Variant report

Variant	nsv1006688
Chromosome Location	chr2:57822953-58030203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1113)
CpG islands
(count:366)
Chromatin interactive
region (count:27)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:57987011-57987296	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:58004102-58004565	K562	blood:	n/a	n/a
3	ATF1	chr2:57903557-57903607	K562	blood:	n/a	n/a
4	ATF2	chr2:58023643-58024051	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:58023548-58024173	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:57987004-57987361	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:57928447-57928865	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:57986897-57987440	A549	lung:	n/a	n/a
9	BATF	chr2:57987600-57987899	GM12878	blood:	n/a	n/a
10	BATF	chr2:57987544-57987875	GM12878	blood:	n/a	n/a
11	BATF	chr2:57987032-57987313	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:58023700-58023881	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr2:57844520-57844727	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:58023688-58023959	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr2:57947138-57947445	GM12878	blood:	n/a	n/a
16	BCL3	chr2:57986988-57987518	A549	lung:	n/a	n/a
17	BCLAF1	chr2:57986905-57987354	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:57844449-57844837	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:57987004-57987358	GM12878	blood:	n/a	chr2:57987168-57987184
20	BHLHE40	chr2:57926172-57926504	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:57987037-57987376	K562	blood:	n/a	chr2:57987168-57987184
22	BRCA1	chr2:57987082-57987288	HepG2	liver:	n/a	n/a
23	BRCA1	chr2:57987020-57987264	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr2:57954496-57954499	HepG2	liver:	n/a	n/a
25	BRCA1	chr2:57966964-57966999	HepG2	liver:	n/a	n/a
26	CBX3	chr2:58025644-58026095	HCT-116	colon:	n/a	n/a
27	CBX3	chr2:57986961-57987351	K562	blood:	n/a	n/a
28	CCNT2	chr2:58003915-58004345	K562	blood:	n/a	chr2:58004252-58004272
29	CCNT2	chr2:57961224-57961472	K562	blood:	n/a	n/a
30	CEBPB	chr2:57919565-57919890	K562	blood:	n/a	chr2:57919729-57919740
31	CEBPB	chr2:57886690-57886972	A549	lung:	n/a	chr2:57886823-57886834
32	CEBPB	chr2:57904502-57904768	IMR90	lung:	n/a	chr2:57904638-57904649 chr2:57904637-57904650
33	CEBPB	chr2:57881951-57882199	A549	lung:	n/a	n/a
34	CEBPB	chr2:57971419-57971633	HepG2	liver:	n/a	chr2:57971568-57971579 chr2:57971490-57971507
35	CEBPB	chr2:57904502-57904799	HepG2	liver:	n/a	chr2:57904638-57904649 chr2:57904637-57904650
36	CEBPB	chr2:57946773-57947091	IMR90	lung:	n/a	chr2:57946944-57946955
37	CEBPB	chr2:57955818-57956241	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:57886735-57886961	H1-hESC	embryonic stem cell:	n/a	chr2:57886823-57886834
39	CEBPB	chr2:57954252-57954261	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:57919562-57919916	IMR90	lung:	n/a	chr2:57919729-57919740
41	CEBPB	chr2:57919552-57919915	HepG2	liver:	n/a	chr2:57919729-57919740
42	CEBPB	chr2:57992915-57993112	HepG2	liver:	n/a	chr2:57993006-57993015 chr2:57993004-57993017 chr2:57993006-57993015 chr2:57993006-57993015
43	CEBPB	chr2:57968600-57968855	HepG2	liver:	n/a	chr2:57968742-57968755 chr2:57968742-57968753
44	CEBPB	chr2:57881885-57882193	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:57919620-57919909	H1-hESC	embryonic stem cell:	n/a	chr2:57919729-57919740
46	CEBPB	chr2:57919540-57919918	A549	lung:	n/a	chr2:57919729-57919740
47	CEBPB	chr2:57904631-57904671	H1-hESC	embryonic stem cell:	n/a	chr2:57904638-57904649 chr2:57904637-57904650
48	CEBPB	chr2:57924198-57924398	HepG2	liver:	n/a	chr2:57924283-57924294
49	CEBPB	chr2:57954085-57954285	K562	blood:	n/a	n/a
50	CEBPB	chr2:57871823-57872040	HepG2	liver:	n/a	chr2:57871961-57871972

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:57987263-57987313	GM19239	blood:	n/a
2	chr2:57938135-57938185	ECC-1	luminal epithelium:	n/a
3	chr2:58023996-58024046	AG04450	lung:	fetal
4	chr2:58023996-58024046	HCT-116	colon:	n/a
5	chr2:57938135-57938185	HRCEpiC	kidney:	n/a
6	chr2:57938135-57938185	HCM	heart:	n/a
7	chr2:57938135-57938185	HRE	kidney:	n/a
8	chr2:58029565-58029615	HAEpiC	amniotic membrane:	n/a
9	chr2:57986550-57986600	NB4	blood:	n/a
10	chr2:58029565-58029615	GM12878	blood:	n/a
11	chr2:58029503-58029553	HCT-116	colon:	n/a
12	chr2:57938135-57938185	Hepatocyte	liver:	n/a
13	chr2:57938135-57938185	HAEpiC	amniotic membrane:	n/a
14	chr2:58023996-58024046	HL-60	blood:	n/a
15	chr2:57987263-57987313	AoSMC	blood vessel:	n/a
16	chr2:58029565-58029615	NH-A	brain:	n/a
17	chr2:57987263-57987313	HRCEpiC	kidney:	n/a
18	chr2:58029503-58029553	HRE	kidney:	n/a
19	chr2:57987263-57987313	NH-A	brain:	n/a
20	chr2:58023996-58024046	PANC-1	pancreas:	n/a
21	chr2:58023996-58024046	NHDF-neo	bronchial:	n/a
22	chr2:58023996-58024046	AoSMC	blood vessel:	n/a
23	chr2:58023996-58024046	SK-N-SH_RA	brain:	n/a
24	chr2:58029503-58029553	HEK293	kidney:	embryo
25	chr2:58029565-58029615	GM12891	blood:	n/a
26	chr2:58029503-58029553	ECC-1	luminal epithelium:	n/a
27	chr2:57986550-57986600	Caco-2	colon:	n/a
28	chr2:58023996-58024046	MCF10A-Er-Src	breast:	n/a
29	chr2:57986550-57986600	HAEpiC	amniotic membrane:	n/a
30	chr2:58029503-58029553	HAEpiC	amniotic membrane:	n/a
31	chr2:57986550-57986600	HCM	heart:	n/a
32	chr2:57986550-57986600	PFSK-1	brain:	n/a
33	chr2:58029503-58029553	HNPCEpiC	eye:	n/a
34	chr2:57938135-57938185	ovcar-3	ovarian:	n/a
35	chr2:58029503-58029553	SK-N-SH	brain:	n/a
36	chr2:58029503-58029553	HL-60	blood:	n/a
37	chr2:57987263-57987313	Hepatocyte	liver:	n/a
38	chr2:57986550-57986600	H1-hESC	embryonic stem cell:	embryo
39	chr2:58029565-58029615	GM19239	blood:	n/a
40	chr2:58023996-58024046	SK-N-MC	brain:	n/a
41	chr2:58029565-58029615	GM12892	blood:	n/a
42	chr2:57938135-57938185	SK-N-SH	brain:	n/a
43	chr2:58029503-58029553	LNCaP	prostate:	n/a
44	chr2:57986550-57986600	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:57987263-57987313	HepG2	liver:	n/a
46	chr2:57987263-57987313	HAEpiC	amniotic membrane:	n/a
47	chr2:57986550-57986600	HIPEpiC	eye:	n/a
48	chr2:57986550-57986600	HNPCEpiC	eye:	n/a
49	chr2:58029565-58029615	AG09309	skin:	n/a
50	chr2:58023996-58024046	HRPEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:57850261..57851990-chr2:57852642..57855006,2	K562	blood:
2	chr2:57835362..57837031-chr2:57842743..57844296,2	MCF-7	breast:
3	chr2:58003897..58005970-chr2:58009303..58012151,2	K562	blood:
4	chr2:57958445..57960288-chr2:57963171..57964699,2	K562	blood:
5	chr2:57940740..57942738-chr2:57945191..57947948,2	K562	blood:
6	chr2:57986795..57987623-chr2:58674835..58675860,4	MCF-7	breast:
7	chr2:58003897..58005970-chr2:58009303..58012151,2	K562	blood:
8	chr2:57947786..57948883-chr2:58675068..58675903,3	MCF-7	breast:
9	chr2:57967586..57970326-chr2:57972561..57975358,2	K562	blood:
10	chr18:9766125..9766938-chr2:57948061..57948667,2	MCF-7	breast:
11	chr2:58025264..58027443-chr2:58030430..58032051,2	MCF-7	breast:
12	chr2:57958445..57960288-chr2:57963171..57964699,2	K562	blood:
13	chr2:57988184..57990505-chr2:57993308..57996155,2	K562	blood:
14	chr2:57967586..57970326-chr2:57972561..57975358,2	K562	blood:
15	chr2:57923440..57925046-chr2:57926940..57929497,2	K562	blood:
16	chr2:57835362..57837031-chr2:57842743..57844296,2	MCF-7	breast:
17	chr2:57947756..57948609-chr2:57986675..57987249,2	MCF-7	breast:
18	chr2:57986735..57987942-chr2:58674900..58675939,5	MCF-7	breast:
19	chr2:57947756..57948609-chr2:57986675..57987249,2	MCF-7	breast:
20	chr2:57925926..57927856-chr2:57928524..57930468,2	K562	blood:
21	chr2:57988189..57989874-chr2:57990120..57992632,2	K562	blood:
22	chr2:57923440..57925046-chr2:57926940..57929497,2	K562	blood:
23	chr2:57986668..57987445-chr2:58674884..58675821,3	K562	blood:
24	chr2:57988184..57990505-chr2:57993308..57996155,2	K562	blood:
25	chr2:57940740..57942738-chr2:57945191..57947948,2	K562	blood:
26	chr2:57925926..57927856-chr2:57928524..57930468,2	K562	blood:
27	chr2:57850261..57851990-chr2:57852642..57855006,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK2-3	chr2:57940101-57940316	NONHSAT070836
2	lnc-VRK2-3	chr2:57933558-57933718	XLOC_001483
3	lnc-VRK2-10	chr2:57991847-57992345	NONHSAT070842
4	lnc-VRK2-10	chr2:57982563-57982922	NONHSAT070842
5	lnc-VRK2-3	chr2:57928888-57928926	XLOC_001483
6	lnc-VRK2-12	chr2:57826063-57826269	uc_51_+
7	lnc-VRK2-3	chr2:57928210-57928749	NONHSAT070836
8	lnc-VRK2-3	chr2:57933557-57933718	NONHSAT070836
9	lnc-VRK2-3	chr2:57940102-57940235	NONHSAT070838
10	lnc-VRK2-2	chr2:57952830-57953284	XLOC_001484
11	lnc-VRK2-3	chr2:57928667-57928926	NONHSAT070838
12	lnc-VRK2-2	chr2:57950063-57950087	XLOC_001484
13	lnc-VRK2-3	chr2:57940102-57940273	XLOC_001483
14	lnc-VRK2-3	chr2:57940102-57940316	XLOC_001483
15	lnc-FANCL-7	chr2:57826063-57826269	uc_51_-
16	lnc-VRK2-11	chr2:57972558-57972765	NONHSAT147090
17	lnc-VRK2-3	chr2:57928211-57928749	XLOC_001483
18	lnc-VRK2-3	chr2:57933558-57933718	XLOC_001483

No data

Variant related genes	Relation type
ENSG00000271615	TF binding region
ENSG00000271615	CpG island
ENSG00000271615	chromatin interactions

Extended variants
information (count: 6228 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6228 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544614275	chr2:57824053-57824054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564413731	chr2:57824287-57824288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577989056	chr2:57824290-57824291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187757850	chr2:57824291-57824292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376869800	chr2:57824296-57824297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13014264	chr2:57824299-57824300	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549063925	chr2:57824302-57824303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562239332	chr2:57824306-57824307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531243981	chr2:57824327-57824328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191475476	chr2:57824436-57824437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570838052	chr2:57824462-57824463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139317979	chr2:57824464-57824465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372633575	chr2:57824469-57824470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563376452	chr2:57824476-57824477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577473110	chr2:57824478-57824479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567062351	chr2:57824515-57824516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530039559	chr2:57824517-57824518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555945028	chr2:57824528-57824529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77367374	chr2:57824537-57824538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538277199	chr2:57824554-57824555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558164412	chr2:57824610-57824611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs578052667	chr2:57824614-57824615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59251805	chr2:57824657-57824658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs67387703	chr2:57824688-57824689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149546818	chr2:57824691-57824692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560149079	chr2:57824737-57824738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573823553	chr2:57824749-57824750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542445816	chr2:57824753-57824754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562232251	chr2:57824757-57824758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149710101	chr2:57824768-57824769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551033237	chr2:57824769-57824770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4672218	chr2:57824784-57824785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375681219	chr2:57824794-57824795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527249470	chr2:57824802-57824803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1358361	chr2:57824814-57824815	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73943554	chr2:57824845-57824846	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145568361	chr2:57824906-57824907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549582737	chr2:57824941-57824942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148890174	chr2:57824974-57824975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538366931	chr2:57824980-57824981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558251919	chr2:57824990-57824991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577978429	chr2:57825019-57825020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377453385	chr2:57825043-57825044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533935248	chr2:57825062-57825063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145294005	chr2:57825077-57825078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573835891	chr2:57825097-57825098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542832417	chr2:57825099-57825100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372406854	chr2:57825140-57825141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551722470	chr2:57825144-57825145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7577676	chr2:57825147-57825148	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57824000-57825400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr2:57824200-57828200	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr2:57824200-57828200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:57824400-57824800	Enhancers	Thymus	Thymus
5	chr2:57824400-57826000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:57824400-57826000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:57824800-57825200	Weak transcription	Thymus	Thymus
8	chr2:57824800-57828200	Enhancers	Primary hematopoietic stem cells	blood
9	chr2:57825000-57825400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr2:57825000-57830200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr2:57825000-57830200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr2:57825200-57826000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:57825200-57826000	Enhancers	Thymus	Thymus
14	chr2:57825400-57825600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:57825400-57826200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:57825400-57826200	Enhancers	Fetal Thymus	thymus
17	chr2:57825400-57826200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr2:57826000-57826200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr2:57826000-57827200	Weak transcription	Thymus	Thymus
20	chr2:57826000-57829800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:57826200-57826600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr2:57826200-57827200	Weak transcription	Fetal Thymus	thymus
23	chr2:57826200-57828600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:57826400-57827400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:57826600-57827000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr2:57827000-57828000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr2:57827000-57828600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:57827200-57827400	Enhancers	Thymus	Thymus
29	chr2:57827200-57828000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:57827200-57828000	Enhancers	Fetal Thymus	thymus
31	chr2:57827400-57827800	Weak transcription	Thymus	Thymus
32	chr2:57827400-57828200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr2:57827400-57828600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:57827800-57828000	Enhancers	Thymus	Thymus
35	chr2:57828000-57829600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr2:57828000-57831600	Weak transcription	Fetal Thymus	thymus
37	chr2:57828000-57842200	Weak transcription	Thymus	Thymus
38	chr2:57828200-57829000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr2:57828200-57829200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr2:57828200-57829200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:57828200-57829600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr2:57828600-57829600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:57829000-57830400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr2:57829200-57829400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:57829200-57830200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:57829600-57830000	Enhancers	Primary hematopoietic stem cells	blood
47	chr2:57829600-57830000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr2:57829600-57830400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:57829800-57830200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:57836000-57836600	Active TSS	ES-I3 Cell Line	embryonic stem cell

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