Variant report

Variant	nsv875527
Chromosome Location	chr2:186272059-186475590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:367)
Chromatin interactive
region (count:18)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
3	BCL3	chr2:186338970-186339324	GM12878	blood:	n/a	n/a
4	CBX3	chr2:186447908-186448538	HCT-116	colon:	n/a	n/a
5	CBX3	chr2:186447981-186448661	HCT-116	colon:	n/a	n/a
6	CBX3	chr2:186321328-186321586	HCT-116	colon:	n/a	n/a
7	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
8	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
9	CEBPB	chr2:186465657-186465842	A549	lung:	n/a	n/a
10	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
11	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:186301535-186301733	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:186448257-186448571	A549	lung:	n/a	n/a
14	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
15	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
16	CEBPB	chr2:186448144-186448607	MCF-7	breast:	n/a	n/a
17	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
19	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
20	CEBPB	chr2:186448129-186448586	A549	lung:	n/a	n/a
21	CEBPB	chr2:186300444-186300644	H1-hESC	embryonic stem cell:	n/a	chr2:186300612-186300623
22	CEBPB	chr2:186448052-186448719	HCT-116	colon:	n/a	n/a
23	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
24	CEBPB	chr2:186296738-186297007	A549	lung:	n/a	n/a
25	CEBPB	chr2:186301521-186301830	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
27	CEBPB	chr2:186448257-186448516	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
29	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
30	CEBPB	chr2:186448119-186448613	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
32	CEBPB	chr2:186448143-186448675	HCT-116	colon:	n/a	n/a
33	CEBPB	chr2:186296703-186297026	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
35	CEBPB	chr2:186296748-186297009	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
37	CEBPB	chr2:186300587-186300787	HepG2	liver:	n/a	chr2:186300612-186300623
38	CEBPB	chr2:186447957-186448588	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
42	CHD1	chr2:186290086-186290487	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
44	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr2:186448192-186448572	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr2:186473624-186473816	MCF-7	breast:	n/a	chr2:186473696-186473704
47	CTCF	chr2:186387352-186387400	GM10266	blood:	n/a	n/a
48	CTCF	chr2:186473680-186473830	NHEK	skin:	n/a	chr2:186473696-186473704
49	CTCF	chr2:186473640-186473790	MCF-7	breast:	n/a	chr2:186473696-186473704
50	CTCF	chr2:186306380-186306530	NHEK	skin:	n/a	chr2:186306416-186306424 chr2:186306417-186306425

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186289849-186289899	Hepatocyte	liver:	n/a
2	chr2:186289849-186289899	Hepatocyte	liver:	n/a
3	chr2:186412073-186412123	SK-N-SH_RA	brain:	n/a
4	chr2:186443903-186443953	PrEC	prostate:	n/a
5	chr2:186443903-186443953	RPTEC	kidney:	n/a
6	chr2:186412305-186412355	Hepatocyte	liver:	n/a
7	chr2:186443903-186443953	HNPCEpiC	eye:	n/a
8	chr2:186295841-186295891	BE2_C	brain:	n/a
9	chr2:186412305-186412355	AG04450	lung:	fetal
10	chr2:186295841-186295891	AG04450	lung:	fetal
11	chr2:186412612-186412662	HEK293	kidney:	embryo
12	chr2:186412073-186412123	GM06990	blood:	n/a
13	chr2:186289849-186289899	GM12878	blood:	n/a
14	chr2:186295841-186295891	PANC-1	pancreas:	n/a
15	chr2:186412073-186412123	K562	blood:	n/a
16	chr2:186295841-186295891	T-47D	breast:	n/a
17	chr2:186443903-186443953	GM12891	blood:	n/a
18	chr2:186412073-186412123	HRPEpiC	eye:	n/a
19	chr2:186443903-186443953	HEK293	kidney:	embryo
20	chr2:186443903-186443953	AG10803	skin:	n/a
21	chr2:186295841-186295891	RPTEC	kidney:	n/a
22	chr2:186412305-186412355	HCPEpiC	choroid plexus:	n/a
23	chr2:186443903-186443953	HAEpiC	amniotic membrane:	n/a
24	chr2:186412305-186412355	GM06990	blood:	n/a
25	chr2:186289849-186289899	CMK	blood:	n/a
26	chr2:186443903-186443953	HCM	heart:	n/a
27	chr2:186443903-186443953	NH-A	brain:	n/a
28	chr2:186412073-186412123	LNCaP	prostate:	n/a
29	chr2:186412612-186412662	RPTEC	kidney:	n/a
30	chr2:186412305-186412355	SK-N-SH	brain:	n/a
31	chr2:186412612-186412662	ECC-1	luminal epithelium:	n/a
32	chr2:186289849-186289899	AG09319	gingival:	n/a
33	chr2:186295841-186295891	HAEpiC	amniotic membrane:	n/a
34	chr2:186289849-186289899	NB4	blood:	n/a
35	chr2:186443903-186443953	PANC-1	pancreas:	n/a
36	chr2:186412073-186412123	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:186443903-186443953	ovcar-3	ovarian:	n/a
38	chr2:186412305-186412355	HEEpiC	esophagus:	n/a
39	chr2:186412305-186412355	AG09319	gingival:	n/a
40	chr2:186443903-186443953	AG04449	skin:	fetal
41	chr2:186443903-186443953	HMEC	breast:	n/a
42	chr2:186412612-186412662	HUVEC	blood vessel:	n/a
43	chr2:186412073-186412123	AG10803	skin:	n/a
44	chr2:186289849-186289899	Caco-2	colon:	n/a
45	chr2:186412305-186412355	CMK	blood:	n/a
46	chr2:186443903-186443953	HCT-116	colon:	n/a
47	chr2:186443903-186443953	HepG2	liver:	n/a
48	chr2:186412073-186412123	HIPEpiC	eye:	n/a
49	chr2:186412612-186412662	SK-N-SH	brain:	n/a
50	chr2:186443903-186443953	AG04450	lung:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
2	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:
3	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
4	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
5	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:
6	chr2:186473268..186473794-chr2:186603435..186603983,2	MCF-7	breast:
7	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
8	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
9	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
10	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
11	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
12	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
13	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:
14	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
15	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
16	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
17	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
18	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
2	lnc-FSIP2-5	chr2:186327396-186327672	NONHSAT075962
3	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
4	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
5	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962
6	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
7	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
8	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
9	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
10	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
11	lnc-FSIP2-5	chr2:186298824-186298920	NONHSAT075962
12	lnc-ZSWIM2-15	chr2:186311542-186311686	ucscGeneNc_uc002upi_2
13	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963
14	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
15	lnc-ZSWIM2-15	chr2:186302301-186302409	ucscGeneNc_uc002upi_2
16	lnc-ZSWIM2-15	chr2:186292850-186293692	ucscGeneNc_uc002upi_2
17	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
18	lnc-ZSWIM2-15	chr2:186309034-186309104	ucscGeneNc_uc002upi_2
19	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
20	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000226747	chromatin interactions
ENSG00000188738	chromatin interactions

Extended variants
information (count: 6932 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6932 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576008242	chr2:186281613-186281614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374504364	chr2:186281633-186281634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202189334	chr2:186281648-186281649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557685076	chr2:186281682-186281683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575853134	chr2:186281701-186281702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114704188	chr2:186281717-186281718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564540692	chr2:186281768-186281769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532217780	chr2:186281799-186281800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541155633	chr2:186281860-186281861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191771551	chr2:186281889-186281890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546887008	chr2:186281951-186281952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116565068	chr2:186281958-186281959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571580483	chr2:186282036-186282037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529756137	chr2:186282058-186282059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548498347	chr2:186282135-186282136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182392510	chr2:186282157-186282158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17403498	chr2:186282227-186282228	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552313614	chr2:186282260-186282261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570572956	chr2:186282287-186282288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534770956	chr2:186282306-186282307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72892419	chr2:186282310-186282311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs568114325	chr2:186282312-186282313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535414305	chr2:186282341-186282342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557089909	chr2:186282406-186282407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575861602	chr2:186282436-186282437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546203551	chr2:186282450-186282451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545093555	chr2:186282480-186282481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145805359	chr2:186282547-186282548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555052421	chr2:186282575-186282576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545130351	chr2:186282589-186282590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573331202	chr2:186282591-186282592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188819058	chr2:186282605-186282606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558812518	chr2:186282620-186282621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559536419	chr2:186282631-186282632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529815614	chr2:186282642-186282643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541767805	chr2:186282663-186282664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138294196	chr2:186282785-186282786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192894804	chr2:186282789-186282790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6712463	chr2:186282807-186282808	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs6712480	chr2:186282856-186282857	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs528320099	chr2:186282861-186282862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546396228	chr2:186282975-186282976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185794437	chr2:186283052-186283053	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535571418	chr2:186283070-186283071	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs72892423	chr2:186283088-186283089	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190318285	chr2:186283110-186283111	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs540110692	chr2:186283116-186283117	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs376466874	chr2:186283184-186283185	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs149270171	chr2:186283185-186283186	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs192399613	chr2:186283188-186283189	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186281600-186282200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:186281800-186283000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:186282200-186282600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:186282600-186283600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:186283000-186283400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:186283400-186283800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:186289600-186290200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:186289600-186290200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:186289600-186290200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:186289600-186290200	Active TSS	Adipose Nuclei	Adipose
11	chr2:186289600-186290600	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr2:186289600-186291200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:186289600-186291600	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr2:186289600-186291800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr2:186289600-186291800	Active TSS	H1 Cell Line	embryonic stem cell
16	chr2:186289600-186291800	Active TSS	H9 Cell Line	embryonic stem cell
17	chr2:186289600-186291800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:186289600-186291800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:186289600-186291800	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr2:186289600-186292000	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr2:186289600-186292000	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr2:186289600-186292000	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr2:186289600-186292200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:186289800-186290200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:186289800-186290200	Active TSS	Fetal Muscle Trunk	muscle
26	chr2:186289800-186290200	Active TSS	Placenta	Placenta
27	chr2:186289800-186290600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:186289800-186291000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:186289800-186291400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr2:186289800-186292400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:186290000-186290600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:186290000-186291200	Active TSS	Muscle Satellite Cultured Cells	--
33	chr2:186290200-186290600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr2:186290200-186290600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:186290200-186290600	Active TSS	Rectal Mucosa Donor 31	rectum
36	chr2:186290200-186290800	Active TSS	HUVEC	blood vessel
37	chr2:186290200-186291000	Active TSS	Primary T cells from cord blood	blood
38	chr2:186290200-186291400	Active TSS	GM12878-XiMat	blood
39	chr2:186290200-186292000	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr2:186290400-186290600	Enhancers	Primary B cells from cord blood	blood
41	chr2:186290400-186290800	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr2:186290400-186291000	Active TSS	Fetal Intestine Large	intestine
43	chr2:186290600-186290800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr2:186290800-186291000	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr2:186291000-186292200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr2:186291000-186295600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:186291200-186297800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:186291600-186291800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr2:186291800-186292000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:186291800-186292000	Flanking Active TSS	H1 Cell Line	embryonic stem cell

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