Variant report

Variant	nsv592983
Chromosome Location	chr3:194987569-194995096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1166)
CpG islands
(count:429)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1166 , 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	chr3:194991804-194992816	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:194992303-194992837	K562	blood:	n/a	n/a
3	ARID3A	chr3:194991883-194991959	K562	blood:	n/a	n/a
4	ATF2	chr3:194992025-194992675	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:194992137-194992571	GM12878	blood:	n/a	n/a
6	ATF2	chr3:194992006-194992656	GM12878	blood:	n/a	n/a
7	ATF3	chr3:194991316-194991783	K562	blood:	n/a	n/a
8	ATF3	chr3:194992312-194992691	K562	blood:	n/a	n/a
9	ATF3	chr3:194992230-194992793	GM12878	blood:	n/a	n/a
10	BACH1	chr3:194992131-194992767	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:194991531-194991603	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:194992845-194992878	K562	blood:	n/a	n/a
13	BCL3	chr3:194992110-194993094	GM12878	blood:	n/a	chr3:194992411-194992420
14	BCL3	chr3:194992062-194992494	A549	lung:	n/a	chr3:194992411-194992420
15	BCL3	chr3:194991640-194992930	K562	blood:	n/a	chr3:194991896-194991909 chr3:194992411-194992420 chr3:194991873-194991886
16	BCL3	chr3:194991989-194992815	A549	lung:	n/a	chr3:194992411-194992420
17	BCLAF1	chr3:194991338-194991985	GM12878	blood:	n/a	chr3:194991896-194991909 chr3:194991873-194991886
18	BCLAF1	chr3:194992139-194992737	GM12878	blood:	n/a	chr3:194992411-194992420
19	BCLAF1	chr3:194991221-194992703	GM12878	blood:	n/a	chr3:194991896-194991909 chr3:194992411-194992420 chr3:194991873-194991886 chr3:194991263-194991276
20	BHLHE40	chr3:194991577-194993187	GM12878	blood:	n/a	chr3:194992401-194992417
21	BHLHE40	chr3:194991314-194992882	K562	blood:	n/a	chr3:194992401-194992417
22	BHLHE40	chr3:194991377-194992822	HepG2	liver:	n/a	chr3:194992401-194992417
23	BRCA1	chr3:194991798-194991802	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr3:194992317-194992476	HepG2	liver:	n/a	n/a
25	BRCA1	chr3:194991686-194991875	HepG2	liver:	n/a	n/a
26	BRCA1	chr3:194992292-194992626	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr3:194992260-194992733	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:194991716-194991742	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr3:194992244-194992470	GM12878	blood:	n/a	n/a
30	BRCA1	chr3:194991027-194991328	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr3:194990825-194992873	K562	blood:	n/a	n/a
32	CBX3	chr3:194992210-194992665	K562	blood:	n/a	n/a
33	CCNT2	chr3:194995040-194995208	K562	blood:	n/a	n/a
34	CCNT2	chr3:194990575-194992714	K562	blood:	n/a	chr3:194991892-194991901
35	CEBPB	chr3:194992030-194992892	GM12878	blood:	n/a	n/a
36	CEBPB	chr3:194991093-194991615	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:194992178-194992791	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:194992542-194992826	K562	blood:	n/a	n/a
39	CEBPB	chr3:194991830-194991838	Hela-S3	cervix:	n/a	n/a
40	CEBPD	chr3:194991663-194992219	HepG2	liver:	n/a	n/a
41	CHD1	chr3:194992047-194992350	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr3:194990920-194991008	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr3:194991442-194991688	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:194990786-194993337	IMR90	lung:	n/a	n/a
45	CHD1	chr3:194992007-194992641	GM12878	blood:	n/a	n/a
46	CHD2	chr3:194991344-194992625	GM12878	blood:	n/a	n/a
47	CHD2	chr3:194991067-194992609	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:194991477-194991842	HepG2	liver:	n/a	n/a
49	CHD2	chr3:194991613-194991653	K562	blood:	n/a	n/a
50	CHD2	chr3:194991137-194992613	H1-hESC	embryonic stem cell:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:194990988-194991038	AG04449	skin:	fetal
2	chr3:194992644-194992694	PrEC	prostate:	n/a
3	chr3:194990988-194991038	AG04449	skin:	fetal
4	chr3:194992644-194992694	PrEC	prostate:	n/a
5	chr3:194992095-194992145	SAEC	small airway:	n/a
6	chr3:194992260-194992310	HCM	heart:	n/a
7	chr3:194990988-194991038	H1-hESC	embryonic stem cell:	embryo
8	chr3:194992644-194992694	SK-N-SH	brain:	n/a
9	chr3:194989568-194989618	GM12878	blood:	n/a
10	chr3:194992095-194992145	HIPEpiC	eye:	n/a
11	chr3:194992260-194992310	HCT-116	colon:	n/a
12	chr3:194992095-194992145	HCM	heart:	n/a
13	chr3:194990988-194991038	ovcar-3	ovarian:	n/a
14	chr3:194991500-194991550	GM12878	blood:	n/a
15	chr3:194990988-194991038	NT2-D1	testis:	n/a
16	chr3:194991500-194991550	NHBE	bronchial:	n/a
17	chr3:194992644-194992694	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:194989568-194989618	HMEC	breast:	n/a
19	chr3:194991685-194991735	PANC-1	pancreas:	n/a
20	chr3:194992260-194992310	AG09309	skin:	n/a
21	chr3:194992260-194992310	CMK	blood:	n/a
22	chr3:194992260-194992310	ovcar-3	ovarian:	n/a
23	chr3:194991500-194991550	H1-hESC	embryonic stem cell:	embryo
24	chr3:194989568-194989618	ECC-1	luminal epithelium:	n/a
25	chr3:194992095-194992145	NHDF-neo	bronchial:	n/a
26	chr3:194992644-194992694	HMEC	breast:	n/a
27	chr3:194992095-194992145	PFSK-1	brain:	n/a
28	chr3:194992644-194992694	HIPEpiC	eye:	n/a
29	chr3:194992644-194992694	HEEpiC	esophagus:	n/a
30	chr3:194992644-194992694	U87	brain:	n/a
31	chr3:194989568-194989618	HRE	kidney:	n/a
32	chr3:194990988-194991038	SAEC	small airway:	n/a
33	chr3:194992095-194992145	NB4	blood:	n/a
34	chr3:194992095-194992145	Hela-S3	cervix:	n/a
35	chr3:194989568-194989618	HCPEpiC	choroid plexus:	n/a
36	chr3:194991500-194991550	HAEpiC	amniotic membrane:	n/a
37	chr3:194991685-194991735	ovcar-3	ovarian:	n/a
38	chr3:194992260-194992310	MCF10A-Er-Src	breast:	n/a
39	chr3:194992644-194992694	IMR90	lung:	fetal
40	chr3:194992095-194992145	HCPEpiC	choroid plexus:	n/a
41	chr3:194992644-194992694	NT2-D1	testis:	n/a
42	chr3:194989568-194989618	HNPCEpiC	eye:	n/a
43	chr3:194992644-194992694	HUVEC	blood vessel:	n/a
44	chr3:194989568-194989618	GM19239	blood:	n/a
45	chr3:194991500-194991550	PrEC	prostate:	n/a
46	chr3:194991500-194991550	HepG2	liver:	n/a
47	chr3:194991500-194991550	SKMC	muscle:	n/a
48	chr3:194992095-194992145	HCF	heart:	n/a
49	chr3:194991500-194991550	SK-N-SH_RA	brain:	n/a
50	chr3:194992260-194992310	Caco-2	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:194990164..194994201-chr3:195268703..195270348,3	K562	blood:
2	chr3:194986029..194989766-chr3:194990279..194993841,6	K562	blood:
3	chr3:194990474..194992109-chr3:195269592..195271685,2	MCF-7	breast:
4	chr3:194985883..194988240-chr3:195267670..195269662,2	K562	blood:
5	chr3:194989462..194991407-chr3:195163007..195164718,2	MCF-7	breast:
6	chr3:194991996..194992502-chr3:195248815..195249691,2	MCF-7	breast:
7	chr3:194992899..194995747-chr3:195244217..195245876,2	K562	blood:
8	chr3:194990296..194992305-chr3:195248848..195251348,4	MCF-7	breast:
9	chr3:194990271..194992764-chr3:194994105..194997544,4	K562	blood:
10	chr3:194989426..194991874-chr3:195268477..195270198,3	MCF-7	breast:
11	chr3:194990005..194994037-chr3:194997788..195001012,5	K562	blood:
12	chr3:194979343..194983092-chr3:194989595..194993137,5	K562	blood:
13	chr3:194990545..194994377-chr3:195246139..195250306,5	K562	blood:
14	chr3:194979343..194985907-chr3:194989595..194992143,7	K562	blood:
15	chr1:43855268..43855853-chr3:194991704..194992499,2	HCT-116	colon:
16	chr3:194851287..194852978-chr3:194986422..194989063,2	K562	blood:
17	chr3:194991198..194994178-chr3:195162096..195163902,2	K562	blood:
18	chr3:194992469..194994554-chr5:42297852..42299758,2	MCF-7	breast:
19	chr3:194989967..194994399-chr3:195244037..195248390,6	K562	blood:
20	chr3:194991144..194993841-chr3:195162528..195164078,2	MCF-7	breast:
21	chr3:194990825..194992800-chr3:195162290..195164935,2	K562	blood:

No data

Variant related genes	Relation type
XXYLT1	TF binding region
XXYLT1	CpG island
ENSG00000173950	chromatin interactions
ENSG00000198198	chromatin interactions
ENSG00000223711	chromatin interactions
ENSG00000184203	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000159479	chromatin interactions
ENSG00000252620	chromatin interactions

Extended variants
information (count: 252 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4677666	chr3:194987569-194987570	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200613044	chr3:194987573-194987574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529348810	chr3:194987589-194987590	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373948221	chr3:194987634-194987635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570192169	chr3:194987792-194987793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145066587	chr3:194987796-194987797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540146565	chr3:194987863-194987864	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558448479	chr3:194987917-194987918	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142005576	chr3:194987939-194987940	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35987872	chr3:194987984-194987985	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183655773	chr3:194987989-194987990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555668527	chr3:194988012-194988013	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569406580	chr3:194988060-194988061	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539900032	chr3:194988138-194988139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375254758	chr3:194988176-194988177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574520313	chr3:194988245-194988246	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535189955	chr3:194988290-194988291	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553358354	chr3:194988317-194988318	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571659422	chr3:194988339-194988340	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545713352	chr3:194988345-194988346	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187765940	chr3:194988362-194988363	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576240447	chr3:194988368-194988369	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543632169	chr3:194988439-194988440	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs6780743	chr3:194988441-194988442	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529430310	chr3:194988457-194988458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369932869	chr3:194988510-194988511	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547872562	chr3:194988514-194988515	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114098105	chr3:194988527-194988528	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192637271	chr3:194988528-194988529	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573375080	chr3:194988593-194988594	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534090612	chr3:194988627-194988628	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs72607893	chr3:194988672-194988673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs200515466	chr3:194988730-194988731	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184902986	chr3:194988758-194988759	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10933704	chr3:194988873-194988874	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs567712805	chr3:194988884-194988885	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535536353	chr3:194988888-194988889	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553421799	chr3:194988896-194988897	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189706971	chr3:194988921-194988922	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374383144	chr3:194988926-194988927	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12695049	chr3:194988940-194988941	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs111779525	chr3:194988941-194988942	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147799935	chr3:194988945-194988946	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575295911	chr3:194989004-194989005	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35537878	chr3:194989005-194989006	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181668090	chr3:194989025-194989026	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561931134	chr3:194989029-194989030	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573708042	chr3:194989052-194989053	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541561496	chr3:194989068-194989069	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141180769	chr3:194989156-194989157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194981400-194987800	Weak transcription	Psoas Muscle	Psoas
2	chr3:194981400-194990000	Weak transcription	HSMMtube	muscle
3	chr3:194981400-194990800	Weak transcription	Aorta	Aorta
4	chr3:194981600-194989600	Weak transcription	Right Ventricle	heart
5	chr3:194981600-194989800	Weak transcription	Brain Substantia Nigra	brain
6	chr3:194981600-194990000	Weak transcription	A549	lung
7	chr3:194981600-194990200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:194981600-194990200	Weak transcription	HSMM	muscle
9	chr3:194981600-194990600	Weak transcription	Ovary	ovary
10	chr3:194981800-194987800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr3:194981800-194987800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:194981800-194987800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr3:194981800-194989400	Weak transcription	Brain Angular Gyrus	brain
14	chr3:194981800-194989400	Weak transcription	Brain Hippocampus Middle	brain
15	chr3:194981800-194989400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr3:194981800-194989600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:194981800-194989600	Weak transcription	Liver	Liver
18	chr3:194981800-194989600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr3:194981800-194989600	Weak transcription	Colon Smooth Muscle	Colon
20	chr3:194981800-194989600	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr3:194981800-194989600	Weak transcription	Fetal Heart	heart
22	chr3:194981800-194989600	Weak transcription	Lung	lung
23	chr3:194981800-194989600	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr3:194981800-194989800	Weak transcription	Adipose Nuclei	Adipose
25	chr3:194981800-194989800	Weak transcription	Colonic Mucosa	Colon
26	chr3:194981800-194989800	Weak transcription	Fetal Brain Female	brain
27	chr3:194981800-194989800	Weak transcription	Gastric	stomach
28	chr3:194981800-194989800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr3:194981800-194989800	Weak transcription	NHDF-Ad	bronchial
30	chr3:194981800-194990000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:194981800-194990000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:194981800-194990000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr3:194981800-194990000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr3:194981800-194990000	Weak transcription	Brain Anterior Caudate	brain
35	chr3:194981800-194990000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr3:194981800-194990000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:194981800-194990000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr3:194981800-194990200	Weak transcription	Fetal Lung	lung
39	chr3:194981800-194990200	Weak transcription	Right Atrium	heart
40	chr3:194981800-194990200	Weak transcription	NH-A	brain
41	chr3:194981800-194990200	Weak transcription	Osteobl	bone
42	chr3:194981800-194990400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr3:194981800-194990400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr3:194981800-194990400	Weak transcription	Thymus	Thymus
45	chr3:194981800-194991200	Weak transcription	Small Intestine	intestine
46	chr3:194982000-194989800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr3:194982200-194987800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:194982200-194989400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr3:194982200-194989600	Weak transcription	Fetal Brain Male	brain
50	chr3:194982200-194989600	Weak transcription	Placenta	Placenta

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