Variant report

Variant	nsv997601
Chromosome Location	chr1:84609346-84672859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:444)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:444 , 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	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
8	BATF	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:84618235-84618750	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:84618300-84618565	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	chr1:84612000-84612544	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:84612020-84612700	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
18	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
19	CBX3	chr1:84609716-84610267	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:84621648-84622549	HCT-116	colon:	n/a	n/a
22	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
23	CEBPB	chr1:84614426-84614628	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
26	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
28	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
29	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:84611961-84612846	HCT-116	colon:	n/a	n/a
31	CEBPB	chr1:84619166-84619515	IMR90	lung:	n/a	chr1:84619337-84619348
32	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
33	CEBPB	chr1:84621953-84622346	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
35	CTCF	chr1:84651926-84651993	NHEK	skin:	n/a	n/a
36	CTCF	chr1:84651942-84651996	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:84651897-84651999	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:84609540-84609690	AG10803	skin:	n/a	n/a
39	CTCF	chr1:84651900-84652050	AG09319	gingival:	n/a	n/a
40	CTCF	chr1:84651920-84652070	GM12872	blood:	n/a	n/a
41	CTCF	chr1:84619100-84619250	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:84651840-84651990	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr1:84653585-84653620	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:84651952-84651975	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:84658864-84658893	Lung_OC	lung:	n/a	n/a
47	CTCF	chr1:84651923-84651989	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:84609959-84609983	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
50	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
2	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
3	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
4	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
5	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
6	chr1:84545204..84547427-chr1:84607809..84609728,2	K562	blood:
7	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
8	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
9	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
10	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
11	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
12	chr1:84606589..84609383-chr1:85086485..85089260,2	MCF-7	breast:
13	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
14	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
15	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
16	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
17	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:

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

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

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: 2023 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2023 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563319189	chr1:84609354-84609355	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184033378	chr1:84609379-84609380	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs188564990	chr1:84609421-84609422	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs41300502	chr1:84609423-84609424	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528147655	chr1:84609497-84609498	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs532059760	chr1:84609547-84609548	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs369805166	chr1:84609548-84609549	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs41300504	chr1:84609556-84609557	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs113112773	chr1:84609718-84609719	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199516588	chr1:84609742-84609743	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs138856622	chr1:84609746-84609747	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530755525	chr1:84609819-84609820	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs1980270	chr1:84609864-84609865	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs559810767	chr1:84609867-84609868	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs569746539	chr1:84609873-84609874	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535443683	chr1:84609921-84609922	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs113718480	chr1:84609960-84609961	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs555443685	chr1:84609981-84609982	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566166385	chr1:84609984-84609985	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs112540650	chr1:84609991-84609992	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs374988248	chr1:84610007-84610008	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534766641	chr1:84610009-84610010	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs112013822	chr1:84610020-84610021	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs200815670	chr1:84610057-84610058	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368743693	chr1:84610070-84610071	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs372658798	chr1:84610102-84610103	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377304636	chr1:84610106-84610107	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201081253	chr1:84610120-84610121	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs369569393	chr1:84610126-84610127	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs374156039	chr1:84610128-84610129	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs376000902	chr1:84610149-84610150	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs369346119	chr1:84610154-84610155	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs77697668	chr1:84610160-84610161	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs139854250	chr1:84610200-84610201	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373002031	chr1:84610267-84610268	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs373371564	chr1:84610310-84610311	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140720001	chr1:84610386-84610387	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570228291	chr1:84610420-84610421	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577374899	chr1:84610444-84610445	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs141454751	chr1:84610522-84610523	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs150855988	chr1:84610524-84610525	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs542628020	chr1:84610630-84610631	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs559041093	chr1:84610647-84610648	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs528200722	chr1:84610656-84610657	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs544767971	chr1:84610659-84610660	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564786108	chr1:84610726-84610727	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs373405459	chr1:84610755-84610756	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373729023	chr1:84610760-84610761	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs41300506	chr1:84610762-84610763	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs368016133	chr1:84610780-84610781	Enhancers Weak transcription 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:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84584000-84609600	Weak transcription	HSMM	muscle
2	chr1:84584000-84609800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:84588000-84618400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:84606800-84609400	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr1:84607000-84613600	Weak transcription	Brain Angular Gyrus	brain
6	chr1:84607200-84609600	Enhancers	Primary hematopoietic stem cells	blood
7	chr1:84607200-84609600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr1:84607200-84609600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:84607200-84609800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:84607200-84609800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr1:84607200-84609800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:84607400-84609400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr1:84607400-84609600	Enhancers	HUVEC	blood vessel
14	chr1:84607400-84610000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:84607600-84609400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr1:84607600-84609800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:84607800-84610000	Weak transcription	Liver	Liver
18	chr1:84608200-84609600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:84608200-84609800	Weak transcription	A549	lung
20	chr1:84608400-84609400	Enhancers	Dnd41	blood
21	chr1:84608400-84609800	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr1:84608600-84609400	Enhancers	Primary T cells fromperipheralblood	blood
23	chr1:84608600-84609400	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr1:84608800-84609800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:84608800-84609800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:84609000-84609400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr1:84609000-84609600	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr1:84609000-84609600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr1:84609000-84609800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:84609000-84609800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr1:84609000-84609800	Enhancers	Fetal Thymus	thymus
32	chr1:84609000-84610000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:84609000-84610000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:84609000-84610800	Weak transcription	Gastric	stomach
35	chr1:84609200-84609600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:84609200-84609800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr1:84609200-84609800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:84609200-84609800	Weak transcription	Brain Substantia Nigra	brain
39	chr1:84609400-84609600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr1:84609400-84609600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr1:84609400-84609800	Enhancers	Primary B cells from cord blood	blood
42	chr1:84609400-84609800	Enhancers	Primary B cells from peripheral blood	blood
43	chr1:84609400-84609800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr1:84609400-84609800	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr1:84609400-84610200	Flanking Active TSS	Dnd41	blood
46	chr1:84609400-84610400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr1:84609400-84610400	Enhancers	Fetal Kidney	kidney
48	chr1:84609400-84612800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:84609400-84612800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:84609600-84609800	Active TSS	Primary T cells from cord blood	blood

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