Variant report

Variant	nsv877306
Chromosome Location	chr3:105372196-105495841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:105375613-105375817	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:105407913-105408076	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:105405206-105405556	K562	blood:	n/a	n/a
4	ATF2	chr3:105441592-105442539	GM12878	blood:	n/a	n/a
5	ATF2	chr3:105483253-105483868	GM12878	blood:	n/a	n/a
6	ATF2	chr3:105483224-105483608	GM12878	blood:	n/a	n/a
7	ATF2	chr3:105441559-105442445	GM12878	blood:	n/a	n/a
8	ATF2	chr3:105493244-105493687	GM12878	blood:	n/a	n/a
9	ATF2	chr3:105471808-105472363	GM12878	blood:	n/a	n/a
10	ATF2	chr3:105493136-105493706	GM12878	blood:	n/a	n/a
11	BACH1	chr3:105438790-105438901	H1-hESC	embryonic stem cell:	n/a	chr3:105438804-105438818
12	BATF	chr3:105482183-105482519	GM12878	blood:	n/a	n/a
13	BATF	chr3:105492176-105492536	GM12878	blood:	n/a	chr3:105492369-105492379 chr3:105492406-105492415 chr3:105492368-105492379
14	BATF	chr3:105493281-105493650	GM12878	blood:	n/a	n/a
15	BATF	chr3:105442092-105442360	GM12878	blood:	n/a	chr3:105442227-105442238 chr3:105442228-105442238
16	BATF	chr3:105441735-105442039	GM12878	blood:	n/a	n/a
17	BATF	chr3:105449914-105450106	GM12878	blood:	n/a	n/a
18	BATF	chr3:105442084-105442403	GM12878	blood:	n/a	chr3:105442227-105442238 chr3:105442228-105442238
19	BATF	chr3:105493258-105493654	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:105493269-105493642	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:105441762-105442353	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
22	BCL3	chr3:105407608-105408148	A549	lung:	n/a	n/a
23	BCL3	chr3:105493306-105493673	GM12878	blood:	n/a	n/a
24	BCL3	chr3:105442069-105442429	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
25	BCLAF1	chr3:105441666-105442424	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
26	BCLAF1	chr3:105491471-105491958	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:105483867-105484184	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:105441702-105442406	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:105405215-105405457	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:105472150-105472218	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:105389966-105390094	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:105417156-105417285	GM12878	blood:	n/a	n/a
33	BRCA1	chr3:105459233-105459283	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:105426446-105426711	A549	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
35	CEBPB	chr3:105472761-105473043	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr3:105434341-105434547	A549	lung:	n/a	chr3:105434439-105434452
37	CEBPB	chr3:105472741-105473094	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:105472751-105473087	K562	blood:	n/a	n/a
39	CEBPB	chr3:105423688-105423827	HepG2	liver:	n/a	chr3:105423741-105423752 chr3:105423743-105423754 chr3:105423741-105423754 chr3:105423741-105423754
40	CEBPB	chr3:105434263-105434621	IMR90	lung:	n/a	chr3:105434439-105434452
41	CEBPB	chr3:105472775-105473017	A549	lung:	n/a	n/a
42	CEBPB	chr3:105426429-105426670	A549	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
43	CEBPB	chr3:105472737-105473017	MCF-7	breast:	n/a	n/a
44	CEBPB	chr3:105426427-105426731	K562	blood:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
45	CEBPB	chr3:105472768-105473078	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:105472774-105473077	A549	lung:	n/a	n/a
47	CEBPB	chr3:105426417-105426701	IMR90	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
48	CEBPB	chr3:105375539-105375739	IMR90	lung:	n/a	chr3:105375617-105375628
49	CEBPB	chr3:105375508-105375758	Hela-S3	cervix:	n/a	chr3:105375617-105375628
50	CEBPB	chr3:105423663-105423882	A549	lung:	n/a	chr3:105423741-105423752 chr3:105423743-105423754 chr3:105423741-105423754 chr3:105423741-105423754

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:105377640-105377690	HIPEpiC	eye:	n/a
2	chr3:105466016-105466066	HUVEC	blood vessel:	n/a
3	chr3:105377640-105377690	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:105377640-105377690	SAEC	small airway:	n/a
5	chr3:105377640-105377690	PrEC	prostate:	n/a
6	chr3:105466016-105466066	GM19239	blood:	n/a
7	chr3:105466016-105466066	HCT-116	colon:	n/a
8	chr3:105377640-105377690	HepG2	liver:	n/a
9	chr3:105377640-105377690	A549	lung:	n/a
10	chr3:105466016-105466066	Caco-2	colon:	n/a
11	chr3:105466016-105466066	HCM	heart:	n/a
12	chr3:105377640-105377690	NHDF-neo	bronchial:	n/a
13	chr3:105377640-105377690	SK-N-SH	brain:	n/a
14	chr3:105466016-105466066	A549	lung:	n/a
15	chr3:105466016-105466066	HNPCEpiC	eye:	n/a
16	chr3:105466016-105466066	PrEC	prostate:	n/a
17	chr3:105466016-105466066	HEEpiC	esophagus:	n/a
18	chr3:105377640-105377690	HEEpiC	esophagus:	n/a
19	chr3:105377640-105377690	T-47D	breast:	n/a
20	chr3:105466016-105466066	T-47D	breast:	n/a
21	chr3:105377640-105377690	U87	brain:	n/a
22	chr3:105466016-105466066	SK-N-SH	brain:	n/a
23	chr3:105466016-105466066	SKMC	muscle:	n/a
24	chr3:105466016-105466066	LNCaP	prostate:	n/a
25	chr3:105377640-105377690	AG04450	lung:	fetal
26	chr3:105466016-105466066	PFSK-1	brain:	n/a
27	chr3:105377640-105377690	HRE	kidney:	n/a
28	chr3:105466016-105466066	SK-N-MC	brain:	n/a
29	chr3:105377640-105377690	HCM	heart:	n/a
30	chr3:105377640-105377690	SK-N-SH_RA	brain:	n/a
31	chr3:105466016-105466066	AoSMC	blood vessel:	n/a
32	chr3:105466016-105466066	BJ	skin:	n/a
33	chr3:105377640-105377690	SK-N-MC	brain:	n/a
34	chr3:105377640-105377690	MCF-7	breast:	n/a
35	chr3:105377640-105377690	H1-hESC	embryonic stem cell:	embryo
36	chr3:105377640-105377690	HMEC	breast:	n/a
37	chr3:105466016-105466066	NHBE	bronchial:	n/a
38	chr3:105466016-105466066	ECC-1	luminal epithelium:	n/a
39	chr3:105466016-105466066	AG09319	gingival:	n/a
40	chr3:105377640-105377690	GM12891	blood:	n/a
41	chr3:105377640-105377690	ECC-1	luminal epithelium:	n/a
42	chr3:105466016-105466066	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:105466016-105466066	HCPEpiC	choroid plexus:	n/a
44	chr3:105377640-105377690	MCF10A-Er-Src	breast:	n/a
45	chr3:105466016-105466066	NB4	blood:	n/a
46	chr3:105466016-105466066	Hela-S3	cervix:	n/a
47	chr3:105466016-105466066	AG04450	lung:	fetal
48	chr3:105466016-105466066	HL-60	blood:	n/a
49	chr3:105466016-105466066	CMK	blood:	n/a
50	chr3:105466016-105466066	GM12878	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:105405012..105405745-chr3:106328493..106329187,4	MCF-7	breast:
2	chr3:105438428..105441312-chr3:105441392..105443154,2	K562	blood:
3	chr3:105435086..105438281-chr3:105439598..105442695,3	MCF-7	breast:
4	chr13:35938087..35938941-chr3:105372532..105373470,2	MCF-7	breast:
5	chr3:105391728..105394638-chr3:105395821..105398573,2	MCF-7	breast:
6	chr3:105481713..105484437-chr7:147483253..147485905,2	MCF-7	breast:
7	chr3:105429146..105430827-chr3:105431044..105433948,2	K562	blood:
8	chr3:105431222..105434203-chr3:105434765..105437080,2	MCF-7	breast:
9	chr3:105404868..105405453-chr3:105840594..105841272,3	MCF-7	breast:
10	chr3:105435161..105438047-chr3:105586543..105588230,2	MCF-7	breast:
11	chr3:105384518..105386462-chr3:105388169..105391773,3	MCF-7	breast:
12	chr3:105373222..105375120-chr3:105379511..105381347,2	K562	blood:
13	chr3:105404910..105406047-chr3:105927670..105928468,4	MCF-7	breast:
14	chr3:105409741..105412023-chr3:105415903..105417976,2	K562	blood:
15	chr3:105404856..105405756-chr3:105840513..105841376,2	MCF-7	breast:
16	chr3:105409741..105412023-chr3:105415903..105417976,2	K562	blood:
17	chr3:105388597..105390954-chr3:105393490..105396667,3	MCF-7	breast:
18	chr3:105388584..105391376-chr3:105413040..105414567,2	MCF-7	breast:
19	chr3:105452868..105454661-chr3:105463117..105465166,2	K562	blood:
20	chr3:105388597..105390954-chr3:105393490..105396667,3	MCF-7	breast:
21	chr3:105435086..105438281-chr3:105439598..105442695,3	MCF-7	breast:
22	chr3:105404907..105405695-chr3:106836814..106837354,2	K562	blood:
23	chr3:105373294..105375257-chr9:136126002..136127894,2	MCF-7	breast:
24	chr3:105404904..105405760-chr3:106328270..106329152,3	MCF-7	breast:
25	chr3:105452868..105454661-chr3:105463117..105465166,2	K562	blood:
26	chr3:105429146..105430827-chr3:105431044..105433948,2	K562	blood:
27	chr3:105406789..105409317-chr3:105420283..105423244,2	MCF-7	breast:
28	chr3:105438428..105441312-chr3:105441392..105443154,2	K562	blood:
29	chr3:105388584..105391376-chr3:105413040..105414567,2	MCF-7	breast:
30	chr3:105384518..105386462-chr3:105388169..105391773,3	MCF-7	breast:
31	chr3:105431222..105434203-chr3:105434765..105437080,2	MCF-7	breast:
32	chr3:105373222..105375120-chr3:105379511..105381347,2	K562	blood:

No data

Variant related genes	Relation type
CBLB	TF binding region
CBLB	CpG island
ENSG00000114423	chromatin interactions

Extended variants
information (count: 4757 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4757 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11706098	chr3:105372196-105372197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116967950	chr3:105372221-105372222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs16851391	chr3:105372226-105372227	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184016745	chr3:105372246-105372247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13061321	chr3:105372266-105372267	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9868363	chr3:105372307-105372308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573539697	chr3:105372327-105372328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188950998	chr3:105372339-105372340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201842372	chr3:105372411-105372412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528763082	chr3:105372425-105372426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs33939500	chr3:105372427-105372428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192518139	chr3:105372507-105372508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79147496	chr3:105372519-105372520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530872737	chr3:105372527-105372528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546104554	chr3:105372608-105372609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146351928	chr3:105372627-105372628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139770711	chr3:105372672-105372673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184378392	chr3:105372721-105372722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546763496	chr3:105372754-105372755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568580276	chr3:105372762-105372763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529267368	chr3:105372781-105372782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550946040	chr3:105372800-105372801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569282816	chr3:105372821-105372822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144482864	chr3:105372845-105372846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558103071	chr3:105372882-105372883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566525665	chr3:105372907-105372908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534024315	chr3:105372944-105372945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186875853	chr3:105372958-105372959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73854349	chr3:105372966-105372967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs35744952	chr3:105373006-105373007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191598024	chr3:105373007-105373008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555709223	chr3:105373008-105373009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577240109	chr3:105373026-105373027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546067627	chr3:105373028-105373029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184120364	chr3:105373057-105373058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573349119	chr3:105373058-105373059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540867684	chr3:105373088-105373089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148821355	chr3:105373098-105373099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530912528	chr3:105373103-105373104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529345754	chr3:105373104-105373105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551107389	chr3:105373137-105373138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562842057	chr3:105373152-105373153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546275540	chr3:105373190-105373191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs16851395	chr3:105373208-105373209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370829801	chr3:105373325-105373326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566797904	chr3:105373331-105373332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77715978	chr3:105373342-105373343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188913035	chr3:105373349-105373350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549121254	chr3:105373363-105373364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566926161	chr3:105373370-105373371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3362 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105366000-105377200	Weak transcription	NHDF-Ad	bronchial
2	chr3:105366600-105373600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr3:105366600-105375400	Weak transcription	NH-A	brain
4	chr3:105366800-105375200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:105366800-105375400	Weak transcription	Osteobl	bone
6	chr3:105367400-105377600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:105368600-105376800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:105368800-105376800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr3:105368800-105377600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:105368800-105388400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:105368800-105393400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:105369200-105375800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr3:105369400-105375600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:105369600-105375800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr3:105371000-105374800	Weak transcription	Fetal Heart	heart
16	chr3:105371400-105377400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr3:105371400-105382200	Weak transcription	Lung	lung
18	chr3:105371800-105377200	Weak transcription	Fetal Stomach	stomach
19	chr3:105372000-105372200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr3:105372000-105372200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:105372000-105372200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:105372000-105372200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr3:105372000-105381800	Weak transcription	Pancreas	Pancrea
24	chr3:105372200-105372400	Enhancers	Primary B cells from peripheral blood	blood
25	chr3:105372200-105373800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:105372200-105376000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr3:105372200-105377000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr3:105372200-105380800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr3:105372200-105387400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr3:105372400-105376000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr3:105372400-105376400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr3:105372400-105388000	Weak transcription	Stomach Mucosa	stomach
33	chr3:105372600-105374600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:105372800-105373000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:105372800-105373000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:105372800-105373000	Enhancers	Gastric	stomach
37	chr3:105372800-105373000	Enhancers	Right Ventricle	heart
38	chr3:105372800-105373400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr3:105373000-105377200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:105373000-105377600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:105373000-105381800	Weak transcription	Right Ventricle	heart
42	chr3:105373000-105387800	Weak transcription	Gastric	stomach
43	chr3:105373000-105419600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr3:105373200-105376400	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr3:105373400-105375600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:105373400-105376200	Weak transcription	Primary B cells from cord blood	blood
47	chr3:105373400-105376600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:105373400-105376600	Weak transcription	Placenta	Placenta
49	chr3:105373400-105401600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:105373600-105373800	Enhancers	Fetal Lung	lung

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