Variant report

Variant	nsv1014021
Chromosome Location	chr3:158554615-158635122
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	ARID3A	chr3:158563639-158563883	K562	blood:	n/a	n/a
2	ATF2	chr3:158581068-158581475	GM12878	blood:	n/a	n/a
3	BACH1	chr3:158583620-158583623	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:158556443-158556457	K562	blood:	n/a	n/a
5	BATF	chr3:158564928-158565198	GM12878	blood:	n/a	n/a
6	CBX3	chr3:158574938-158575181	K562	blood:	n/a	n/a
7	CEBPB	chr3:158626927-158627182	A549	lung:	n/a	n/a
8	CEBPB	chr3:158586395-158586410	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr3:158630100-158630250	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr3:158563660-158563810	NHEK	skin:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
11	CTCF	chr3:158563680-158563830	HBMEC	blood vessel:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
12	CTCF	chr3:158563676-158563847	MCF-7	breast:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
13	CTCF	chr3:158630073-158630348	K562	blood:	n/a	n/a
14	CTCF	chr3:158564000-158564150	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr3:158563640-158563790	SK-N-SH_RA	brain:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
16	CTCF	chr3:158563980-158564130	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:158630060-158630210	GM12873	blood:	n/a	n/a
18	CTCF	chr3:158626440-158626590	GM12872	blood:	n/a	chr3:158626518-158626527
19	CTCF	chr3:158563660-158563810	WERI-Rb-1	eye:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
20	CTCF	chr3:158563620-158563770	BE2_C	brain:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
21	CTCF	chr3:158563640-158563790	HCM	heart:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
22	CTCF	chr3:158563940-158564090	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr3:158563598-158563863	K562	blood:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
24	CTCF	chr3:158563680-158563830	GM12867	blood:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
25	CTCF	chr3:158563229-158564304	A549	lung:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
26	CTCF	chr3:158630180-158630330	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr3:158563720-158563870	HAc	cerebellar:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
28	CTCF	chr3:158626440-158626590	NHEK	skin:	n/a	chr3:158626518-158626527
29	CTCF	chr3:158563540-158563899	A549	lung:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
30	CTCF	chr3:158563633-158563842	GM10266	blood:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
31	CTCF	chr3:158563640-158563790	AoAF	blood vessel:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
32	CTCF	chr3:158563504-158563953	H1-hESC	embryonic stem cell:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
33	CTCF	chr3:158563656-158563865	Fibrobl	skin:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
34	CTCF	chr3:158630140-158630290	HCT-116	colon:	n/a	n/a
35	CTCF	chr3:158630260-158630410	WI-38	lung:	n/a	n/a
36	CTCF	chr3:158630240-158630390	GM12872	blood:	n/a	n/a
37	CTCF	chr3:158563280-158563430	AG04450	lung:	n/a	n/a
38	CTCF	chr3:158630180-158630330	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr3:158563640-158563790	WERI-Rb-1	eye:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
40	CTCF	chr3:158563652-158563860	MCF-7	breast:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
41	CTCF	chr3:158630097-158630323	K562	blood:	n/a	n/a
42	CTCF	chr3:158630140-158630290	AG09309	skin:	n/a	n/a
43	CTCF	chr3:158630120-158630270	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr3:158575780-158575930	HepG2	liver:	n/a	n/a
45	CTCF	chr3:158563660-158563810	HVMF	connective:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
46	CTCF	chr3:158563645-158563860	A549	lung:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
47	CTCF	chr3:158630100-158630340	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:158563610-158563872	LNCaP	prostate:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749
49	CTCF	chr3:158630120-158630270	HCT-116	colon:	n/a	n/a
50	CTCF	chr3:158563620-158563770	GM12871	blood:	n/a	chr3:158563726-158563744 chr3:158563727-158563743 chr3:158563730-158563737 chr3:158563728-158563749

No.	Distal block	Cell Line	Cell type
1	chr3:158563780..158564295-chr3:158629761..158630543,2	MCF-7	breast:
2	chr3:158624831..158626643-chr3:158626673..158628308,2	K562	blood:
3	chr3:158563260..158563874-chr3:158970247..158971020,2	MCF-7	breast:
4	chr3:158565428..158568080-chr3:158631507..158633757,2	K562	blood:
5	chr3:158624831..158626643-chr3:158626673..158628308,2	K562	blood:
6	chr3:158604339..158606646-chr3:158644177..158645762,2	K562	blood:
7	chr3:158596511..158598135-chr3:158626376..158629235,2	MCF-7	breast:
8	chr3:158634871..158637670-chr3:158645869..158648578,2	MCF-7	breast:
9	chr3:158553808..158556556-chr3:158560756..158562852,2	K562	blood:
10	chr3:158567936..158569622-chr3:158570978..158572826,2	MCF-7	breast:
11	chr3:158596511..158598135-chr3:158626376..158629235,2	MCF-7	breast:
12	chr3:158554664..158556817-chr3:158563538..158566180,3	K562	blood:
13	chr3:158552403..158553952-chr3:158554364..158557250,2	K562	blood:
14	chr3:158563514..158564079-chr3:158981208..158981999,2	MCF-7	breast:
15	chr3:158563487..158564229-chr3:158977992..158978845,2	MCF-7	breast:
16	chr3:158581079..158584266-chr3:158585250..158589082,3	MCF-7	breast:
17	chr3:158581820..158584871-chr3:158586596..158591446,4	K562	blood:
18	chr3:158591633..158593498-chr3:159330967..159333508,2	MCF-7	breast:
19	chr3:158556502..158558155-chr3:158560493..158562217,2	MCF-7	breast:
20	chr3:158538746..158540414-chr3:158596755..158599583,2	K562	blood:
21	chr3:158581820..158584871-chr3:158586596..158591446,4	K562	blood:
22	chr3:158563458..158564296-chr3:158976821..158978499,10	MCF-7	breast:
23	chr3:158552150..158554007-chr3:158577726..158580202,2	K562	blood:
24	chr3:158553808..158556556-chr3:158560756..158562852,2	K562	blood:
25	chr3:158563274..158564252-chr3:158977565..158978464,8	K562	blood:
26	chr3:158629756..158630668-chr3:158970292..158971225,2	MCF-7	breast:
27	chr3:158565428..158568080-chr3:158631507..158633757,2	K562	blood:
28	chr3:158554664..158556817-chr3:158563538..158566180,3	K562	blood:
29	chr3:158567936..158569622-chr3:158570978..158572826,2	MCF-7	breast:
30	chr3:158563780..158564295-chr3:158629761..158630543,2	MCF-7	breast:
31	chr3:158556502..158558155-chr3:158560493..158562217,2	MCF-7	breast:
32	chr3:158581079..158584266-chr3:158585250..158589082,3	MCF-7	breast:
33	chr3:158565121..158565952-chr3:158977538..158978210,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD1-1	chr3:158586305-158586387	XLOC_002897
2	lnc-MFSD1-1	chr3:158587027-158587531	NONHSAT092954
3	lnc-MFSD1-1	chr3:158586304-158586387	NONHSAT092954
4	lnc-MFSD1-1	chr3:158586273-158586387	XLOC_002897
5	lnc-MFSD1-1	chr3:158602069-158602973	XLOC_002897
6	lnc-MFSD1-1	chr3:158587028-158587143	XLOC_002897
7	lnc-MFSD1-3	chr3:158587689-158589595	NONHSAT092956
8	lnc-MFSD1-1	chr3:158587028-158587531	XLOC_002897

Variant related genes	Relation type
GPR79	TF binding region
ENSG00000118855	chromatin interactions
AP2B1	miRNA target sites
TTPAL	miRNA target sites
STK35	miRNA target sites
STK36	miRNA target sites

Extended variants
information (count: 2447 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2447 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7651532	chr3:158554615-158554616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577437891	chr3:158554721-158554722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541372996	chr3:158554780-158554781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533902064	chr3:158554784-158554785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180709208	chr3:158554826-158554827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187276661	chr3:158554862-158554863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369918470	chr3:158554906-158554907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1870829	chr3:158554978-158554979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs563759995	chr3:158554994-158554995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140616837	chr3:158555027-158555028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34756072	chr3:158555064-158555065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377237958	chr3:158555095-158555096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552321761	chr3:158555148-158555149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114588440	chr3:158555165-158555166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145615383	chr3:158555166-158555167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546581142	chr3:158555182-158555183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568059284	chr3:158555241-158555242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535073615	chr3:158555242-158555243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28385458	chr3:158555264-158555265	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs373104295	chr3:158555274-158555275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538147624	chr3:158555298-158555299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77684473	chr3:158555329-158555330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190534359	chr3:158555375-158555376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559071857	chr3:158555387-158555388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577373263	chr3:158555388-158555389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541660239	chr3:158555399-158555400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373119744	chr3:158555531-158555532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116286112	chr3:158555556-158555557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575246049	chr3:158555592-158555593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542225479	chr3:158555646-158555647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182010103	chr3:158555664-158555665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531000906	chr3:158555810-158555811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575038437	chr3:158555816-158555817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545992568	chr3:158555819-158555820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187114782	chr3:158555842-158555843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528270503	chr3:158555954-158555955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6776106	chr3:158555971-158555972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190465754	chr3:158555989-158555990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182705318	chr3:158556071-158556072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553875073	chr3:158556085-158556086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78737803	chr3:158556139-158556140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550129520	chr3:158556206-158556207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112731548	chr3:158556220-158556221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545918476	chr3:158556227-158556228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539477810	chr3:158556233-158556234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185302439	chr3:158556247-158556248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566605275	chr3:158556263-158556264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189771549	chr3:158556272-158556273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9839548	chr3:158556280-158556281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs575158176	chr3:158556283-158556284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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	22032731	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
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158532400-158557800	Weak transcription	Gastric	stomach
2	chr3:158533000-158556400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:158533000-158559600	Weak transcription	Right Ventricle	heart
4	chr3:158541800-158555000	Weak transcription	Spleen	Spleen
5	chr3:158541800-158560200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:158542000-158556400	Weak transcription	Brain Germinal Matrix	brain
7	chr3:158542200-158561000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:158542600-158558000	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:158543600-158555200	Weak transcription	Esophagus	oesophagus
10	chr3:158544000-158556200	Weak transcription	Small Intestine	intestine
11	chr3:158546400-158565200	Weak transcription	Osteobl	bone
12	chr3:158548600-158554800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:158548600-158555400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr3:158548600-158559000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr3:158548600-158569400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:158548600-158571200	Weak transcription	Pancreas	Pancrea
17	chr3:158548800-158555000	Weak transcription	Psoas Muscle	Psoas
18	chr3:158548800-158563800	Weak transcription	Brain Anterior Caudate	brain
19	chr3:158548800-158576400	Weak transcription	Left Ventricle	heart
20	chr3:158549800-158564800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr3:158550200-158586600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr3:158550600-158556800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr3:158550800-158555200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr3:158550800-158562000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:158550800-158565200	Weak transcription	Primary T cells from cord blood	blood
26	chr3:158551000-158559000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr3:158551000-158565400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr3:158551200-158561000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:158554600-158554800	Enhancers	Fetal Lung	lung
30	chr3:158555000-158555200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:158555000-158555200	Enhancers	Psoas Muscle	Psoas
32	chr3:158555000-158555200	Enhancers	Spleen	Spleen
33	chr3:158555200-158555400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr3:158555200-158555400	Enhancers	Esophagus	oesophagus
35	chr3:158555600-158556000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:158555600-158565600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:158556200-158556400	Enhancers	Small Intestine	intestine
38	chr3:158556200-158556600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:158556400-158557000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr3:158556800-158557000	Enhancers	Brain Germinal Matrix	brain
41	chr3:158557800-158558200	Enhancers	Gastric	stomach
42	chr3:158557800-158558200	Enhancers	K562	blood
43	chr3:158558000-158558200	Enhancers	HepG2	liver
44	chr3:158558000-158558400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:158558000-158558400	Enhancers	Brain Hippocampus Middle	brain
46	chr3:158559400-158559600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr3:158559600-158560000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:158560200-158560400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:158561000-158561200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr3:158561000-158561600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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