Variant report

Variant	rs12879905
Chromosome Location	chr14:69825614-69825615
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:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:69808456..69811857-chr14:69822855..69826097,4	MCF-7	breast:
2	chr14:69821172..69826934-chr14:69835934..69842143,9	MCF-7	breast:
3	chr14:69825390..69827894-chr14:69869921..69871865,2	MCF-7	breast:
4	chr14:69823108..69825691-chr14:69865001..69866828,2	MCF-7	breast:
5	chr14:69824235..69826782-chr14:69843380..69845607,3	MCF-7	breast:
6	chr14:69820575..69822363-chr14:69824777..69827563,2	MCF-7	breast:
7	chr14:69810682..69812571-chr14:69823617..69825729,2	MCF-7	breast:
8	chr14:69822349..69827857-chr14:69829114..69832930,7	MCF-7	breast:
9	chr14:69791053..69792994-chr14:69824210..69827110,2	MCF-7	breast:
10	chr14:69824029..69825880-chr14:69851725..69853417,2	MCF-7	breast:
11	chr14:69823834..69826023-chr14:69826399..69829100,3	MCF-7	breast:
12	chr14:69811705..69814388-chr14:69822919..69825901,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALNTL1-1	chr14:69823727-69826025	NONHSAT037522

No data

No data

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1026385	1.00[AFR][1000 genomes]
rs12884741	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12890434	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12893308	1.00[AFR][1000 genomes]
rs17106981	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17107007	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34112413	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34531312	1.00[AFR][1000 genomes]
rs34531959	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34644391	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34765661	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35593122	1.00[AFR][1000 genomes]
rs35876363	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs45557240	1.00[AFR][1000 genomes]
rs59831177	1.00[AFR][1000 genomes]
rs71423358	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423359	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423360	1.00[AFR][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	nsv456334	chr14:69793624-69831037	Strong transcription Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv564966	chr14:69793624-69831037	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69815600-69838800	Weak transcription	Brain Germinal Matrix	brain
2	chr14:69818400-69827400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:69818600-69842800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr14:69821000-69838800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:69821000-69839600	Weak transcription	Fetal Brain Female	brain
6	chr14:69821800-69827200	Weak transcription	Fetal Intestine Small	intestine
7	chr14:69821800-69852400	Weak transcription	Spleen	Spleen
8	chr14:69822000-69829600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr14:69822600-69825800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr14:69823000-69827000	Weak transcription	Primary B cells from cord blood	blood
11	chr14:69823000-69827000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr14:69823000-69829200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr14:69823200-69827400	Weak transcription	NHDF-Ad	bronchial
14	chr14:69824200-69826000	Enhancers	GM12878-XiMat	blood
15	chr14:69824200-69864000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:69825200-69825800	Enhancers	Brain Anterior Caudate	brain
17	chr14:69825400-69825800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:69825600-69825800	Enhancers	Stomach Mucosa	stomach

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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