Variant report

Variant	esv3341217
Chromosome Location	chr3:195972755-195975953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:195973801-195974026	GM12878	blood:	n/a	n/a
2	BCL11A	chr3:195973611-195974028	GM12878	blood:	n/a	n/a
3	CTCF	chr3:195974880-195975030	MCF-7	breast:	n/a	n/a
4	CTCF	chr3:195973220-195973370	GM12867	blood:	n/a	n/a
5	CTCF	chr3:195975100-195975250	HBMEC	blood vessel:	n/a	n/a
6	CUX1	chr3:195973789-195973835	GM12878	blood:	n/a	n/a
7	EBF1	chr3:195973512-195973797	GM12878	blood:	n/a	chr3:195973626-195973637
8	EBF1	chr3:195973524-195974001	GM12878	blood:	n/a	chr3:195973626-195973637
9	EBF1	chr3:195973501-195973984	GM12878	blood:	n/a	chr3:195973626-195973637
10	FOS	chr3:195973685-195974201	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr3:195973865-195974169	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr3:195973724-195974263	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr3:195973802-195974271	MCF10A-Er-Src	breast:	n/a	n/a
14	GABPA	chr3:195973815-195974294	HL-60	blood:	n/a	n/a
15	IRF4	chr3:195973557-195974004	GM12878	blood:	n/a	n/a
16	MYC	chr3:195973800-195974123	MCF10A-Er-Src	breast:	n/a	n/a
17	PAX5	chr3:195973618-195973961	GM12878	blood:	n/a	n/a
18	PAX5	chr3:195973526-195974077	GM12878	blood:	n/a	n/a
19	PAX5	chr3:195973636-195974007	GM12878	blood:	n/a	n/a
20	PAX5	chr3:195975658-195975961	GM12878	blood:	n/a	n/a
21	POLR2A	chr3:195973514-195974080	GM12878	blood:	n/a	n/a
22	POLR2A	chr3:195973408-195974406	HL-60	blood:	n/a	n/a
23	POLR2A	chr3:195973643-195973922	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr3:195975337-195975503	HepG2	liver:	n/a	n/a
25	POLR2A	chr3:195974523-195974672	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:195972696-195972759	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:195973664-195974323	U87	brain:	n/a	n/a
28	POLR2A	chr3:195973685-195974244	U87	brain:	n/a	n/a
29	POLR2A	chr3:195973062-195973266	K562	blood:	n/a	n/a
30	POLR2A	chr3:195973456-195974400	HL-60	blood:	n/a	n/a
31	POLR2A	chr3:195973818-195974244	U87	brain:	n/a	n/a
32	POU2F2	chr3:195973565-195974083	GM12878	blood:	n/a	n/a
33	RXRA	chr3:195973605-195973960	GM12878	blood:	n/a	n/a
34	SIN3AK20	chr3:195975725-195975861	HepG2	liver:	n/a	n/a
35	SIX5	chr3:195973658-195973996	K562	blood:	n/a	n/a
36	SP1	chr3:195973678-195973971	GM12878	blood:	n/a	n/a
37	SPI1	chr3:195975661-195975832	GM12878	blood:	n/a	n/a
38	SPI1	chr3:195973608-195974007	GM12878	blood:	n/a	n/a
39	SPI1	chr3:195973840-195974283	HL-60	blood:	n/a	n/a
40	STAT3	chr3:195973894-195974088	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr3:195974322-195974454	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr3:195973416-195974297	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr3:195973862-195974179	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr3:195973484-195974179	MCF10A-Er-Src	breast:	n/a	n/a
45	TCF12	chr3:195973558-195973946	GM12878	blood:	n/a	n/a
46	TCF12	chr3:195973560-195973964	GM12878	blood:	n/a	n/a
47	USF1	chr3:195975717-195975898	HepG2	liver:	n/a	n/a
48	ZBTB33	chr3:195973682-195973959	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195974329-195974379	HRPEpiC	eye:	n/a
2	chr3:195974258-195974308	AG04449	skin:	fetal
3	chr3:195974329-195974379	AoSMC	blood vessel:	n/a
4	chr3:195974258-195974308	ProgFib	skin:	n/a
5	chr3:195974329-195974379	Hela-S3	cervix:	n/a
6	chr3:195974258-195974308	HAEpiC	amniotic membrane:	n/a
7	chr3:195974258-195974308	GM12878	blood:	n/a
8	chr3:195974329-195974379	GM06990	blood:	n/a
9	chr3:195974258-195974308	HepG2	liver:	n/a
10	chr3:195974258-195974308	NHDF-neo	bronchial:	n/a
11	chr3:195974258-195974308	ECC-1	luminal epithelium:	n/a
12	chr3:195974300-195974350	Caco-2	colon:	n/a
13	chr3:195974258-195974308	PANC-1	pancreas:	n/a
14	chr3:195974329-195974379	AG04449	skin:	fetal
15	chr3:195974258-195974308	AG09309	skin:	n/a
16	chr3:195974300-195974350	AG04450	lung:	fetal
17	chr3:195974300-195974350	HNPCEpiC	eye:	n/a
18	chr3:195974258-195974308	HEEpiC	esophagus:	n/a
19	chr3:195974329-195974379	RPTEC	kidney:	n/a
20	chr3:195974300-195974350	Hepatocyte	liver:	n/a
21	chr3:195974258-195974308	GM19239	blood:	n/a
22	chr3:195974329-195974379	MCF-7	breast:	n/a
23	chr3:195974258-195974308	HUVEC	blood vessel:	n/a
24	chr3:195974300-195974350	U87	brain:	n/a
25	chr3:195974329-195974379	HRCEpiC	kidney:	n/a
26	chr3:195974300-195974350	PrEC	prostate:	n/a
27	chr3:195974329-195974379	SAEC	small airway:	n/a
28	chr3:195974300-195974350	MCF-7	breast:	n/a
29	chr3:195974258-195974308	AG04450	lung:	fetal
30	chr3:195974258-195974308	HCF	heart:	n/a
31	chr3:195974329-195974379	SK-N-SH_RA	brain:	n/a
32	chr3:195974329-195974379	HepG2	liver:	n/a
33	chr3:195974300-195974350	AG10803	skin:	n/a
34	chr3:195974300-195974350	AG04449	skin:	fetal
35	chr3:195974300-195974350	HRE	kidney:	n/a
36	chr3:195974329-195974379	NH-A	brain:	n/a
37	chr3:195974258-195974308	Jurkat	blood:	n/a
38	chr3:195974300-195974350	HCPEpiC	choroid plexus:	n/a
39	chr3:195974300-195974350	BE2_C	brain:	n/a
40	chr3:195974300-195974350	HRCEpiC	kidney:	n/a
41	chr3:195974300-195974350	GM19239	blood:	n/a
42	chr3:195974258-195974308	Hepatocyte	liver:	n/a
43	chr3:195974300-195974350	HCF	heart:	n/a
44	chr3:195974329-195974379	GM12891	blood:	n/a
45	chr3:195974258-195974308	K562	blood:	n/a
46	chr3:195974329-195974379	H1-hESC	embryonic stem cell:	embryo
47	chr3:195974300-195974350	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:195974329-195974379	PANC-1	pancreas:	n/a
49	chr3:195974258-195974308	GM12892	blood:	n/a
50	chr3:195974329-195974379	AG04450	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195958884..195960424-chr3:195972113..195974415,2	K562	blood:
2	chr3:195952863..195955052-chr3:195973498..195975966,2	K562	blood:
3	chr3:195971988..195973828-chr3:195999663..196002125,2	MCF-7	breast:
4	chr3:195971582..195973149-chr3:195978489..195981811,3	MCF-7	breast:
5	chr3:195970824..195973413-chr3:196244591..196247031,2	K562	blood:
6	chr3:195961871..195964800-chr3:195972048..195973919,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228028	TF binding region
PCYT1A	TF binding region
ENSG00000228028	CpG island
PCYT1A	CpG island
ENSG00000163959	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542425642	chr3:195972762-195972763	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374233358	chr3:195972763-195972764	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550879860	chr3:195972770-195972771	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182437041	chr3:195972778-195972779	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199568554	chr3:195972822-195972823	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544660993	chr3:195972841-195972842	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555193280	chr3:195972865-195972866	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539532070	chr3:195972884-195972885	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188302949	chr3:195972907-195972908	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534340654	chr3:195972971-195972972	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139130889	chr3:195973031-195973032	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577186888	chr3:195973078-195973079	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545287855	chr3:195973082-195973083	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75302827	chr3:195973083-195973084	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191168500	chr3:195973092-195973093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149963927	chr3:195973117-195973118	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561176800	chr3:195973155-195973156	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528153310	chr3:195973187-195973188	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568453168	chr3:195973231-195973232	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7639752	chr3:195973244-195973245	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs145072368	chr3:195973344-195973345	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545546595	chr3:195973372-195973373	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370670800	chr3:195973387-195973388	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148621347	chr3:195973426-195973427	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569207619	chr3:195973449-195973450	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs183819875	chr3:195973474-195973475	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116781471	chr3:195973568-195973569	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142056924	chr3:195973572-195973573	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534005916	chr3:195973596-195973597	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559022954	chr3:195973615-195973616	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs75499981	chr3:195973667-195973668	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs188311691	chr3:195973672-195973673	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556640547	chr3:195973681-195973682	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377432414	chr3:195973692-195973693	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369880567	chr3:195973767-195973768	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575600145	chr3:195973789-195973790	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs542978184	chr3:195973840-195973841	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554439230	chr3:195973883-195973884	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573009925	chr3:195973894-195973895	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539909738	chr3:195973895-195973896	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564997086	chr3:195973918-195973919	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192612606	chr3:195973955-195973956	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543797566	chr3:195973968-195973969	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs562180862	chr3:195973977-195973978	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184771760	chr3:195973978-195973979	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187598930	chr3:195974015-195974016	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs566915405	chr3:195974116-195974117	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs527912095	chr3:195974117-195974118	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs527893599	chr3:195974166-195974167	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs191307761	chr3:195974169-195974170	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195959600-195978200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr3:195961600-195973800	Weak transcription	Stomach Mucosa	stomach
3	chr3:195962400-195977000	Strong transcription	Fetal Stomach	stomach
4	chr3:195962400-195979400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:195964000-195975000	Strong transcription	Fetal Brain Female	brain
6	chr3:195965200-195994200	Weak transcription	A549	lung
7	chr3:195965600-195975800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr3:195965800-195976600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:195965800-196012400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr3:195966400-195973600	Weak transcription	Esophagus	oesophagus
11	chr3:195967000-195975200	Strong transcription	Aorta	Aorta
12	chr3:195967200-195988600	Strong transcription	Fetal Intestine Small	intestine
13	chr3:195967400-195975600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:195968400-195976400	Strong transcription	Spleen	Spleen
15	chr3:195968800-195993400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr3:195969000-195972800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr3:195969000-195973000	Weak transcription	Small Intestine	intestine
18	chr3:195969000-195973200	Weak transcription	Pancreas	Pancrea
19	chr3:195969200-195974000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:195969200-195978200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:195969400-195973200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:195969400-195973400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:195969400-195973800	Weak transcription	Brain Germinal Matrix	brain
24	chr3:195969400-195974000	Weak transcription	Primary B cells from cord blood	blood
25	chr3:195969600-195972800	Weak transcription	HUVEC	blood vessel
26	chr3:195969600-195973000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr3:195969600-195973000	Weak transcription	Brain Angular Gyrus	brain
28	chr3:195969600-195974000	Weak transcription	Hela-S3	cervix
29	chr3:195969600-195974200	Weak transcription	Psoas Muscle	Psoas
30	chr3:195969600-195974400	Weak transcription	Fetal Kidney	kidney
31	chr3:195969600-195982400	Weak transcription	Fetal Heart	heart
32	chr3:195969600-196012400	Weak transcription	Fetal Brain Male	brain
33	chr3:195969800-195972800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr3:195969800-195972800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr3:195969800-195973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr3:195969800-195973000	Weak transcription	HMEC	breast
37	chr3:195969800-195973000	Weak transcription	HSMM	muscle
38	chr3:195969800-195973200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr3:195969800-195973200	Weak transcription	Brain Hippocampus Middle	brain
40	chr3:195969800-195973600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr3:195969800-195973600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr3:195969800-195974200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr3:195969800-195974200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr3:195970000-195972800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr3:195970000-195973200	Weak transcription	NHEK	skin
46	chr3:195970000-195973600	Weak transcription	Gastric	stomach
47	chr3:195970200-195972800	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr3:195970400-195972800	Weak transcription	Liver	Liver
49	chr3:195970400-195973800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:195970800-195975200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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