Variant report

Variant	nsv584017
Chromosome Location	chr2:186352959-186515328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:244)
Chromatin interactive
region (count:18)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186510210-186510829	HepG2	liver:	n/a	n/a
2	ATF2	chr2:186509544-186509954	GM12878	blood:	n/a	n/a
3	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
4	BATF	chr2:186509574-186509959	GM12878	blood:	n/a	n/a
5	BCLAF1	chr2:186509649-186509904	GM12878	blood:	n/a	n/a
6	CBX3	chr2:186447981-186448661	HCT-116	colon:	n/a	n/a
7	CBX3	chr2:186447908-186448538	HCT-116	colon:	n/a	n/a
8	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
9	CCNT2	chr2:186508599-186508741	K562	blood:	n/a	n/a
10	CEBPB	chr2:186448257-186448516	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:186478620-186478884	HepG2	liver:	n/a	chr2:186478732-186478743
12	CEBPB	chr2:186447957-186448588	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
15	CEBPB	chr2:186448129-186448586	A549	lung:	n/a	n/a
16	CEBPB	chr2:186510298-186510570	HepG2	liver:	n/a	chr2:186510394-186510405
17	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
18	CEBPB	chr2:186448119-186448613	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:186448144-186448607	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:186448257-186448571	A549	lung:	n/a	n/a
22	CEBPB	chr2:186465657-186465842	A549	lung:	n/a	n/a
23	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:186448143-186448675	HCT-116	colon:	n/a	n/a
25	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
26	CEBPB	chr2:186478710-186478888	A549	lung:	n/a	chr2:186478732-186478743
27	CEBPB	chr2:186448052-186448719	HCT-116	colon:	n/a	n/a
28	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
29	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
30	CEBPB	chr2:186510221-186510640	HepG2	liver:	n/a	chr2:186510394-186510405
31	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
32	CEBPB	chr2:186510299-186510509	HepG2	liver:	n/a	chr2:186510394-186510405
33	CEBPB	chr2:186510245-186510608	HepG2	liver:	n/a	chr2:186510394-186510405
34	CEBPD	chr2:186510309-186510546	HepG2	liver:	n/a	chr2:186510394-186510405
35	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
36	CHD2	chr2:186510399-186510485	HepG2	liver:	n/a	n/a
37	CHD2	chr2:186448192-186448572	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr2:186387220-186387370	GM12865	blood:	n/a	n/a
39	CTCF	chr2:186483540-186483690	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr2:186493970-186494090	A549	lung:	n/a	n/a
41	CTCF	chr2:186493715-186493768	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:186483676-186483698	A549	lung:	n/a	n/a
43	CTCF	chr2:186387280-186387430	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr2:186494020-186494170	HCT-116	colon:	n/a	n/a
45	CTCF	chr2:186493940-186494090	GM12865	blood:	n/a	n/a
46	CTCF	chr2:186493922-186494087	K562	blood:	n/a	n/a
47	CTCF	chr2:186416060-186416210	HepG2	liver:	n/a	n/a
48	CTCF	chr2:186483560-186483710	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr2:186483580-186483730	NHEK	skin:	n/a	n/a
50	CTCF	chr2:186473680-186473830	HA-sp	spinal cord:	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	chr2:186412305-186412355	GM12878	blood:	n/a
2	chr2:186412305-186412355	HUVEC	blood vessel:	n/a
3	chr2:186443903-186443953	LNCaP	prostate:	n/a
4	chr2:186412073-186412123	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:186412073-186412123	HRCEpiC	kidney:	n/a
6	chr2:186412305-186412355	NHBE	bronchial:	n/a
7	chr2:186412073-186412123	HAEpiC	amniotic membrane:	n/a
8	chr2:186443903-186443953	Hepatocyte	liver:	n/a
9	chr2:186412612-186412662	HCF	heart:	n/a
10	chr2:186412612-186412662	AoSMC	blood vessel:	n/a
11	chr2:186412073-186412123	GM19239	blood:	n/a
12	chr2:186412612-186412662	SK-N-MC	brain:	n/a
13	chr2:186412305-186412355	AG09309	skin:	n/a
14	chr2:186412073-186412123	AG09309	skin:	n/a
15	chr2:186443903-186443953	SK-N-MC	brain:	n/a
16	chr2:186412612-186412662	HEEpiC	esophagus:	n/a
17	chr2:186412612-186412662	AG04449	skin:	fetal
18	chr2:186443903-186443953	AG04449	skin:	fetal
19	chr2:186443903-186443953	HAEpiC	amniotic membrane:	n/a
20	chr2:186412305-186412355	SKMC	muscle:	n/a
21	chr2:186443903-186443953	T-47D	breast:	n/a
22	chr2:186412612-186412662	NB4	blood:	n/a
23	chr2:186412612-186412662	GM06990	blood:	n/a
24	chr2:186412073-186412123	HEEpiC	esophagus:	n/a
25	chr2:186443903-186443953	NHBE	bronchial:	n/a
26	chr2:186412305-186412355	ovcar-3	ovarian:	n/a
27	chr2:186412612-186412662	Caco-2	colon:	n/a
28	chr2:186412305-186412355	Hepatocyte	liver:	n/a
29	chr2:186412073-186412123	HNPCEpiC	eye:	n/a
30	chr2:186412073-186412123	ProgFib	skin:	n/a
31	chr2:186412073-186412123	HEK293	kidney:	embryo
32	chr2:186412612-186412662	HMEC	breast:	n/a
33	chr2:186412073-186412123	NB4	blood:	n/a
34	chr2:186412305-186412355	PANC-1	pancreas:	n/a
35	chr2:186412612-186412662	K562	blood:	n/a
36	chr2:186443903-186443953	AG10803	skin:	n/a
37	chr2:186412612-186412662	HRCEpiC	kidney:	n/a
38	chr2:186412612-186412662	BJ	skin:	n/a
39	chr2:186412305-186412355	AG10803	skin:	n/a
40	chr2:186412305-186412355	HepG2	liver:	n/a
41	chr2:186443903-186443953	AoSMC	blood vessel:	n/a
42	chr2:186412612-186412662	AG04450	lung:	fetal
43	chr2:186412305-186412355	CMK	blood:	n/a
44	chr2:186412612-186412662	HIPEpiC	eye:	n/a
45	chr2:186412073-186412123	HCT-116	colon:	n/a
46	chr2:186412073-186412123	HRE	kidney:	n/a
47	chr2:186443903-186443953	Hela-S3	cervix:	n/a
48	chr2:186412305-186412355	HAEpiC	amniotic membrane:	n/a
49	chr2:186412612-186412662	AG09309	skin:	n/a
50	chr2:186443903-186443953	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
2	chr16:88876629..88878732-chr2:186490716..186492785,2	MCF-7	breast:
3	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
4	chr2:186492938..186493701-chr2:186603922..186604721,2	MCF-7	breast:
5	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
6	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
7	chr2:186493592..186494450-chr2:186603275..186603898,3	MCF-7	breast:
8	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
9	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
10	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
11	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
12	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
13	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
14	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
15	chr2:186473268..186473794-chr2:186603435..186603983,2	MCF-7	breast:
16	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
17	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
18	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:

(count:13 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000226747	chromatin interactions
ENSG00000188738	chromatin interactions
ENSG00000198931	chromatin interactions

Extended variants
information (count: 5541 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5541 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1424523	chr2:186352959-186352960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34784476	chr2:186353011-186353012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535327019	chr2:186353025-186353026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553334038	chr2:186353029-186353030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568625154	chr2:186353098-186353099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573559681	chr2:186353133-186353134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535968773	chr2:186353210-186353211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376596809	chr2:186353246-186353247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200035525	chr2:186353257-186353258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554214624	chr2:186353312-186353313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575645843	chr2:186353325-186353326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75976561	chr2:186353348-186353349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558817575	chr2:186353352-186353353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192137789	chr2:186353367-186353368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541308264	chr2:186353383-186353384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559317124	chr2:186353409-186353410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373293837	chr2:186353420-186353421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542360404	chr2:186353437-186353438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147595004	chr2:186353443-186353444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530931922	chr2:186353459-186353460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182656049	chr2:186353488-186353489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528010298	chr2:186353509-186353510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543105904	chr2:186353536-186353537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564499906	chr2:186353563-186353564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528819047	chr2:186353573-186353574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377082823	chr2:186353608-186353609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554769591	chr2:186353627-186353628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142287976	chr2:186353687-186353688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547252034	chr2:186353737-186353738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568336481	chr2:186353741-186353742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535617691	chr2:186353806-186353807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547887625	chr2:186353854-186353855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569361924	chr2:186353885-186353886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536746477	chr2:186354038-186354039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6715687	chr2:186354049-186354050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558308581	chr2:186354138-186354139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373366821	chr2:186354169-186354170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576756360	chr2:186354170-186354171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141916110	chr2:186354224-186354225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545269655	chr2:186354252-186354253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187690363	chr2:186354255-186354256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191714705	chr2:186354257-186354258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539133727	chr2:186354264-186354265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541999355	chr2:186354279-186354280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542943795	chr2:186354283-186354284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563472842	chr2:186354329-186354330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575852287	chr2:186354405-186354406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371093794	chr2:186354410-186354411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201858160	chr2:186354420-186354421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564353550	chr2:186354447-186354448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186321400-186358600	Weak transcription	HMEC	breast
2	chr2:186339200-186358400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:186339200-186358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:186342800-186368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:186348000-186358600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:186348800-186358800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:186348800-186358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:186350000-186358400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr2:186350000-186358400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:186350000-186360600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr2:186350000-186360800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:186350200-186358800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:186350400-186361000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr2:186358400-186359000	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr2:186358400-186359200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:186358400-186359400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:186358400-186359400	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:186358600-186359200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:186358600-186359400	Strong transcription	HMEC	breast
20	chr2:186358800-186359200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:186358800-186359600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:186358800-186359800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:186359000-186359200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr2:186359200-186360000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr2:186359200-186360800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:186359200-186361000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:186359200-186361000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:186359200-186368200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:186359400-186361800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:186359400-186364800	Weak transcription	HMEC	breast
31	chr2:186359400-186367200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:186359600-186368000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:186359800-186393400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:186360600-186360800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr2:186361000-186361400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:186361400-186368000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:186365800-186374600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:186367200-186368400	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr2:186368000-186368600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:186368000-186369400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:186368200-186368600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
42	chr2:186368400-186368800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr2:186368600-186371400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:186368800-186372600	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr2:186369400-186372400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:186371400-186372400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:186372400-186372800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:186372400-186372800	ZNF genes & repeats	Pancreas	Pancrea
49	chr2:186372400-186373000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:186372400-186373000	ZNF genes & repeats	HMEC	breast

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