Variant report

Variant	esv1823728
Chromosome Location	chr3:53046712-53080351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:429)
Chromatin interactive
region (count:32)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:53079923-53080078	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:53066637-53066919	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:53074378-53074816	HepG2	liver:	n/a	n/a
4	BACH1	chr3:53065056-53065448	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:53079417-53081172	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:53078839-53078970	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr3:53078329-53079258	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:53079955-53080354	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:53079770-53081260	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:53079792-53080082	K562	blood:	n/a	n/a
11	BHLHE40	chr3:53053064-53053368	K562	blood:	n/a	n/a
12	CCNT2	chr3:53079023-53080645	K562	blood:	n/a	chr3:53080122-53080131
13	CEBPB	chr3:53067264-53067276	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr3:53060779-53061025	HepG2	liver:	n/a	chr3:53060872-53060883
15	CEBPB	chr3:53056688-53057024	K562	blood:	n/a	chr3:53056861-53056872
16	CEBPB	chr3:53060839-53060890	A549	lung:	n/a	chr3:53060872-53060883
17	CEBPB	chr3:53056695-53057040	IMR90	lung:	n/a	chr3:53056861-53056872
18	CEBPB	chr3:53056725-53057013	A549	lung:	n/a	chr3:53056861-53056872
19	CEBPB	chr3:53060696-53061014	H1-hESC	embryonic stem cell:	n/a	chr3:53060872-53060883
20	CEBPB	chr3:53073480-53073654	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:53074601-53074898	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:53074242-53074861	Hela-S3	cervix:	n/a	chr3:53074381-53074392 chr3:53074381-53074392
23	CEBPB	chr3:53056711-53057039	HepG2	liver:	n/a	chr3:53056861-53056872
24	CEBPB	chr3:53060857-53060870	K562	blood:	n/a	n/a
25	CEBPD	chr3:53079891-53080235	HepG2	liver:	n/a	n/a
26	CEBPD	chr3:53079153-53079403	HepG2	liver:	n/a	n/a
27	CHD1	chr3:53079000-53079253	GM12878	blood:	n/a	n/a
28	CHD1	chr3:53079807-53080192	GM12878	blood:	n/a	chr3:53080160-53080170
29	CHD2	chr3:53079835-53080238	K562	blood:	n/a	chr3:53080160-53080170
30	CHD2	chr3:53079452-53079597	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr3:53079807-53080211	GM12878	blood:	n/a	chr3:53080160-53080170
32	CHD2	chr3:53079844-53080219	Hela-S3	cervix:	n/a	chr3:53080160-53080170
33	CREB1	chr3:53079985-53080258	A549	lung:	n/a	n/a
34	CREB1	chr3:53079009-53079348	A549	lung:	n/a	n/a
35	CREB1	chr3:53079608-53080444	HepG2	liver:	n/a	n/a
36	CTBP2	chr3:53080311-53081173	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:53070200-53070350	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr3:53079400-53079550	GM12873	blood:	n/a	n/a
39	CTCF	chr3:53060610-53060686	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:53078980-53079130	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr3:53080152-53080157	GM19240	blood:	n/a	n/a
42	CTCF	chr3:53079360-53079510	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr3:53051126-53051162	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr3:53070140-53070290	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr3:53070120-53070270	HFF	foreskin:	n/a	n/a
46	CTCF	chr3:53080020-53080170	GM12870	blood:	n/a	n/a
47	CTCF	chr3:53070200-53070350	AG04450	lung:	n/a	n/a
48	CTCF	chr3:53079400-53079550	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr3:53070260-53070410	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr3:53060600-53060627	Fibrobl	skin:	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	chr3:53051694-53051744	GM12891	blood:	n/a
2	chr3:53080176-53080226	SK-N-SH	brain:	n/a
3	chr3:53051694-53051744	GM12891	blood:	n/a
4	chr3:53080176-53080226	SK-N-SH	brain:	n/a
5	chr3:53075834-53075884	BE2_C	brain:	n/a
6	chr3:53079796-53079846	HUVEC	blood vessel:	n/a
7	chr3:53078990-53079040	NB4	blood:	n/a
8	chr3:53079105-53079155	HIPEpiC	eye:	n/a
9	chr3:53080176-53080226	AG04450	lung:	fetal
10	chr3:53078218-53078268	AG10803	skin:	n/a
11	chr3:53078218-53078268	ProgFib	skin:	n/a
12	chr3:53075834-53075884	HIPEpiC	eye:	n/a
13	chr3:53079796-53079846	A549	lung:	n/a
14	chr3:53079796-53079846	BE2_C	brain:	n/a
15	chr3:53078218-53078268	K562	blood:	n/a
16	chr3:53078218-53078268	HAEpiC	amniotic membrane:	n/a
17	chr3:53078990-53079040	AG04449	skin:	fetal
18	chr3:53075834-53075884	HepG2	liver:	n/a
19	chr3:53078218-53078268	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:53079796-53079846	HCT-116	colon:	n/a
21	chr3:53079105-53079155	ECC-1	luminal epithelium:	n/a
22	chr3:53078990-53079040	BJ	skin:	n/a
23	chr3:53080176-53080226	NH-A	brain:	n/a
24	chr3:53079105-53079155	HEEpiC	esophagus:	n/a
25	chr3:53079796-53079846	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:53078218-53078268	T-47D	breast:	n/a
27	chr3:53078990-53079040	HCPEpiC	choroid plexus:	n/a
28	chr3:53078218-53078268	BE2_C	brain:	n/a
29	chr3:53075834-53075884	NB4	blood:	n/a
30	chr3:53075834-53075884	HAEpiC	amniotic membrane:	n/a
31	chr3:53078990-53079040	Hepatocyte	liver:	n/a
32	chr3:53075834-53075884	PFSK-1	brain:	n/a
33	chr3:53079796-53079846	GM12878	blood:	n/a
34	chr3:53078218-53078268	HUVEC	blood vessel:	n/a
35	chr3:53078218-53078268	GM12892	blood:	n/a
36	chr3:53075834-53075884	HMEC	breast:	n/a
37	chr3:53079105-53079155	HCF	heart:	n/a
38	chr3:53078990-53079040	NHDF-neo	bronchial:	n/a
39	chr3:53078218-53078268	A549	lung:	n/a
40	chr3:53075834-53075884	MCF10A-Er-Src	breast:	n/a
41	chr3:53080176-53080226	NHDF-neo	bronchial:	n/a
42	chr3:53075834-53075884	NHBE	bronchial:	n/a
43	chr3:53079796-53079846	GM19239	blood:	n/a
44	chr3:53075834-53075884	HCPEpiC	choroid plexus:	n/a
45	chr3:53078218-53078268	RPTEC	kidney:	n/a
46	chr3:53080176-53080226	LNCaP	prostate:	n/a
47	chr3:53079796-53079846	AG04450	lung:	fetal
48	chr3:53079796-53079846	ECC-1	luminal epithelium:	n/a
49	chr3:53051694-53051744	MCF10A-Er-Src	breast:	n/a
50	chr3:53079796-53079846	HEK293	kidney:	embryo

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:53045411..53048406-chr3:53050370..53052257,2	K562	blood:
2	chr3:53074151..53077350-chr3:53077899..53081125,4	K562	blood:
3	chr3:53056126..53058134-chr3:53061359..53063994,2	K562	blood:
4	chr3:53059584..53062030-chr3:53075790..53077753,2	K562	blood:
5	chr3:53045411..53048406-chr3:53050370..53052257,2	K562	blood:
6	chr3:53077653..53079153-chr3:53079208..53080925,2	K562	blood:
7	chr3:53053108..53056030-chr3:53104834..53107226,3	K562	blood:
8	chr20:33999620..34000214-chr3:53080089..53080662,2	Hela-S3	cervix:
9	chr3:53069872..53071542-chr3:53073094..53075949,2	K562	blood:
10	chr3:53064347..53066735-chr3:53078484..53080283,2	K562	blood:
11	chr3:53068314..53070606-chr3:53078738..53080578,2	MCF-7	breast:
12	chr3:53071101..53072947-chr3:53077681..53080413,2	K562	blood:
13	chr3:53060296..53062382-chr3:53075868..53077771,2	MCF-7	breast:
14	chr3:53047316..53051698-chr3:53056732..53062167,5	MCF-7	breast:
15	chr3:53058305..53064318-chr3:53075790..53081540,9	K562	blood:
16	chr3:53065348..53067602-chr3:53078678..53080712,2	MCF-7	breast:
17	chr3:53072702..53076307-chr3:53077847..53082050,5	MCF-7	breast:
18	chr3:53066267..53068975-chr3:53075224..53077291,2	K562	blood:
19	chr3:53069872..53071542-chr3:53073094..53075949,2	K562	blood:
20	chr3:53058305..53060040-chr3:53077970..53080050,2	K562	blood:
21	chr3:53055176..53056730-chr3:53078490..53080404,2	MCF-7	breast:
22	chr3:52964018..52964668-chr3:53072552..53073141,2	MCF-7	breast:
23	chr3:53047316..53051698-chr3:53056732..53062167,5	MCF-7	breast:
24	chr3:53059584..53062030-chr3:53075790..53077753,2	K562	blood:
25	chr3:53066267..53068975-chr3:53075224..53077291,2	K562	blood:
26	chr3:53054569..53056705-chr3:53106775..53108496,2	MCF-7	breast:
27	chr19:46273919..46274424-chr3:53078893..53079893,2	Hela-S3	cervix:
28	chr3:53060296..53062382-chr3:53075868..53077771,2	MCF-7	breast:
29	chr3:53061590..53065851-chr3:53079689..53082481,4	K562	blood:
30	chr3:53071049..53072587-chr3:53078204..53080217,2	MCF-7	breast:
31	chr3:53056801..53057547-chr3:53179048..53179588,2	MCF-7	breast:
32	chr3:53056126..53058134-chr3:53061359..53063994,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFT1-5	chr3:53077152-53077270	NONHSAT089976
2	lnc-RFT1-5	chr3:53077152-53077270	NONHSAT089975
3	lnc-RFT1-5	chr3:53052102-53052244	NONHSAT089975
4	lnc-RFT1-5	chr3:53079832-53080073	NONHSAT089976
5	lnc-PRKCD-2	chr3:53080091-53082182	NONHSAT089977

No data

Variant related genes	Relation type
SFMBT1	TF binding region
SFMBT1	CpG island
ENSG00000267395	chromatin interactions
ENSG00000163935	chromatin interactions
ENSG00000101019	chromatin interactions

Extended variants
information (count: 1172 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56665986	chr3:53046717-53046718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568003499	chr3:53046720-53046721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376951608	chr3:53046838-53046839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62255892	chr3:53046904-53046905	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs571867807	chr3:53046931-53046932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577145309	chr3:53046987-53046988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151332802	chr3:53047006-53047007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529351167	chr3:53047041-53047042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561093468	chr3:53047092-53047093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529753118	chr3:53047103-53047104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140038778	chr3:53047120-53047121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550756945	chr3:53047124-53047125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547896490	chr3:53047142-53047143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369231375	chr3:53047145-53047146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561959289	chr3:53047212-53047213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9819608	chr3:53047213-53047214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs117496343	chr3:53047386-53047387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79139223	chr3:53047417-53047418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185476450	chr3:53047454-53047455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2564948	chr3:53047469-53047470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546780231	chr3:53047501-53047502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145569678	chr3:53047502-53047503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529546895	chr3:53047524-53047525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189323044	chr3:53047529-53047530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2564949	chr3:53047545-53047546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192540992	chr3:53047549-53047550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567981922	chr3:53047597-53047598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2564950	chr3:53047611-53047612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537037257	chr3:53047621-53047622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374769860	chr3:53047630-53047631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567690944	chr3:53047660-53047661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397989629	chr3:53047662-53047663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147737904	chr3:53047676-53047677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375856678	chr3:53047684-53047685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368886018	chr3:53047692-53047693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183597104	chr3:53047693-53047694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55794978	chr3:53047708-53047709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs551614655	chr3:53047747-53047748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369675904	chr3:53047794-53047795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374112955	chr3:53047802-53047803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573045455	chr3:53047805-53047806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377006639	chr3:53047806-53047807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142263737	chr3:53047832-53047833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188468008	chr3:53047833-53047834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181240278	chr3:53047941-53047942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570038694	chr3:53047956-53047957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544591057	chr3:53047992-53047993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186704392	chr3:53048013-53048014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577725460	chr3:53048030-53048031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112069786	chr3:53048049-53048050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53019000-53057200	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:53019600-53056400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr3:53020600-53057000	Weak transcription	Dnd41	blood
4	chr3:53022600-53050400	Weak transcription	Primary B cells from cord blood	blood
5	chr3:53025600-53061600	Weak transcription	Lung	lung
6	chr3:53027600-53061600	Weak transcription	Liver	Liver
7	chr3:53027800-53051000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr3:53030200-53059400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:53030400-53052400	Weak transcription	Primary T cells from cord blood	blood
10	chr3:53030800-53050400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr3:53032800-53051600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:53033000-53078400	Weak transcription	Aorta	Aorta
13	chr3:53033200-53057000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr3:53033600-53056200	Weak transcription	Fetal Stomach	stomach
15	chr3:53033800-53052800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr3:53033800-53053800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr3:53033800-53060400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:53033800-53065000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:53037000-53065000	Weak transcription	Fetal Intestine Small	intestine
20	chr3:53040800-53065000	Weak transcription	Fetal Intestine Large	intestine
21	chr3:53041400-53053600	Weak transcription	Fetal Thymus	thymus
22	chr3:53043800-53064800	Weak transcription	Stomach Mucosa	stomach
23	chr3:53044400-53050400	Weak transcription	A549	lung
24	chr3:53044400-53052400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr3:53044400-53056000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr3:53044600-53048800	Weak transcription	Pancreas	Pancrea
27	chr3:53044600-53050200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:53044600-53051200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr3:53044600-53055600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:53044600-53065000	Weak transcription	Gastric	stomach
31	chr3:53045000-53050400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr3:53045200-53049800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr3:53045200-53050200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:53045200-53050200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:53045200-53061400	Weak transcription	Fetal Heart	heart
36	chr3:53045400-53049600	Weak transcription	Fetal Muscle Trunk	muscle
37	chr3:53045400-53050200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr3:53045400-53052600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:53045400-53057200	Weak transcription	Psoas Muscle	Psoas
40	chr3:53045400-53061600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:53045600-53050600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr3:53045600-53052400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr3:53045600-53057000	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr3:53045600-53057600	Weak transcription	Left Ventricle	heart
45	chr3:53045800-53050400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr3:53045800-53061400	Weak transcription	HepG2	liver
47	chr3:53046000-53051800	Weak transcription	GM12878-XiMat	blood
48	chr3:53046000-53052400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr3:53046000-53057600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr3:53046200-53052600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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