Variant report

Variant	rs73771110
Chromosome Location	chr5:90192654-90192655
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:90186001..90188260-chr5:90191699..90193353,2	MCF-7	breast:
2	chr5:90189989..90193986-chr5:90677446..90680190,4	K562	blood:
3	chr5:90162422..90165076-chr5:90191582..90194100,2	MCF-7	breast:
4	chr5:90190412..90192818-chr5:90363374..90365459,2	K562	blood:
5	chr5:90185745..90188136-chr5:90190208..90193028,2	K562	blood:

Variant related genes	Relation type
ENSG00000113369	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10942615	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10942616	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10942617	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11948100	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11956677	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12658466	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16869291	0.81[EUR][1000 genomes]
rs1818350	0.89[EUR][1000 genomes]
rs1828175	0.83[EUR][1000 genomes]
rs36088173	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4362971	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4382198	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4916692	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4916824	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4916825	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4916830	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56851353	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58258039	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59665236	0.81[EUR][1000 genomes]
rs61006221	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61130831	0.81[EUR][1000 genomes]
rs6863794	0.81[EUR][1000 genomes]
rs6886778	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6889598	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6893164	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73771113	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73771115	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73771117	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73771118	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73771119	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv517049	chr5:90003131-90262475	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	esv2754394	chr5:90181320-90225796	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90163600-90194400	Weak transcription	Pancreas	Pancrea
2	chr5:90185000-90226600	Weak transcription	K562	blood
3	chr5:90186400-90218000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr5:90186600-90193600	Weak transcription	Hela-S3	cervix
5	chr5:90190400-90194400	Weak transcription	Stomach Mucosa	stomach
6	chr5:90191000-90194400	Enhancers	Liver	Liver
7	chr5:90191400-90192800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr5:90191400-90193800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:90191600-90192800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:90191800-90192800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr5:90191800-90192800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:90191800-90193400	Weak transcription	HepG2	liver
13	chr5:90191800-90193600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:90191800-90195000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:90192000-90192800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr5:90192000-90193600	Weak transcription	Esophagus	oesophagus
17	chr5:90192200-90192800	Enhancers	Gastric	stomach
18	chr5:90192600-90192800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:90192600-90192800	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr5:90192600-90193000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr5:90192600-90193600	Weak transcription	Fetal Intestine Small	intestine
22	chr5:90192600-90193600	Enhancers	A549	lung

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