Variant report

Variant	nsv875780
Chromosome Location	chr2:212350245-212415948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:212363692-212363815	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
3	CEBPB	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
7	CEBPB	chr2:212363575-212363885	H1-hESC	embryonic stem cell:	n/a	chr2:212363681-212363692
8	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
9	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:212357683-212357979	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
12	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
13	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:212368720-212368870	GM12870	blood:	n/a	n/a
15	CTCF	chr2:212368687-212368856	K562	blood:	n/a	n/a
16	CTCF	chr2:212368700-212368850	GM12874	blood:	n/a	n/a
17	CTCF	chr2:212368683-212368861	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:212368720-212368870	HEK293	kidney:	n/a	n/a
19	CTCF	chr2:212368680-212368830	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr2:212368691-212368835	A549	lung:	n/a	n/a
21	CTCF	chr2:212406424-212406426	GM12878	blood:	n/a	n/a
22	CTCF	chr2:212368600-212368750	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr2:212368700-212368850	HAc	cerebellar:	n/a	n/a
24	CTCF	chr2:212368740-212368890	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr2:212368633-212368869	GM12892	blood:	n/a	n/a
26	CTCF	chr2:212368720-212368870	HCT-116	colon:	n/a	n/a
27	CTCF	chr2:212368680-212368830	GM12873	blood:	n/a	n/a
28	CTCF	chr2:212368720-212368870	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr2:212389640-212389790	BE2_C	brain:	n/a	n/a
30	CTCF	chr2:212368621-212368821	K562	blood:	n/a	n/a
31	CTCF	chr2:212368596-212368939	GM12878	blood:	n/a	n/a
32	CTCF	chr2:212368680-212368830	HEK293	kidney:	n/a	n/a
33	CTCF	chr2:212368720-212368870	GM12878	blood:	n/a	n/a
34	CTCF	chr2:212368640-212368790	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr2:212368691-212368854	HepG2	liver:	n/a	n/a
36	CTCF	chr2:212368680-212368830	HMF	breast:	n/a	n/a
37	CTCF	chr2:212368707-212368832	GM10248	blood:	n/a	n/a
38	CTCF	chr2:212368640-212368790	K562	blood:	n/a	n/a
39	CTCF	chr2:212368682-212368877	Gliobla	brain:	n/a	n/a
40	CTCF	chr2:212368700-212368850	GM12872	blood:	n/a	n/a
41	CTCF	chr2:212368720-212368870	GM12864	blood:	n/a	n/a
42	CTCF	chr2:212368649-212368893	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:212368740-212368890	HCFaa	heart:	n/a	n/a
44	CTCF	chr2:212368700-212368850	GM12871	blood:	n/a	n/a
45	CTCF	chr2:212368740-212368890	HRE	kidney:	n/a	n/a
46	CTCF	chr2:212368700-212368850	GM12868	blood:	n/a	n/a
47	CTCF	chr2:212368660-212368810	GM12801	blood:	n/a	n/a
48	CTCF	chr2:212368700-212368850	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr2:212368680-212368830	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr2:212354920-212355070	BE2_C	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212389424-212389474	Jurkat	blood:	n/a
2	chr2:212363715-212363765	HCF	heart:	n/a
3	chr2:212389424-212389474	GM12892	blood:	n/a
4	chr2:212363715-212363765	MCF10A-Er-Src	breast:	n/a
5	chr2:212388373-212388423	SK-N-MC	brain:	n/a
6	chr2:212363715-212363765	HRE	kidney:	n/a
7	chr2:212389424-212389474	BJ	skin:	n/a
8	chr2:212389424-212389474	IMR90	lung:	fetal
9	chr2:212388373-212388423	MCF-7	breast:	n/a
10	chr2:212389424-212389474	ProgFib	skin:	n/a
11	chr2:212363715-212363765	SK-N-SH	brain:	n/a
12	chr2:212388373-212388423	CMK	blood:	n/a
13	chr2:212388373-212388423	SAEC	small airway:	n/a
14	chr2:212389424-212389474	NH-A	brain:	n/a
15	chr2:212389424-212389474	HCT-116	colon:	n/a
16	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
17	chr2:212389424-212389474	HepG2	liver:	n/a
18	chr2:212388373-212388423	AG09309	skin:	n/a
19	chr2:212388373-212388423	NB4	blood:	n/a
20	chr2:212389424-212389474	PANC-1	pancreas:	n/a
21	chr2:212388373-212388423	HUVEC	blood vessel:	n/a
22	chr2:212388373-212388423	SKMC	muscle:	n/a
23	chr2:212363715-212363765	RPTEC	kidney:	n/a
24	chr2:212389424-212389474	AG04449	skin:	fetal
25	chr2:212363715-212363765	Jurkat	blood:	n/a
26	chr2:212363715-212363765	HCT-116	colon:	n/a
27	chr2:212389424-212389474	GM12878	blood:	n/a
28	chr2:212389424-212389474	HEK293	kidney:	embryo
29	chr2:212363715-212363765	GM06990	blood:	n/a
30	chr2:212388373-212388423	PANC-1	pancreas:	n/a
31	chr2:212388373-212388423	HepG2	liver:	n/a
32	chr2:212363715-212363765	AG09309	skin:	n/a
33	chr2:212388373-212388423	Hela-S3	cervix:	n/a
34	chr2:212363715-212363765	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:212388373-212388423	HL-60	blood:	n/a
36	chr2:212389424-212389474	AG09319	gingival:	n/a
37	chr2:212388373-212388423	HRPEpiC	eye:	n/a
38	chr2:212363715-212363765	U87	brain:	n/a
39	chr2:212388373-212388423	ovcar-3	ovarian:	n/a
40	chr2:212389424-212389474	HL-60	blood:	n/a
41	chr2:212363715-212363765	ECC-1	luminal epithelium:	n/a
42	chr2:212363715-212363765	SAEC	small airway:	n/a
43	chr2:212388373-212388423	AG09319	gingival:	n/a
44	chr2:212363715-212363765	MCF-7	breast:	n/a
45	chr2:212363715-212363765	HRPEpiC	eye:	n/a
46	chr2:212363715-212363765	HNPCEpiC	eye:	n/a
47	chr2:212389424-212389474	GM06990	blood:	n/a
48	chr2:212389424-212389474	LNCaP	prostate:	n/a
49	chr2:212388373-212388423	AG04449	skin:	fetal
50	chr2:212389424-212389474	SK-N-SH	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
2	chr2:212288710..212290756-chr2:212380740..212383126,2	MCF-7	breast:
3	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
4	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
5	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
6	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
7	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:
8	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
9	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
10	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP119	TF binding region
RNA5SP119	CpG island
ENSG00000159388	chromatin interactions
ENSG00000233791	chromatin interactions

Extended variants
information (count: 2855 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2855 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13021324	chr2:212350245-212350246	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544721886	chr2:212350294-212350295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561354233	chr2:212350338-212350339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12995574	chr2:212350341-212350342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536298195	chr2:212350371-212350372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373251737	chr2:212350406-212350407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190104933	chr2:212350446-212350447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566442424	chr2:212350447-212350448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560345653	chr2:212350448-212350449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12995615	chr2:212350489-212350490	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs13021911	chr2:212350497-212350498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568879201	chr2:212350499-212350500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34675508	chr2:212350582-212350583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199816954	chr2:212350587-212350588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs36112233	chr2:212350588-212350589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548414117	chr2:212350589-212350590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537418893	chr2:212350590-212350591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538905240	chr2:212350601-212350602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181408776	chr2:212350617-212350618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545494542	chr2:212350622-212350623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557530299	chr2:212350633-212350634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12989822	chr2:212350641-212350642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs559020062	chr2:212350649-212350650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553153856	chr2:212350706-212350707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543071206	chr2:212350715-212350716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566683093	chr2:212350740-212350741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184802394	chr2:212350742-212350743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558965279	chr2:212350799-212350800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575630166	chr2:212350833-212350834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370272757	chr2:212350836-212350837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373719147	chr2:212350844-212350845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13013923	chr2:212350863-212350864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs540693989	chr2:212350915-212350916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572928392	chr2:212350929-212350930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188472095	chr2:212350932-212350933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143716700	chr2:212350978-212350979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180849412	chr2:212351126-212351127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185152268	chr2:212351166-212351167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531598859	chr2:212351176-212351177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34631772	chr2:212351185-212351186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567672231	chr2:212351186-212351187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115268559	chr2:212351201-212351202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547087789	chr2:212351206-212351207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79107438	chr2:212351229-212351230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538842978	chr2:212351236-212351237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374318692	chr2:212351302-212351303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538486215	chr2:212351314-212351315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35330898	chr2:212351335-212351336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574879597	chr2:212351341-212351342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189480620	chr2:212351352-212351353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
Breast cancer	17603634	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
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
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	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
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212347000-212352400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:212350000-212350400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:212350400-212352400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:212352200-212353000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:212352200-212353000	Enhancers	Brain Angular Gyrus	brain
6	chr2:212352400-212352800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:212352400-212352800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:212352400-212352800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:212352400-212352800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:212352400-212353000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:212352400-212353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:212352400-212353000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:212352400-212353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:212352400-212353200	Enhancers	Brain Anterior Caudate	brain
15	chr2:212352400-212353200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr2:212352400-212353800	Enhancers	Brain Substantia Nigra	brain
17	chr2:212352600-212353000	Enhancers	Brain Hippocampus Middle	brain
18	chr2:212352800-212353000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:212352800-212362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:212353000-212363400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:212358600-212359200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:212358800-212359400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:212359200-212363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr2:212359400-212363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:212362000-212365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:212362200-212362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:212362200-212364000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:212362600-212363800	Enhancers	Brain Angular Gyrus	brain
29	chr2:212362800-212363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:212362800-212363800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:212362800-212363800	Enhancers	Brain Hippocampus Middle	brain
32	chr2:212362800-212368600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:212363200-212363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr2:212363200-212363800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr2:212363200-212363800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:212363200-212363800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr2:212363200-212364000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr2:212363200-212364000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:212363200-212364000	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:212363200-212364000	Enhancers	Brain Substantia Nigra	brain
41	chr2:212363400-212363600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:212363400-212363800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:212363400-212363800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr2:212363400-212363800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:212363400-212363800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:212363400-212364000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr2:212363600-212363800	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:212363800-212364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr2:212363800-212364000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr2:212364000-212364400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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