Variant report

Variant	nsv584300
Chromosome Location	chr2:209033557-209054928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:245)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 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	chr2:209040035-209040305	GM12878	blood:	n/a	n/a
6	BCLAF1	chr2:209040059-209040456	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:209036792-209037173	HepG2	liver:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
8	BHLHE40	chr2:209036991-209037029	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:209040130-209040348	K562	blood:	n/a	n/a
10	BHLHE40	chr2:209036726-209037189	K562	blood:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
11	BHLHE40	chr2:209039203-209039447	K562	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	chr2:209037690-209037847	HepG2	liver:	n/a	chr2:209037793-209037804
15	CEBPB	chr2:209040017-209040455	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:209040042-209040396	K562	blood:	n/a	n/a
17	CEBPB	chr2:209043880-209044312	MCF-7	breast:	n/a	chr2:209044080-209044091
18	CEBPB	chr2:209040025-209040475	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:209040071-209040454	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:209037651-209037883	A549	lung:	n/a	chr2:209037793-209037804
21	CEBPB	chr2:209043905-209044275	HepG2	liver:	n/a	chr2:209044080-209044091
22	CEBPB	chr2:209040104-209040463	A549	lung:	n/a	n/a
23	CEBPB	chr2:209048700-209048981	H1-hESC	embryonic stem cell:	n/a	chr2:209048819-209048830
24	CEBPB	chr2:209040079-209040454	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:209039968-209040482	K562	blood:	n/a	n/a
26	CEBPB	chr2:209043908-209044263	H1-hESC	embryonic stem cell:	n/a	chr2:209044080-209044091
27	CEBPB	chr2:209040049-209040477	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:209043915-209044258	K562	blood:	n/a	chr2:209044080-209044091
29	CEBPB	chr2:209037644-209037894	K562	blood:	n/a	chr2:209037793-209037804
30	CEBPB	chr2:209039992-209040447	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:209039995-209040438	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:209048683-209048969	HepG2	liver:	n/a	chr2:209048819-209048830
33	CEBPB	chr2:209040087-209040406	A549	lung:	n/a	n/a
34	CEBPB	chr2:209043922-209044294	HepG2	liver:	n/a	chr2:209044080-209044091
35	CEBPB	chr2:209043897-209044285	HepG2	liver:	n/a	chr2:209044080-209044091
36	CEBPB	chr2:209040135-209040344	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:209037671-209037918	K562	blood:	n/a	chr2:209037793-209037804
38	CEBPB	chr2:209037731-209037841	H1-hESC	embryonic stem cell:	n/a	chr2:209037793-209037804
39	CEBPB	chr2:209048718-209048898	HepG2	liver:	n/a	chr2:209048819-209048830
40	CEBPB	chr2:209037544-209037877	IMR90	lung:	n/a	chr2:209037793-209037804
41	CEBPB	chr2:209040062-209040418	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:209043891-209044214	K562	blood:	n/a	chr2:209044080-209044091
43	CEBPB	chr2:209043994-209044214	HepG2	liver:	n/a	chr2:209044080-209044091
44	CEBPB	chr2:209040063-209040484	A549	lung:	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	chr2:209040089-209040370	GM19240	blood:	n/a	chr2:209040227-209040245 chr2:209040229-209040250

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209048830-209048880	AG09319	gingival:	n/a
2	chr2:209048830-209048880	AG09319	gingival:	n/a
3	chr2:209054740-209054790	A549	lung:	n/a
4	chr2:209040082-209040132	HIPEpiC	eye:	n/a
5	chr2:209048830-209048880	MCF10A-Er-Src	breast:	n/a
6	chr2:209054740-209054790	PFSK-1	brain:	n/a
7	chr2:209048830-209048880	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:209054740-209054790	HIPEpiC	eye:	n/a
9	chr2:209048830-209048880	Hela-S3	cervix:	n/a
10	chr2:209054740-209054790	NH-A	brain:	n/a
11	chr2:209054740-209054790	HepG2	liver:	n/a
12	chr2:209054740-209054790	U87	brain:	n/a
13	chr2:209054670-209054720	ProgFib	skin:	n/a
14	chr2:209040082-209040132	GM12892	blood:	n/a
15	chr2:209048830-209048880	BJ	skin:	n/a
16	chr2:209054670-209054720	AG09319	gingival:	n/a
17	chr2:209040082-209040132	HEEpiC	esophagus:	n/a
18	chr2:209048830-209048880	GM12891	blood:	n/a
19	chr2:209048830-209048880	HCPEpiC	choroid plexus:	n/a
20	chr2:209040082-209040132	HRPEpiC	eye:	n/a
21	chr2:209054670-209054720	HCF	heart:	n/a
22	chr2:209054740-209054790	Hepatocyte	liver:	n/a
23	chr2:209054670-209054720	HEEpiC	esophagus:	n/a
24	chr2:209054670-209054720	NHBE	bronchial:	n/a
25	chr2:209054740-209054790	AG10803	skin:	n/a
26	chr2:209040082-209040132	NH-A	brain:	n/a
27	chr2:209054670-209054720	HL-60	blood:	n/a
28	chr2:209040082-209040132	HCT-116	colon:	n/a
29	chr2:209040082-209040132	NB4	blood:	n/a
30	chr2:209054740-209054790	HMEC	breast:	n/a
31	chr2:209048830-209048880	SK-N-MC	brain:	n/a
32	chr2:209048830-209048880	AG04449	skin:	fetal
33	chr2:209054670-209054720	GM06990	blood:	n/a
34	chr2:209048830-209048880	HEEpiC	esophagus:	n/a
35	chr2:209048830-209048880	GM19239	blood:	n/a
36	chr2:209054740-209054790	CMK	blood:	n/a
37	chr2:209054670-209054720	NB4	blood:	n/a
38	chr2:209054670-209054720	AG04450	lung:	fetal
39	chr2:209054670-209054720	NHDF-neo	bronchial:	n/a
40	chr2:209040082-209040132	HUVEC	blood vessel:	n/a
41	chr2:209040082-209040132	HCM	heart:	n/a
42	chr2:209054740-209054790	Jurkat	blood:	n/a
43	chr2:209040082-209040132	NHDF-neo	bronchial:	n/a
44	chr2:209048830-209048880	HUVEC	blood vessel:	n/a
45	chr2:209040082-209040132	AoSMC	blood vessel:	n/a
46	chr2:209048830-209048880	Hepatocyte	liver:	n/a
47	chr2:209054670-209054720	HAEpiC	amniotic membrane:	n/a
48	chr2:209040082-209040132	PFSK-1	brain:	n/a
49	chr2:209054740-209054790	BJ	skin:	n/a
50	chr2:209048830-209048880	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
2	chr17:19991747..19994521-chr2:209032147..209035018,4	K562	blood:
3	chr2:209034002..209036462-chr2:209130730..209132491,2	K562	blood:
4	chr17:19995540..19998202-chr2:209032220..209035134,2	MCF-7	breast:
5	chr2:209039733..209040833-chr2:209118699..209120498,12	MCF-7	breast:
6	chr2:209050833..209051384-chr5:23573266..23573766,2	MCF-7	breast:
7	chr2:209039807..209040681-chr2:209119247..209120525,5	MCF-7	breast:
8	chr2:209049851..209051700-chr2:209064881..209067497,2	K562	blood:
9	chr2:209027080..209028800-chr2:209034737..209037524,2	K562	blood:
10	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
11	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
12	chr2:209028147..209030842-chr2:209033531..209035644,2	MCF-7	breast:
13	chr2:209043347..209044006-chr2:209118780..209119320,2	MCF-7	breast:
14	chr2:209045281..209046929-chr2:209048317..209050730,2	K562	blood:
15	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
16	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
17	chr17:19991773..19994998-chr2:209032034..209035004,3	K562	blood:
18	chr2:209040088..209040688-chr2:209118748..209120316,4	K562	blood:
19	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
20	chr2:209048413..209050423-chr2:209125192..209127904,2	K562	blood:
21	chr2:209039776..209040279-chr2:209119196..209119817,2	MCF-7	breast:
22	chr2:209040053..209040651-chr2:209133538..209134369,3	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
C2orf80	TF binding region
C2orf80	CpG island
ENSG00000138413	chromatin interactions
ENSG00000115020	chromatin interactions
ENSG00000231908	chromatin interactions
ENSG00000188674	chromatin interactions
ENSG00000168582	chromatin interactions

Extended variants
information (count: 1028 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1028 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7589531	chr2:209033557-209033558	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4366892	chr2:209033567-209033568	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs373077808	chr2:209033583-209033584	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561083247	chr2:209033659-209033660	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377551146	chr2:209033661-209033662	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547204821	chr2:209033663-209033664	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4589738	chr2:209033799-209033800	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs6435419	chr2:209033834-209033835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs138217521	chr2:209033867-209033868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538289579	chr2:209033885-209033886	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191720823	chr2:209033918-209033919	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114292062	chr2:209033921-209033922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2166447	chr2:209033923-209033924	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554208976	chr2:209033925-209033926	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572952659	chr2:209033934-209033935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544762760	chr2:209033939-209033940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564874246	chr2:209033941-209033942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2166448	chr2:209033944-209033945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543832142	chr2:209033959-209033960	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs5838108	chr2:209033960-209033961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147866211	chr2:209033961-209033962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs10658929	chr2:209033993-209033994	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs71036985	chr2:209034013-209034014	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs141052983	chr2:209034019-209034020	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs199776752	chr2:209034021-209034022	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112446076	chr2:209034091-209034092	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs529657530	chr2:209034104-209034105	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539955820	chr2:209034151-209034152	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2166449	chr2:209034351-209034352	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184313035	chr2:209034361-209034362	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs552801541	chr2:209034395-209034396	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs569601850	chr2:209034397-209034398	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs186787730	chr2:209034405-209034406	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs548832305	chr2:209034415-209034416	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs9288388	chr2:209034437-209034438	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs76075865	chr2:209034439-209034440	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs397872784	chr2:209034451-209034452	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs10706960	chr2:209034466-209034467	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs568386367	chr2:209034488-209034489	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs534147700	chr2:209034490-209034491	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs553980734	chr2:209034503-209034504	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs570600918	chr2:209034564-209034565	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs191443346	chr2:209034594-209034595	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185404151	chr2:209034597-209034598	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs577407462	chr2:209034645-209034646	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs190710627	chr2:209034699-209034700	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs1374208	chr2:209034715-209034716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143362685	chr2:209034720-209034721	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs115378315	chr2:209034724-209034725	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs540214486	chr2:209034732-209034733	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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

Chromatin state (count:361 , 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	chr2:209033400-209033600	Enhancers	K562	blood
10	chr2:209033400-209033800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:209033600-209036400	Weak transcription	K562	blood
12	chr2:209033600-209040000	Weak transcription	Brain Germinal Matrix	brain
13	chr2:209034600-209035000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:209034800-209035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:209035200-209040400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:209036400-209036600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:209036400-209036800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr2:209036400-209037400	Enhancers	Primary hematopoietic stem cells	blood
19	chr2:209036400-209037800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr2:209036400-209037800	Enhancers	K562	blood
21	chr2:209036400-209038600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr2:209036600-209037600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:209036600-209037800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr2:209036600-209038000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:209036600-209040200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:209036800-209037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:209036800-209037200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr2:209036800-209037400	Bivalent Enhancer	HepG2	liver
29	chr2:209037000-209037200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr2:209037000-209038000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:209037000-209039800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:209037200-209040000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:209037200-209040800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr2:209037400-209037600	Enhancers	Liver	Liver
35	chr2:209037400-209039800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr2:209037600-209039000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:209037600-209040000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:209037800-209038400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr2:209037800-209039000	Weak transcription	K562	blood
40	chr2:209037800-209040000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr2:209038000-209040600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:209038000-209048200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:209038400-209040000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr2:209038600-209040000	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr2:209038800-209039200	Bivalent Enhancer	HepG2	liver
46	chr2:209039000-209039600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:209039000-209039600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:209039000-209040800	Enhancers	K562	blood
49	chr2:209039200-209039400	Flanking Bivalent TSS/Enh	HepG2	liver
50	chr2:209039200-209039800	Enhancers	A549	lung

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