Variant report

Variant	nsv875802
Chromosome Location	chr2:212867291-213004603
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	BACH1	chr2:212886803-212886915	K562	blood:	n/a	n/a
2	BACH1	chr2:212886715-212887065	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr2:212888724-212889019	GM12878	blood:	n/a	n/a
4	BCL3	chr2:212896799-212897040	GM12878	blood:	n/a	chr2:212896895-212896904
5	BHLHE40	chr2:212870003-212870157	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:212953108-212953412	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:212947372-212947380	HepG2	liver:	n/a	n/a
8	CBX3	chr2:212869803-212870344	HCT-116	colon:	n/a	n/a
9	CEBPB	chr2:213001096-213001402	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:212929226-212929301	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:212880354-212880789	HepG2	liver:	n/a	chr2:212880658-212880669
12	CEBPB	chr2:212953137-212953338	H1-hESC	embryonic stem cell:	n/a	chr2:212953227-212953238
13	CEBPB	chr2:212953173-212953409	K562	blood:	n/a	chr2:212953227-212953238
14	CEBPB	chr2:212892491-212892798	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:212869891-212870388	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:212870037-212870315	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:212931464-212931465	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:213001168-213001365	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:212932362-212932724	HepG2	liver:	n/a	chr2:212932534-212932545
20	CEBPB	chr2:212989415-212989703	A549	lung:	n/a	n/a
21	CEBPB	chr2:212948234-212948578	IMR90	lung:	n/a	chr2:212948418-212948427 chr2:212948416-212948429 chr2:212948418-212948427 chr2:212948418-212948427 chr2:212948416-212948427 chr2:212948418-212948427 chr2:212948418-212948429 chr2:212948416-212948429
22	CEBPB	chr2:212989378-212989756	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:212989374-212989746	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:212880553-212880788	H1-hESC	embryonic stem cell:	n/a	chr2:212880658-212880669
25	CEBPB	chr2:212948334-212948534	H1-hESC	embryonic stem cell:	n/a	chr2:212948418-212948427 chr2:212948416-212948429 chr2:212948418-212948427 chr2:212948418-212948427 chr2:212948416-212948427 chr2:212948418-212948427 chr2:212948418-212948429 chr2:212948416-212948429
26	CEBPB	chr2:212902723-212902900	A549	lung:	n/a	n/a
27	CEBPB	chr2:212917150-212917896	IMR90	lung:	n/a	chr2:212917260-212917272
28	CEBPB	chr2:212880496-212880738	A549	lung:	n/a	chr2:212880658-212880669
29	CEBPB	chr2:212893121-212893310	HepG2	liver:	n/a	chr2:212893203-212893214
30	CEBPB	chr2:213001057-213001257	A549	lung:	n/a	n/a
31	CEBPB	chr2:212870053-212870336	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:212896765-212897085	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:212897579-212897938	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:212953045-212953411	A549	lung:	n/a	chr2:212953227-212953238
35	CEBPB	chr2:212948246-212948581	A549	lung:	n/a	chr2:212948418-212948427 chr2:212948416-212948429 chr2:212948418-212948427 chr2:212948418-212948427 chr2:212948416-212948427 chr2:212948418-212948427 chr2:212948418-212948429 chr2:212948416-212948429
36	CEBPB	chr2:212880485-212880821	IMR90	lung:	n/a	chr2:212880658-212880669
37	CEBPB	chr2:212893105-212893256	H1-hESC	embryonic stem cell:	n/a	chr2:212893203-212893214
38	CEBPB	chr2:212953060-212953419	HepG2	liver:	n/a	chr2:212953227-212953238
39	CEBPB	chr2:212989367-212989751	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:213001895-213002095	A549	lung:	n/a	n/a
41	CEBPB	chr2:212989412-212989664	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:212989451-212989648	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:212897580-212897962	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:212886692-212887013	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:212989374-212989770	MCF-7	breast:	n/a	n/a
46	CEBPB	chr2:212953044-212953411	IMR90	lung:	n/a	chr2:212953227-212953238
47	CEBPB	chr2:212948242-212948605	HepG2	liver:	n/a	chr2:212948418-212948427 chr2:212948416-212948429 chr2:212948418-212948427 chr2:212948418-212948427 chr2:212948416-212948427 chr2:212948418-212948427 chr2:212948418-212948429 chr2:212948416-212948429
48	CEBPB	chr2:212989403-212989713	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr2:212892366-212892819	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:212932270-212932722	IMR90	lung:	n/a	chr2:212932534-212932545

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212895973-212896023	A549	lung:	n/a
2	chr2:212895973-212896023	RPTEC	kidney:	n/a
3	chr2:212895973-212896023	Caco-2	colon:	n/a
4	chr2:212938740-212938790	HepG2	liver:	n/a
5	chr2:212895973-212896023	SAEC	small airway:	n/a
6	chr2:212917701-212917751	ovcar-3	ovarian:	n/a
7	chr2:212938740-212938790	IMR90	lung:	fetal
8	chr2:212938740-212938790	AG09319	gingival:	n/a
9	chr2:212895973-212896023	LNCaP	prostate:	n/a
10	chr2:212938740-212938790	LNCaP	prostate:	n/a
11	chr2:212917701-212917751	NT2-D1	testis:	n/a
12	chr2:212938740-212938790	AG09309	skin:	n/a
13	chr2:212938740-212938790	GM12878	blood:	n/a
14	chr2:212895973-212896023	H1-hESC	embryonic stem cell:	embryo
15	chr2:212917701-212917751	GM12878	blood:	n/a
16	chr2:212938740-212938790	HRCEpiC	kidney:	n/a
17	chr2:212895973-212896023	PFSK-1	brain:	n/a
18	chr2:212895973-212896023	HNPCEpiC	eye:	n/a
19	chr2:212938740-212938790	ProgFib	skin:	n/a
20	chr2:212895973-212896023	HepG2	liver:	n/a
21	chr2:212917701-212917751	GM06990	blood:	n/a
22	chr2:212895973-212896023	NHBE	bronchial:	n/a
23	chr2:212917701-212917751	HCPEpiC	choroid plexus:	n/a
24	chr2:212938740-212938790	SKMC	muscle:	n/a
25	chr2:212938740-212938790	HCT-116	colon:	n/a
26	chr2:212938740-212938790	AG04450	lung:	fetal
27	chr2:212895973-212896023	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:212895973-212896023	MCF10A-Er-Src	breast:	n/a
29	chr2:212895973-212896023	HMEC	breast:	n/a
30	chr2:212895973-212896023	ProgFib	skin:	n/a
31	chr2:212938740-212938790	HAEpiC	amniotic membrane:	n/a
32	chr2:212895973-212896023	NH-A	brain:	n/a
33	chr2:212895973-212896023	Hepatocyte	liver:	n/a
34	chr2:212895973-212896023	Jurkat	blood:	n/a
35	chr2:212917701-212917751	AG04450	lung:	fetal
36	chr2:212938740-212938790	Caco-2	colon:	n/a
37	chr2:212917701-212917751	SK-N-SH_RA	brain:	n/a
38	chr2:212938740-212938790	HNPCEpiC	eye:	n/a
39	chr2:212938740-212938790	NB4	blood:	n/a
40	chr2:212895973-212896023	T-47D	breast:	n/a
41	chr2:212895973-212896023	U87	brain:	n/a
42	chr2:212917701-212917751	RPTEC	kidney:	n/a
43	chr2:212938740-212938790	ovcar-3	ovarian:	n/a
44	chr2:212917701-212917751	SKMC	muscle:	n/a
45	chr2:212895973-212896023	BJ	skin:	n/a
46	chr2:212938740-212938790	GM12891	blood:	n/a
47	chr2:212917701-212917751	H1-hESC	embryonic stem cell:	embryo
48	chr2:212938740-212938790	HCM	heart:	n/a
49	chr2:212895973-212896023	HRCEpiC	kidney:	n/a
50	chr2:212917701-212917751	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:212932110..212934697-chr2:212936693..212938362,2	MCF-7	breast:
2	chr2:212891576..212893248-chr2:212907537..212909277,2	K562	blood:
3	chr2:212891168..212892898-chr5:170814131..170816510,2	MCF-7	breast:
4	chr2:212982925..212985652-chr2:212994637..212996884,2	K562	blood:
5	chr2:212891576..212893248-chr2:212907537..212909277,2	K562	blood:
6	chr2:212932110..212934697-chr2:212936693..212938362,2	MCF-7	breast:
7	chr2:212982925..212985652-chr2:212994637..212996884,2	K562	blood:

Variant related genes	Relation type
ERBB4	TF binding region
ERBB4	CpG island
ENSG00000181163	chromatin interactions

Extended variants
information (count: 3748 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3748 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73081394	chr2:212872622-212872623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563456459	chr2:212872624-212872625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551567659	chr2:212872691-212872692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571461251	chr2:212872751-212872752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192296553	chr2:212872768-212872769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62183383	chr2:212872784-212872785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567731516	chr2:212872858-212872859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536276167	chr2:212872878-212872879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73988936	chr2:212872937-212872938	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148678953	chr2:212872948-212872949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538891362	chr2:212872958-212872959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558891668	chr2:212872962-212872963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144530144	chr2:212872991-212872992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544382524	chr2:212873014-212873015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147815127	chr2:212873024-212873025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574446242	chr2:212873030-212873031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115019428	chr2:212873147-212873148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559679080	chr2:212873209-212873210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111565140	chr2:212873217-212873218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187984969	chr2:212873243-212873244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74980316	chr2:212873259-212873260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531045158	chr2:212873327-212873328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369114113	chr2:212873332-212873333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543098059	chr2:212873457-212873458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115123153	chr2:212873497-212873498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567673048	chr2:212873529-212873530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191292943	chr2:212873541-212873542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75691445	chr2:212873590-212873591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566919829	chr2:212873647-212873648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539027278	chr2:212873660-212873661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs66523936	chr2:212873755-212873756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1949645	chr2:212873790-212873791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62183384	chr2:212873793-212873794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs62183385	chr2:212873797-212873798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2888039	chr2:212873799-212873800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3037280	chr2:212873803-212873804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs57847013	chr2:212873808-212873809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2888040	chr2:212873823-212873824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560568341	chr2:212873824-212873825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2371437	chr2:212873831-212873832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3037289	chr2:212873833-212873834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs3037292	chr2:212873837-212873838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202228282	chr2:212873840-212873841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368561151	chr2:212873841-212873842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71054163	chr2:212873843-212873844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200459195	chr2:212873844-212873845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569113588	chr2:212873859-212873860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183781548	chr2:212873882-212873883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189638746	chr2:212873890-212873891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574459348	chr2:212873909-212873910	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212872600-212874400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:212874200-212874800	Enhancers	Brain Angular Gyrus	brain
3	chr2:212874400-212875800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:212877200-212877400	ZNF genes & repeats	Aorta	Aorta
5	chr2:212877400-212877800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:212877400-212878600	Enhancers	Aorta	Aorta
7	chr2:212877400-212879000	Enhancers	Osteobl	bone
8	chr2:212877600-212877800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:212877600-212878000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:212877600-212881200	Enhancers	Fetal Heart	heart
11	chr2:212878000-212878400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:212878000-212878400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:212878000-212878400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:212878000-212878600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:212878400-212878600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:212878400-212878600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:212878400-212879000	Enhancers	HMEC	breast
18	chr2:212878400-212880200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:212878400-212881600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:212878600-212880200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:212878600-212882600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:212879000-212880200	Weak transcription	Osteobl	bone
23	chr2:212880200-212880600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:212880200-212880600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:212880200-212880600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:212880200-212880600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:212880200-212880600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:212880200-212880600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:212880200-212880600	Enhancers	Brain Germinal Matrix	brain
30	chr2:212880200-212880600	Enhancers	HSMMtube	muscle
31	chr2:212880200-212881200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:212880200-212883800	Enhancers	Osteobl	bone
33	chr2:212880400-212880600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:212881000-212884400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:212881200-212882400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:212881200-212883600	Weak transcription	Fetal Heart	heart
37	chr2:212881600-212883000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:212882200-212883200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr2:212882400-212883600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:212882600-212882800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:212882800-212892000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:212883200-212886600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr2:212883600-212884200	Enhancers	Fetal Heart	heart
44	chr2:212883800-212892000	Weak transcription	Osteobl	bone
45	chr2:212884200-212889800	Weak transcription	Fetal Heart	heart
46	chr2:212886600-212887000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:212886600-212887200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr2:212886600-212887200	Enhancers	HUVEC	blood vessel
49	chr2:212887000-212887400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:212887000-212887400	Enhancers	HMEC	breast

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