Variant report

Variant	rs41267082
Chromosome Location	chr6:31830593-31830594
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:183)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr6:31830298-31831020	K562	blood:	n/a	n/a
2	YY1	chr6:31830299-31831014	K562	blood:	n/a	n/a
3	SPI1	chr6:31830481-31830976	HL-60	blood:	n/a	n/a
4	ATF3	chr6:31830357-31831033	HepG2	liver:	n/a	chr6:31830879-31830892 chr6:31830648-31830657 chr6:31830881-31830901 chr6:31830717-31830737
5	E2F6	chr6:31830226-31831034	K562	blood:	n/a	chr6:31830862-31830871
6	RCOR1	chr6:31830291-31831058	K562	blood:	n/a	n/a
7	POLR2A	chr6:31830116-31831878	H1-hESC	embryonic stem cell:	n/a	n/a
8	FOSL1	chr6:31830153-31831079	K562	blood:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
9	POLR2A	chr6:31830349-31830722	SK-N-SH	brain:	n/a	n/a
10	RELA	chr6:31830314-31830917	GM15510	blood:	n/a	n/a
11	FOXM1	chr6:31830284-31831169	GM12878	blood:	n/a	n/a
12	CREB1	chr6:31830295-31831050	GM12878	blood:	n/a	chr6:31830879-31830892
13	TCF12	chr6:31830281-31831200	ECC-1	luminal epithelium:	n/a	n/a
14	SP2	chr6:31830405-31831004	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:31830316-31830999	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr6:31830467-31831054	Hela-S3	cervix:	n/a	n/a
17	ETS1	chr6:31830367-31830730	GM12878	blood:	n/a	chr6:31830673-31830684
18	TCF3	chr6:31830290-31830713	GM12878	blood:	n/a	n/a
19	NFYA	chr6:31830511-31830902	GM12878	blood:	n/a	chr6:31830858-31830873 chr6:31830858-31830873 chr6:31830862-31830874 chr6:31830746-31830764 chr6:31830859-31830873
20	PML	chr6:31830274-31830764	MCF-7	breast:	n/a	n/a
21	JUND	chr6:31830543-31831075	H1-hESC	embryonic stem cell:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830953-31830964 chr6:31830860-31830869
22	FOSL2	chr6:31830105-31831112	SK-N-SH	brain:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
23	SP1	chr6:31830399-31831106	A549	lung:	n/a	chr6:31830892-31830901 chr6:31830892-31830901 chr6:31830647-31830656 chr6:31830890-31830902 chr6:31830890-31830902 chr6:31830678-31830699 chr6:31830891-31830900 chr6:31830851-31830872 chr6:31830891-31830901 chr6:31830891-31830901
24	SP4	chr6:31830294-31831077	H1-hESC	embryonic stem cell:	n/a	chr6:31830888-31830904
25	EP300	chr6:31830351-31831019	HepG2	liver:	n/a	chr6:31830956-31830965
26	SMC3	chr6:31830366-31830679	K562	blood:	n/a	n/a
27	SIN3AK20	chr6:31830376-31831064	A549	lung:	n/a	n/a
28	USF1	chr6:31830334-31831018	SK-N-SH	brain:	n/a	chr6:31830715-31830728
29	GTF2F1	chr6:31830494-31831152	Hela-S3	cervix:	n/a	n/a
30	USF1	chr6:31830372-31830985	A549	lung:	n/a	chr6:31830715-31830728
31	E2F6	chr6:31830235-31830986	K562	blood:	n/a	chr6:31830862-31830871
32	GATA1	chr6:31830424-31832058	PBDE	blood:	n/a	chr6:31830604-31830611 chr6:31830955-31830964
33	JUND	chr6:31830244-31831121	H1-hESC	embryonic stem cell:	n/a	chr6:31830384-31830395 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
34	TAF1	chr6:31830359-31830778	GM12891	blood:	n/a	n/a
35	POLR2A	chr6:31830203-31830871	HepG2	liver:	n/a	n/a
36	TBP	chr6:31830315-31831083	HepG2	liver:	n/a	n/a
37	MAX	chr6:31829919-31830983	HepG2	liver:	n/a	chr6:31830956-31830965
38	USF1	chr6:31830371-31831000	A549	lung:	n/a	chr6:31830715-31830728
39	CREB1	chr6:31830090-31831928	K562	blood:	n/a	chr6:31830879-31830892
40	HDAC2	chr6:31830181-31830975	K562	blood:	n/a	n/a
41	SIN3AK20	chr6:31830167-31831136	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr6:31830249-31830902	MCF-7	breast:	n/a	n/a
43	POLR2A	chr6:31830142-31830946	HUVEC	blood vessel:	n/a	n/a
44	BHLHE40	chr6:31830294-31830942	HepG2	liver:	n/a	chr6:31830715-31830728
45	POLR2A	chr6:31830374-31830768	NB4	blood:	n/a	n/a
46	POLR2A	chr6:31830382-31830755	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr6:31830255-31830875	ProgFib	skin:	n/a	n/a
48	TAF1	chr6:31830300-31830957	H1-neurons	neurons:	n/a	n/a
49	SIN3AK20	chr6:31830083-31831000	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr6:31830248-31830825	PANC-1	pancreas:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31830561-31830611	NH-A	brain:	n/a
2	chr6:31830561-31830611	PrEC	prostate:	n/a
3	chr6:31830561-31830611	BJ	skin:	n/a
4	chr6:31830570-31830620	U87	brain:	n/a
5	chr6:31830561-31830611	Hepatocyte	liver:	n/a
6	chr6:31830572-31830622	RPTEC	kidney:	n/a
7	chr6:31830570-31830620	AoSMC	blood vessel:	n/a
8	chr6:31830570-31830620	Hela-S3	cervix:	n/a
9	chr6:31830570-31830620	AG10803	skin:	n/a
10	chr6:31830572-31830622	H1-hESC	embryonic stem cell:	embryo
11	chr6:31830570-31830620	AG09309	skin:	n/a
12	chr6:31830572-31830622	AG04449	skin:	fetal
13	chr6:31830572-31830622	GM19239	blood:	n/a
14	chr6:31830570-31830620	HCPEpiC	choroid plexus:	n/a
15	chr6:31830572-31830622	HRE	kidney:	n/a
16	chr6:31830572-31830622	HepG2	liver:	n/a
17	chr6:31830572-31830622	ProgFib	skin:	n/a
18	chr6:31830572-31830622	IMR90	lung:	fetal
19	chr6:31830561-31830611	AG09319	gingival:	n/a
20	chr6:31830570-31830620	GM19239	blood:	n/a
21	chr6:31830572-31830622	Jurkat	blood:	n/a
22	chr6:31830570-31830620	K562	blood:	n/a
23	chr6:31830570-31830620	ProgFib	skin:	n/a
24	chr6:31830561-31830611	MCF-7	breast:	n/a
25	chr6:31830572-31830622	NT2-D1	testis:	n/a
26	chr6:31830561-31830611	ProgFib	skin:	n/a
27	chr6:31830561-31830611	HRCEpiC	kidney:	n/a
28	chr6:31830561-31830611	Jurkat	blood:	n/a
29	chr6:31830570-31830620	MCF10A-Er-Src	breast:	n/a
30	chr6:31830561-31830611	AG10803	skin:	n/a
31	chr6:31830561-31830611	AG04450	lung:	fetal
32	chr6:31830570-31830620	LNCaP	prostate:	n/a
33	chr6:31830572-31830622	ECC-1	luminal epithelium:	n/a
34	chr6:31830561-31830611	BE2_C	brain:	n/a
35	chr6:31830572-31830622	HCT-116	colon:	n/a
36	chr6:31830570-31830620	GM12891	blood:	n/a
37	chr6:31830572-31830622	SAEC	small airway:	n/a
38	chr6:31830561-31830611	NT2-D1	testis:	n/a
39	chr6:31830572-31830622	Caco-2	colon:	n/a
40	chr6:31830572-31830622	ovcar-3	ovarian:	n/a
41	chr6:31830572-31830622	SK-N-SH	brain:	n/a
42	chr6:31830572-31830622	HMEC	breast:	n/a
43	chr6:31830561-31830611	AG04449	skin:	fetal
44	chr6:31830570-31830620	NH-A	brain:	n/a
45	chr6:31830570-31830620	HEEpiC	esophagus:	n/a
46	chr6:31830561-31830611	HUVEC	blood vessel:	n/a
47	chr6:31830570-31830620	AG04450	lung:	fetal
48	chr6:31830572-31830622	K562	blood:	n/a
49	chr6:31830561-31830611	SAEC	small airway:	n/a
50	chr6:31830561-31830611	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31619018..31621668-chr6:31828535..31831298,4	MCF-7	breast:
2	chr6:31761047..31764270-chr6:31827785..31831725,4	MCF-7	breast:
3	chr6:31514420..31518271-chr6:31830053..31832008,3	K562	blood:
4	chr6:31748274..31750464-chr6:31829000..31831442,2	MCF-7	breast:
5	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
6	chr6:31828758..31831666-chr6:31853611..31856072,2	MCF-7	breast:
7	chr6:31734752..31736298-chr6:31828518..31831343,2	K562	blood:
8	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
9	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
10	chr6:31774091..31776344-chr6:31828893..31831277,2	K562	blood:
11	chr6:31827799..31831011-chr6:31868395..31870845,5	MCF-7	breast:
12	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
13	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
14	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
15	chr6:31750326..31751829-chr6:31829443..31831754,2	MCF-7	breast:
16	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
17	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
18	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
19	chr6:31829900..31830743-chr6:31865500..31866056,2	MCF-7	breast:
20	chr6:31703656..31706945-chr6:31827756..31831598,5	MCF-7	breast:
21	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
22	chr6:31830083..31833987-chr6:31862759..31865610,4	MCF-7	breast:
23	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
24	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
25	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:
26	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
27	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
28	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
29	chr6:31829731..31832430-chr6:31863949..31866099,3	K562	blood:
30	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
31	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
32	chr6:31828952..31831553-chr6:31912715..31914981,2	K562	blood:
33	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
34	chr6:31827981..31830842-chr6:31915280..31917835,3	K562	blood:
35	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
36	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:
37	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
38	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
39	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
40	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
41	chr6:31701938..31704638-chr6:31828885..31832061,3	K562	blood:
42	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
43	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
44	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
45	chr6:31694971..31696688-chr6:31829211..31832001,2	MCF-7	breast:
46	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
47	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:
48	chr6:31794986..31795591-chr6:31830132..31830996,2	K562	blood:
49	chr6:31626270..31630199-chr6:31829030..31832230,7	K562	blood:
50	chr6:31780821..31784746-chr6:31829825..31831701,4	MCF-7	breast:

No data

Variant related genes	Relation type
NEU1	TF binding region
NEU1	CpG island
ENSG00000204348	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000204394	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11576013	0.81[ASN][1000 genomes]
rs17201248	0.81[ASN][1000 genomes]
rs3911893	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' 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	197 gene(s)	inside rSNPs	diseases
18	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
19	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
20	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 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	chr6:31829200-31831200	Active TSS	NHLF	lung
2	chr6:31829200-31832000	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr6:31829200-31832400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:31829400-31832200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr6:31829400-31832400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:31829600-31830600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:31829600-31830600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:31829600-31830600	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr6:31829600-31831000	Active TSS	NH-A	brain
10	chr6:31829600-31832200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:31829600-31832200	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr6:31829600-31832200	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr6:31829600-31832200	Active TSS	HSMM	muscle
14	chr6:31829600-31832200	Active TSS	HSMMtube	muscle
15	chr6:31829600-31832200	Active TSS	NHDF-Ad	bronchial
16	chr6:31829600-31832400	Active TSS	H9 Cell Line	embryonic stem cell
17	chr6:31829800-31830600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr6:31829800-31830600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:31829800-31831000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:31829800-31831800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr6:31829800-31832200	Active TSS	Fetal Kidney	kidney
22	chr6:31829800-31832400	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr6:31829800-31832400	Active TSS	A549	lung
24	chr6:31830000-31830600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:31830000-31830600	Active TSS	Aorta	Aorta
26	chr6:31830000-31830800	Active TSS	Gastric	stomach
27	chr6:31830000-31830800	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr6:31830000-31830800	Active TSS	Small Intestine	intestine
29	chr6:31830000-31831000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:31830000-31831000	Active TSS	Pancreas	Pancrea
31	chr6:31830000-31831200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:31830000-31831200	Active TSS	Lung	lung
33	chr6:31830000-31831200	Active TSS	HMEC	breast
34	chr6:31830000-31832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr6:31830000-31832000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:31830000-31832000	Active TSS	Ovary	ovary
37	chr6:31830000-31832000	Active TSS	Right Atrium	heart
38	chr6:31830000-31832200	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr6:31830000-31832200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:31830000-31832200	Active TSS	Right Ventricle	heart
41	chr6:31830000-31832400	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr6:31830000-31832400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr6:31830000-31832400	Bivalent/Poised TSS	HepG2	liver
44	chr6:31830200-31830600	Active TSS	Fetal Heart	heart
45	chr6:31830200-31830600	Active TSS	Stomach Mucosa	stomach
46	chr6:31830200-31831000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:31830200-31831000	Active TSS	Primary B cells from cord blood	blood
48	chr6:31830200-31831000	Active TSS	Muscle Satellite Cultured Cells	--
49	chr6:31830200-31831000	Active TSS	Brain Anterior Caudate	brain
50	chr6:31830200-31831000	Active TSS	Brain Hippocampus Middle	brain

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