Variant report

Variant	nsv1010448
Chromosome Location	chr2:34525955-34604094
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	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:34575982-34576211	HepG2	liver:	n/a	chr2:34576118-34576129
4	CEBPB	chr2:34541175-34541372	HepG2	liver:	n/a	chr2:34541344-34541357 chr2:34541346-34541357 chr2:34541341-34541358 chr2:34541344-34541355
5	CEBPB	chr2:34531788-34532038	A549	lung:	n/a	n/a
6	CEBPB	chr2:34590884-34591363	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr2:34562713-34562834	GM12878	blood:	n/a	n/a
8	CHD2	chr2:34590960-34591415	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr2:34578800-34578950	RPTEC	kidney:	n/a	n/a
10	CTCF	chr2:34591160-34591310	HepG2	liver:	n/a	chr2:34591235-34591243
11	CTCF	chr2:34591160-34591310	HRPEpiC	eye:	n/a	chr2:34591235-34591243
12	CTCF	chr2:34591200-34591350	HAc	cerebellar:	n/a	chr2:34591235-34591243
13	CTCF	chr2:34591140-34591290	HRE	kidney:	n/a	chr2:34591235-34591243
14	CTCF	chr2:34591140-34591290	RPTEC	kidney:	n/a	chr2:34591235-34591243
15	CTCF	chr2:34556672-34556747	MCF-7	breast:	n/a	n/a
16	CTCF	chr2:34578878-34579039	HUVEC	blood vessel:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
17	CTCF	chr2:34600840-34600990	GM12874	blood:	n/a	n/a
18	CTCF	chr2:34591180-34591330	WERI-Rb-1	eye:	n/a	chr2:34591235-34591243
19	CTCF	chr2:34578860-34579010	HRPEpiC	eye:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
20	CTCF	chr2:34591160-34591310	HRE	kidney:	n/a	chr2:34591235-34591243
21	CTCF	chr2:34578820-34578970	RPTEC	kidney:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
22	CTCF	chr2:34578840-34578990	HRE	kidney:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
23	CTCF	chr2:34578820-34578970	GM06990	blood:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
24	CTCF	chr2:34578975-34578990	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr2:34591220-34591370	RPTEC	kidney:	n/a	chr2:34591235-34591243
26	CTCF	chr2:34578907-34579021	GM12878	blood:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
27	CTCF	chr2:34591220-34591370	HRPEpiC	eye:	n/a	chr2:34591235-34591243
28	CTCF	chr2:34562578-34562644	GM12878	blood:	n/a	n/a
29	CTCF	chr2:34578933-34578999	Pancreas_OC	pancreas:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
30	CTCF	chr2:34591200-34591350	WERI-Rb-1	eye:	n/a	chr2:34591235-34591243
31	CTCF	chr2:34591202-34591372	Medullo	brain:	n/a	chr2:34591235-34591243
32	CTCF	chr2:34578900-34579050	HepG2	liver:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
33	CTCF	chr2:34578860-34579010	HRE	kidney:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
34	CTCF	chr2:34578940-34579090	MCF-7	breast:	n/a	chr2:34578949-34578957
35	CTCF	chr2:34591200-34591350	HEK293	kidney:	n/a	chr2:34591235-34591243
36	EGR1	chr2:34591033-34591395	H1-hESC	embryonic stem cell:	n/a	n/a
37	EP300	chr2:34591054-34591427	H1-hESC	embryonic stem cell:	n/a	n/a
38	EP300	chr2:34590952-34591438	H1-hESC	embryonic stem cell:	n/a	n/a
39	FAM48A	chr2:34549938-34550074	GM12878	blood:	n/a	n/a
40	FOS	chr2:34541912-34542134	MCF10A-Er-Src	breast:	n/a	chr2:34542046-34542054 chr2:34542044-34542056 chr2:34542047-34542054 chr2:34542045-34542055
41	FOS	chr2:34541911-34542214	MCF10A-Er-Src	breast:	n/a	chr2:34542046-34542054 chr2:34542044-34542056 chr2:34542047-34542054 chr2:34542045-34542055
42	FOS	chr2:34562915-34563115	MCF10A-Er-Src	breast:	n/a	chr2:34563007-34563016 chr2:34562980-34562988
43	FOS	chr2:34562847-34563152	MCF10A-Er-Src	breast:	n/a	chr2:34563007-34563016 chr2:34562980-34562988
44	FOS	chr2:34562894-34563146	MCF10A-Er-Src	breast:	n/a	chr2:34563007-34563016 chr2:34562980-34562988
45	FOS	chr2:34541924-34542181	MCF10A-Er-Src	breast:	n/a	chr2:34542046-34542054 chr2:34542044-34542056 chr2:34542047-34542054 chr2:34542045-34542055
46	FOS	chr2:34541985-34542214	MCF10A-Er-Src	breast:	n/a	chr2:34542046-34542054 chr2:34542044-34542056 chr2:34542047-34542054 chr2:34542045-34542055
47	FOXA1	chr2:34530777-34531034	T-47D	breast:	n/a	n/a
48	FOXA1	chr2:34598898-34599346	HepG2	liver:	n/a	chr2:34599104-34599119
49	FOXA1	chr2:34578562-34579166	HepG2	liver:	n/a	chr2:34578934-34578946
50	FOXA1	chr2:34552749-34552965	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34590591-34590641	MCF10A-Er-Src	breast:	n/a
2	chr2:34590591-34590641	HRE	kidney:	n/a
3	chr2:34590591-34590641	HEK293	kidney:	embryo
4	chr2:34590591-34590641	GM12878	blood:	n/a
5	chr2:34590591-34590641	HL-60	blood:	n/a
6	chr2:34590591-34590641	U87	brain:	n/a
7	chr2:34590591-34590641	HCT-116	colon:	n/a
8	chr2:34590591-34590641	MCF-7	breast:	n/a
9	chr2:34590591-34590641	AG09319	gingival:	n/a
10	chr2:34590591-34590641	Jurkat	blood:	n/a
11	chr2:34590591-34590641	K562	blood:	n/a
12	chr2:34590591-34590641	PrEC	prostate:	n/a
13	chr2:34590591-34590641	NT2-D1	testis:	n/a
14	chr2:34590591-34590641	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:34590591-34590641	RPTEC	kidney:	n/a
16	chr2:34590591-34590641	PANC-1	pancreas:	n/a
17	chr2:34590591-34590641	Caco-2	colon:	n/a
18	chr2:34590591-34590641	NHDF-neo	bronchial:	n/a
19	chr2:34590591-34590641	AG04450	lung:	fetal
20	chr2:34590591-34590641	SKMC	muscle:	n/a
21	chr2:34590591-34590641	HRPEpiC	eye:	n/a
22	chr2:34590591-34590641	AoSMC	blood vessel:	n/a
23	chr2:34590591-34590641	HCF	heart:	n/a
24	chr2:34590591-34590641	HNPCEpiC	eye:	n/a
25	chr2:34590591-34590641	PFSK-1	brain:	n/a
26	chr2:34590591-34590641	ovcar-3	ovarian:	n/a
27	chr2:34590591-34590641	AG10803	skin:	n/a
28	chr2:34590591-34590641	HEEpiC	esophagus:	n/a
29	chr2:34590591-34590641	ProgFib	skin:	n/a
30	chr2:34590591-34590641	HepG2	liver:	n/a
31	chr2:34590591-34590641	GM12891	blood:	n/a
32	chr2:34590591-34590641	HUVEC	blood vessel:	n/a
33	chr2:34590591-34590641	H1-hESC	embryonic stem cell:	embryo
34	chr2:34590591-34590641	HMEC	breast:	n/a
35	chr2:34590591-34590641	HCPEpiC	choroid plexus:	n/a
36	chr2:34590591-34590641	Hela-S3	cervix:	n/a
37	chr2:34590591-34590641	SK-N-SH	brain:	n/a
38	chr2:34590591-34590641	AG04449	skin:	fetal
39	chr2:34590591-34590641	Hepatocyte	liver:	n/a
40	chr2:34590591-34590641	LNCaP	prostate:	n/a
41	chr2:34590591-34590641	HAEpiC	amniotic membrane:	n/a
42	chr2:34590591-34590641	HIPEpiC	eye:	n/a
43	chr2:34590591-34590641	GM19239	blood:	n/a
44	chr2:34590591-34590641	SAEC	small airway:	n/a
45	chr2:34590591-34590641	HRCEpiC	kidney:	n/a
46	chr2:34590591-34590641	NB4	blood:	n/a
47	chr2:34590591-34590641	GM06990	blood:	n/a
48	chr2:34590591-34590641	NHBE	bronchial:	n/a
49	chr2:34590591-34590641	HCM	heart:	n/a
50	chr2:34590591-34590641	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
2	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
3	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
4	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:
5	chr2:34520994..34523413-chr2:34524356..34526580,2	MCF-7	breast:
6	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:

Variant related genes	Relation type
ENSG00000226785	TF binding region
ENSG00000226785	CpG island
ENSG00000258096	chromatin interactions
ENSG00000134294	chromatin interactions

Extended variants
information (count: 1275 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7592195	chr2:34528345-34528346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180935749	chr2:34528371-34528372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72786805	chr2:34528373-34528374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148134354	chr2:34528401-34528402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7592495	chr2:34528416-34528417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530800719	chr2:34528462-34528463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572696030	chr2:34528466-34528467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142026391	chr2:34528492-34528493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538045481	chr2:34528494-34528495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539933822	chr2:34528497-34528498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546357685	chr2:34528513-34528514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566353401	chr2:34528529-34528530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535297303	chr2:34528530-34528531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190249778	chr2:34528576-34528577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116887563	chr2:34528585-34528586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537440492	chr2:34528586-34528587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117348818	chr2:34528590-34528591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574344637	chr2:34536414-34536415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181131488	chr2:34536418-34536419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539313862	chr2:34536440-34536441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186028411	chr2:34536442-34536443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs60918451	chr2:34536455-34536456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190487359	chr2:34536459-34536460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551529072	chr2:34536480-34536481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565113634	chr2:34536500-34536501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56204539	chr2:34536531-34536532	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs202003255	chr2:34536534-34536535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79740583	chr2:34536563-34536564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375561917	chr2:34536565-34536566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560053880	chr2:34536571-34536572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567995489	chr2:34536574-34536575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536205100	chr2:34536576-34536577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183388133	chr2:34536577-34536578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571950341	chr2:34536595-34536596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550171399	chr2:34537218-34537219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186206797	chr2:34537223-34537224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1594836	chr2:34537236-34537237	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552694992	chr2:34537256-34537257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372884172	chr2:34537276-34537277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552526944	chr2:34537324-34537325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6146707	chr2:34537326-34537327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62163180	chr2:34537334-34537335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200218992	chr2:34537335-34537336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566213730	chr2:34537336-34537337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62163181	chr2:34537337-34537338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534473902	chr2:34537338-34537339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199782494	chr2:34537339-34537340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs67646541	chr2:34537349-34537350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367702737	chr2:34537352-34537353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199603797	chr2:34537353-34537354	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34528200-34528600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:34536400-34536600	Enhancers	HUVEC	blood vessel
3	chr2:34537200-34537400	Enhancers	HUVEC	blood vessel
4	chr2:34542000-34542400	Bivalent Enhancer	Fetal Heart	heart
5	chr2:34542400-34543600	Enhancers	Fetal Heart	heart
6	chr2:34549600-34550200	Bivalent Enhancer	Fetal Heart	heart
7	chr2:34553600-34560400	Weak transcription	Fetal Kidney	kidney
8	chr2:34556600-34556800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:34560400-34560800	Enhancers	Fetal Kidney	kidney
10	chr2:34570200-34571000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:34570200-34571000	Enhancers	Fetal Brain Female	brain
12	chr2:34570400-34570600	Enhancers	Fetal Heart	heart
13	chr2:34570400-34571200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:34571000-34571400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:34573400-34575400	Enhancers	Fetal Heart	heart
16	chr2:34578200-34579000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr2:34578400-34579200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:34578600-34579000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:34578600-34579400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:34578800-34579200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:34578800-34579200	Enhancers	Liver	Liver
22	chr2:34581600-34582000	Enhancers	Fetal Heart	heart
23	chr2:34584200-34584800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr2:34587400-34591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:34587800-34590000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:34587800-34590800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:34588000-34588600	Enhancers	Fetal Kidney	kidney
28	chr2:34588000-34590600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:34588000-34590800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr2:34588200-34588400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:34588200-34590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:34588400-34589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:34588600-34589000	Weak transcription	Fetal Kidney	kidney
34	chr2:34588800-34589000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr2:34588800-34589400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:34588800-34590800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:34589000-34589200	Enhancers	Fetal Kidney	kidney
38	chr2:34589000-34589600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:34589000-34589800	Enhancers	Colon Smooth Muscle	Colon
40	chr2:34589000-34590200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:34589000-34590800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:34589000-34592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:34589200-34589400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr2:34589200-34589400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:34589200-34589600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:34589200-34590800	Weak transcription	Fetal Kidney	kidney
47	chr2:34589200-34591200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:34589400-34590800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr2:34589400-34590800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr2:34589600-34590000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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