Variant report

Variant	rs146537871
Chromosome Location	chr11:67806375-67806376
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:297)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PML	chr11:67806327-67806736	K562	blood:	n/a	n/a
2	POLR2A	chr11:67806109-67806769	GM12892	blood:	n/a	n/a
3	NR2F2	chr11:67805554-67806651	K562	blood:	n/a	n/a
4	STAT3	chr11:67806317-67806543	MCF10A-Er-Src	breast:	n/a	chr11:67806396-67806403
5	TAF1	chr11:67806241-67806841	K562	blood:	n/a	n/a
6	POLR2A	chr11:67806193-67806707	K562	blood:	n/a	n/a
7	POLR2A	chr11:67806231-67806688	K562	blood:	n/a	n/a
8	SIN3AK20	chr11:67806362-67806981	K562	blood:	n/a	n/a
9	RCOR1	chr11:67806064-67808274	IMR90	lung:	n/a	n/a
10	ELF1	chr11:67806056-67806645	HepG2	liver:	n/a	n/a
11	YY1	chr11:67806221-67806646	HCT-116	colon:	n/a	chr11:67806427-67806436 chr11:67806424-67806438
12	BHLHE40	chr11:67806324-67807679	GM12878	blood:	n/a	chr11:67806545-67806561 chr11:67806553-67806569
13	CCNT2	chr11:67805793-67806848	K562	blood:	n/a	chr11:67806427-67806436
14	TAF1	chr11:67806315-67806629	GM12891	blood:	n/a	n/a
15	IRF1	chr11:67806237-67806582	K562	blood:	n/a	chr11:67806426-67806440
16	YY1	chr11:67806250-67806669	K562	blood:	n/a	chr11:67806427-67806436 chr11:67806424-67806438
17	POLR2A	chr11:67806185-67806685	H1-hESC	embryonic stem cell:	n/a	n/a
18	YY1	chr11:67805420-67806783	HepG2	liver:	n/a	chr11:67805655-67805666 chr11:67806427-67806436 chr11:67806424-67806438
19	POLR2A	chr11:67806140-67806753	K562	blood:	n/a	n/a
20	TAF1	chr11:67806215-67806627	K562	blood:	n/a	n/a
21	POLR2A	chr11:67805531-67806728	HepG2	liver:	n/a	n/a
22	MYC	chr11:67806230-67806955	K562	blood:	n/a	n/a
23	POLR2A	chr11:67806151-67806756	MCF10A-Er-Src	breast:	n/a	n/a
24	PML	chr11:67806102-67806967	K562	blood:	n/a	n/a
25	SMARCB1	chr11:67805474-67806918	Hela-S3	cervix:	n/a	chr11:67805613-67805622
26	REST	chr11:67806228-67806678	A549	lung:	n/a	chr11:67806573-67806586 chr11:67806253-67806266
27	RAD21	chr11:67806048-67806626	ECC-1	luminal epithelium:	n/a	chr11:67806289-67806301
28	POLR2A	chr11:67806083-67806794	HCT-116	colon:	n/a	n/a
29	ZNF143	chr11:67806226-67807045	K562	blood:	n/a	n/a
30	ELF1	chr11:67806050-67806667	MCF-7	breast:	n/a	n/a
31	TBP	chr11:67805513-67806669	HepG2	liver:	n/a	n/a
32	POLR2A	chr11:67806160-67806754	NB4	blood:	n/a	n/a
33	MYC	chr11:67806356-67806496	HepG2	liver:	n/a	n/a
34	TCF12	chr11:67805624-67806779	ECC-1	luminal epithelium:	n/a	chr11:67805897-67805904 chr11:67805928-67805938
35	E2F6	chr11:67806276-67806697	A549	lung:	n/a	chr11:67806560-67806569 chr11:67806663-67806673 chr11:67806427-67806436
36	GTF2F1	chr11:67806183-67806531	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:67806146-67806751	K562	blood:	n/a	n/a
38	YY1	chr11:67806146-67806558	A549	lung:	n/a	chr11:67806427-67806436 chr11:67806424-67806438
39	RAD21	chr11:67806244-67806546	Hela-S3	cervix:	n/a	chr11:67806289-67806301
40	POLR2A	chr11:67806116-67806626	A549	lung:	n/a	n/a
41	POLR2A	chr11:67806092-67806682	H1-hESC	embryonic stem cell:	n/a	n/a
42	MXI1	chr11:67806301-67806656	Hela-S3	cervix:	n/a	n/a
43	RUNX3	chr11:67806131-67807082	GM12878	blood:	n/a	n/a
44	SMC3	chr11:67805771-67806728	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr11:67805800-67806818	MCF-7	breast:	n/a	n/a
46	SRF	chr11:67806304-67806609	K562	blood:	n/a	n/a
47	GTF2F1	chr11:67806145-67806555	K562	blood:	n/a	n/a
48	CTCF	chr11:67806300-67806450	K562	blood:	n/a	n/a
49	REST	chr11:67806177-67806551	K562	blood:	n/a	chr11:67806253-67806266
50	JUND	chr11:67805950-67806571	A549	lung:	n/a	chr11:67806177-67806188

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67806363-67806413	A549	lung:	n/a
2	chr11:67806337-67806387	GM06990	blood:	n/a
3	chr11:67806363-67806413	ProgFib	skin:	n/a
4	chr11:67806363-67806413	GM06990	blood:	n/a
5	chr11:67806337-67806387	ProgFib	skin:	n/a
6	chr11:67806337-67806387	H1-hESC	embryonic stem cell:	embryo
7	chr11:67806363-67806413	CMK	blood:	n/a
8	chr11:67806337-67806387	MCF10A-Er-Src	breast:	n/a
9	chr11:67806347-67806397	AG04450	lung:	fetal
10	chr11:67806363-67806413	HCPEpiC	choroid plexus:	n/a
11	chr11:67806347-67806397	ovcar-3	ovarian:	n/a
12	chr11:67806337-67806387	K562	blood:	n/a
13	chr11:67806347-67806397	HCF	heart:	n/a
14	chr11:67806347-67806397	PFSK-1	brain:	n/a
15	chr11:67806363-67806413	HAEpiC	amniotic membrane:	n/a
16	chr11:67806363-67806413	HCT-116	colon:	n/a
17	chr11:67806337-67806387	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:67806337-67806387	GM12878	blood:	n/a
19	chr11:67806337-67806387	ECC-1	luminal epithelium:	n/a
20	chr11:67806363-67806413	LNCaP	prostate:	n/a
21	chr11:67806363-67806413	Caco-2	colon:	n/a
22	chr11:67806337-67806387	CMK	blood:	n/a
23	chr11:67806363-67806413	AoSMC	blood vessel:	n/a
24	chr11:67806337-67806387	HRE	kidney:	n/a
25	chr11:67806337-67806387	NB4	blood:	n/a
26	chr11:67806347-67806397	GM19239	blood:	n/a
27	chr11:67806363-67806413	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:67806337-67806387	GM12892	blood:	n/a
29	chr11:67806337-67806387	Hela-S3	cervix:	n/a
30	chr11:67806347-67806397	HCT-116	colon:	n/a
31	chr11:67806337-67806387	AG04449	skin:	fetal
32	chr11:67806337-67806387	HRCEpiC	kidney:	n/a
33	chr11:67806363-67806413	HepG2	liver:	n/a
34	chr11:67806337-67806387	AoSMC	blood vessel:	n/a
35	chr11:67806347-67806397	SKMC	muscle:	n/a
36	chr11:67806347-67806397	SK-N-SH_RA	brain:	n/a
37	chr11:67806363-67806413	BJ	skin:	n/a
38	chr11:67806363-67806413	BE2_C	brain:	n/a
39	chr11:67806363-67806413	AG10803	skin:	n/a
40	chr11:67806337-67806387	LNCaP	prostate:	n/a
41	chr11:67806337-67806387	HIPEpiC	eye:	n/a
42	chr11:67806363-67806413	Hela-S3	cervix:	n/a
43	chr11:67806363-67806413	NT2-D1	testis:	n/a
44	chr11:67806337-67806387	HMEC	breast:	n/a
45	chr11:67806337-67806387	HAEpiC	amniotic membrane:	n/a
46	chr11:67806337-67806387	T-47D	breast:	n/a
47	chr11:67806347-67806397	AG09309	skin:	n/a
48	chr11:67806337-67806387	ovcar-3	ovarian:	n/a
49	chr11:67806363-67806413	GM12878	blood:	n/a
50	chr11:67806347-67806397	CMK	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67805173..67809189-chr11:67886289..67889765,4	K562	blood:
2	chr11:67803641..67806455-chr11:67892940..67895598,3	MCF-7	breast:
3	chr11:67805993..67806840-chr3:73160072..73160591,2	Hela-S3	cervix:
4	chr11:67803003..67807692-chr11:67979461..67982180,5	MCF-7	breast:
5	chr11:67805971..67806654-chr8:126442470..126443020,2	Hela-S3	cervix:
6	chr11:67770218..67773172-chr11:67805064..67808057,3	K562	blood:
7	chr11:67803608..67807840-chr11:67979633..67982182,3	K562	blood:
8	chr11:67805532..67808187-chr11:67887312..67890096,4	MCF-7	breast:
9	chr11:67805173..67807792-chr11:67887405..67889765,3	K562	blood:
10	chr11:67791829..67792701-chr11:67805432..67806435,3	MCF-7	breast:

No data

Variant related genes	Relation type
TCIRG1	TF binding region
TCIRG1	CpG island
ENSG00000255236	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000110057	Chromatin interaction
ENSG00000173334	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000110066	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
9	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
10	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
12	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
13	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
14	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
16	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
17	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
20	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking 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	61 gene(s)	inside rSNPs	diseases
21	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
22	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
23	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
24	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
25	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
26	nsv555279	chr11:67789553-67816936	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
27	nsv897848	chr11:67789837-67816936	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
28	nsv897849	chr11:67789837-67821036	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
29	nsv555280	chr11:67793014-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
30	nsv897851	chr11:67793448-67821036	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
31	nsv897852	chr11:67795066-67833543	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
32	nsv555281	chr11:67796691-67821036	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
33	nsv555282	chr11:67798567-67818325	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
34	nsv555283	chr11:67804074-67816936	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
35	nsv897853	chr11:67804074-67817876	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
36	nsv897854	chr11:67805476-67818325	Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
37	nsv897855	chr11:67805563-67842369	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 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	chr11:67799800-67806400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:67802000-67807400	Weak transcription	Dnd41	blood
3	chr11:67803600-67806400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr11:67803600-67806400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr11:67804000-67807400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:67805200-67808000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr11:67805200-67808800	Flanking Active TSS	Stomach Smooth Muscle	stomach
8	chr11:67805400-67807800	Flanking Active TSS	Liver	Liver
9	chr11:67805400-67808200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:67805400-67808600	Enhancers	Fetal Heart	heart
11	chr11:67805600-67806400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr11:67805600-67806400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:67805600-67806400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:67805600-67806400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
15	chr11:67805600-67808800	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr11:67805800-67806400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr11:67805800-67806400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
18	chr11:67805800-67806400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:67805800-67806400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr11:67805800-67806400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:67805800-67806400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr11:67805800-67806400	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr11:67805800-67806400	Flanking Active TSS	Fetal Intestine Large	intestine
24	chr11:67805800-67806400	Flanking Active TSS	Pancreas	Pancrea
25	chr11:67805800-67806400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr11:67805800-67806400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr11:67805800-67806400	Flanking Active TSS	Rectal Smooth Muscle	rectum
28	chr11:67805800-67806400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr11:67805800-67806400	Flanking Active TSS	GM12878-XiMat	blood
30	chr11:67805800-67806400	Flanking Active TSS	HSMM	muscle
31	chr11:67805800-67806400	Flanking Active TSS	Osteobl	bone
32	chr11:67805800-67806800	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr11:67805800-67807000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:67805800-67807200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:67805800-67807200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:67805800-67807200	Flanking Active TSS	Right Ventricle	heart
37	chr11:67805800-67807800	Flanking Active TSS	Fetal Intestine Small	intestine
38	chr11:67805800-67808200	Active TSS	HepG2	liver
39	chr11:67805800-67808400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:67805800-67808400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:67805800-67808400	Flanking Active TSS	Fetal Muscle Trunk	muscle
42	chr11:67805800-67808600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:67805800-67808600	Flanking Active TSS	Colonic Mucosa	Colon
44	chr11:67805800-67808600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr11:67805800-67808600	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr11:67805800-67808800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:67806000-67806400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr11:67806000-67806400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:67806000-67806400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr11:67806000-67806400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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