Variant report

Variant	rs11037878
Chromosome Location	chr11:5527218-5527219
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:5525497-5527420	K562	blood:	n/a	n/a
2	ZNF143	chr11:5526409-5527277	K562	blood:	n/a	n/a
3	POLR2A	chr11:5524438-5527237	K562	blood:	n/a	n/a
4	MAX	chr11:5526712-5527233	K562	blood:	n/a	n/a
5	SIN3AK20	chr11:5526362-5527542	HCT-116	colon:	n/a	n/a
6	POLR2A	chr11:5526603-5527265	HCT-116	colon:	n/a	n/a
7	POLR2A	chr11:5526550-5527231	HCT-116	colon:	n/a	n/a
8	TBL1XR1	chr11:5525561-5527529	K562	blood:	n/a	n/a
9	CBX3	chr11:5526652-5527237	K562	blood:	n/a	n/a
10	ZBTB33	chr11:5526613-5527220	K562	blood:	n/a	n/a
11	HCFC1	chr11:5526655-5527466	K562	blood:	n/a	n/a
12	MYC	chr11:5526577-5527249	K562	blood:	n/a	n/a
13	CHD2	chr11:5526388-5527678	K562	blood:	n/a	n/a
14	POLR2A	chr11:5525399-5527227	K562	blood:	n/a	n/a
15	MYC	chr11:5526657-5527325	K562	blood:	n/a	n/a
16	HEY1	chr11:5525385-5527240	K562	blood:	n/a	n/a
17	GTF2B	chr11:5526589-5527331	K562	blood:	n/a	n/a
18	POLR2A	chr11:5523226-5527268	K562	blood:	n/a	n/a
19	ZBTB33	chr11:5526501-5527233	HCT-116	colon:	n/a	n/a
20	TBP	chr11:5525476-5527354	K562	blood:	n/a	n/a
21	POLR2A	chr11:5519727-5527234	K562	blood:	n/a	n/a
22	POLR2A	chr11:5525344-5527317	HCT-116	colon:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:5524818..5527723-chr11:5704615..5707499,2	K562	blood:
2	chr11:5526007..5528692-chr11:5548871..5550699,2	K562	blood:
3	chr11:5526297..5528707-chr11:5655729..5658397,2	K562	blood:
4	chr11:5522829..5527225-chr11:5617678..5621647,5	K562	blood:
5	chr11:5523660..5528079-chr11:5704615..5707879,4	K562	blood:
6	chr11:5526569..5527262-chr7:148580950..148581596,2	HCT-116	colon:
7	chr11:5523708..5530495-chr11:5543485..5554743,19	K562	blood:
8	chr11:5527022..5529491-chr11:5577103..5579456,2	K562	blood:
9	chr11:5525343..5528294-chr11:5586982..5589014,2	K562	blood:
10	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000167355	TF binding region
HBE1	TF binding region
HBG2	TF binding region
ENSG00000224091	Chromatin interaction
ENSG00000258588	Chromatin interaction
ENSG00000224295	Chromatin interaction
ENSG00000233646	Chromatin interaction
ENSG00000249633	Chromatin interaction
ENSG00000258659	Chromatin interaction
ENSG00000106462	Chromatin interaction
ENSG00000121236	Chromatin interaction
ENSG00000132256	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11037877	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11037879	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16931951	0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16931955	0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048608	chr11:5328516-5645179	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
2	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers 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 target site	89 gene(s)	inside rSNPs	diseases
3	nsv832057	chr11:5375585-5576200	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
4	nsv896939	chr11:5497799-5809548	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv467670	chr11:5506034-5550630	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv553240	chr11:5506034-5550630	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv553241	chr11:5506034-6203685	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5527200-5527400	Flanking Active TSS	K562	blood

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