Variant report

Variant	nsv1008421
Chromosome Location	chr2:67417384-67476219
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	chr2:67468017-67468028	K562	blood:	n/a	n/a
2	BACH1	chr2:67431528-67431811	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:67442430-67442736	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:67461612-67461951	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:67448459-67448715	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:67467663-67468009	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:67467702-67467993	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:67461642-67461936	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:67475050-67475149	H1-hESC	embryonic stem cell:	n/a	chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475099-67475110 chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475098-67475111 chr2:67475098-67475109
10	CEBPB	chr2:67448430-67448709	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:67461538-67462050	MCF-7	breast:	n/a	n/a
12	CEBPB	chr2:67461620-67461957	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:67474945-67475210	HepG2	liver:	n/a	chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475099-67475110 chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475098-67475111 chr2:67475098-67475109
14	CEBPB	chr2:67474978-67475233	IMR90	lung:	n/a	chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475099-67475110 chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475098-67475111 chr2:67475098-67475109
15	CEBPB	chr2:67474970-67475217	A549	lung:	n/a	chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475099-67475110 chr2:67475100-67475109 chr2:67475100-67475109 chr2:67475098-67475111 chr2:67475098-67475109
16	CEBPB	chr2:67449561-67449793	HepG2	liver:	n/a	n/a
17	CTCF	chr2:67442550-67442598	GM10266	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
18	CTCF	chr2:67437620-67437770	HCFaa	heart:	n/a	n/a
19	CTCF	chr2:67437680-67437830	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr2:67461720-67461870	HCFaa	heart:	n/a	n/a
21	CTCF	chr2:67464620-67464770	HRE	kidney:	n/a	n/a
22	CTCF	chr2:67442540-67442690	Hela-S3	cervix:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
23	CTCF	chr2:67464640-67464790	HCM	heart:	n/a	n/a
24	CTCF	chr2:67442440-67442590	GM12870	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
25	CTCF	chr2:67442378-67442695	SK-N-SH_RA	brain:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
26	CTCF	chr2:67442520-67442670	AG10803	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
27	CTCF	chr2:67442520-67442670	RPTEC	kidney:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
28	CTCF	chr2:67461700-67461850	HCM	heart:	n/a	n/a
29	CTCF	chr2:67464620-67464770	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr2:67442322-67442805	IMR90	lung:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
31	CTCF	chr2:67461700-67461850	HCT-116	colon:	n/a	n/a
32	CTCF	chr2:67422318-67422369	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:67437580-67437730	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:67464490-67464722	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:67442466-67442719	Medullo	brain:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
36	CTCF	chr2:67442480-67442630	GM12865	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
37	CTCF	chr2:67464547-67464663	HepG2	liver:	n/a	n/a
38	CTCF	chr2:67464600-67464750	HVMF	connective:	n/a	n/a
39	CTCF	chr2:67442500-67442650	HUVEC	blood vessel:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
40	CTCF	chr2:67442400-67442550	WI-38	lung:	n/a	n/a
41	CTCF	chr2:67461700-67461850	HRE	kidney:	n/a	n/a
42	CTCF	chr2:67461720-67461870	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr2:67442540-67442690	NB4	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
44	CTCF	chr2:67442550-67442638	GM13977	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
45	CTCF	chr2:67461740-67461890	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr2:67469747-67469797	IMR90	lung:	n/a	n/a
47	CTCF	chr2:67461720-67461870	HAc	cerebellar:	n/a	n/a
48	CTCF	chr2:67442480-67442630	HepG2	liver:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
49	CTCF	chr2:67461630-67461920	A549	lung:	n/a	n/a
50	CTCF	chr2:67461676-67461891	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:67443148-67443198	PFSK-1	brain:	n/a
2	chr2:67443148-67443198	PFSK-1	brain:	n/a
3	chr2:67443148-67443198	SAEC	small airway:	n/a
4	chr2:67461943-67461993	SK-N-SH_RA	brain:	n/a
5	chr2:67443148-67443198	NHBE	bronchial:	n/a
6	chr2:67443148-67443198	BE2_C	brain:	n/a
7	chr2:67442562-67442612	SK-N-SH	brain:	n/a
8	chr2:67461943-67461993	SK-N-SH	brain:	n/a
9	chr2:67442562-67442612	HIPEpiC	eye:	n/a
10	chr2:67461943-67461993	ECC-1	luminal epithelium:	n/a
11	chr2:67461943-67461993	NHBE	bronchial:	n/a
12	chr2:67442559-67442609	NB4	blood:	n/a
13	chr2:67442559-67442609	AG04450	lung:	fetal
14	chr2:67442562-67442612	MCF-7	breast:	n/a
15	chr2:67443148-67443198	AG10803	skin:	n/a
16	chr2:67442559-67442609	Hela-S3	cervix:	n/a
17	chr2:67442559-67442609	T-47D	breast:	n/a
18	chr2:67442559-67442609	MCF-7	breast:	n/a
19	chr2:67442559-67442609	HEEpiC	esophagus:	n/a
20	chr2:67443148-67443198	HIPEpiC	eye:	n/a
21	chr2:67442562-67442612	Jurkat	blood:	n/a
22	chr2:67443148-67443198	SKMC	muscle:	n/a
23	chr2:67442562-67442612	HNPCEpiC	eye:	n/a
24	chr2:67443148-67443198	HEEpiC	esophagus:	n/a
25	chr2:67443148-67443198	RPTEC	kidney:	n/a
26	chr2:67442562-67442612	ovcar-3	ovarian:	n/a
27	chr2:67442559-67442609	BJ	skin:	n/a
28	chr2:67443148-67443198	SK-N-SH_RA	brain:	n/a
29	chr2:67443148-67443198	NH-A	brain:	n/a
30	chr2:67461943-67461993	HRPEpiC	eye:	n/a
31	chr2:67443148-67443198	HNPCEpiC	eye:	n/a
32	chr2:67461943-67461993	HCPEpiC	choroid plexus:	n/a
33	chr2:67443148-67443198	ECC-1	luminal epithelium:	n/a
34	chr2:67443148-67443198	Hepatocyte	liver:	n/a
35	chr2:67461943-67461993	NB4	blood:	n/a
36	chr2:67443148-67443198	HepG2	liver:	n/a
37	chr2:67443148-67443198	GM12892	blood:	n/a
38	chr2:67461943-67461993	MCF10A-Er-Src	breast:	n/a
39	chr2:67442562-67442612	HRE	kidney:	n/a
40	chr2:67442562-67442612	HCM	heart:	n/a
41	chr2:67442562-67442612	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:67461943-67461993	AoSMC	blood vessel:	n/a
43	chr2:67442559-67442609	Jurkat	blood:	n/a
44	chr2:67443148-67443198	HCT-116	colon:	n/a
45	chr2:67443148-67443198	NHDF-neo	bronchial:	n/a
46	chr2:67443148-67443198	NB4	blood:	n/a
47	chr2:67442559-67442609	GM12892	blood:	n/a
48	chr2:67442559-67442609	H1-hESC	embryonic stem cell:	embryo
49	chr2:67442559-67442609	HRCEpiC	kidney:	n/a
50	chr2:67461943-67461993	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:67464250..67465118-chr2:67877852..67878567,2	MCF-7	breast:
2	chr2:66660597..66662328-chr2:67444081..67446040,2	MCF-7	breast:
3	chr2:66660289..66660808-chr2:67461184..67461830,2	MCF-7	breast:
4	chr2:67442796..67445118-chr2:67455798..67458502,2	MCF-7	breast:
5	chr2:67442796..67445118-chr2:67455798..67458502,2	MCF-7	breast:
6	chr2:67464144..67464961-chr2:68067459..68068253,2	MCF-7	breast:
7	chr2:67428374..67430346-chr2:67431827..67434171,3	K562	blood:
8	chr2:66813989..66814981-chr2:67461210..67462180,4	MCF-7	breast:
9	chr2:67464167..67465140-chr2:68067336..68068083,4	MCF-7	breast:
10	chr2:67464314..67465913-chr2:67549538..67550435,4	MCF-7	breast:
11	chr2:67428374..67430346-chr2:67431827..67434171,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1D-3	chr2:67442360-67442451	XLOC_002142
2	lnc-C1D-3	chr2:67432641-67432695	XLOC_002142
3	lnc-C1D-3	chr2:67440771-67440900	XLOC_002142
4	lnc-C1D-3	chr2:67430248-67430305	XLOC_002142
5	lnc-C1D-3	chr2:67432641-67432695	XLOC_002142
6	lnc-C1D-3	chr2:67442360-67442409	XLOC_002142
7	lnc-C1D-3	chr2:67442360-67442466	XLOC_002142
8	lnc-C1D-3	chr2:67432641-67432695	XLOC_002142
9	lnc-ETAA1-3	chr2:67470411-67470493	ENSG00000230906
10	lnc-C1D-3	chr2:67430248-67430305	XLOC_002142
11	lnc-C1D-3	chr2:67432641-67432695	XLOC_002142
12	lnc-C1D-3	chr2:67440771-67440848	XLOC_002142
13	lnc-ETAA1-3	chr2:67440540-67440627	ENSG00000230906
14	lnc-C1D-3	chr2:67430248-67430305	XLOC_002142
15	lnc-C1D-3	chr2:67432641-67432695	XLOC_002142
16	lnc-ETAA1-6	chr2:67456531-67456627	ENSG00000230906.2
17	lnc-ETAA1-3	chr2:67456531-67456627	ENSG00000230906
18	lnc-ETAA1-3	chr2:67471444-67471706	ENSG00000230906

Variant related genes	Relation type
ENSG00000230906	TF binding region
ENSG00000236780	TF binding region
ENSG00000230906	CpG island
ENSG00000236780	CpG island
ENSG00000143995	chromatin interactions
ENSG00000226819	chromatin interactions

Extended variants
information (count: 2469 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2469 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113617147	chr2:67417399-67417400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369427433	chr2:67417409-67417410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113004666	chr2:67417415-67417416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185612133	chr2:67417423-67417424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189465591	chr2:67417450-67417451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181926579	chr2:67417480-67417481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547350449	chr2:67417553-67417554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570545330	chr2:67417559-67417560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184973276	chr2:67417560-67417561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189730646	chr2:67417565-67417566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375764942	chr2:67417598-67417599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538005399	chr2:67417669-67417670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554471811	chr2:67417674-67417675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534417103	chr2:67417705-67417706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147444307	chr2:67417713-67417714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181056157	chr2:67417714-67417715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574100283	chr2:67417738-67417739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560178855	chr2:67417744-67417745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576945106	chr2:67417762-67417763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186513115	chr2:67417768-67417769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563075281	chr2:67417769-67417770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531913540	chr2:67417772-67417773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542379842	chr2:67417779-67417780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543362223	chr2:67417786-67417787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199853392	chr2:67417789-67417790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562157001	chr2:67417793-67417794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527762585	chr2:67417947-67417948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547512924	chr2:67417963-67417964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570509046	chr2:67417964-67417965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533193249	chr2:67418007-67418008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549915710	chr2:67418214-67418215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569087081	chr2:67418249-67418250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537773131	chr2:67418254-67418255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373510638	chr2:67418259-67418260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554715920	chr2:67418364-67418365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7368804	chr2:67418377-67418378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533853777	chr2:67418390-67418391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553958550	chr2:67418432-67418433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191746098	chr2:67418442-67418443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545734746	chr2:67418471-67418472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183576243	chr2:67418526-67418527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188719373	chr2:67418527-67418528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140656292	chr2:67418583-67418584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542190400	chr2:67418658-67418659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372687045	chr2:67418660-67418661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149320883	chr2:67418670-67418671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527927296	chr2:67418674-67418675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541116204	chr2:67418700-67418701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564199990	chr2:67418733-67418734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533255217	chr2:67418740-67418741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Colorectal cancer	16272173	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67396400-67422000	Weak transcription	Pancreas	Pancrea
2	chr2:67422000-67423800	ZNF genes & repeats	Pancreas	Pancrea
3	chr2:67422200-67422400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:67423800-67437400	Weak transcription	Pancreas	Pancrea
5	chr2:67430000-67437400	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:67432400-67432800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:67432800-67434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:67434600-67435000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:67434600-67435200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:67434800-67435200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:67434800-67435200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr2:67434800-67435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr2:67435200-67442200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr2:67435400-67436000	Enhancers	Fetal Lung	lung
15	chr2:67436000-67436400	Weak transcription	Fetal Lung	lung
16	chr2:67436200-67436400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr2:67436400-67436600	Enhancers	Fetal Lung	lung
18	chr2:67436400-67440400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr2:67436600-67439000	Weak transcription	Fetal Lung	lung
20	chr2:67437400-67437600	Flanking Active TSS	Colon Smooth Muscle	Colon
21	chr2:67437400-67437600	Enhancers	Fetal Stomach	stomach
22	chr2:67437400-67439000	Enhancers	Pancreas	Pancrea
23	chr2:67437600-67437800	Active TSS	Colon Smooth Muscle	Colon
24	chr2:67437600-67438200	Weak transcription	Fetal Stomach	stomach
25	chr2:67437800-67440400	Weak transcription	Colon Smooth Muscle	Colon
26	chr2:67438200-67438800	Enhancers	Fetal Stomach	stomach
27	chr2:67438800-67440400	Weak transcription	Fetal Stomach	stomach
28	chr2:67439000-67439200	Weak transcription	Pancreas	Pancrea
29	chr2:67439000-67439400	Enhancers	Fetal Kidney	kidney
30	chr2:67439000-67440600	Enhancers	Fetal Lung	lung
31	chr2:67439200-67439600	Active TSS	Pancreas	Pancrea
32	chr2:67439400-67441000	Weak transcription	Fetal Kidney	kidney
33	chr2:67439400-67442600	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr2:67439600-67440400	Weak transcription	Pancreas	Pancrea
35	chr2:67440200-67440600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:67440400-67440600	Active TSS	Fetal Stomach	stomach
37	chr2:67440400-67440800	Active TSS	Colon Smooth Muscle	Colon
38	chr2:67440400-67440800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr2:67440400-67442600	Active TSS	Pancreas	Pancrea
40	chr2:67440600-67440800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:67440600-67441000	Flanking Active TSS	Fetal Stomach	stomach
42	chr2:67440600-67441000	Active TSS	Rectal Smooth Muscle	rectum
43	chr2:67440600-67441200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:67440600-67441400	Flanking Active TSS	Fetal Lung	lung
45	chr2:67440600-67442200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:67440800-67441000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:67440800-67441000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:67440800-67441000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr2:67440800-67441000	Bivalent Enhancer	Fetal Brain Male	brain
50	chr2:67440800-67441200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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