Variant report

Variant	nsv999772
Chromosome Location	chr1:84611207-84667218
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 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	ATF1	chr1:84625274-84625597	K562	blood:	n/a	n/a
2	ATF2	chr1:84618224-84618863	GM12878	blood:	n/a	n/a
3	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
4	ATF3	chr1:84621649-84622441	HCT-116	colon:	n/a	n/a
5	BATF	chr1:84618291-84618802	GM12878	blood:	n/a	n/a
6	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
7	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
8	BATF	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:84618300-84618565	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:84618235-84618750	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:84618223-84618787	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:84622132-84622332	A549	lung:	n/a	n/a
13	CBX3	chr1:84612020-84612700	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:84612000-84612544	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
18	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
19	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
20	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:84619166-84619515	IMR90	lung:	n/a	chr1:84619337-84619348
22	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
23	CEBPB	chr1:84614426-84614628	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
25	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
27	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
28	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:84621648-84622549	HCT-116	colon:	n/a	n/a
30	CEBPB	chr1:84621953-84622346	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:84611961-84612846	HCT-116	colon:	n/a	n/a
32	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
33	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
34	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a
35	CTCF	chr1:84651941-84651966	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
37	CTCF	chr1:84651941-84652037	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:84651952-84651975	ProgFib	skin:	n/a	n/a
39	CTCF	chr1:84651880-84652030	HEK293	kidney:	n/a	n/a
40	CTCF	chr1:84653585-84653620	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr1:84651897-84651999	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr1:84651926-84651993	NHEK	skin:	n/a	n/a
43	CTCF	chr1:84651840-84651990	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:84629400-84629550	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
46	CTCF	chr1:84651800-84651950	AG09319	gingival:	n/a	n/a
47	CTCF	chr1:84651840-84651990	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr1:84651820-84651970	GM06990	blood:	n/a	n/a
49	CTCF	chr1:84651740-84651890	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:84651920-84652070	MCF-7	breast:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
2	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
3	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
4	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
5	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
6	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
7	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
8	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
9	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
10	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
11	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
12	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
13	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
2	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
3	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
4	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
5	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188
6	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190
7	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
8	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
9	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
10	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
11	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
12	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
13	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190

No data

Variant related genes	Relation type
PRKACB	TF binding region
ENSG00000142875	chromatin interactions
GCNT2	miRNA target sites
GCH1	miRNA target sites
GCFC1	miRNA target sites

Extended variants
information (count: 1801 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149574269	chr1:84611264-84611265	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs192987894	chr1:84611350-84611351	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs535164499	chr1:84611378-84611379	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs557947783	chr1:84611379-84611380	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs114685579	chr1:84611401-84611402	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574600984	chr1:84611563-84611564	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374823322	chr1:84611578-84611579	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs543404892	chr1:84611685-84611686	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs557560603	chr1:84611798-84611799	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149821464	chr1:84611824-84611825	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs201540445	chr1:84611825-84611826	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11381377	chr1:84611826-84611827	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs200802696	chr1:84611827-84611828	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs201750311	chr1:84611828-84611829	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs199773746	chr1:84611830-84611831	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs71097834	chr1:84611838-84611839	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372721982	chr1:84611857-84611858	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs542912520	chr1:84611870-84611871	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs368878904	chr1:84611901-84611902	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs368350792	chr1:84611927-84611928	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs563722472	chr1:84611982-84611983	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs6576963	chr1:84611998-84611999	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs115154355	chr1:84612006-84612007	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs185328051	chr1:84612018-84612019	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs371742859	chr1:84612066-84612067	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs530489630	chr1:84612127-84612128	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs186845462	chr1:84612156-84612157	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs111504412	chr1:84612187-84612188	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs530042353	chr1:84612188-84612189	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs546571400	chr1:84612223-84612224	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs559722813	chr1:84612238-84612239	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs78788513	chr1:84612276-84612277	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs551763655	chr1:84612289-84612290	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs573237345	chr1:84612385-84612386	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs191782985	chr1:84612430-84612431	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs552140149	chr1:84612436-84612437	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537495300	chr1:84612443-84612444	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs376872228	chr1:84612465-84612466	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs567849919	chr1:84612470-84612471	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs374145638	chr1:84612516-84612517	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373113923	chr1:84612555-84612556	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs537001176	chr1:84612589-84612590	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs75521526	chr1:84612678-84612679	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs139799659	chr1:84612732-84612733	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs538272269	chr1:84612741-84612742	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs183509113	chr1:84612744-84612745	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs55968149	chr1:84612820-84612821	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369107544	chr1:84612859-84612860	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs575002681	chr1:84612864-84612865	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545183048	chr1:84612893-84612894	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84588000-84618400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr1:84607000-84613600	Weak transcription	Brain Angular Gyrus	brain
3	chr1:84609400-84612800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:84609400-84612800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr1:84609600-84611400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr1:84609600-84612600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:84609600-84612600	Enhancers	NHDF-Ad	bronchial
8	chr1:84609600-84612600	Enhancers	NHEK	skin
9	chr1:84609600-84612600	Enhancers	Osteobl	bone
10	chr1:84609600-84612800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:84609600-84613000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
12	chr1:84609600-84613800	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr1:84609600-84614000	Active TSS	Primary T cells fromperipheralblood	blood
14	chr1:84609800-84611400	Active TSS	Primary B cells from peripheral blood	blood
15	chr1:84609800-84611400	Active TSS	Adipose Nuclei	Adipose
16	chr1:84609800-84611600	Active TSS	HUVEC	blood vessel
17	chr1:84609800-84612400	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr1:84609800-84612400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
19	chr1:84609800-84612400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
20	chr1:84609800-84612400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:84609800-84612800	Active TSS	Primary T killer memory cells from peripheral blood	blood
22	chr1:84609800-84612800	Active TSS	Fetal Thymus	thymus
23	chr1:84609800-84612800	Active TSS	Thymus	Thymus
24	chr1:84609800-84612800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr1:84609800-84613000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr1:84609800-84613000	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr1:84609800-84613400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr1:84609800-84613800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:84610000-84611600	Active TSS	Primary T cells from cord blood	blood
30	chr1:84610000-84611600	Active TSS	Fetal Stomach	stomach
31	chr1:84610000-84612600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:84610000-84612600	Active TSS	Colonic Mucosa	Colon
33	chr1:84610000-84612600	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr1:84610000-84612600	Active TSS	Rectal Smooth Muscle	rectum
35	chr1:84610200-84611400	Active TSS	Liver	Liver
36	chr1:84610200-84611600	Active TSS	Primary monocytes fromperipheralblood	blood
37	chr1:84610200-84611600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:84610200-84611600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:84610200-84611800	Active TSS	Primary hematopoietic stem cells	blood
40	chr1:84610200-84611800	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr1:84610200-84611800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr1:84610200-84611800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:84610200-84611800	Weak transcription	Brain Hippocampus Middle	brain
44	chr1:84610200-84612000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr1:84610200-84612000	Active TSS	Dnd41	blood
46	chr1:84610200-84612200	Active TSS	Duodenum Mucosa	Duodenum
47	chr1:84610200-84613800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr1:84610200-84621800	Weak transcription	Aorta	Aorta
49	chr1:84610200-84621800	Weak transcription	Small Intestine	intestine
50	chr1:84610200-84622000	Weak transcription	HSMM	muscle

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