Variant report

Variant	nsv871375
Chromosome Location	chr1:84622793-84678418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

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	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	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
7	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
8	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
9	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
11	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
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	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
16	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
17	CTCF	chr1:84651942-84651996	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:84651880-84652030	GM12875	blood:	n/a	n/a
19	CTCF	chr1:84651897-84651999	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr1:84651941-84652037	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:84651923-84651989	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:84651840-84651990	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr1:84651840-84651990	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr1:84651876-84652020	K562	blood:	n/a	n/a
25	CTCF	chr1:84651900-84652050	AG04449	skin:	n/a	n/a
26	CTCF	chr1:84651820-84651970	HCFaa	heart:	n/a	n/a
27	CTCF	chr1:84651926-84651993	NHEK	skin:	n/a	n/a
28	CTCF	chr1:84651820-84651970	GM06990	blood:	n/a	n/a
29	CTCF	chr1:84651820-84651970	HMF	breast:	n/a	n/a
30	CTCF	chr1:84651900-84652050	AG09319	gingival:	n/a	n/a
31	CTCF	chr1:84651860-84652010	HVMF	connective:	n/a	n/a
32	CTCF	chr1:84651800-84651950	AG09319	gingival:	n/a	n/a
33	CTCF	chr1:84651860-84652010	BJ	skin:	n/a	n/a
34	CTCF	chr1:84651947-84652024	GM19238	blood:	n/a	n/a
35	CTCF	chr1:84651933-84652005	GM10266	blood:	n/a	n/a
36	CTCF	chr1:84653585-84653620	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
38	CTCF	chr1:84651840-84651990	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr1:84651961-84651988	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr1:84629400-84629550	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr1:84651940-84652090	RPTEC	kidney:	n/a	n/a
42	CTCF	chr1:84651880-84652030	HEK293	kidney:	n/a	n/a
43	CTCF	chr1:84651740-84651890	RPTEC	kidney:	n/a	n/a
44	CTCF	chr1:84651860-84652010	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr1:84652020-84652022	A549	lung:	n/a	n/a
46	CTCF	chr1:84651883-84652042	Gliobla	brain:	n/a	n/a
47	CTCF	chr1:84651895-84652005	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:84651840-84651990	AG10803	skin:	n/a	n/a
49	CTCF	chr1:84651946-84652019	A549	lung:	n/a	n/a
50	CTCF	chr1:84651880-84652030	HL-60	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
2	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
3	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
4	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
5	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
6	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
7	chr1:84662036..84663948-chr1:84669561..84672181,4	K562	blood:
8	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
9	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
10	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
11	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
12	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
13	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
14	chr1:84642752..84644786-chr1:84646959..84648659,2	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	chr1:84640716-84640739	NONHSAT004188
3	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
4	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
5	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190
6	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
7	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
8	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
9	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
10	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
11	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
12	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
13	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190

No data

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

Extended variants
information (count: 1799 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1799 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55781344	chr1:84622793-84622794	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs533979670	chr1:84622795-84622796	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs372826445	chr1:84622830-84622831	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs553981158	chr1:84622838-84622839	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs189469396	chr1:84622843-84622844	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539727932	chr1:84622865-84622866	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs77977524	chr1:84622866-84622867	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs575589458	chr1:84622882-84622883	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs372224818	chr1:84622918-84622919	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs181459995	chr1:84622974-84622975	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552845743	chr1:84622979-84622980	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs561440701	chr1:84622981-84622982	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs116772572	chr1:84623034-84623035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540445294	chr1:84623072-84623073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560299922	chr1:84623081-84623082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374796387	chr1:84623123-84623124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532697799	chr1:84623199-84623200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538728084	chr1:84623247-84623248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141250500	chr1:84623249-84623250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558720272	chr1:84623306-84623307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370261528	chr1:84623385-84623386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562386131	chr1:84623422-84623423	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs575291508	chr1:84623440-84623441	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs531347020	chr1:84623443-84623444	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs547829223	chr1:84623484-84623485	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs375272241	chr1:84623494-84623495	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs568169728	chr1:84623497-84623498	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs72710864	chr1:84623565-84623566	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs150779078	chr1:84623596-84623597	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs570637754	chr1:84623679-84623680	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs539788871	chr1:84623701-84623702	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs80044544	chr1:84623725-84623726	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs576214440	chr1:84623748-84623749	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs35694160	chr1:84623757-84623758	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs538239703	chr1:84623763-84623764	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs397751886	chr1:84623768-84623769	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs61766378	chr1:84623772-84623773	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs554634992	chr1:84623815-84623816	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs139159961	chr1:84623858-84623859	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs144025358	chr1:84623864-84623865	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs374223195	chr1:84623870-84623871	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs560363646	chr1:84623881-84623882	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs185894570	chr1:84623893-84623894	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs545950652	chr1:84623903-84623904	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs563200335	chr1:84623913-84623914	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs531883025	chr1:84623919-84623920	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs189570789	chr1:84623964-84623965	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs561510835	chr1:84624012-84624013	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs145973286	chr1:84624016-84624017	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs61766379	chr1:84624033-84624034	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	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:1461 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	chr1:84613200-84623400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:84614000-84633800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr1:84614600-84625600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr1:84614800-84629000	Weak transcription	Brain Hippocampus Middle	brain
8	chr1:84615800-84623800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr1:84615800-84634800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:84616000-84623000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr1:84616200-84622800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr1:84616200-84635200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:84616400-84623000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr1:84618200-84623800	Weak transcription	Thymus	Thymus
15	chr1:84618600-84623000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr1:84618800-84623000	Enhancers	Primary T cells from cord blood	blood
17	chr1:84618800-84623600	Weak transcription	Fetal Thymus	thymus
18	chr1:84618800-84630400	Weak transcription	Primary B cells from cord blood	blood
19	chr1:84619000-84628800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:84619000-84628800	Weak transcription	Gastric	stomach
21	chr1:84619200-84630200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:84620000-84623200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:84621000-84622800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr1:84621000-84623000	Enhancers	HUVEC	blood vessel
25	chr1:84621200-84622800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:84621200-84623000	Enhancers	A549	lung
27	chr1:84621200-84623200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr1:84621400-84622800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:84621400-84624400	Weak transcription	Dnd41	blood
30	chr1:84621600-84622800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr1:84621600-84622800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr1:84621600-84622800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:84621600-84622800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:84621600-84623000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:84621600-84623000	Enhancers	Primary B cells from peripheral blood	blood
36	chr1:84621600-84623000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:84621600-84623000	Enhancers	NHEK	skin
38	chr1:84621800-84622800	Enhancers	NH-A	brain
39	chr1:84621800-84622800	Enhancers	Osteobl	bone
40	chr1:84621800-84623000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:84621800-84623000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:84621800-84625400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:84622000-84622800	Enhancers	HMEC	breast
44	chr1:84622000-84622800	Enhancers	HSMM	muscle
45	chr1:84622000-84628800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:84622200-84626000	Strong transcription	Primary hematopoietic stem cells	blood
47	chr1:84622200-84630000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr1:84622400-84623600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr1:84622400-84625400	Weak transcription	Aorta	Aorta
50	chr1:84622400-84635800	Weak transcription	Small Intestine	intestine

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