Variant report

Variant	nsv869592
Chromosome Location	chr2:209029861-209060862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:367)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr2:209036726-209037189	K562	blood:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
8	BHLHE40	chr2:209040130-209040348	K562	blood:	n/a	n/a
9	BHLHE40	chr2:209036792-209037173	HepG2	liver:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
10	BHLHE40	chr2:209039203-209039447	K562	blood:	n/a	n/a
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	chr2:209043891-209044214	K562	blood:	n/a	chr2:209044080-209044091
15	CEBPB	chr2:209048683-209048969	HepG2	liver:	n/a	chr2:209048819-209048830
16	CEBPB	chr2:209040049-209040477	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr2:209037644-209037894	K562	blood:	n/a	chr2:209037793-209037804
18	CEBPB	chr2:209043908-209044263	H1-hESC	embryonic stem cell:	n/a	chr2:209044080-209044091
19	CEBPB	chr2:209040079-209040454	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:209048718-209048898	HepG2	liver:	n/a	chr2:209048819-209048830
21	CEBPB	chr2:209040135-209040344	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:209040017-209040455	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:209043905-209044275	HepG2	liver:	n/a	chr2:209044080-209044091
24	CEBPB	chr2:209037671-209037918	K562	blood:	n/a	chr2:209037793-209037804
25	CEBPB	chr2:209040104-209040463	A549	lung:	n/a	n/a
26	CEBPB	chr2:209048700-209048981	H1-hESC	embryonic stem cell:	n/a	chr2:209048819-209048830
27	CEBPB	chr2:209043880-209044312	MCF-7	breast:	n/a	chr2:209044080-209044091
28	CEBPB	chr2:209039995-209040438	MCF-7	breast:	n/a	n/a
29	CEBPB	chr2:209037544-209037877	IMR90	lung:	n/a	chr2:209037793-209037804
30	CEBPB	chr2:209039992-209040447	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:209040087-209040406	A549	lung:	n/a	n/a
32	CEBPB	chr2:209043922-209044294	HepG2	liver:	n/a	chr2:209044080-209044091
33	CEBPB	chr2:209037690-209037847	HepG2	liver:	n/a	chr2:209037793-209037804
34	CEBPB	chr2:209040062-209040418	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:209037731-209037841	H1-hESC	embryonic stem cell:	n/a	chr2:209037793-209037804
36	CEBPB	chr2:209037651-209037883	A549	lung:	n/a	chr2:209037793-209037804
37	CEBPB	chr2:209040063-209040484	A549	lung:	n/a	n/a
38	CEBPB	chr2:209039968-209040482	K562	blood:	n/a	n/a
39	CEBPB	chr2:209043994-209044214	HepG2	liver:	n/a	chr2:209044080-209044091
40	CEBPB	chr2:209040025-209040475	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:209040071-209040454	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:209043915-209044258	K562	blood:	n/a	chr2:209044080-209044091
43	CEBPB	chr2:209040042-209040396	K562	blood:	n/a	n/a
44	CEBPB	chr2:209043897-209044285	HepG2	liver:	n/a	chr2:209044080-209044091
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	chr2:209040180-209040330	Hela-S3	cervix:	n/a	chr2:209040227-209040245 chr2:209040229-209040250

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209040082-209040132	BJ	skin:	n/a
2	chr2:209040082-209040132	BJ	skin:	n/a
3	chr2:209054740-209054790	LNCaP	prostate:	n/a
4	chr2:209040082-209040132	AoSMC	blood vessel:	n/a
5	chr2:209055251-209055301	H1-hESC	embryonic stem cell:	embryo
6	chr2:209055151-209055201	BE2_C	brain:	n/a
7	chr2:209055151-209055201	AG10803	skin:	n/a
8	chr2:209048830-209048880	Caco-2	colon:	n/a
9	chr2:209054670-209054720	HCF	heart:	n/a
10	chr2:209055151-209055201	H1-hESC	embryonic stem cell:	embryo
11	chr2:209054670-209054720	HUVEC	blood vessel:	n/a
12	chr2:209040082-209040132	AG09319	gingival:	n/a
13	chr2:209040082-209040132	Caco-2	colon:	n/a
14	chr2:209054740-209054790	MCF-7	breast:	n/a
15	chr2:209040082-209040132	HRE	kidney:	n/a
16	chr2:209040082-209040132	SKMC	muscle:	n/a
17	chr2:209054740-209054790	BE2_C	brain:	n/a
18	chr2:209054670-209054720	HepG2	liver:	n/a
19	chr2:209048830-209048880	NHBE	bronchial:	n/a
20	chr2:209054670-209054720	HCM	heart:	n/a
21	chr2:209055251-209055301	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:209048830-209048880	SAEC	small airway:	n/a
23	chr2:209055251-209055301	SK-N-SH	brain:	n/a
24	chr2:209054670-209054720	HRCEpiC	kidney:	n/a
25	chr2:209055151-209055201	GM12892	blood:	n/a
26	chr2:209048830-209048880	Hepatocyte	liver:	n/a
27	chr2:209055151-209055201	HL-60	blood:	n/a
28	chr2:209048830-209048880	HMEC	breast:	n/a
29	chr2:209054740-209054790	HMEC	breast:	n/a
30	chr2:209055151-209055201	GM19239	blood:	n/a
31	chr2:209048830-209048880	HAEpiC	amniotic membrane:	n/a
32	chr2:209054740-209054790	GM12891	blood:	n/a
33	chr2:209040082-209040132	GM12891	blood:	n/a
34	chr2:209048830-209048880	NH-A	brain:	n/a
35	chr2:209040082-209040132	ovcar-3	ovarian:	n/a
36	chr2:209054670-209054720	AG09309	skin:	n/a
37	chr2:209040082-209040132	Hepatocyte	liver:	n/a
38	chr2:209055251-209055301	AG10803	skin:	n/a
39	chr2:209054670-209054720	HIPEpiC	eye:	n/a
40	chr2:209040082-209040132	HCM	heart:	n/a
41	chr2:209048830-209048880	HCM	heart:	n/a
42	chr2:209055251-209055301	SKMC	muscle:	n/a
43	chr2:209048830-209048880	BE2_C	brain:	n/a
44	chr2:209054670-209054720	GM06990	blood:	n/a
45	chr2:209055151-209055201	T-47D	breast:	n/a
46	chr2:209055251-209055301	NB4	blood:	n/a
47	chr2:209054670-209054720	NHBE	bronchial:	n/a
48	chr2:209055251-209055301	NT2-D1	testis:	n/a
49	chr2:209054740-209054790	GM19239	blood:	n/a
50	chr2:209054670-209054720	HRPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
2	chr2:209040088..209040688-chr2:209118748..209120316,4	K562	blood:
3	chr2:209039776..209040279-chr2:209119196..209119817,2	MCF-7	breast:
4	chr2:209058168..209060792-chr2:209061919..209063895,2	K562	blood:
5	chr2:209043347..209044006-chr2:209118780..209119320,2	MCF-7	breast:
6	chr17:19995540..19998202-chr2:209032220..209035134,2	MCF-7	breast:
7	chr2:209049851..209051700-chr2:209064881..209067497,2	K562	blood:
8	chr2:209039733..209040833-chr2:209118699..209120498,12	MCF-7	breast:
9	chr2:209028147..209030842-chr2:209033531..209035644,2	MCF-7	breast:
10	chr17:19991773..19994998-chr2:209032034..209035004,3	K562	blood:
11	chr2:209060491..209062065-chr2:209066501..209069096,2	K562	blood:
12	chr17:19991747..19994521-chr2:209032147..209035018,4	K562	blood:
13	chr2:209027080..209028800-chr2:209034737..209037524,2	K562	blood:
14	chr2:209059939..209061469-chr2:209069888..209071988,2	K562	blood:
15	chr2:209034002..209036462-chr2:209130730..209132491,2	K562	blood:
16	chr2:209045281..209046929-chr2:209048317..209050730,2	K562	blood:
17	chr2:209039807..209040681-chr2:209119247..209120525,5	MCF-7	breast:
18	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
19	chr2:209058318..209061036-chr2:209107934..209110316,2	MCF-7	breast:
20	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
21	chr2:209050833..209051384-chr5:23573266..23573766,2	MCF-7	breast:
22	chr2:209040053..209040651-chr2:209133538..209134369,3	K562	blood:
23	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
24	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
25	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
26	chr2:209048413..209050423-chr2:209125192..209127904,2	K562	blood:

(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
CRYGA	TF binding region
C2orf80	TF binding region
CRYGA	CpG island
C2orf80	CpG island
ENSG00000168582	chromatin interactions
ENSG00000115020	chromatin interactions
ENSG00000138413	chromatin interactions
ENSG00000188674	chromatin interactions
ENSG00000231908	chromatin interactions

Extended variants
information (count: 1402 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554677397	chr2:209029870-209029871	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs572835726	chr2:209029878-209029879	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs79635315	chr2:209029899-209029900	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541652322	chr2:209029927-209029928	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs532322465	chr2:209029967-209029968	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs141949050	chr2:209029991-209029992	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs554080542	chr2:209030025-209030026	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs10191088	chr2:209030050-209030051	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10178748	chr2:209030068-209030069	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542864793	chr2:209030110-209030111	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs556084696	chr2:209030112-209030113	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547568116	chr2:209030140-209030141	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs570680853	chr2:209030195-209030196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539727681	chr2:209030238-209030239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556460938	chr2:209030239-209030240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545261066	chr2:209030275-209030276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563362783	chr2:209030295-209030296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34111482	chr2:209030330-209030331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397755731	chr2:209030341-209030342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76084234	chr2:209030343-209030344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200790495	chr2:209030344-209030345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73986528	chr2:209030400-209030401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs367917289	chr2:209030408-209030409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574292522	chr2:209030475-209030476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75916583	chr2:209030520-209030521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61737639	chr2:209030540-209030541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181904127	chr2:209030558-209030559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6721025	chr2:209030572-209030573	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs796281	chr2:209030578-209030579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370442285	chr2:209030586-209030587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543728846	chr2:209030596-209030597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185882181	chr2:209030597-209030598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528571421	chr2:209030657-209030658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140035789	chr2:209030672-209030673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541058646	chr2:209030673-209030674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548958441	chr2:209030748-209030749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559639630	chr2:209030795-209030796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528562080	chr2:209030840-209030841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368169583	chr2:209030843-209030844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189814578	chr2:209030858-209030859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74456262	chr2:209030875-209030876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566741826	chr2:209030941-209030942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570638757	chr2:209031050-209031051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539612581	chr2:209031069-209031070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546775077	chr2:209031084-209031085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370032594	chr2:209031091-209031092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373285953	chr2:209031148-209031149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35548052	chr2:209031155-209031156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564892048	chr2:209031209-209031210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569925381	chr2:209031285-209031286	Weak transcription Enhancers	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:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209028200-209030400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:209028200-209030600	Enhancers	Fetal Brain Female	brain
3	chr2:209028200-209031800	Enhancers	Fetal Brain Male	brain
4	chr2:209028200-209033200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:209028600-209031600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:209028600-209033400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:209028600-209040400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:209028800-209034800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:209029800-209040000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:209030600-209040400	Weak transcription	Fetal Brain Female	brain
11	chr2:209031600-209039400	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr2:209031800-209039800	Weak transcription	Fetal Brain Male	brain
13	chr2:209032400-209032800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:209032800-209040600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:209033200-209037600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:209033400-209033600	Enhancers	K562	blood
17	chr2:209033400-209033800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:209033600-209036400	Weak transcription	K562	blood
19	chr2:209033600-209040000	Weak transcription	Brain Germinal Matrix	brain
20	chr2:209034600-209035000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:209034800-209035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:209035200-209040400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:209036400-209036600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr2:209036400-209036800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:209036400-209037400	Enhancers	Primary hematopoietic stem cells	blood
26	chr2:209036400-209037800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr2:209036400-209037800	Enhancers	K562	blood
28	chr2:209036400-209038600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr2:209036600-209037600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:209036600-209037800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr2:209036600-209038000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:209036600-209040200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr2:209036800-209037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:209036800-209037200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr2:209036800-209037400	Bivalent Enhancer	HepG2	liver
36	chr2:209037000-209037200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr2:209037000-209038000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:209037000-209039800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:209037200-209040000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:209037200-209040800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr2:209037400-209037600	Enhancers	Liver	Liver
42	chr2:209037400-209039800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr2:209037600-209039000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:209037600-209040000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:209037800-209038400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr2:209037800-209039000	Weak transcription	K562	blood
47	chr2:209037800-209040000	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr2:209038000-209040600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:209038000-209048200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:209038400-209040000	Weak transcription	Monocytes-CD14+_RO01746	blood

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