Variant report

Variant	nsv10297
Chromosome Location	chr3:103721772-104050133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1173)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:103724705-103724974	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:103925893-103926002	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:103991942-103992244	HepG2	liver:	n/a	n/a
4	BACH1	chr3:103884809-103885080	K562	blood:	n/a	chr3:103884906-103884920
5	BACH1	chr3:104042194-104042390	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:103884749-103885041	H1-hESC	embryonic stem cell:	n/a	chr3:103884906-103884920
7	BHLHE40	chr3:103759961-103759976	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:103821208-103821464	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:103810880-103810900	GM12878	blood:	n/a	n/a
10	CEBPB	chr3:103796855-103796941	A549	lung:	n/a	n/a
11	CEBPB	chr3:104011498-104011752	HepG2	liver:	n/a	chr3:104011674-104011685 chr3:104011676-104011687 chr3:104011676-104011685
12	CEBPB	chr3:103939250-103939605	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:103785596-103785936	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:103897556-103897933	A549	lung:	n/a	chr3:103897701-103897712 chr3:103897765-103897776
15	CEBPB	chr3:103724727-103724957	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:103934828-103934918	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:103785603-103785893	A549	lung:	n/a	n/a
18	CEBPB	chr3:103924619-103924818	A549	lung:	n/a	chr3:103924684-103924693 chr3:103924682-103924693
19	CEBPB	chr3:103785580-103785896	IMR90	lung:	n/a	n/a
20	CEBPB	chr3:103785574-103785961	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:103883444-103883622	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr3:104043708-104043981	HepG2	liver:	n/a	chr3:104043849-104043860
23	CEBPB	chr3:103857054-103857254	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:103856039-103856350	HepG2	liver:	n/a	chr3:103856132-103856145 chr3:103856180-103856193
25	CEBPB	chr3:104043811-104043974	A549	lung:	n/a	chr3:104043849-104043860
26	CEBPB	chr3:103811784-103812069	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:103897592-103897940	IMR90	lung:	n/a	chr3:103897701-103897712 chr3:103897765-103897776
28	CEBPB	chr3:103897563-103897926	HepG2	liver:	n/a	chr3:103897701-103897712 chr3:103897765-103897776
29	CEBPB	chr3:103855958-103856371	Hela-S3	cervix:	n/a	chr3:103856132-103856145 chr3:103856180-103856193
30	CEBPB	chr3:103869532-103869863	HepG2	liver:	n/a	chr3:103869676-103869687
31	CEBPB	chr3:103821162-103821469	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:103785587-103785944	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr3:103992011-103992184	HepG2	liver:	n/a	n/a
34	CREB1	chr3:103821148-103821581	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:103821280-103821430	HCT-116	colon:	n/a	n/a
36	CTCF	chr3:103992000-103992150	MCF-7	breast:	n/a	chr3:103992074-103992092 chr3:103992076-103992097 chr3:103992075-103992091
37	CTCF	chr3:103821260-103821410	GM12868	blood:	n/a	n/a
38	CTCF	chr3:103991920-103992070	GM12864	blood:	n/a	n/a
39	CTCF	chr3:103821140-103821598	HCT-116	colon:	n/a	n/a
40	CTCF	chr3:103868064-103868280	T-47D	breast:	n/a	n/a
41	CTCF	chr3:103821260-103821410	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:103991960-103992110	BJ	skin:	n/a	chr3:103992074-103992092 chr3:103992076-103992097 chr3:103992075-103992091
43	CTCF	chr3:103991980-103992130	GM06990	blood:	n/a	chr3:103992074-103992092 chr3:103992076-103992097 chr3:103992075-103992091
44	CTCF	chr3:103821340-103821490	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr3:103821225-103821434	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr3:103821222-103821491	GM13977	blood:	n/a	n/a
47	CTCF	chr3:103821174-103821480	K562	blood:	n/a	n/a
48	CTCF	chr3:103991937-103992207	Spleen_OC	spleen:	n/a	chr3:103992074-103992092 chr3:103992076-103992097 chr3:103992075-103992091
49	CTCF	chr3:103821150-103821544	IMR90	lung:	n/a	n/a
50	CTCF	chr3:103738020-103738170	HBMEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:103930387-103930437	MCF10A-Er-Src	breast:	n/a
2	chr3:103930387-103930437	HAEpiC	amniotic membrane:	n/a
3	chr3:103930387-103930437	MCF-7	breast:	n/a
4	chr3:103930387-103930437	GM12878	blood:	n/a
5	chr3:103926553-103926603	HRPEpiC	eye:	n/a
6	chr3:104009869-104009919	HRCEpiC	kidney:	n/a
7	chr3:103930387-103930437	HIPEpiC	eye:	n/a
8	chr3:103926553-103926603	ProgFib	skin:	n/a
9	chr3:104009869-104009919	PFSK-1	brain:	n/a
10	chr3:103926553-103926603	U87	brain:	n/a
11	chr3:104009869-104009919	K562	blood:	n/a
12	chr3:103926553-103926603	HMEC	breast:	n/a
13	chr3:104009869-104009919	NH-A	brain:	n/a
14	chr3:103930387-103930437	GM12891	blood:	n/a
15	chr3:103926553-103926603	HCF	heart:	n/a
16	chr3:103926553-103926603	GM12891	blood:	n/a
17	chr3:103926553-103926603	MCF10A-Er-Src	breast:	n/a
18	chr3:103930387-103930437	HNPCEpiC	eye:	n/a
19	chr3:103930387-103930437	LNCaP	prostate:	n/a
20	chr3:104009869-104009919	NHDF-neo	bronchial:	n/a
21	chr3:104009869-104009919	GM12892	blood:	n/a
22	chr3:103930387-103930437	SAEC	small airway:	n/a
23	chr3:103926553-103926603	GM12892	blood:	n/a
24	chr3:104009869-104009919	HEEpiC	esophagus:	n/a
25	chr3:103926553-103926603	SAEC	small airway:	n/a
26	chr3:103926553-103926603	HRE	kidney:	n/a
27	chr3:103930387-103930437	Hela-S3	cervix:	n/a
28	chr3:103930387-103930437	Jurkat	blood:	n/a
29	chr3:103926553-103926603	AG04449	skin:	fetal
30	chr3:103926553-103926603	IMR90	lung:	fetal
31	chr3:103926553-103926603	AG04450	lung:	fetal
32	chr3:103926553-103926603	BE2_C	brain:	n/a
33	chr3:104009869-104009919	ovcar-3	ovarian:	n/a
34	chr3:104009869-104009919	AG04450	lung:	fetal
35	chr3:104009869-104009919	GM19239	blood:	n/a
36	chr3:104009869-104009919	HIPEpiC	eye:	n/a
37	chr3:103926553-103926603	HAEpiC	amniotic membrane:	n/a
38	chr3:103926553-103926603	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:103930387-103930437	SK-N-SH	brain:	n/a
40	chr3:103926553-103926603	HIPEpiC	eye:	n/a
41	chr3:103926553-103926603	SK-N-SH	brain:	n/a
42	chr3:103926553-103926603	SK-N-SH_RA	brain:	n/a
43	chr3:103930387-103930437	NHDF-neo	bronchial:	n/a
44	chr3:103930387-103930437	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:104009869-104009919	HL-60	blood:	n/a
46	chr3:104009869-104009919	U87	brain:	n/a
47	chr3:103930387-103930437	ProgFib	skin:	n/a
48	chr3:103930387-103930437	HEEpiC	esophagus:	n/a
49	chr3:103926553-103926603	Caco-2	colon:	n/a
50	chr3:103926553-103926603	T-47D	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:104019759..104021466-chr3:104032792..104034849,2	MCF-7	breast:
2	chr3:103880993..103882582-chr3:103882964..103884489,2	MCF-7	breast:
3	chr3:103991921..103992642-chr3:104110921..104111912,5	MCF-7	breast:
4	chr3:103826755..103828262-chr3:103828801..103830471,2	MCF-7	breast:
5	chr3:103880993..103882582-chr3:103882964..103884489,2	MCF-7	breast:
6	chr3:103994526..103998414-chr3:104000524..104003642,3	MCF-7	breast:
7	chr3:103994526..103998414-chr3:104000524..104003642,3	MCF-7	breast:
8	chr3:104019759..104021466-chr3:104032792..104034849,2	MCF-7	breast:
9	chr3:103709950..103710945-chr3:103925530..103926295,2	MCF-7	breast:
10	chr3:103821229..103821749-chr3:103925613..103926201,2	MCF-7	breast:
11	chr2:43448083..43448937-chr3:103955529..103956134,2	MCF-7	breast:
12	chr3:103801464..103801966-chr9:129631201..129631808,2	MCF-7	breast:
13	chr3:103821229..103821749-chr3:103925613..103926201,2	MCF-7	breast:
14	chr3:103826755..103828262-chr3:103828801..103830471,2	MCF-7	breast:
15	chr3:103672576..103675146-chr3:103946117..103948469,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALCAM-13	chr3:103994987-103995208	NONHSAT090953
2	lnc-CBLB-16	chr3:103875288-103875520	l_2422_chr3:103870374-103876716_testes
3	lnc-ALCAM-17	chr3:103927315-103927591	l_2423_chr3:103927314-103929100_testes
4	lnc-ALCAM-16	chr3:103999604-104000347	NONHSAT090950
5	lnc-ALCAM-18	chr3:103781883-103782426	NONHSAT090947
6	lnc-ALCAM-16	chr3:103984584-103984654	FPKM1_group_21625_transcript_5
7	lnc-ALCAM-15	chr3:103987096-103987447	NONHSAT090951
8	lnc-ALCAM-16	chr3:103986086-103986829	FPKM1_group_21625_transcript_5
9	lnc-ALCAM-16	chr3:103984584-103984654	NONHSAT090950
10	lnc-ALCAM-17	chr3:103928928-103929115	l_2423_chr3:103927314-103929100_testes
11	lnc-CBLB-16	chr3:103870375-103870796	l_2422_chr3:103870374-103876716_testes
12	lnc-CBLB-16	chr3:103876500-103876716	l_2422_chr3:103870374-103876716_testes
13	lnc-ALCAM-3	chr3:103730436-103730568	XLOC_002744
14	lnc-ALCAM-14	chr3:103990116-103990678	NONHSAT090952

No data

Variant related genes	Relation type
ENSG00000265076	TF binding region
ENSG00000214405	TF binding region
ENSG00000265076	CpG island
ENSG00000214405	CpG island

Extended variants
information (count: 5383 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5383 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191467329	chr3:103724012-103724013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555264584	chr3:103724052-103724053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533514379	chr3:103724071-103724072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575911379	chr3:103724117-103724118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548999719	chr3:103724134-103724135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567429555	chr3:103724135-103724136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563746202	chr3:103724184-103724185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538188067	chr3:103724207-103724208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556076449	chr3:103724257-103724258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200426054	chr3:103724305-103724306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144935287	chr3:103724306-103724307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538839895	chr3:103724317-103724318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535394002	chr3:103724342-103724343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558254366	chr3:103724353-103724354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573390851	chr3:103724368-103724369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75359362	chr3:103724398-103724399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13315965	chr3:103724400-103724401	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557600173	chr3:103730490-103730491	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs184313543	chr3:103730495-103730496	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs188644129	chr3:103730500-103730501	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs533730625	chr3:103730506-103730507	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs34378710	chr3:103730558-103730559	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs73162444	chr3:103730567-103730568	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35598422	chr3:103737125-103737126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566333695	chr3:103737129-103737130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542242179	chr3:103737131-103737132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557432377	chr3:103737149-103737150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533797004	chr3:103737171-103737172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562165971	chr3:103737175-103737176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575559712	chr3:103737182-103737183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546432694	chr3:103737257-103737258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564650368	chr3:103737267-103737268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148787235	chr3:103737303-103737304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116788772	chr3:103737344-103737345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186510542	chr3:103737372-103737373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561422832	chr3:103737405-103737406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372331831	chr3:103737425-103737426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115621600	chr3:103737466-103737467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191408870	chr3:103737470-103737471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568471202	chr3:103737478-103737479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78820024	chr3:103737549-103737550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551625765	chr3:103737562-103737563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369903526	chr3:103737583-103737584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72982861	chr3:103749207-103749208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182544481	chr3:103749259-103749260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72982863	chr3:103749287-103749288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138928970	chr3:103749329-103749330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189254698	chr3:103749335-103749336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544226011	chr3:103749363-103749364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149037170	chr3:103749376-103749377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:103724000-103724400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:103737000-103737600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:103749200-103750400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:103749600-103749800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:103749600-103751200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:103749800-103751400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:103750000-103750200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:103750400-103750800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:103750400-103750800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr3:103750400-103751000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr3:103750400-103751600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:103750600-103751000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:103750600-103751200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:103750600-103751400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:103750600-103751400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:103750600-103751400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:103750600-103752400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:103750800-103751200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:103750800-103751600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr3:103750800-103751800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:103751200-103751600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:103751400-103751800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:103751800-103752200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:103767000-103767200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:103767200-103772200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:103770200-103772000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:103772000-103772400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:103781000-103787600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr3:103785000-103785200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:103785000-103786400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:103785000-103786600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:103785200-103786200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:103785200-103789800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr3:103785400-103786400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:103785600-103786000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:103785600-103786200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:103785600-103786200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:103785600-103786600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:103785800-103786200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:103785800-103786600	Enhancers	H9 Cell Line	embryonic stem cell
41	chr3:103786000-103794600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:103786200-103786600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr3:103786200-103786600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr3:103786200-103787600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr3:103786200-103789800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr3:103786600-103787600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:103786600-103787600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr3:103786600-103787800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr3:103787600-103787800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr3:103787600-103788000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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