Variant report

Variant	nsv875539
Chromosome Location	chr2:186345148-186475590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
2	CBX3	chr2:186447981-186448661	HCT-116	colon:	n/a	n/a
3	CBX3	chr2:186447908-186448538	HCT-116	colon:	n/a	n/a
4	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
5	CEBPB	chr2:186448119-186448613	MCF-7	breast:	n/a	n/a
6	CEBPB	chr2:186448143-186448675	HCT-116	colon:	n/a	n/a
7	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
8	CEBPB	chr2:186447957-186448588	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:186448257-186448516	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:186465657-186465842	A549	lung:	n/a	n/a
11	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
12	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:186448052-186448719	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
17	CEBPB	chr2:186448257-186448571	A549	lung:	n/a	n/a
18	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
19	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
20	CEBPB	chr2:186448144-186448607	MCF-7	breast:	n/a	n/a
21	CEBPB	chr2:186448129-186448586	A549	lung:	n/a	n/a
22	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
23	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
24	CHD2	chr2:186448192-186448572	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:186473681-186473750	MCF-7	breast:	n/a	chr2:186473696-186473704
27	CTCF	chr2:186473660-186473810	GM12872	blood:	n/a	chr2:186473696-186473704
28	CTCF	chr2:186473660-186473810	SK-N-SH_RA	brain:	n/a	chr2:186473696-186473704
29	CTCF	chr2:186387280-186387430	HRE	kidney:	n/a	n/a
30	CTCF	chr2:186455420-186455486	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr2:186473608-186473805	HepG2	liver:	n/a	chr2:186473696-186473704
32	CTCF	chr2:186473620-186473770	SK-N-SH_RA	brain:	n/a	chr2:186473696-186473704
33	CTCF	chr2:186473560-186473710	HEEpiC	esophagus:	n/a	chr2:186473696-186473704
34	CTCF	chr2:186387320-186387470	GM12874	blood:	n/a	n/a
35	CTCF	chr2:186473640-186473790	BE2_C	brain:	n/a	chr2:186473696-186473704
36	CTCF	chr2:186387260-186387410	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr2:186388999-186389045	LNCaP	prostate:	n/a	n/a
38	CTCF	chr2:186387220-186387370	GM12865	blood:	n/a	n/a
39	CTCF	chr2:186387331-186387451	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr2:186381425-186381497	Medullo	brain:	n/a	n/a
41	CTCF	chr2:186347600-186347681	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:186387260-186387410	GM12869	blood:	n/a	n/a
43	CTCF	chr2:186473640-186473790	HRE	kidney:	n/a	chr2:186473696-186473704
44	CTCF	chr2:186473685-186473776	GM12878	blood:	n/a	chr2:186473696-186473704
45	CTCF	chr2:186387300-186387450	GM06990	blood:	n/a	n/a
46	CTCF	chr2:186387352-186387400	GM10266	blood:	n/a	n/a
47	CTCF	chr2:186387200-186387350	A549	lung:	n/a	n/a
48	CTCF	chr2:186387360-186387510	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr2:186411005-186411020	GM10248	blood:	n/a	n/a
50	CTCF	chr2:186473680-186473830	A549	lung:	n/a	chr2:186473696-186473704

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186443903-186443953	H1-hESC	embryonic stem cell:	embryo
2	chr2:186412305-186412355	SKMC	muscle:	n/a
3	chr2:186412073-186412123	AG04449	skin:	fetal
4	chr2:186412073-186412123	SKMC	muscle:	n/a
5	chr2:186412073-186412123	HAEpiC	amniotic membrane:	n/a
6	chr2:186443903-186443953	NHDF-neo	bronchial:	n/a
7	chr2:186412073-186412123	BE2_C	brain:	n/a
8	chr2:186412305-186412355	K562	blood:	n/a
9	chr2:186443903-186443953	NB4	blood:	n/a
10	chr2:186443903-186443953	BE2_C	brain:	n/a
11	chr2:186443903-186443953	Hela-S3	cervix:	n/a
12	chr2:186443903-186443953	SKMC	muscle:	n/a
13	chr2:186412612-186412662	HRCEpiC	kidney:	n/a
14	chr2:186412073-186412123	T-47D	breast:	n/a
15	chr2:186412073-186412123	SK-N-SH	brain:	n/a
16	chr2:186412073-186412123	RPTEC	kidney:	n/a
17	chr2:186443903-186443953	HCF	heart:	n/a
18	chr2:186412305-186412355	HCT-116	colon:	n/a
19	chr2:186412305-186412355	MCF10A-Er-Src	breast:	n/a
20	chr2:186412073-186412123	HCM	heart:	n/a
21	chr2:186443903-186443953	NT2-D1	testis:	n/a
22	chr2:186443903-186443953	AG09319	gingival:	n/a
23	chr2:186412305-186412355	Hepatocyte	liver:	n/a
24	chr2:186443903-186443953	AG04449	skin:	fetal
25	chr2:186412612-186412662	GM19239	blood:	n/a
26	chr2:186412612-186412662	HCT-116	colon:	n/a
27	chr2:186412073-186412123	AoSMC	blood vessel:	n/a
28	chr2:186412073-186412123	AG04450	lung:	fetal
29	chr2:186412305-186412355	SK-N-MC	brain:	n/a
30	chr2:186443903-186443953	GM19239	blood:	n/a
31	chr2:186412073-186412123	HEK293	kidney:	embryo
32	chr2:186412612-186412662	PANC-1	pancreas:	n/a
33	chr2:186412305-186412355	NT2-D1	testis:	n/a
34	chr2:186412305-186412355	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:186412612-186412662	U87	brain:	n/a
36	chr2:186443903-186443953	HRPEpiC	eye:	n/a
37	chr2:186443903-186443953	LNCaP	prostate:	n/a
38	chr2:186412612-186412662	LNCaP	prostate:	n/a
39	chr2:186443903-186443953	HCT-116	colon:	n/a
40	chr2:186412305-186412355	ECC-1	luminal epithelium:	n/a
41	chr2:186412305-186412355	GM12892	blood:	n/a
42	chr2:186412612-186412662	NB4	blood:	n/a
43	chr2:186443903-186443953	BJ	skin:	n/a
44	chr2:186412073-186412123	ProgFib	skin:	n/a
45	chr2:186412073-186412123	GM19239	blood:	n/a
46	chr2:186412305-186412355	SK-N-SH	brain:	n/a
47	chr2:186443903-186443953	RPTEC	kidney:	n/a
48	chr2:186412612-186412662	Hepatocyte	liver:	n/a
49	chr2:186412073-186412123	HRE	kidney:	n/a
50	chr2:186443903-186443953	HepG2	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
2	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
3	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
4	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
5	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
6	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
7	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
8	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
9	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
10	chr2:186473268..186473794-chr2:186603435..186603983,2	MCF-7	breast:
11	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
12	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 4703 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4703 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11675192	chr2:186345148-186345149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570015616	chr2:186345235-186345236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537447876	chr2:186345250-186345251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71405629	chr2:186345262-186345263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72125659	chr2:186345263-186345264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147875787	chr2:186345270-186345271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552654025	chr2:186345292-186345293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs60386699	chr2:186345294-186345295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35420495	chr2:186345295-186345296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367791799	chr2:186345341-186345342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570851174	chr2:186345342-186345343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148150910	chr2:186345361-186345362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553369652	chr2:186345378-186345379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577627591	chr2:186345418-186345419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535638802	chr2:186345570-186345571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35885633	chr2:186345605-186345606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187445156	chr2:186345610-186345611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575685201	chr2:186345629-186345630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543109861	chr2:186345659-186345660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80046362	chr2:186345683-186345684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576412395	chr2:186345713-186345714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34492105	chr2:186345714-186345715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140190972	chr2:186345766-186345767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146963995	chr2:186345786-186345787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375468492	chr2:186345819-186345820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192934460	chr2:186345842-186345843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541615870	chr2:186345844-186345845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563472850	chr2:186345857-186345858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547050289	chr2:186345863-186345864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552688855	chr2:186345866-186345867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369623819	chr2:186345888-186345889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528449422	chr2:186345963-186345964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543082887	chr2:186345979-186345980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561483961	chr2:186345988-186345989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547288351	chr2:186346104-186346105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184740819	chr2:186346152-186346153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536049946	chr2:186346183-186346184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565786204	chr2:186346246-186346247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573734418	chr2:186346275-186346276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569096244	chr2:186346276-186346277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114007209	chr2:186346299-186346300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558205828	chr2:186346360-186346361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376117276	chr2:186346524-186346525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567634437	chr2:186346536-186346537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60161170	chr2:186346574-186346575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369932237	chr2:186346656-186346657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137888116	chr2:186346660-186346661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368929115	chr2:186346696-186346697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540630463	chr2:186346755-186346756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553237261	chr2:186346810-186346811	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:226 , 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	chr2:186321400-186358600	Weak transcription	HMEC	breast
3	chr2:186339200-186347600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:186339200-186358400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:186339200-186358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:186341200-186349600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:186342200-186347600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:186342200-186349000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:186342200-186349800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:186342800-186368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:186343000-186346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:186343200-186349600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:186343800-186347400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:186343800-186348600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:186343800-186348800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:186344000-186349200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:186344800-186349000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:186345200-186345400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:186345400-186345600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:186346800-186348800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:186347400-186348800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr2:186347600-186348800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr2:186347600-186348800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:186348000-186358600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:186348400-186348800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr2:186348600-186350000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:186348800-186349000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:186348800-186349000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr2:186348800-186349600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr2:186348800-186350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:186348800-186358800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:186348800-186358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:186349000-186349800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:186349000-186350000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:186349000-186350000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr2:186349000-186350000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:186349000-186350000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:186349200-186350000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:186349400-186349800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:186349600-186350000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:186349600-186350000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:186349600-186350000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:186349600-186350200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:186349800-186350000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr2:186350000-186358400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr2:186350000-186358400	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:186350000-186360600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr2:186350000-186360800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr2:186350200-186358800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:186350400-186361000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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