Variant report

Variant	esv1795045
Chromosome Location	chr1:174273004-174346276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 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	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
2	CBX3	chr1:174284403-174284874	K562	blood:	n/a	n/a
3	CBX3	chr1:174284427-174284759	K562	blood:	n/a	n/a
4	CBX3	chr1:174289992-174290425	K562	blood:	n/a	n/a
5	CBX3	chr1:174295373-174295772	K562	blood:	n/a	n/a
6	CBX3	chr1:174290094-174290435	K562	blood:	n/a	n/a
7	CEBPB	chr1:174277808-174278120	K562	blood:	n/a	n/a
8	CEBPB	chr1:174321250-174321613	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:174338881-174339140	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:174334174-174334306	K562	blood:	n/a	n/a
11	CEBPB	chr1:174338872-174339172	A549	lung:	n/a	n/a
12	CEBPB	chr1:174277440-174277448	A549	lung:	n/a	n/a
13	CEBPB	chr1:174325741-174325974	K562	blood:	n/a	chr1:174325840-174325851 chr1:174325840-174325849 chr1:174325838-174325851
14	CEBPB	chr1:174277885-174278089	K562	blood:	n/a	n/a
15	CEBPB	chr1:174277912-174277999	A549	lung:	n/a	n/a
16	CEBPB	chr1:174277825-174278104	K562	blood:	n/a	n/a
17	CEBPB	chr1:174291213-174291328	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:174277430-174277450	K562	blood:	n/a	n/a
19	CEBPB	chr1:174334085-174334410	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:174338902-174339102	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:174328100-174328168	K562	blood:	n/a	n/a
22	CTCF	chr1:174328020-174328170	GM12870	blood:	n/a	n/a
23	CTCF	chr1:174328080-174328230	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:174327920-174328070	A549	lung:	n/a	n/a
25	CTCF	chr1:174328000-174328150	K562	blood:	n/a	n/a
26	CTCF	chr1:174328000-174328150	AG04450	lung:	n/a	n/a
27	CTCF	chr1:174328100-174328250	HCT-116	colon:	n/a	n/a
28	CTCF	chr1:174334797-174334861	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:174328140-174328290	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:174328060-174328210	BE2_C	brain:	n/a	n/a
31	CTCF	chr1:174328060-174328210	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:174327960-174328110	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:174328040-174328190	GM06990	blood:	n/a	n/a
34	CTCF	chr1:174328020-174328170	GM12871	blood:	n/a	n/a
35	CTCF	chr1:174281132-174281271	Medullo	brain:	n/a	n/a
36	CTCF	chr1:174328100-174328250	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:174328105-174328135	HepG2	liver:	n/a	n/a
38	CTCF	chr1:174308340-174308490	GM12874	blood:	n/a	n/a
39	CTCF	chr1:174328040-174328190	K562	blood:	n/a	n/a
40	CTCF	chr1:174328300-174328450	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:174334805-174334873	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:174328085-174328128	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:174328140-174328290	GM12872	blood:	n/a	n/a
44	CTCF	chr1:174334780-174334930	HepG2	liver:	n/a	n/a
45	CTCF	chr1:174327960-174328110	GM12866	blood:	n/a	n/a
46	CTCF	chr1:174328120-174328270	GM12868	blood:	n/a	n/a
47	CTCF	chr1:174280210-174280274	GM13976	blood:	n/a	n/a
48	CTCF	chr1:174337192-174337245	Fibrobl	skin:	n/a	n/a
49	CTCF	chr1:174328015-174328251	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:174328004-174328280	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174319673-174319723	HNPCEpiC	eye:	n/a
2	chr1:174319673-174319723	AG09319	gingival:	n/a
3	chr1:174319673-174319723	ProgFib	skin:	n/a
4	chr1:174319673-174319723	NH-A	brain:	n/a
5	chr1:174319673-174319723	Caco-2	colon:	n/a
6	chr1:174319673-174319723	SAEC	small airway:	n/a
7	chr1:174319673-174319723	HRPEpiC	eye:	n/a
8	chr1:174319673-174319723	NB4	blood:	n/a
9	chr1:174319673-174319723	GM12892	blood:	n/a
10	chr1:174319673-174319723	SK-N-SH_RA	brain:	n/a
11	chr1:174319673-174319723	HMEC	breast:	n/a
12	chr1:174319673-174319723	HCPEpiC	choroid plexus:	n/a
13	chr1:174319673-174319723	SK-N-MC	brain:	n/a
14	chr1:174319673-174319723	T-47D	breast:	n/a
15	chr1:174319673-174319723	HCT-116	colon:	n/a
16	chr1:174319673-174319723	MCF-7	breast:	n/a
17	chr1:174319673-174319723	HEEpiC	esophagus:	n/a
18	chr1:174319673-174319723	AG04450	lung:	fetal
19	chr1:174319673-174319723	K562	blood:	n/a
20	chr1:174319673-174319723	SK-N-SH	brain:	n/a
21	chr1:174319673-174319723	HUVEC	blood vessel:	n/a
22	chr1:174319673-174319723	HepG2	liver:	n/a
23	chr1:174319673-174319723	PrEC	prostate:	n/a
24	chr1:174319673-174319723	HIPEpiC	eye:	n/a
25	chr1:174319673-174319723	BE2_C	brain:	n/a
26	chr1:174319673-174319723	HAEpiC	amniotic membrane:	n/a
27	chr1:174319673-174319723	GM12891	blood:	n/a
28	chr1:174319673-174319723	AG10803	skin:	n/a
29	chr1:174319673-174319723	HEK293	kidney:	embryo
30	chr1:174319673-174319723	NHDF-neo	bronchial:	n/a
31	chr1:174319673-174319723	ECC-1	luminal epithelium:	n/a
32	chr1:174319673-174319723	Jurkat	blood:	n/a
33	chr1:174319673-174319723	LNCaP	prostate:	n/a
34	chr1:174319673-174319723	AoSMC	blood vessel:	n/a
35	chr1:174319673-174319723	BJ	skin:	n/a
36	chr1:174319673-174319723	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:174319673-174319723	PANC-1	pancreas:	n/a
38	chr1:174319673-174319723	Hela-S3	cervix:	n/a
39	chr1:174319673-174319723	NT2-D1	testis:	n/a
40	chr1:174319673-174319723	HL-60	blood:	n/a
41	chr1:174319673-174319723	NHBE	bronchial:	n/a
42	chr1:174319673-174319723	IMR90	lung:	fetal
43	chr1:174319673-174319723	HCF	heart:	n/a
44	chr1:174319673-174319723	HRCEpiC	kidney:	n/a
45	chr1:174319673-174319723	RPTEC	kidney:	n/a
46	chr1:174319673-174319723	AG09309	skin:	n/a
47	chr1:174319673-174319723	CMK	blood:	n/a
48	chr1:174319673-174319723	SKMC	muscle:	n/a
49	chr1:174319673-174319723	A549	lung:	n/a
50	chr1:174319673-174319723	HRE	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:174302180..174304421-chr1:174305573..174307627,2	K562	blood:
2	chr1:174293187..174295185-chr1:174300416..174302383,2	K562	blood:
3	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
4	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
5	chr1:174292133..174293963-chr1:174301470..174303626,2	MCF-7	breast:
6	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
7	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
8	chr1:174302180..174304421-chr1:174305573..174307627,2	K562	blood:
9	chr1:174292133..174293963-chr1:174301470..174303626,2	MCF-7	breast:
10	chr1:174269404..174272933-chr1:174275940..174280582,4	MCF-7	breast:
11	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
12	chr1:174328732..174330689-chr1:174332303..174334086,2	K562	blood:
13	chr1:174328732..174330689-chr1:174332303..174334086,2	K562	blood:
14	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
15	chr1:174293187..174295185-chr1:174300416..174302383,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-4	chr1:174336243-174337177	NONHSAT007733

No data

Variant related genes	Relation type
ENSG00000237317	TF binding region
RABGAP1L	TF binding region
ENSG00000266125	TF binding region
ENSG00000237317	CpG island
RABGAP1L	CpG island
ENSG00000266125	CpG island

Extended variants
information (count: 2639 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2639 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12069450	chr1:174273004-174273005	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77053067	chr1:174273043-174273044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74128340	chr1:174273057-174273058	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546362415	chr1:174273058-174273059	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76912418	chr1:174273097-174273098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556293091	chr1:174273124-174273125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531489936	chr1:174273200-174273201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576340857	chr1:174273204-174273205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545194298	chr1:174273221-174273222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565004224	chr1:174273341-174273342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145457884	chr1:174273342-174273343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145229324	chr1:174273344-174273345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561135237	chr1:174273348-174273349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181501295	chr1:174273400-174273401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550400640	chr1:174273434-174273435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6693198	chr1:174273439-174273440	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs531299101	chr1:174273501-174273502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12030642	chr1:174273510-174273511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116427604	chr1:174273549-174273550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186181769	chr1:174273558-174273559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533873828	chr1:174273660-174273661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73036669	chr1:174273664-174273665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148722710	chr1:174273670-174273671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561987051	chr1:174273702-174273703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536159598	chr1:174273708-174273709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564496632	chr1:174273770-174273771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377306030	chr1:174273789-174273790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576376648	chr1:174273838-174273839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539058856	chr1:174273897-174273898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183310687	chr1:174273906-174273907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572245239	chr1:174273946-174273947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112218795	chr1:174273986-174273987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373474076	chr1:174274006-174274007	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs2142864	chr1:174274062-174274063	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs115229836	chr1:174274065-174274066	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs142728115	chr1:174274146-174274147	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs370068818	chr1:174274163-174274164	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373960756	chr1:174274185-174274186	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs199975855	chr1:174274195-174274196	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs377380635	chr1:174274202-174274203	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs142260750	chr1:174274224-174274225	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs187569532	chr1:174274302-174274303	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs374228345	chr1:174274317-174274318	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs2860909	chr1:174274349-174274350	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs570150928	chr1:174274382-174274383	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs114953875	chr1:174274440-174274441	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs151230481	chr1:174274444-174274445	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs567372265	chr1:174274482-174274483	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs140387301	chr1:174274488-174274489	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs145288245	chr1:174274518-174274519	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174242800-174277200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr1:174243800-174275800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:174244400-174274000	Weak transcription	Fetal Heart	heart
4	chr1:174246200-174284200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:174251200-174275800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:174251400-174276000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:174259600-174276200	Weak transcription	Brain Anterior Caudate	brain
8	chr1:174259600-174277800	Weak transcription	K562	blood
9	chr1:174259800-174273800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr1:174259800-174274000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:174260200-174274000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:174260200-174275800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr1:174260400-174276200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr1:174260400-174277200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:174260600-174275600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:174262000-174274000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:174264800-174275400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:174270600-174274000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:174270600-174275400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:174270600-174279200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:174270800-174274000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:174270800-174274000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr1:174270800-174274000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:174270800-174274000	Weak transcription	Fetal Intestine Large	intestine
25	chr1:174270800-174274200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr1:174270800-174274200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:174270800-174274200	Weak transcription	Left Ventricle	heart
28	chr1:174270800-174274200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:174270800-174275600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr1:174270800-174275800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr1:174270800-174276600	Weak transcription	Esophagus	oesophagus
32	chr1:174270800-174276800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:174270800-174281400	Weak transcription	Right Ventricle	heart
34	chr1:174270800-174284200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr1:174270800-174285800	Weak transcription	Aorta	Aorta
36	chr1:174270800-174289800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:174271000-174274000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr1:174271000-174274000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr1:174271000-174274600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr1:174271000-174275800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:174271000-174276200	Weak transcription	Adipose Nuclei	Adipose
42	chr1:174271000-174276800	Weak transcription	Thymus	Thymus
43	chr1:174271000-174279400	Weak transcription	Fetal Stomach	stomach
44	chr1:174271000-174286400	Weak transcription	Spleen	Spleen
45	chr1:174271200-174274000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:174271200-174274000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr1:174271200-174274000	Weak transcription	Pancreas	Pancrea
48	chr1:174271200-174274200	Weak transcription	Primary T cells from cord blood	blood
49	chr1:174271200-174274200	Weak transcription	Ovary	ovary
50	chr1:174271200-174274400	Weak transcription	Fetal Intestine Small	intestine

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