Variant report

Variant	nsv871866
Chromosome Location	chr1:86726619-86851420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:86726776-86727165	HepG2	liver:	n/a	n/a
2	ATF1	chr1:86762113-86762313	K562	blood:	n/a	n/a
3	BHLHE40	chr1:86845967-86846318	GM12878	blood:	n/a	n/a
4	CBX3	chr1:86843074-86843437	K562	blood:	n/a	n/a
5	CBX3	chr1:86843060-86843358	K562	blood:	n/a	n/a
6	CEBPB	chr1:86844524-86844880	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:86822191-86822196	K562	blood:	n/a	n/a
8	CEBPB	chr1:86836535-86836833	K562	blood:	n/a	chr1:86836660-86836669 chr1:86836660-86836671
9	CEBPB	chr1:86791799-86792053	IMR90	lung:	n/a	chr1:86791908-86791921
10	CEBPB	chr1:86817786-86818113	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:86728656-86728889	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:86836580-86836823	HepG2	liver:	n/a	chr1:86836660-86836669 chr1:86836660-86836671
13	CEBPB	chr1:86745851-86746051	IMR90	lung:	n/a	chr1:86745963-86745976
14	CEBPB	chr1:86844570-86844826	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:86844520-86844854	A549	lung:	n/a	n/a
16	CEBPB	chr1:86745867-86746032	A549	lung:	n/a	chr1:86745963-86745976
17	CEBPB	chr1:86817806-86818107	A549	lung:	n/a	n/a
18	CEBPB	chr1:86836478-86836842	IMR90	lung:	n/a	chr1:86836660-86836669 chr1:86836660-86836671
19	CEBPB	chr1:86844521-86844826	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:86817767-86818125	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:86817785-86817986	K562	blood:	n/a	n/a
22	CEBPB	chr1:86817853-86818061	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:86791934-86791940	A549	lung:	n/a	n/a
24	CEBPB	chr1:86805176-86805274	K562	blood:	n/a	n/a
25	CHD2	chr1:86794698-86794884	K562	blood:	n/a	n/a
26	CTCF	chr1:86821980-86822130	HPAF	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
27	CTCF	chr1:86822003-86822114	LNCaP	prostate:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
28	CTCF	chr1:86821960-86822110	SAEC	small airway:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
29	CTCF	chr1:86789660-86789810	HRE	kidney:	n/a	n/a
30	CTCF	chr1:86846000-86846150	GM12868	blood:	n/a	n/a
31	CTCF	chr1:86828600-86828750	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:86770834-86770854	GM13976	blood:	n/a	n/a
33	CTCF	chr1:86846080-86846230	GM12873	blood:	n/a	n/a
34	CTCF	chr1:86845934-86846331	K562	blood:	n/a	n/a
35	CTCF	chr1:86821960-86822110	NHDF-neo	bronchial:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
36	CTCF	chr1:86846003-86846225	HepG2	liver:	n/a	n/a
37	CTCF	chr1:86789680-86789830	RPTEC	kidney:	n/a	n/a
38	CTCF	chr1:86821988-86822147	HepG2	liver:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
39	CTCF	chr1:86846055-86846197	A549	lung:	n/a	n/a
40	CTCF	chr1:86821960-86822110	AG04449	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
41	CTCF	chr1:86821960-86822110	AG10803	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
42	CTCF	chr1:86846060-86846210	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:86845980-86846130	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr1:86828700-86828850	HMF	breast:	n/a	n/a
45	CTCF	chr1:86828600-86828750	GM12870	blood:	n/a	n/a
46	CTCF	chr1:86759085-86759138	GM20000	blood:	n/a	n/a
47	CTCF	chr1:86846060-86846210	HEK293	kidney:	n/a	n/a
48	CTCF	chr1:86822000-86822150	HPF	lung:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
49	CTCF	chr1:86828560-86828710	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr1:86822020-86822170	MCF-7	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86819371-86819421	HAEpiC	amniotic membrane:	n/a
2	chr1:86819371-86819421	HUVEC	blood vessel:	n/a
3	chr1:86819371-86819421	CMK	blood:	n/a
4	chr1:86819371-86819421	NT2-D1	testis:	n/a
5	chr1:86819371-86819421	SKMC	muscle:	n/a
6	chr1:86819371-86819421	SAEC	small airway:	n/a
7	chr1:86819371-86819421	A549	lung:	n/a
8	chr1:86819371-86819421	GM06990	blood:	n/a
9	chr1:86819371-86819421	AoSMC	blood vessel:	n/a
10	chr1:86819371-86819421	HIPEpiC	eye:	n/a
11	chr1:86819371-86819421	Caco-2	colon:	n/a
12	chr1:86819371-86819421	K562	blood:	n/a
13	chr1:86819371-86819421	ECC-1	luminal epithelium:	n/a
14	chr1:86819371-86819421	T-47D	breast:	n/a
15	chr1:86819371-86819421	AG04449	skin:	fetal
16	chr1:86819371-86819421	PrEC	prostate:	n/a
17	chr1:86819371-86819421	GM19239	blood:	n/a
18	chr1:86819371-86819421	GM12892	blood:	n/a
19	chr1:86819371-86819421	GM12891	blood:	n/a
20	chr1:86819371-86819421	HRPEpiC	eye:	n/a
21	chr1:86819371-86819421	ovcar-3	ovarian:	n/a
22	chr1:86819371-86819421	HCF	heart:	n/a
23	chr1:86819371-86819421	SK-N-SH	brain:	n/a
24	chr1:86819371-86819421	HCPEpiC	choroid plexus:	n/a
25	chr1:86819371-86819421	HEK293	kidney:	embryo
26	chr1:86819371-86819421	PANC-1	pancreas:	n/a
27	chr1:86819371-86819421	HCT-116	colon:	n/a
28	chr1:86819371-86819421	H1-hESC	embryonic stem cell:	embryo
29	chr1:86819371-86819421	AG04450	lung:	fetal
30	chr1:86819371-86819421	LNCaP	prostate:	n/a
31	chr1:86819371-86819421	HCM	heart:	n/a
32	chr1:86819371-86819421	ProgFib	skin:	n/a
33	chr1:86819371-86819421	NH-A	brain:	n/a
34	chr1:86819371-86819421	GM12878	blood:	n/a
35	chr1:86819371-86819421	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:86819371-86819421	AG10803	skin:	n/a
37	chr1:86819371-86819421	SK-N-MC	brain:	n/a
38	chr1:86819371-86819421	MCF10A-Er-Src	breast:	n/a
39	chr1:86819371-86819421	IMR90	lung:	fetal
40	chr1:86819371-86819421	U87	brain:	n/a
41	chr1:86819371-86819421	PFSK-1	brain:	n/a
42	chr1:86819371-86819421	Hepatocyte	liver:	n/a
43	chr1:86819371-86819421	BJ	skin:	n/a
44	chr1:86819371-86819421	NB4	blood:	n/a
45	chr1:86819371-86819421	Jurkat	blood:	n/a
46	chr1:86819371-86819421	SK-N-SH_RA	brain:	n/a
47	chr1:86819371-86819421	NHBE	bronchial:	n/a
48	chr1:86819371-86819421	AG09319	gingival:	n/a
49	chr1:86819371-86819421	HMEC	breast:	n/a
50	chr1:86819371-86819421	HepG2	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:86821077..86823352-chr1:86861196..86863227,2	K562	blood:
2	chr1:86845633..86846612-chr1:86965720..86966238,3	K562	blood:
3	chr1:86774306..86776171-chr1:86780419..86782294,2	K562	blood:
4	chr1:86782319..86784371-chr1:86788176..86791110,3	K562	blood:
5	chr1:86774306..86776171-chr1:86780419..86782294,2	K562	blood:
6	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
7	chr1:86732233..86735923-chr1:86736339..86739151,3	K562	blood:
8	chr1:86845689..86846553-chr1:86965309..86966983,5	MCF-7	breast:
9	chr1:86823768..86826042-chr1:86827235..86830172,2	MCF-7	breast:
10	chr1:86732233..86735923-chr1:86736339..86739151,3	K562	blood:
11	chr1:86846140..86846692-chr1:86967603..86968149,2	MCF-7	breast:
12	chr1:86845700..86846558-chr1:86939625..86940177,2	MCF-7	breast:
13	chr1:86782319..86784371-chr1:86788176..86791110,3	K562	blood:
14	chr1:86817766..86820014-chr1:86820204..86822305,3	K562	blood:
15	chr1:86834879..86837302-chr1:86845447..86847463,2	K562	blood:
16	chr1:86825572..86828967-chr1:86833765..86835448,3	K562	blood:
17	chr1:86823768..86826042-chr1:86827235..86830172,2	MCF-7	breast:
18	chr1:86817633..86819266-chr1:86820612..86822159,2	K562	blood:
19	chr1:86767271..86769500-chr1:86772874..86775446,2	MCF-7	breast:
20	chr1:86767271..86769500-chr1:86772874..86775446,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL24A1-3	chr1:86823623-86823788	NONHSAT004267
2	lnc-COL24A1-3	chr1:86826109-86826219	NONHSAT004267
3	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004267
4	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004266
5	lnc-COL24A1-3	chr1:86822259-86822285	NONHSAT004266
6	lnc-COL24A1-3	chr1:86826109-86826604	NONHSAT004266

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7856-5p	chr1:86823348-86823368	MIMAT0030431

No data

Variant related genes	Relation type
ODF2L	TF binding region
ODF2L	CpG island
ENSG00000122417	chromatin interactions

Extended variants
information (count: 3916 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:3916 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192854158	chr1:86728813-86728814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115574999	chr1:86728829-86728830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185158017	chr1:86728852-86728853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541846369	chr1:86728892-86728893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74446387	chr1:86728914-86728915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538539035	chr1:86728918-86728919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115773566	chr1:86728920-86728921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564386255	chr1:86728923-86728924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558533031	chr1:86728963-86728964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549996547	chr1:86729005-86729006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563228150	chr1:86729039-86729040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541589642	chr1:86729060-86729061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529019711	chr1:86729111-86729112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548682594	chr1:86729119-86729120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565311211	chr1:86729137-86729138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372450771	chr1:86731258-86731259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148413315	chr1:86731259-86731260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190129024	chr1:86731331-86731332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557176505	chr1:86731357-86731358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551847072	chr1:86731383-86731384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182521986	chr1:86731396-86731397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114255047	chr1:86736229-86736230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574652174	chr1:86736293-86736294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185368477	chr1:86736303-86736304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs386633149	chr1:86736513-86736514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34167094	chr1:86736524-86736525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565408694	chr1:86736533-86736534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191306578	chr1:86736541-86736542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112793555	chr1:86736558-86736559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577309540	chr1:86736581-86736582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180908052	chr1:86736601-86736602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562932314	chr1:86736618-86736619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576524400	chr1:86736632-86736633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185918510	chr1:86736644-86736645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142348270	chr1:86736657-86736658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372573076	chr1:86736699-86736700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527434271	chr1:86736730-86736731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7546158	chr1:86736880-86736881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs17129031	chr1:86736892-86736893	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533082183	chr1:86736915-86736916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549489839	chr1:86736918-86736919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542943008	chr1:86736923-86736924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569600176	chr1:86736934-86736935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528868461	chr1:86736938-86736939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548427698	chr1:86737021-86737022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530239457	chr1:86737096-86737097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191971208	chr1:86737123-86737124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559932682	chr1:86737153-86737154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534119025	chr1:86737158-86737159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531248351	chr1:86737183-86737184	Enhancers	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
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
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86728800-86729000	Enhancers	Fetal Kidney	kidney
2	chr1:86729000-86729200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:86731200-86731400	Enhancers	GM12878-XiMat	blood
4	chr1:86736200-86738000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:86738000-86742400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:86742200-86743800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:86742400-86744200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:86743200-86743600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:86743200-86744200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:86743400-86743800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr1:86743400-86744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:86743400-86744000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:86743400-86744200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:86743600-86744000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:86743800-86744200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:86743800-86746400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:86743800-86747200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:86744200-86747200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:86747200-86747600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:86747200-86748000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:86747600-86748600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr1:86748000-86754800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:86748600-86748800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:86753400-86755200	Enhancers	Fetal Stomach	stomach
25	chr1:86753600-86754800	Enhancers	Fetal Muscle Leg	muscle
26	chr1:86754600-86754800	Enhancers	Fetal Muscle Trunk	muscle
27	chr1:86754800-86755600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:86754800-86756400	Weak transcription	Fetal Muscle Leg	muscle
29	chr1:86755000-86756000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:86755200-86756400	Weak transcription	Fetal Stomach	stomach
31	chr1:86755600-86761600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:86756400-86757000	Enhancers	Fetal Stomach	stomach
33	chr1:86756600-86756800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:86756600-86756800	Enhancers	Fetal Muscle Leg	muscle
35	chr1:86757000-86762000	Weak transcription	Fetal Stomach	stomach
36	chr1:86758600-86758800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr1:86761600-86761800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr1:86761600-86762600	Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr1:86761600-86762800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:86761600-86762800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:86761600-86762800	Enhancers	Psoas Muscle	Psoas
42	chr1:86761600-86763200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:86761800-86762200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr1:86761800-86762400	Enhancers	Fetal Heart	heart
45	chr1:86761800-86762800	Enhancers	Primary hematopoietic stem cells	blood
46	chr1:86761800-86763200	Enhancers	HSMMtube	muscle
47	chr1:86762000-86762600	Enhancers	Fetal Stomach	stomach
48	chr1:86762000-86762800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:86762000-86762800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:86762000-86763200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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