Variant report

Variant	nsv1021789
Chromosome Location	chr6:141024733-141284394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1309)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:141263537-141263547	K562	blood:	n/a	n/a
2	ARID3A	chr6:141219526-141219833	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:141233801-141234207	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:141219654-141219754	K562	blood:	n/a	n/a
5	ATF1	chr6:141242769-141243022	K562	blood:	n/a	n/a
6	ATF1	chr6:141095400-141095672	K562	blood:	n/a	n/a
7	ATF1	chr6:141218607-141218807	K562	blood:	n/a	n/a
8	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
9	ATF1	chr6:141057542-141057722	K562	blood:	n/a	n/a
10	ATF1	chr6:141236361-141236561	K562	blood:	n/a	n/a
11	ATF1	chr6:141178980-141179277	K562	blood:	n/a	n/a
12	ATF2	chr6:141130615-141131385	GM12878	blood:	n/a	n/a
13	ATF2	chr6:141095241-141095760	GM12878	blood:	n/a	n/a
14	ATF2	chr6:141130657-141131259	GM12878	blood:	n/a	n/a
15	ATF2	chr6:141095239-141095755	GM12878	blood:	n/a	n/a
16	BACH1	chr6:141066249-141066420	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:141066206-141066385	K562	blood:	n/a	n/a
18	BATF	chr6:141095289-141095760	GM12878	blood:	n/a	chr6:141095560-141095570 chr6:141095559-141095570
19	BATF	chr6:141130673-141131290	GM12878	blood:	n/a	n/a
20	BATF	chr6:141066029-141066341	GM12878	blood:	n/a	chr6:141066245-141066256
21	BATF	chr6:141065980-141066438	GM12878	blood:	n/a	chr6:141066245-141066256
22	BATF	chr6:141095303-141095730	GM12878	blood:	n/a	chr6:141095560-141095570 chr6:141095559-141095570
23	BATF	chr6:141130703-141131094	GM12878	blood:	n/a	n/a
24	BATF	chr6:141179510-141179919	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:141130675-141131273	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:141130716-141131254	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:141095314-141095662	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
28	BCL11A	chr6:141095345-141095639	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
29	BCL11A	chr6:141079725-141079897	GM12878	blood:	n/a	n/a
30	BCL3	chr6:141095338-141095693	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
31	BCL3	chr6:141130776-141131187	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:141095199-141095818	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
33	BCLAF1	chr6:141130632-141131257	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:141179621-141179991	K562	blood:	n/a	n/a
35	BHLHE40	chr6:141178965-141179291	K562	blood:	n/a	n/a
36	BHLHE40	chr6:141218694-141218754	K562	blood:	n/a	n/a
37	BHLHE40	chr6:141219396-141219402	K562	blood:	n/a	n/a
38	BHLHE40	chr6:141233841-141234246	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
40	BRCA1	chr6:141236422-141236424	HepG2	liver:	n/a	n/a
41	CBX3	chr6:141068268-141068538	K562	blood:	n/a	n/a
42	CBX3	chr6:141089349-141089584	K562	blood:	n/a	n/a
43	CBX3	chr6:141265947-141266292	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:141095286-141095712	HCT-116	colon:	n/a	n/a
45	CBX3	chr6:141265879-141266203	K562	blood:	n/a	n/a
46	CCNT2	chr6:141281282-141281459	K562	blood:	n/a	n/a
47	CEBPB	chr6:141233993-141234197	H1-hESC	embryonic stem cell:	n/a	chr6:141234069-141234082 chr6:141234070-141234081
48	CEBPB	chr6:141111270-141111595	IMR90	lung:	n/a	chr6:141111439-141111450
49	CEBPB	chr6:141137825-141138049	HepG2	liver:	n/a	chr6:141137965-141137976
50	CEBPB	chr6:141111286-141111595	A549	lung:	n/a	chr6:141111439-141111450

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141167819-141167869	SAEC	small airway:	n/a
2	chr6:141167819-141167869	HEK293	kidney:	embryo
3	chr6:141167819-141167869	HNPCEpiC	eye:	n/a
4	chr6:141167819-141167869	HCF	heart:	n/a
5	chr6:141167819-141167869	AG10803	skin:	n/a
6	chr6:141167819-141167869	MCF-7	breast:	n/a
7	chr6:141167819-141167869	ProgFib	skin:	n/a
8	chr6:141167819-141167869	U87	brain:	n/a
9	chr6:141167819-141167869	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:141167819-141167869	ovcar-3	ovarian:	n/a
11	chr6:141167819-141167869	NH-A	brain:	n/a
12	chr6:141167819-141167869	MCF10A-Er-Src	breast:	n/a
13	chr6:141167819-141167869	PANC-1	pancreas:	n/a
14	chr6:141167819-141167869	SK-N-SH	brain:	n/a
15	chr6:141167819-141167869	HepG2	liver:	n/a
16	chr6:141167819-141167869	NHDF-neo	bronchial:	n/a
17	chr6:141167819-141167869	HIPEpiC	eye:	n/a
18	chr6:141167819-141167869	SK-N-SH_RA	brain:	n/a
19	chr6:141167819-141167869	Hepatocyte	liver:	n/a
20	chr6:141167819-141167869	HEEpiC	esophagus:	n/a
21	chr6:141167819-141167869	BE2_C	brain:	n/a
22	chr6:141167819-141167869	AG04450	lung:	fetal
23	chr6:141167819-141167869	HMEC	breast:	n/a
24	chr6:141167819-141167869	AG09309	skin:	n/a
25	chr6:141167819-141167869	Caco-2	colon:	n/a
26	chr6:141167819-141167869	HRPEpiC	eye:	n/a
27	chr6:141167819-141167869	HUVEC	blood vessel:	n/a
28	chr6:141167819-141167869	Hela-S3	cervix:	n/a
29	chr6:141167819-141167869	HCPEpiC	choroid plexus:	n/a
30	chr6:141167819-141167869	ECC-1	luminal epithelium:	n/a
31	chr6:141167819-141167869	CMK	blood:	n/a
32	chr6:141167819-141167869	GM12892	blood:	n/a
33	chr6:141167819-141167869	PrEC	prostate:	n/a
34	chr6:141167819-141167869	NB4	blood:	n/a
35	chr6:141167819-141167869	H1-hESC	embryonic stem cell:	embryo
36	chr6:141167819-141167869	NT2-D1	testis:	n/a
37	chr6:141167819-141167869	PFSK-1	brain:	n/a
38	chr6:141167819-141167869	AoSMC	blood vessel:	n/a
39	chr6:141167819-141167869	SK-N-MC	brain:	n/a
40	chr6:141167819-141167869	RPTEC	kidney:	n/a
41	chr6:141167819-141167869	IMR90	lung:	fetal
42	chr6:141167819-141167869	GM12891	blood:	n/a
43	chr6:141167819-141167869	A549	lung:	n/a
44	chr6:141167819-141167869	K562	blood:	n/a
45	chr6:141167819-141167869	AG09319	gingival:	n/a
46	chr6:141167819-141167869	T-47D	breast:	n/a
47	chr6:141167819-141167869	HL-60	blood:	n/a
48	chr6:141167819-141167869	HAEpiC	amniotic membrane:	n/a
49	chr6:141167819-141167869	HRCEpiC	kidney:	n/a
50	chr6:141167819-141167869	HCT-116	colon:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141225214..141229759-chr6:141230098..141233300,4	K562	blood:
2	chr6:141225214..141229759-chr6:141230098..141233300,4	K562	blood:
3	chr6:141220439..141223347-chr6:141228844..141230950,2	MCF-7	breast:
4	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
5	chr6:141142470..141143996-chr6:141149245..141150819,2	K562	blood:
6	chr6:141069422..141072199-chr6:141082873..141085142,2	K562	blood:
7	chr6:141220439..141223347-chr6:141228844..141230950,2	MCF-7	breast:
8	chr6:141231506..141233804-chr6:141236593..141238127,2	K562	blood:
9	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
10	chr6:141212244..141214629-chr6:141219189..141220964,2	MCF-7	breast:
11	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
12	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
13	chr6:141212244..141214629-chr6:141219189..141220964,2	MCF-7	breast:
14	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
15	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
16	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
17	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
18	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
19	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
20	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
21	chr6:141147468..141149344-chr6:141153230..141155525,2	K562	blood:
22	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
23	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
24	chr6:141218727..141221164-chr6:141224854..141227033,2	K562	blood:
25	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
26	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
27	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
28	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
29	chr6:141147468..141149344-chr6:141153230..141155525,2	K562	blood:
30	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
31	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
32	chr6:141245976..141248049-chr6:141253125..141254687,2	MCF-7	breast:
33	chr6:141142470..141143996-chr6:141149245..141150819,2	K562	blood:
34	chr6:140128805..140131673-chr6:141152750..141154839,2	K562	blood:
35	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
36	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
37	chr6:141069422..141072199-chr6:141082873..141085142,2	K562	blood:
38	chr6:141231506..141233804-chr6:141236593..141238127,2	K562	blood:
39	chr6:141210884..141213823-chr6:141384643..141387034,2	K562	blood:
40	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
41	chr6:140202949..140203456-chr6:141242488..141243293,2	MCF-7	breast:
42	chr2:225923916..225924696-chr6:141138966..141139702,2	MCF-7	breast:
43	chr6:141245976..141248049-chr6:141253125..141254687,2	MCF-7	breast:
44	chr6:141218727..141221164-chr6:141224854..141227033,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-2	chr6:141216940-141217067	NONHSAT115288
2	lnc-NMBR-2	chr6:141219325-141219567	NONHSAT115288
3	lnc-NMBR-2	chr6:141184986-141185033	NONHSAT115288
4	lnc-NMBR-2	chr6:141185039-141185580	NONHSAT115288
5	lnc-NMBR-8	chr6:141208788-141209134	NONHSAT115290
6	lnc-NMBR-2	chr6:141137269-141138214	NONHSAT115288
7	lnc-NMBR-8	chr6:141215649-141215754	NONHSAT115290
8	lnc-NMBR-2	chr6:141167095-141167471	NONHSAT115288
9	lnc-NMBR-2	chr6:141173956-141174061	ENSG00000234147
10	lnc-NMBR-2	chr6:141167095-141167441	ENSG00000234147
11	lnc-NMBR-2	chr6:141128740-141128958	NONHSAT115288
12	lnc-NMBR-2	chr6:141173956-141174059	NONHSAT115288
13	lnc-NMBR-2	chr6:141184950-141184976	NONHSAT115288
14	lnc-GJE1-8	chr6:141082666-141083399	NONHSAT115287

No data

Variant related genes	Relation type
RPS3AP24	TF binding region
ENSG00000216548	TF binding region
ENSG00000234147	TF binding region
RPS3AP24	CpG island
ENSG00000216548	CpG island
ENSG00000234147	CpG island

Extended variants
information (count: 7535 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7535 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188789553	chr6:141029223-141029224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1521149	chr6:141029235-141029236	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540598353	chr6:141029278-141029279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562048770	chr6:141029312-141029313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529348390	chr6:141029328-141029329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548471980	chr6:141029350-141029351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551093003	chr6:141029353-141029354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563027789	chr6:141029399-141029400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146181712	chr6:141029428-141029429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181206254	chr6:141029475-141029476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76293787	chr6:141029481-141029482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184702989	chr6:141029504-141029505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534893338	chr6:141029529-141029530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546522972	chr6:141029532-141029533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189069863	chr6:141029703-141029704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182148189	chr6:141029728-141029729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556599663	chr6:141029735-141029736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2139826	chr6:141029818-141029819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140533391	chr6:141029826-141029827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558309031	chr6:141029859-141029860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573392021	chr6:141029889-141029890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116274587	chr6:141029902-141029903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150032083	chr6:141029933-141029934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564050207	chr6:141030019-141030020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533076385	chr6:141030031-141030032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546262395	chr6:141030036-141030037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs202070840	chr6:141030080-141030081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115428016	chr6:141030098-141030099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544626080	chr6:141030100-141030101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2506872	chr6:141030143-141030144	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs118011053	chr6:141030153-141030154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551609999	chr6:141030221-141030222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373603733	chr6:141030362-141030363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564287719	chr6:141030390-141030391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114410233	chr6:141030708-141030709	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568791763	chr6:141030757-141030758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs539504070	chr6:141030765-141030766	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs145367861	chr6:141030793-141030794	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189250017	chr6:141030799-141030800	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs534396690	chr6:141030842-141030843	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548868128	chr6:141030848-141030849	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs149217722	chr6:141030879-141030880	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574399922	chr6:141030913-141030914	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs576085095	chr6:141030941-141030942	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs544589285	chr6:141030971-141030972	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs556496766	chr6:141031018-141031019	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs564894453	chr6:141031023-141031024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534954441	chr6:141031107-141031108	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs553879585	chr6:141032042-141032043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529094362	chr6:141032059-141032060	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141029200-141030000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:141029200-141030400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:141029200-141030400	Enhancers	Fetal Lung	lung
4	chr6:141029400-141029800	Enhancers	Brain Substantia Nigra	brain
5	chr6:141029400-141030000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:141029400-141030400	Enhancers	Fetal Stomach	stomach
7	chr6:141029600-141030000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:141029600-141030000	Enhancers	HSMMtube	muscle
9	chr6:141029600-141030200	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr6:141029800-141030000	Enhancers	Fetal Heart	heart
11	chr6:141030600-141031200	Active TSS	Fetal Heart	heart
12	chr6:141032000-141033200	Enhancers	Primary B cells from cord blood	blood
13	chr6:141032600-141032800	Enhancers	GM12878-XiMat	blood
14	chr6:141038800-141039400	Enhancers	Ovary	ovary
15	chr6:141039000-141039200	Enhancers	Adipose Nuclei	Adipose
16	chr6:141039000-141039400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:141039200-141039400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:141041800-141042000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr6:141042000-141050600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr6:141046200-141049200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:141047400-141047600	Enhancers	NHDF-Ad	bronchial
22	chr6:141047600-141054800	Weak transcription	NHDF-Ad	bronchial
23	chr6:141049800-141051800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr6:141050200-141051200	Enhancers	Primary T cells from cord blood	blood
25	chr6:141050600-141051000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr6:141051000-141052600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr6:141051200-141051800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:141051600-141051800	Enhancers	Psoas Muscle	Psoas
29	chr6:141051800-141053000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:141052400-141053800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr6:141052600-141052800	Enhancers	Osteobl	bone
32	chr6:141052600-141053200	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr6:141052600-141053400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:141052800-141053200	Enhancers	Rectal Smooth Muscle	rectum
35	chr6:141053000-141053600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:141053200-141057600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:141053400-141057200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:141053800-141057400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr6:141054600-141055000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:141054800-141055200	Enhancers	NHDF-Ad	bronchial
41	chr6:141054800-141055200	Enhancers	Osteobl	bone
42	chr6:141055000-141057200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:141055200-141057200	Weak transcription	Osteobl	bone
44	chr6:141055200-141057600	Weak transcription	NHDF-Ad	bronchial
45	chr6:141057200-141057800	Enhancers	Fetal Kidney	kidney
46	chr6:141057200-141058000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:141057200-141058000	Enhancers	Osteobl	bone
48	chr6:141057200-141058200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:141057400-141057800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:141057400-141058200	Enhancers	Muscle Satellite Cultured Cells	--

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