Variant report

Variant	rs17773381
Chromosome Location	chr11:16981213-16981214
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:16759050..16760785-chr11:16980346..16982493,2	MCF-7	breast:
2	chr11:16980702..16983607-chr11:16983722..16985302,2	MCF-7	breast:
3	chr11:16975602..16978503-chr11:16980370..16983065,3	MCF-7	breast:
4	chr11:16980966..16983226-chr11:17033903..17037153,3	MCF-7	breast:
5	chr11:16980630..16982721-chr11:16985840..16988789,2	MCF-7	breast:
6	chr11:16970516..16973330-chr11:16980967..16983342,2	K562	blood:
7	chr11:16978536..16981349-chr11:16989679..16991819,2	K562	blood:
8	chr11:16980989..16984063-chr11:16991605..16994714,3	MCF-7	breast:
9	chr11:16978286..16981863-chr11:16983113..16986432,3	K562	blood:
10	chr11:16971713..16981548-chr11:17031573..17039006,21	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000110696	Chromatin interaction
ENSG00000166689	Chromatin interaction
ENSG00000184669	Chromatin interaction
ENSG00000110693	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs10741714	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10741715	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10766361	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.90[MKK][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10766363	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832702	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832704	0.89[CEU][hapmap];0.90[GIH][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs10832705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11024080	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs11024085	0.87[EUR][1000 genomes]
rs11827202	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12362815	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs17700056	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs1860026	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756877	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757448	0.89[CEU][hapmap];0.86[GIH][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs4757455	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6486327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7104003	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117795	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7119088	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7130314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72865768	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7934117	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832077	chr11:16834545-17059176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv7689	chr11:16945953-16990852	Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17773381	TEAD1	cis	parietal	SCAN
rs17773381	TSG101	cis	cerebellum	SCAN

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16955600-16991000	Weak transcription	Right Atrium	heart
2	chr11:16964200-16981400	Weak transcription	Gastric	stomach
3	chr11:16968000-16989800	Weak transcription	Esophagus	oesophagus
4	chr11:16968800-16984400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:16973600-16982600	Enhancers	Fetal Intestine Large	intestine
6	chr11:16975400-16990600	Weak transcription	Spleen	Spleen
7	chr11:16978000-16981400	Enhancers	Fetal Intestine Small	intestine
8	chr11:16978600-16981600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:16978600-16987600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr11:16978600-16988400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:16979800-16982200	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr11:16979800-16983400	Enhancers	Stomach Mucosa	stomach
13	chr11:16980000-16982400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr11:16980200-16982200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr11:16980200-16982400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:16980200-16982600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr11:16980200-16983800	Enhancers	HepG2	liver
18	chr11:16980400-16981800	Enhancers	Small Intestine	intestine
19	chr11:16980400-16982000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:16980400-16982600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr11:16980600-16981400	Enhancers	Brain Anterior Caudate	brain
22	chr11:16980600-16981400	Weak transcription	Placenta	Placenta
23	chr11:16980600-16982000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:16980600-16982200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr11:16980600-16982200	Enhancers	Fetal Lung	lung
26	chr11:16980600-16982400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:16980600-16982800	Enhancers	Duodenum Mucosa	Duodenum
28	chr11:16980600-16983200	Enhancers	Fetal Heart	heart
29	chr11:16980800-16981600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr11:16981000-16981600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr11:16981000-16981800	Weak transcription	Liver	Liver
32	chr11:16981000-16982400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:16981000-16982600	Enhancers	Pancreas	Pancrea
34	chr11:16981200-16981600	Enhancers	Thymus	Thymus
35	chr11:16981200-16982000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:16981200-16982400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:16981200-16984400	Weak transcription	GM12878-XiMat	blood
38	chr11:16981200-16987800	Weak transcription	Fetal Kidney	kidney

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