Variant report

Variant	nsv875781
Chromosome Location	chr2:212351667-212418110
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	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:212363575-212363885	H1-hESC	embryonic stem cell:	n/a	chr2:212363681-212363692
5	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
8	CEBPB	chr2:212357683-212357979	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
10	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
11	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
12	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
13	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:212368700-212368850	GM12868	blood:	n/a	n/a
15	CTCF	chr2:212368620-212368770	HepG2	liver:	n/a	n/a
16	CTCF	chr2:212368620-212368770	NHEK	skin:	n/a	n/a
17	CTCF	chr2:212368700-212368850	GM12864	blood:	n/a	n/a
18	CTCF	chr2:212368713-212368825	GM20000	blood:	n/a	n/a
19	CTCF	chr2:212368700-212368850	HAc	cerebellar:	n/a	n/a
20	CTCF	chr2:212368720-212368870	GM12878	blood:	n/a	n/a
21	CTCF	chr2:212368680-212368830	RPTEC	kidney:	n/a	n/a
22	CTCF	chr2:212368720-212368870	SAEC	small airway:	n/a	n/a
23	CTCF	chr2:212368691-212368854	HepG2	liver:	n/a	n/a
24	CTCF	chr2:212368620-212368770	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:212368680-212368830	GM12873	blood:	n/a	n/a
26	CTCF	chr2:212368720-212368870	GM12874	blood:	n/a	n/a
27	CTCF	chr2:212368700-212368850	GM12867	blood:	n/a	n/a
28	CTCF	chr2:212368640-212368790	HPF	lung:	n/a	n/a
29	CTCF	chr2:212387121-212387172	Medullo	brain:	n/a	n/a
30	CTCF	chr2:212368680-212368830	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:212368740-212368890	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr2:212368320-212368470	GM12873	blood:	n/a	n/a
33	CTCF	chr2:212368660-212368863	GM19240	blood:	n/a	n/a
34	CTCF	chr2:212368633-212368869	GM12892	blood:	n/a	n/a
35	CTCF	chr2:212368720-212368870	GM12865	blood:	n/a	n/a
36	CTCF	chr2:212368720-212368870	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:212368660-212368810	GM12801	blood:	n/a	n/a
38	CTCF	chr2:212368767-212368820	Medullo	brain:	n/a	n/a
39	CTCF	chr2:212368520-212368670	RPTEC	kidney:	n/a	n/a
40	CTCF	chr2:212368686-212368846	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:212368740-212368890	GM12870	blood:	n/a	n/a
42	CTCF	chr2:212368747-212368867	LNCaP	prostate:	n/a	n/a
43	CTCF	chr2:212368574-212368963	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:212368660-212368810	HL-60	blood:	n/a	n/a
45	CTCF	chr2:212368596-212368939	GM12878	blood:	n/a	n/a
46	CTCF	chr2:212368620-212368770	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr2:212368660-212368810	HMF	breast:	n/a	n/a
48	CTCF	chr2:212368720-212368870	NHEK	skin:	n/a	n/a
49	CTCF	chr2:212368700-212368850	GM12871	blood:	n/a	n/a
50	CTCF	chr2:212368681-212368872	GM19239	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212388373-212388423	HAEpiC	amniotic membrane:	n/a
2	chr2:212388373-212388423	SKMC	muscle:	n/a
3	chr2:212388373-212388423	AG10803	skin:	n/a
4	chr2:212389424-212389474	NT2-D1	testis:	n/a
5	chr2:212363715-212363765	AG10803	skin:	n/a
6	chr2:212363715-212363765	HRPEpiC	eye:	n/a
7	chr2:212388373-212388423	AG09319	gingival:	n/a
8	chr2:212389424-212389474	Jurkat	blood:	n/a
9	chr2:212389424-212389474	A549	lung:	n/a
10	chr2:212363715-212363765	ProgFib	skin:	n/a
11	chr2:212363715-212363765	NHBE	bronchial:	n/a
12	chr2:212363715-212363765	HIPEpiC	eye:	n/a
13	chr2:212363715-212363765	GM12878	blood:	n/a
14	chr2:212388373-212388423	NT2-D1	testis:	n/a
15	chr2:212389424-212389474	MCF10A-Er-Src	breast:	n/a
16	chr2:212363715-212363765	PFSK-1	brain:	n/a
17	chr2:212388373-212388423	PANC-1	pancreas:	n/a
18	chr2:212363715-212363765	HL-60	blood:	n/a
19	chr2:212363715-212363765	HRCEpiC	kidney:	n/a
20	chr2:212388373-212388423	NB4	blood:	n/a
21	chr2:212389424-212389474	BJ	skin:	n/a
22	chr2:212389424-212389474	HNPCEpiC	eye:	n/a
23	chr2:212363715-212363765	HRE	kidney:	n/a
24	chr2:212363715-212363765	GM12891	blood:	n/a
25	chr2:212389424-212389474	SK-N-SH	brain:	n/a
26	chr2:212388373-212388423	GM12891	blood:	n/a
27	chr2:212388373-212388423	BJ	skin:	n/a
28	chr2:212363715-212363765	NH-A	brain:	n/a
29	chr2:212363715-212363765	HCF	heart:	n/a
30	chr2:212389424-212389474	Caco-2	colon:	n/a
31	chr2:212388373-212388423	GM12878	blood:	n/a
32	chr2:212388373-212388423	MCF-7	breast:	n/a
33	chr2:212389424-212389474	IMR90	lung:	fetal
34	chr2:212363715-212363765	HEEpiC	esophagus:	n/a
35	chr2:212389424-212389474	U87	brain:	n/a
36	chr2:212389424-212389474	HEEpiC	esophagus:	n/a
37	chr2:212388373-212388423	PrEC	prostate:	n/a
38	chr2:212389424-212389474	K562	blood:	n/a
39	chr2:212388373-212388423	HUVEC	blood vessel:	n/a
40	chr2:212388373-212388423	HMEC	breast:	n/a
41	chr2:212363715-212363765	Caco-2	colon:	n/a
42	chr2:212388373-212388423	SK-N-SH_RA	brain:	n/a
43	chr2:212363715-212363765	HNPCEpiC	eye:	n/a
44	chr2:212363715-212363765	SK-N-SH_RA	brain:	n/a
45	chr2:212363715-212363765	HCM	heart:	n/a
46	chr2:212388373-212388423	ECC-1	luminal epithelium:	n/a
47	chr2:212363715-212363765	U87	brain:	n/a
48	chr2:212363715-212363765	HCT-116	colon:	n/a
49	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
50	chr2:212363715-212363765	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
2	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
3	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
4	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:
5	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
6	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
7	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
8	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
9	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
10	chr2:212288710..212290756-chr2:212380740..212383126,2	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: 2887 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2887 , 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	rs9941626	chr2:212351667-212351668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538581879	chr2:212351670-212351671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114440717	chr2:212351673-212351674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183124246	chr2:212351678-212351679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534166188	chr2:212351706-212351707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201552066	chr2:212351707-212351708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554172647	chr2:212351759-212351760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577288264	chr2:212351769-212351770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369389580	chr2:212351791-212351792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539873904	chr2:212351811-212351812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13020659	chr2:212351828-212351829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9941687	chr2:212351832-212351833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs9941688	chr2:212351843-212351844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541750877	chr2:212351845-212351846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111906571	chr2:212351862-212351863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9941562	chr2:212351870-212351871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs13020699	chr2:212351873-212351874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71422745	chr2:212351877-212351878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs9941563	chr2:212351885-212351886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs141201676	chr2:212351908-212351909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116526002	chr2:212351913-212351914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13020725	chr2:212351937-212351938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200623551	chr2:212351942-212351943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185424755	chr2:212351952-212351953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548931310	chr2:212351964-212351965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189940364	chr2:212351968-212351969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569402379	chr2:212351969-212351970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534464149	chr2:212351996-212351997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547476330	chr2:212352035-212352036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs67577312	chr2:212352061-212352062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs71397130	chr2:212352095-212352096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72933599	chr2:212352098-212352099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199530496	chr2:212352109-212352110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs59961819	chr2:212352112-212352113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576192005	chr2:212352200-212352201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535284085	chr2:212352220-212352221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573034240	chr2:212352224-212352225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555116580	chr2:212352248-212352249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572012955	chr2:212352249-212352250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112229997	chr2:212352289-212352290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146958517	chr2:212352324-212352325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs60523925	chr2:212352332-212352333	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543184163	chr2:212352344-212352345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113317514	chr2:212352356-212352357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563378184	chr2:212352392-212352393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75318016	chr2:212352401-212352402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200486224	chr2:212352423-212352424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149469826	chr2:212352505-212352506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144119983	chr2:212352515-212352516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74654817	chr2:212352518-212352519	Enhancers	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:118 , 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	chr2:212350400-212352400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:212352200-212353000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:212352200-212353000	Enhancers	Brain Angular Gyrus	brain
5	chr2:212352400-212352800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:212352400-212352800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:212352400-212352800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:212352400-212352800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:212352400-212353000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:212352400-212353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:212352400-212353000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:212352400-212353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:212352400-212353200	Enhancers	Brain Anterior Caudate	brain
14	chr2:212352400-212353200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr2:212352400-212353800	Enhancers	Brain Substantia Nigra	brain
16	chr2:212352600-212353000	Enhancers	Brain Hippocampus Middle	brain
17	chr2:212352800-212353000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:212352800-212362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:212353000-212363400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:212358600-212359200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:212358800-212359400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:212359200-212363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:212359400-212363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:212362000-212365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:212362200-212362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:212362200-212364000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:212362600-212363800	Enhancers	Brain Angular Gyrus	brain
28	chr2:212362800-212363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:212362800-212363800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:212362800-212363800	Enhancers	Brain Hippocampus Middle	brain
31	chr2:212362800-212368600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:212363200-212363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:212363200-212363800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:212363200-212363800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:212363200-212363800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr2:212363200-212364000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:212363200-212364000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr2:212363200-212364000	Enhancers	Brain Cingulate Gyrus	brain
39	chr2:212363200-212364000	Enhancers	Brain Substantia Nigra	brain
40	chr2:212363400-212363600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:212363400-212363800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:212363400-212363800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr2:212363400-212363800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr2:212363400-212363800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr2:212363400-212364000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:212363600-212363800	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:212363800-212364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr2:212363800-212364000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:212364000-212364400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:212364000-212364400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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