Variant report

Variant	nsv536300
Chromosome Location	chr3:578914-880722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:707)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:599789-600089	GM12878	blood:	n/a	chr3:599953-599962
2	BATF	chr3:638972-639242	GM12878	blood:	n/a	chr3:639093-639102
3	BATF	chr3:599827-600084	GM12878	blood:	n/a	chr3:599953-599962
4	BCLAF1	chr3:599656-600200	GM12878	blood:	n/a	chr3:599779-599788 chr3:599826-599835
5	BHLHE40	chr3:846853-846863	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:649451-649478	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr3:817416-817453	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr3:674381-674581	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr3:638578-639330	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr3:754720-755580	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr3:815996-816027	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:639591-639851	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:638934-639824	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:754275-756263	Hela-S3	cervix:	n/a	chr3:754384-754393 chr3:754382-754393 chr3:755103-755114
15	CEBPB	chr3:780130-780267	K562	blood:	n/a	chr3:780198-780209
16	CEBPB	chr3:591255-591764	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:674328-674574	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:700968-701307	HepG2	liver:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
19	CEBPB	chr3:672472-672697	A549	lung:	n/a	chr3:672554-672567 chr3:672555-672566
20	CEBPB	chr3:697395-697928	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:650024-650224	A549	lung:	n/a	chr3:650073-650084 chr3:650075-650084
22	CEBPB	chr3:780119-780347	HepG2	liver:	n/a	chr3:780198-780209
23	CEBPB	chr3:879534-879816	A549	lung:	n/a	n/a
24	CEBPB	chr3:780178-780270	H1-hESC	embryonic stem cell:	n/a	chr3:780198-780209
25	CEBPB	chr3:834255-834315	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:872412-872499	A549	lung:	n/a	n/a
27	CEBPB	chr3:766028-766169	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:754295-754516	HepG2	liver:	n/a	chr3:754384-754393 chr3:754382-754393
29	CEBPB	chr3:672488-672700	HepG2	liver:	n/a	chr3:672554-672567 chr3:672555-672566
30	CEBPB	chr3:700965-701296	IMR90	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
31	CEBPB	chr3:649124-649464	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:637765-638119	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:649955-650248	IMR90	lung:	n/a	chr3:650073-650084 chr3:650075-650084
34	CEBPB	chr3:816945-817493	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:650039-650244	HepG2	liver:	n/a	chr3:650073-650084 chr3:650075-650084
36	CEBPB	chr3:611097-611344	HepG2	liver:	n/a	chr3:611201-611212
37	CEBPB	chr3:775096-775429	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:701078-701278	A549	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
39	CEBPB	chr3:766071-766268	HepG2	liver:	n/a	chr3:766173-766184
40	CEBPB	chr3:700997-701241	H1-hESC	embryonic stem cell:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
41	CEBPB	chr3:700961-701300	Hela-S3	cervix:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
42	CEBPB	chr3:746911-747209	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:795219-795424	K562	blood:	n/a	n/a
44	CHD1	chr3:660628-660658	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr3:639101-639345	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr3:754899-755419	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr3:834356-834507	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:612787-612876	GM13976	blood:	n/a	n/a
49	CTCF	chr3:674374-674510	MCF-7	breast:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
50	CTCF	chr3:662427-662492	GM20000	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:782757-782807	K562	blood:	n/a
2	chr3:782757-782807	AG09309	skin:	n/a
3	chr3:782757-782807	BJ	skin:	n/a
4	chr3:782757-782807	GM12891	blood:	n/a
5	chr3:782757-782807	HRE	kidney:	n/a
6	chr3:782757-782807	BE2_C	brain:	n/a
7	chr3:782757-782807	GM12878	blood:	n/a
8	chr3:782757-782807	HEK293	kidney:	embryo
9	chr3:782757-782807	A549	lung:	n/a
10	chr3:782757-782807	Jurkat	blood:	n/a
11	chr3:782757-782807	Caco-2	colon:	n/a
12	chr3:782757-782807	NH-A	brain:	n/a
13	chr3:782757-782807	ovcar-3	ovarian:	n/a
14	chr3:782757-782807	AG04450	lung:	fetal
15	chr3:782757-782807	MCF-7	breast:	n/a
16	chr3:782757-782807	GM12892	blood:	n/a
17	chr3:782757-782807	HRPEpiC	eye:	n/a
18	chr3:782757-782807	HAEpiC	amniotic membrane:	n/a
19	chr3:782757-782807	NHDF-neo	bronchial:	n/a
20	chr3:782757-782807	SK-N-SH_RA	brain:	n/a
21	chr3:782757-782807	AG09319	gingival:	n/a
22	chr3:782757-782807	HRCEpiC	kidney:	n/a
23	chr3:782757-782807	HUVEC	blood vessel:	n/a
24	chr3:782757-782807	HCF	heart:	n/a
25	chr3:782757-782807	RPTEC	kidney:	n/a
26	chr3:782757-782807	SK-N-SH	brain:	n/a
27	chr3:782757-782807	HCM	heart:	n/a
28	chr3:782757-782807	U87	brain:	n/a
29	chr3:782757-782807	NHBE	bronchial:	n/a
30	chr3:782757-782807	HEEpiC	esophagus:	n/a
31	chr3:782757-782807	SKMC	muscle:	n/a
32	chr3:782757-782807	SAEC	small airway:	n/a
33	chr3:782757-782807	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:782757-782807	HepG2	liver:	n/a
35	chr3:782757-782807	Hela-S3	cervix:	n/a
36	chr3:782757-782807	LNCaP	prostate:	n/a
37	chr3:782757-782807	CMK	blood:	n/a
38	chr3:782757-782807	HCT-116	colon:	n/a
39	chr3:782757-782807	IMR90	lung:	fetal
40	chr3:782757-782807	PrEC	prostate:	n/a
41	chr3:782757-782807	AG10803	skin:	n/a
42	chr3:782757-782807	HCPEpiC	choroid plexus:	n/a
43	chr3:782757-782807	AG04449	skin:	fetal
44	chr3:782757-782807	AoSMC	blood vessel:	n/a
45	chr3:782757-782807	SK-N-MC	brain:	n/a
46	chr3:782757-782807	NT2-D1	testis:	n/a
47	chr3:782757-782807	Hepatocyte	liver:	n/a
48	chr3:782757-782807	HIPEpiC	eye:	n/a
49	chr3:782757-782807	H1-hESC	embryonic stem cell:	embryo
50	chr3:782757-782807	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
2	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
3	chr3:805612..808013-chr3:811141..813375,2	K562	blood:
4	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
5	chr12:101154422..101155178-chr3:753774..754622,2	MCF-7	breast:
6	chr20:14175439..14177996-chr3:730394..733241,2	MCF-7	breast:
7	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
8	chr3:674217..674800-chr3:1123463..1123990,2	MCF-7	breast:
9	chr3:726576..727076-chr3:11025934..11026463,2	MCF-7	breast:
10	chr3:674203..674975-chr3:2197712..2198482,2	MCF-7	breast:
11	chr20:12921782..12922300-chr3:762237..762760,2	MCF-7	breast:
12	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
13	chr21:9517250..9519290-chr3:632442..635070,2	MCF-7	breast:
14	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
15	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
16	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
17	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
18	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
19	chr21:9537493..9539688-chr3:612236..614804,2	MCF-7	breast:
20	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
21	chr1:229050784..229051693-chr3:758018..758663,2	MCF-7	breast:
22	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
23	chr21:9533639..9536328-chr3:614645..617390,2	MCF-7	breast:
24	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
25	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
26	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
27	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
28	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
29	chr3:805612..808013-chr3:811141..813375,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:868690-868816	ENSG00000224957
2	lnc-CHL1-3	chr3:633788-633866	NR_110118
3	lnc-IL5RA-14	chr3:659472-659997	NONHSAT087571
4	lnc-CHL1-3	chr3:633788-633866	ENSG00000224957
5	lnc-CHL1-6	chr3:608788-608866	ucscGeneNc_uc003boy_1
6	lnc-CHL1-3	chr3:791898-791933	ENSG00000224957
7	lnc-CHL1-6	chr3:857398-857493	ucscGeneNc_uc003boy_1
8	lnc-CHL1-6	chr3:766898-766933	ucscGeneNc_uc003boy_1
9	lnc-CHL1-6	chr3:859059-862698	ucscGeneNc_uc003boy_1
10	lnc-CHL1-3	chr3:791898-791933	NR_110118
11	lnc-CHL1-3	chr3:577941-579275	NONHSAT087570

No data

Variant related genes	Relation type
ENSG00000238075	TF binding region
ENSG00000238075	CpG island
IL10	miRNA target sites
DCBLD2	miRNA target sites
HIF1A	miRNA target sites

Extended variants
information (count: 4204 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4204 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541243098	chr3:579005-579006	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs559250392	chr3:579028-579029	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs77498446	chr3:579031-579032	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs541677636	chr3:579069-579070	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs563241467	chr3:579074-579075	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs530467326	chr3:579152-579153	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs72991423	chr3:579153-579154	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs371681781	chr3:579161-579162	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs4685874	chr3:579178-579179	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77730999	chr3:579198-579199	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs184703246	chr3:579205-579206	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs566092062	chr3:579206-579207	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs576422588	chr3:579224-579225	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs115720412	chr3:579233-579234	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs558925905	chr3:579241-579242	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs4684467	chr3:579260-579261	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs4685876	chr3:579313-579314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537470262	chr3:579372-579373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558964430	chr3:579394-579395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541923331	chr3:579400-579401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570940342	chr3:579402-579403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13327178	chr3:579414-579415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569428192	chr3:579423-579424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574594311	chr3:579431-579432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541617233	chr3:579455-579456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376139716	chr3:579503-579504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4684468	chr3:579515-579516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs6800552	chr3:579540-579541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545407816	chr3:579550-579551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563883510	chr3:579578-579579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13322154	chr3:579584-579585	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542437195	chr3:579596-579597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148466087	chr3:579633-579634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190597766	chr3:579674-579675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555704890	chr3:579698-579699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575760927	chr3:579699-579700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73092890	chr3:579723-579724	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548778148	chr3:579752-579753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182160632	chr3:579785-579786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531197597	chr3:579817-579818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543552391	chr3:579820-579821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528802238	chr3:579868-579869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546989343	chr3:579889-579890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73092892	chr3:579914-579915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553234153	chr3:579971-579972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568483342	chr3:579974-579975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535564741	chr3:580009-580010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7616596	chr3:580021-580022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535297517	chr3:580022-580023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563327375	chr3:580026-580027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:577200-579000	Active TSS	Brain Hippocampus Middle	brain
2	chr3:577400-579000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:577400-579000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:577400-579000	Active TSS	Fetal Kidney	kidney
5	chr3:577400-579000	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr3:577400-579000	Active TSS	Stomach Smooth Muscle	stomach
7	chr3:577400-579000	Active TSS	NHLF	lung
8	chr3:577600-579000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:577600-579000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:577600-579000	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr3:577600-579000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr3:577600-579000	Active TSS	Right Atrium	heart
13	chr3:578400-583000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:578800-579000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr3:578800-579000	Flanking Active TSS	Fetal Lung	lung
16	chr3:578800-582800	Weak transcription	Fetal Muscle Leg	muscle
17	chr3:578800-583000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:579000-579200	Enhancers	Fetal Lung	lung
19	chr3:579200-581800	Weak transcription	Fetal Lung	lung
20	chr3:581800-582800	Enhancers	Fetal Lung	lung
21	chr3:582800-583000	Enhancers	Ovary	ovary
22	chr3:582800-583200	Flanking Active TSS	Fetal Lung	lung
23	chr3:582800-583400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr3:582800-583400	Active TSS	Fetal Kidney	kidney
25	chr3:582800-584000	Enhancers	Fetal Muscle Leg	muscle
26	chr3:583000-583200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:583000-583200	Enhancers	Fetal Stomach	stomach
28	chr3:583000-583400	Flanking Active TSS	Ovary	ovary
29	chr3:583000-585000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:583200-584200	Enhancers	Fetal Lung	lung
31	chr3:583200-584800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr3:583400-583800	Weak transcription	Fetal Kidney	kidney
33	chr3:583400-584000	Enhancers	Ovary	ovary
34	chr3:583800-584000	Enhancers	Fetal Kidney	kidney
35	chr3:584000-584200	Enhancers	Fetal Stomach	stomach
36	chr3:584000-584600	Weak transcription	Fetal Kidney	kidney
37	chr3:584000-584600	Weak transcription	Fetal Muscle Leg	muscle
38	chr3:584600-584800	Enhancers	Fetal Kidney	kidney
39	chr3:584600-584800	Enhancers	Fetal Muscle Leg	muscle
40	chr3:584800-585800	Weak transcription	Fetal Muscle Leg	muscle
41	chr3:584800-587400	Weak transcription	Fetal Kidney	kidney
42	chr3:585800-587800	Enhancers	Fetal Muscle Leg	muscle
43	chr3:586800-588800	Enhancers	Hela-S3	cervix
44	chr3:587200-587600	Enhancers	Fetal Brain Male	brain
45	chr3:587400-587800	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr3:587400-588800	Active TSS	Fetal Muscle Trunk	muscle
47	chr3:587600-587800	Enhancers	Fetal Kidney	kidney
48	chr3:587600-587800	Enhancers	Psoas Muscle	Psoas
49	chr3:587800-588000	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr3:587800-588000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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