Variant report

Variant	nsv875779
Chromosome Location	chr2:212340740-212415948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

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	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:212357683-212357979	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	chr2:212342586-212342717	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:212341207-212341417	HepG2	liver:	n/a	chr2:212341327-212341338
7	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
8	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
10	CEBPB	chr2:212342461-212342725	A549	lung:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
11	CEBPB	chr2:212342377-212343109	HepG2	liver:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
12	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
13	CEBPB	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
15	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
16	CEBPB	chr2:212342486-212342714	IMR90	lung:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
17	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
18	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:212368720-212368870	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:212368720-212368870	AG09309	skin:	n/a	n/a
21	CTCF	chr2:212368694-212368843	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:212368720-212368870	GM12864	blood:	n/a	n/a
23	CTCF	chr2:212368700-212368850	A549	lung:	n/a	n/a
24	CTCF	chr2:212368740-212368890	HCFaa	heart:	n/a	n/a
25	CTCF	chr2:212368640-212368790	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr2:212368621-212368821	K562	blood:	n/a	n/a
27	CTCF	chr2:212368720-212368870	GM12870	blood:	n/a	n/a
28	CTCF	chr2:212368640-212368790	GM12878	blood:	n/a	n/a
29	CTCF	chr2:212368675-212368892	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr2:212368700-212368850	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr2:212368683-212368858	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:212368680-212368830	HMF	breast:	n/a	n/a
33	CTCF	chr2:212368637-212368886	GM19238	blood:	n/a	n/a
34	CTCF	chr2:212368700-212368850	GM12868	blood:	n/a	n/a
35	CTCF	chr2:212368720-212368870	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr2:212368720-212368870	GM12865	blood:	n/a	n/a
37	CTCF	chr2:212368680-212368830	BE2_C	brain:	n/a	n/a
38	CTCF	chr2:212368640-212368790	K562	blood:	n/a	n/a
39	CTCF	chr2:212368640-212368790	HPF	lung:	n/a	n/a
40	CTCF	chr2:212368683-212368861	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:212368750-212368829	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr2:212368660-212368810	HL-60	blood:	n/a	n/a
43	CTCF	chr2:212368660-212368810	GM12868	blood:	n/a	n/a
44	CTCF	chr2:212368707-212368832	GM10248	blood:	n/a	n/a
45	CTCF	chr2:212368720-212368870	NHEK	skin:	n/a	n/a
46	CTCF	chr2:212354920-212355070	BE2_C	brain:	n/a	n/a
47	CTCF	chr2:212368640-212368790	HMEC	breast:	n/a	n/a
48	CTCF	chr2:212368700-212368850	HAc	cerebellar:	n/a	n/a
49	CTCF	chr2:212368767-212368820	Medullo	brain:	n/a	n/a
50	CTCF	chr2:212368678-212368869	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212363715-212363765	Caco-2	colon:	n/a
2	chr2:212388373-212388423	HCF	heart:	n/a
3	chr2:212363715-212363765	AG09319	gingival:	n/a
4	chr2:212389424-212389474	HIPEpiC	eye:	n/a
5	chr2:212388373-212388423	ovcar-3	ovarian:	n/a
6	chr2:212363715-212363765	NT2-D1	testis:	n/a
7	chr2:212389424-212389474	ProgFib	skin:	n/a
8	chr2:212363715-212363765	AG10803	skin:	n/a
9	chr2:212388373-212388423	HUVEC	blood vessel:	n/a
10	chr2:212389424-212389474	ovcar-3	ovarian:	n/a
11	chr2:212388373-212388423	SK-N-SH_RA	brain:	n/a
12	chr2:212389424-212389474	LNCaP	prostate:	n/a
13	chr2:212389424-212389474	AG04450	lung:	fetal
14	chr2:212389424-212389474	AG09319	gingival:	n/a
15	chr2:212389424-212389474	BJ	skin:	n/a
16	chr2:212363715-212363765	HCM	heart:	n/a
17	chr2:212389424-212389474	IMR90	lung:	fetal
18	chr2:212389424-212389474	AG09309	skin:	n/a
19	chr2:212363715-212363765	HEEpiC	esophagus:	n/a
20	chr2:212388373-212388423	AG04450	lung:	fetal
21	chr2:212388373-212388423	CMK	blood:	n/a
22	chr2:212388373-212388423	BJ	skin:	n/a
23	chr2:212363715-212363765	HAEpiC	amniotic membrane:	n/a
24	chr2:212388373-212388423	Jurkat	blood:	n/a
25	chr2:212388373-212388423	U87	brain:	n/a
26	chr2:212389424-212389474	ECC-1	luminal epithelium:	n/a
27	chr2:212389424-212389474	HEEpiC	esophagus:	n/a
28	chr2:212388373-212388423	NB4	blood:	n/a
29	chr2:212363715-212363765	K562	blood:	n/a
30	chr2:212388373-212388423	NH-A	brain:	n/a
31	chr2:212388373-212388423	HEK293	kidney:	embryo
32	chr2:212363715-212363765	HRPEpiC	eye:	n/a
33	chr2:212363715-212363765	ECC-1	luminal epithelium:	n/a
34	chr2:212363715-212363765	Jurkat	blood:	n/a
35	chr2:212388373-212388423	RPTEC	kidney:	n/a
36	chr2:212388373-212388423	HAEpiC	amniotic membrane:	n/a
37	chr2:212389424-212389474	HMEC	breast:	n/a
38	chr2:212363715-212363765	SAEC	small airway:	n/a
39	chr2:212388373-212388423	AoSMC	blood vessel:	n/a
40	chr2:212389424-212389474	RPTEC	kidney:	n/a
41	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
42	chr2:212363715-212363765	HCF	heart:	n/a
43	chr2:212389424-212389474	Hepatocyte	liver:	n/a
44	chr2:212389424-212389474	A549	lung:	n/a
45	chr2:212389424-212389474	SK-N-MC	brain:	n/a
46	chr2:212363715-212363765	BE2_C	brain:	n/a
47	chr2:212388373-212388423	BE2_C	brain:	n/a
48	chr2:212363715-212363765	Hepatocyte	liver:	n/a
49	chr2:212388373-212388423	HCT-116	colon:	n/a
50	chr2:212389424-212389474	HNPCEpiC	eye:	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	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:
3	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
4	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
5	chr2:212288710..212290756-chr2:212380740..212383126,2	MCF-7	breast:
6	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
7	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
8	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
9	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
10	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:

No data

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

Extended variants
information (count: 3213 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3213 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13030346	chr2:212340740-212340741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116410062	chr2:212340821-212340822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556888003	chr2:212340848-212340849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570082588	chr2:212340863-212340864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529403121	chr2:212340915-212340916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547882786	chr2:212340920-212340921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566156705	chr2:212340950-212340951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535462927	chr2:212340989-212340990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555864246	chr2:212340999-212341000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572464878	chr2:212341004-212341005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533398742	chr2:212341015-212341016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376489523	chr2:212341043-212341044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551790209	chr2:212341051-212341052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569981413	chr2:212341075-212341076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541488589	chr2:212341091-212341092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557535007	chr2:212341093-212341094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577376134	chr2:212341095-212341096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371188961	chr2:212341150-212341151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563239238	chr2:212341196-212341197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111820088	chr2:212341199-212341200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536903359	chr2:212341234-212341235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528910193	chr2:212341238-212341239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542239575	chr2:212341286-212341287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559264535	chr2:212341296-212341297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371822953	chr2:212341306-212341307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397987658	chr2:212341307-212341308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191181446	chr2:212341348-212341349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551447145	chr2:212341403-212341404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145166881	chr2:212341407-212341408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199627516	chr2:212341421-212341422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528977981	chr2:212341453-212341454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575834696	chr2:212341462-212341463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533566495	chr2:212341518-212341519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180882090	chr2:212341526-212341527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114993299	chr2:212341655-212341656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536113368	chr2:212341676-212341677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116181210	chr2:212341678-212341679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115178473	chr2:212341763-212341764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185896039	chr2:212341807-212341808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557820682	chr2:212341863-212341864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577461661	chr2:212341913-212341914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536828124	chr2:212341967-212341968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557254196	chr2:212341992-212341993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145801142	chr2:212342023-212342024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192034420	chr2:212342038-212342039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146542040	chr2:212342039-212342040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542877226	chr2:212342077-212342078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559087716	chr2:212342089-212342090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555548394	chr2:212342095-212342096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142193404	chr2:212342109-212342110	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:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212333800-212343400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:212338600-212342800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:212342800-212344600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:212344600-212346400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:212346400-212346600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:212346600-212346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:212346800-212347000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:212347000-212347200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:212347000-212352400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:212347200-212350000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:212348400-212348600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:212350000-212350400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:212350400-212352400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:212352200-212353000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:212352200-212353000	Enhancers	Brain Angular Gyrus	brain
16	chr2:212352400-212352800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:212352400-212352800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:212352400-212352800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:212352400-212352800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:212352400-212353000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:212352400-212353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:212352400-212353000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr2:212352400-212353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:212352400-212353200	Enhancers	Brain Anterior Caudate	brain
25	chr2:212352400-212353200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:212352400-212353800	Enhancers	Brain Substantia Nigra	brain
27	chr2:212352600-212353000	Enhancers	Brain Hippocampus Middle	brain
28	chr2:212352800-212353000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:212352800-212362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:212353000-212363400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:212358600-212359200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:212358800-212359400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:212359200-212363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:212359400-212363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:212362000-212365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:212362200-212362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:212362200-212364000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:212362600-212363800	Enhancers	Brain Angular Gyrus	brain
39	chr2:212362800-212363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:212362800-212363800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:212362800-212363800	Enhancers	Brain Hippocampus Middle	brain
42	chr2:212362800-212368600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:212363200-212363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:212363200-212363800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:212363200-212363800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr2:212363200-212363800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr2:212363200-212364000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr2:212363200-212364000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr2:212363200-212364000	Enhancers	Brain Cingulate Gyrus	brain
50	chr2:212363200-212364000	Enhancers	Brain Substantia Nigra	brain

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