Variant report

Variant	nsv536664
Chromosome Location	chr3:98815244-98947271
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	chr3:98892032-98892087	HepG2	liver:	n/a	n/a
2	BATF	chr3:98830078-98830466	GM12878	blood:	n/a	chr3:98830301-98830312
3	BATF	chr3:98830193-98830469	GM12878	blood:	n/a	chr3:98830301-98830312
4	BCL3	chr3:98827422-98827724	GM12878	blood:	n/a	n/a
5	BRCA1	chr3:98930300-98930345	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:98869565-98869661	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:98945624-98945864	HepG2	liver:	n/a	chr3:98945722-98945733
8	CEBPB	chr3:98827333-98827860	IMR90	lung:	n/a	n/a
9	CEBPB	chr3:98827512-98827736	A549	lung:	n/a	n/a
10	CEBPB	chr3:98895292-98895657	IMR90	lung:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
11	CEBPB	chr3:98827449-98827723	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:98847617-98848596	IMR90	lung:	n/a	chr3:98848200-98848208
13	CEBPB	chr3:98895351-98895574	A549	lung:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
14	CEBPB	chr3:98895381-98895526	Hela-S3	cervix:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
15	CEBPB	chr3:98837356-98837695	IMR90	lung:	n/a	chr3:98837560-98837573
16	CEBPB	chr3:98897865-98898056	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:98848521-98848696	A549	lung:	n/a	n/a
18	CEBPB	chr3:98927039-98927064	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:98888858-98889087	HepG2	liver:	n/a	chr3:98889001-98889012
20	CEBPB	chr3:98895313-98895658	HepG2	liver:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
21	CEBPB	chr3:98888891-98889173	A549	lung:	n/a	chr3:98889001-98889012
22	CEBPB	chr3:98847729-98847776	A549	lung:	n/a	n/a
23	CHD1	chr3:98833214-98833953	IMR90	lung:	n/a	n/a
24	CHD2	chr3:98829994-98829996	GM12878	blood:	n/a	n/a
25	CHD2	chr3:98891868-98891881	HepG2	liver:	n/a	n/a
26	CTCF	chr3:98891923-98892227	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:98867980-98868130	HAc	cerebellar:	n/a	n/a
28	CTCF	chr3:98838020-98838170	HAc	cerebellar:	n/a	n/a
29	CTCF	chr3:98891963-98892190	GM10248	blood:	n/a	n/a
30	CTCF	chr3:98891938-98892211	GM12878	blood:	n/a	n/a
31	CTCF	chr3:98817716-98817865	A549	lung:	n/a	n/a
32	CTCF	chr3:98891860-98892010	WI-38	lung:	n/a	n/a
33	CTCF	chr3:98892000-98892150	HepG2	liver:	n/a	n/a
34	CTCF	chr3:98833520-98833670	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:98833496-98833692	GM12891	blood:	n/a	n/a
36	CTCF	chr3:98833560-98833710	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr3:98817556-98817922	K562	blood:	n/a	n/a
38	CTCF	chr3:98817693-98817894	GM12892	blood:	n/a	n/a
39	CTCF	chr3:98833520-98833670	SAEC	small airway:	n/a	n/a
40	CTCF	chr3:98833460-98833610	HMEC	breast:	n/a	n/a
41	CTCF	chr3:98833480-98833630	GM12865	blood:	n/a	n/a
42	CTCF	chr3:98833500-98833650	AG09319	gingival:	n/a	n/a
43	CTCF	chr3:98833500-98833650	GM12869	blood:	n/a	n/a
44	CTCF	chr3:98891956-98892198	LNCaP	prostate:	n/a	n/a
45	CTCF	chr3:98833500-98833650	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr3:98892000-98892150	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr3:98833460-98833610	GM12870	blood:	n/a	n/a
48	CTCF	chr3:98891960-98892110	HCM	heart:	n/a	n/a
49	CTCF	chr3:98833457-98833741	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:98833471-98833712	GM12892	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98848062-98848112	HCT-116	colon:	n/a
2	chr3:98848062-98848112	AG04449	skin:	fetal
3	chr3:98848062-98848112	NH-A	brain:	n/a
4	chr3:98848062-98848112	U87	brain:	n/a
5	chr3:98848062-98848112	ovcar-3	ovarian:	n/a
6	chr3:98848062-98848112	BJ	skin:	n/a
7	chr3:98848062-98848112	MCF-7	breast:	n/a
8	chr3:98848062-98848112	CMK	blood:	n/a
9	chr3:98848062-98848112	SK-N-SH	brain:	n/a
10	chr3:98848062-98848112	IMR90	lung:	fetal
11	chr3:98848062-98848112	PFSK-1	brain:	n/a
12	chr3:98848062-98848112	HepG2	liver:	n/a
13	chr3:98848062-98848112	AG04450	lung:	fetal
14	chr3:98848062-98848112	AG09319	gingival:	n/a
15	chr3:98848062-98848112	HAEpiC	amniotic membrane:	n/a
16	chr3:98848062-98848112	GM19239	blood:	n/a
17	chr3:98848062-98848112	T-47D	breast:	n/a
18	chr3:98848062-98848112	HL-60	blood:	n/a
19	chr3:98848062-98848112	SAEC	small airway:	n/a
20	chr3:98848062-98848112	HUVEC	blood vessel:	n/a
21	chr3:98848062-98848112	HCM	heart:	n/a
22	chr3:98848062-98848112	ECC-1	luminal epithelium:	n/a
23	chr3:98848062-98848112	PrEC	prostate:	n/a
24	chr3:98848062-98848112	LNCaP	prostate:	n/a
25	chr3:98848062-98848112	GM12892	blood:	n/a
26	chr3:98848062-98848112	RPTEC	kidney:	n/a
27	chr3:98848062-98848112	SKMC	muscle:	n/a
28	chr3:98848062-98848112	SK-N-SH_RA	brain:	n/a
29	chr3:98848062-98848112	GM12878	blood:	n/a
30	chr3:98848062-98848112	AG09309	skin:	n/a
31	chr3:98848062-98848112	HIPEpiC	eye:	n/a
32	chr3:98848062-98848112	ProgFib	skin:	n/a
33	chr3:98848062-98848112	K562	blood:	n/a
34	chr3:98848062-98848112	A549	lung:	n/a
35	chr3:98848062-98848112	GM06990	blood:	n/a
36	chr3:98848062-98848112	Hela-S3	cervix:	n/a
37	chr3:98848062-98848112	HRPEpiC	eye:	n/a
38	chr3:98848062-98848112	NHDF-neo	bronchial:	n/a
39	chr3:98848062-98848112	PANC-1	pancreas:	n/a
40	chr3:98848062-98848112	NB4	blood:	n/a
41	chr3:98848062-98848112	HEEpiC	esophagus:	n/a
42	chr3:98848062-98848112	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:98848062-98848112	MCF10A-Er-Src	breast:	n/a
44	chr3:98848062-98848112	SK-N-MC	brain:	n/a
45	chr3:98848062-98848112	HNPCEpiC	eye:	n/a
46	chr3:98848062-98848112	HCF	heart:	n/a
47	chr3:98848062-98848112	NHBE	bronchial:	n/a
48	chr3:98848062-98848112	Caco-2	colon:	n/a
49	chr3:98848062-98848112	HMEC	breast:	n/a
50	chr3:98848062-98848112	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
2	chr3:98822685..98824986-chr3:98826352..98828099,2	K562	blood:
3	chr3:98833143..98834039-chr3:99250824..99251730,3	MCF-7	breast:
4	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
5	chr3:98833207..98833983-chr3:99472028..99472879,3	MCF-7	breast:
6	chr3:98839672..98842383-chr3:98845089..98846835,2	K562	blood:
7	chr3:98819273..98821037-chr3:98825327..98828696,3	K562	blood:
8	chr3:98819273..98821037-chr3:98825327..98828696,3	K562	blood:
9	chr3:98742229..98743324-chr3:98833134..98833747,3	MCF-7	breast:
10	chr3:98833031..98833794-chr3:98891585..98892473,5	MCF-7	breast:
11	chr3:98839672..98842383-chr3:98845089..98846835,2	K562	blood:
12	chr3:98833031..98833794-chr3:98891585..98892473,5	MCF-7	breast:
13	chr3:98833374..98834517-chr3:99507971..99508723,4	MCF-7	breast:
14	chr3:98742090..98742958-chr3:98891307..98892432,5	MCF-7	breast:
15	chr3:98742225..98743062-chr3:98891577..98892142,2	MCF-7	breast:
16	chr3:98822685..98824986-chr3:98826352..98828099,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCBLD2-2	chr3:98934068-98935110	NONHSAT090839
2	lnc-ST3GAL6-6	chr3:98904502-98904611	NONHSAT090838
3	lnc-ST3GAL6-6	chr3:98899387-98899480	NONHSAT090838
4	lnc-ST3GAL6-6	chr3:98896222-98896357	NONHSAT090838

Variant related genes	Relation type
ACTG1P13	TF binding region
ACTG1P13	CpG island

Extended variants
information (count: 4822 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4822 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377754911	chr3:98815276-98815277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75252945	chr3:98815468-98815469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544778116	chr3:98815506-98815507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181866401	chr3:98815528-98815529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548977845	chr3:98815564-98815565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6778584	chr3:98815640-98815641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs77805077	chr3:98815659-98815660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115302843	chr3:98815741-98815742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77175873	chr3:98815742-98815743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375740997	chr3:98815749-98815750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561465494	chr3:98815760-98815761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185232178	chr3:98815825-98815826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556950441	chr3:98815843-98815844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573870522	chr3:98815907-98815908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567130445	chr3:98815938-98815939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190828755	chr3:98816003-98816004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532088223	chr3:98816026-98816027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9836746	chr3:98816037-98816038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs182630685	chr3:98816128-98816129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186467237	chr3:98816150-98816151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558382664	chr3:98816166-98816167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555892162	chr3:98816196-98816197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368774311	chr3:98816222-98816223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs578174801	chr3:98816259-98816260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191294658	chr3:98816260-98816261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563722181	chr3:98816261-98816262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573914433	chr3:98816272-98816273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542914168	chr3:98816273-98816274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571674009	chr3:98816294-98816295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79430252	chr3:98816348-98816349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7635255	chr3:98816357-98816358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs112088793	chr3:98816378-98816379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551201540	chr3:98816390-98816391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183123807	chr3:98816407-98816408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2222444	chr3:98816409-98816410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550377566	chr3:98816421-98816422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567270256	chr3:98816443-98816444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535832605	chr3:98816462-98816463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145355650	chr3:98816480-98816481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549702861	chr3:98816505-98816506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566425942	chr3:98816603-98816604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11706893	chr3:98816659-98816660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536327329	chr3:98816717-98816718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558426729	chr3:98816736-98816737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571782608	chr3:98816801-98816802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541249134	chr3:98816803-98816804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148763674	chr3:98816949-98816950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557132943	chr3:98816960-98816961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187500268	chr3:98816987-98816988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376786927	chr3:98817025-98817026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98815000-98817400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:98817400-98818000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:98818000-98828600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:98822400-98827200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:98823400-98826600	Weak transcription	NHDF-Ad	bronchial
6	chr3:98826400-98827800	Enhancers	NHLF	lung
7	chr3:98826400-98828200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:98826600-98827600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr3:98826600-98828000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:98826600-98828000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:98826600-98828000	Enhancers	HMEC	breast
12	chr3:98826600-98828200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr3:98826600-98828400	Enhancers	NHDF-Ad	bronchial
14	chr3:98826800-98827000	Enhancers	HSMMtube	muscle
15	chr3:98826800-98827200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:98826800-98828000	Enhancers	NHEK	skin
17	chr3:98826800-98828800	Enhancers	HUVEC	blood vessel
18	chr3:98827000-98827800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:98827000-98828000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:98827000-98828000	Enhancers	HSMM	muscle
21	chr3:98827000-98828000	Enhancers	NH-A	brain
22	chr3:98827000-98828000	Enhancers	Osteobl	bone
23	chr3:98827200-98827800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:98827200-98828000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:98827400-98828000	Enhancers	Adipose Nuclei	Adipose
26	chr3:98827600-98827800	Enhancers	HSMMtube	muscle
27	chr3:98827600-98836600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr3:98827800-98830000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:98828000-98829600	Weak transcription	HMEC	breast
30	chr3:98828000-98830000	Weak transcription	Osteobl	bone
31	chr3:98828000-98830200	Weak transcription	NHEK	skin
32	chr3:98828000-98830400	Weak transcription	HSMM	muscle
33	chr3:98828000-98837800	Weak transcription	NH-A	brain
34	chr3:98828000-98838000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:98828200-98829600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:98828200-98837200	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:98828600-98829200	Enhancers	Fetal Brain Male	brain
38	chr3:98829200-98832200	Weak transcription	Fetal Brain Male	brain
39	chr3:98829600-98830600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:98829600-98831200	Enhancers	HMEC	breast
41	chr3:98830000-98830200	Enhancers	Osteobl	bone
42	chr3:98830000-98830600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:98830200-98830600	Enhancers	NHEK	skin
44	chr3:98830200-98830600	Weak transcription	Osteobl	bone
45	chr3:98830400-98830600	Enhancers	HSMM	muscle
46	chr3:98832200-98832400	Enhancers	Fetal Brain Male	brain
47	chr3:98833600-98834000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr3:98833600-98834400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr3:98833800-98834400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr3:98833800-98834400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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