Variant report

Variant	esv3448405
Chromosome Location	chr1:67360980-67393830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:832)
CpG islands
(count:915)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:67390774-67391360	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:67381958-67382504	K562	blood:	n/a	n/a
3	ARID3A	chr1:67390496-67391144	K562	blood:	n/a	n/a
4	ARID3A	chr1:67393745-67393896	K562	blood:	n/a	n/a
5	ARID3A	chr1:67391399-67392405	K562	blood:	n/a	chr1:67392384-67392400
6	ATF1	chr1:67382000-67382335	K562	blood:	n/a	n/a
7	ATF2	chr1:67390438-67390994	GM12878	blood:	n/a	n/a
8	ATF3	chr1:67382026-67382429	K562	blood:	n/a	n/a
9	BACH1	chr1:67390952-67391423	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr1:67390252-67391317	GM12878	blood:	n/a	chr1:67390950-67390963 chr1:67390654-67390667
11	BCLAF1	chr1:67390270-67391325	GM12878	blood:	n/a	chr1:67390950-67390963 chr1:67390654-67390667
12	BHLHE40	chr1:67381990-67382444	K562	blood:	n/a	n/a
13	BHLHE40	chr1:67390327-67391273	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:67390300-67391363	K562	blood:	n/a	n/a
15	BHLHE40	chr1:67382087-67382259	HepG2	liver:	n/a	n/a
16	BHLHE40	chr1:67390347-67391446	HepG2	liver:	n/a	n/a
17	BRCA1	chr1:67390697-67391240	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:67390584-67391075	GM12878	blood:	n/a	n/a
19	BRCA1	chr1:67390357-67391467	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr1:67383195-67383567	K562	blood:	n/a	n/a
21	CBX3	chr1:67385658-67386087	K562	blood:	n/a	n/a
22	CBX3	chr1:67390365-67391591	K562	blood:	n/a	n/a
23	CBX3	chr1:67383198-67383551	K562	blood:	n/a	n/a
24	CCNT2	chr1:67382031-67382347	K562	blood:	n/a	n/a
25	CCNT2	chr1:67390337-67391502	K562	blood:	n/a	chr1:67390870-67390879
26	CEBPB	chr1:67390928-67390962	K562	blood:	n/a	n/a
27	CEBPB	chr1:67381921-67382453	K562	blood:	n/a	n/a
28	CEBPB	chr1:67382111-67382355	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:67381862-67382574	K562	blood:	n/a	n/a
30	CEBPB	chr1:67392419-67392756	K562	blood:	n/a	chr1:67392577-67392590 chr1:67392677-67392694
31	CEBPB	chr1:67382154-67382373	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:67366218-67366446	HepG2	liver:	n/a	chr1:67366346-67366357
33	CEBPB	chr1:67382147-67382411	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:67382005-67382508	K562	blood:	n/a	n/a
35	CEBPB	chr1:67390376-67391877	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:67368343-67368557	K562	blood:	n/a	n/a
37	CEBPB	chr1:67390756-67391261	K562	blood:	n/a	n/a
38	CEBPB	chr1:67366232-67366447	IMR90	lung:	n/a	chr1:67366346-67366357
39	CEBPB	chr1:67390873-67391263	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPD	chr1:67390992-67391391	HepG2	liver:	n/a	n/a
41	CEBPD	chr1:67390332-67390710	HepG2	liver:	n/a	n/a
42	CEBPD	chr1:67381849-67382570	K562	blood:	n/a	n/a
43	CEBPD	chr1:67381887-67382489	K562	blood:	n/a	n/a
44	CHD1	chr1:67390913-67391331	GM12878	blood:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
45	CHD2	chr1:67390367-67391693	HepG2	liver:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
46	CHD2	chr1:67390370-67391361	H1-hESC	embryonic stem cell:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
47	CHD2	chr1:67390211-67391333	GM12878	blood:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
48	CHD2	chr1:67390329-67391425	Hela-S3	cervix:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
49	CHD2	chr1:67390344-67391500	K562	blood:	n/a	chr1:67391072-67391082 chr1:67390964-67390971
50	CREB1	chr1:67390295-67391283	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:67389884-67389934	MCF10A-Er-Src	breast:	n/a
2	chr1:67391082-67391132	RPTEC	kidney:	n/a
3	chr1:67389884-67389934	SKMC	muscle:	n/a
4	chr1:67390436-67390486	Jurkat	blood:	n/a
5	chr1:67391091-67391141	HUVEC	blood vessel:	n/a
6	chr1:67390768-67390818	HEK293	kidney:	embryo
7	chr1:67389698-67389748	GM12892	blood:	n/a
8	chr1:67390436-67390486	PANC-1	pancreas:	n/a
9	chr1:67390937-67390987	Hela-S3	cervix:	n/a
10	chr1:67390436-67390486	Hepatocyte	liver:	n/a
11	chr1:67390436-67390486	GM12878	blood:	n/a
12	chr1:67390937-67390987	HRCEpiC	kidney:	n/a
13	chr1:67390436-67390486	RPTEC	kidney:	n/a
14	chr1:67390768-67390818	PFSK-1	brain:	n/a
15	chr1:67390937-67390987	HNPCEpiC	eye:	n/a
16	chr1:67390937-67390987	Caco-2	colon:	n/a
17	chr1:67390349-67390399	HEK293	kidney:	embryo
18	chr1:67387618-67387668	HMEC	breast:	n/a
19	chr1:67390349-67390399	HIPEpiC	eye:	n/a
20	chr1:67391835-67391885	HRE	kidney:	n/a
21	chr1:67390768-67390818	SK-N-SH	brain:	n/a
22	chr1:67390732-67390782	PFSK-1	brain:	n/a
23	chr1:67390349-67390399	HCM	heart:	n/a
24	chr1:67390732-67390782	AG04450	lung:	fetal
25	chr1:67391144-67391194	HepG2	liver:	n/a
26	chr1:67391091-67391141	MCF10A-Er-Src	breast:	n/a
27	chr1:67390759-67390809	SK-N-MC	brain:	n/a
28	chr1:67391082-67391132	HepG2	liver:	n/a
29	chr1:67390436-67390486	AG09319	gingival:	n/a
30	chr1:67387618-67387668	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:67389698-67389748	AoSMC	blood vessel:	n/a
32	chr1:67389884-67389934	HRCEpiC	kidney:	n/a
33	chr1:67389698-67389748	SK-N-SH	brain:	n/a
34	chr1:67390937-67390987	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:67391144-67391194	HCT-116	colon:	n/a
36	chr1:67389698-67389748	HEK293	kidney:	embryo
37	chr1:67391835-67391885	SK-N-SH	brain:	n/a
38	chr1:67390768-67390818	AG10803	skin:	n/a
39	chr1:67391082-67391132	HAEpiC	amniotic membrane:	n/a
40	chr1:67391091-67391141	HMEC	breast:	n/a
41	chr1:67391091-67391141	SAEC	small airway:	n/a
42	chr1:67390759-67390809	PrEC	prostate:	n/a
43	chr1:67391144-67391194	RPTEC	kidney:	n/a
44	chr1:67390732-67390782	HEEpiC	esophagus:	n/a
45	chr1:67390349-67390399	SK-N-SH_RA	brain:	n/a
46	chr1:67391091-67391141	HAEpiC	amniotic membrane:	n/a
47	chr1:67389733-67389783	RPTEC	kidney:	n/a
48	chr1:67391835-67391885	HAEpiC	amniotic membrane:	n/a
49	chr1:67390768-67390818	U87	brain:	n/a
50	chr1:67390349-67390399	Caco-2	colon:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:67356978..67359079-chr1:67361266..67364100,2	K562	blood:
2	chr1:67390712..67391423-chr5:94061472..94061972,2	NB4	blood:
3	chr1:67363985..67367919-chr1:67368695..67372358,4	K562	blood:
4	chr1:67376441..67378103-chr1:67389443..67391844,2	K562	blood:
5	chr1:67379651..67382405-chr1:67394284..67396739,2	K562	blood:
6	chr1:67374324..67377212-chr1:67396474..67398489,3	K562	blood:
7	chr1:67366082..67368708-chr1:67375984..67378961,2	K562	blood:
8	chr1:67372987..67375149-chr1:67375633..67379902,4	K562	blood:
9	chr1:67389047..67393171-chr1:67393255..67399137,11	MCF-7	breast:
10	chr1:67391025..67391990-chr12:123465066..123465658,2	Hela-S3	cervix:
11	chr1:52194759..52195337-chr1:67390414..67391320,2	Hela-S3	cervix:
12	chr1:67389047..67393171-chr1:67393255..67399137,11	MCF-7	breast:
13	chr1:67369227..67371783-chr1:67374860..67376638,2	K562	blood:
14	chr1:67390775..67391349-chr7:337412..337913,2	Hela-S3	cervix:
15	chr1:67390720..67392859-chr1:67459230..67461663,2	K562	blood:
16	chr1:65608373..65610541-chr1:67391827..67393625,2	MCF-7	breast:
17	chr1:67385997..67392679-chr1:67394416..67400305,9	MCF-7	breast:
18	chr1:67374136..67376779-chr1:67384902..67386423,2	K562	blood:
19	chr1:67366082..67368708-chr1:67375984..67378961,2	K562	blood:
20	chr1:67351495..67353743-chr1:67373492..67375346,2	K562	blood:
21	chr1:67381959..67383522-chr1:67390509..67392299,2	K562	blood:
22	chr1:67385809..67388238-chr1:67388654..67390836,2	MCF-7	breast:
23	chr1:67374136..67376779-chr1:67384902..67386423,2	K562	blood:
24	chr1:67371066..67372897-chr1:67378097..67380047,2	K562	blood:
25	chr1:67372987..67375149-chr1:67375633..67379902,4	K562	blood:
26	chr1:67385327..67388250-chr1:67504419..67506337,2	MCF-7	breast:

No data

Variant related genes	Relation type
WDR78	TF binding region
MIER1	TF binding region
WDR78	CpG island
MIER1	CpG island
ENSG00000182196	chromatin interactions
ENSG00000198160	chromatin interactions
ENSG00000117859	chromatin interactions
ENSG00000152763	chromatin interactions

Extended variants
information (count: 1134 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1134 , 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	rs565975272	chr1:67360991-67360992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192230409	chr1:67361034-67361035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554969826	chr1:67361037-67361038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575051729	chr1:67361054-67361055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561757540	chr1:67361067-67361068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535887752	chr1:67361091-67361092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556155099	chr1:67361140-67361141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576082972	chr1:67361144-67361145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184615244	chr1:67361171-67361172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545907581	chr1:67361172-67361173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12122364	chr1:67361195-67361196	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs558592198	chr1:67361197-67361198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189394951	chr1:67361220-67361221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138234983	chr1:67361234-67361235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561046998	chr1:67361257-67361258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180708165	chr1:67361286-67361287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543329613	chr1:67361360-67361361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184500248	chr1:67361378-67361379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144881690	chr1:67361411-67361412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189369767	chr1:67361418-67361419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532363562	chr1:67361464-67361465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552265514	chr1:67361497-67361498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551658205	chr1:67361498-67361499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374101390	chr1:67361551-67361552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565791078	chr1:67361560-67361561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181288356	chr1:67361568-67361569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186497076	chr1:67361575-67361576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559243650	chr1:67361589-67361590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142954122	chr1:67361590-67361591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537774355	chr1:67361592-67361593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146135835	chr1:67361603-67361604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535498968	chr1:67361605-67361606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372225130	chr1:67361606-67361607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569706830	chr1:67361628-67361629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538596227	chr1:67361657-67361658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1925407	chr1:67361670-67361671	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs72671687	chr1:67361671-67361672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549057979	chr1:67361757-67361758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540884535	chr1:67361764-67361765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554777337	chr1:67361767-67361768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574545112	chr1:67361769-67361770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79690474	chr1:67361831-67361832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190556746	chr1:67361858-67361859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543741685	chr1:67361864-67361865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563202739	chr1:67361873-67361874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532375340	chr1:67361886-67361887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545766307	chr1:67361913-67361914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181672438	chr1:67361944-67361945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575142166	chr1:67361947-67361948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548368070	chr1:67362178-67362179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67346800-67363200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:67348400-67389000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:67349400-67389600	Weak transcription	Aorta	Aorta
4	chr1:67350000-67369400	Weak transcription	Fetal Kidney	kidney
5	chr1:67352200-67372600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:67352800-67385600	Weak transcription	Ovary	ovary
7	chr1:67354600-67362600	Weak transcription	Brain Substantia Nigra	brain
8	chr1:67355800-67369400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:67359400-67389600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:67360000-67367800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:67362600-67362800	Enhancers	Brain Substantia Nigra	brain
12	chr1:67362600-67363000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:67362600-67363200	Enhancers	Brain Anterior Caudate	brain
14	chr1:67363200-67363800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:67363200-67368600	Weak transcription	Brain Anterior Caudate	brain
16	chr1:67363800-67365400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:67364000-67382000	Weak transcription	Fetal Intestine Small	intestine
18	chr1:67364000-67385800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:67364000-67389000	Weak transcription	Osteobl	bone
20	chr1:67364600-67372000	Weak transcription	Left Ventricle	heart
21	chr1:67364800-67388800	Weak transcription	NHDF-Ad	bronchial
22	chr1:67365000-67383200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:67365400-67369600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:67366400-67369200	Weak transcription	Liver	Liver
25	chr1:67366600-67389000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:67367200-67369400	Weak transcription	Primary T cells from cord blood	blood
27	chr1:67367600-67374600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:67367800-67369200	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr1:67367800-67385400	Weak transcription	Fetal Stomach	stomach
30	chr1:67369200-67371200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:67369600-67385600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:67374600-67374800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr1:67374800-67377000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:67376400-67377200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr1:67376600-67377200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:67376600-67377200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:67376800-67377200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr1:67376800-67377400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:67377000-67377200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:67377000-67377200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:67377000-67377400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:67377000-67378400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:67377200-67377400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:67377200-67378800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:67377200-67384800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:67377200-67389200	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr1:67377400-67378800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:67377400-67378800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr1:67377400-67382800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:67378800-67379000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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