Variant report

Variant	nsv437315
Chromosome Location	chr2:209204714-209249613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:635)
CpG islands
(count:671)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209238174-209238580	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:209210719-209210725	K562	blood:	n/a	n/a
3	ARID3A	chr2:209235877-209236505	K562	blood:	n/a	n/a
4	ARID3A	chr2:209233745-209234164	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:209228572-209228578	K562	blood:	n/a	n/a
6	ARID3A	chr2:209238240-209238613	K562	blood:	n/a	n/a
7	ATF1	chr2:209235807-209236248	K562	blood:	n/a	n/a
8	BATF	chr2:209228257-209228621	GM12878	blood:	n/a	chr2:209228435-209228446
9	BATF	chr2:209228294-209228554	GM12878	blood:	n/a	chr2:209228435-209228446
10	BCL11A	chr2:209228223-209228612	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:209228247-209228618	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:209231458-209231762	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:209216655-209216677	A549	lung:	n/a	n/a
14	BHLHE40	chr2:209235865-209236444	K562	blood:	n/a	n/a
15	CCNT2	chr2:209235684-209236200	K562	blood:	n/a	n/a
16	CCNT2	chr2:209224399-209224784	K562	blood:	n/a	n/a
17	CCNT2	chr2:209243607-209243784	K562	blood:	n/a	n/a
18	CCNT2	chr2:209223879-209224079	K562	blood:	n/a	n/a
19	CEBPB	chr2:209235790-209236138	K562	blood:	n/a	n/a
20	CEBPB	chr2:209233827-209234132	A549	lung:	n/a	chr2:209233922-209233933
21	CEBPB	chr2:209228317-209228584	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:209228292-209228627	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:209212356-209212384	K562	blood:	n/a	n/a
24	CEBPB	chr2:209215280-209215912	IMR90	lung:	n/a	chr2:209215746-209215759
25	CEBPB	chr2:209226193-209226409	HepG2	liver:	n/a	chr2:209226260-209226271 chr2:209226224-209226235
26	CEBPB	chr2:209233734-209234186	Hela-S3	cervix:	n/a	chr2:209233922-209233933
27	CEBPB	chr2:209233774-209234153	MCF-7	breast:	n/a	chr2:209233922-209233933
28	CEBPB	chr2:209219785-209220071	A549	lung:	n/a	chr2:209219897-209219910
29	CEBPB	chr2:209233738-209234200	HepG2	liver:	n/a	chr2:209233922-209233933
30	CEBPB	chr2:209233800-209234152	MCF-7	breast:	n/a	chr2:209233922-209233933
31	CEBPB	chr2:209238250-209238569	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:209219673-209220160	HepG2	liver:	n/a	chr2:209219897-209219910
33	CEBPB	chr2:209233720-209234122	A549	lung:	n/a	chr2:209233922-209233933
34	CEBPB	chr2:209233813-209234182	IMR90	lung:	n/a	chr2:209233922-209233933
35	CEBPB	chr2:209213707-209213952	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:209215660-209215728	A549	lung:	n/a	n/a
37	CEBPB	chr2:209233797-209234153	A549	lung:	n/a	chr2:209233922-209233933
38	CEBPB	chr2:209234443-209234834	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:209219230-209219440	HepG2	liver:	n/a	chr2:209219335-209219346
40	CEBPB	chr2:209233818-209234101	HepG2	liver:	n/a	chr2:209233922-209233933
41	CEBPB	chr2:209233870-209234062	HepG2	liver:	n/a	chr2:209233922-209233933
42	CEBPB	chr2:209235768-209236174	K562	blood:	n/a	n/a
43	CEBPD	chr2:209235812-209236227	K562	blood:	n/a	n/a
44	CEBPD	chr2:209235741-209236189	K562	blood:	n/a	n/a
45	CHD2	chr2:209224018-209224650	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr2:209224345-209224464	K562	blood:	n/a	n/a
47	CREB1	chr2:209231397-209231883	GM12878	blood:	n/a	n/a
48	CREB1	chr2:209235820-209236371	K562	blood:	n/a	n/a
49	CREB1	chr2:209231367-209231831	GM12878	blood:	n/a	n/a
50	CTCF	chr2:209238257-209238481	LNCaP	prostate:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209225872-209225922	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:209225600-209225650	GM12891	blood:	n/a
3	chr2:209225600-209225650	PFSK-1	brain:	n/a
4	chr2:209225183-209225233	HUVEC	blood vessel:	n/a
5	chr2:209224657-209224707	AG10803	skin:	n/a
6	chr2:209225123-209225173	BE2_C	brain:	n/a
7	chr2:209240193-209240243	CMK	blood:	n/a
8	chr2:209224676-209224726	U87	brain:	n/a
9	chr2:209225872-209225922	ovcar-3	ovarian:	n/a
10	chr2:209225600-209225650	HIPEpiC	eye:	n/a
11	chr2:209206217-209206267	PANC-1	pancreas:	n/a
12	chr2:209224999-209225049	Caco-2	colon:	n/a
13	chr2:209206217-209206267	ECC-1	luminal epithelium:	n/a
14	chr2:209224225-209224275	HCM	heart:	n/a
15	chr2:209242596-209242646	K562	blood:	n/a
16	chr2:209224999-209225049	GM06990	blood:	n/a
17	chr2:209225872-209225922	U87	brain:	n/a
18	chr2:209225600-209225650	GM06990	blood:	n/a
19	chr2:209224676-209224726	NH-A	brain:	n/a
20	chr2:209224225-209224275	SKMC	muscle:	n/a
21	chr2:209225872-209225922	Caco-2	colon:	n/a
22	chr2:209224225-209224275	PANC-1	pancreas:	n/a
23	chr2:209225872-209225922	HCT-116	colon:	n/a
24	chr2:209240193-209240243	PFSK-1	brain:	n/a
25	chr2:209225183-209225233	RPTEC	kidney:	n/a
26	chr2:209240193-209240243	H1-hESC	embryonic stem cell:	embryo
27	chr2:209225123-209225173	HEK293	kidney:	embryo
28	chr2:209225183-209225233	T-47D	breast:	n/a
29	chr2:209224999-209225049	HCT-116	colon:	n/a
30	chr2:209224999-209225049	BE2_C	brain:	n/a
31	chr2:209240193-209240243	NH-A	brain:	n/a
32	chr2:209225872-209225922	HRCEpiC	kidney:	n/a
33	chr2:209225123-209225173	GM06990	blood:	n/a
34	chr2:209242596-209242646	ECC-1	luminal epithelium:	n/a
35	chr2:209224225-209224275	AG04449	skin:	fetal
36	chr2:209224999-209225049	RPTEC	kidney:	n/a
37	chr2:209225872-209225922	Hepatocyte	liver:	n/a
38	chr2:209224225-209224275	GM12891	blood:	n/a
39	chr2:209224999-209225049	HRE	kidney:	n/a
40	chr2:209225183-209225233	HEK293	kidney:	embryo
41	chr2:209225123-209225173	BJ	skin:	n/a
42	chr2:209225183-209225233	NT2-D1	testis:	n/a
43	chr2:209224225-209224275	AG09319	gingival:	n/a
44	chr2:209206217-209206267	NHBE	bronchial:	n/a
45	chr2:209224225-209224275	NH-A	brain:	n/a
46	chr2:209242596-209242646	NH-A	brain:	n/a
47	chr2:209224999-209225049	HRCEpiC	kidney:	n/a
48	chr2:209225872-209225922	GM06990	blood:	n/a
49	chr2:209225872-209225922	HEEpiC	esophagus:	n/a
50	chr2:209224225-209224275	AG09309	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209210530..209214066-chr2:209215409..209218725,4	K562	blood:
2	chr2:209209485..209212181-chr2:209212474..209214962,2	MCF-7	breast:
3	chr2:209210530..209214066-chr2:209215409..209218725,4	K562	blood:
4	chr2:209220629..209223614-chr2:209226035..209228837,2	MCF-7	breast:
5	chr2:209244985..209246550-chr2:209250823..209252697,2	MCF-7	breast:
6	chr2:209175774..209177934-chr2:209202859..209205730,2	K562	blood:
7	chr19:46270760..46271644-chr2:209219267..209220010,2	NB4	blood:
8	chr2:209210530..209212074-chr2:209215409..209217883,2	K562	blood:
9	chr2:209209485..209212181-chr2:209212474..209214962,2	MCF-7	breast:
10	chr2:209210530..209212074-chr2:209215409..209217883,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDH1-2	chr2:209225356-209226094	NONHSAT076639

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIKFYVE	hsa-miR-26a-5p	chr2:209221645-209221665

Variant related genes	Relation type
PTH2R	TF binding region
ENSG00000213081	TF binding region
ENSG00000265454	TF binding region
PTH2R	CpG island
ENSG00000213081	CpG island
ENSG00000265454	CpG island
ENSG00000213081	chromatin interactions
ENSG00000267395	chromatin interactions

Extended variants
information (count: 1652 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2289171	chr2:209204714-209204715	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148173811	chr2:209204726-209204727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201255886	chr2:209204728-209204729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61752191	chr2:209204738-209204739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371531193	chr2:209204769-209204770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376623357	chr2:209204787-209204788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369050968	chr2:209204791-209204792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199929403	chr2:209204794-209204795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552454414	chr2:209204888-209204889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373998871	chr2:209204912-209204913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538037402	chr2:209204914-209204915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554896495	chr2:209204931-209204932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551803521	chr2:209204953-209204954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181224267	chr2:209205125-209205126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554104668	chr2:209205215-209205216	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577322506	chr2:209205254-209205255	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184997007	chr2:209205315-209205316	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189681145	chr2:209205316-209205317	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557637487	chr2:209205378-209205379	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150261708	chr2:209205390-209205391	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540531824	chr2:209205434-209205435	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560946182	chr2:209205457-209205458	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180748141	chr2:209205461-209205462	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574438243	chr2:209205463-209205464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537231935	chr2:209205491-209205492	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138667896	chr2:209205524-209205525	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559672630	chr2:209205544-209205545	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531975365	chr2:209205619-209205620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185123216	chr2:209205624-209205625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562824908	chr2:209205643-209205644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28503455	chr2:209205645-209205646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531908551	chr2:209205647-209205648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549168631	chr2:209205677-209205678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561160021	chr2:209205686-209205687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548737622	chr2:209205690-209205691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569387149	chr2:209205762-209205763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568578832	chr2:209205802-209205803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142671081	chr2:209205862-209205863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547580939	chr2:209205869-209205870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571004293	chr2:209205881-209205882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555730473	chr2:209205903-209205904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539834427	chr2:209205951-209205952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556630190	chr2:209205952-209205953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6435448	chr2:209205973-209205974	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537765087	chr2:209205977-209205978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554707824	chr2:209206013-209206014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116097593	chr2:209206015-209206016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534893210	chr2:209206025-209206026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540467423	chr2:209206120-209206121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559804310	chr2:209206167-209206168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Acute lymphoblastic leukemia	22237106	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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209147400-209225600	Weak transcription	Stomach Mucosa	stomach
2	chr2:209179000-209220600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr2:209180600-209224600	Strong transcription	Fetal Thymus	thymus
4	chr2:209182400-209224200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:209185600-209224000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:209188400-209213400	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr2:209188400-209221400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:209188400-209223400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr2:209188600-209214200	Strong transcription	Placenta	Placenta
10	chr2:209188800-209208400	Strong transcription	Skeletal Muscle Female	skeletal muscle
11	chr2:209188800-209208600	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr2:209188800-209211200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:209188800-209211200	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr2:209188800-209212000	Strong transcription	Adipose Nuclei	Adipose
15	chr2:209188800-209212400	Strong transcription	NH-A	brain
16	chr2:209188800-209213200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:209188800-209214000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr2:209188800-209215400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:209188800-209220400	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr2:209188800-209221200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:209188800-209221200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr2:209188800-209221800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr2:209188800-209222200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:209188800-209222400	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr2:209188800-209222600	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr2:209188800-209223600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:209188800-209223800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr2:209188800-209224000	Strong transcription	Primary B cells from cord blood	blood
29	chr2:209188800-209224000	Strong transcription	Primary hematopoietic stem cells	blood
30	chr2:209188800-209224200	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr2:209188800-209224400	Strong transcription	Dnd41	blood
32	chr2:209189200-209209000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr2:209190600-209224200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:209191000-209212600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:209191000-209218000	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr2:209191200-209206200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:209191200-209211600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:209191200-209212600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:209191200-209215400	Weak transcription	Right Ventricle	heart
40	chr2:209191200-209215600	Weak transcription	Aorta	Aorta
41	chr2:209191200-209224200	Strong transcription	Primary B cells from peripheral blood	blood
42	chr2:209192400-209218600	Weak transcription	Hela-S3	cervix
43	chr2:209192600-209214200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:209194000-209209000	Strong transcription	Fetal Muscle Trunk	muscle
45	chr2:209194400-209214000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:209194400-209220600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr2:209194800-209208600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:209195400-209210600	Weak transcription	K562	blood
49	chr2:209195400-209220000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:209195400-209223800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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