Variant report

Variant	nsv871643
Chromosome Location	chr1:84628655-84705481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:84691434-84691612	K562	blood:	n/a	n/a
2	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
3	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
4	CBX3	chr1:84674603-84675127	HCT-116	colon:	n/a	n/a
5	CBX3	chr1:84688887-84689091	K562	blood:	n/a	n/a
6	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
7	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
9	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
11	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
12	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
16	CTCF	chr1:84689800-84689950	GM12878	blood:	n/a	n/a
17	CTCF	chr1:84651860-84652010	BJ	skin:	n/a	n/a
18	CTCF	chr1:84651876-84652020	K562	blood:	n/a	n/a
19	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
20	CTCF	chr1:84689740-84689890	HCT-116	colon:	n/a	n/a
21	CTCF	chr1:84689780-84689930	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:84689760-84689910	GM12865	blood:	n/a	n/a
23	CTCF	chr1:84689960-84690110	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr1:84651860-84652010	HVMF	connective:	n/a	n/a
25	CTCF	chr1:84651860-84652010	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr1:84689840-84689990	HCT-116	colon:	n/a	n/a
27	CTCF	chr1:84689900-84690050	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr1:84651883-84652042	Gliobla	brain:	n/a	n/a
29	CTCF	chr1:84651920-84652070	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:84689800-84689950	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
32	CTCF	chr1:84689780-84689930	GM12873	blood:	n/a	n/a
33	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:84689820-84689970	SAEC	small airway:	n/a	n/a
35	CTCF	chr1:84651947-84652024	GM19238	blood:	n/a	n/a
36	CTCF	chr1:84689880-84690030	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:84689794-84690026	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:84689840-84689990	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr1:84689840-84689990	HCFaa	heart:	n/a	n/a
40	CTCF	chr1:84651933-84652005	GM10266	blood:	n/a	n/a
41	CTCF	chr1:84651961-84651988	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:84651900-84652050	AG09319	gingival:	n/a	n/a
43	CTCF	chr1:84689920-84690070	GM12874	blood:	n/a	n/a
44	CTCF	chr1:84689858-84689909	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:84689840-84689990	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr1:84651952-84651975	ProgFib	skin:	n/a	n/a
47	CTCF	chr1:84651840-84651990	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:84689840-84689990	HMEC	breast:	n/a	n/a
49	CTCF	chr1:84689820-84689970	GM12868	blood:	n/a	n/a
50	CTCF	chr1:84651820-84651970	HMF	breast:	n/a	n/a

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
2	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
3	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
4	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
5	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
6	chr1:84703877..84705548-chr1:84707085..84709584,2	K562	blood:
7	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
8	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
9	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
10	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
11	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
12	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
13	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
14	chr1:84701446..84703629-chr1:84722658..84725060,2	MCF-7	breast:
15	chr1:84699628..84701684-chr1:84763119..84765204,2	MCF-7	breast:
16	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
17	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:

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

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

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PRKACB	hsa-miR-19b-3p	chr1:84702375-84702399
2	PRKACB	hsa-miR-93-5p	chr1:84702387-84702393
3	PRKACB	hsa-miR-93-5p	chr1:84702372-84702394
4	PRKACB	hsa-miR-19b-3p	chr1:84701025-84701031

Variant related genes	Relation type
ENSG00000226970	TF binding region
PRKACB	TF binding region
ENSG00000203943	chromatin interactions
ENSG00000142875	chromatin interactions
GCNT2	miRNA target sites
GCH1	miRNA target sites
GCFC1	miRNA target sites

Extended variants
information (count: 2611 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2611 , 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	rs12129768	chr1:84628655-84628656	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544823104	chr1:84628697-84628698	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2684915	chr1:84628700-84628701	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs575481340	chr1:84628722-84628723	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371988893	chr1:84628723-84628724	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562751829	chr1:84628738-84628739	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139046753	chr1:84628791-84628792	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116143582	chr1:84628814-84628815	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114764842	chr1:84628835-84628836	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542999025	chr1:84628882-84628883	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188805612	chr1:84628891-84628892	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528562898	chr1:84628925-84628926	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369396818	chr1:84628971-84628972	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12752859	chr1:84629005-84629006	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551722067	chr1:84629041-84629042	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571791244	chr1:84629061-84629062	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs12731933	chr1:84629064-84629065	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs12731935	chr1:84629066-84629067	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs12753033	chr1:84629090-84629091	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192640088	chr1:84629127-84629128	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs12753168	chr1:84629140-84629141	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs12732075	chr1:84629156-84629157	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs12733303	chr1:84629157-84629158	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs372693110	chr1:84629171-84629172	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs12732084	chr1:84629178-84629179	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs185072279	chr1:84629179-84629180	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs75611394	chr1:84629202-84629203	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs574720865	chr1:84629340-84629341	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs539821066	chr1:84629393-84629394	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551245785	chr1:84629402-84629403	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs567578267	chr1:84629493-84629494	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs140916425	chr1:84629539-84629540	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs189140933	chr1:84629548-84629549	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs553386875	chr1:84629554-84629555	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538328544	chr1:84629665-84629666	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs113391999	chr1:84629709-84629710	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs144867427	chr1:84629754-84629755	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542355563	chr1:84629841-84629842	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs12030564	chr1:84629845-84629846	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs141675932	chr1:84629852-84629853	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs574759821	chr1:84629853-84629854	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543062091	chr1:84629898-84629899	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs559768656	chr1:84629919-84629920	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs573403164	chr1:84630003-84630004	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369513745	chr1:84630051-84630052	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs565380126	chr1:84630064-84630065	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs369345269	chr1:84630135-84630136	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565439699	chr1:84630156-84630157	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs180706399	chr1:84630188-84630189	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs376705048	chr1:84630204-84630205	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84610400-84633400	Weak transcription	Fetal Kidney	kidney
2	chr1:84611600-84629800	Weak transcription	Fetal Stomach	stomach
3	chr1:84612800-84628800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:84614000-84633800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:84614800-84629000	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:84615800-84634800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:84616200-84635200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:84618800-84630400	Weak transcription	Primary B cells from cord blood	blood
9	chr1:84619000-84628800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:84619000-84628800	Weak transcription	Gastric	stomach
11	chr1:84619200-84630200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:84622000-84628800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:84622200-84630000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:84622400-84635800	Weak transcription	Small Intestine	intestine
15	chr1:84622600-84628800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:84623000-84629800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr1:84623000-84639200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:84623800-84630000	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr1:84624000-84628800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:84624000-84629200	Weak transcription	Fetal Thymus	thymus
21	chr1:84624000-84651800	Weak transcription	Thymus	Thymus
22	chr1:84624200-84630800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:84624800-84633200	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr1:84625200-84629600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:84625600-84629800	Weak transcription	Right Atrium	heart
26	chr1:84625600-84635600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr1:84625800-84628800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:84625800-84634000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:84626000-84628800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:84626000-84630000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr1:84626200-84628800	Weak transcription	Dnd41	blood
32	chr1:84626400-84630400	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr1:84626600-84629000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr1:84626800-84628800	Weak transcription	Brain Anterior Caudate	brain
35	chr1:84627200-84631000	Weak transcription	HUVEC	blood vessel
36	chr1:84627600-84635400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr1:84627800-84629400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:84628200-84628800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:84628200-84628800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:84628200-84628800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:84628600-84628800	Active TSS	Primary T cells from cord blood	blood
42	chr1:84628600-84628800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr1:84628800-84629000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:84628800-84629000	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr1:84628800-84629000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr1:84628800-84629000	Enhancers	Brain Germinal Matrix	brain
47	chr1:84628800-84629000	Enhancers	Gastric	stomach
48	chr1:84628800-84629000	Enhancers	Left Ventricle	heart
49	chr1:84628800-84629000	Enhancers	Dnd41	blood
50	chr1:84628800-84629000	Weak transcription	NHLF	lung

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