Variant report

Variant	rs56710909
Chromosome Location	chr10:27538072-27538073
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:27529615..27533136-chr10:27533477..27538101,8	K562	blood:
2	chr10:27442115..27444569-chr10:27537853..27541412,3	K562	blood:
3	chr10:27536677..27538349-chr10:27539935..27542436,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACBD5-1	chr10:27534782-27541235	NR_003525

Variant related genes	Relation type
ENSG00000230445	Chromatin interaction
ENSG00000120539	Chromatin interaction
ENSG00000136758	Chromatin interaction
ENSG00000107897	Chromatin interaction
ENSG00000262412	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs3818962	0.85[ASN][1000 genomes]
rs3818965	0.85[ASN][1000 genomes]
rs3818968	0.85[ASN][1000 genomes]
rs55872244	0.85[ASN][1000 genomes]
rs55884764	0.85[ASN][1000 genomes]
rs56787693	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57563582	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59935135	0.85[ASN][1000 genomes]
rs59947739	0.85[ASN][1000 genomes]
rs61607571	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61644623	1.00[EUR][1000 genomes]
rs61737707	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61737928	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7069127	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7069761	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7070377	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7070508	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7087198	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7091897	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7092591	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7092612	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs74126946	0.85[ASN][1000 genomes]
rs74126948	0.90[ASN][1000 genomes]
rs7898820	0.85[ASN][1000 genomes]
rs7912056	0.85[ASN][1000 genomes]
rs7913638	0.85[ASN][1000 genomes]
rs7914017	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422253	chr10:27431366-27575370	Strong transcription Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3337781	chr10:27472216-27666703	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv947786	chr10:27535141-27541912	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27532600-27540400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:27532600-27541200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:27532600-27541200	Weak transcription	Esophagus	oesophagus
4	chr10:27532600-27541200	Weak transcription	Pancreas	Pancrea
5	chr10:27532600-27541200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr10:27532800-27541000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr10:27532800-27541000	Weak transcription	Adipose Nuclei	Adipose
8	chr10:27532800-27541200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr10:27532800-27541200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr10:27532800-27541200	Weak transcription	Right Ventricle	heart
11	chr10:27533000-27541000	Weak transcription	Hela-S3	cervix
12	chr10:27533000-27541200	Weak transcription	Primary T cells from cord blood	blood
13	chr10:27533000-27541200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:27533000-27541200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:27533000-27541200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr10:27533000-27541200	Weak transcription	Brain Substantia Nigra	brain
17	chr10:27533000-27541200	Weak transcription	Fetal Kidney	kidney
18	chr10:27536400-27541200	Weak transcription	Fetal Intestine Large	intestine
19	chr10:27536400-27541200	Weak transcription	Fetal Intestine Small	intestine
20	chr10:27537000-27538200	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr10:27537200-27541200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:27537200-27541200	Weak transcription	Fetal Muscle Leg	muscle
23	chr10:27537200-27541200	Weak transcription	Right Atrium	heart
24	chr10:27537200-27541400	Weak transcription	Psoas Muscle	Psoas
25	chr10:27538000-27538400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:27538000-27541200	Weak transcription	Left Ventricle	heart
27	chr10:27538000-27541200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr10:27538000-27547200	Weak transcription	Fetal Heart	heart

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