Variant report

Variant	nsv533110
Chromosome Location	chr2:189354436-189462552
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	chr2:189377267-189377455	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:189377238-189377522	K562	blood:	n/a	n/a
3	ARID3A	chr2:189389327-189389620	HepG2	liver:	n/a	n/a
4	ATF1	chr2:189416446-189416727	K562	blood:	n/a	n/a
5	BACH1	chr2:189444453-189444475	K562	blood:	n/a	n/a
6	BACH1	chr2:189408352-189408359	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:189377279-189377523	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:189360824-189361028	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr2:189359445-189360194	HCT-116	colon:	n/a	n/a
10	CBX3	chr2:189360540-189361698	HCT-116	colon:	n/a	n/a
11	CCNT2	chr2:189360712-189360977	K562	blood:	n/a	n/a
12	CEBPB	chr2:189436224-189436625	MCF-7	breast:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
13	CEBPB	chr2:189436279-189436619	A549	lung:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
14	CEBPB	chr2:189387289-189387619	Hela-S3	cervix:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
15	CEBPB	chr2:189409728-189409827	H1-hESC	embryonic stem cell:	n/a	chr2:189409795-189409806
16	CEBPB	chr2:189360552-189361211	Hela-S3	cervix:	n/a	chr2:189360734-189360745 chr2:189360686-189360699
17	CEBPB	chr2:189360649-189361245	IMR90	lung:	n/a	chr2:189360734-189360745 chr2:189360686-189360699
18	CEBPB	chr2:189436225-189436725	A549	lung:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
19	CEBPB	chr2:189399866-189400127	IMR90	lung:	n/a	chr2:189399971-189399982
20	CEBPB	chr2:189416029-189416182	A549	lung:	n/a	chr2:189416104-189416115
21	CEBPB	chr2:189355030-189355092	A549	lung:	n/a	n/a
22	CEBPB	chr2:189399808-189400136	HepG2	liver:	n/a	chr2:189399971-189399982
23	CEBPB	chr2:189409748-189409897	A549	lung:	n/a	chr2:189409795-189409806
24	CEBPB	chr2:189436285-189436668	A549	lung:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
25	CEBPB	chr2:189409661-189409950	HepG2	liver:	n/a	chr2:189409795-189409806
26	CEBPB	chr2:189436294-189436757	HepG2	liver:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
27	CEBPB	chr2:189435045-189435508	ECC-1	luminal epithelium:	n/a	chr2:189435436-189435447
28	CEBPB	chr2:189387295-189387607	IMR90	lung:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
29	CEBPB	chr2:189436324-189436540	K562	blood:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
30	CEBPB	chr2:189399876-189400138	A549	lung:	n/a	chr2:189399971-189399982
31	CEBPB	chr2:189435116-189435486	ECC-1	luminal epithelium:	n/a	chr2:189435436-189435447
32	CEBPB	chr2:189387308-189387584	A549	lung:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
33	CEBPB	chr2:189436339-189436621	H1-hESC	embryonic stem cell:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
34	CEBPB	chr2:189387300-189387560	K562	blood:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
35	CEBPB	chr2:189374918-189375107	HepG2	liver:	n/a	chr2:189375049-189375058
36	CEBPB	chr2:189436249-189436545	MCF-7	breast:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
37	CEBPB	chr2:189409696-189409893	IMR90	lung:	n/a	chr2:189409795-189409806
38	CEBPB	chr2:189387383-189387520	H1-hESC	embryonic stem cell:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
39	CEBPB	chr2:189431000-189431028	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:189436287-189436738	IMR90	lung:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
41	CEBPB	chr2:189362658-189362762	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:189360552-189361317	HCT-116	colon:	n/a	chr2:189360734-189360745 chr2:189360686-189360699
43	CEBPB	chr2:189391303-189391492	HepG2	liver:	n/a	chr2:189391401-189391414
44	CEBPB	chr2:189360413-189361332	HCT-116	colon:	n/a	chr2:189360734-189360745 chr2:189360686-189360699
45	CEBPB	chr2:189436314-189437008	Hela-S3	cervix:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
46	CEBPB	chr2:189387273-189387600	HepG2	liver:	n/a	chr2:189387400-189387413 chr2:189387424-189387435 chr2:189387400-189387413 chr2:189387401-189387412
47	CEBPB	chr2:189436301-189436746	K562	blood:	n/a	chr2:189436473-189436482 chr2:189436472-189436483
48	CEBPB	chr2:189416031-189416167	HepG2	liver:	n/a	chr2:189416104-189416115
49	CEBPD	chr2:189360679-189361050	K562	blood:	n/a	n/a
50	CEBPD	chr2:189360634-189360995	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:189433317-189433367	BJ	skin:	n/a
2	chr2:189433317-189433367	NH-A	brain:	n/a
3	chr2:189434064-189434114	HCF	heart:	n/a
4	chr2:189382445-189382495	AG04450	lung:	fetal
5	chr2:189361842-189361892	H1-hESC	embryonic stem cell:	embryo
6	chr2:189361842-189361892	IMR90	lung:	fetal
7	chr2:189361842-189361892	HMEC	breast:	n/a
8	chr2:189433317-189433367	PANC-1	pancreas:	n/a
9	chr2:189382445-189382495	AoSMC	blood vessel:	n/a
10	chr2:189434064-189434114	LNCaP	prostate:	n/a
11	chr2:189382445-189382495	HCF	heart:	n/a
12	chr2:189433317-189433367	NHDF-neo	bronchial:	n/a
13	chr2:189361842-189361892	HEEpiC	esophagus:	n/a
14	chr2:189433317-189433367	LNCaP	prostate:	n/a
15	chr2:189382445-189382495	LNCaP	prostate:	n/a
16	chr2:189434064-189434114	HRCEpiC	kidney:	n/a
17	chr2:189361842-189361892	HIPEpiC	eye:	n/a
18	chr2:189433317-189433367	HIPEpiC	eye:	n/a
19	chr2:189361842-189361892	GM12878	blood:	n/a
20	chr2:189382445-189382495	NHDF-neo	bronchial:	n/a
21	chr2:189434064-189434114	SK-N-SH	brain:	n/a
22	chr2:189434064-189434114	AG09309	skin:	n/a
23	chr2:189434064-189434114	SK-N-MC	brain:	n/a
24	chr2:189382445-189382495	K562	blood:	n/a
25	chr2:189382445-189382495	SK-N-MC	brain:	n/a
26	chr2:189434064-189434114	HEEpiC	esophagus:	n/a
27	chr2:189434064-189434114	HMEC	breast:	n/a
28	chr2:189434064-189434114	RPTEC	kidney:	n/a
29	chr2:189434064-189434114	BJ	skin:	n/a
30	chr2:189382445-189382495	SK-N-SH_RA	brain:	n/a
31	chr2:189433317-189433367	A549	lung:	n/a
32	chr2:189434064-189434114	NH-A	brain:	n/a
33	chr2:189382445-189382495	Hepatocyte	liver:	n/a
34	chr2:189434064-189434114	GM06990	blood:	n/a
35	chr2:189434064-189434114	AG04449	skin:	fetal
36	chr2:189361842-189361892	A549	lung:	n/a
37	chr2:189433317-189433367	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:189434064-189434114	BE2_C	brain:	n/a
39	chr2:189434064-189434114	ECC-1	luminal epithelium:	n/a
40	chr2:189361842-189361892	NHBE	bronchial:	n/a
41	chr2:189361842-189361892	PFSK-1	brain:	n/a
42	chr2:189434064-189434114	HCPEpiC	choroid plexus:	n/a
43	chr2:189382445-189382495	A549	lung:	n/a
44	chr2:189433317-189433367	GM12878	blood:	n/a
45	chr2:189382445-189382495	SAEC	small airway:	n/a
46	chr2:189361842-189361892	SAEC	small airway:	n/a
47	chr2:189361842-189361892	GM12891	blood:	n/a
48	chr2:189382445-189382495	MCF10A-Er-Src	breast:	n/a
49	chr2:189361842-189361892	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:189361842-189361892	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:189388967..189389813-chr2:189842832..189843620,3	MCF-7	breast:
2	chr2:189378377..189379197-chr2:189842327..189843215,2	MCF-7	breast:
3	chr2:189366557..189368547-chr2:189369752..189373297,3	MCF-7	breast:
4	chr2:189410342..189413264-chr2:189419173..189420949,2	K562	blood:
5	chr2:189366557..189368547-chr2:189369752..189373297,3	MCF-7	breast:
6	chr13:92777089..92778054-chr2:189460184..189460902,2	MCF-7	breast:
7	chr2:189437275..189439743-chr2:189454053..189456620,2	MCF-7	breast:
8	chr2:189460991..189463243-chr2:189840556..189843059,2	MCF-7	breast:
9	chr2:189436897..189438874-chr2:189440329..189441944,2	K562	blood:
10	chr2:189449607..189454566-chr2:189458525..189463315,5	MCF-7	breast:
11	chr2:189457452..189459622-chr2:189465915..189469641,4	MCF-7	breast:
12	chr2:188363035..188364690-chr2:189379831..189382772,2	MCF-7	breast:
13	chr2:189439657..189442123-chr2:189444360..189445883,2	K562	blood:
14	chr2:189439657..189442123-chr2:189444360..189445883,2	K562	blood:
15	chr2:189378368..189379278-chr2:189848607..189850003,3	MCF-7	breast:
16	chr2:189389338..189392140-chr2:189468251..189470739,2	MCF-7	breast:
17	chr2:188446227..188446782-chr2:189376811..189377413,2	K562	blood:
18	chr2:189410342..189413264-chr2:189419173..189420949,2	K562	blood:
19	chr2:189461232..189465911-chr2:189467782..189472229,8	MCF-7	breast:
20	chr2:189396716..189399685-chr2:189460866..189462803,2	MCF-7	breast:
21	chr2:189350444..189353078-chr2:189355041..189357306,2	MCF-7	breast:
22	chr2:189389248..189389928-chr2:190276695..190277389,2	K562	blood:
23	chr2:189402975..189404996-chr2:189407067..189409618,2	K562	blood:
24	chr2:189157000..189158643-chr2:189362497..189364899,2	MCF-7	breast:
25	chr2:188707921..188708505-chr2:189376811..189377638,2	MCF-7	breast:
26	chr2:188458841..188460185-chr2:189376734..189377597,3	MCF-7	breast:
27	chr2:189389424..189389930-chr2:189841189..189841702,2	MCF-7	breast:
28	chr2:189357879..189360494-chr2:189362422..189365223,2	K562	blood:
29	chr2:189460620..189463074-chr2:189843714..189846986,3	MCF-7	breast:
30	chr2:189402975..189404996-chr2:189407067..189409618,2	K562	blood:
31	chr2:189389325..189390214-chr2:190152713..190153216,2	K562	blood:
32	chr2:189378325..189379323-chr2:190276804..190277370,2	K562	blood:
33	chr2:189357879..189360494-chr2:189362422..189365223,2	K562	blood:
34	chr2:189396716..189399685-chr2:189460866..189462803,2	MCF-7	breast:
35	chr2:189436897..189438874-chr2:189440329..189441944,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL3A1-2	chr2:189454318-189454477	NONHSAT076034
2	lnc-COL3A1-2	chr2:189458667-189459095	NONHSAT076034

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GULP1	hsa-miR-335-5p	chr2:189459027-189459048

Variant related genes	Relation type
GULP1	TF binding region
GULP1	CpG island
ENSG00000221502	chromatin interactions
ENSG00000144366	chromatin interactions

Extended variants
information (count: 3488 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3488 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527953198	chr2:189354441-189354442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10931363	chr2:189354533-189354534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs142947578	chr2:189354620-189354621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537986625	chr2:189354655-189354656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12477723	chr2:189354662-189354663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576598598	chr2:189354760-189354761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571323346	chr2:189354789-189354790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540013432	chr2:189354791-189354792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34278190	chr2:189354813-189354814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538458517	chr2:189354845-189354846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553902743	chr2:189354846-189354847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572264539	chr2:189354853-189354854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536528548	chr2:189354864-189354865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555368370	chr2:189354915-189354916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543978928	chr2:189354968-189354969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573692118	chr2:189355038-189355039	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78220788	chr2:189355054-189355055	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556244319	chr2:189355151-189355152	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186260034	chr2:189355244-189355245	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13402873	chr2:189355295-189355296	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562575559	chr2:189355333-189355334	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545290629	chr2:189355408-189355409	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560722587	chr2:189355421-189355422	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376165045	chr2:189355437-189355438	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376568551	chr2:189355438-189355439	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528004814	chr2:189355498-189355499	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78606799	chr2:189355560-189355561	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573244131	chr2:189355571-189355572	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543341325	chr2:189355622-189355623	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191554835	chr2:189355637-189355638	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370876711	chr2:189355651-189355652	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145383305	chr2:189355653-189355654	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549749573	chr2:189355679-189355680	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6434284	chr2:189355687-189355688	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs532197899	chr2:189355703-189355704	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367858492	chr2:189355726-189355727	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115227710	chr2:189355744-189355745	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530199502	chr2:189355751-189355752	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542004090	chr2:189355767-189355768	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536197074	chr2:189355792-189355793	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182254251	chr2:189355894-189355895	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186959948	chr2:189355947-189355948	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116727587	chr2:189355952-189355953	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202212348	chr2:189355985-189355986	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537873081	chr2:189355991-189355992	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs137925262	chr2:189355994-189355995	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578062388	chr2:189356018-189356019	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545463315	chr2:189356052-189356053	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554118331	chr2:189356076-189356077	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575220913	chr2:189356161-189356162	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	16912164	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189329200-189399000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:189330600-189356600	Weak transcription	Fetal Intestine Small	intestine
3	chr2:189334600-189367600	Weak transcription	Fetal Lung	lung
4	chr2:189338600-189360600	Weak transcription	Ovary	ovary
5	chr2:189341200-189358800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:189343800-189355000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr2:189343800-189355600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:189343800-189355800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:189344000-189358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:189344000-189370200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:189344200-189390400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:189348400-189358400	Weak transcription	Placenta	Placenta
13	chr2:189352800-189355000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:189353000-189355200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:189353000-189366400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr2:189353600-189355400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:189354000-189355000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:189354000-189355200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:189354200-189355000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr2:189354200-189355600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:189355000-189355600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:189355000-189356400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:189355000-189356400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:189355000-189356400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:189355200-189356000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:189355200-189357800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:189355400-189356600	Genic enhancers	HUES64 Cell Line	embryonic stem cell
28	chr2:189355600-189355800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:189355600-189355800	Enhancers	Gastric	stomach
30	chr2:189355600-189356600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:189355600-189356800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:189355600-189356800	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr2:189355800-189356000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:189355800-189357400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:189355800-189382400	Weak transcription	Gastric	stomach
36	chr2:189356000-189370800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:189356400-189370000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr2:189356400-189371200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:189356400-189373600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr2:189356600-189357000	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:189356600-189358200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:189356800-189362600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:189356800-189371000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr2:189357000-189370000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr2:189357800-189371000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:189358200-189359200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:189358400-189358800	Strong transcription	Placenta	Placenta
48	chr2:189358400-189359000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:189358600-189359400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:189358800-189362400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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