Variant report

Variant	nsv915689
Chromosome Location	chr3:191244719-191479974
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:641)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:641 , 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	chr3:191459594-191460185	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:191445136-191445516	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:191336838-191336975	K562	blood:	n/a	n/a
4	ARID3A	chr3:191479890-191480846	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:191338258-191338275	K562	blood:	n/a	n/a
6	BACH1	chr3:191420009-191420174	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:191446031-191446343	K562	blood:	n/a	chr3:191446165-191446179
8	BACH1	chr3:191408309-191408323	K562	blood:	n/a	n/a
9	BACH1	chr3:191446042-191446336	H1-hESC	embryonic stem cell:	n/a	chr3:191446165-191446179
10	BCL11A	chr3:191406611-191406868	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr3:191406564-191406904	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr3:191267361-191267367	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:191462896-191462914	GM12878	blood:	n/a	n/a
14	CBX3	chr3:191265982-191266246	K562	blood:	n/a	n/a
15	CEBPB	chr3:191299666-191299695	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:191261816-191262094	HepG2	liver:	n/a	chr3:191261956-191261967 chr3:191261966-191261979 chr3:191261956-191261969 chr3:191261966-191261977
17	CEBPB	chr3:191247832-191248129	MCF-7	breast:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
18	CEBPB	chr3:191261916-191262065	H1-hESC	embryonic stem cell:	n/a	chr3:191261956-191261967 chr3:191261966-191261979 chr3:191261956-191261969 chr3:191261966-191261977
19	CEBPB	chr3:191406631-191406933	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:191349962-191350121	K562	blood:	n/a	n/a
21	CEBPB	chr3:191448306-191448658	HepG2	liver:	n/a	chr3:191448536-191448547
22	CEBPB	chr3:191247829-191248180	K562	blood:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
23	CEBPB	chr3:191256881-191257173	A549	lung:	n/a	chr3:191257002-191257015 chr3:191257003-191257014
24	CEBPB	chr3:191248488-191248729	HepG2	liver:	n/a	chr3:191248567-191248584
25	CEBPB	chr3:191256934-191257057	HepG2	liver:	n/a	chr3:191257002-191257015 chr3:191257003-191257014
26	CEBPB	chr3:191459609-191459782	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:191306695-191306999	HepG2	liver:	n/a	chr3:191306833-191306844
28	CEBPB	chr3:191306776-191306998	H1-hESC	embryonic stem cell:	n/a	chr3:191306833-191306844
29	CEBPB	chr3:191414196-191414568	MCF-7	breast:	n/a	n/a
30	CEBPB	chr3:191247828-191248170	IMR90	lung:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
31	CEBPB	chr3:191370057-191370102	K562	blood:	n/a	n/a
32	CEBPB	chr3:191459547-191459959	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:191369922-191370232	IMR90	lung:	n/a	n/a
34	CEBPB	chr3:191312566-191312831	HepG2	liver:	n/a	chr3:191312703-191312714 chr3:191312705-191312716
35	CEBPB	chr3:191407982-191408028	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:191247811-191248162	HepG2	liver:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
37	CEBPB	chr3:191445203-191445571	HepG2	liver:	n/a	chr3:191445385-191445396
38	CEBPB	chr3:191439007-191439776	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr3:191247940-191248164	H1-hESC	embryonic stem cell:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
40	CEBPB	chr3:191445246-191445446	A549	lung:	n/a	chr3:191445385-191445396
41	CEBPB	chr3:191247903-191248056	HepG2	liver:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
42	CEBPB	chr3:191248434-191248709	K562	blood:	n/a	chr3:191248485-191248498 chr3:191248567-191248584
43	CEBPB	chr3:191247886-191248127	A549	lung:	n/a	chr3:191247991-191248004 chr3:191247992-191248003 chr3:191247991-191248002 chr3:191247993-191248002
44	CEBPB	chr3:191445281-191445453	HepG2	liver:	n/a	chr3:191445385-191445396
45	CHD2	chr3:191406425-191406970	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr3:191286108-191286206	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr3:191419966-191420207	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:191359420-191359570	GM12875	blood:	n/a	n/a
49	CTCF	chr3:191419951-191420252	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr3:191314695-191314731	GM13976	blood:	n/a	n/a

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191282988..191286150-chr3:191301534..191304296,3	K562	blood:
2	chr3:191295509..191298991-chr3:191304819..191308022,4	K562	blood:
3	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
4	chr3:191401415..191403217-chr3:191403592..191405646,2	K562	blood:
5	chr3:191295509..191298991-chr3:191304819..191308022,4	K562	blood:
6	chr3:191371142..191373244-chr3:191374844..191377761,2	K562	blood:
7	chr3:191415298..191416937-chr3:191418603..191420214,2	K562	blood:
8	chr3:191235981..191238025-chr3:191243524..191245044,2	K562	blood:
9	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
10	chr3:191245150..191247720-chr3:191249087..191253104,4	K562	blood:
11	chr3:191401415..191403217-chr3:191403592..191405646,2	K562	blood:
12	chr3:191415298..191416937-chr3:191418603..191420214,2	K562	blood:
13	chr17:56736314..56737969-chr3:191250717..191252860,2	MCF-7	breast:
14	chr3:191371142..191373244-chr3:191374844..191377761,2	K562	blood:
15	chr3:191395265..191397942-chr3:191403159..191405641,2	MCF-7	breast:
16	chr3:191395265..191397942-chr3:191403159..191405641,2	MCF-7	breast:
17	chr3:191243722..191246308-chr3:191248023..191250359,2	MCF-7	breast:
18	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
19	chr3:191305970..191308801-chr3:191310773..191313195,2	K562	blood:
20	chr3:191282988..191286150-chr3:191301534..191304296,3	K562	blood:
21	chr3:191414615..191416798-chr3:191418714..191420918,2	K562	blood:
22	chr3:191243722..191246308-chr3:191248023..191250359,2	MCF-7	breast:
23	chr3:191305970..191308801-chr3:191310773..191313195,2	K562	blood:
24	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
25	chr3:191285914..191288424-chr3:191291658..191293344,2	K562	blood:
26	chr3:191414615..191416798-chr3:191418714..191420918,2	K562	blood:
27	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
28	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
29	chr3:191245150..191247720-chr3:191249087..191253104,4	K562	blood:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PYDC2-2	chr3:191470957-191471124	XLOC_002969
2	lnc-PYDC2-1	chr3:191263839-191263904	NONHSAT093969
3	lnc-PYDC2-1	chr3:191287389-191287613	XLOC_002968
4	lnc-PYDC2-1	chr3:191291103-191291263	NONHSAT093976
5	lnc-PYDC2-2	chr3:191477303-191477492	XLOC_002969
6	lnc-PYDC2-1	chr3:191279232-191279277	XLOC_002968
7	lnc-PYDC2-1	chr3:191274951-191275173	NONHSAT093969
8	lnc-PYDC2-1	chr3:191307692-191307790	NONHSAT093976
9	lnc-PYDC2-1	chr3:191277402-191277543	NONHSAT093973
10	lnc-PYDC2-1	chr3:191286323-191286396	NONHSAT093969
11	lnc-PYDC2-1	chr3:191286324-191286396	XLOC_002968
12	lnc-PYDC2-1	chr3:191291103-191291298	XLOC_002968
13	lnc-PYDC2-1	chr3:191279231-191279277	NONHSAT093969
14	lnc-PYDC2-1	chr3:191277467-191277543	XLOC_002968
15	lnc-PYDC2-1	chr3:191287349-191287613	NONHSAT093976
16	lnc-PYDC2-6	chr3:191249358-191250570	NONHSAT093968
17	lnc-PYDC2-1	chr3:191307692-191307826	NONHSAT093973
18	lnc-PYDC2-1	chr3:191285974-191286130	XLOC_002968
19	lnc-FGF12-1	chr3:191469931-191470131	XLOC_003375
20	lnc-PYDC2-1	chr3:191274952-191275173	XLOC_002968
21	lnc-PYDC2-6	chr3:191248615-191248639	NONHSAT093968
22	lnc-PYDC2-1	chr3:191277467-191277543	XLOC_002968
23	lnc-PYDC2-1	chr3:191274952-191275173	XLOC_002968
24	lnc-PYDC2-1	chr3:191291103-191291263	XLOC_002968
25	lnc-PYDC2-1	chr3:191307691-191309646	NONHSAT093969
26	lnc-PYDC2-1	chr3:191291103-191291263	NONHSAT093973
27	lnc-PYDC2-2	chr3:191470956-191471124	NONHSAT093985
28	lnc-PYDC2-1	chr3:191285973-191286130	NONHSAT093969
29	lnc-FGF12-1	chr3:191469930-191470131	NONHSAT093983
30	lnc-FGF12-2	chr3:191466402-191466767	XLOC_003374
31	lnc-PYDC2-1	chr3:191307692-191309646	XLOC_002968
32	lnc-PYDC2-1	chr3:191291103-191291263	XLOC_002968
33	lnc-PYDC2-1	chr3:191287389-191287613	XLOC_002968
34	lnc-PYDC2-1	chr3:191287389-191287613	XLOC_002968
35	lnc-PYDC2-1	chr3:191287389-191287613	XLOC_002968
36	lnc-PYDC2-1	chr3:191291102-191291298	NONHSAT093969
37	lnc-PYDC2-1	chr3:191307692-191308145	XLOC_002968
38	lnc-PYDC2-1	chr3:191275113-191275173	XLOC_002968
39	lnc-PYDC2-2	chr3:191477302-191477492	NONHSAT093985
40	lnc-PYDC2-1	chr3:191307692-191309646	XLOC_002968
41	lnc-PYDC2-1	chr3:191287389-191287613	NONHSAT093973
42	lnc-PYDC2-1	chr3:191291103-191291263	XLOC_002968
43	lnc-PYDC2-1	chr3:191277466-191277543	NONHSAT093969
44	lnc-FGF12-2	chr3:191467745-191467882	XLOC_003374
45	lnc-PYDC2-1	chr3:191287351-191287616	NONHSAT093969

No data

Variant related genes	Relation type
ENSG00000223812	TF binding region
ENSG00000201860	TF binding region
ENSG00000200270	TF binding region
ENSG00000202077	chromatin interactions
ENSG00000223812	chromatin interactions
ATP11C	miRNA target sites
ATP13A3	miRNA target sites
ZEB1	miRNA target sites

Extended variants
information (count: 7528 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7528 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199797072	chr3:191244804-191244805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566837724	chr3:191244812-191244813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533885470	chr3:191244933-191244934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538902769	chr3:191244947-191244948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57832083	chr3:191244962-191244963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529194021	chr3:191244971-191244972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553715788	chr3:191244972-191244973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550903607	chr3:191245032-191245033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371139334	chr3:191245037-191245038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369055520	chr3:191245161-191245162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558884801	chr3:191245344-191245345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570702638	chr3:191245374-191245375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573766245	chr3:191245388-191245389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373253011	chr3:191245389-191245390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542379577	chr3:191245402-191245403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562464406	chr3:191245437-191245438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28501420	chr3:191245459-191245460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148775083	chr3:191245466-191245467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184090268	chr3:191245467-191245468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564495924	chr3:191245494-191245495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533310269	chr3:191245517-191245518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6795769	chr3:191245532-191245533	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79158395	chr3:191245565-191245566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144797261	chr3:191245629-191245630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370673794	chr3:191245675-191245676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549569982	chr3:191245681-191245682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555076580	chr3:191245686-191245687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140492741	chr3:191245689-191245690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78452400	chr3:191245693-191245694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538531259	chr3:191245720-191245721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7620357	chr3:191245735-191245736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571203456	chr3:191245776-191245777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533687741	chr3:191245822-191245823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370940382	chr3:191245911-191245912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540647369	chr3:191245946-191245947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs151142453	chr3:191245957-191245958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs66474337	chr3:191245989-191245990	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555901296	chr3:191245997-191245998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79726554	chr3:191246037-191246038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374605821	chr3:191246119-191246120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376416546	chr3:191246123-191246124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2365028	chr3:191246141-191246142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs190582470	chr3:191246183-191246184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564351411	chr3:191246205-191246206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546166094	chr3:191246218-191246219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201610850	chr3:191246273-191246274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72400618	chr3:191246274-191246275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9876209	chr3:191246277-191246278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138295791	chr3:191246289-191246290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201664950	chr3:191246291-191246292	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191244200-191247000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:191249400-191249600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:191254200-191256800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:191264800-191265400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:191268200-191270400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:191270400-191271200	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:191271200-191274600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:191272400-191301400	Weak transcription	K562	blood
9	chr3:191272800-191273600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:191273000-191273600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr3:191274600-191275400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr3:191274600-191276200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:191277800-191279200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:191282000-191283000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:191282400-191283000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:191282400-191283000	Enhancers	HMEC	breast
17	chr3:191282400-191283200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:191282600-191283200	Enhancers	NHEK	skin
19	chr3:191282800-191283000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:191282800-191283200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:191283000-191284400	Weak transcription	HMEC	breast
22	chr3:191283000-191284600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:191283000-191284800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:191283200-191284400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:191283200-191284400	Weak transcription	NHEK	skin
26	chr3:191283200-191285800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:191284400-191285000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:191284400-191285000	Enhancers	NHEK	skin
29	chr3:191284400-191285200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:191284400-191285200	Enhancers	HMEC	breast
31	chr3:191284600-191285200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:191284600-191285200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr3:191284800-191285200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:191285200-191287600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:191285800-191286000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:191286400-191286800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:191299600-191300800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr3:191300800-191305800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr3:191301600-191302000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr3:191305800-191309400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr3:191311000-191312800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:191325200-191332400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr3:191332400-191332600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr3:191334200-191335000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:191336200-191336600	Active TSS	K562	blood
46	chr3:191342200-191342600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:191342600-191342800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:191342600-191343600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:191343400-191344800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr3:191343600-191344600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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