Variant report

Variant	nsv932954
Chromosome Location	chr1:45975022-45976755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:128)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:128 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr1:45972281-45975128	A549	lung:	n/a	chr1:45972464-45972473
2	CCNT2	chr1:45975882-45976177	K562	blood:	n/a	n/a
3	CTCF	chr1:45976705-45977109	T-47D	breast:	n/a	n/a
4	EP300	chr1:45976667-45977048	T-47D	breast:	n/a	n/a
5	FOSL2	chr1:45975760-45976665	HepG2	liver:	n/a	n/a
6	GATA3	chr1:45973660-45975100	A549	lung:	n/a	n/a
7	HEY1	chr1:45975715-45976693	HepG2	liver:	n/a	n/a
8	HEY1	chr1:45974760-45975050	HepG2	liver:	n/a	n/a
9	HEY1	chr1:45975682-45976733	HepG2	liver:	n/a	n/a
10	HEY1	chr1:45973515-45975037	HepG2	liver:	n/a	n/a
11	JUND	chr1:45973695-45975056	HCT-116	colon:	n/a	n/a
12	JUND	chr1:45972871-45975112	A549	lung:	n/a	chr1:45973476-45973490
13	MBD4	chr1:45975767-45976508	HepG2	liver:	n/a	n/a
14	MTA3	chr1:45973568-45975082	GM12878	blood:	n/a	n/a
15	NFYA	chr1:45975971-45976171	GM12878	blood:	n/a	n/a
16	NFYB	chr1:45975910-45976068	GM12878	blood:	n/a	n/a
17	NFYB	chr1:45975846-45976072	K562	blood:	n/a	n/a
18	PML	chr1:45973923-45975170	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:45973921-45975042	K562	blood:	n/a	n/a
20	POLR2A	chr1:45972877-45977732	HepG2	liver:	n/a	n/a
21	POLR2A	chr1:45975978-45976169	A549	lung:	n/a	n/a
22	POLR2A	chr1:45972974-45979094	K562	blood:	n/a	n/a
23	POLR2A	chr1:45975816-45976525	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr1:45973262-45977737	PFSK-1	brain:	n/a	n/a
25	POLR2A	chr1:45975273-45976635	K562	blood:	n/a	n/a
26	POLR2A	chr1:45973256-45975023	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr1:45972931-45975038	HepG2	liver:	n/a	n/a
28	POLR2A	chr1:45975210-45975649	HCT-116	colon:	n/a	n/a
29	POLR2A	chr1:45973985-45975233	HepG2	liver:	n/a	n/a
30	POLR2A	chr1:45976699-45977067	HCT-116	colon:	n/a	n/a
31	POLR2A	chr1:45976427-45976526	A549	lung:	n/a	n/a
32	POLR2A	chr1:45976398-45976632	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr1:45972867-45979125	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr1:45975572-45976645	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr1:45976004-45976179	HepG2	liver:	n/a	n/a
36	POLR2A	chr1:45975539-45975717	A549	lung:	n/a	n/a
37	POLR2A	chr1:45975594-45976524	MCF-7	breast:	n/a	n/a
38	POLR2A	chr1:45975229-45976315	GM12891	blood:	n/a	n/a
39	POLR2A	chr1:45975782-45975998	HepG2	liver:	n/a	n/a
40	POLR2A	chr1:45972840-45975205	K562	blood:	n/a	n/a
41	POLR2A	chr1:45975248-45976666	HepG2	liver:	n/a	n/a
42	POLR2A	chr1:45976194-45976275	A549	lung:	n/a	n/a
43	POLR2A	chr1:45976129-45976340	GM12878	blood:	n/a	n/a
44	POLR2A	chr1:45973197-45975216	GM12891	blood:	n/a	n/a
45	POLR2A	chr1:45975066-45975074	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr1:45975871-45976287	GM12878	blood:	n/a	n/a
47	POLR2A	chr1:45973763-45976656	K562	blood:	n/a	n/a
48	POLR2A	chr1:45972821-45976692	GM12878	blood:	n/a	n/a
49	POLR2A	chr1:45972161-45977648	HepG2	liver:	n/a	n/a
50	POLR2A	chr1:45972866-45975153	HCT-116	colon:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45975796-45975846	H1-hESC	embryonic stem cell:	embryo
2	chr1:45975796-45975846	HAEpiC	amniotic membrane:	n/a
3	chr1:45975796-45975846	Hepatocyte	liver:	n/a
4	chr1:45975796-45975846	HIPEpiC	eye:	n/a
5	chr1:45975796-45975846	AG10803	skin:	n/a
6	chr1:45975796-45975846	HCPEpiC	choroid plexus:	n/a
7	chr1:45975796-45975846	HMEC	breast:	n/a
8	chr1:45975796-45975846	SK-N-SH	brain:	n/a
9	chr1:45975796-45975846	Caco-2	colon:	n/a
10	chr1:45975796-45975846	BJ	skin:	n/a
11	chr1:45975796-45975846	PFSK-1	brain:	n/a
12	chr1:45975796-45975846	MCF10A-Er-Src	breast:	n/a
13	chr1:45975796-45975846	T-47D	breast:	n/a
14	chr1:45975796-45975846	Jurkat	blood:	n/a
15	chr1:45975796-45975846	ovcar-3	ovarian:	n/a
16	chr1:45975796-45975846	IMR90	lung:	fetal
17	chr1:45975796-45975846	AG04450	lung:	fetal
18	chr1:45975796-45975846	SK-N-SH_RA	brain:	n/a
19	chr1:45975796-45975846	HEEpiC	esophagus:	n/a
20	chr1:45975796-45975846	HNPCEpiC	eye:	n/a
21	chr1:45975796-45975846	NHBE	bronchial:	n/a
22	chr1:45975796-45975846	PANC-1	pancreas:	n/a
23	chr1:45975796-45975846	ProgFib	skin:	n/a
24	chr1:45975796-45975846	RPTEC	kidney:	n/a
25	chr1:45975796-45975846	GM12891	blood:	n/a
26	chr1:45975796-45975846	CMK	blood:	n/a
27	chr1:45975796-45975846	LNCaP	prostate:	n/a
28	chr1:45975796-45975846	AG04449	skin:	fetal
29	chr1:45975796-45975846	SKMC	muscle:	n/a
30	chr1:45975796-45975846	NHDF-neo	bronchial:	n/a
31	chr1:45975796-45975846	NB4	blood:	n/a
32	chr1:45975796-45975846	K562	blood:	n/a
33	chr1:45975796-45975846	AG09309	skin:	n/a
34	chr1:45975796-45975846	NT2-D1	testis:	n/a
35	chr1:45975796-45975846	GM06990	blood:	n/a
36	chr1:45975796-45975846	HUVEC	blood vessel:	n/a
37	chr1:45975796-45975846	PrEC	prostate:	n/a
38	chr1:45975796-45975846	HRPEpiC	eye:	n/a
39	chr1:45975796-45975846	AoSMC	blood vessel:	n/a
40	chr1:45975796-45975846	SK-N-MC	brain:	n/a
41	chr1:45975796-45975846	GM12892	blood:	n/a
42	chr1:45975796-45975846	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:45975796-45975846	HRCEpiC	kidney:	n/a
44	chr1:45975796-45975846	HEK293	kidney:	embryo
45	chr1:45975796-45975846	SAEC	small airway:	n/a
46	chr1:45975796-45975846	A549	lung:	n/a
47	chr1:45975796-45975846	HCT-116	colon:	n/a
48	chr1:45975796-45975846	HCM	heart:	n/a
49	chr1:45975796-45975846	HL-60	blood:	n/a
50	chr1:45975796-45975846	BE2_C	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45974971..45980027-chr1:46048272..46053531,9	K562	blood:
2	chr1:45973182..45975128-chr1:45984664..45989019,3	MCF-7	breast:
3	chr1:45976468..45980834-chr1:46032613..46036060,5	MCF-7	breast:
4	chr1:45973068..45975148-chr1:46049390..46051110,2	MCF-7	breast:
5	chr1:45976261..45980461-chr1:45986473..45989288,6	MCF-7	breast:
6	chr1:45975860..45989626-chr1:46030076..46041078,36	K562	blood:
7	chr1:45805983..45807549-chr1:45973532..45975768,2	K562	blood:
8	chr1:45965671..45969478-chr1:45972057..45975317,5	MCF-7	breast:
9	chr1:45975860..45980379-chr1:46034172..46039771,7	K562	blood:
10	chr1:45976649..45978583-chr1:45986125..45989012,2	MCF-7	breast:
11	chr1:45974939..45977846-chr1:46015282..46017928,2	MCF-7	breast:
12	chr1:45974558..45995867-chr1:46046173..46057010,94	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1A1-3	chr1:45975105-45975180	NONHSAT002944
2	lnc-AKR1A1-3	chr1:45975647-45976177	NONHSAT002944

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MMACHC	hsa-let-7b-5p	chr1:45975754-45975776
2	MMACHC	hsa-miR-98-5p	chr1:45975755-45975776

Variant related genes	Relation type
MMACHC	TF binding region
MMACHC	CpG island
ENSG00000117448	chromatin interactions
ENSG00000132780	chromatin interactions
ENSG00000132773	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000132763	chromatin interactions
ENSG00000132781	chromatin interactions
ENSG00000236624	chromatin interactions

Extended variants
information (count: 83 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566121791	chr1:45975056-45975057	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs544461302	chr1:45975058-45975059	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs150453039	chr1:45975072-45975073	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs56934185	chr1:45975104-45975105	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs199894635	chr1:45975105-45975106	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
6	rs35067820	chr1:45975156-45975157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs9729395	chr1:45975166-45975167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs371534152	chr1:45975175-45975176	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
9	rs146159774	chr1:45975197-45975198	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs372606078	chr1:45975238-45975239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs529318996	chr1:45975289-45975290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs12021717	chr1:45975300-45975301	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs569118214	chr1:45975320-45975321	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs34448673	chr1:45975337-45975338	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs551671089	chr1:45975354-45975355	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs571481152	chr1:45975373-45975374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs371142358	chr1:45975390-45975391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs533957977	chr1:45975435-45975436	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs34296447	chr1:45975452-45975453	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs368679330	chr1:45975463-45975464	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs553614581	chr1:45975520-45975521	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs567350715	chr1:45975526-45975527	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs4660865	chr1:45975541-45975542	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs535908216	chr1:45975556-45975557	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs184478450	chr1:45975579-45975580	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs111591157	chr1:45975589-45975590	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs115045133	chr1:45975605-45975606	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs374495859	chr1:45975617-45975618	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs537216133	chr1:45975638-45975639	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs544520513	chr1:45975650-45975651	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs558013685	chr1:45975671-45975672	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs577844439	chr1:45975686-45975687	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs540427267	chr1:45975705-45975706	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs189360408	chr1:45975708-45975709	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs34005380	chr1:45975732-45975733	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs33996053	chr1:45975740-45975741	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs201001791	chr1:45975741-45975742	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs398052965	chr1:45975742-45975743	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs148748387	chr1:45975744-45975745	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs145881323	chr1:45975747-45975748	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs150301205	chr1:45975748-45975749	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs201643497	chr1:45975764-45975765	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA miRNA target site	5 gene(s)	Overlapped CNVs	n/a
43	rs35495485	chr1:45975765-45975766	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA miRNA target site	5 gene(s)	Overlapped CNVs	n/a
44	rs542710084	chr1:45975796-45975797	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs181264318	chr1:45975849-45975850	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs11580609	chr1:45975856-45975857	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs551730972	chr1:45975862-45975863	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs571540873	chr1:45975888-45975889	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs185604515	chr1:45975936-45975937	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs547560812	chr1:45975942-45975943	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45966400-45975600	Weak transcription	HSMMtube	muscle
2	chr1:45966400-45975800	Weak transcription	Aorta	Aorta
3	chr1:45966600-45984600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:45966800-45975800	Weak transcription	HSMM	muscle
5	chr1:45966800-45975800	Weak transcription	NHDF-Ad	bronchial
6	chr1:45966800-45976000	Weak transcription	Fetal Brain Male	brain
7	chr1:45966800-45976000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:45966800-45980200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr1:45966800-45984800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:45967000-45975400	Weak transcription	NH-A	brain
11	chr1:45967000-45975600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:45967000-45975800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:45967000-45977200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:45967200-45975200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:45967200-45975400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr1:45967200-45975400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:45967200-45975600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr1:45967200-45975600	Weak transcription	Psoas Muscle	Psoas
19	chr1:45967200-45975800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr1:45967200-45976200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:45967200-45976200	Weak transcription	Fetal Lung	lung
22	chr1:45967400-45975600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr1:45967400-45975800	Weak transcription	Stomach Mucosa	stomach
24	chr1:45971600-45985000	Strong transcription	Fetal Stomach	stomach
25	chr1:45971800-45980400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:45971800-45982000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:45972800-45978200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:45972800-45978400	Strong transcription	Fetal Intestine Small	intestine
29	chr1:45972800-45980400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:45972800-45982200	Strong transcription	K562	blood
31	chr1:45972800-45982400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:45972800-45984400	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:45972800-45984400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:45972800-45984400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr1:45972800-45984600	Strong transcription	Fetal Thymus	thymus
36	chr1:45973000-45976800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr1:45973000-45981800	Strong transcription	Dnd41	blood
38	chr1:45973000-45983000	Strong transcription	Fetal Brain Female	brain
39	chr1:45973000-45983200	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr1:45973000-45983200	Strong transcription	Sigmoid Colon	Sigmoid Colon
41	chr1:45973000-45983400	Strong transcription	Primary B cells from peripheral blood	blood
42	chr1:45973000-45983800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr1:45973000-45983800	Strong transcription	Spleen	Spleen
44	chr1:45973000-45984000	Strong transcription	Primary T cells from cord blood	blood
45	chr1:45973000-45984000	Strong transcription	Fetal Muscle Trunk	muscle
46	chr1:45973000-45984000	Strong transcription	Fetal Muscle Leg	muscle
47	chr1:45973000-45984400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr1:45973000-45984400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr1:45973000-45984600	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr1:45973200-45975800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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