Variant report

Variant	nsv1002578
Chromosome Location	chr2:209836205-210026339
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:433)
CpG islands
(count:611)
Chromatin interactive
region (count:13)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209850333-209850752	K562	blood:	n/a	n/a
2	ATF1	chr2:209906096-209906295	K562	blood:	n/a	n/a
3	ATF1	chr2:209850478-209850694	K562	blood:	n/a	n/a
4	BACH1	chr2:209875885-209876024	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:209986398-209986748	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:210002834-210003125	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr2:209986484-209986694	GM12878	blood:	n/a	chr2:209986623-209986632
8	BHLHE40	chr2:209954270-209954587	K562	blood:	n/a	n/a
9	BHLHE40	chr2:209906062-209906412	K562	blood:	n/a	n/a
10	CEBPB	chr2:210012739-210013035	A549	lung:	n/a	chr2:210012850-210012861
11	CEBPB	chr2:209848087-209848667	MCF-7	breast:	n/a	n/a
12	CEBPB	chr2:209864598-209865094	MCF-7	breast:	n/a	chr2:209864704-209864715 chr2:209864704-209864715
13	CEBPB	chr2:209875950-209876151	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:210012705-210013038	HepG2	liver:	n/a	chr2:210012850-210012861
15	CEBPB	chr2:209883491-209883673	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:209840198-209840398	HepG2	liver:	n/a	chr2:209840308-209840319
17	CEBPB	chr2:209925339-209925581	HepG2	liver:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
18	CEBPB	chr2:210012758-210013109	MCF-7	breast:	n/a	chr2:210012850-210012861
19	CEBPB	chr2:209935544-209935609	HepG2	liver:	n/a	chr2:209935580-209935591
20	CEBPB	chr2:210011134-210011376	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:210012714-210013010	IMR90	lung:	n/a	chr2:210012850-210012861
22	CEBPB	chr2:209851799-209851995	HepG2	liver:	n/a	chr2:209851907-209851918
23	CEBPB	chr2:209864574-209864995	MCF-7	breast:	n/a	chr2:209864704-209864715 chr2:209864704-209864715
24	CEBPB	chr2:209925435-209925658	A549	lung:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
25	CEBPB	chr2:209848245-209848598	MCF-7	breast:	n/a	n/a
26	CEBPB	chr2:209955124-209955199	A549	lung:	n/a	chr2:209955162-209955175 chr2:209955162-209955173
27	CEBPB	chr2:210012736-210013044	MCF-7	breast:	n/a	chr2:210012850-210012861
28	CEBPB	chr2:210012759-210013067	Hela-S3	cervix:	n/a	chr2:210012850-210012861
29	CEBPD	chr2:209850457-209850711	K562	blood:	n/a	n/a
30	CHD2	chr2:210025669-210025708	HepG2	liver:	n/a	n/a
31	CTCF	chr2:209962008-209962196	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:209902520-209902670	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:209895620-209895770	RPTEC	kidney:	n/a	n/a
34	CTCF	chr2:209895600-209895750	GM12875	blood:	n/a	n/a
35	CTCF	chr2:209873753-209873831	LNCaP	prostate:	n/a	n/a
36	CTCF	chr2:209962004-209962171	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:209873756-209873828	NHEK	skin:	n/a	n/a
38	CTCF	chr2:209873757-209873843	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:209902720-209902870	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:209914480-209914630	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr2:209961920-209962070	GM12878	blood:	n/a	n/a
42	CTCF	chr2:209895600-209895750	GM12878	blood:	n/a	n/a
43	CTCF	chr2:209902719-209902871	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:209870799-209870845	GM13976	blood:	n/a	n/a
45	CTCF	chr2:209914560-209914710	NHEK	skin:	n/a	n/a
46	CTCF	chr2:209895671-209895709	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:209873768-209873825	HepG2	liver:	n/a	n/a
48	CTCF	chr2:209977900-209978050	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr2:209948063-209948098	GM20000	blood:	n/a	n/a
50	CTCF	chr2:209961973-209962135	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210011147-210011197	MCF10A-Er-Src	breast:	n/a
2	chr2:210011147-210011197	MCF10A-Er-Src	breast:	n/a
3	chr2:210010124-210010174	HCT-116	colon:	n/a
4	chr2:209981979-209982029	HRE	kidney:	n/a
5	chr2:210008092-210008142	Caco-2	colon:	n/a
6	chr2:210010193-210010243	AG04450	lung:	fetal
7	chr2:209854267-209854317	GM06990	blood:	n/a
8	chr2:210010325-210010375	AG10803	skin:	n/a
9	chr2:209874962-209875012	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:210003746-210003796	ovcar-3	ovarian:	n/a
11	chr2:209854267-209854317	AG04449	skin:	fetal
12	chr2:210010193-210010243	BJ	skin:	n/a
13	chr2:210008092-210008142	GM12892	blood:	n/a
14	chr2:210010228-210010278	HNPCEpiC	eye:	n/a
15	chr2:210010193-210010243	PFSK-1	brain:	n/a
16	chr2:210010228-210010278	SKMC	muscle:	n/a
17	chr2:210008092-210008142	NH-A	brain:	n/a
18	chr2:210003746-210003796	AG04449	skin:	fetal
19	chr2:210003746-210003796	A549	lung:	n/a
20	chr2:210010228-210010278	A549	lung:	n/a
21	chr2:210008092-210008142	NHBE	bronchial:	n/a
22	chr2:209981979-209982029	NHDF-neo	bronchial:	n/a
23	chr2:210003746-210003796	HEK293	kidney:	embryo
24	chr2:209874962-209875012	ECC-1	luminal epithelium:	n/a
25	chr2:210010325-210010375	GM06990	blood:	n/a
26	chr2:210010325-210010375	Jurkat	blood:	n/a
27	chr2:209981979-209982029	SK-N-SH	brain:	n/a
28	chr2:210010193-210010243	NH-A	brain:	n/a
29	chr2:210003746-210003796	ProgFib	skin:	n/a
30	chr2:210010124-210010174	AoSMC	blood vessel:	n/a
31	chr2:209981979-209982029	HAEpiC	amniotic membrane:	n/a
32	chr2:210010193-210010243	Hepatocyte	liver:	n/a
33	chr2:210010193-210010243	Caco-2	colon:	n/a
34	chr2:210010228-210010278	ProgFib	skin:	n/a
35	chr2:210010124-210010174	H1-hESC	embryonic stem cell:	embryo
36	chr2:210011147-210011197	HCPEpiC	choroid plexus:	n/a
37	chr2:209981979-209982029	HRPEpiC	eye:	n/a
38	chr2:210011147-210011197	HAEpiC	amniotic membrane:	n/a
39	chr2:210010228-210010278	HUVEC	blood vessel:	n/a
40	chr2:209981979-209982029	NH-A	brain:	n/a
41	chr2:210008092-210008142	ovcar-3	ovarian:	n/a
42	chr2:210010124-210010174	HUVEC	blood vessel:	n/a
43	chr2:210010228-210010278	HEEpiC	esophagus:	n/a
44	chr2:210003746-210003796	SKMC	muscle:	n/a
45	chr2:210010193-210010243	NHBE	bronchial:	n/a
46	chr2:209854267-209854317	HL-60	blood:	n/a
47	chr2:210010228-210010278	HAEpiC	amniotic membrane:	n/a
48	chr2:210010325-210010375	Hepatocyte	liver:	n/a
49	chr2:210003746-210003796	CMK	blood:	n/a
50	chr2:209981979-209982029	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:209852263..209854117-chr2:209855293..209858192,2	K562	blood:
2	chr2:209962059..209962630-chr8:88609274..88609836,2	MCF-7	breast:
3	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
4	chr2:209331311..209331890-chr2:209961645..209962198,2	MCF-7	breast:
5	chr2:209878244..209880957-chr2:209882078..209884649,2	MCF-7	breast:
6	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
7	chr2:209878244..209880957-chr2:209882078..209884649,2	MCF-7	breast:
8	chr2:209852263..209854117-chr2:209855293..209858192,2	K562	blood:
9	chr2:209984149..209984947-chr8:69366893..69367419,2	MCF-7	breast:
10	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
11	chr2:209736383..209738259-chr2:210013383..210015250,2	MCF-7	breast:
12	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
13	chr2:209684682..209685324-chr2:209961529..209962479,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH2R-2	chr2:209896369-209898538	l_2022_chr2:209894596-209898538_76bGuttman_hES
2	lnc-IDH1-4	chr2:209907730-209907770	NONHSAT076653
3	lnc-IDH1-4	chr2:210016969-210017110	NONHSAT076653
4	lnc-PTH2R-2	chr2:209894597-209894764	l_2022_chr2:209894596-209898538_76bGuttman_hES
5	lnc-IDH1-4	chr2:209914528-209914662	NONHSAT076653

No data

Variant related genes	Relation type
HSPA8P6	TF binding region
CRYGFP	TF binding region
HSPA8P6	CpG island
CRYGFP	CpG island
ENSG00000227430	chromatin interactions

Extended variants
information (count: 3459 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3459 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568677605	chr2:209842819-209842820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs13391279	chr2:209842842-209842843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs143803857	chr2:209842843-209842844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567974145	chr2:209842857-209842858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377437560	chr2:209842889-209842890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570198934	chr2:209842891-209842892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533777533	chr2:209842947-209842948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538006358	chr2:209842994-209842995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549520465	chr2:209843012-209843013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28607870	chr2:209843029-209843030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577595332	chr2:209843030-209843031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140681815	chr2:209843114-209843115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556816281	chr2:209843115-209843116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576661693	chr2:209843138-209843139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113320493	chr2:209843198-209843199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180781334	chr2:209843204-209843205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10084387	chr2:209843211-209843212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541392957	chr2:209843234-209843235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186271529	chr2:209843242-209843243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190347849	chr2:209843265-209843266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552027042	chr2:209843462-209843463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562347498	chr2:209843520-209843521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531363993	chr2:209843545-209843546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548023043	chr2:209843667-209843668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568147064	chr2:209843722-209843723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111718173	chr2:209843790-209843791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547381777	chr2:209843823-209843824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570432279	chr2:209843831-209843832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540138181	chr2:209843883-209843884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556854912	chr2:209843982-209843983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75512273	chr2:209844052-209844053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536045427	chr2:209844060-209844061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555607310	chr2:209844076-209844077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200352201	chr2:209844084-209844085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181772479	chr2:209844136-209844137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541132137	chr2:209844165-209844166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557753372	chr2:209844186-209844187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7564538	chr2:209844211-209844212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186504391	chr2:209844217-209844218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562435616	chr2:209844257-209844258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577962854	chr2:209844277-209844278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531456102	chr2:209844337-209844338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138715605	chr2:209844343-209844344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142729966	chr2:209844421-209844422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368389663	chr2:209844440-209844441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527400585	chr2:209844444-209844445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553425959	chr2:209844446-209844447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573132825	chr2:209844510-209844511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114597267	chr2:209844514-209844515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190496891	chr2:209844542-209844543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209842800-209843000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:209843000-209853600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:209843800-209844200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:209843800-209844200	Enhancers	NHEK	skin
5	chr2:209844200-209847000	Weak transcription	NHEK	skin
6	chr2:209844200-209848600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:209847000-209850000	Enhancers	NHEK	skin
8	chr2:209847200-209848000	Enhancers	Placenta Amnion	Placenta Amnion
9	chr2:209847200-209848000	Enhancers	HMEC	breast
10	chr2:209847200-209849800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:209847800-209848000	Enhancers	Placenta	Placenta
12	chr2:209847800-209849800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:209848000-209849000	Weak transcription	Placenta	Placenta
14	chr2:209848000-209849000	Weak transcription	HMEC	breast
15	chr2:209848000-209851000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr2:209848600-209850200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:209849000-209849800	Enhancers	Placenta	Placenta
18	chr2:209849000-209849800	Enhancers	HMEC	breast
19	chr2:209849000-209850600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:209849200-209849400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:209849200-209849800	Enhancers	Pancreas	Pancrea
22	chr2:209849600-209850000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:209849600-209850000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:209849800-209853600	Weak transcription	Pancreas	Pancrea
25	chr2:209850000-209850800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:209850400-209850800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:209851000-209851200	Enhancers	Placenta Amnion	Placenta Amnion
28	chr2:209851200-209856800	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr2:209853600-209853800	Enhancers	Pancreas	Pancrea
30	chr2:209853600-209854000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr2:209853600-209854000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:209853600-209854200	Enhancers	Fetal Brain Male	brain
33	chr2:209853800-209854800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:209853800-209855000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:209854200-209855800	Weak transcription	Fetal Brain Male	brain
36	chr2:209855800-209856200	Enhancers	Fetal Brain Male	brain
37	chr2:209863400-209866000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr2:209864400-209864600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:209864400-209865200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr2:209864600-209865000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:209865000-209865200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:209865200-209866000	Enhancers	Fetal Brain Male	brain
43	chr2:209865200-209868800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:209866000-209868400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr2:209868400-209869200	Enhancers	Placenta Amnion	Placenta Amnion
46	chr2:209868800-209869200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:209869200-209870200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr2:209870200-209871000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr2:209871000-209871400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:209873600-209874200	Enhancers	HUES48 Cell Line	embryonic stem cell

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