Variant report

Variant	nsv875537
Chromosome Location	chr2:186336529-186422662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:289)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
3	BCL3	chr2:186338970-186339324	GM12878	blood:	n/a	n/a
4	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
5	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
6	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
8	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
10	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
11	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
13	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
14	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:186387200-186387350	A549	lung:	n/a	n/a
16	CTCF	chr2:186411871-186411904	Medullo	brain:	n/a	n/a
17	CTCF	chr2:186387260-186387410	GM12864	blood:	n/a	n/a
18	CTCF	chr2:186387300-186387450	HepG2	liver:	n/a	n/a
19	CTCF	chr2:186340700-186340850	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:186340680-186340830	Caco-2	colon:	n/a	n/a
21	CTCF	chr2:186387260-186387410	GM06990	blood:	n/a	n/a
22	CTCF	chr2:186387201-186387561	GM12878	blood:	n/a	n/a
23	CTCF	chr2:186387322-186387485	LNCaP	prostate:	n/a	n/a
24	CTCF	chr2:186340740-186340890	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr2:186387380-186387530	GM12875	blood:	n/a	n/a
26	CTCF	chr2:186387300-186387450	GM06990	blood:	n/a	n/a
27	CTCF	chr2:186340680-186340830	HCT-116	colon:	n/a	n/a
28	CTCF	chr2:186340660-186340810	NHEK	skin:	n/a	n/a
29	CTCF	chr2:186394437-186394585	GM12878	blood:	n/a	n/a
30	CTCF	chr2:186387260-186387410	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr2:186387260-186387410	SAEC	small airway:	n/a	n/a
32	CTCF	chr2:186387360-186387510	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr2:186387320-186387470	GM12864	blood:	n/a	n/a
34	CTCF	chr2:186387244-186387623	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:186387360-186387510	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr2:186387320-186387470	HMEC	breast:	n/a	n/a
37	CTCF	chr2:186340680-186340830	NHEK	skin:	n/a	n/a
38	CTCF	chr2:186387320-186387470	GM12874	blood:	n/a	n/a
39	CTCF	chr2:186347614-186347651	NHEK	skin:	n/a	n/a
40	CTCF	chr2:186340640-186340790	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:186387260-186387410	GM12865	blood:	n/a	n/a
42	CTCF	chr2:186387308-186387447	GM12878	blood:	n/a	n/a
43	CTCF	chr2:186387352-186387400	GM10266	blood:	n/a	n/a
44	CTCF	chr2:186340640-186340790	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr2:186340780-186340930	HRE	kidney:	n/a	n/a
46	CTCF	chr2:186387280-186387430	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:186387280-186387430	GM12872	blood:	n/a	n/a
48	CTCF	chr2:186387305-186387478	Medullo	brain:	n/a	n/a
49	CTCF	chr2:186387272-186387522	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:186340620-186340770	HRE	kidney:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412305-186412355	HCM	heart:	n/a
2	chr2:186412305-186412355	HCM	heart:	n/a
3	chr2:186412305-186412355	Hela-S3	cervix:	n/a
4	chr2:186412612-186412662	SAEC	small airway:	n/a
5	chr2:186412612-186412662	GM12891	blood:	n/a
6	chr2:186412612-186412662	GM12878	blood:	n/a
7	chr2:186412305-186412355	GM19239	blood:	n/a
8	chr2:186412073-186412123	T-47D	breast:	n/a
9	chr2:186412612-186412662	GM19239	blood:	n/a
10	chr2:186412305-186412355	AG10803	skin:	n/a
11	chr2:186412073-186412123	HAEpiC	amniotic membrane:	n/a
12	chr2:186412612-186412662	HAEpiC	amniotic membrane:	n/a
13	chr2:186412612-186412662	HCM	heart:	n/a
14	chr2:186412073-186412123	CMK	blood:	n/a
15	chr2:186412612-186412662	HCT-116	colon:	n/a
16	chr2:186412612-186412662	HNPCEpiC	eye:	n/a
17	chr2:186412073-186412123	HUVEC	blood vessel:	n/a
18	chr2:186412612-186412662	NT2-D1	testis:	n/a
19	chr2:186412305-186412355	BE2_C	brain:	n/a
20	chr2:186412612-186412662	HRPEpiC	eye:	n/a
21	chr2:186412612-186412662	HIPEpiC	eye:	n/a
22	chr2:186412612-186412662	BE2_C	brain:	n/a
23	chr2:186412612-186412662	HCPEpiC	choroid plexus:	n/a
24	chr2:186412612-186412662	U87	brain:	n/a
25	chr2:186412073-186412123	Hela-S3	cervix:	n/a
26	chr2:186412305-186412355	HMEC	breast:	n/a
27	chr2:186412305-186412355	Jurkat	blood:	n/a
28	chr2:186412073-186412123	HMEC	breast:	n/a
29	chr2:186412612-186412662	RPTEC	kidney:	n/a
30	chr2:186412073-186412123	MCF-7	breast:	n/a
31	chr2:186412305-186412355	NHBE	bronchial:	n/a
32	chr2:186412305-186412355	MCF-7	breast:	n/a
33	chr2:186412073-186412123	NB4	blood:	n/a
34	chr2:186412073-186412123	AG09319	gingival:	n/a
35	chr2:186412612-186412662	MCF-7	breast:	n/a
36	chr2:186412305-186412355	Caco-2	colon:	n/a
37	chr2:186412073-186412123	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:186412073-186412123	PFSK-1	brain:	n/a
39	chr2:186412305-186412355	PFSK-1	brain:	n/a
40	chr2:186412073-186412123	GM06990	blood:	n/a
41	chr2:186412612-186412662	NHBE	bronchial:	n/a
42	chr2:186412073-186412123	PANC-1	pancreas:	n/a
43	chr2:186412305-186412355	HRPEpiC	eye:	n/a
44	chr2:186412073-186412123	HNPCEpiC	eye:	n/a
45	chr2:186412073-186412123	AoSMC	blood vessel:	n/a
46	chr2:186412612-186412662	K562	blood:	n/a
47	chr2:186412073-186412123	BJ	skin:	n/a
48	chr2:186412073-186412123	GM12878	blood:	n/a
49	chr2:186412073-186412123	SK-N-SH_RA	brain:	n/a
50	chr2:186412305-186412355	T-47D	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
2	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
3	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
4	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
5	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
6	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
7	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
8	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
9	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
10	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
11	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:
12	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
13	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
14	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
15	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
2	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
3	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
4	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
5	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
6	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
7	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
8	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962
9	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
10	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
11	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
12	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
13	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
14	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000188738	chromatin interactions
ENSG00000226747	chromatin interactions

Extended variants
information (count: 3092 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3092 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs731374	chr2:186336529-186336530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527432014	chr2:186336599-186336600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549091082	chr2:186336604-186336605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374646040	chr2:186336628-186336629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185678360	chr2:186336655-186336656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537827318	chr2:186336656-186336657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35518949	chr2:186336657-186336658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3054725	chr2:186336663-186336664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201748042	chr2:186336665-186336666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72894499	chr2:186336720-186336721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373231132	chr2:186336762-186336763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190688818	chr2:186336803-186336804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193041723	chr2:186336857-186336858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571904678	chr2:186336971-186336972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571749891	chr2:186337005-186337006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34107286	chr2:186337022-186337023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548253851	chr2:186337035-186337036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542554787	chr2:186337042-186337043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555029266	chr2:186337057-186337058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576384468	chr2:186337108-186337109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146987626	chr2:186337111-186337112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543768422	chr2:186337112-186337113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374212948	chr2:186337116-186337117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs202082382	chr2:186337128-186337129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558999591	chr2:186337182-186337183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184482403	chr2:186337230-186337231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541745669	chr2:186337234-186337235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372402011	chr2:186337309-186337310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12473280	chr2:186337313-186337314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79577526	chr2:186337317-186337318	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs531366931	chr2:186337327-186337328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542773711	chr2:186337335-186337336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371233534	chr2:186337359-186337360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561010639	chr2:186337360-186337361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12477524	chr2:186337430-186337431	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76278036	chr2:186337432-186337433	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549709738	chr2:186337488-186337489	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72894502	chr2:186337499-186337500	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375485182	chr2:186337563-186337564	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188133727	chr2:186337568-186337569	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547279004	chr2:186337598-186337599	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565572038	chr2:186337603-186337604	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371849729	chr2:186337649-186337650	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375798984	chr2:186337661-186337662	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113708147	chr2:186337681-186337682	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554785772	chr2:186337694-186337695	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1345931	chr2:186337702-186337703	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs537056295	chr2:186337728-186337729	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79833693	chr2:186337739-186337740	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs577304016	chr2:186337749-186337750	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Autism	22543975	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186314400-186345200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:186317000-186337400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:186321400-186358600	Weak transcription	HMEC	breast
4	chr2:186331800-186337400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:186331800-186342000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:186332600-186340800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:186336200-186337400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:186336200-186340800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:186337400-186337600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr2:186337400-186337600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:186337400-186338800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:186337400-186339200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:186337400-186339200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:186337400-186340800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr2:186337600-186337800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:186337600-186337800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
17	chr2:186337600-186338600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:186337600-186339000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:186337600-186340600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr2:186337800-186340800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:186338600-186338800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr2:186338600-186340800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:186338800-186339200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:186338800-186341000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:186339000-186339200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:186339200-186339600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr2:186339200-186339800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:186339200-186347600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:186339200-186358400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:186339200-186358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:186340200-186340800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:186340600-186341000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr2:186340600-186341600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr2:186340600-186343800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:186340800-186341200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:186340800-186341200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:186340800-186341400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr2:186340800-186341400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:186340800-186342200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr2:186340800-186342200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr2:186340800-186342200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:186340800-186344000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr2:186341000-186341200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr2:186341000-186342000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:186341000-186343800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:186341200-186343000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:186341200-186349600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:186341400-186341800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr2:186341400-186342400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr2:186341600-186342000	Weak transcription	H1 Cell Line	embryonic stem cell

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