Variant report

Variant	nsv875585
Chromosome Location	chr2:188424525-188626214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1413)
CpG islands
(count:183)
Chromatin interactive
region (count:75)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188441711-188441904	K562	blood:	n/a	n/a
2	ARID3A	chr2:188445189-188446578	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:188445260-188446786	K562	blood:	n/a	n/a
4	ARID3A	chr2:188439872-188439983	K562	blood:	n/a	n/a
5	ARID3A	chr2:188513230-188513415	K562	blood:	n/a	n/a
6	ARID3A	chr2:188459686-188459815	K562	blood:	n/a	n/a
7	ATF1	chr2:188551050-188551187	K562	blood:	n/a	n/a
8	ATF1	chr2:188451755-188452052	K562	blood:	n/a	n/a
9	ATF1	chr2:188461274-188461426	K562	blood:	n/a	n/a
10	ATF1	chr2:188558759-188558891	K562	blood:	n/a	n/a
11	ATF3	chr2:188445322-188445922	A549	lung:	n/a	n/a
12	ATF3	chr2:188445228-188445831	K562	blood:	n/a	n/a
13	BACH1	chr2:188445366-188445738	K562	blood:	n/a	n/a
14	BHLHE40	chr2:188521903-188522037	K562	blood:	n/a	n/a
15	BHLHE40	chr2:188441708-188441986	K562	blood:	n/a	n/a
16	CBX3	chr2:188455967-188456347	K562	blood:	n/a	n/a
17	CBX3	chr2:188505670-188506206	K562	blood:	n/a	n/a
18	CBX3	chr2:188446052-188446586	HCT-116	colon:	n/a	n/a
19	CBX3	chr2:188441997-188442525	HCT-116	colon:	n/a	n/a
20	CBX3	chr2:188445256-188445756	K562	blood:	n/a	n/a
21	CBX3	chr2:188445170-188445891	HCT-116	colon:	n/a	chr2:188445792-188445803
22	CCNT2	chr2:188441728-188441994	K562	blood:	n/a	n/a
23	CCNT2	chr2:188505985-188506183	K562	blood:	n/a	n/a
24	CEBPB	chr2:188431954-188432276	MCF-7	breast:	n/a	n/a
25	CEBPB	chr2:188439803-188440204	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:188442123-188442378	A549	lung:	n/a	n/a
27	CEBPB	chr2:188446939-188447125	A549	lung:	n/a	chr2:188447035-188447046
28	CEBPB	chr2:188439691-188440208	MCF-7	breast:	n/a	n/a
29	CEBPB	chr2:188431820-188432178	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:188473851-188474022	A549	lung:	n/a	n/a
31	CEBPB	chr2:188431966-188432159	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:188481857-188482003	A549	lung:	n/a	n/a
33	CEBPB	chr2:188439726-188440252	A549	lung:	n/a	n/a
34	CEBPB	chr2:188450663-188451420	A549	lung:	n/a	chr2:188450941-188450950 chr2:188450941-188450950 chr2:188450941-188450950 chr2:188450941-188450950
35	CEBPB	chr2:188481870-188482145	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:188446033-188446598	HCT-116	colon:	n/a	n/a
37	CEBPB	chr2:188451207-188451339	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:188446919-188447136	H1-hESC	embryonic stem cell:	n/a	chr2:188447035-188447046
39	CEBPB	chr2:188431938-188432299	MCF-7	breast:	n/a	n/a
40	CEBPB	chr2:188608563-188608828	HepG2	liver:	n/a	chr2:188608676-188608687
41	CEBPB	chr2:188431924-188432168	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:188445888-188446561	HCT-116	colon:	n/a	n/a
43	CEBPB	chr2:188479419-188479729	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:188581048-188581245	A549	lung:	n/a	n/a
45	CEBPB	chr2:188431814-188432338	A549	lung:	n/a	n/a
46	CEBPB	chr2:188481903-188482085	K562	blood:	n/a	n/a
47	CEBPB	chr2:188450791-188451308	HCT-116	colon:	n/a	chr2:188450941-188450950 chr2:188450941-188450950 chr2:188450941-188450950 chr2:188450941-188450950
48	CEBPB	chr2:188439793-188440464	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr2:188431887-188432244	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:188431898-188432228	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188583082-188583132	RPTEC	kidney:	n/a
2	chr2:188483530-188483580	Hela-S3	cervix:	n/a
3	chr2:188583082-188583132	MCF10A-Er-Src	breast:	n/a
4	chr2:188481707-188481757	ProgFib	skin:	n/a
5	chr2:188481707-188481757	HRE	kidney:	n/a
6	chr2:188483530-188483580	PrEC	prostate:	n/a
7	chr2:188583082-188583132	BJ	skin:	n/a
8	chr2:188483530-188483580	ProgFib	skin:	n/a
9	chr2:188483530-188483580	CMK	blood:	n/a
10	chr2:188483530-188483580	SK-N-SH	brain:	n/a
11	chr2:188481707-188481757	LNCaP	prostate:	n/a
12	chr2:188483530-188483580	HRPEpiC	eye:	n/a
13	chr2:188481707-188481757	NHDF-neo	bronchial:	n/a
14	chr2:188481707-188481757	NB4	blood:	n/a
15	chr2:188483530-188483580	T-47D	breast:	n/a
16	chr2:188481707-188481757	GM19239	blood:	n/a
17	chr2:188483530-188483580	IMR90	lung:	fetal
18	chr2:188481707-188481757	HCT-116	colon:	n/a
19	chr2:188481707-188481757	PrEC	prostate:	n/a
20	chr2:188483530-188483580	AG04450	lung:	fetal
21	chr2:188483530-188483580	GM12891	blood:	n/a
22	chr2:188483530-188483580	SKMC	muscle:	n/a
23	chr2:188583082-188583132	SK-N-SH	brain:	n/a
24	chr2:188583082-188583132	AG04449	skin:	fetal
25	chr2:188583082-188583132	K562	blood:	n/a
26	chr2:188583082-188583132	HRCEpiC	kidney:	n/a
27	chr2:188481707-188481757	RPTEC	kidney:	n/a
28	chr2:188483530-188483580	RPTEC	kidney:	n/a
29	chr2:188583082-188583132	H1-hESC	embryonic stem cell:	embryo
30	chr2:188481707-188481757	HMEC	breast:	n/a
31	chr2:188483530-188483580	AG09309	skin:	n/a
32	chr2:188481707-188481757	GM06990	blood:	n/a
33	chr2:188583082-188583132	PFSK-1	brain:	n/a
34	chr2:188481707-188481757	AG09309	skin:	n/a
35	chr2:188583082-188583132	BE2_C	brain:	n/a
36	chr2:188481707-188481757	Hela-S3	cervix:	n/a
37	chr2:188483530-188483580	MCF10A-Er-Src	breast:	n/a
38	chr2:188481707-188481757	H1-hESC	embryonic stem cell:	embryo
39	chr2:188483530-188483580	HL-60	blood:	n/a
40	chr2:188481707-188481757	SK-N-SH_RA	brain:	n/a
41	chr2:188481707-188481757	HUVEC	blood vessel:	n/a
42	chr2:188583082-188583132	PrEC	prostate:	n/a
43	chr2:188483530-188483580	PFSK-1	brain:	n/a
44	chr2:188481707-188481757	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:188483530-188483580	Jurkat	blood:	n/a
46	chr2:188583082-188583132	ovcar-3	ovarian:	n/a
47	chr2:188481707-188481757	AG10803	skin:	n/a
48	chr2:188483530-188483580	GM19239	blood:	n/a
49	chr2:188481707-188481757	HepG2	liver:	n/a
50	chr2:188481707-188481757	AG04449	skin:	fetal

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
2	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
3	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:
4	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
5	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
6	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
7	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
8	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
9	chr2:188363950..188366399-chr2:188445083..188446553,13	MCF-7	breast:
10	chr2:188360925..188366256-chr2:188443265..188447959,7	K562	blood:
11	chr2:188366835..188367676-chr2:188445069..188445969,2	MCF-7	breast:
12	chr16:73088044..73089636-chr2:188441847..188444162,2	MCF-7	breast:
13	chr2:188440243..188443082-chr2:188444632..188448024,3	K562	blood:
14	chr2:188523465..188524329-chr2:188707490..188708173,2	MCF-7	breast:
15	chr2:188601026..188603906-chr2:188607326..188609061,2	K562	blood:
16	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
17	chr2:188445112..188445612-chr2:223767773..223768610,2	K562	blood:
18	chr2:188549053..188550995-chr2:188552944..188555111,2	K562	blood:
19	chr2:188459276..188460160-chr2:189841055..189841647,2	MCF-7	breast:
20	chr2:188363922..188366266-chr2:188444694..188447033,35	MCF-7	breast:
21	chr2:188411707..188414780-chr2:188445119..188447288,3	K562	blood:
22	chr2:188440243..188443082-chr2:188444632..188448024,3	K562	blood:
23	chr2:188433750..188436567-chr2:188440064..188442739,2	K562	blood:
24	chr2:188362272..188363211-chr2:188445966..188446643,3	MCF-7	breast:
25	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
26	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
27	chr2:188363929..188365341-chr2:188444758..188446502,16	K562	blood:
28	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
29	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
30	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
31	chr2:188430133..188432200-chr2:188438721..188440616,2	K562	blood:
32	chr2:188363780..188367877-chr2:188441342..188445875,5	MCF-7	breast:
33	chr2:188445783..188446859-chr2:188707667..188708674,8	MCF-7	breast:
34	chr2:188366744..188369184-chr2:188446137..188447850,2	K562	blood:
35	chr2:188506449..188508323-chr2:188511407..188513734,2	K562	blood:
36	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
37	chr2:188433750..188436567-chr2:188440064..188442739,2	K562	blood:
38	chr2:188506973..188509886-chr2:188511524..188513522,2	MCF-7	breast:
39	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:
40	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
41	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
42	chr2:188544173..188545945-chr2:188547538..188549082,2	K562	blood:
43	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
44	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
45	chr2:188458841..188460185-chr2:189376734..189377597,3	MCF-7	breast:
46	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
47	chr2:188449920..188452608-chr2:188452638..188454975,2	K562	blood:
48	chr2:188560452..188562867-chr2:188563141..188566315,4	K562	blood:
49	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
50	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRC1-2	chr2:188577543-188577606	ENSG00000231689

No data

Variant related genes	Relation type
ENSG00000252004	TF binding region
TFPI	TF binding region
ENSG00000252004	CpG island
TFPI	CpG island
ENSG00000224063	chromatin interactions
ENSG00000003436	chromatin interactions
ENSG00000143727	chromatin interactions
ENSG00000252004	chromatin interactions
ENSG00000035115	chromatin interactions
ENSG00000131778	chromatin interactions

Extended variants
information (count: 5900 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:5900 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10191373	chr2:188424525-188424526	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542588961	chr2:188424544-188424545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561605620	chr2:188424566-188424567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115780031	chr2:188424707-188424708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550468284	chr2:188424722-188424723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145071200	chr2:188424733-188424734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12998073	chr2:188424763-188424764	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs547614656	chr2:188424774-188424775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571209810	chr2:188424792-188424793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141994307	chr2:188424795-188424796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554525350	chr2:188424839-188424840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569677199	chr2:188424848-188424849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537769492	chr2:188424905-188424906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555991352	chr2:188424933-188424934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185733406	chr2:188424948-188424949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545186865	chr2:188424949-188424950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553616801	chr2:188424955-188424956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572093673	chr2:188424984-188424985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189659280	chr2:188425024-188425025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34908365	chr2:188425058-188425059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182748224	chr2:188425059-188425060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531287553	chr2:188425083-188425084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189011145	chr2:188425112-188425113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs71432493	chr2:188425124-188425125	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532641419	chr2:188425140-188425141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4380190	chr2:188425141-188425142	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372114616	chr2:188425199-188425200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566075402	chr2:188425212-188425213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193131672	chr2:188425220-188425221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183570737	chr2:188425234-188425235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548245391	chr2:188425258-188425259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187264825	chr2:188425331-188425332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537006607	chr2:188425345-188425346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192144752	chr2:188425363-188425364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571498808	chr2:188425403-188425404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538494758	chr2:188425404-188425405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145892654	chr2:188425420-188425421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572119805	chr2:188425466-188425467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536356338	chr2:188425475-188425476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554665796	chr2:188425479-188425480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576146286	chr2:188425485-188425486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543436917	chr2:188425489-188425490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4567898	chr2:188425505-188425506	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577449890	chr2:188425515-188425516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541325781	chr2:188425570-188425571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201778944	chr2:188425590-188425591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572839760	chr2:188425652-188425653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559916253	chr2:188425663-188425664	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530183615	chr2:188425674-188425675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367899531	chr2:188425687-188425688	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188415000-188431200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:188419200-188429200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:188419400-188428000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr2:188419400-188445400	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:188420600-188428000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr2:188420600-188430800	Weak transcription	HepG2	liver
7	chr2:188421200-188425600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:188421800-188428400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:188422800-188426400	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:188422800-188426400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:188423000-188427000	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:188423400-188426000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:188424000-188426800	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr2:188424400-188426800	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr2:188425600-188426600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
16	chr2:188426000-188428200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:188426400-188427000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:188426400-188427600	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
19	chr2:188426600-188426800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:188426800-188427200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:188426800-188427400	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr2:188426800-188427400	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
23	chr2:188427000-188427200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:188427000-188429000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:188427200-188430800	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr2:188427200-188431000	Active TSS	H1 Cell Line	embryonic stem cell
27	chr2:188427400-188428000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:188427400-188430800	Active TSS	H9 Cell Line	embryonic stem cell
29	chr2:188427400-188430800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:188427600-188431000	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr2:188428000-188430800	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr2:188428000-188431000	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr2:188428000-188431000	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr2:188428200-188431000	Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr2:188428400-188430600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr2:188429000-188430800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:188429200-188429800	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr2:188429400-188430200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:188429800-188431200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr2:188430200-188431000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:188430800-188431200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr2:188430800-188431600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr2:188430800-188431800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr2:188430800-188431800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:188430800-188432000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:188430800-188432600	Enhancers	HepG2	liver
47	chr2:188431000-188431200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr2:188431000-188431200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr2:188431000-188431600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:188431000-188431800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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