Variant report

Variant	nsv875525
Chromosome Location	chr2:186223503-186434458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:608)
CpG islands
(count:307)
Chromatin interactive
region (count:18)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:186267472-186267561	K562	blood:	n/a	n/a
2	BACH1	chr2:186257731-186257792	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
5	BCL3	chr2:186338970-186339324	GM12878	blood:	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	chr2:186267331-186267556	K562	blood:	n/a	chr2:186267407-186267418
9	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
10	CEBPB	chr2:186300444-186300644	H1-hESC	embryonic stem cell:	n/a	chr2:186300612-186300623
11	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
12	CEBPB	chr2:186236934-186237305	HepG2	liver:	n/a	chr2:186237151-186237162
13	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:186301521-186301830	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
16	CEBPB	chr2:186296703-186297026	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:186239668-186240013	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:186301535-186301733	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
21	CEBPB	chr2:186300587-186300787	HepG2	liver:	n/a	chr2:186300612-186300623
22	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
23	CEBPB	chr2:186236984-186237244	ECC-1	luminal epithelium:	n/a	chr2:186237151-186237162
24	CEBPB	chr2:186236965-186237314	A549	lung:	n/a	chr2:186237151-186237162
25	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
26	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
27	CEBPB	chr2:186248706-186248830	HepG2	liver:	n/a	chr2:186248752-186248763
28	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
29	CEBPB	chr2:186267262-186267587	IMR90	lung:	n/a	chr2:186267407-186267418
30	CEBPB	chr2:186259086-186259195	HepG2	liver:	n/a	chr2:186259151-186259162
31	CEBPB	chr2:186267231-186267588	HepG2	liver:	n/a	chr2:186267407-186267418
32	CEBPB	chr2:186296748-186297009	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
35	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
36	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
37	CEBPB	chr2:186296738-186297007	A549	lung:	n/a	n/a
38	CEBPB	chr2:186259033-186259232	H1-hESC	embryonic stem cell:	n/a	chr2:186259151-186259162
39	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
41	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
42	CEBPB	chr2:186255982-186256182	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:186236942-186237179	H1-hESC	embryonic stem cell:	n/a	chr2:186237151-186237162
44	CEBPB	chr2:186253170-186253363	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:186267257-186267558	A549	lung:	n/a	chr2:186267407-186267418
46	CEBPB	chr2:186236885-186237330	Hela-S3	cervix:	n/a	chr2:186237151-186237162
47	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
48	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
49	CHD1	chr2:186290086-186290487	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412612-186412662	GM12891	blood:	n/a
2	chr2:186289849-186289899	AG04450	lung:	fetal
3	chr2:186412612-186412662	GM12891	blood:	n/a
4	chr2:186289849-186289899	AG04450	lung:	fetal
5	chr2:186412305-186412355	SAEC	small airway:	n/a
6	chr2:186412073-186412123	GM06990	blood:	n/a
7	chr2:186412073-186412123	HepG2	liver:	n/a
8	chr2:186295841-186295891	SAEC	small airway:	n/a
9	chr2:186412073-186412123	AG04450	lung:	fetal
10	chr2:186295841-186295891	AG10803	skin:	n/a
11	chr2:186412305-186412355	HRPEpiC	eye:	n/a
12	chr2:186412612-186412662	Hepatocyte	liver:	n/a
13	chr2:186412073-186412123	HNPCEpiC	eye:	n/a
14	chr2:186412073-186412123	SK-N-MC	brain:	n/a
15	chr2:186412612-186412662	AoSMC	blood vessel:	n/a
16	chr2:186289849-186289899	MCF10A-Er-Src	breast:	n/a
17	chr2:186412305-186412355	HUVEC	blood vessel:	n/a
18	chr2:186412073-186412123	HUVEC	blood vessel:	n/a
19	chr2:186412073-186412123	NB4	blood:	n/a
20	chr2:186412305-186412355	PrEC	prostate:	n/a
21	chr2:186289849-186289899	IMR90	lung:	fetal
22	chr2:186412612-186412662	ProgFib	skin:	n/a
23	chr2:186412073-186412123	HMEC	breast:	n/a
24	chr2:186295841-186295891	NB4	blood:	n/a
25	chr2:186412073-186412123	BJ	skin:	n/a
26	chr2:186289849-186289899	HL-60	blood:	n/a
27	chr2:186412305-186412355	HMEC	breast:	n/a
28	chr2:186295841-186295891	K562	blood:	n/a
29	chr2:186412073-186412123	NHBE	bronchial:	n/a
30	chr2:186412305-186412355	SKMC	muscle:	n/a
31	chr2:186295841-186295891	HIPEpiC	eye:	n/a
32	chr2:186295841-186295891	SKMC	muscle:	n/a
33	chr2:186289849-186289899	K562	blood:	n/a
34	chr2:186289849-186289899	PANC-1	pancreas:	n/a
35	chr2:186295841-186295891	SK-N-SH	brain:	n/a
36	chr2:186412073-186412123	PANC-1	pancreas:	n/a
37	chr2:186412305-186412355	GM12878	blood:	n/a
38	chr2:186289849-186289899	ProgFib	skin:	n/a
39	chr2:186289849-186289899	HEEpiC	esophagus:	n/a
40	chr2:186289849-186289899	NHDF-neo	bronchial:	n/a
41	chr2:186412305-186412355	MCF-7	breast:	n/a
42	chr2:186289849-186289899	AG09309	skin:	n/a
43	chr2:186412073-186412123	RPTEC	kidney:	n/a
44	chr2:186412612-186412662	AG09309	skin:	n/a
45	chr2:186412305-186412355	HNPCEpiC	eye:	n/a
46	chr2:186412073-186412123	HIPEpiC	eye:	n/a
47	chr2:186295841-186295891	HMEC	breast:	n/a
48	chr2:186289849-186289899	BE2_C	brain:	n/a
49	chr2:186295841-186295891	ProgFib	skin:	n/a
50	chr2:186412305-186412355	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:
2	chr2:186094342..186094913-chr2:186257717..186258552,2	MCF-7	breast:
3	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
4	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
5	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
6	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
7	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
8	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:
9	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
10	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
11	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
12	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
13	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
14	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
15	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
16	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
17	chr2:186291344..186293651-chr2:186297486..186299914,2	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	chr2:186298824-186298920	NONHSAT075962
2	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
3	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
4	lnc-FSIP2-5	chr2:186327396-186327672	NONHSAT075962
5	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
6	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
7	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
8	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
9	lnc-ZSWIM2-15	chr2:186292850-186293692	ucscGeneNc_uc002upi_2
10	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
11	lnc-ZSWIM2-15	chr2:186302301-186302409	ucscGeneNc_uc002upi_2
12	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
13	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962
14	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963
15	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
16	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
17	lnc-ZSWIM2-15	chr2:186311542-186311686	ucscGeneNc_uc002upi_2
18	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
19	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
20	lnc-ZSWIM2-15	chr2:186309034-186309104	ucscGeneNc_uc002upi_2

No data

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

Extended variants
information (count: 5674 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5674 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548816629	chr2:186236810-186236811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572698529	chr2:186236820-186236821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191742417	chr2:186236834-186236835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376970066	chr2:186236842-186236843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74726003	chr2:186236855-186236856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556005852	chr2:186236889-186236890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577550763	chr2:186236932-186236933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538426725	chr2:186236939-186236940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553595541	chr2:186236940-186236941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181839677	chr2:186236951-186236952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34831915	chr2:186236955-186236956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572539739	chr2:186236973-186236974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373081329	chr2:186236974-186236975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142715764	chr2:186236986-186236987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117487603	chr2:186237015-186237016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558440195	chr2:186237021-186237022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576733104	chr2:186237030-186237031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190825438	chr2:186237055-186237056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183114466	chr2:186237112-186237113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186728271	chr2:186237114-186237115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532905309	chr2:186237125-186237126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190876546	chr2:186237149-186237150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559946679	chr2:186237182-186237183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530234249	chr2:186237208-186237209	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549036988	chr2:186237265-186237266	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562527413	chr2:186237281-186237282	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574624225	chr2:186237322-186237323	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74497182	chr2:186237368-186237369	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546526765	chr2:186237370-186237371	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549395536	chr2:186237485-186237486	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542042175	chr2:186237490-186237491	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62198830	chr2:186237536-186237537	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183177848	chr2:186237619-186237620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538585524	chr2:186237682-186237683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566339731	chr2:186237717-186237718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188256195	chr2:186237724-186237725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147421822	chr2:186237754-186237755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536079683	chr2:186237798-186237799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113980931	chr2:186237803-186237804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555012846	chr2:186237811-186237812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560417187	chr2:186237823-186237824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139787486	chr2:186237907-186237908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543815498	chr2:186237915-186237916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78143749	chr2:186237931-186237932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575201494	chr2:186237948-186237949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567229464	chr2:186237972-186237973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142437969	chr2:186238003-186238004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537481012	chr2:186238072-186238073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78997943	chr2:186238095-186238096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374302401	chr2:186238097-186238098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186236800-186237200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr2:186236800-186237800	Enhancers	Adipose Nuclei	Adipose
3	chr2:186237200-186237600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:186237200-186237600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr2:186237600-186238000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:186237600-186238600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:186238000-186238200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:186239200-186239400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:186241200-186241400	Enhancers	Pancreas	Pancrea
10	chr2:186241200-186242000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:186242000-186242200	Enhancers	Pancreas	Pancrea
12	chr2:186249800-186250200	Enhancers	Fetal Kidney	kidney
13	chr2:186250600-186250800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr2:186255400-186256200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:186255400-186256600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:186255800-186256200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:186256000-186256400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:186259800-186261200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:186261200-186261400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:186261200-186261800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr2:186281600-186282200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr2:186281800-186283000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:186282200-186282600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr2:186282600-186283600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:186283000-186283400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:186283400-186283800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr2:186289600-186290200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:186289600-186290200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:186289600-186290200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:186289600-186290200	Active TSS	Adipose Nuclei	Adipose
31	chr2:186289600-186290600	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr2:186289600-186291200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr2:186289600-186291600	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr2:186289600-186291800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr2:186289600-186291800	Active TSS	H1 Cell Line	embryonic stem cell
36	chr2:186289600-186291800	Active TSS	H9 Cell Line	embryonic stem cell
37	chr2:186289600-186291800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:186289600-186291800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:186289600-186291800	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr2:186289600-186292000	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr2:186289600-186292000	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr2:186289600-186292000	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr2:186289600-186292200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:186289800-186290200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:186289800-186290200	Active TSS	Fetal Muscle Trunk	muscle
46	chr2:186289800-186290200	Active TSS	Placenta	Placenta
47	chr2:186289800-186290600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:186289800-186291000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:186289800-186291400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:186289800-186292400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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