Variant report

Variant	nsv1005225
Chromosome Location	chr1:84609871-84667950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
8	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
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	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
14	CBX3	chr1:84609716-84610267	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:84612020-84612700	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
18	CBX3	chr1:84612000-84612544	HCT-116	colon:	n/a	n/a
19	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
21	CEBPB	chr1:84621648-84622549	HCT-116	colon:	n/a	n/a
22	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:84611961-84612846	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
28	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
29	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
30	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
31	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
32	CEBPB	chr1:84619166-84619515	IMR90	lung:	n/a	chr1:84619337-84619348
33	CEBPB	chr1:84614426-84614628	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:84621953-84622346	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:84629400-84629550	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr1:84609959-84609983	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr1:84651923-84651989	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:84609866-84609954	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
40	CTCF	chr1:84651860-84652010	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr1:84651900-84652050	AG04449	skin:	n/a	n/a
42	CTCF	chr1:84651795-84651989	K562	blood:	n/a	n/a
43	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:84609860-84610010	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
46	CTCF	chr1:84651942-84651996	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:84652020-84652022	A549	lung:	n/a	n/a
48	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a
49	CTCF	chr1:84658864-84658893	Lung_OC	lung:	n/a	n/a
50	CTCF	chr1:84651800-84651950	AG09319	gingival:	n/a	n/a

No data

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

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

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

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

No data

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

Extended variants
information (count: 1869 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1869 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569746539	chr1:84609873-84609874	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs535443683	chr1:84609921-84609922	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113718480	chr1:84609960-84609961	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555443685	chr1:84609981-84609982	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566166385	chr1:84609984-84609985	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112540650	chr1:84609991-84609992	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374988248	chr1:84610007-84610008	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534766641	chr1:84610009-84610010	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs112013822	chr1:84610020-84610021	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200815670	chr1:84610057-84610058	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs368743693	chr1:84610070-84610071	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs372658798	chr1:84610102-84610103	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs377304636	chr1:84610106-84610107	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs201081253	chr1:84610120-84610121	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs369569393	chr1:84610126-84610127	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs374156039	chr1:84610128-84610129	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs376000902	chr1:84610149-84610150	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs369346119	chr1:84610154-84610155	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs77697668	chr1:84610160-84610161	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139854250	chr1:84610200-84610201	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs373002031	chr1:84610267-84610268	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs373371564	chr1:84610310-84610311	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs140720001	chr1:84610386-84610387	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs570228291	chr1:84610420-84610421	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs577374899	chr1:84610444-84610445	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs141454751	chr1:84610522-84610523	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs150855988	chr1:84610524-84610525	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542628020	chr1:84610630-84610631	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs559041093	chr1:84610647-84610648	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs528200722	chr1:84610656-84610657	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs544767971	chr1:84610659-84610660	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs564786108	chr1:84610726-84610727	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373405459	chr1:84610755-84610756	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373729023	chr1:84610760-84610761	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs41300506	chr1:84610762-84610763	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368016133	chr1:84610780-84610781	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs375343031	chr1:84610795-84610796	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs532105714	chr1:84610821-84610822	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550497677	chr1:84610829-84610830	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563075210	chr1:84610890-84610891	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs2684912	chr1:84610974-84610975	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs567240666	chr1:84610978-84610979	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs572284190	chr1:84611162-84611163	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs139233222	chr1:84611174-84611175	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs149574269	chr1:84611264-84611265	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs192987894	chr1:84611350-84611351	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535164499	chr1:84611378-84611379	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs557947783	chr1:84611379-84611380	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs114685579	chr1:84611401-84611402	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs574600984	chr1:84611563-84611564	Weak transcription Enhancers Active TSS Flanking 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:1677 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

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	chr1:84607400-84610000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:84607800-84610000	Weak transcription	Liver	Liver
5	chr1:84609000-84610000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:84609000-84610000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:84609000-84610800	Weak transcription	Gastric	stomach
8	chr1:84609400-84610200	Flanking Active TSS	Dnd41	blood
9	chr1:84609400-84610400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
10	chr1:84609400-84610400	Enhancers	Fetal Kidney	kidney
11	chr1:84609400-84612800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:84609400-84612800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:84609600-84610000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:84609600-84610000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:84609600-84610000	Enhancers	Duodenum Mucosa	Duodenum
16	chr1:84609600-84610000	Enhancers	NH-A	brain
17	chr1:84609600-84610200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:84609600-84610200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:84609600-84610200	Enhancers	HSMM	muscle
20	chr1:84609600-84610600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:84609600-84611000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:84609600-84611400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:84609600-84612600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:84609600-84612600	Enhancers	NHDF-Ad	bronchial
25	chr1:84609600-84612600	Enhancers	NHEK	skin
26	chr1:84609600-84612600	Enhancers	Osteobl	bone
27	chr1:84609600-84612800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:84609600-84613000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr1:84609600-84613800	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr1:84609600-84614000	Active TSS	Primary T cells fromperipheralblood	blood
31	chr1:84609800-84610000	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr1:84609800-84610000	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr1:84609800-84610000	Active TSS	Primary hematopoietic stem cells	blood
34	chr1:84609800-84610000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr1:84609800-84610000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr1:84609800-84610200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr1:84609800-84610200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:84609800-84610200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr1:84609800-84610200	Enhancers	Brain Hippocampus Middle	brain
40	chr1:84609800-84610200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr1:84609800-84610200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:84609800-84610200	Enhancers	Fetal Heart	heart
43	chr1:84609800-84610400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:84609800-84610400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:84609800-84610400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:84609800-84610400	Enhancers	Brain Substantia Nigra	brain
47	chr1:84609800-84610400	Enhancers	A549	lung
48	chr1:84609800-84611200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:84609800-84611200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:84609800-84611200	Active TSS	Duodenum Smooth Muscle	Duodenum

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