Variant report

Variant	nsv584298
Chromosome Location	chr2:209021232-209052303
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:549)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 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	chr2:209040041-209040430	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:209040108-209040387	K562	blood:	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	chr2:209040130-209040348	K562	blood:	n/a	n/a
8	BHLHE40	chr2:209036792-209037173	HepG2	liver:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
9	BHLHE40	chr2:209039203-209039447	K562	blood:	n/a	n/a
10	BHLHE40	chr2:209036726-209037189	K562	blood:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
11	BHLHE40	chr2:209036991-209037029	GM12878	blood:	n/a	n/a
12	CBX3	chr2:209039958-209040402	K562	blood:	n/a	n/a
13	CBX3	chr2:209036804-209037150	K562	blood:	n/a	n/a
14	CEBPB	chr2:209043994-209044214	HepG2	liver:	n/a	chr2:209044080-209044091
15	CEBPB	chr2:209040017-209040455	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:209040079-209040454	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:209040062-209040418	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:209048718-209048898	HepG2	liver:	n/a	chr2:209048819-209048830
19	CEBPB	chr2:209040104-209040463	A549	lung:	n/a	n/a
20	CEBPB	chr2:209048683-209048969	HepG2	liver:	n/a	chr2:209048819-209048830
21	CEBPB	chr2:209040071-209040454	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:209043922-209044294	HepG2	liver:	n/a	chr2:209044080-209044091
23	CEBPB	chr2:209039992-209040447	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:209043891-209044214	K562	blood:	n/a	chr2:209044080-209044091
25	CEBPB	chr2:209043915-209044258	K562	blood:	n/a	chr2:209044080-209044091
26	CEBPB	chr2:209040135-209040344	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:209043905-209044275	HepG2	liver:	n/a	chr2:209044080-209044091
28	CEBPB	chr2:209040049-209040477	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr2:209021185-209021537	HepG2	liver:	n/a	chr2:209021351-209021362
30	CEBPB	chr2:209043880-209044312	MCF-7	breast:	n/a	chr2:209044080-209044091
31	CEBPB	chr2:209043897-209044285	HepG2	liver:	n/a	chr2:209044080-209044091
32	CEBPB	chr2:209037644-209037894	K562	blood:	n/a	chr2:209037793-209037804
33	CEBPB	chr2:209039968-209040482	K562	blood:	n/a	n/a
34	CEBPB	chr2:209028041-209028161	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:209037731-209037841	H1-hESC	embryonic stem cell:	n/a	chr2:209037793-209037804
36	CEBPB	chr2:209040087-209040406	A549	lung:	n/a	n/a
37	CEBPB	chr2:209037651-209037883	A549	lung:	n/a	chr2:209037793-209037804
38	CEBPB	chr2:209040042-209040396	K562	blood:	n/a	n/a
39	CEBPB	chr2:209037690-209037847	HepG2	liver:	n/a	chr2:209037793-209037804
40	CEBPB	chr2:209021266-209021445	K562	blood:	n/a	chr2:209021351-209021362
41	CEBPB	chr2:209037671-209037918	K562	blood:	n/a	chr2:209037793-209037804
42	CEBPB	chr2:209040063-209040484	A549	lung:	n/a	n/a
43	CEBPB	chr2:209037544-209037877	IMR90	lung:	n/a	chr2:209037793-209037804
44	CEBPB	chr2:209048700-209048981	H1-hESC	embryonic stem cell:	n/a	chr2:209048819-209048830
45	CEBPB	chr2:209040025-209040475	MCF-7	breast:	n/a	n/a
46	CEBPB	chr2:209043908-209044263	H1-hESC	embryonic stem cell:	n/a	chr2:209044080-209044091
47	CEBPB	chr2:209039995-209040438	MCF-7	breast:	n/a	n/a
48	CEBPD	chr2:209043968-209044174	HepG2	liver:	n/a	n/a
49	CEBPD	chr2:209043978-209044221	HepG2	liver:	n/a	n/a
50	CHD2	chr2:209044056-209044267	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209025539-209025589	SK-N-SH	brain:	n/a
2	chr2:209029594-209029644	CMK	blood:	n/a
3	chr2:209029690-209029740	Caco-2	colon:	n/a
4	chr2:209040082-209040132	Jurkat	blood:	n/a
5	chr2:209028478-209028528	GM06990	blood:	n/a
6	chr2:209029782-209029832	Caco-2	colon:	n/a
7	chr2:209028059-209028109	BE2_C	brain:	n/a
8	chr2:209048830-209048880	NHDF-neo	bronchial:	n/a
9	chr2:209028399-209028449	ProgFib	skin:	n/a
10	chr2:209029782-209029832	HUVEC	blood vessel:	n/a
11	chr2:209028478-209028528	ProgFib	skin:	n/a
12	chr2:209025539-209025589	HAEpiC	amniotic membrane:	n/a
13	chr2:209028399-209028449	GM12892	blood:	n/a
14	chr2:209028478-209028528	Hela-S3	cervix:	n/a
15	chr2:209029594-209029644	AG09319	gingival:	n/a
16	chr2:209028059-209028109	HCPEpiC	choroid plexus:	n/a
17	chr2:209029594-209029644	NT2-D1	testis:	n/a
18	chr2:209029594-209029644	MCF-7	breast:	n/a
19	chr2:209048830-209048880	HRPEpiC	eye:	n/a
20	chr2:209028478-209028528	PANC-1	pancreas:	n/a
21	chr2:209029782-209029832	Jurkat	blood:	n/a
22	chr2:209028059-209028109	HPAEpiC	pulmonary alveolar:	n/a
23	chr2:209029594-209029644	HCM	heart:	n/a
24	chr2:209029690-209029740	GM12878	blood:	n/a
25	chr2:209040082-209040132	BE2_C	brain:	n/a
26	chr2:209028399-209028449	GM19239	blood:	n/a
27	chr2:209029782-209029832	AG04450	lung:	fetal
28	chr2:209028059-209028109	HCM	heart:	n/a
29	chr2:209028478-209028528	HCPEpiC	choroid plexus:	n/a
30	chr2:209029690-209029740	HCF	heart:	n/a
31	chr2:209029782-209029832	HCPEpiC	choroid plexus:	n/a
32	chr2:209040082-209040132	IMR90	lung:	fetal
33	chr2:209028478-209028528	HL-60	blood:	n/a
34	chr2:209025539-209025589	ECC-1	luminal epithelium:	n/a
35	chr2:209029782-209029832	HCF	heart:	n/a
36	chr2:209025539-209025589	AG04449	skin:	fetal
37	chr2:209028399-209028449	HEEpiC	esophagus:	n/a
38	chr2:209029690-209029740	AG09319	gingival:	n/a
39	chr2:209040082-209040132	HRCEpiC	kidney:	n/a
40	chr2:209028478-209028528	AG04450	lung:	fetal
41	chr2:209029594-209029644	PANC-1	pancreas:	n/a
42	chr2:209025539-209025589	NB4	blood:	n/a
43	chr2:209029690-209029740	AG04450	lung:	fetal
44	chr2:209028478-209028528	HEK293	kidney:	embryo
45	chr2:209040082-209040132	SAEC	small airway:	n/a
46	chr2:209028478-209028528	HIPEpiC	eye:	n/a
47	chr2:209028059-209028109	HAEpiC	amniotic membrane:	n/a
48	chr2:209028478-209028528	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:209048830-209048880	K562	blood:	n/a
50	chr2:209028478-209028528	GM19239	blood:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIKFYVE-4	chr2:209021271-209021486	NONHSAT076632
2	lnc-PIKFYVE-4	chr2:209048753-209048776	NONHSAT076630

No data

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

Extended variants
information (count: 1248 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs796271	chr2:209021232-209021233	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78890386	chr2:209021236-209021237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs796272	chr2:209021301-209021302	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537349117	chr2:209021314-209021315	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs192108289	chr2:209021324-209021325	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs183836854	chr2:209021353-209021354	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs188611577	chr2:209021359-209021360	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs114550653	chr2:209021364-209021365	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs80248582	chr2:209021371-209021372	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs117602648	chr2:209021421-209021422	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs16840606	chr2:209021457-209021458	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180778507	chr2:209021486-209021487	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs185886697	chr2:209021488-209021489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189614844	chr2:209021521-209021522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs16840611	chr2:209021523-209021524	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs574910022	chr2:209021534-209021535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540587072	chr2:209021586-209021587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560578235	chr2:209021587-209021588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139782294	chr2:209021601-209021602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546734437	chr2:209021604-209021605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79759452	chr2:209021623-209021624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs796273	chr2:209021625-209021626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs373458054	chr2:209021654-209021655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs796274	chr2:209021665-209021666	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs368104772	chr2:209021667-209021668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74600413	chr2:209021699-209021700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139243756	chr2:209021700-209021701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113242794	chr2:209021732-209021733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186448300	chr2:209021736-209021737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538708371	chr2:209021748-209021749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74664891	chr2:209021752-209021753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375136997	chr2:209026817-209026818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369507981	chr2:209026819-209026820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190623391	chr2:209026841-209026842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575021924	chr2:209026862-209026863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534633358	chr2:209026863-209026864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369627570	chr2:209026932-209026933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113422245	chr2:209026940-209026941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560356502	chr2:209026960-209026961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62194805	chr2:209027278-209027279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187640046	chr2:209027304-209027305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558884588	chr2:209027307-209027308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199579622	chr2:209027346-209027347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148014189	chr2:209027347-209027348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs66517860	chr2:209027348-209027349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71036984	chr2:209027352-209027353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147239549	chr2:209027353-209027354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs796278	chr2:209027424-209027425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538523056	chr2:209027468-209027469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190811055	chr2:209027477-209027478	Weak transcription	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209020400-209021400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:209021000-209021600	Enhancers	HMEC	breast
3	chr2:209021600-209021800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:209026800-209027000	Enhancers	Fetal Brain Female	brain
5	chr2:209027200-209028200	Weak transcription	Fetal Brain Female	brain
6	chr2:209028000-209028200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:209028000-209028400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:209028000-209028600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:209028000-209028600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:209028000-209028800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:209028200-209028600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:209028200-209028600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:209028200-209029600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr2:209028200-209030400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:209028200-209030600	Enhancers	Fetal Brain Female	brain
16	chr2:209028200-209031800	Enhancers	Fetal Brain Male	brain
17	chr2:209028200-209033200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:209028600-209028800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:209028600-209029000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:209028600-209031600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:209028600-209033400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr2:209028600-209040400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:209028800-209034800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:209029000-209029400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:209029400-209029600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:209029400-209029600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr2:209029800-209040000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:209030600-209040400	Weak transcription	Fetal Brain Female	brain
29	chr2:209031600-209039400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:209031800-209039800	Weak transcription	Fetal Brain Male	brain
31	chr2:209032400-209032800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:209032800-209040600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:209033200-209037600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:209033400-209033600	Enhancers	K562	blood
35	chr2:209033400-209033800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:209033600-209036400	Weak transcription	K562	blood
37	chr2:209033600-209040000	Weak transcription	Brain Germinal Matrix	brain
38	chr2:209034600-209035000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:209034800-209035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:209035200-209040400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:209036400-209036600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr2:209036400-209036800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:209036400-209037400	Enhancers	Primary hematopoietic stem cells	blood
44	chr2:209036400-209037800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr2:209036400-209037800	Enhancers	K562	blood
46	chr2:209036400-209038600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr2:209036600-209037600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:209036600-209037800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr2:209036600-209038000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:209036600-209040200	Weak transcription	Brain Cingulate Gyrus	brain

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