Variant report

Variant	rs56194675
Chromosome Location	chr6:31632527-31632528
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HCFC1	chr6:31632027-31634910	Hela-S3	cervix:	n/a	n/a
2	MAFK	chr6:31632292-31634152	K562	blood:	n/a	n/a
3	REST	chr6:31632240-31634048	H1-neurons	neurons:	n/a	chr6:31633472-31633492 chr6:31633479-31633492
4	CUX1	chr6:31631866-31634258	K562	blood:	n/a	chr6:31633594-31633608
5	BCLAF1	chr6:31632487-31634355	K562	blood:	n/a	chr6:31633646-31633655 chr6:31634115-31634124 chr6:31634061-31634070
6	YY1	chr6:31632356-31634157	GM12892	blood:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
7	POLR2A	chr6:31632353-31634300	SK-N-MC	brain:	n/a	n/a
8	ELK1	chr6:31631742-31634144	K562	blood:	n/a	chr6:31633646-31633655 chr6:31633646-31633655
9	STAT5A	chr6:31632431-31634415	GM12878	blood:	n/a	chr6:31634066-31634078 chr6:31633551-31633563 chr6:31633839-31633851 chr6:31633070-31633078
10	MAX	chr6:31632427-31634207	SK-N-SH	brain:	n/a	chr6:31634058-31634068
11	POLR2A	chr6:31632451-31634149	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr6:31632506-31634185	PANC-1	pancreas:	n/a	n/a
13	ATF3	chr6:31631679-31633915	K562	blood:	n/a	chr6:31633492-31633501 chr6:31632951-31632971 chr6:31632950-31632959
14	TRIM28	chr6:31631410-31634096	K562	blood:	n/a	chr6:31633746-31633754
15	TCF7L2	chr6:31632379-31632988	HEK293	kidney:	n/a	n/a
16	YY1	chr6:31632381-31633935	H1-hESC	embryonic stem cell:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172
17	HNF4G	chr6:31632495-31634203	HepG2	liver:	n/a	chr6:31633191-31633205 chr6:31633814-31633827 chr6:31633810-31633822 chr6:31633814-31633827 chr6:31633809-31633831 chr6:31633191-31633205 chr6:31633193-31633205 chr6:31633191-31633204
18	YY1	chr6:31631619-31634169	K562	blood:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
19	MTA3	chr6:31632175-31634692	GM12878	blood:	n/a	n/a
20	ATF2	chr6:31632493-31633150	GM12878	blood:	n/a	n/a
21	TEAD4	chr6:31631617-31634618	K562	blood:	n/a	n/a
22	HCFC1	chr6:31631398-31634556	K562	blood:	n/a	n/a
23	CBX3	chr6:31631090-31634828	K562	blood:	n/a	chr6:31632567-31632578
24	POLR2A	chr6:31632511-31634079	MCF10A-Er-Src	breast:	n/a	n/a
25	YY1	chr6:31632251-31633210	SK-N-SH_RA	brain:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172
26	RUNX3	chr6:31632348-31634430	GM12878	blood:	n/a	chr6:31632844-31632861 chr6:31632853-31632862 chr6:31632853-31632862 chr6:31632853-31632868
27	NFIC	chr6:31631978-31634355	HepG2	liver:	n/a	n/a
28	ZNF384	chr6:31632430-31634255	K562	blood:	n/a	n/a
29	REST	chr6:31632512-31634174	HL-60	blood:	n/a	chr6:31633472-31633492 chr6:31633479-31633492
30	TAF7	chr6:31632506-31633754	K562	blood:	n/a	n/a
31	MXI1	chr6:31632296-31634473	K562	blood:	n/a	n/a
32	POLR2A	chr6:31631672-31634628	IMR90	lung:	n/a	n/a
33	YY1	chr6:31632415-31633942	ECC-1	luminal epithelium:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172
34	RFX5	chr6:31632427-31634053	K562	blood:	n/a	n/a
35	MAX	chr6:31632508-31634254	ECC-1	luminal epithelium:	n/a	chr6:31634058-31634068 chr6:31634235-31634244
36	TAF1	chr6:31632365-31634241	ECC-1	luminal epithelium:	n/a	n/a
37	YY1	chr6:31632334-31634168	H1-hESC	embryonic stem cell:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
38	EGR1	chr6:31632472-31634352	K562	blood:	n/a	chr6:31633003-31633025 chr6:31633009-31633020 chr6:31633783-31633807 chr6:31634061-31634074 chr6:31633301-31633308 chr6:31634054-31634069 chr6:31633720-31633744 chr6:31634060-31634070 chr6:31634055-31634068 chr6:31633008-31633021 chr6:31634058-31634068 chr6:31634055-31634068 chr6:31633007-31633022 chr6:31633300-31633315
39	YY1	chr6:31632327-31634021	SK-N-SH	brain:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172
40	YY1	chr6:31632354-31634161	GM12878	blood:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
41	TEAD4	chr6:31630958-31634869	K562	blood:	n/a	n/a
42	ATF2	chr6:31632449-31633543	GM12878	blood:	n/a	n/a
43	TAL1	chr6:31631121-31634369	K562	blood:	n/a	n/a
44	SREBP1	chr6:31631677-31634839	GM12878	blood:	n/a	n/a
45	POLR2A	chr6:31632521-31634059	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr6:31631018-31634754	K562	blood:	n/a	n/a
47	POLR2A	chr6:31632386-31634258	HUVEC	blood vessel:	n/a	n/a
48	MXI1	chr6:31632275-31634555	HepG2	liver:	n/a	n/a
49	ARID3A	chr6:31631879-31633884	K562	blood:	n/a	chr6:31632907-31632915 chr6:31632494-31632510
50	YY1	chr6:31632463-31633729	A549	lung:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31632477-31632527	PrEC	prostate:	n/a
2	chr6:31632477-31632527	H1-hESC	embryonic stem cell:	embryo
3	chr6:31632477-31632527	AG04450	lung:	fetal
4	chr6:31632477-31632527	IMR90	lung:	fetal
5	chr6:31632477-31632527	ovcar-3	ovarian:	n/a
6	chr6:31632477-31632527	U87	brain:	n/a
7	chr6:31632477-31632527	HAEpiC	amniotic membrane:	n/a
8	chr6:31632477-31632527	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:31632477-31632527	AG04449	skin:	fetal
10	chr6:31632477-31632527	HEEpiC	esophagus:	n/a
11	chr6:31632477-31632527	AG09319	gingival:	n/a
12	chr6:31632477-31632527	HMEC	breast:	n/a
13	chr6:31632477-31632527	HNPCEpiC	eye:	n/a
14	chr6:31632477-31632527	LNCaP	prostate:	n/a
15	chr6:31632477-31632527	Hepatocyte	liver:	n/a
16	chr6:31632477-31632527	A549	lung:	n/a
17	chr6:31632477-31632527	HRPEpiC	eye:	n/a
18	chr6:31632477-31632527	SKMC	muscle:	n/a
19	chr6:31632477-31632527	CMK	blood:	n/a
20	chr6:31632477-31632527	BE2_C	brain:	n/a
21	chr6:31632477-31632527	HCM	heart:	n/a
22	chr6:31632477-31632527	GM12892	blood:	n/a
23	chr6:31632477-31632527	SAEC	small airway:	n/a
24	chr6:31632477-31632527	Hela-S3	cervix:	n/a
25	chr6:31632477-31632527	HIPEpiC	eye:	n/a
26	chr6:31632477-31632527	NHBE	bronchial:	n/a
27	chr6:31632477-31632527	HRE	kidney:	n/a
28	chr6:31632477-31632527	SK-N-SH_RA	brain:	n/a
29	chr6:31632477-31632527	GM12878	blood:	n/a
30	chr6:31632477-31632527	SK-N-MC	brain:	n/a
31	chr6:31632477-31632527	Caco-2	colon:	n/a
32	chr6:31632477-31632527	AG10803	skin:	n/a
33	chr6:31632477-31632527	BJ	skin:	n/a
34	chr6:31632477-31632527	K562	blood:	n/a
35	chr6:31632477-31632527	NT2-D1	testis:	n/a
36	chr6:31632477-31632527	PANC-1	pancreas:	n/a
37	chr6:31632477-31632527	NHDF-neo	bronchial:	n/a
38	chr6:31632477-31632527	NB4	blood:	n/a
39	chr6:31632477-31632527	MCF10A-Er-Src	breast:	n/a
40	chr6:31632477-31632527	HL-60	blood:	n/a
41	chr6:31632477-31632527	HRCEpiC	kidney:	n/a
42	chr6:31632477-31632527	MCF-7	breast:	n/a
43	chr6:31632477-31632527	HEK293	kidney:	embryo
44	chr6:31632477-31632527	Jurkat	blood:	n/a
45	chr6:31632477-31632527	HUVEC	blood vessel:	n/a
46	chr6:31632477-31632527	HepG2	liver:	n/a
47	chr6:31632477-31632527	PFSK-1	brain:	n/a
48	chr6:31632477-31632527	ECC-1	luminal epithelium:	n/a
49	chr6:31632477-31632527	AG09309	skin:	n/a
50	chr6:31632477-31632527	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
2	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
3	chr6:31631113..31634365-chr6:31867924..31871902,6	K562	blood:
4	chr6:31506496..31512275-chr6:31630248..31634828,11	K562	blood:
5	chr10:33247123..33247949-chr6:31632509..31633366,2	Hela-S3	cervix:
6	chr6:31631384..31635745-chr6:32161942..32163949,3	K562	blood:
7	chr6:31630940..31635916-chr6:31782579..31784659,6	MCF-7	breast:
8	chr6:31632296..31634965-chr6:31685541..31687886,2	MCF-7	breast:
9	chr6:31631824..31634552-chr6:31668867..31671892,6	MCF-7	breast:
10	chr6:31547676..31550388-chr6:31631712..31633963,2	K562	blood:
11	chr6:31631207..31634109-chr6:31926807..31929140,3	K562	blood:
12	chr6:31630921..31635353-chr6:31802314..31807064,6	MCF-7	breast:
13	chr6:31505350..31512312-chr6:31630543..31635379,11	K562	blood:
14	chr6:31631384..31634257-chr6:32162297..32163949,2	K562	blood:
15	chr6:31630896..31633436-chr6:31799776..31802391,2	MCF-7	breast:
16	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
17	chr6:31632061..31634821-chr6:31925160..31927798,3	MCF-7	breast:
18	chr6:31632509..31634236-chr6:31853959..31856343,2	K562	blood:
19	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
20	chr6:31628509..31634075-chr6:31935054..31938547,6	K562	blood:
21	chr6:31632488..31634160-chr6:31845506..31848503,2	MCF-7	breast:
22	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
23	chr6:31632318..31634134-chr6:31707864..31709911,2	MCF-7	breast:
24	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
25	chr6:31632224..31633782-chr6:32938836..32940645,2	K562	blood:
26	chr6:31630138..31633537-chr6:31702184..31707226,4	MCF-7	breast:
27	chr6:31512174..31516924-chr6:31632110..31634699,4	MCF-7	breast:
28	chr6:31548503..31550806-chr6:31631619..31633429,4	MCF-7	breast:
29	chr6:31631741..31634123-chr6:32936470..32938783,3	MCF-7	breast:
30	chr6:31631447..31633355-chr6:32013677..32016476,2	K562	blood:
31	chr6:31632509..31634091-chr6:31794981..31797016,2	MCF-7	breast:
32	chr6:31632206..31634072-chr6:31697899..31700595,2	MCF-7	breast:
33	chr6:31632223..31634660-chr6:31938839..31941215,3	K562	blood:
34	chr6:31632360..31634286-chr7:148580319..148582667,2	K562	blood:
35	chr6:31631608..31633822-chr6:31656164..31658364,2	MCF-7	breast:
36	chr6:31632122..31634257-chr7:1497327..1499894,2	K562	blood:
37	chr6:31631495..31634660-chr6:31935613..31943206,9	K562	blood:
38	chr6:31512487..31516692-chr6:31630820..31634965,11	K562	blood:

Variant related genes	Relation type
C6orf47	TF binding region
ENSG00000263020	TF binding region
CSNK2B	TF binding region
ENSG00000263020	CpG island
CSNK2B	CpG island
C6orf47	CpG island
ENSG00000204388	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000150093	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000225981	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000229656	Chromatin interaction
ENSG00000106462	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000164877	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204498	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10947225	0.87[AFR][1000 genomes]
rs28445017	1.00[AMR][1000 genomes]
rs58368425	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59402363	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73728948	1.00[AMR][1000 genomes]
rs73728988	0.87[AFR][1000 genomes]
rs73728991	0.87[AFR][1000 genomes]
rs9282875	1.00[AMR][1000 genomes]
rs9332712	0.87[AFR][1000 genomes]
rs9461723	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9461730	0.87[AFR][1000 genomes]
rs9469030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469039	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469048	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501148	1.00[AMR][1000 genomes]
rs9501150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
10	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
11	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
13	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
14	nsv884419	chr6:31585000-31632651	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
15	nsv884420	chr6:31586827-31632651	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
16	nsv884424	chr6:31593729-31632651	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
17	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
18	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31630800-31632600	Flanking Active TSS	HMEC	breast
2	chr6:31631000-31632600	Flanking Active TSS	NH-A	brain
3	chr6:31631000-31633200	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr6:31631200-31632600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:31631200-31632600	Flanking Active TSS	Fetal Brain Male	brain
6	chr6:31631200-31633200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:31631200-31633400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:31631200-31634800	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr6:31631400-31632600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr6:31631400-31633200	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr6:31631400-31634200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
12	chr6:31631400-31634400	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr6:31631400-31634600	Active TSS	H9 Cell Line	embryonic stem cell
14	chr6:31631400-31634600	Active TSS	Aorta	Aorta
15	chr6:31631600-31632600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr6:31631600-31632600	Flanking Active TSS	Fetal Brain Female	brain
17	chr6:31631600-31632600	Flanking Active TSS	Osteobl	bone
18	chr6:31631600-31633200	Flanking Active TSS	HUVEC	blood vessel
19	chr6:31631600-31634400	Active TSS	Fetal Kidney	kidney
20	chr6:31631600-31634600	Active TSS	Ovary	ovary
21	chr6:31631600-31634800	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr6:31631800-31632600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr6:31631800-31632600	Flanking Active TSS	Primary T cells from cord blood	blood
24	chr6:31631800-31632600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr6:31631800-31632600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr6:31631800-31632600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr6:31631800-31632600	Active TSS	Right Atrium	heart
28	chr6:31631800-31632800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr6:31631800-31633000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:31631800-31633200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr6:31631800-31634600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr6:31631800-31634600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:31631800-31634600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:31631800-31634600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:31631800-31634800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:31632000-31632600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr6:31632000-31632600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:31632000-31632600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr6:31632000-31632600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr6:31632000-31632600	Flanking Active TSS	NHLF	lung
41	chr6:31632000-31632800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
42	chr6:31632000-31632800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr6:31632000-31633000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr6:31632000-31633200	Flanking Active TSS	Primary B cells from cord blood	blood
45	chr6:31632000-31634200	Active TSS	Fetal Lung	lung
46	chr6:31632000-31634400	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr6:31632000-31634400	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr6:31632000-31634400	Active TSS	Colon Smooth Muscle	Colon
49	chr6:31632000-31634400	Active TSS	Fetal Heart	heart
50	chr6:31632000-31634400	Active TSS	Fetal Intestine Large	intestine

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