Variant report

Variant	nsv10672
Chromosome Location	chr1:120386985-120410007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:361)
CpG islands
(count:549)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120402048-120402592	K562	blood:	n/a	n/a
2	ARID3A	chr1:120392364-120392392	K562	blood:	n/a	n/a
3	ARID3A	chr1:120386952-120387123	K562	blood:	n/a	n/a
4	ATF1	chr1:120398236-120398340	K562	blood:	n/a	n/a
5	ATF1	chr1:120391966-120392057	K562	blood:	n/a	n/a
6	ATF1	chr1:120402001-120402616	K562	blood:	n/a	n/a
7	ATF3	chr1:120402162-120402649	K562	blood:	n/a	n/a
8	BATF	chr1:120386780-120387005	GM12878	blood:	n/a	n/a
9	BATF	chr1:120386771-120387113	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:120387330-120387656	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:120387086-120387158	K562	blood:	n/a	n/a
12	BHLHE40	chr1:120402075-120402625	K562	blood:	n/a	n/a
13	BHLHE40	chr1:120386765-120387007	HepG2	liver:	n/a	n/a
14	CBX3	chr1:120402018-120402716	K562	blood:	n/a	n/a
15	CEBPB	chr1:120409436-120409447	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:120402181-120402652	K562	blood:	n/a	n/a
17	CEBPB	chr1:120402260-120402530	K562	blood:	n/a	n/a
18	CEBPB	chr1:120408184-120408568	IMR90	lung:	n/a	n/a
19	CEBPD	chr1:120402145-120402665	K562	blood:	n/a	n/a
20	CTCF	chr1:120386940-120387090	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr1:120387100-120387250	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr1:120386940-120387090	HRE	kidney:	n/a	n/a
23	CTCF	chr1:120386992-120387062	GM12878	blood:	n/a	n/a
24	CTCF	chr1:120386960-120387110	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr1:120386956-120387078	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr1:120386940-120387090	AG09319	gingival:	n/a	n/a
27	CTCF	chr1:120386940-120387090	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr1:120386960-120387110	GM12869	blood:	n/a	n/a
29	CTCF	chr1:120386960-120387110	NHEK	skin:	n/a	n/a
30	CTCF	chr1:120386784-120387140	A549	lung:	n/a	n/a
31	CTCF	chr1:120386960-120387110	HMF	breast:	n/a	n/a
32	CTCF	chr1:120386890-120387142	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:120386940-120387090	HVMF	connective:	n/a	n/a
34	CTCF	chr1:120386960-120387110	AG04449	skin:	n/a	n/a
35	CTCF	chr1:120386980-120387130	GM12874	blood:	n/a	n/a
36	CTCF	chr1:120386940-120387090	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr1:120386980-120387130	HMF	breast:	n/a	n/a
38	CTCF	chr1:120386931-120387072	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr1:120386940-120387090	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:120386980-120387130	HCT-116	colon:	n/a	n/a
41	CTCF	chr1:120386920-120387070	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:120386958-120387103	Gliobla	brain:	n/a	n/a
43	CTCF	chr1:120387060-120387210	HFF	foreskin:	n/a	n/a
44	CTCF	chr1:120386980-120387130	GM12878	blood:	n/a	n/a
45	CTCF	chr1:120386940-120387090	GM12878	blood:	n/a	n/a
46	CTCF	chr1:120386960-120387110	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:120386980-120387130	GM06990	blood:	n/a	n/a
48	CTCF	chr1:120386867-120387203	A549	lung:	n/a	n/a
49	CTCF	chr1:120386831-120387195	IMR90	lung:	n/a	n/a
50	CTCF	chr1:120401504-120401616	Kidney_OC	kidney:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120395857-120395907	GM12892	blood:	n/a
2	chr1:120396074-120396124	LNCaP	prostate:	n/a
3	chr1:120394120-120394170	MCF10A-Er-Src	breast:	n/a
4	chr1:120387299-120387349	CMK	blood:	n/a
5	chr1:120389211-120389261	SK-N-MC	brain:	n/a
6	chr1:120387083-120387133	LNCaP	prostate:	n/a
7	chr1:120394120-120394170	GM12892	blood:	n/a
8	chr1:120396167-120396217	HNPCEpiC	eye:	n/a
9	chr1:120387083-120387133	IMR90	lung:	fetal
10	chr1:120396167-120396217	PrEC	prostate:	n/a
11	chr1:120395943-120395993	GM12891	blood:	n/a
12	chr1:120387299-120387349	HMEC	breast:	n/a
13	chr1:120395857-120395907	RPTEC	kidney:	n/a
14	chr1:120396167-120396217	ProgFib	skin:	n/a
15	chr1:120396074-120396124	NHBE	bronchial:	n/a
16	chr1:120395943-120395993	HCT-116	colon:	n/a
17	chr1:120395943-120395993	AG04449	skin:	fetal
18	chr1:120394120-120394170	HCPEpiC	choroid plexus:	n/a
19	chr1:120387965-120388015	SK-N-MC	brain:	n/a
20	chr1:120387083-120387133	PANC-1	pancreas:	n/a
21	chr1:120387083-120387133	AG04449	skin:	fetal
22	chr1:120387299-120387349	SK-N-MC	brain:	n/a
23	chr1:120395943-120395993	SKMC	muscle:	n/a
24	chr1:120395943-120395993	AoSMC	blood vessel:	n/a
25	chr1:120396074-120396124	HNPCEpiC	eye:	n/a
26	chr1:120389211-120389261	Caco-2	colon:	n/a
27	chr1:120387299-120387349	HEEpiC	esophagus:	n/a
28	chr1:120387083-120387133	HCF	heart:	n/a
29	chr1:120396074-120396124	HRE	kidney:	n/a
30	chr1:120396074-120396124	SKMC	muscle:	n/a
31	chr1:120387965-120388015	AG04450	lung:	fetal
32	chr1:120396074-120396124	Hela-S3	cervix:	n/a
33	chr1:120389211-120389261	AG09319	gingival:	n/a
34	chr1:120394120-120394170	HL-60	blood:	n/a
35	chr1:120389211-120389261	AG10803	skin:	n/a
36	chr1:120387299-120387349	HCT-116	colon:	n/a
37	chr1:120396074-120396124	HUVEC	blood vessel:	n/a
38	chr1:120395943-120395993	GM12878	blood:	n/a
39	chr1:120387965-120388015	LNCaP	prostate:	n/a
40	chr1:120387965-120388015	GM06990	blood:	n/a
41	chr1:120387965-120388015	ovcar-3	ovarian:	n/a
42	chr1:120389211-120389261	LNCaP	prostate:	n/a
43	chr1:120395857-120395907	PFSK-1	brain:	n/a
44	chr1:120387083-120387133	Hela-S3	cervix:	n/a
45	chr1:120387299-120387349	SAEC	small airway:	n/a
46	chr1:120387299-120387349	ECC-1	luminal epithelium:	n/a
47	chr1:120395943-120395993	A549	lung:	n/a
48	chr1:120396074-120396124	ECC-1	luminal epithelium:	n/a
49	chr1:120395943-120395993	NH-A	brain:	n/a
50	chr1:120394120-120394170	Jurkat	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120400389..120402381-chr1:120411990..120414876,2	MCF-7	breast:
2	chr1:120396123..120397960-chr1:120398634..120401481,2	MCF-7	breast:
3	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
4	chr1:120396123..120397960-chr1:120398634..120401481,2	MCF-7	breast:
5	chr1:120370478..120372574-chr1:120394062..120395720,2	MCF-7	breast:
6	chr1:120395050..120396919-chr1:120400456..120403382,2	K562	blood:
7	chr1:120401899..120403872-chr1:120404616..120406616,2	K562	blood:
8	chr1:120401899..120403872-chr1:120404616..120406616,2	K562	blood:
9	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:
10	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:
11	chr1:120400878..120403434-chr1:120429544..120432344,2	MCF-7	breast:
12	chr1:120407227..120409866-chr1:120411448..120413775,3	K562	blood:
13	chr1:120409955..120411545-chr1:120412072..120413806,2	MCF-7	breast:
14	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
15	chr1:120401746..120405481-chr1:120411089..120413247,3	K562	blood:
16	chr1:120402638..120409843-chr1:120411143..120414879,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM30-1	chr1:120390862-120391484	ENSG00000247433
2	lnc-PHGDH-2	chr1:120389145-120389383	XLOC_000371
3	lnc-PHGDH-2	chr1:120388521-120388629	XLOC_000371

No data

Variant related genes	Relation type
NBPF7	TF binding region
PFN1P9	TF binding region
NBPF7	CpG island
PFN1P9	CpG island
ENSG00000227205	chromatin interactions
ZDHHC2	miRNA target sites

Extended variants
information (count: 747 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200602121	chr1:120387000-120387001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs202043705	chr1:120387006-120387007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372571788	chr1:120387009-120387010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200625495	chr1:120387025-120387026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72469596	chr1:120387039-120387040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587601069	chr1:120387041-120387042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140448413	chr1:120387057-120387058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375970796	chr1:120387083-120387084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200955537	chr1:120387084-120387085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371109790	chr1:120387104-120387105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374251758	chr1:120387107-120387108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12405228	chr1:120387120-120387121	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs201495038	chr1:120387150-120387151	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189728424	chr1:120387163-120387164	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373843587	chr1:120387201-120387202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs12731358	chr1:120387211-120387212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs12745903	chr1:120387212-120387213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs587682392	chr1:120387219-120387220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs587742290	chr1:120387230-120387231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs587634188	chr1:120387231-120387232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs587622084	chr1:120387261-120387262	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs587697410	chr1:120387286-120387287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs181791046	chr1:120387300-120387301	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs371192284	chr1:120387350-120387351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs587673191	chr1:120387371-120387372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs2153676	chr1:120387376-120387377	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs587775386	chr1:120387388-120387389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs375485181	chr1:120387402-120387403	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200663081	chr1:120387408-120387409	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs186770144	chr1:120387424-120387425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs587706586	chr1:120387462-120387463	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs587758907	chr1:120387536-120387537	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs587640225	chr1:120387543-120387544	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190474272	chr1:120387549-120387550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs587595049	chr1:120387578-120387579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs587671322	chr1:120387582-120387583	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs587706151	chr1:120387731-120387732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs587606573	chr1:120387768-120387769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs185205568	chr1:120387966-120387967	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs189768156	chr1:120387980-120387981	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs112697682	chr1:120387997-120387998	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs587775524	chr1:120388185-120388186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs141356318	chr1:120388214-120388215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs186511524	chr1:120388217-120388218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs6675042	chr1:120388218-120388219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs191379751	chr1:120388227-120388228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs145104834	chr1:120388238-120388239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs587753443	chr1:120388245-120388246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs183466256	chr1:120388285-120388286	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs587714154	chr1:120388324-120388325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Aortic dissecting aneurysms	22263138	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120387000-120387200	Enhancers	K562	blood
2	chr1:120389600-120390800	Enhancers	GM12878-XiMat	blood
3	chr1:120390600-120390800	Enhancers	NHEK	skin
4	chr1:120395000-120400400	Weak transcription	Fetal Intestine Small	intestine
5	chr1:120395800-120396000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:120395800-120396200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:120396000-120402400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:120397800-120398000	Enhancers	K562	blood
9	chr1:120398000-120398200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:120398200-120398600	Enhancers	HepG2	liver
11	chr1:120398200-120400600	Weak transcription	K562	blood
12	chr1:120398600-120400600	Weak transcription	HepG2	liver
13	chr1:120398600-120400800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:120400200-120402400	Enhancers	Fetal Intestine Large	intestine
15	chr1:120400400-120402600	Enhancers	Fetal Intestine Small	intestine
16	chr1:120400600-120401000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:120400600-120401000	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr1:120400600-120401400	Enhancers	HepG2	liver
19	chr1:120400600-120401800	Enhancers	K562	blood
20	chr1:120400800-120401000	Enhancers	Duodenum Mucosa	Duodenum
21	chr1:120400800-120401000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr1:120400800-120401800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:120400800-120401800	Enhancers	Dnd41	blood
24	chr1:120400800-120402400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:120400800-120403200	Enhancers	HUVEC	blood vessel
26	chr1:120400800-120404000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:120400800-120404200	Enhancers	Fetal Muscle Leg	muscle
28	chr1:120400800-120405000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:120401000-120401400	Enhancers	Fetal Kidney	kidney
30	chr1:120401000-120402000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr1:120401000-120402000	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr1:120401000-120402200	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr1:120401000-120404800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:120401200-120401400	Enhancers	Small Intestine	intestine
35	chr1:120401200-120401600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr1:120401200-120403200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr1:120401400-120401600	Enhancers	Fetal Muscle Trunk	muscle
38	chr1:120401400-120402400	Enhancers	Primary hematopoietic stem cells	blood
39	chr1:120401400-120403400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:120401400-120415000	Weak transcription	Fetal Kidney	kidney
41	chr1:120401600-120402600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr1:120401600-120403000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:120401800-120402000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr1:120401800-120402200	Flanking Active TSS	Dnd41	blood
45	chr1:120401800-120402600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:120401800-120402600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:120401800-120402600	Enhancers	Osteobl	bone
48	chr1:120401800-120402800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:120401800-120402800	Enhancers	HMEC	breast
50	chr1:120401800-120402800	Enhancers	HSMMtube	muscle

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