Variant report

Variant	nsv1012174
Chromosome Location	chr2:184956114-185316664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:948)
CpG islands
(count:61)
Chromatin interactive
region (count:92)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:185069593-185070127	K562	blood:	n/a	n/a
2	ARID3A	chr2:185060092-185060099	K562	blood:	n/a	n/a
3	ARID3A	chr2:185068347-185068808	K562	blood:	n/a	n/a
4	ARID3A	chr2:185136996-185137081	K562	blood:	n/a	n/a
5	ARID3A	chr2:185234055-185234428	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:185060541-185060558	K562	blood:	n/a	n/a
7	ATF1	chr2:185039540-185039740	K562	blood:	n/a	n/a
8	ATF2	chr2:185308834-185309398	GM12878	blood:	n/a	n/a
9	ATF2	chr2:185308801-185309526	GM12878	blood:	n/a	n/a
10	ATF2	chr2:185187340-185187651	GM12878	blood:	n/a	n/a
11	BACH1	chr2:185068420-185068484	K562	blood:	n/a	n/a
12	BACH1	chr2:185051246-185051364	K562	blood:	n/a	n/a
13	BACH1	chr2:184984541-184984607	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr2:185308921-185309210	GM12878	blood:	n/a	n/a
15	BATF	chr2:184978754-184979078	GM12878	blood:	n/a	n/a
16	BATF	chr2:185308924-185309328	GM12878	blood:	n/a	n/a
17	BATF	chr2:184978819-184979004	GM12878	blood:	n/a	n/a
18	BATF	chr2:185187318-185187665	GM12878	blood:	n/a	n/a
19	BATF	chr2:185290327-185290619	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:185289883-185290123	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:185308850-185309390	GM12878	blood:	n/a	n/a
22	BCL11A	chr2:185308935-185309247	GM12878	blood:	n/a	n/a
23	BCL3	chr2:185308945-185309370	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:185308913-185309383	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:185308886-185309417	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:185137191-185137291	K562	blood:	n/a	n/a
27	BHLHE40	chr2:185227990-185228275	HepG2	liver:	n/a	n/a
28	BHLHE40	chr2:185289855-185290047	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:184982837-184982965	K562	blood:	n/a	n/a
30	BHLHE40	chr2:185251589-185251715	K562	blood:	n/a	n/a
31	BRCA1	chr2:185234005-185234016	HepG2	liver:	n/a	n/a
32	CBX3	chr2:185271763-185272041	K562	blood:	n/a	n/a
33	CCNT2	chr2:185106876-185106964	K562	blood:	n/a	n/a
34	CCNT2	chr2:185075725-185075820	K562	blood:	n/a	n/a
35	CEBPB	chr2:185251635-185251802	K562	blood:	n/a	chr2:185251752-185251763
36	CEBPB	chr2:185069906-185070466	K562	blood:	n/a	chr2:185070115-185070128 chr2:185070115-185070126
37	CEBPB	chr2:185302568-185302810	HepG2	liver:	n/a	chr2:185302693-185302704
38	CEBPB	chr2:185207047-185207335	A549	lung:	n/a	chr2:185207173-185207184 chr2:185207208-185207219 chr2:185207173-185207182
39	CEBPB	chr2:185228101-185228119	K562	blood:	n/a	n/a
40	CEBPB	chr2:185132408-185132718	HepG2	liver:	n/a	chr2:185132561-185132572
41	CEBPB	chr2:185117823-185117990	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:185284749-185284771	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:185112478-185112662	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:185234071-185234445	HepG2	liver:	n/a	chr2:185234227-185234240 chr2:185234228-185234239 chr2:185234227-185234240 chr2:185234205-185234216
45	CEBPB	chr2:185167273-185167627	Hela-S3	cervix:	n/a	chr2:185167453-185167464
46	CEBPB	chr2:185135546-185135816	H1-hESC	embryonic stem cell:	n/a	chr2:185135672-185135689 chr2:185135675-185135686
47	CEBPB	chr2:185104623-185104834	HepG2	liver:	n/a	chr2:185104729-185104742 chr2:185104731-185104742 chr2:185104729-185104740 chr2:185104731-185104742 chr2:185104729-185104742
48	CEBPB	chr2:185067380-185067637	K562	blood:	n/a	n/a
49	CEBPB	chr2:185072144-185072389	HepG2	liver:	n/a	chr2:185072268-185072279
50	CEBPB	chr2:184961355-184961543	HepG2	liver:	n/a	chr2:184961443-184961454

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:185019269-185019319	HAEpiC	amniotic membrane:	n/a
2	chr2:185019269-185019319	HCT-116	colon:	n/a
3	chr2:185019269-185019319	NB4	blood:	n/a
4	chr2:185019269-185019319	NT2-D1	testis:	n/a
5	chr2:185019269-185019319	NHBE	bronchial:	n/a
6	chr2:185019269-185019319	H1-hESC	embryonic stem cell:	embryo
7	chr2:185019269-185019319	HMEC	breast:	n/a
8	chr2:185019269-185019319	SAEC	small airway:	n/a
9	chr2:185019269-185019319	LNCaP	prostate:	n/a
10	chr2:185019269-185019319	SK-N-SH_RA	brain:	n/a
11	chr2:185019269-185019319	PANC-1	pancreas:	n/a
12	chr2:185019269-185019319	ECC-1	luminal epithelium:	n/a
13	chr2:185019269-185019319	NH-A	brain:	n/a
14	chr2:185019269-185019319	BE2_C	brain:	n/a
15	chr2:185019269-185019319	PFSK-1	brain:	n/a
16	chr2:185019269-185019319	CMK	blood:	n/a
17	chr2:185019269-185019319	MCF-7	breast:	n/a
18	chr2:185019269-185019319	HRE	kidney:	n/a
19	chr2:185019269-185019319	A549	lung:	n/a
20	chr2:185019269-185019319	Caco-2	colon:	n/a
21	chr2:185019269-185019319	AG09319	gingival:	n/a
22	chr2:185019269-185019319	HL-60	blood:	n/a
23	chr2:185019269-185019319	GM12891	blood:	n/a
24	chr2:185019269-185019319	SK-N-MC	brain:	n/a
25	chr2:185019269-185019319	HEEpiC	esophagus:	n/a
26	chr2:185019269-185019319	BJ	skin:	n/a
27	chr2:185019269-185019319	ProgFib	skin:	n/a
28	chr2:185019269-185019319	HCF	heart:	n/a
29	chr2:185019269-185019319	GM12892	blood:	n/a
30	chr2:185019269-185019319	MCF10A-Er-Src	breast:	n/a
31	chr2:185019269-185019319	GM19239	blood:	n/a
32	chr2:185019269-185019319	HIPEpiC	eye:	n/a
33	chr2:185019269-185019319	U87	brain:	n/a
34	chr2:185019269-185019319	HRCEpiC	kidney:	n/a
35	chr2:185019269-185019319	AG10803	skin:	n/a
36	chr2:185019269-185019319	PrEC	prostate:	n/a
37	chr2:185019269-185019319	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:185019269-185019319	NHDF-neo	bronchial:	n/a
39	chr2:185019269-185019319	HNPCEpiC	eye:	n/a
40	chr2:185019269-185019319	RPTEC	kidney:	n/a
41	chr2:185019269-185019319	SKMC	muscle:	n/a
42	chr2:185019269-185019319	AG09309	skin:	n/a
43	chr2:185019269-185019319	GM06990	blood:	n/a
44	chr2:185019269-185019319	Hepatocyte	liver:	n/a
45	chr2:185019269-185019319	K562	blood:	n/a
46	chr2:185019269-185019319	HRPEpiC	eye:	n/a
47	chr2:185019269-185019319	AG04450	lung:	fetal
48	chr2:185019269-185019319	HCM	heart:	n/a
49	chr2:185019269-185019319	HUVEC	blood vessel:	n/a
50	chr2:185019269-185019319	AG04449	skin:	fetal

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:185017191..185018721-chr2:185022322..185025318,2	K562	blood:
2	chr2:185069331..185071140-chr2:185086941..185089740,2	K562	blood:
3	chr2:185063557..185066298-chr2:185074059..185077042,2	K562	blood:
4	chr2:185160917..185163331-chr2:185190953..185193318,2	K562	blood:
5	chr2:185073490..185075521-chr2:185077251..185078979,2	K562	blood:
6	chr2:185030293..185033303-chr2:185042017..185046003,4	K562	blood:
7	chr2:185030205..185032507-chr2:185041818..185044084,3	K562	blood:
8	chr2:185020880..185023021-chr2:185080890..185083971,3	K562	blood:
9	chr16:57227705..57228253-chr2:185151504..185152004,2	NB4	blood:
10	chr2:185223918..185225918-chr2:185227977..185230621,2	K562	blood:
11	chr2:185068138..185070964-chr2:185088334..185090815,2	K562	blood:
12	chr2:185039166..185041142-chr2:185069813..185071820,2	K562	blood:
13	chr2:185299549..185301224-chr2:185314147..185316677,2	K562	blood:
14	chr2:185201237..185203817-chr2:185332460..185335138,2	K562	blood:
15	chr2:185039166..185041142-chr2:185069813..185071820,2	K562	blood:
16	chr2:185068138..185070964-chr2:185088334..185090815,2	K562	blood:
17	chr2:185299549..185301224-chr2:185314147..185316677,2	K562	blood:
18	chr2:185086289..185087889-chr2:185091229..185094182,2	K562	blood:
19	chr2:185053723..185055741-chr2:185058684..185061541,2	K562	blood:
20	chr2:185049732..185051441-chr2:185066416..185068378,2	K562	blood:
21	chr2:184738935..184741579-chr2:185018317..185019872,2	K562	blood:
22	chr2:185017202..185019755-chr2:185059188..185062172,2	K562	blood:
23	chr2:185030293..185033303-chr2:185042017..185046003,4	K562	blood:
24	chr2:185017202..185019755-chr2:185059188..185062172,2	K562	blood:
25	chr2:185226895..185229045-chr2:185330186..185332070,2	K562	blood:
26	chr2:45032907..45033761-chr2:185301029..185301683,2	MCF-7	breast:
27	chr2:185223918..185225918-chr2:185227977..185230621,2	K562	blood:
28	chr2:185056201..185058411-chr2:185059740..185062010,3	K562	blood:
29	chr2:185128748..185131745-chr2:185134110..185138355,3	K562	blood:
30	chr2:185230131..185232758-chr2:185233211..185235341,2	MCF-7	breast:
31	chr2:127533916..127534758-chr2:185187632..185188334,2	MCF-7	breast:
32	chr2:185299545..185302161-chr2:185314147..185317606,4	K562	blood:
33	chr2:185020880..185023021-chr2:185080890..185083971,3	K562	blood:
34	chr2:185050606..185053529-chr2:185055758..185057591,2	K562	blood:
35	chr2:185052728..185055643-chr2:185086397..185088845,2	K562	blood:
36	chr15:41186270..41188900-chr2:185100150..185103068,2	K562	blood:
37	chr2:185048995..185051495-chr2:185054071..185055731,2	K562	blood:
38	chr2:185027163..185028822-chr2:185041434..185043457,2	K562	blood:
39	chr2:184975933..184978535-chr2:184980820..184983519,2	K562	blood:
40	chr2:185052728..185055643-chr2:185086397..185088845,2	K562	blood:
41	chr2:185073976..185076039-chr2:185080302..185082080,2	K562	blood:
42	chr2:185056201..185058976-chr2:185059740..185064773,6	K562	blood:
43	chr2:185056201..185058411-chr2:185059740..185062010,3	K562	blood:
44	chr2:185115001..185116702-chr2:185121013..185123546,2	K562	blood:
45	chr2:185030205..185032507-chr2:185041818..185044084,3	K562	blood:
46	chr2:185204369..185206130-chr2:185218623..185221505,2	K562	blood:
47	chr2:185069331..185071140-chr2:185086941..185089740,2	K562	blood:
48	chr2:185103488..185105465-chr2:185244326..185245928,2	K562	blood:
49	chr2:185295330..185297259-chr2:185298334..185299844,2	K562	blood:
50	chr2:185265120..185267657-chr2:185268029..185269760,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF804A-3	chr2:185244856-185245013	NONHSAT075951
2	lnc-NCKAP1-4	chr2:185169187-185169348	l_2003_chr2:185169076-185171314_76bGuttman_hLF
3	lnc-NCKAP1-4	chr2:185169077-185169159	l_2003_chr2:185169076-185171314_76bGuttman_hLF
4	lnc-NCKAP1-4	chr2:185171240-185171314	l_2003_chr2:185169076-185171314_76bGuttman_hLF
5	lnc-ZNF804A-3	chr2:185246875-185247280	NONHSAT075951

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548ae	chr2:185243744-185243764	MIMAT0018954

No data

Variant related genes	Relation type
MIR548AE1	TF binding region
MIR548AE1	CpG island
ENSG00000104142	chromatin interactions

Extended variants
information (count: 4078 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4078 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79356075	chr2:184975601-184975602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190287066	chr2:184975656-184975657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74685609	chr2:184975687-184975688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140463006	chr2:184975705-184975706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76677453	chr2:184975764-184975765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571926440	chr2:184975765-184975766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6751918	chr2:184975795-184975796	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs181684480	chr2:184975881-184975882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6751841	chr2:184975888-184975889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536737563	chr2:184975897-184975898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553123577	chr2:184975919-184975920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144378521	chr2:184975962-184975963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76682354	chr2:184975990-184975991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs398080884	chr2:184975991-184975992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201051631	chr2:184975993-184975994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538596969	chr2:184976013-184976014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185857461	chr2:184976020-184976021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575149499	chr2:184976034-184976035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544016732	chr2:184976036-184976037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554326891	chr2:184976058-184976059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574475892	chr2:184976115-184976116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376667290	chr2:184976129-184976130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540319937	chr2:184976133-184976134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17500558	chr2:184976157-184976158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532140451	chr2:184976205-184976206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138067839	chr2:184976264-184976265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190999758	chr2:184976380-184976381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545766968	chr2:184976422-184976423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565597699	chr2:184976423-184976424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181832723	chr2:184976476-184976477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573811952	chr2:184976478-184976479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2369200	chr2:184976536-184976537	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs567828461	chr2:184976587-184976588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2369201	chr2:184976591-184976592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547062324	chr2:184976629-184976630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556311300	chr2:184976650-184976651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186151693	chr2:184976660-184976661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538652246	chr2:184976721-184976722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78036359	chr2:184976742-184976743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190666257	chr2:184976766-184976767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183282199	chr2:184976772-184976773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17615865	chr2:184976775-184976776	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs143406271	chr2:184976794-184976795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577091245	chr2:184979201-184979202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368404324	chr2:184979222-184979223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376220766	chr2:184979224-184979225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181114637	chr2:184979248-184979249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573805505	chr2:184979267-184979268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575127777	chr2:184979318-184979319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77246138	chr2:184979319-184979320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Intellectual disability	22102821	CNVD
Autism	18522746	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
low-grade B-cell lymphoma tumor	18367492	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
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Psychiatric disorder	20548289	CNVD
Psychosis	20048749	CNVD
Rectal cancer	20877625	CNVD
Schizophrenia	20548289	CNVD
anxiety disorder	20548289	CNVD
Autism	20548289	CNVD
Bipolar disorder	20548289	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184975600-184976000	Enhancers	Fetal Brain Female	brain
2	chr2:184975800-184976600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr2:184976200-184976800	Enhancers	Brain Germinal Matrix	brain
4	chr2:184979200-184986800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:184982800-184983200	Enhancers	Fetal Stomach	stomach
6	chr2:184983200-184984800	Weak transcription	Fetal Stomach	stomach
7	chr2:184984400-184985200	Enhancers	Fetal Brain Male	brain
8	chr2:184984800-184985200	Enhancers	Colon Smooth Muscle	Colon
9	chr2:184984800-184985600	Enhancers	Fetal Stomach	stomach
10	chr2:185009000-185018400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr2:185009200-185009800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:185009600-185010200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr2:185013800-185014200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:185018400-185018600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr2:185018400-185019000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:185018400-185019000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr2:185018600-185019200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr2:185018800-185019600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:185019000-185019800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr2:185019200-185019400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr2:185019200-185019600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:185019200-185019600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:185019200-185019600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:185019200-185019600	Enhancers	HMEC	breast
25	chr2:185019600-185019800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:185019600-185022000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:185019800-185020000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr2:185019800-185020400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:185020000-185020400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr2:185020400-185020800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:185020400-185021000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:185021800-185022200	Enhancers	HUVEC	blood vessel
33	chr2:185022000-185023200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:185033400-185034400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr2:185033400-185034600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:185033600-185034400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:185034000-185034400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:185034000-185034600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:185034200-185034600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:185039200-185039800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:185039400-185039800	Active TSS	Hela-S3	cervix
42	chr2:185039400-185039800	Active TSS	K562	blood
43	chr2:185039800-185043000	Weak transcription	Hela-S3	cervix
44	chr2:185043000-185043400	Enhancers	Liver	Liver
45	chr2:185043000-185043800	Enhancers	Hela-S3	cervix
46	chr2:185052200-185052600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:185052400-185052600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:185055400-185057600	Active TSS	K562	blood
49	chr2:185057600-185063400	Weak transcription	K562	blood
50	chr2:185060600-185061200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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