Variant report

Variant	esv3515393
Chromosome Location	chr1:85437980-85465392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:915)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:85439375-85440116	GM12878	blood:	n/a	n/a
2	ATF2	chr1:85461001-85462170	GM12878	blood:	n/a	n/a
3	ATF2	chr1:85454138-85454764	GM12878	blood:	n/a	n/a
4	ATF2	chr1:85460975-85462328	GM12878	blood:	n/a	n/a
5	ATF2	chr1:85437537-85438676	GM12878	blood:	n/a	n/a
6	ATF2	chr1:85456684-85457419	GM12878	blood:	n/a	n/a
7	ATF2	chr1:85439191-85440151	GM12878	blood:	n/a	n/a
8	ATF2	chr1:85456557-85457627	GM12878	blood:	n/a	n/a
9	ATF2	chr1:85454171-85454687	GM12878	blood:	n/a	n/a
10	ATF2	chr1:85437628-85438125	GM12878	blood:	n/a	n/a
11	BACH1	chr1:85463795-85463995	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:85463401-85463435	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:85462556-85462963	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:85461580-85461958	GM12878	blood:	n/a	n/a
15	BATF	chr1:85439501-85439958	GM12878	blood:	n/a	n/a
16	BATF	chr1:85444292-85444525	GM12878	blood:	n/a	n/a
17	BATF	chr1:85454290-85454675	GM12878	blood:	n/a	n/a
18	BATF	chr1:85461189-85461461	GM12878	blood:	n/a	n/a
19	BATF	chr1:85461158-85462031	GM12878	blood:	n/a	chr1:85461561-85461572
20	BATF	chr1:85454206-85454722	GM12878	blood:	n/a	n/a
21	BATF	chr1:85456748-85457237	GM12878	blood:	n/a	n/a
22	BATF	chr1:85456799-85457126	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:85456748-85457352	GM12878	blood:	n/a	chr1:85457303-85457312
24	BCL11A	chr1:85461179-85461538	GM12878	blood:	n/a	chr1:85461391-85461400
25	BCL11A	chr1:85461223-85461445	GM12878	blood:	n/a	chr1:85461391-85461400
26	BCL3	chr1:85458788-85459114	GM12878	blood:	n/a	n/a
27	BCL3	chr1:85454182-85454690	GM12878	blood:	n/a	n/a
28	BCL3	chr1:85461098-85462125	GM12878	blood:	n/a	chr1:85461391-85461400
29	BCL3	chr1:85456757-85457167	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:85456720-85457651	GM12878	blood:	n/a	chr1:85457537-85457546 chr1:85457303-85457312
31	BCLAF1	chr1:85454133-85454869	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:85461500-85462338	GM12878	blood:	n/a	n/a
33	BCLAF1	chr1:85460942-85462854	GM12878	blood:	n/a	chr1:85461391-85461400
34	BCLAF1	chr1:85439367-85439960	GM12878	blood:	n/a	n/a
35	BCLAF1	chr1:85462352-85462829	GM12878	blood:	n/a	n/a
36	BCLAF1	chr1:85456733-85457651	GM12878	blood:	n/a	chr1:85457537-85457546 chr1:85457303-85457312
37	BCLAF1	chr1:85461001-85461484	GM12878	blood:	n/a	chr1:85461391-85461400
38	BCLAF1	chr1:85437641-85438370	GM12878	blood:	n/a	chr1:85438198-85438207
39	BCLAF1	chr1:85439247-85440063	GM12878	blood:	n/a	n/a
40	BCLAF1	chr1:85454155-85454815	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:85437716-85438437	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:85439396-85439729	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:85454227-85454773	GM12878	blood:	n/a	n/a
44	BHLHE40	chr1:85456704-85457551	GM12878	blood:	n/a	n/a
45	BHLHE40	chr1:85462315-85463615	GM12878	blood:	n/a	chr1:85463418-85463434 chr1:85463404-85463420
46	BHLHE40	chr1:85461025-85462056	GM12878	blood:	n/a	n/a
47	BRCA1	chr1:85463618-85463875	GM12878	blood:	n/a	n/a
48	CEBPB	chr1:85439190-85439542	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:85439122-85439956	GM12878	blood:	n/a	n/a
50	CEBPB	chr1:85456657-85457311	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85462953-85463003	CMK	blood:	n/a
2	chr1:85462483-85462533	ProgFib	skin:	n/a
3	chr1:85462812-85462862	HRCEpiC	kidney:	n/a
4	chr1:85463364-85463414	SK-N-SH_RA	brain:	n/a
5	chr1:85461303-85461353	A549	lung:	n/a
6	chr1:85464261-85464311	A549	lung:	n/a
7	chr1:85462892-85462942	HCM	heart:	n/a
8	chr1:85462857-85462907	HCF	heart:	n/a
9	chr1:85462700-85462750	GM12878	blood:	n/a
10	chr1:85462939-85462989	RPTEC	kidney:	n/a
11	chr1:85462953-85463003	Jurkat	blood:	n/a
12	chr1:85458682-85458732	GM12892	blood:	n/a
13	chr1:85458682-85458732	NH-A	brain:	n/a
14	chr1:85464000-85464050	U87	brain:	n/a
15	chr1:85462812-85462862	CMK	blood:	n/a
16	chr1:85458682-85458732	HCT-116	colon:	n/a
17	chr1:85462700-85462750	HCPEpiC	choroid plexus:	n/a
18	chr1:85458682-85458732	K562	blood:	n/a
19	chr1:85461303-85461353	Hepatocyte	liver:	n/a
20	chr1:85458682-85458732	GM19239	blood:	n/a
21	chr1:85464166-85464216	RPTEC	kidney:	n/a
22	chr1:85464261-85464311	HL-60	blood:	n/a
23	chr1:85463364-85463414	HAEpiC	amniotic membrane:	n/a
24	chr1:85464110-85464160	PFSK-1	brain:	n/a
25	chr1:85458682-85458732	SKMC	muscle:	n/a
26	chr1:85462953-85463003	SKMC	muscle:	n/a
27	chr1:85464110-85464160	AG04450	lung:	fetal
28	chr1:85462857-85462907	BJ	skin:	n/a
29	chr1:85462483-85462533	H1-hESC	embryonic stem cell:	embryo
30	chr1:85462939-85462989	ovcar-3	ovarian:	n/a
31	chr1:85462700-85462750	SK-N-MC	brain:	n/a
32	chr1:85462812-85462862	Hepatocyte	liver:	n/a
33	chr1:85464166-85464216	MCF-7	breast:	n/a
34	chr1:85463364-85463414	AG04449	skin:	fetal
35	chr1:85462700-85462750	HCT-116	colon:	n/a
36	chr1:85462700-85462750	PFSK-1	brain:	n/a
37	chr1:85462939-85462989	SK-N-SH_RA	brain:	n/a
38	chr1:85464110-85464160	MCF-7	breast:	n/a
39	chr1:85462939-85462989	SK-N-SH	brain:	n/a
40	chr1:85464166-85464216	NB4	blood:	n/a
41	chr1:85462953-85463003	HNPCEpiC	eye:	n/a
42	chr1:85464166-85464216	PrEC	prostate:	n/a
43	chr1:85464000-85464050	AG09319	gingival:	n/a
44	chr1:85463364-85463414	HEK293	kidney:	embryo
45	chr1:85462857-85462907	A549	lung:	n/a
46	chr1:85458682-85458732	A549	lung:	n/a
47	chr1:85462812-85462862	U87	brain:	n/a
48	chr1:85464110-85464160	SK-N-SH_RA	brain:	n/a
49	chr1:85462812-85462862	HRE	kidney:	n/a
50	chr1:85463364-85463414	MCF10A-Er-Src	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:85434009..85435841-chr1:85437123..85439359,2	K562	blood:
2	chr1:85455345..85457020-chr1:85460582..85462706,2	K562	blood:
3	chr1:85457596..85460591-chr1:85461678..85464189,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR63-1	chr1:85463140-85463597	XLOC_000274
2	lnc-WDR63-1	chr1:85463022-85463042	XLOC_000274

No data

Variant related genes	Relation type
MCOLN2	TF binding region
WDR63	TF binding region
MCOLN2	CpG island
WDR63	CpG island
ENSG00000153898	chromatin interactions

Extended variants
information (count: 1126 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374292868	chr1:85437985-85437986	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12743055	chr1:85437996-85437997	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs527532965	chr1:85438024-85438025	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs663843	chr1:85438032-85438033	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs113540863	chr1:85438105-85438106	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs372598693	chr1:85438107-85438108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs138219135	chr1:85438188-85438189	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs541897	chr1:85438243-85438244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs182941291	chr1:85438249-85438250	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs187238192	chr1:85438319-85438320	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77610892	chr1:85438409-85438410	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533685876	chr1:85438450-85438451	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs537869138	chr1:85438470-85438471	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190087269	chr1:85438479-85438480	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs568420113	chr1:85438576-85438577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs182312956	chr1:85438618-85438619	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553782845	chr1:85438620-85438621	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs371075293	chr1:85438662-85438663	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs534220900	chr1:85438720-85438721	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs553988266	chr1:85438724-85438725	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs573727830	chr1:85438725-85438726	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577353197	chr1:85438855-85438856	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs149552151	chr1:85438857-85438858	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs377632052	chr1:85438899-85438900	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs555998678	chr1:85438921-85438922	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs576045478	chr1:85438948-85438949	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs541460745	chr1:85438992-85438993	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs561664513	chr1:85439015-85439016	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs112803316	chr1:85439039-85439040	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs513430	chr1:85439059-85439060	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs375142056	chr1:85439081-85439082	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs541316128	chr1:85439095-85439096	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs679167	chr1:85439147-85439148	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs533004426	chr1:85439212-85439213	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs589227	chr1:85439228-85439229	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs569262963	chr1:85439231-85439232	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs187774044	chr1:85439246-85439247	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs548227393	chr1:85439260-85439261	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs558085141	chr1:85439261-85439262	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs534258403	chr1:85439265-85439266	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs115696596	chr1:85439266-85439267	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs74689037	chr1:85439268-85439269	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs589653	chr1:85439304-85439305	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs556668586	chr1:85439332-85439333	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs145005856	chr1:85439369-85439370	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs72944599	chr1:85439370-85439371	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs488710	chr1:85439454-85439455	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs376233401	chr1:85439585-85439586	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs75236845	chr1:85439611-85439612	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs527769332	chr1:85439614-85439615	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	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
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:745 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85435200-85440400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:85435600-85438400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:85436800-85438000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr1:85436800-85438000	Weak transcription	Osteobl	bone
5	chr1:85436800-85438200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:85437200-85438800	Flanking Active TSS	GM12878-XiMat	blood
7	chr1:85437400-85438000	Enhancers	Primary T cells fromperipheralblood	blood
8	chr1:85437400-85438800	Enhancers	Fetal Intestine Large	intestine
9	chr1:85437400-85438800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr1:85437400-85441200	Enhancers	Primary B cells from peripheral blood	blood
11	chr1:85437400-85441200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:85437600-85438000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:85437600-85438200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:85437600-85441200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:85437800-85438600	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr1:85437800-85438600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:85437800-85438800	Enhancers	Fetal Intestine Small	intestine
18	chr1:85437800-85438800	Enhancers	Hela-S3	cervix
19	chr1:85437800-85439200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr1:85437800-85439600	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr1:85437800-85439600	Enhancers	NHDF-Ad	bronchial
22	chr1:85437800-85440000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:85438000-85438400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr1:85438000-85438600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr1:85438000-85438800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:85438000-85439200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr1:85438000-85439600	Enhancers	Osteobl	bone
28	chr1:85438000-85440200	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr1:85438200-85438400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:85438200-85438400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:85438200-85438600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:85438200-85438600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr1:85438200-85438600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr1:85438200-85438800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:85438400-85438600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:85438400-85439200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr1:85438400-85439600	Enhancers	Primary T cells fromperipheralblood	blood
38	chr1:85438400-85439800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:85438600-85438800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:85438600-85439000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr1:85438600-85439600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:85438600-85439800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr1:85438600-85440600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr1:85438600-85441000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:85438800-85440000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr1:85438800-85440400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:85438800-85441200	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
48	chr1:85439000-85439600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:85439200-85439600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:85439400-85439800	Enhancers	HUES48 Cell Line	embryonic stem cell

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