Variant report

Variant	nsv508408
Chromosome Location	chr6:56735681-56773285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:876)
CpG islands
(count:122)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56769406-56769670	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:56740789-56741128	HepG2	liver:	n/a	n/a
3	ATF1	chr6:56771564-56771849	K562	blood:	n/a	n/a
4	ATF1	chr6:56755431-56755724	K562	blood:	n/a	n/a
5	ATF2	chr6:56755252-56755956	GM12878	blood:	n/a	n/a
6	ATF2	chr6:56755239-56756256	GM12878	blood:	n/a	n/a
7	ATF3	chr6:56755485-56755648	K562	blood:	n/a	n/a
8	ATF3	chr6:56755397-56755867	K562	blood:	n/a	n/a
9	BACH1	chr6:56755379-56755755	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:56755369-56755962	K562	blood:	n/a	n/a
11	BATF	chr6:56755437-56755801	GM12878	blood:	n/a	chr6:56755573-56755583
12	BATF	chr6:56755432-56755930	GM12878	blood:	n/a	chr6:56755573-56755583
13	BCL11A	chr6:56755415-56755814	GM12878	blood:	n/a	n/a
14	BCL3	chr6:56755419-56755885	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:56755418-56756042	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:56740732-56741167	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:56755351-56755906	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:56767786-56768032	GM12878	blood:	n/a	n/a
19	BRCA1	chr6:56769475-56769626	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr6:56767817-56768016	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:56769361-56769732	MCF-7	breast:	n/a	chr6:56769643-56769654
22	CEBPB	chr6:56769396-56769883	K562	blood:	n/a	chr6:56769643-56769654
23	CEBPB	chr6:56769402-56769715	ECC-1	luminal epithelium:	n/a	chr6:56769643-56769654
24	CEBPB	chr6:56771544-56771887	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:56769456-56769796	H1-hESC	embryonic stem cell:	n/a	chr6:56769643-56769654
26	CEBPB	chr6:56740846-56741198	A549	lung:	n/a	n/a
27	CEBPB	chr6:56755458-56755859	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:56740831-56741257	A549	lung:	n/a	n/a
29	CEBPB	chr6:56769440-56769844	K562	blood:	n/a	chr6:56769643-56769654
30	CEBPB	chr6:56772637-56772894	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr6:56740842-56741205	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:56769431-56769717	A549	lung:	n/a	chr6:56769643-56769654
33	CEBPB	chr6:56769415-56769809	Hela-S3	cervix:	n/a	chr6:56769643-56769654
34	CEBPB	chr6:56771591-56771874	A549	lung:	n/a	n/a
35	CEBPB	chr6:56769457-56769811	A549	lung:	n/a	chr6:56769643-56769654
36	CEBPB	chr6:56769456-56769824	IMR90	lung:	n/a	chr6:56769643-56769654
37	CEBPB	chr6:56769530-56769709	K562	blood:	n/a	chr6:56769643-56769654
38	CEBPB	chr6:56768756-56769905	HCT-116	colon:	n/a	chr6:56769643-56769654
39	CEBPB	chr6:56769441-56769715	MCF-7	breast:	n/a	chr6:56769643-56769654
40	CEBPB	chr6:56771647-56771832	K562	blood:	n/a	n/a
41	CEBPB	chr6:56769508-56769800	HepG2	liver:	n/a	chr6:56769643-56769654
42	CEBPB	chr6:56769534-56769688	HepG2	liver:	n/a	chr6:56769643-56769654
43	CEBPB	chr6:56769331-56769741	A549	lung:	n/a	chr6:56769643-56769654
44	CHD1	chr6:56755632-56756081	GM12878	blood:	n/a	n/a
45	CHD2	chr6:56755444-56755751	GM12878	blood:	n/a	n/a
46	CHD2	chr6:56767494-56767513	GM12878	blood:	n/a	n/a
47	CREB1	chr6:56755360-56756099	GM12878	blood:	n/a	n/a
48	CTCF	chr6:56769520-56769670	NHLF	lung:	n/a	chr6:56769547-56769563 chr6:56769548-56769569 chr6:56769546-56769564
49	CTCF	chr6:56769442-56769663	Pancreas_OC	pancreas:	n/a	chr6:56769547-56769563 chr6:56769548-56769569 chr6:56769546-56769564
50	CTCF	chr6:56768040-56768190	GM12867	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56765087-56765137	AG09309	skin:	n/a
2	chr6:56755566-56755616	LNCaP	prostate:	n/a
3	chr6:56755566-56755616	Hela-S3	cervix:	n/a
4	chr6:56765087-56765137	AG04449	skin:	fetal
5	chr6:56765087-56765137	HRE	kidney:	n/a
6	chr6:56765087-56765137	NH-A	brain:	n/a
7	chr6:56755566-56755616	GM12892	blood:	n/a
8	chr6:56765087-56765137	Caco-2	colon:	n/a
9	chr6:56755566-56755616	HEK293	kidney:	embryo
10	chr6:56755566-56755616	NH-A	brain:	n/a
11	chr6:56755566-56755616	AG09319	gingival:	n/a
12	chr6:56765087-56765137	AG04450	lung:	fetal
13	chr6:56755566-56755616	CMK	blood:	n/a
14	chr6:56755566-56755616	GM12878	blood:	n/a
15	chr6:56755566-56755616	SKMC	muscle:	n/a
16	chr6:56755566-56755616	AG04449	skin:	fetal
17	chr6:56755566-56755616	T-47D	breast:	n/a
18	chr6:56765087-56765137	GM06990	blood:	n/a
19	chr6:56765087-56765137	Jurkat	blood:	n/a
20	chr6:56755566-56755616	HCPEpiC	choroid plexus:	n/a
21	chr6:56765087-56765137	GM12891	blood:	n/a
22	chr6:56765087-56765137	HRPEpiC	eye:	n/a
23	chr6:56755566-56755616	GM19239	blood:	n/a
24	chr6:56755566-56755616	ovcar-3	ovarian:	n/a
25	chr6:56765087-56765137	HCM	heart:	n/a
26	chr6:56765087-56765137	SK-N-MC	brain:	n/a
27	chr6:56755566-56755616	GM12891	blood:	n/a
28	chr6:56755566-56755616	SAEC	small airway:	n/a
29	chr6:56765087-56765137	HRCEpiC	kidney:	n/a
30	chr6:56765087-56765137	HIPEpiC	eye:	n/a
31	chr6:56755566-56755616	ECC-1	luminal epithelium:	n/a
32	chr6:56755566-56755616	PANC-1	pancreas:	n/a
33	chr6:56765087-56765137	HNPCEpiC	eye:	n/a
34	chr6:56765087-56765137	Hepatocyte	liver:	n/a
35	chr6:56765087-56765137	SK-N-SH_RA	brain:	n/a
36	chr6:56765087-56765137	BE2_C	brain:	n/a
37	chr6:56765087-56765137	ECC-1	luminal epithelium:	n/a
38	chr6:56765087-56765137	HCT-116	colon:	n/a
39	chr6:56755566-56755616	HepG2	liver:	n/a
40	chr6:56755566-56755616	HCM	heart:	n/a
41	chr6:56765087-56765137	PrEC	prostate:	n/a
42	chr6:56755566-56755616	H1-hESC	embryonic stem cell:	embryo
43	chr6:56765087-56765137	GM12892	blood:	n/a
44	chr6:56765087-56765137	LNCaP	prostate:	n/a
45	chr6:56765087-56765137	CMK	blood:	n/a
46	chr6:56765087-56765137	AoSMC	blood vessel:	n/a
47	chr6:56765087-56765137	T-47D	breast:	n/a
48	chr6:56755566-56755616	HCT-116	colon:	n/a
49	chr6:56755566-56755616	Hepatocyte	liver:	n/a
50	chr6:56765087-56765137	HMEC	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:56769552..56770203-chr6:57189093..57189825,2	MCF-7	breast:
2	chr6:56767335..56769579-chr6:56770902..56774646,3	K562	blood:
3	chr6:56734484..56737042-chr6:56741473..56744438,2	K562	blood:
4	chr6:56769038..56769893-chr6:57181008..57181695,4	K562	blood:
5	chr6:56763562..56765199-chr6:56770424..56772449,2	MCF-7	breast:
6	chr6:56741671..56743522-chr6:56818559..56820649,2	K562	blood:
7	chr6:56768468..56773680-chr6:56817098..56821672,5	MCF-7	breast:
8	chr6:56743268..56744831-chr6:56747772..56749482,2	MCF-7	breast:
9	chr6:56767504..56768223-chr6:56819760..56820310,2	MCF-7	breast:
10	chr6:56772967..56775962-chr6:56913388..56915663,2	K562	blood:
11	chr6:56769451..56770050-chr6:56819340..56821302,7	MCF-7	breast:
12	chr6:56707848..56709523-chr6:56741887..56744401,2	MCF-7	breast:
13	chr6:56763562..56765199-chr6:56770424..56772449,2	MCF-7	breast:
14	chr6:56767444..56768237-chr6:57180983..57181496,2	K562	blood:
15	chr1:182807964..182808769-chr6:56751629..56752198,2	MCF-7	breast:
16	chr6:56765319..56768240-chr6:56782219..56784389,2	K562	blood:
17	chr6:56767586..56771762-chr6:56818503..56821591,4	K562	blood:
18	chr6:56767464..56768319-chr6:56820397..56821373,5	MCF-7	breast:
19	chr6:56773027..56775523-chr6:56776633..56778873,3	K562	blood:
20	chr6:56769047..56769912-chr6:56885790..56886530,2	MCF-7	breast:
21	chr6:56770313..56772562-chr6:56773630..56775659,2	K562	blood:
22	chr6:56767380..56768433-chr6:56825743..56826632,5	MCF-7	breast:
23	chr6:56766600..56772134-chr6:56817595..56821119,8	MCF-7	breast:
24	chr6:56748598..56751509-chr6:56763693..56765656,2	K562	blood:
25	chr6:56748598..56751509-chr6:56763693..56765656,2	K562	blood:
26	chr6:56748557..56750730-chr6:57036166..57038744,2	K562	blood:
27	chr6:56773281..56775523-chr6:56776609..56780879,5	K562	blood:
28	chr6:56743268..56744831-chr6:56747772..56749482,2	MCF-7	breast:
29	chr6:56767335..56769579-chr6:56770902..56774646,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BEND6-2	chr6:56735989-56736541	NONHSAT113251

No data

Variant related genes	Relation type
RPL17P26	TF binding region
RPL17P26	CpG island
ENSG00000151917	chromatin interactions
ENSG00000231441	chromatin interactions
ENSG00000216854	chromatin interactions
ENSG00000135829	chromatin interactions
ENSG00000112208	chromatin interactions
ENSG00000226803	chromatin interactions
ENSG00000151914	chromatin interactions

Extended variants
information (count: 1292 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187833810	chr6:56735701-56735702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145986814	chr6:56735703-56735704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533189176	chr6:56735754-56735755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561999771	chr6:56735798-56735799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546358623	chr6:56735837-56735838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574180068	chr6:56735919-56735920	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544523066	chr6:56735923-56735924	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560242568	chr6:56735996-56735997	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs192433188	chr6:56736056-56736057	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs551635075	chr6:56736076-56736077	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs563756608	chr6:56736172-56736173	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs528037109	chr6:56736178-56736179	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs546680162	chr6:56736221-56736222	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs536877274	chr6:56736222-56736223	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs370478339	chr6:56736233-56736234	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs535525103	chr6:56736294-56736295	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs550537090	chr6:56736331-56736332	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs57178695	chr6:56736345-56736346	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539768082	chr6:56736368-56736369	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs184570877	chr6:56736384-56736385	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs573283500	chr6:56736434-56736435	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs139167701	chr6:56736525-56736526	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs555728943	chr6:56736531-56736532	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs539397119	chr6:56736536-56736537	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs574088470	chr6:56736547-56736548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544674973	chr6:56736551-56736552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375186552	chr6:56736558-56736559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187490518	chr6:56736569-56736570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371120676	chr6:56736573-56736574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372236624	chr6:56736574-56736575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192916822	chr6:56736589-56736590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545307863	chr6:56736590-56736591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs57792744	chr6:56736593-56736594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201411712	chr6:56736594-56736595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13218414	chr6:56736595-56736596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9464401	chr6:56736655-56736656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs527984863	chr6:56736681-56736682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184745916	chr6:56736709-56736710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561711972	chr6:56736721-56736722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529009266	chr6:56736749-56736750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149952706	chr6:56736795-56736796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368341065	chr6:56736815-56736816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189093361	chr6:56736837-56736838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145118449	chr6:56736845-56736846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181485033	chr6:56736882-56736883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149024827	chr6:56736942-56736943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548955993	chr6:56736949-56736950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568870368	chr6:56736972-56736973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184790497	chr6:56736977-56736978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534085199	chr6:56736981-56736982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD

Chromatin state (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56730400-56740400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr6:56732600-56736000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:56734200-56755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:56734600-56750200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:56734600-56755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:56734800-56740400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:56734800-56740400	Weak transcription	A549	lung
8	chr6:56734800-56740600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:56734800-56740600	Weak transcription	NHLF	lung
10	chr6:56734800-56754200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:56734800-56754400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:56735000-56736000	Weak transcription	GM12878-XiMat	blood
13	chr6:56735000-56736000	Weak transcription	NHDF-Ad	bronchial
14	chr6:56735200-56740600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:56735600-56740800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:56736000-56736200	Enhancers	NHDF-Ad	bronchial
17	chr6:56736000-56736400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:56736000-56736400	Enhancers	GM12878-XiMat	blood
19	chr6:56736200-56740400	Weak transcription	NHDF-Ad	bronchial
20	chr6:56736400-56755800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:56738000-56738200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:56738200-56743000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:56740400-56740600	Enhancers	HepG2	liver
24	chr6:56740400-56740800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr6:56740400-56741400	Enhancers	Fetal Intestine Large	intestine
26	chr6:56740400-56741600	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr6:56740400-56741600	Flanking Active TSS	A549	lung
28	chr6:56740400-56742000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:56740400-56742000	Genic enhancers	NHDF-Ad	bronchial
30	chr6:56740600-56740800	Flanking Active TSS	HepG2	liver
31	chr6:56740600-56741000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:56740600-56741000	Strong transcription	NHLF	lung
33	chr6:56740600-56741400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:56740800-56741000	Enhancers	HepG2	liver
35	chr6:56740800-56741600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr6:56740800-56742000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:56740800-56742000	Enhancers	Osteobl	bone
38	chr6:56741000-56741200	Flanking Active TSS	HepG2	liver
39	chr6:56741000-56741600	Genic enhancers	NHLF	lung
40	chr6:56741000-56741800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:56741200-56741600	Enhancers	HepG2	liver
42	chr6:56741200-56754600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr6:56741400-56750600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:56741600-56742000	Enhancers	A549	lung
45	chr6:56741600-56754200	Weak transcription	NHLF	lung
46	chr6:56741800-56743000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:56742000-56743000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:56742000-56743400	Strong transcription	NHDF-Ad	bronchial
49	chr6:56742000-56750000	Weak transcription	Osteobl	bone
50	chr6:56742000-56750800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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