Variant report

Variant	nsv457407
Chromosome Location	chr2:48414735-48493182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1062)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1062 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:48477046-48478513	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:48430164-48430486	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:48475747-48476038	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:48448813-48449551	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:48484484-48484520	K562	blood:	n/a	n/a
6	ARID3A	chr2:48433217-48433475	K562	blood:	n/a	n/a
7	ARID3A	chr2:48463565-48464093	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:48492181-48492668	K562	blood:	n/a	n/a
9	ARID3A	chr2:48427791-48428233	K562	blood:	n/a	n/a
10	ARID3A	chr2:48446581-48447667	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:48432221-48433107	HepG2	liver:	n/a	chr2:48432400-48432416
12	ATF1	chr2:48491931-48493102	K562	blood:	n/a	n/a
13	ATF2	chr2:48454623-48455253	GM12878	blood:	n/a	n/a
14	ATF2	chr2:48454572-48455439	GM12878	blood:	n/a	n/a
15	ATF2	chr2:48475582-48476108	GM12878	blood:	n/a	n/a
16	ATF2	chr2:48475608-48476169	GM12878	blood:	n/a	n/a
17	ATF2	chr2:48478029-48478492	GM12878	blood:	n/a	n/a
18	ATF3	chr2:48492226-48492663	K562	blood:	n/a	n/a
19	ATF3	chr2:48475723-48476146	HCT-116	colon:	n/a	n/a
20	ATF3	chr2:48448870-48449538	HepG2	liver:	n/a	n/a
21	BACH1	chr2:48493009-48493011	K562	blood:	n/a	n/a
22	BACH1	chr2:48475704-48476068	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr2:48475730-48476062	GM12878	blood:	n/a	chr2:48475910-48475921 chr2:48475882-48475890
24	BATF	chr2:48460150-48460423	GM12878	blood:	n/a	n/a
25	BATF	chr2:48475749-48476094	GM12878	blood:	n/a	chr2:48475910-48475921 chr2:48475882-48475890
26	BATF	chr2:48454704-48455022	GM12878	blood:	n/a	n/a
27	BATF	chr2:48478102-48478372	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:48460148-48460384	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:48454785-48455079	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:48454672-48455139	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:48475759-48476096	GM12878	blood:	n/a	chr2:48475946-48475954
32	BCL11A	chr2:48475758-48476036	GM12878	blood:	n/a	chr2:48475946-48475954
33	BCL3	chr2:48475733-48476014	GM12878	blood:	n/a	chr2:48475946-48475954
34	BCLAF1	chr2:48455381-48455759	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:48434518-48434748	K562	blood:	n/a	n/a
36	BHLHE40	chr2:48432815-48432958	K562	blood:	n/a	n/a
37	BHLHE40	chr2:48416954-48417363	K562	blood:	n/a	n/a
38	BHLHE40	chr2:48422434-48422515	K562	blood:	n/a	n/a
39	BHLHE40	chr2:48454747-48455103	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:48492225-48493171	K562	blood:	n/a	n/a
41	BHLHE40	chr2:48446906-48447658	HepG2	liver:	n/a	n/a
42	BHLHE40	chr2:48448860-48449489	HepG2	liver:	n/a	n/a
43	CBX3	chr2:48492199-48492656	K562	blood:	n/a	n/a
44	CCNT2	chr2:48427785-48428096	K562	blood:	n/a	chr2:48428042-48428051
45	CCNT2	chr2:48480165-48480611	K562	blood:	n/a	n/a
46	CCNT2	chr2:48492154-48492782	K562	blood:	n/a	chr2:48492418-48492438
47	CCNT2	chr2:48433392-48433460	K562	blood:	n/a	n/a
48	CEBPB	chr2:48478181-48478401	HepG2	liver:	n/a	chr2:48478348-48478359
49	CEBPB	chr2:48477117-48477489	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:48424425-48424606	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48434367-48434417	T-47D	breast:	n/a
2	chr2:48434367-48434417	RPTEC	kidney:	n/a
3	chr2:48434367-48434417	H1-hESC	embryonic stem cell:	embryo
4	chr2:48434367-48434417	AG04450	lung:	fetal
5	chr2:48434367-48434417	AG04449	skin:	fetal
6	chr2:48434367-48434417	U87	brain:	n/a
7	chr2:48434367-48434417	HRCEpiC	kidney:	n/a
8	chr2:48434367-48434417	Hela-S3	cervix:	n/a
9	chr2:48434367-48434417	HAEpiC	amniotic membrane:	n/a
10	chr2:48434367-48434417	HCT-116	colon:	n/a
11	chr2:48434367-48434417	PFSK-1	brain:	n/a
12	chr2:48434367-48434417	SAEC	small airway:	n/a
13	chr2:48434367-48434417	GM06990	blood:	n/a
14	chr2:48434367-48434417	AG10803	skin:	n/a
15	chr2:48434367-48434417	HNPCEpiC	eye:	n/a
16	chr2:48434367-48434417	HMEC	breast:	n/a
17	chr2:48434367-48434417	HRPEpiC	eye:	n/a
18	chr2:48434367-48434417	AG09319	gingival:	n/a
19	chr2:48434367-48434417	HUVEC	blood vessel:	n/a
20	chr2:48434367-48434417	HL-60	blood:	n/a
21	chr2:48434367-48434417	GM12892	blood:	n/a
22	chr2:48434367-48434417	HCF	heart:	n/a
23	chr2:48434367-48434417	NHBE	bronchial:	n/a
24	chr2:48434367-48434417	MCF10A-Er-Src	breast:	n/a
25	chr2:48434367-48434417	SK-N-MC	brain:	n/a
26	chr2:48434367-48434417	HCM	heart:	n/a
27	chr2:48434367-48434417	AoSMC	blood vessel:	n/a
28	chr2:48434367-48434417	SKMC	muscle:	n/a
29	chr2:48434367-48434417	NHDF-neo	bronchial:	n/a
30	chr2:48434367-48434417	K562	blood:	n/a
31	chr2:48434367-48434417	BJ	skin:	n/a
32	chr2:48434367-48434417	AG09309	skin:	n/a
33	chr2:48434367-48434417	HEK293	kidney:	embryo
34	chr2:48434367-48434417	HIPEpiC	eye:	n/a
35	chr2:48434367-48434417	NT2-D1	testis:	n/a
36	chr2:48434367-48434417	CMK	blood:	n/a
37	chr2:48434367-48434417	ovcar-3	ovarian:	n/a
38	chr2:48434367-48434417	GM12878	blood:	n/a
39	chr2:48434367-48434417	GM12891	blood:	n/a
40	chr2:48434367-48434417	MCF-7	breast:	n/a
41	chr2:48434367-48434417	ECC-1	luminal epithelium:	n/a
42	chr2:48434367-48434417	Hepatocyte	liver:	n/a
43	chr2:48434367-48434417	SK-N-SH_RA	brain:	n/a
44	chr2:48434367-48434417	LNCaP	prostate:	n/a
45	chr2:48434367-48434417	SK-N-SH	brain:	n/a
46	chr2:48434367-48434417	NH-A	brain:	n/a
47	chr2:48434367-48434417	PANC-1	pancreas:	n/a
48	chr2:48434367-48434417	Jurkat	blood:	n/a
49	chr2:48434367-48434417	Caco-2	colon:	n/a
50	chr2:48434367-48434417	GM19239	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:48492137..48494411-chr2:48542775..48545328,2	K562	blood:
2	chr14:81611696..81613196-chr2:48488940..48490546,2	MCF-7	breast:
3	chr2:48436276..48438962-chr2:48439621..48441170,3	K562	blood:
4	chr2:48432585..48437809-chr2:48438116..48442314,6	K562	blood:
5	chr2:48492280..48493854-chr2:48539785..48541732,2	K562	blood:
6	chr2:48430653..48432447-chr2:48432583..48435502,2	K562	blood:
7	chr2:48475740..48478459-chr2:48481350..48483573,2	K562	blood:
8	chr2:48415132..48417658-chr2:48422363..48423907,2	MCF-7	breast:
9	chr2:48431668..48433629-chr2:48442154..48444145,2	MCF-7	breast:
10	chr2:48442344..48444202-chr2:48446205..48448068,2	K562	blood:
11	chr2:48415132..48417658-chr2:48422363..48423907,2	MCF-7	breast:
12	chr2:48432585..48437809-chr2:48438116..48442314,6	K562	blood:
13	chr2:48456981..48457558-chr8:144780788..144781293,2	MCF-7	breast:
14	chr2:48463548..48466435-chr2:48483353..48486334,2	K562	blood:
15	chr2:48475740..48478459-chr2:48481350..48483573,2	K562	blood:
16	chr2:48444859..48447446-chr2:48460629..48462297,2	K562	blood:
17	chr2:48420748..48422643-chr2:48628237..48631229,2	K562	blood:
18	chr2:48463548..48466435-chr2:48483353..48486334,2	K562	blood:
19	chr2:48430653..48432447-chr2:48432583..48435502,2	K562	blood:
20	chr2:48436276..48438962-chr2:48439621..48441170,3	K562	blood:
21	chr2:48434273..48436933-chr2:48509087..48510604,2	K562	blood:
22	chr2:48431668..48433629-chr2:48442154..48444145,2	MCF-7	breast:
23	chr2:48457105..48459838-chr2:48462699..48465520,3	K562	blood:
24	chr2:48457105..48459838-chr2:48462699..48465520,3	K562	blood:
25	chr2:48475464..48477949-chr2:48504616..48506328,2	K562	blood:
26	chr1:8360834..8361754-chr2:48483082..48483582,2	NB4	blood:
27	chr2:48487519..48489450-chr2:48489934..48492138,2	K562	blood:
28	chr2:48444859..48447446-chr2:48460629..48462297,2	K562	blood:
29	chr2:48487519..48489450-chr2:48489934..48492138,2	K562	blood:
30	chr2:48442344..48444202-chr2:48446205..48448068,2	K562	blood:
31	chr2:48444197..48446382-chr2:48474210..48475992,2	MCF-7	breast:
32	chr2:48480909..48483204-chr2:48540042..48542458,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXN2-4	chr2:48425532-48425603	NONHSAT070616
2	lnc-FOXN2-4	chr2:48423238-48423721	NONHSAT070616
3	lnc-FBXO11-1	chr2:48468067-48468122	ENSG00000230773
4	lnc-FBXO11-1	chr2:48468067-48468141	NONHSAT070610
5	lnc-FOXN2-3	chr2:48444714-48445038	NONHSAT070617

No data

Variant related genes	Relation type
RN7SKP224	TF binding region
ENSG00000230773	TF binding region
RN7SKP224	CpG island
ENSG00000230773	CpG island
ENSG00000201010	chromatin interactions
ENSG00000170802	chromatin interactions

Extended variants
information (count: 3161 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3161 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12621844	chr2:48414735-48414736	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138809690	chr2:48414752-48414753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560899468	chr2:48414757-48414758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532558782	chr2:48414768-48414769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570742438	chr2:48414784-48414785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531220407	chr2:48414786-48414787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549803733	chr2:48414793-48414794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12612417	chr2:48414875-48414876	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539214902	chr2:48414916-48414917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547633228	chr2:48414921-48414922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78984405	chr2:48414935-48414936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371081540	chr2:48414948-48414949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554858607	chr2:48414971-48414972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561369522	chr2:48414972-48414973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537054131	chr2:48414994-48414995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558967957	chr2:48414996-48414997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62137432	chr2:48414997-48414998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545182869	chr2:48415017-48415018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115798576	chr2:48415034-48415035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184164560	chr2:48415042-48415043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542906708	chr2:48415054-48415055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564038861	chr2:48415089-48415090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376758719	chr2:48415092-48415093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561172866	chr2:48415108-48415109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34213876	chr2:48415112-48415113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370706081	chr2:48415115-48415116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547976242	chr2:48415117-48415118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75569594	chr2:48415131-48415132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564991726	chr2:48415146-48415147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72883976	chr2:48415214-48415215	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs374700055	chr2:48415217-48415218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547571497	chr2:48415288-48415289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62137433	chr2:48415347-48415348	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4953560	chr2:48415351-48415352	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548427414	chr2:48415397-48415398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11693267	chr2:48415449-48415450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187549612	chr2:48415473-48415474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558727428	chr2:48415508-48415509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570901165	chr2:48415597-48415598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535125123	chr2:48415657-48415658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4953561	chr2:48415708-48415709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568481079	chr2:48415720-48415721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191493605	chr2:48415736-48415737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572240074	chr2:48415739-48415740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147508556	chr2:48415765-48415766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182577415	chr2:48415841-48415842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187199944	chr2:48415855-48415856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369397341	chr2:48415876-48415877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114898860	chr2:48415878-48415879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564764125	chr2:48415882-48415883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Bladder cancer	21909424	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
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48412000-48418600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:48412200-48415200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:48412600-48415200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:48412600-48416800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr2:48413000-48416200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr2:48413200-48415200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:48413200-48416000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr2:48413200-48417000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr2:48413600-48415200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:48413600-48415200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:48414200-48415000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:48414200-48415200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr2:48414200-48415200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:48414200-48415200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr2:48414200-48415400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:48414400-48415000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:48415000-48415200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:48415000-48423200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:48416000-48418200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr2:48416200-48416800	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr2:48416800-48417000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:48416800-48417200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:48416800-48417600	Enhancers	Primary B cells from peripheral blood	blood
24	chr2:48416800-48417600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:48416800-48417600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr2:48417000-48418200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr2:48417600-48418000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr2:48417600-48423400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr2:48417800-48418200	Enhancers	HepG2	liver
30	chr2:48418000-48423200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr2:48418200-48422000	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr2:48418200-48423200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr2:48418400-48419000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:48418400-48419000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:48418600-48419000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:48418600-48419000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:48418600-48419000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:48418600-48419000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:48418800-48423200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:48419000-48423200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:48419000-48423200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:48419000-48423200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:48419000-48423400	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr2:48419000-48423600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:48421200-48421600	Enhancers	Brain Substantia Nigra	brain
46	chr2:48421400-48421600	Enhancers	Brain Anterior Caudate	brain
47	chr2:48421400-48422200	Enhancers	Fetal Brain Male	brain
48	chr2:48421400-48424600	Enhancers	Brain Hippocampus Middle	brain
49	chr2:48421600-48422000	Weak transcription	Brain Substantia Nigra	brain
50	chr2:48421800-48422000	Enhancers	Brain Cingulate Gyrus	brain

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