Variant report

Variant	nsv873795
Chromosome Location	chr2:33939941-34064746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:33989933-33989937	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:33992471-33992698	GM12878	blood:	n/a	n/a
3	BATF	chr2:33992376-33992627	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:33992452-33992619	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:33992459-33992730	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:34010355-34011098	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:34009927-34010076	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:33950219-33950224	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:33954808-33954914	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:33992456-33992639	HepG2	liver:	n/a	n/a
11	CBX3	chr2:33986046-33986247	K562	blood:	n/a	n/a
12	CEBPB	chr2:34050115-34050323	HepG2	liver:	n/a	chr2:34050219-34050230
13	CEBPB	chr2:34046826-34047351	HepG2	liver:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
14	CEBPB	chr2:33944249-33944412	MCF-7	breast:	n/a	chr2:33944333-33944350 chr2:33944334-33944347 chr2:33944335-33944346
15	CEBPB	chr2:34016775-34017034	A549	lung:	n/a	n/a
16	CEBPB	chr2:34063261-34063570	HepG2	liver:	n/a	chr2:34063436-34063447
17	CEBPB	chr2:34027732-34028058	A549	lung:	n/a	n/a
18	CEBPB	chr2:33944152-33944511	A549	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
19	CEBPB	chr2:34050108-34050338	A549	lung:	n/a	chr2:34050219-34050230
20	CEBPB	chr2:34062049-34062067	A549	lung:	n/a	n/a
21	CEBPB	chr2:34046847-34047396	IMR90	lung:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
22	CEBPB	chr2:33956627-33956689	K562	blood:	n/a	n/a
23	CEBPB	chr2:33944156-33944511	IMR90	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
24	CEBPB	chr2:34016763-34016978	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:34016725-34017098	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:33944200-33944431	H1-hESC	embryonic stem cell:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
27	CEBPB	chr2:34027728-34028064	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:34046885-34047345	A549	lung:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
29	CEBPB	chr2:34062064-34062078	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:34047164-34047373	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:34016736-34017067	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:33944156-33944508	HepG2	liver:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
33	CEBPB	chr2:33944196-33944468	K562	blood:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
34	CEBPB	chr2:34063300-34063564	IMR90	lung:	n/a	chr2:34063436-34063447
35	CEBPD	chr2:33992469-33992658	K562	blood:	n/a	n/a
36	CHD2	chr2:34010211-34010613	GM12878	blood:	n/a	n/a
37	CHD2	chr2:34010971-34011007	GM12878	blood:	n/a	n/a
38	CTCF	chr2:34008060-34008210	HMF	breast:	n/a	chr2:34008113-34008131
39	CTCF	chr2:34008003-34008218	H1-hESC	embryonic stem cell:	n/a	chr2:34008113-34008131
40	CTCF	chr2:34008060-34008210	GM12873	blood:	n/a	chr2:34008113-34008131
41	CTCF	chr2:33990180-33990330	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:34008060-34008210	HEK293	kidney:	n/a	chr2:34008113-34008131
43	CTCF	chr2:34008077-34008186	MCF-7	breast:	n/a	chr2:34008113-34008131
44	CTCF	chr2:34008050-34008191	GM19240	blood:	n/a	chr2:34008113-34008131
45	CTCF	chr2:34007960-34008110	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr2:34008114-34008143	Fibrobl	skin:	n/a	n/a
47	CTCF	chr2:34045840-34045990	GM12875	blood:	n/a	chr2:34045928-34045946
48	CTCF	chr2:34045911-34045994	MCF-7	breast:	n/a	chr2:34045928-34045946
49	CTCF	chr2:33992537-33992633	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr2:34008041-34008214	GM12878	blood:	n/a	chr2:34008113-34008131

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33954347-33954397	HRPEpiC	eye:	n/a
2	chr2:33954347-33954397	HRPEpiC	eye:	n/a
3	chr2:33951647-33951697	Hepatocyte	liver:	n/a
4	chr2:33952673-33952723	PANC-1	pancreas:	n/a
5	chr2:33954735-33954785	HAEpiC	amniotic membrane:	n/a
6	chr2:33953195-33953245	GM12878	blood:	n/a
7	chr2:33953437-33953487	GM12892	blood:	n/a
8	chr2:33952423-33952473	ovcar-3	ovarian:	n/a
9	chr2:33954043-33954093	A549	lung:	n/a
10	chr2:33948457-33948507	SK-N-SH	brain:	n/a
11	chr2:33953370-33953420	Hela-S3	cervix:	n/a
12	chr2:33954347-33954397	HCPEpiC	choroid plexus:	n/a
13	chr2:33953437-33953487	HL-60	blood:	n/a
14	chr2:33954735-33954785	GM12878	blood:	n/a
15	chr2:33952673-33952723	HRE	kidney:	n/a
16	chr2:33952423-33952473	HMEC	breast:	n/a
17	chr2:33952509-33952559	T-47D	breast:	n/a
18	chr2:33954347-33954397	SK-N-SH_RA	brain:	n/a
19	chr2:33954043-33954093	SK-N-SH	brain:	n/a
20	chr2:33954735-33954785	H1-hESC	embryonic stem cell:	embryo
21	chr2:33952488-33952538	SK-N-SH	brain:	n/a
22	chr2:33952423-33952473	AoSMC	blood vessel:	n/a
23	chr2:33954043-33954093	GM19239	blood:	n/a
24	chr2:33948457-33948507	CMK	blood:	n/a
25	chr2:33952509-33952559	HEEpiC	esophagus:	n/a
26	chr2:33952673-33952723	SAEC	small airway:	n/a
27	chr2:33953203-33953253	HRCEpiC	kidney:	n/a
28	chr2:33951647-33951697	NHDF-neo	bronchial:	n/a
29	chr2:33948457-33948507	RPTEC	kidney:	n/a
30	chr2:33953437-33953487	GM06990	blood:	n/a
31	chr2:33953203-33953253	HCF	heart:	n/a
32	chr2:33952509-33952559	HCF	heart:	n/a
33	chr2:33953437-33953487	RPTEC	kidney:	n/a
34	chr2:33952509-33952559	RPTEC	kidney:	n/a
35	chr2:33952509-33952559	HMEC	breast:	n/a
36	chr2:33948457-33948507	HCM	heart:	n/a
37	chr2:33953437-33953487	CMK	blood:	n/a
38	chr2:33953370-33953420	GM12878	blood:	n/a
39	chr2:33954735-33954785	ProgFib	skin:	n/a
40	chr2:33948457-33948507	NB4	blood:	n/a
41	chr2:33952423-33952473	HEK293	kidney:	embryo
42	chr2:33952673-33952723	GM19239	blood:	n/a
43	chr2:33952488-33952538	HAEpiC	amniotic membrane:	n/a
44	chr2:33952423-33952473	ProgFib	skin:	n/a
45	chr2:33951647-33951697	AoSMC	blood vessel:	n/a
46	chr2:33953370-33953420	AG04450	lung:	fetal
47	chr2:33953203-33953253	NHBE	bronchial:	n/a
48	chr2:33952423-33952473	BE2_C	brain:	n/a
49	chr2:33953370-33953420	NHDF-neo	bronchial:	n/a
50	chr2:33954347-33954397	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:34033415..34035422-chr2:34038221..34040306,2	MCF-7	breast:
2	chr2:33973736..33977470-chr2:33981372..33984191,3	K562	blood:
3	chr2:34033415..34035422-chr2:34038221..34040306,2	MCF-7	breast:
4	chr2:34056369..34058032-chr2:34058034..34060009,2	K562	blood:
5	chr2:34056369..34058032-chr2:34058034..34060009,2	K562	blood:
6	chr2:33994888..33996887-chr2:34002074..34004966,2	MCF-7	breast:
7	chr2:34008516..34010441-chr2:34014849..34016681,2	MCF-7	breast:
8	chr2:33973736..33977470-chr2:33981372..33984191,3	K562	blood:
9	chr2:34008516..34010441-chr2:34014849..34016681,2	MCF-7	breast:
10	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
11	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
12	chr2:33994888..33996887-chr2:34002074..34004966,2	MCF-7	breast:
13	chr11:62608939..62609489-chr2:34040620..34041120,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM98A-4	chr2:33948350-33948577	NONHSAT147081
2	lnc-FAM98A-4	chr2:33947328-33947937	NONHSAT147081

Variant related genes	Relation type
ENSG00000264267	TF binding region
MYADML	TF binding region
ENSG00000264267	CpG island
MYADML	CpG island
ENSG00000133316	chromatin interactions

Extended variants
information (count: 3657 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3657 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2367955	chr2:33939941-33939942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76978264	chr2:33939943-33939944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148155676	chr2:33939988-33939989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114998340	chr2:33940017-33940018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141650765	chr2:33940019-33940020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150508520	chr2:33940020-33940021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1448553	chr2:33940043-33940044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543505503	chr2:33940077-33940078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138539694	chr2:33940079-33940080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374748845	chr2:33940144-33940145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562074859	chr2:33940159-33940160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531183158	chr2:33940161-33940162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6750177	chr2:33940162-33940163	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs142760227	chr2:33940184-33940185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115475359	chr2:33940217-33940218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192361376	chr2:33940243-33940244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184042537	chr2:33940264-33940265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528968940	chr2:33940269-33940270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188972114	chr2:33940292-33940293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79168312	chr2:33940296-33940297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537745211	chr2:33940298-33940299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557807612	chr2:33940306-33940307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147371308	chr2:33940314-33940315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190973742	chr2:33940407-33940408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553949117	chr2:33940424-33940425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573334973	chr2:33940433-33940434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542346317	chr2:33940440-33940441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80157640	chr2:33940458-33940459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72787883	chr2:33940471-33940472	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182180894	chr2:33940489-33940490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56843641	chr2:33940506-33940507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536882135	chr2:33940509-33940510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555218076	chr2:33940515-33940516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145194225	chr2:33940517-33940518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187053319	chr2:33940563-33940564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560322063	chr2:33940573-33940574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528907186	chr2:33940594-33940595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368506365	chr2:33940604-33940605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576579927	chr2:33940609-33940610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116036891	chr2:33940641-33940642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111940862	chr2:33940656-33940657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191502857	chr2:33940676-33940677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571417638	chr2:33940746-33940747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184379412	chr2:33940786-33940787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547229604	chr2:33940798-33940799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558872167	chr2:33940851-33940852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577212080	chr2:33940869-33940870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114806670	chr2:33940895-33940896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555932919	chr2:33940910-33940911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12988770	chr2:33940918-33940919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33938400-33941800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:33938600-33942200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:33943800-33945200	Enhancers	HUVEC	blood vessel
4	chr2:33951400-33951600	Enhancers	K562	blood
5	chr2:33952200-33952400	Enhancers	K562	blood
6	chr2:33952200-33953200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:33952200-33953200	ZNF genes & repeats	Spleen	Spleen
8	chr2:33954800-33955200	Enhancers	GM12878-XiMat	blood
9	chr2:33955000-33955800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr2:33955200-33955600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:33955200-33955800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:33955400-33955800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:33955400-33955800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:33955800-33960200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:33960200-33960600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:33984200-33984400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:33986800-33987000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
18	chr2:33986800-33987000	Active TSS	Gastric	stomach
19	chr2:33986800-33987200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:33987000-33987200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:33987000-34000200	Weak transcription	Gastric	stomach
22	chr2:33987200-33987600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr2:33987200-33988400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:33988000-33988800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr2:33988000-33992200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:33988200-33988400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:33988200-33988800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:33988200-33989200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:33988200-33991200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:33988400-33989000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:33988400-33989000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:33988400-33989000	Enhancers	Lung	lung
33	chr2:33988400-33989800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:33988400-33991000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:33988600-33988800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:33988600-33988800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:33988800-33989400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:33988800-33989800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:33988800-33990000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:33988800-33991000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:33989200-33989600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:33989400-33990000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:33989600-33990200	Enhancers	Fetal Kidney	kidney
44	chr2:33989600-33990400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:33989800-33990000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:33989800-33990200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:33989800-33990400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr2:33989800-33990600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:33989800-33990800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:33989800-33990800	Enhancers	Cortex derived primary cultured neurospheres	brain

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