Variant report

Variant	rs7743957
Chromosome Location	chr6:26103998-26103999
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:542)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr6:26103424-26104403	HUVEC	blood vessel:	n/a	chr6:26104005-26104014 chr6:26103578-26103588 chr6:26103580-26103587 chr6:26103579-26103587 chr6:26103579-26103588
2	REST	chr6:26103962-26104508	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr6:26103998-26105005	GM12878	blood:	n/a	n/a
4	PML	chr6:26103929-26104901	MCF-7	breast:	n/a	n/a
5	YY1	chr6:26103834-26104655	SK-N-SH_RA	brain:	n/a	n/a
6	CEBPD	chr6:26103764-26105313	K562	blood:	n/a	n/a
7	POLR2A	chr6:26103939-26104928	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr6:26103814-26104965	Hela-S3	cervix:	n/a	n/a
9	SIN3AK20	chr6:26103685-26105020	HCT-116	colon:	n/a	n/a
10	STAT3	chr6:26103533-26104320	MCF10A-Er-Src	breast:	n/a	chr6:26103889-26103896 chr6:26103578-26103587 chr6:26103579-26103588 chr6:26103971-26103983
11	RELA	chr6:26103940-26104815	GM18951	blood:	n/a	n/a
12	WRNIP1	chr6:26103941-26104840	GM12878	blood:	n/a	n/a
13	MTA3	chr6:26103868-26104919	GM12878	blood:	n/a	n/a
14	ELF1	chr6:26103846-26104651	MCF-7	breast:	n/a	chr6:26104312-26104325
15	STAT3	chr6:26103487-26104535	Hela-S3	cervix:	n/a	chr6:26103889-26103896 chr6:26103578-26103587 chr6:26103579-26103588 chr6:26103971-26103983
16	RELA	chr6:26103831-26104814	GM10847	blood:	n/a	n/a
17	CEBPB	chr6:26103902-26104479	A549	lung:	n/a	n/a
18	NFIC	chr6:26103825-26105046	SK-N-SH	brain:	n/a	n/a
19	ETS1	chr6:26103903-26105369	K562	blood:	n/a	n/a
20	CREB1	chr6:26103764-26104513	H1-hESC	embryonic stem cell:	n/a	n/a
21	RCOR1	chr6:26103985-26104813	HepG2	liver:	n/a	n/a
22	RELA	chr6:26103912-26104874	GM19099	blood:	n/a	n/a
23	FOXA1	chr6:26103805-26104385	HepG2	liver:	n/a	n/a
24	MTA3	chr6:26103764-26105088	GM12878	blood:	n/a	n/a
25	TRIM28	chr6:26103826-26104461	K562	blood:	n/a	n/a
26	ELF1	chr6:26103957-26104610	K562	blood:	n/a	chr6:26104312-26104325
27	BCL3	chr6:26103878-26104932	K562	blood:	n/a	n/a
28	POLR2A	chr6:26103793-26105147	K562	blood:	n/a	n/a
29	FOS	chr6:26103407-26104403	MCF10A-Er-Src	breast:	n/a	chr6:26104005-26104014 chr6:26103578-26103588 chr6:26103577-26103588 chr6:26103580-26103587 chr6:26103579-26103587 chr6:26103579-26103588
30	POLR2A	chr6:26103691-26105363	HL-60	blood:	n/a	n/a
31	CBX3	chr6:26103818-26104740	K562	blood:	n/a	n/a
32	MYC	chr6:26103963-26104030	HUVEC	blood vessel:	n/a	n/a
33	JUND	chr6:26103976-26104560	H1-hESC	embryonic stem cell:	n/a	chr6:26104005-26104014
34	MAFK	chr6:26103925-26104389	HepG2	liver:	n/a	n/a
35	RUNX3	chr6:26103790-26104883	GM12878	blood:	n/a	n/a
36	CREB1	chr6:26103777-26104833	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr6:26103807-26104784	Hela-S3	cervix:	n/a	n/a
38	RAD21	chr6:26103950-26104638	IMR90	lung:	n/a	n/a
39	BCL3	chr6:26103895-26104819	A549	lung:	n/a	n/a
40	MAX	chr6:26103879-26104689	GM12878	blood:	n/a	n/a
41	EP300	chr6:26103769-26104690	HepG2	liver:	n/a	n/a
42	SP4	chr6:26103761-26104727	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr6:26103840-26105317	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr6:26103909-26104618	K562	blood:	n/a	n/a
45	POLR2A	chr6:26103942-26105054	GM12891	blood:	n/a	n/a
46	SIN3AK20	chr6:26103844-26104759	K562	blood:	n/a	n/a
47	POU2F2	chr6:26103952-26104796	GM12878	blood:	n/a	chr6:26104061-26104082
48	SRF	chr6:26103941-26104267	H1-hESC	embryonic stem cell:	n/a	n/a
49	JUND	chr6:26103300-26104758	HCT-116	colon:	n/a	chr6:26104005-26104014 chr6:26103578-26103588 chr6:26103580-26103587 chr6:26103579-26103587 chr6:26103577-26103588 chr6:26103579-26103588
50	SIN3AK20	chr6:26103765-26104750	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26103952-26104002	HL-60	blood:	n/a
2	chr6:26103952-26104002	NHBE	bronchial:	n/a
3	chr6:26103952-26104002	NH-A	brain:	n/a
4	chr6:26103952-26104002	AG09309	skin:	n/a
5	chr6:26103952-26104002	BJ	skin:	n/a
6	chr6:26103952-26104002	AG04449	skin:	fetal
7	chr6:26103952-26104002	HCF	heart:	n/a
8	chr6:26103952-26104002	LNCaP	prostate:	n/a
9	chr6:26103952-26104002	HIPEpiC	eye:	n/a
10	chr6:26103952-26104002	Hela-S3	cervix:	n/a
11	chr6:26103952-26104002	Caco-2	colon:	n/a
12	chr6:26103952-26104002	PrEC	prostate:	n/a
13	chr6:26103952-26104002	HMEC	breast:	n/a
14	chr6:26103952-26104002	U87	brain:	n/a
15	chr6:26103952-26104002	PANC-1	pancreas:	n/a
16	chr6:26103952-26104002	HRE	kidney:	n/a
17	chr6:26103952-26104002	AG10803	skin:	n/a
18	chr6:26103952-26104002	SKMC	muscle:	n/a
19	chr6:26103952-26104002	HNPCEpiC	eye:	n/a
20	chr6:26103952-26104002	GM19239	blood:	n/a
21	chr6:26103952-26104002	HCM	heart:	n/a
22	chr6:26103952-26104002	SK-N-SH_RA	brain:	n/a
23	chr6:26103952-26104002	GM12878	blood:	n/a
24	chr6:26103952-26104002	RPTEC	kidney:	n/a
25	chr6:26103952-26104002	K562	blood:	n/a
26	chr6:26103952-26104002	AG09319	gingival:	n/a
27	chr6:26103952-26104002	T-47D	breast:	n/a
28	chr6:26103952-26104002	ovcar-3	ovarian:	n/a
29	chr6:26103952-26104002	GM06990	blood:	n/a
30	chr6:26103952-26104002	A549	lung:	n/a
31	chr6:26103952-26104002	HEEpiC	esophagus:	n/a
32	chr6:26103952-26104002	Jurkat	blood:	n/a
33	chr6:26103952-26104002	NB4	blood:	n/a
34	chr6:26103952-26104002	MCF-7	breast:	n/a
35	chr6:26103952-26104002	HRPEpiC	eye:	n/a
36	chr6:26103952-26104002	AG04450	lung:	fetal
37	chr6:26103952-26104002	AoSMC	blood vessel:	n/a
38	chr6:26103952-26104002	ProgFib	skin:	n/a
39	chr6:26103952-26104002	PFSK-1	brain:	n/a
40	chr6:26103952-26104002	NT2-D1	testis:	n/a
41	chr6:26103952-26104002	SK-N-SH	brain:	n/a
42	chr6:26103952-26104002	HRCEpiC	kidney:	n/a
43	chr6:26103952-26104002	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:26103952-26104002	HCT-116	colon:	n/a
45	chr6:26103952-26104002	SK-N-MC	brain:	n/a
46	chr6:26103952-26104002	HEK293	kidney:	embryo
47	chr6:26103952-26104002	BE2_C	brain:	n/a
48	chr6:26103952-26104002	GM12891	blood:	n/a
49	chr6:26103952-26104002	ECC-1	luminal epithelium:	n/a
50	chr6:26103952-26104002	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:26102660..26104205-chr6:27804912..27807560,2	MCF-7	breast:
2	chr17:79826314..79826980-chr6:26103771..26104517,2	HCT-116	colon:
3	chr19:33793219..33794086-chr6:26103698..26104271,2	NB4	blood:
4	chr10:74033615..74034131-chr6:26103848..26104489,2	Hela-S3	cervix:
5	chr6:26101409..26106036-chr6:27098701..27102040,8	K562	blood:
6	chr4:90032248..90033146-chr6:26103791..26104616,2	Hela-S3	cervix:
7	chr19:10654465..10655067-chr6:26103887..26104848,2	NB4	blood:
8	chr6:26103772..26104616-chr8:134308982..134309567,2	Hela-S3	cervix:
9	chr6:26103055..26105911-chr6:27113369..27117045,6	K562	blood:
10	chr6:26103926..26104502-chr6:150038578..150039176,2	Hela-S3	cervix:
11	chr17:56708534..56710943-chr6:26103089..26104740,2	MCF-7	breast:
12	chr14:20937170..20938090-chr6:26103896..26104570,2	Hela-S3	cervix:
13	chr3:187871474..187872032-chr6:26103716..26104440,2	Hela-S3	cervix:
14	chr15:43622697..43623448-chr6:26103718..26104631,2	Hela-S3	cervix:
15	chr6:26052762..26068184-chr6:26093226..26113078,68	MCF-7	breast:
16	chr6:26042662..26045122-chr6:26102656..26104697,2	MCF-7	breast:
17	chr6:26101462..26104336-chr6:26520946..26522887,2	MCF-7	breast:
18	chr6:26026694..26027650-chr6:26103682..26104243,2	NB4	blood:
19	chr12:57039254..57039982-chr6:26103866..26104750,2	Hela-S3	cervix:
20	chr15:71407014..71408733-chr6:26102615..26104813,2	MCF-7	breast:
21	chr6:26103941..26105937-chr6:27113043..27115556,2	MCF-7	breast:
22	chr6:26019620..26034082-chr6:26100355..26110400,33	MCF-7	breast:
23	chr22:43011043..43011628-chr6:26103546..26104483,2	Hela-S3	cervix:
24	chr12:49524716..49525586-chr6:26103705..26104546,2	Hela-S3	cervix:
25	chr20:57554671..57557045-chr6:26103566..26105565,2	MCF-7	breast:
26	chr18:33709608..33710404-chr6:26103817..26104463,2	NB4	blood:
27	chr6:26103870..26104690-chr9:128003459..128004003,2	Hela-S3	cervix:
28	chr2:190648081..190648767-chr6:26103962..26104723,2	Hela-S3	cervix:
29	chr12:46662594..46663567-chr6:26103738..26104255,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
HIST1H4C	TF binding region
HIST1H4C	CpG island
ENSG00000104419	Chromatin interaction
ENSG00000225362	Chromatin interaction
ENSG00000271359	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000141522	Chromatin interaction
ENSG00000168803	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000270022	Chromatin interaction
ENSG00000196226	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000131023	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000044574	Chromatin interaction
ENSG00000101158	Chromatin interaction
ENSG00000267296	Chromatin interaction
ENSG00000134759	Chromatin interaction
ENSG00000123416	Chromatin interaction
ENSG00000198805	Chromatin interaction
ENSG00000110955	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000258017	Chromatin interaction
ENSG00000239705	Chromatin interaction
ENSG00000270959	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000168806	Chromatin interaction
ENSG00000168209	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000145012	Chromatin interaction
ENSG00000230259	Chromatin interaction
ENSG00000111371	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000128699	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000130734	Chromatin interaction
ENSG00000138640	Chromatin interaction
ENSG00000178863	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000245848	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1800708	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2050947	0.90[AFR][1000 genomes]
rs2051542	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2051543	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2282848	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3752418	0.86[AFR][1000 genomes]
rs3830054	0.83[AFR][1000 genomes]
rs6908263	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6927689	0.82[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7747040	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7760713	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7771690	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9295682	0.81[AFR][1000 genomes]
rs933199	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9366637	0.90[AFR][1000 genomes]
rs9366638	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9379826	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9393682	0.83[AFR][1000 genomes]
rs9393685	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9461234	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9461235	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9467667	0.86[AFR][1000 genomes]
rs9467675	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9467677	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
8	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
9	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
10	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
11	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
12	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
13	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
14	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
15	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
16	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
17	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
18	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26088400-26104000	Weak transcription	Esophagus	oesophagus
2	chr6:26090000-26104200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:26093200-26104200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:26099600-26104200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:26102600-26104000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:26103200-26104000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:26103200-26104000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:26103200-26104000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:26103200-26104000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr6:26103200-26104000	Active TSS	Aorta	Aorta
11	chr6:26103200-26104000	Flanking Active TSS	Dnd41	blood
12	chr6:26103200-26104000	Flanking Active TSS	Osteobl	bone
13	chr6:26103200-26104800	Flanking Active TSS	NHEK	skin
14	chr6:26103200-26105000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:26103400-26104000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:26103400-26104000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr6:26103400-26104000	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:26103400-26104000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:26103400-26104000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr6:26103400-26104000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:26103400-26104000	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr6:26103400-26104000	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr6:26103400-26104000	Flanking Active TSS	Fetal Kidney	kidney
24	chr6:26103400-26104000	Enhancers	Left Ventricle	heart
25	chr6:26103400-26104000	Active TSS	Right Atrium	heart
26	chr6:26103400-26104000	Flanking Active TSS	HMEC	breast
27	chr6:26103400-26104600	Active TSS	Thymus	Thymus
28	chr6:26103400-26104800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:26103400-26104800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:26103400-26104800	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr6:26103400-26104800	Flanking Active TSS	HUVEC	blood vessel
32	chr6:26103400-26104800	Active TSS	NHDF-Ad	bronchial
33	chr6:26103400-26105000	Active TSS	NHLF	lung
34	chr6:26103400-26105200	Active TSS	A549	lung
35	chr6:26103600-26104000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:26103600-26104000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr6:26103600-26104000	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr6:26103600-26104000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr6:26103600-26104000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:26103600-26104000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr6:26103600-26104000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr6:26103600-26104000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr6:26103600-26104000	Flanking Active TSS	HSMM	muscle
44	chr6:26103600-26104200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr6:26103600-26104200	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr6:26103600-26104200	Active TSS	HepG2	liver
47	chr6:26103600-26104200	Active TSS	K562	blood
48	chr6:26103600-26104400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:26103600-26104400	Active TSS	Fetal Muscle Leg	muscle
50	chr6:26103600-26104400	Active TSS	Placenta	Placenta

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