPTEC	kidney:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
25	CTCF	chr1:62416086-62416443	K562	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
26	CTCF	chr1:62416101-62416363	SK-N-SH_RA	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
27	CTCF	chr1:62415995-62416610	A549	lung:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
28	CTCF	chr1:62416160-62416310	GM06990	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
29	CTCF	chr1:62416180-62416330	GM12869	blood:	n/a	chr1:62416250-62416271 chr1:62416249-62416265 chr1:62416248-62416266
30	CTCF	chr1:62416184-62416348	Kidney_OC	kidney:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
31	CTCF	chr1:62415860-62416010	HMEC	breast:	n/a	n/a
32	CTCF	chr1:62416200-62416350	GM12874	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
33	CTCF	chr1:62416180-62416330	HA-sp	spinal cord:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
34	CTCF	chr1:62416220-62416370	HFF	foreskin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
35	CTCF	chr1:62416100-62416250	K562	blood:	n/a	n/a
36	CTCF	chr1:62416160-62416310	NHEK	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
37	CTCF	chr1:62415980-62416130	BJ	skin:	n/a	n/a
38	CTCF	chr1:62416160-62416310	HCFaa	heart:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
39	CTCF	chr1:62416200-62416350	GM12801	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
40	CTCF	chr1:62416140-62416290	GM12872	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
41	CTCF	chr1:62416120-62416270	HBMEC	blood vessel:	n/a	chr1:62416248-62416266 chr1:62416249-62416265
42	CTCF	chr1:62416180-62416330	HEK293	kidney:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
43	CTCF	chr1:62416200-62416350	GM12878	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
44	CTCF	chr1:62416100-62416250	HPF	lung:	n/a	n/a
45	CTCF	chr1:62416220-62416370	GM12865	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
46	CTCF	chr1:62416239-62416284	GM10248	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
47	CTCF	chr1:62416166-62416346	HepG2	liver:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
48	CTCF	chr1:62416190-62416338	HepG2	liver:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
49	CTCF	chr1:62416175-62416324	GM10266	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
50	CTCF	chr1:62410015-62410050	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62416593-62416643	Hepatocyte	liver:	n/a
2	chr1:62416593-62416643	GM12878	blood:	n/a
3	chr1:62416593-62416643	IMR90	lung:	fetal
4	chr1:62416593-62416643	HCM	heart:	n/a
5	chr1:62416593-62416643	NT2-D1	testis:	n/a
6	chr1:62416593-62416643	PFSK-1	brain:	n/a
7	chr1:62416593-62416643	BE2_C	brain:	n/a
8	chr1:62416593-62416643	SKMC	muscle:	n/a
9	chr1:62416593-62416643	HCPEpiC	choroid plexus:	n/a
10	chr1:62416593-62416643	HRCEpiC	kidney:	n/a
11	chr1:62416593-62416643	ovcar-3	ovarian:	n/a
12	chr1:62416593-62416643	HIPEpiC	eye:	n/a
13	chr1:62416593-62416643	GM12892	blood:	n/a
14	chr1:62416593-62416643	HEEpiC	esophagus:	n/a
15	chr1:62416593-62416643	PrEC	prostate:	n/a
16	chr1:62416593-62416643	HCT-116	colon:	n/a
17	chr1:62416593-62416643	AoSMC	blood vessel:	n/a
18	chr1:62416593-62416643	SK-N-SH	brain:	n/a
19	chr1:62416593-62416643	BJ	skin:	n/a
20	chr1:62416593-62416643	HMEC	breast:	n/a
21	chr1:62416593-62416643	AG10803	skin:	n/a
22	chr1:62416593-62416643	HUVEC	blood vessel:	n/a
23	chr1:62416593-62416643	A549	lung:	n/a
24	chr1:62416593-62416643	HepG2	liver:	n/a
25	chr1:62416593-62416643	AG09309	skin:	n/a
26	chr1:62416593-62416643	ECC-1	luminal epithelium:	n/a
27	chr1:62416593-62416643	NHBE	bronchial:	n/a
28	chr1:62416593-62416643	NH-A	brain:	n/a
29	chr1:62416593-62416643	Caco-2	colon:	n/a
30	chr1:62416593-62416643	HRE	kidney:	n/a
31	chr1:62416593-62416643	SK-N-SH_RA	brain:	n/a
32	chr1:62416593-62416643	HNPCEpiC	eye:	n/a
33	chr1:62416593-62416643	U87	brain:	n/a
34	chr1:62416593-62416643	T-47D	breast:	n/a
35	chr1:62416593-62416643	AG09319	gingival:	n/a
36	chr1:62416593-62416643	Jurkat	blood:	n/a
37	chr1:62416593-62416643	ProgFib	skin:	n/a
38	chr1:62416593-62416643	CMK	blood:	n/a
39	chr1:62416593-62416643	SK-N-MC	brain:	n/a
40	chr1:62416593-62416643	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:62416593-62416643	PANC-1	pancreas:	n/a
42	chr1:62416593-62416643	MCF10A-Er-Src	breast:	n/a
43	chr1:62416593-62416643	H1-hESC	embryonic stem cell:	embryo
44	chr1:62416593-62416643	HAEpiC	amniotic membrane:	n/a
45	chr1:62416593-62416643	K562	blood:	n/a
46	chr1:62416593-62416643	GM06990	blood:	n/a
47	chr1:62416593-62416643	HL-60	blood:	n/a
48	chr1:62416593-62416643	LNCaP	prostate:	n/a
49	chr1:62416593-62416643	NHDF-neo	bronchial:	n/a
50	chr1:62416593-62416643	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
2	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
3	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: 1129 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11807297	chr1:62405873-62405874	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76738047	chr1:62405874-62405875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539881412	chr1:62405911-62405912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371544767	chr1:62405931-62405932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558278903	chr1:62405965-62405966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537920798	chr1:62406030-62406031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556318491	chr1:62406051-62406052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11207873	chr1:62406053-62406054	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545031188	chr1:62406121-62406122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190860230	chr1:62406155-62406156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11802946	chr1:62406159-62406160	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542993932	chr1:62406173-62406174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561515394	chr1:62406187-62406188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142912926	chr1:62406202-62406203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183447978	chr1:62406203-62406204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573291257	chr1:62406215-62406216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147438075	chr1:62406258-62406259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112616491	chr1:62406259-62406260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187296068	chr1:62406270-62406271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199639048	chr1:62406292-62406293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190634304	chr1:62406312-62406313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182840574	chr1:62406313-62406314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12069154	chr1:62406349-62406350	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs547927537	chr1:62406393-62406394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369859908	chr1:62406452-62406453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538057225	chr1:62406532-62406533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549865359	chr1:62406588-62406589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571368906	chr1:62406598-62406599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538786150	chr1:62406620-62406621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553721006	chr1:62406641-62406642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571982960	chr1:62406645-62406646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12135923	chr1:62406650-62406651	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188359701	chr1:62406655-62406656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2482866	chr1:62406661-62406662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192156877	chr1:62406676-62406677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6693783	chr1:62406679-62406680	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs56283855	chr1:62406696-62406697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541167249	chr1:62406725-62406726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373982557	chr1:62406738-62406739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148639604	chr1:62406809-62406810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549227141	chr1:62406810-62406811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2482867	chr1:62406930-62406931	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs565051122	chr1:62406972-62406973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537982417	chr1:62407044-62407045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186964500	chr1:62407045-62407046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531490498	chr1:62407053-62407054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554665770	chr1:62407058-62407059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192442409	chr1:62407107-62407108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571510414	chr1:62407126-62407127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371114419	chr1:62407138-62407139	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:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62336000-62408600	Weak transcription	Pancreas	Pancrea
2	chr1:62346200-62417600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:62350800-62417600	Weak transcription	Ovary	ovary
5	chr1:62353800-62408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:62361600-62408800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:62362000-62408600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:62372400-62408800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:62372400-62417600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr1:62374600-62410600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:62376200-62417600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:62380600-62408600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr1:62380800-62410000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr1:62381000-62408200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr1:62381000-62416000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr1:62381200-62417400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:62381200-62418400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr1:62383400-62408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:62384600-62408200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:62384600-62408800	Weak transcription	Fetal Intestine Large	intestine
21	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
22	chr1:62385400-62408400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:62385400-62408600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:62386000-62408600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr1:62391800-62409000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr1:62392000-62408800	Weak transcription	Gastric	stomach
27	chr1:62392600-62408600	Weak transcription	Stomach Mucosa	stomach
28	chr1:62392600-62408800	Weak transcription	Left Ventricle	heart
29	chr1:62393800-62422400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr1:62395000-62408600	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr1:62395000-62410800	Weak transcription	Liver	Liver
32	chr1:62395800-62408200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr1:62396200-62408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr1:62396200-62416000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:62396200-62417200	Weak transcription	HMEC	breast
36	chr1:62396400-62408200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:62396400-62408600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr1:62396400-62418000	Weak transcription	Fetal Kidney	kidney
39	chr1:62397400-62408200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:62397600-62408600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr1:62398000-62408200	Weak transcription	NHEK	skin
42	chr1:62398200-62408400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr1:62398200-62408600	Weak transcription	Esophagus	oesophagus
44	chr1:62398800-62408600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr1:62400600-62417600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:62401000-62406000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:62401400-62408800	Weak transcription	Lung	lung
48	chr1:62403000-62407600	Weak transcription	HepG2	liver
49	chr1:62404200-62407000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:62405200-62406000	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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