Variant report

Variant	rs35126317
Chromosome Location	chr12:119521563-119521564
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:119519961..119522229-chr12:119531990..119534794,2	MCF-7	breast:
2	chr12:119520274..119523110-chr12:119524611..119526386,2	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10775012	0.83[EUR][1000 genomes]
rs10849622	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10851063	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11064650	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11064652	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11609417	0.83[EUR][1000 genomes]
rs11610794	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11612123	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11612183	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11612863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11614635	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11615880	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs12228320	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs12228589	0.83[EUR][1000 genomes]
rs12305005	0.83[EUR][1000 genomes]
rs12305240	0.83[EUR][1000 genomes]
rs4766925	0.96[ASN][1000 genomes]
rs4767769	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4767772	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4767773	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4767774	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57961828	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59060630	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119513800-119523400	Weak transcription	Pancreas	Pancrea
2	chr12:119520600-119525000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:119520600-119525800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:119520600-119526800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:119520800-119525000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr12:119520800-119525800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr12:119520800-119526400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:119521000-119522000	Weak transcription	Left Ventricle	heart
9	chr12:119521000-119526000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:119521000-119535600	Weak transcription	Fetal Brain Female	brain
11	chr12:119521200-119521600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:119521200-119521600	Weak transcription	Fetal Heart	heart
13	chr12:119521200-119525800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:119521200-119537400	Weak transcription	Brain Germinal Matrix	brain

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