Variant report

Variant	nsv886753
Chromosome Location	chr6:147526508-147680291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1455)
CpG islands
(count:305)
Chromatin interactive
region (count:201)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1455 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147529694-147529864	K562	blood:	n/a	n/a
2	ARID3A	chr6:147531050-147531310	K562	blood:	n/a	n/a
3	ARID3A	chr6:147527046-147527225	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:147543293-147543870	K562	blood:	n/a	n/a
5	ARID3A	chr6:147539112-147539472	K562	blood:	n/a	n/a
6	ARID3A	chr6:147526670-147527526	K562	blood:	n/a	chr6:147526834-147526850
7	ARID3A	chr6:147528435-147528992	K562	blood:	n/a	n/a
8	ARID3A	chr6:147539974-147540745	K562	blood:	n/a	n/a
9	ARID3A	chr6:147530188-147530714	K562	blood:	n/a	n/a
10	ARID3A	chr6:147642433-147642696	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:147553185-147553219	K562	blood:	n/a	n/a
12	ARID3A	chr6:147528088-147528191	K562	blood:	n/a	n/a
13	ATF1	chr6:147563836-147563881	K562	blood:	n/a	n/a
14	ATF1	chr6:147526915-147527250	K562	blood:	n/a	n/a
15	ATF1	chr6:147543405-147543852	K562	blood:	n/a	n/a
16	ATF3	chr6:147613024-147613310	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:147528491-147528686	K562	blood:	n/a	n/a
18	BACH1	chr6:147568452-147568564	K562	blood:	n/a	n/a
19	BACH1	chr6:147619125-147619346	K562	blood:	n/a	n/a
20	BACH1	chr6:147668403-147668878	K562	blood:	n/a	n/a
21	BACH1	chr6:147622318-147622405	K562	blood:	n/a	n/a
22	BACH1	chr6:147643267-147643332	K562	blood:	n/a	n/a
23	BACH1	chr6:147562497-147562531	K562	blood:	n/a	n/a
24	BACH1	chr6:147619572-147619745	K562	blood:	n/a	n/a
25	BATF	chr6:147643614-147643982	GM12878	blood:	n/a	chr6:147643753-147643762
26	BATF	chr6:147643559-147643930	GM12878	blood:	n/a	chr6:147643753-147643762
27	BCL3	chr6:147548162-147548567	K562	blood:	n/a	n/a
28	BCL3	chr6:147673487-147674459	K562	blood:	n/a	n/a
29	BCL3	chr6:147666121-147666736	K562	blood:	n/a	n/a
30	BCL3	chr6:147666819-147668873	K562	blood:	n/a	n/a
31	BCLAF1	chr6:147526825-147527464	K562	blood:	n/a	n/a
32	BCLAF1	chr6:147528369-147529033	K562	blood:	n/a	chr6:147528794-147528803
33	BCLAF1	chr6:147533572-147534127	K562	blood:	n/a	n/a
34	BHLHE40	chr6:147547603-147547724	K562	blood:	n/a	n/a
35	BHLHE40	chr6:147549261-147549310	K562	blood:	n/a	n/a
36	BHLHE40	chr6:147543341-147543744	K562	blood:	n/a	n/a
37	BHLHE40	chr6:147546616-147546619	GM12878	blood:	n/a	n/a
38	CBX3	chr6:147618203-147618656	K562	blood:	n/a	n/a
39	CBX3	chr6:147572073-147572608	K562	blood:	n/a	n/a
40	CBX3	chr6:147573399-147574012	K562	blood:	n/a	n/a
41	CBX3	chr6:147625161-147625767	K562	blood:	n/a	n/a
42	CBX3	chr6:147571248-147571606	K562	blood:	n/a	n/a
43	CBX3	chr6:147619319-147620023	K562	blood:	n/a	n/a
44	CBX3	chr6:147617302-147617677	K562	blood:	n/a	n/a
45	CCNT2	chr6:147549586-147549644	K562	blood:	n/a	n/a
46	CCNT2	chr6:147603738-147603823	K562	blood:	n/a	n/a
47	CCNT2	chr6:147546779-147546916	K562	blood:	n/a	n/a
48	CCNT2	chr6:147620532-147620627	K562	blood:	n/a	n/a
49	CCNT2	chr6:147599902-147599989	K562	blood:	n/a	n/a
50	CCNT2	chr6:147600749-147600984	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147605330-147605380	HRPEpiC	eye:	n/a
2	chr6:147527113-147527163	HCPEpiC	choroid plexus:	n/a
3	chr6:147643548-147643598	BE2_C	brain:	n/a
4	chr6:147528521-147528571	ECC-1	luminal epithelium:	n/a
5	chr6:147528521-147528571	PANC-1	pancreas:	n/a
6	chr6:147527113-147527163	NT2-D1	testis:	n/a
7	chr6:147605330-147605380	T-47D	breast:	n/a
8	chr6:147527113-147527163	NHDF-neo	bronchial:	n/a
9	chr6:147570728-147570778	H1-hESC	embryonic stem cell:	embryo
10	chr6:147570728-147570778	HCPEpiC	choroid plexus:	n/a
11	chr6:147605330-147605380	HCF	heart:	n/a
12	chr6:147527113-147527163	GM12892	blood:	n/a
13	chr6:147643548-147643598	GM06990	blood:	n/a
14	chr6:147643548-147643598	AG04449	skin:	fetal
15	chr6:147570728-147570778	HRCEpiC	kidney:	n/a
16	chr6:147605330-147605380	ECC-1	luminal epithelium:	n/a
17	chr6:147570728-147570778	GM12878	blood:	n/a
18	chr6:147643548-147643598	SAEC	small airway:	n/a
19	chr6:147570728-147570778	IMR90	lung:	fetal
20	chr6:147605330-147605380	AG04449	skin:	fetal
21	chr6:147527113-147527163	BJ	skin:	n/a
22	chr6:147528521-147528571	ProgFib	skin:	n/a
23	chr6:147570728-147570778	CMK	blood:	n/a
24	chr6:147643548-147643598	HEK293	kidney:	embryo
25	chr6:147570728-147570778	U87	brain:	n/a
26	chr6:147570728-147570778	SK-N-SH_RA	brain:	n/a
27	chr6:147643548-147643598	AG09319	gingival:	n/a
28	chr6:147528521-147528571	ovcar-3	ovarian:	n/a
29	chr6:147643548-147643598	GM12892	blood:	n/a
30	chr6:147570728-147570778	AG10803	skin:	n/a
31	chr6:147527113-147527163	HCT-116	colon:	n/a
32	chr6:147527113-147527163	HRE	kidney:	n/a
33	chr6:147527113-147527163	RPTEC	kidney:	n/a
34	chr6:147570728-147570778	HNPCEpiC	eye:	n/a
35	chr6:147570728-147570778	MCF-7	breast:	n/a
36	chr6:147528521-147528571	GM12891	blood:	n/a
37	chr6:147570728-147570778	PrEC	prostate:	n/a
38	chr6:147527113-147527163	PANC-1	pancreas:	n/a
39	chr6:147605330-147605380	SK-N-SH_RA	brain:	n/a
40	chr6:147605330-147605380	AG09319	gingival:	n/a
41	chr6:147527113-147527163	MCF10A-Er-Src	breast:	n/a
42	chr6:147605330-147605380	HRE	kidney:	n/a
43	chr6:147643548-147643598	IMR90	lung:	fetal
44	chr6:147570728-147570778	PFSK-1	brain:	n/a
45	chr6:147527113-147527163	SK-N-SH	brain:	n/a
46	chr6:147643548-147643598	SK-N-MC	brain:	n/a
47	chr6:147643548-147643598	PrEC	prostate:	n/a
48	chr6:147528521-147528571	MCF-7	breast:	n/a
49	chr6:147570728-147570778	AG09319	gingival:	n/a
50	chr6:147643548-147643598	Hepatocyte	liver:	n/a

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:147225843..147228171-chr6:147577371..147579455,2	K562	blood:
2	chr6:147628703..147630384-chr6:147656186..147658681,2	K562	blood:
3	chr6:147640420..147643294-chr6:147648350..147651490,3	K562	blood:
4	chr6:147570692..147572642-chr6:147580577..147582832,2	MCF-7	breast:
5	chr6:147598437..147600865-chr6:147608002..147611556,3	K562	blood:
6	chr6:147579954..147581876-chr6:147584142..147585790,2	K562	blood:
7	chr6:147223660..147224280-chr6:147543816..147544342,2	MCF-7	breast:
8	chr6:147614299..147616581-chr6:147618756..147622866,3	K562	blood:
9	chr6:147598044..147601159-chr6:147601266..147602927,3	K562	blood:
10	chr6:147603613..147606358-chr6:147670525..147673088,2	K562	blood:
11	chr6:147514297..147518572-chr6:147531601..147534869,4	K562	blood:
12	chr6:147185541..147187437-chr6:147534820..147537621,2	K562	blood:
13	chr6:147605533..147608299-chr6:147613299..147616141,2	K562	blood:
14	chr6:147522804..147525350-chr6:147604658..147607399,2	MCF-7	breast:
15	chr6:147178650..147179155-chr6:147605934..147606927,2	K562	blood:
16	chr6:147583404..147586719-chr6:147587995..147591992,4	K562	blood:
17	chr6:147565658..147568685-chr6:147568738..147571330,4	K562	blood:
18	chr6:147555348..147557079-chr6:147583607..147585757,2	K562	blood:
19	chr6:147570173..147572962-chr6:147576488..147578515,2	K562	blood:
20	chr6:147562403..147564458-chr6:147565957..147567500,2	K562	blood:
21	chr6:147632934..147634936-chr6:147640228..147643160,2	MCF-7	breast:
22	chr6:147556538..147559509-chr6:147591738..147594515,2	K562	blood:
23	chr6:147223063..147225142-chr6:147528018..147531876,3	K562	blood:
24	chr6:147555348..147557079-chr6:147583607..147585757,2	K562	blood:
25	chr6:147221960..147224216-chr6:147538711..147540256,2	MCF-7	breast:
26	chr6:147205783..147208504-chr6:147543534..147546293,2	K562	blood:
27	chr6:147610982..147613437-chr6:147615648..147618340,2	K562	blood:
28	chr6:147674544..147676430-chr6:147682128..147684379,2	K562	blood:
29	chr6:147593854..147595682-chr6:147603055..147604986,2	MCF-7	breast:
30	chr6:147537663..147540561-chr6:147542025..147543593,2	MCF-7	breast:
31	chr6:147483460..147485748-chr6:147538509..147541125,2	K562	blood:
32	chr6:147603604..147605158-chr9:110248613..110251263,2	MCF-7	breast:
33	chr6:147596142..147599213-chr6:147600887..147603555,4	K562	blood:
34	chr6:147583523..147585752-chr6:147591147..147593959,2	K562	blood:
35	chr6:147583523..147586879-chr6:147592459..147595708,4	K562	blood:
36	chr6:147523543..147527462-chr6:147538561..147541910,5	MCF-7	breast:
37	chr6:147245797..147247698-chr6:147527227..147529725,2	K562	blood:
38	chr6:147649628..147652559-chr6:147657178..147658972,2	K562	blood:
39	chr6:147229677..147239083-chr6:147521152..147530893,22	K562	blood:
40	chr6:147573677..147576082-chr6:147580543..147582067,2	K562	blood:
41	chr6:147478214..147481987-chr6:147524471..147526667,3	MCF-7	breast:
42	chr6:147565658..147568685-chr6:147568738..147571330,4	K562	blood:
43	chr6:147564930..147567300-chr6:147589285..147591858,2	K562	blood:
44	chr6:147579053..147583009-chr6:147587087..147590128,3	K562	blood:
45	chr6:147570173..147572962-chr6:147576488..147578515,2	K562	blood:
46	chr6:147565112..147568685-chr6:147569145..147570967,3	K562	blood:
47	chr6:147180819..147182398-chr6:147544000..147546077,2	K562	blood:
48	chr6:147582141..147584603-chr6:147598166..147600367,2	K562	blood:
49	chr6:147541961..147544233-chr6:147614888..147617069,2	K562	blood:
50	chr6:147522256..147524439-chr6:147601454..147603467,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP5-4	chr6:147543558-147543821	NONHSAT115448
2	lnc-SAMD5-3	chr6:147566472-147566951	expReg_chr6_10923_+
3	lnc-STXBP5-4	chr6:147528560-147528688	NONHSAT115448

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STXBP5	hsa-miR-21-5p	chr6:147636655-147636676

Variant related genes	Relation type
STXBP5-AS1	TF binding region
STXBP5	TF binding region
STXBP5-AS1	CpG island
STXBP5	CpG island
ENSG00000233452	chromatin interactions
ENSG00000136826	chromatin interactions
ENSG00000164506	chromatin interactions
ENSG00000196634	chromatin interactions
ENSG00000227748	chromatin interactions
ENSG00000125846	chromatin interactions

Extended variants
information (count: 5427 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5427 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs398048351	chr6:147526508-147526509	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs200859878	chr6:147526512-147526513	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs66924827	chr6:147526531-147526532	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs145139309	chr6:147526532-147526533	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs570857007	chr6:147526535-147526536	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs192706521	chr6:147526572-147526573	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs556741087	chr6:147526577-147526578	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs547275527	chr6:147526606-147526607	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs567072609	chr6:147526620-147526621	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs535647938	chr6:147526629-147526630	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs184118306	chr6:147526682-147526683	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs568093727	chr6:147526715-147526716	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537138156	chr6:147526729-147526730	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs189390657	chr6:147526808-147526809	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs57284678	chr6:147526933-147526934	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs545700869	chr6:147526955-147526956	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs552814076	chr6:147527034-147527035	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs181795025	chr6:147527040-147527041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs541693286	chr6:147527051-147527052	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs561912735	chr6:147527066-147527067	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs530956843	chr6:147527129-147527130	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141223320	chr6:147527143-147527144	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs372793319	chr6:147527165-147527166	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs377524924	chr6:147527224-147527225	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs74342338	chr6:147527255-147527256	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs62435614	chr6:147527258-147527259	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs144556057	chr6:147527261-147527262	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs79263268	chr6:147527280-147527281	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs567077500	chr6:147527284-147527285	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35138607	chr6:147527346-147527347	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs148421027	chr6:147527368-147527369	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs549349629	chr6:147527399-147527400	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs569428865	chr6:147527431-147527432	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs536750866	chr6:147527455-147527456	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs546239809	chr6:147527492-147527493	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs145131902	chr6:147527531-147527532	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570127943	chr6:147527536-147527537	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs184438773	chr6:147527559-147527560	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549886195	chr6:147527624-147527625	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs78079687	chr6:147527660-147527661	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs375520960	chr6:147527674-147527675	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs143404211	chr6:147527720-147527721	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs538602438	chr6:147527833-147527834	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs563776084	chr6:147527938-147527939	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs12212700	chr6:147527973-147527974	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs373903316	chr6:147527979-147527980	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs377145397	chr6:147528003-147528004	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs555276646	chr6:147528005-147528006	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575356896	chr6:147528076-147528077	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs544736432	chr6:147528113-147528114	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
Gastric cancer	17908304	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3617 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147522800-147528600	Active TSS	Duodenum Mucosa	Duodenum
2	chr6:147522800-147529000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:147523000-147526600	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr6:147523000-147526800	Active TSS	Brain Substantia Nigra	brain
5	chr6:147523000-147526800	Active TSS	Duodenum Smooth Muscle	Duodenum
6	chr6:147523000-147526800	Active TSS	Fetal Brain Male	brain
7	chr6:147523000-147527000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:147523000-147527000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:147523000-147527000	Active TSS	Fetal Stomach	stomach
10	chr6:147523000-147527000	Active TSS	Psoas Muscle	Psoas
11	chr6:147523000-147527000	Active TSS	Rectal Smooth Muscle	rectum
12	chr6:147523000-147527000	Active TSS	Thymus	Thymus
13	chr6:147523000-147527000	Active TSS	GM12878-XiMat	blood
14	chr6:147523000-147527000	Active TSS	NH-A	brain
15	chr6:147523000-147527200	Active TSS	Colonic Mucosa	Colon
16	chr6:147523000-147527200	Active TSS	A549	lung
17	chr6:147523000-147527400	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr6:147523000-147527400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:147523000-147527400	Active TSS	Fetal Intestine Small	intestine
20	chr6:147523000-147527600	Active TSS	Fetal Intestine Large	intestine
21	chr6:147523000-147527800	Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr6:147523000-147528000	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr6:147523000-147528600	Active TSS	Brain Cingulate Gyrus	brain
24	chr6:147523000-147528800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:147523000-147528800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:147523000-147528800	Active TSS	Brain Anterior Caudate	brain
27	chr6:147523000-147528800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr6:147523000-147529000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:147523000-147529200	Active TSS	NHLF	lung
30	chr6:147523000-147529600	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr6:147523000-147529600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr6:147523000-147529800	Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr6:147523200-147526600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:147523200-147527000	Active TSS	Sigmoid Colon	Sigmoid Colon
35	chr6:147523200-147527400	Active TSS	Aorta	Aorta
36	chr6:147523200-147527400	Active TSS	HSMMtube	muscle
37	chr6:147523200-147527800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:147523200-147528400	Active TSS	K562	blood
39	chr6:147523200-147528800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:147523400-147526600	Active TSS	Brain Hippocampus Middle	brain
41	chr6:147523400-147526800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:147523400-147526800	Active TSS	Fetal Thymus	thymus
43	chr6:147523400-147527000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:147523400-147527400	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr6:147523400-147527400	Active TSS	HSMM	muscle
46	chr6:147523400-147528400	Active TSS	Muscle Satellite Cultured Cells	--
47	chr6:147523400-147528600	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr6:147523400-147528600	Active TSS	NHDF-Ad	bronchial
49	chr6:147523400-147528800	Active TSS	Brain Angular Gyrus	brain
50	chr6:147523400-147529000	Active TSS	NHEK	skin

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