Variant report

Variant	nsv584307
Chromosome Location	chr2:209966941-210024938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:209986398-209986748	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:209986484-209986694	GM12878	blood:	n/a	chr2:209986623-209986632
3	BCL11A	chr2:210002834-210003125	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:210012736-210013044	MCF-7	breast:	n/a	chr2:210012850-210012861
5	CEBPB	chr2:210011134-210011376	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:210012705-210013038	HepG2	liver:	n/a	chr2:210012850-210012861
7	CEBPB	chr2:210012739-210013035	A549	lung:	n/a	chr2:210012850-210012861
8	CEBPB	chr2:210012759-210013067	Hela-S3	cervix:	n/a	chr2:210012850-210012861
9	CEBPB	chr2:210012714-210013010	IMR90	lung:	n/a	chr2:210012850-210012861
10	CEBPB	chr2:210012758-210013109	MCF-7	breast:	n/a	chr2:210012850-210012861
11	CTCF	chr2:209977900-209978050	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr2:209977760-209977910	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr2:209977840-209977990	MCF-7	breast:	n/a	n/a
14	CUX1	chr2:209986415-209986736	GM12878	blood:	n/a	n/a
15	E2F4	chr2:209981752-209981950	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr2:210009157-210009305	MCF10A-Er-Src	breast:	n/a	n/a
17	EP300	chr2:210010582-210010906	H1-hESC	embryonic stem cell:	n/a	n/a
18	EP300	chr2:209979376-209979591	K562	blood:	n/a	n/a
19	EP300	chr2:209986484-209986694	GM12878	blood:	n/a	chr2:209986623-209986637
20	FAM48A	chr2:209968028-209968083	GM12878	blood:	n/a	n/a
21	FOS	chr2:209990167-209990318	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr2:210006100-210006150	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr2:210006671-210006766	MCF10A-Er-Src	breast:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718
24	FOS	chr2:210012817-210012986	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr2:210005958-210006172	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr2:210006582-210006818	MCF10A-Er-Src	breast:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718
27	FOS	chr2:210006554-210006870	MCF10A-Er-Src	breast:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718
28	FOS	chr2:210006568-210006781	MCF10A-Er-Src	breast:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718
29	FOXA2	chr2:209993596-209993828	A549	lung:	n/a	n/a
30	FOXA2	chr2:209993356-209994043	A549	lung:	n/a	n/a
31	GATA3	chr2:210017214-210017595	SH-SY5Y	brain:	n/a	chr2:210017343-210017356
32	GATA3	chr2:209979270-209979401	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr2:210017012-210017711	MCF-7	breast:	n/a	chr2:210017343-210017356
34	GATA3	chr2:210017460-210017524	MCF-7	breast:	n/a	n/a
35	GATA3	chr2:210012667-210013301	MCF-7	breast:	n/a	chr2:210012952-210012960
36	HDAC2	chr2:210010656-210010998	H1-hESC	embryonic stem cell:	n/a	n/a
37	HEY1	chr2:210022123-210022396	HepG2	liver:	n/a	n/a
38	JUN	chr2:210006560-210006795	HepG2	liver:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718
39	JUND	chr2:210017585-210017799	HepG2	liver:	n/a	chr2:210017733-210017741 chr2:210017731-210017742 chr2:210017731-210017743
40	JUND	chr2:210006532-210007071	SK-N-SH	brain:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718 chr2:210006708-210006719
41	JUND	chr2:210006552-210006898	HepG2	liver:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718 chr2:210006708-210006719
42	JUND	chr2:210002947-210003227	H1-hESC	embryonic stem cell:	n/a	chr2:210003114-210003126
43	JUND	chr2:210006688-210006826	H1-hESC	embryonic stem cell:	n/a	chr2:210006711-210006718 chr2:210006710-210006719 chr2:210006709-210006718 chr2:210006708-210006720 chr2:210006709-210006719 chr2:210006710-210006718 chr2:210006708-210006719
44	MAFF	chr2:209975772-209976022	HepG2	liver:	n/a	chr2:209975876-209975894
45	MAFF	chr2:209967186-209967336	K562	blood:	n/a	n/a
46	MAFF	chr2:210011079-210011388	HepG2	liver:	n/a	chr2:210011212-210011230
47	MAFF	chr2:209967086-209967420	HepG2	liver:	n/a	n/a
48	MAFK	chr2:209967077-209967405	HepG2	liver:	n/a	chr2:209967239-209967254
49	MAFK	chr2:210011068-210011630	HepG2	liver:	n/a	chr2:210011214-210011229
50	MAFK	chr2:209967088-209967387	IMR90	lung:	n/a	chr2:209967239-209967254

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210010228-210010278	HIPEpiC	eye:	n/a
2	chr2:210010325-210010375	HCF	heart:	n/a
3	chr2:210010124-210010174	AoSMC	blood vessel:	n/a
4	chr2:210003746-210003796	HCF	heart:	n/a
5	chr2:210003746-210003796	HCPEpiC	choroid plexus:	n/a
6	chr2:210010193-210010243	HRPEpiC	eye:	n/a
7	chr2:210010124-210010174	HCF	heart:	n/a
8	chr2:210010193-210010243	HCM	heart:	n/a
9	chr2:210010124-210010174	SK-N-SH	brain:	n/a
10	chr2:210003746-210003796	A549	lung:	n/a
11	chr2:209981979-209982029	GM12892	blood:	n/a
12	chr2:210010325-210010375	SK-N-SH	brain:	n/a
13	chr2:210008092-210008142	A549	lung:	n/a
14	chr2:209981979-209982029	HUVEC	blood vessel:	n/a
15	chr2:210010228-210010278	HEK293	kidney:	embryo
16	chr2:210011147-210011197	HRE	kidney:	n/a
17	chr2:210010193-210010243	U87	brain:	n/a
18	chr2:210010193-210010243	HCPEpiC	choroid plexus:	n/a
19	chr2:210010193-210010243	GM19239	blood:	n/a
20	chr2:210010325-210010375	AG04450	lung:	fetal
21	chr2:210010193-210010243	HepG2	liver:	n/a
22	chr2:210010124-210010174	AG09309	skin:	n/a
23	chr2:210011147-210011197	GM06990	blood:	n/a
24	chr2:210010325-210010375	AG04449	skin:	fetal
25	chr2:210011147-210011197	CMK	blood:	n/a
26	chr2:210008092-210008142	SK-N-SH	brain:	n/a
27	chr2:210003746-210003796	PANC-1	pancreas:	n/a
28	chr2:210010325-210010375	LNCaP	prostate:	n/a
29	chr2:210003746-210003796	ProgFib	skin:	n/a
30	chr2:210010325-210010375	NHDF-neo	bronchial:	n/a
31	chr2:210011147-210011197	GM19239	blood:	n/a
32	chr2:210011147-210011197	U87	brain:	n/a
33	chr2:209981979-209982029	HRPEpiC	eye:	n/a
34	chr2:210010124-210010174	AG10803	skin:	n/a
35	chr2:210011147-210011197	Caco-2	colon:	n/a
36	chr2:210008092-210008142	PrEC	prostate:	n/a
37	chr2:210010325-210010375	T-47D	breast:	n/a
38	chr2:210003746-210003796	NHDF-neo	bronchial:	n/a
39	chr2:210010228-210010278	GM12878	blood:	n/a
40	chr2:210010124-210010174	ProgFib	skin:	n/a
41	chr2:210003746-210003796	AG04449	skin:	fetal
42	chr2:210010325-210010375	AG09309	skin:	n/a
43	chr2:210003746-210003796	AoSMC	blood vessel:	n/a
44	chr2:209981979-209982029	T-47D	breast:	n/a
45	chr2:210010325-210010375	SKMC	muscle:	n/a
46	chr2:210008092-210008142	HNPCEpiC	eye:	n/a
47	chr2:210011147-210011197	HepG2	liver:	n/a
48	chr2:210003746-210003796	SK-N-MC	brain:	n/a
49	chr2:210010193-210010243	NB4	blood:	n/a
50	chr2:210010228-210010278	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:209736383..209738259-chr2:210013383..210015250,2	MCF-7	breast:
2	chr2:209984149..209984947-chr8:69366893..69367419,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDH1-4	chr2:210016969-210017110	NONHSAT076653

Variant related genes	Relation type
CRYGFP	TF binding region
CRYGFP	CpG island

Extended variants
information (count: 1357 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367818430	chr2:209975408-209975409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114027279	chr2:209975446-209975447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4672546	chr2:209975457-209975458	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559632342	chr2:209975497-209975498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528034100	chr2:209975502-209975503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78460963	chr2:209975516-209975517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534468178	chr2:209975527-209975528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565481224	chr2:209975569-209975570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563112160	chr2:209975571-209975572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs397839313	chr2:209975594-209975595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs398060997	chr2:209975595-209975596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191571502	chr2:209975600-209975601	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554605375	chr2:209975622-209975623	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558467138	chr2:209975658-209975659	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144557354	chr2:209975659-209975660	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527647893	chr2:209975737-209975738	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11676613	chr2:209975852-209975853	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530610736	chr2:209975951-209975952	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs550428904	chr2:209975969-209975970	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184055369	chr2:209975981-209975982	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs536073522	chr2:209976073-209976074	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs552547243	chr2:209976111-209976112	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs113522545	chr2:209976126-209976127	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs188101924	chr2:209976150-209976151	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs192445288	chr2:209976163-209976164	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs185638742	chr2:209976164-209976165	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs190213945	chr2:209976165-209976166	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs78722428	chr2:209976174-209976175	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs117643100	chr2:209976228-209976229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145853912	chr2:209976260-209976261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77012781	chr2:209976261-209976262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574139337	chr2:209976263-209976264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1439724	chr2:209976271-209976272	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559564731	chr2:209976325-209976326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182400532	chr2:209976414-209976415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545326806	chr2:209976425-209976426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564515036	chr2:209976432-209976433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530444545	chr2:209976441-209976442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138867120	chr2:209976444-209976445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567258662	chr2:209976477-209976478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529849728	chr2:209976478-209976479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546809054	chr2:209976715-209976716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554861355	chr2:209976717-209976718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371936638	chr2:209976753-209976754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566707632	chr2:209976770-209976771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538915200	chr2:209976777-209976778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142803624	chr2:209976817-209976818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571584350	chr2:209976827-209976828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185976268	chr2:209976831-209976832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557382370	chr2:209976849-209976850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Acute lymphoblastic leukemia	22237106	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209975400-209976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:209975400-209977000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr2:209975400-209977200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:209975400-209978200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:209975400-209978600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:209975600-209976200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:209975600-209978400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:209975800-209978200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr2:209976000-209976200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:209976000-209976800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:209976000-209978200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:209976200-209977200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:209976400-209977400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:209976400-209977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:209976800-209977200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:209977000-209977400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr2:209977200-209977600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr2:209977200-209978000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:209977200-209981200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:209977400-209978200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:209977400-209978200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:209977600-209977800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:209977600-209978000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr2:209977600-209978000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:209977600-209978200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:209977600-209978200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:209977800-209979000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:209978200-209980800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:209978400-209982000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr2:209978600-209980400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr2:209979000-209980400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:209980400-209980600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:209980600-209981000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr2:209980800-209981600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:209981000-209982400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:209981200-209982200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:209981600-209982000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:209982000-209982400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:209982000-209982400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:209986200-209987400	Enhancers	GM12878-XiMat	blood
41	chr2:209986200-209988600	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr2:209986400-209987600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr2:209989400-209990200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:209989800-209991000	Enhancers	NHEK	skin
45	chr2:209990200-209990600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:209990400-209990800	Enhancers	Placenta Amnion	Placenta Amnion
47	chr2:209993200-209993600	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr2:209999000-210003000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr2:210001000-210001400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr2:210001400-210003000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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