Variant report

Variant	nsv584301
Chromosome Location	chr2:209034715-209054928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:471)
CpG islands
(count:244)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209040108-209040387	K562	blood:	n/a	n/a
2	ARID3A	chr2:209040041-209040430	HepG2	liver:	n/a	n/a
3	ATF1	chr2:209036916-209037257	K562	blood:	n/a	n/a
4	BACH1	chr2:209036897-209037049	K562	blood:	n/a	n/a
5	BCLAF1	chr2:209040059-209040456	GM12878	blood:	n/a	n/a
6	BCLAF1	chr2:209040035-209040305	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:209036726-209037189	K562	blood:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
8	BHLHE40	chr2:209039203-209039447	K562	blood:	n/a	n/a
9	BHLHE40	chr2:209040130-209040348	K562	blood:	n/a	n/a
10	BHLHE40	chr2:209036792-209037173	HepG2	liver:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
11	BHLHE40	chr2:209036991-209037029	GM12878	blood:	n/a	n/a
12	CBX3	chr2:209036804-209037150	K562	blood:	n/a	n/a
13	CBX3	chr2:209039958-209040402	K562	blood:	n/a	n/a
14	CEBPB	chr2:209040042-209040396	K562	blood:	n/a	n/a
15	CEBPB	chr2:209040017-209040455	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:209043905-209044275	HepG2	liver:	n/a	chr2:209044080-209044091
17	CEBPB	chr2:209037671-209037918	K562	blood:	n/a	chr2:209037793-209037804
18	CEBPB	chr2:209037544-209037877	IMR90	lung:	n/a	chr2:209037793-209037804
19	CEBPB	chr2:209040087-209040406	A549	lung:	n/a	n/a
20	CEBPB	chr2:209048683-209048969	HepG2	liver:	n/a	chr2:209048819-209048830
21	CEBPB	chr2:209040079-209040454	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:209037644-209037894	K562	blood:	n/a	chr2:209037793-209037804
23	CEBPB	chr2:209040049-209040477	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr2:209043922-209044294	HepG2	liver:	n/a	chr2:209044080-209044091
25	CEBPB	chr2:209043915-209044258	K562	blood:	n/a	chr2:209044080-209044091
26	CEBPB	chr2:209048718-209048898	HepG2	liver:	n/a	chr2:209048819-209048830
27	CEBPB	chr2:209037690-209037847	HepG2	liver:	n/a	chr2:209037793-209037804
28	CEBPB	chr2:209048700-209048981	H1-hESC	embryonic stem cell:	n/a	chr2:209048819-209048830
29	CEBPB	chr2:209043897-209044285	HepG2	liver:	n/a	chr2:209044080-209044091
30	CEBPB	chr2:209043891-209044214	K562	blood:	n/a	chr2:209044080-209044091
31	CEBPB	chr2:209040062-209040418	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:209039968-209040482	K562	blood:	n/a	n/a
33	CEBPB	chr2:209040104-209040463	A549	lung:	n/a	n/a
34	CEBPB	chr2:209040063-209040484	A549	lung:	n/a	n/a
35	CEBPB	chr2:209040071-209040454	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:209043994-209044214	HepG2	liver:	n/a	chr2:209044080-209044091
37	CEBPB	chr2:209043908-209044263	H1-hESC	embryonic stem cell:	n/a	chr2:209044080-209044091
38	CEBPB	chr2:209037731-209037841	H1-hESC	embryonic stem cell:	n/a	chr2:209037793-209037804
39	CEBPB	chr2:209040025-209040475	MCF-7	breast:	n/a	n/a
40	CEBPB	chr2:209040135-209040344	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:209037651-209037883	A549	lung:	n/a	chr2:209037793-209037804
42	CEBPB	chr2:209039995-209040438	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:209043880-209044312	MCF-7	breast:	n/a	chr2:209044080-209044091
44	CEBPB	chr2:209039992-209040447	HepG2	liver:	n/a	n/a
45	CEBPD	chr2:209043968-209044174	HepG2	liver:	n/a	n/a
46	CEBPD	chr2:209043978-209044221	HepG2	liver:	n/a	n/a
47	CHD2	chr2:209044056-209044267	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr2:209040098-209040315	A549	lung:	n/a	n/a
49	CTBP2	chr2:209048380-209049301	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr2:209040080-209040230	HAc	cerebellar:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209054670-209054720	HCPEpiC	choroid plexus:	n/a
2	chr2:209040082-209040132	MCF-7	breast:	n/a
3	chr2:209054740-209054790	AoSMC	blood vessel:	n/a
4	chr2:209040082-209040132	PrEC	prostate:	n/a
5	chr2:209054670-209054720	GM06990	blood:	n/a
6	chr2:209054740-209054790	AG09319	gingival:	n/a
7	chr2:209040082-209040132	ECC-1	luminal epithelium:	n/a
8	chr2:209054740-209054790	HL-60	blood:	n/a
9	chr2:209040082-209040132	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:209054670-209054720	NH-A	brain:	n/a
11	chr2:209054740-209054790	HRCEpiC	kidney:	n/a
12	chr2:209054740-209054790	SK-N-SH_RA	brain:	n/a
13	chr2:209048830-209048880	HRCEpiC	kidney:	n/a
14	chr2:209054740-209054790	HMEC	breast:	n/a
15	chr2:209048830-209048880	GM19239	blood:	n/a
16	chr2:209040082-209040132	PANC-1	pancreas:	n/a
17	chr2:209048830-209048880	NH-A	brain:	n/a
18	chr2:209054670-209054720	NT2-D1	testis:	n/a
19	chr2:209054740-209054790	NT2-D1	testis:	n/a
20	chr2:209048830-209048880	HNPCEpiC	eye:	n/a
21	chr2:209048830-209048880	Hepatocyte	liver:	n/a
22	chr2:209048830-209048880	LNCaP	prostate:	n/a
23	chr2:209040082-209040132	SK-N-SH	brain:	n/a
24	chr2:209054670-209054720	MCF10A-Er-Src	breast:	n/a
25	chr2:209054670-209054720	U87	brain:	n/a
26	chr2:209054670-209054720	HRPEpiC	eye:	n/a
27	chr2:209054740-209054790	HEEpiC	esophagus:	n/a
28	chr2:209054670-209054720	BE2_C	brain:	n/a
29	chr2:209048830-209048880	AG04450	lung:	fetal
30	chr2:209048830-209048880	HUVEC	blood vessel:	n/a
31	chr2:209048830-209048880	HCPEpiC	choroid plexus:	n/a
32	chr2:209054740-209054790	HCF	heart:	n/a
33	chr2:209048830-209048880	NHBE	bronchial:	n/a
34	chr2:209054670-209054720	HMEC	breast:	n/a
35	chr2:209054740-209054790	Caco-2	colon:	n/a
36	chr2:209040082-209040132	SK-N-MC	brain:	n/a
37	chr2:209048830-209048880	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:209048830-209048880	AG09319	gingival:	n/a
39	chr2:209048830-209048880	AG10803	skin:	n/a
40	chr2:209054740-209054790	Hepatocyte	liver:	n/a
41	chr2:209048830-209048880	ECC-1	luminal epithelium:	n/a
42	chr2:209054670-209054720	BJ	skin:	n/a
43	chr2:209048830-209048880	HAEpiC	amniotic membrane:	n/a
44	chr2:209054740-209054790	HNPCEpiC	eye:	n/a
45	chr2:209054740-209054790	HUVEC	blood vessel:	n/a
46	chr2:209054740-209054790	NHBE	bronchial:	n/a
47	chr2:209048830-209048880	AoSMC	blood vessel:	n/a
48	chr2:209054740-209054790	H1-hESC	embryonic stem cell:	embryo
49	chr2:209054670-209054720	SK-N-SH_RA	brain:	n/a
50	chr2:209054670-209054720	PrEC	prostate:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209039733..209040833-chr2:209118699..209120498,12	MCF-7	breast:
2	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
3	chr2:209040088..209040688-chr2:209118748..209120316,4	K562	blood:
4	chr2:209048413..209050423-chr2:209125192..209127904,2	K562	blood:
5	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
6	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
7	chr2:209045281..209046929-chr2:209048317..209050730,2	K562	blood:
8	chr2:209049851..209051700-chr2:209064881..209067497,2	K562	blood:
9	chr2:209039807..209040681-chr2:209119247..209120525,5	MCF-7	breast:
10	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
11	chr2:209034002..209036462-chr2:209130730..209132491,2	K562	blood:
12	chr17:19991747..19994521-chr2:209032147..209035018,4	K562	blood:
13	chr2:209028147..209030842-chr2:209033531..209035644,2	MCF-7	breast:
14	chr17:19991773..19994998-chr2:209032034..209035004,3	K562	blood:
15	chr2:209043347..209044006-chr2:209118780..209119320,2	MCF-7	breast:
16	chr2:209050833..209051384-chr5:23573266..23573766,2	MCF-7	breast:
17	chr2:209039776..209040279-chr2:209119196..209119817,2	MCF-7	breast:
18	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
19	chr2:209027080..209028800-chr2:209034737..209037524,2	K562	blood:
20	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
21	chr2:209040053..209040651-chr2:209133538..209134369,3	K562	blood:
22	chr17:19995540..19998202-chr2:209032220..209035134,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIKFYVE-4	chr2:209048753-209048776	NONHSAT076630

No data

Variant related genes	Relation type
C2orf80	TF binding region
C2orf80	CpG island
ENSG00000115020	chromatin interactions
ENSG00000168582	chromatin interactions
ENSG00000231908	chromatin interactions
ENSG00000138413	chromatin interactions
ENSG00000188674	chromatin interactions

Extended variants
information (count: 982 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:982 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1374208	chr2:209034715-209034716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143362685	chr2:209034720-209034721	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115378315	chr2:209034724-209034725	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540214486	chr2:209034732-209034733	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373504628	chr2:209034746-209034747	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532224006	chr2:209034750-209034751	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs546456184	chr2:209034785-209034786	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs1348751	chr2:209034801-209034802	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200379062	chr2:209034812-209034813	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78933523	chr2:209034815-209034816	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548601831	chr2:209034836-209034837	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs537578730	chr2:209034837-209034838	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs62194833	chr2:209034865-209034866	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs35655799	chr2:209034938-209034939	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs74945130	chr2:209034946-209034947	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs79065780	chr2:209034947-209034948	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs62194834	chr2:209034949-209034950	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148346865	chr2:209034976-209034977	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570639159	chr2:209035002-209035003	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143344328	chr2:209035025-209035026	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs181621478	chr2:209035038-209035039	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs568733139	chr2:209035043-209035044	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs547207433	chr2:209035055-209035056	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs538005282	chr2:209035081-209035082	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376753525	chr2:209035082-209035083	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs7424670	chr2:209035115-209035116	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs554608645	chr2:209035123-209035124	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs78224938	chr2:209035151-209035152	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs533581673	chr2:209035156-209035157	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs115131921	chr2:209035166-209035167	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs7596591	chr2:209035169-209035170	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs570255750	chr2:209035189-209035190	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs7596778	chr2:209035219-209035220	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7596783	chr2:209035224-209035225	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs576717147	chr2:209035345-209035346	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73986533	chr2:209035348-209035349	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562290568	chr2:209035360-209035361	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs185206381	chr2:209035400-209035401	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547507001	chr2:209035403-209035404	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs115994494	chr2:209035408-209035409	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs6435420	chr2:209035485-209035486	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538957672	chr2:209035498-209035499	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs147540325	chr2:209035549-209035550	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569805961	chr2:209035573-209035574	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs189078851	chr2:209035614-209035615	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs372624284	chr2:209035639-209035640	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs140148953	chr2:209035653-209035654	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs568299775	chr2:209035656-209035657	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs6748431	chr2:209035658-209035659	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs371565117	chr2:209035675-209035676	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	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
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
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209028600-209040400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:209028800-209034800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:209029800-209040000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:209030600-209040400	Weak transcription	Fetal Brain Female	brain
5	chr2:209031600-209039400	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:209031800-209039800	Weak transcription	Fetal Brain Male	brain
7	chr2:209032800-209040600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:209033200-209037600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:209033600-209036400	Weak transcription	K562	blood
10	chr2:209033600-209040000	Weak transcription	Brain Germinal Matrix	brain
11	chr2:209034600-209035000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:209034800-209035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:209035200-209040400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:209036400-209036600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr2:209036400-209036800	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr2:209036400-209037400	Enhancers	Primary hematopoietic stem cells	blood
17	chr2:209036400-209037800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr2:209036400-209037800	Enhancers	K562	blood
19	chr2:209036400-209038600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr2:209036600-209037600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:209036600-209037800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr2:209036600-209038000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:209036600-209040200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr2:209036800-209037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:209036800-209037200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr2:209036800-209037400	Bivalent Enhancer	HepG2	liver
27	chr2:209037000-209037200	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr2:209037000-209038000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:209037000-209039800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:209037200-209040000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:209037200-209040800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr2:209037400-209037600	Enhancers	Liver	Liver
33	chr2:209037400-209039800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr2:209037600-209039000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:209037600-209040000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:209037800-209038400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:209037800-209039000	Weak transcription	K562	blood
38	chr2:209037800-209040000	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr2:209038000-209040600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:209038000-209048200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:209038400-209040000	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr2:209038600-209040000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr2:209038800-209039200	Bivalent Enhancer	HepG2	liver
44	chr2:209039000-209039600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:209039000-209039600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:209039000-209040800	Enhancers	K562	blood
47	chr2:209039200-209039400	Flanking Bivalent TSS/Enh	HepG2	liver
48	chr2:209039200-209039800	Enhancers	A549	lung
49	chr2:209039400-209040000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:209039400-209040600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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