Variant report

Variant	esv15440
Chromosome Location	chr3:21793027-21795819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr3:21792301-21793038	H1-hESC	embryonic stem cell:	n/a	n/a
2	CREB1	chr3:21792360-21793085	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr3:21793560-21793710	AG09319	gingival:	n/a	n/a
4	CTCF	chr3:21794340-21794490	GM12878	blood:	n/a	n/a
5	CTCF	chr3:21794360-21794510	AoAF	blood vessel:	n/a	n/a
6	CTCF	chr3:21794420-21794570	BJ	skin:	n/a	n/a
7	CTCF	chr3:21794360-21794510	HPF	lung:	n/a	n/a
8	CTCF	chr3:21794340-21794490	NHLF	lung:	n/a	n/a
9	CTCF	chr3:21794334-21794546	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr3:21794360-21794510	HCM	heart:	n/a	n/a
11	CTCF	chr3:21794360-21794510	HMEC	breast:	n/a	n/a
12	CTCF	chr3:21794314-21794570	Lung_OC	lung:	n/a	n/a
13	CTCF	chr3:21794360-21794510	GM12868	blood:	n/a	n/a
14	CTCF	chr3:21794340-21794490	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr3:21794400-21794550	GM12872	blood:	n/a	n/a
16	CTCF	chr3:21794331-21794540	GM10266	blood:	n/a	n/a
17	CTCF	chr3:21794360-21794510	HRE	kidney:	n/a	n/a
18	CTCF	chr3:21794345-21794540	Fibrobl	skin:	n/a	n/a
19	CTCF	chr3:21794291-21794623	Medullo	brain:	n/a	n/a
20	CTCF	chr3:21794380-21794530	AG04449	skin:	n/a	n/a
21	CTCF	chr3:21794280-21794430	HCM	heart:	n/a	n/a
22	CTCF	chr3:21793580-21793730	HMF	breast:	n/a	n/a
23	CTCF	chr3:21794340-21794490	SAEC	small airway:	n/a	n/a
24	CTCF	chr3:21794368-21794519	GM10248	blood:	n/a	n/a
25	CTCF	chr3:21794302-21794577	LNCaP	prostate:	n/a	n/a
26	CTCF	chr3:21794400-21794550	GM12864	blood:	n/a	n/a
27	CTCF	chr3:21794360-21794510	GM12874	blood:	n/a	n/a
28	CTCF	chr3:21794360-21794510	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr3:21794380-21794530	BJ	skin:	n/a	n/a
30	CTCF	chr3:21793520-21793670	HMF	breast:	n/a	n/a
31	CTCF	chr3:21794400-21794550	GM12865	blood:	n/a	n/a
32	CTCF	chr3:21794360-21794510	K562	blood:	n/a	n/a
33	CTCF	chr3:21794280-21794430	HMEC	breast:	n/a	n/a
34	CTCF	chr3:21794300-21794450	RPTEC	kidney:	n/a	n/a
35	CTCF	chr3:21794380-21794530	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr3:21794360-21794510	HMF	breast:	n/a	n/a
37	CTCF	chr3:21794317-21794569	K562	blood:	n/a	n/a
38	CTCF	chr3:21794340-21794490	GM12867	blood:	n/a	n/a
39	CTCF	chr3:21794440-21794590	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr3:21794423-21794440	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:21794340-21794490	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr3:21794360-21794510	GM12875	blood:	n/a	n/a
43	CTCF	chr3:21794303-21794517	A549	lung:	n/a	n/a
44	CTCF	chr3:21793580-21793730	AG10803	skin:	n/a	n/a
45	CTCF	chr3:21794316-21794572	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr3:21794280-21794430	A549	lung:	n/a	n/a
47	CTCF	chr3:21794280-21794430	BE2_C	brain:	n/a	n/a
48	CTCF	chr3:21794400-21794550	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:21794337-21794564	GM12878	blood:	n/a	n/a
50	CTCF	chr3:21794320-21794470	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21793557-21793607	GM12891	blood:	n/a
2	chr3:21792991-21793041	AoSMC	blood vessel:	n/a
3	chr3:21793557-21793607	HCF	heart:	n/a
4	chr3:21792991-21793041	HRCEpiC	kidney:	n/a
5	chr3:21793557-21793607	Hela-S3	cervix:	n/a
6	chr3:21793557-21793607	U87	brain:	n/a
7	chr3:21792991-21793041	GM19239	blood:	n/a
8	chr3:21792991-21793041	Caco-2	colon:	n/a
9	chr3:21792991-21793041	ovcar-3	ovarian:	n/a
10	chr3:21793557-21793607	NB4	blood:	n/a
11	chr3:21792991-21793041	T-47D	breast:	n/a
12	chr3:21792991-21793041	AG04450	lung:	fetal
13	chr3:21793557-21793607	BJ	skin:	n/a
14	chr3:21793557-21793607	HRPEpiC	eye:	n/a
15	chr3:21793557-21793607	PANC-1	pancreas:	n/a
16	chr3:21793557-21793607	HL-60	blood:	n/a
17	chr3:21792991-21793041	PANC-1	pancreas:	n/a
18	chr3:21793557-21793607	NHBE	bronchial:	n/a
19	chr3:21792991-21793041	ECC-1	luminal epithelium:	n/a
20	chr3:21793557-21793607	MCF-7	breast:	n/a
21	chr3:21792991-21793041	GM06990	blood:	n/a
22	chr3:21793557-21793607	HepG2	liver:	n/a
23	chr3:21793557-21793607	IMR90	lung:	fetal
24	chr3:21793557-21793607	MCF10A-Er-Src	breast:	n/a
25	chr3:21792991-21793041	PFSK-1	brain:	n/a
26	chr3:21793557-21793607	AG10803	skin:	n/a
27	chr3:21793557-21793607	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:21792991-21793041	BJ	skin:	n/a
29	chr3:21793557-21793607	HUVEC	blood vessel:	n/a
30	chr3:21793557-21793607	NH-A	brain:	n/a
31	chr3:21792991-21793041	Hela-S3	cervix:	n/a
32	chr3:21792991-21793041	ProgFib	skin:	n/a
33	chr3:21792991-21793041	AG10803	skin:	n/a
34	chr3:21792991-21793041	GM12878	blood:	n/a
35	chr3:21792991-21793041	HCPEpiC	choroid plexus:	n/a
36	chr3:21792991-21793041	NH-A	brain:	n/a
37	chr3:21792991-21793041	K562	blood:	n/a
38	chr3:21793557-21793607	LNCaP	prostate:	n/a
39	chr3:21792991-21793041	SK-N-SH	brain:	n/a
40	chr3:21793557-21793607	H1-hESC	embryonic stem cell:	embryo
41	chr3:21792991-21793041	SK-N-MC	brain:	n/a
42	chr3:21792991-21793041	BE2_C	brain:	n/a
43	chr3:21793557-21793607	AG09319	gingival:	n/a
44	chr3:21792991-21793041	HCF	heart:	n/a
45	chr3:21793557-21793607	HEEpiC	esophagus:	n/a
46	chr3:21793557-21793607	Jurkat	blood:	n/a
47	chr3:21793557-21793607	AoSMC	blood vessel:	n/a
48	chr3:21792991-21793041	NB4	blood:	n/a
49	chr3:21792991-21793041	HAEpiC	amniotic membrane:	n/a
50	chr3:21793557-21793607	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
2	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:
3	chr3:21793963..21794585-chr3:21876272..21877179,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF385D	TF binding region
ZNF385D	CpG island

Extended variants
information (count: 145 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:145 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549199589	chr3:21793113-21793114	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs561037895	chr3:21793116-21793117	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531881350	chr3:21793131-21793132	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561783627	chr3:21793138-21793139	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550009919	chr3:21793205-21793206	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs571577868	chr3:21793247-21793248	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538674577	chr3:21793258-21793259	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551675050	chr3:21793270-21793271	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566803510	chr3:21793273-21793274	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs66986383	chr3:21793358-21793359	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555644818	chr3:21793381-21793382	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370768487	chr3:21793395-21793396	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12637349	chr3:21793417-21793418	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575240488	chr3:21793431-21793432	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577537130	chr3:21793442-21793443	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139208602	chr3:21793476-21793477	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs375424707	chr3:21793490-21793491	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs35622283	chr3:21793497-21793498	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs143047740	chr3:21793499-21793500	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs71044940	chr3:21793500-21793501	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs71044941	chr3:21793508-21793509	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370679154	chr3:21793517-21793518	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574520758	chr3:21793518-21793519	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs560396503	chr3:21793529-21793530	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572445765	chr3:21793537-21793538	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs183884199	chr3:21793545-21793546	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs561486681	chr3:21793558-21793559	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs531823137	chr3:21793620-21793621	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs62236196	chr3:21793640-21793641	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs116893168	chr3:21793808-21793809	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532530875	chr3:21793812-21793813	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs186727646	chr3:21793820-21793821	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs566766729	chr3:21793827-21793828	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs527532924	chr3:21793851-21793852	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs191829125	chr3:21793873-21793874	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs6804285	chr3:21793901-21793902	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs367785612	chr3:21793908-21793909	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184061489	chr3:21793945-21793946	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs556201778	chr3:21793947-21793948	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571287849	chr3:21793963-21793964	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs538236948	chr3:21794000-21794001	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs62236197	chr3:21794082-21794083	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs6783377	chr3:21794090-21794091	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs554979819	chr3:21794111-21794112	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535184178	chr3:21794115-21794116	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs568957516	chr3:21794121-21794122	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576552662	chr3:21794143-21794144	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543685859	chr3:21794169-21794170	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs565366700	chr3:21794171-21794172	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs13340131	chr3:21794174-21794175	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	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
Oral squamous cell carcinoma	17134496	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
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21786400-21793600	Active TSS	Aorta	Aorta
2	chr3:21788800-21793200	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr3:21789200-21793200	Active TSS	Fetal Brain Female	brain
4	chr3:21789400-21793200	Active TSS	NHDF-Ad	bronchial
5	chr3:21789800-21793200	Active TSS	Stomach Smooth Muscle	stomach
6	chr3:21790000-21793400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:21790200-21793200	Active TSS	Right Atrium	heart
8	chr3:21790200-21793200	Active TSS	Right Ventricle	heart
9	chr3:21790400-21793200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:21790400-21793200	Active TSS	Left Ventricle	heart
11	chr3:21790600-21793200	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr3:21790600-21793200	Active TSS	Fetal Muscle Trunk	muscle
13	chr3:21790600-21793200	Active TSS	Fetal Stomach	stomach
14	chr3:21790800-21793200	Active TSS	Brain Germinal Matrix	brain
15	chr3:21790800-21793200	Active TSS	HMEC	breast
16	chr3:21790800-21793400	Active TSS	Fetal Brain Male	brain
17	chr3:21790800-21793400	Active TSS	Fetal Kidney	kidney
18	chr3:21791400-21793200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:21791400-21793400	Active TSS	H9 Cell Line	embryonic stem cell
20	chr3:21791600-21793200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:21791600-21793200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:21791600-21793200	Active TSS	Osteobl	bone
23	chr3:21791800-21793200	Active TSS	Muscle Satellite Cultured Cells	--
24	chr3:21791800-21793200	Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr3:21791800-21793400	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr3:21792000-21793200	Active TSS	H1 Cell Line	embryonic stem cell
27	chr3:21792000-21793200	Active TSS	Brain Anterior Caudate	brain
28	chr3:21792000-21793200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:21792000-21793400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr3:21792000-21793400	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr3:21792000-21793400	Active TSS	HSMM	muscle
32	chr3:21792200-21793200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:21792200-21793200	Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr3:21792200-21793200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:21792200-21793200	Active TSS	Brain Angular Gyrus	brain
36	chr3:21792200-21793600	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr3:21792400-21793200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr3:21792400-21793200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:21792400-21793200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:21792400-21793200	Active TSS	Brain Cingulate Gyrus	brain
41	chr3:21792400-21793200	Active TSS	HSMMtube	muscle
42	chr3:21792400-21793200	Active TSS	NH-A	brain
43	chr3:21792400-21793400	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr3:21792400-21793400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr3:21792600-21793200	Active TSS	Brain Substantia Nigra	brain
46	chr3:21792600-21793200	Weak transcription	Fetal Heart	heart
47	chr3:21792600-21793400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:21792800-21793200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr3:21792800-21793200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:21792800-21793200	Flanking Active TSS	Fetal Muscle Leg	muscle

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