Variant report

Variant	rs57934416
Chromosome Location	chr16:11919153-11919154
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:11918375..11921492-chr16:11938739..11940419,3	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13338411	0.84[EUR][1000 genomes]
rs16958700	0.83[EUR][1000 genomes]
rs373496	0.83[EUR][1000 genomes]
rs3885011	0.83[EUR][1000 genomes]
rs4780403	1.00[EUR][1000 genomes]
rs4780406	0.83[EUR][1000 genomes]
rs4781160	0.83[EUR][1000 genomes]
rs58472329	1.00[EUR][1000 genomes]
rs7193780	0.83[EUR][1000 genomes]
rs73509738	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73509774	1.00[EUR][1000 genomes]
rs74010441	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482288	chr16:11776491-11946429	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1043909	chr16:11839910-12007435	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1042660	chr16:11846873-12110435	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11916000-11921000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr16:11916600-11928800	Weak transcription	Primary B cells from cord blood	blood
3	chr16:11918000-11919200	Flanking Active TSS	Placenta	Placenta
4	chr16:11918400-11919200	Enhancers	Fetal Intestine Large	intestine
5	chr16:11918600-11922600	Weak transcription	K562	blood
6	chr16:11918600-11929600	Weak transcription	Brain Anterior Caudate	brain
7	chr16:11918600-11929800	Weak transcription	Pancreas	Pancrea
8	chr16:11918600-11930000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr16:11918600-11930200	Weak transcription	Left Ventricle	heart
10	chr16:11918600-11933600	Weak transcription	Stomach Mucosa	stomach
11	chr16:11918600-11943800	Weak transcription	Right Atrium	heart
12	chr16:11918800-11919200	Enhancers	HepG2	liver
13	chr16:11918800-11920200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr16:11918800-11929400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr16:11918800-11930000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr16:11918800-11930000	Weak transcription	Hela-S3	cervix
17	chr16:11918800-11930200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr16:11918800-11930200	Weak transcription	Colon Smooth Muscle	Colon
19	chr16:11919000-11929600	Weak transcription	Brain Hippocampus Middle	brain
20	chr16:11919000-11929800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr16:11919000-11930000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr16:11919000-11930000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr16:11919000-11930200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr16:11919000-11930400	Weak transcription	Right Ventricle	heart
25	chr16:11919000-11931400	Weak transcription	Small Intestine	intestine

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