Variant report

Variant	rs16958292
Chromosome Location	chr15:74097901-74097902
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:73923170..73926616-chr15:74097721..74100835,3	MCF-7	breast:
2	chr15:74087708..74090506-chr15:74096468..74098729,2	MCF-7	breast:
3	chr15:74096413..74099919-chr15:74101380..74103863,3	K562	blood:

Variant related genes	Relation type
ENSG00000156642	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12438304	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442248	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442263	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16958300	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28576159	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28628284	0.82[AFR][1000 genomes]
rs72743363	0.90[EUR][1000 genomes]
rs9920550	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][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	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74088200-74100200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr15:74089600-74101800	Weak transcription	Spleen	Spleen
3	chr15:74092000-74099400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:74092400-74098400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr15:74092600-74099200	Enhancers	Fetal Brain Female	brain
6	chr15:74092800-74099600	Enhancers	Fetal Brain Male	brain
7	chr15:74093600-74099200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr15:74095800-74098000	Enhancers	Brain Cingulate Gyrus	brain
9	chr15:74096400-74099400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:74096400-74103000	Weak transcription	Right Ventricle	heart
11	chr15:74096600-74098600	Enhancers	HepG2	liver
12	chr15:74096600-74101600	Weak transcription	Right Atrium	heart
13	chr15:74096600-74101800	Weak transcription	Left Ventricle	heart
14	chr15:74096600-74102200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr15:74097000-74098000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr15:74097000-74098200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:74097200-74098000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr15:74097400-74099200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:74097400-74100000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:74097800-74098000	Bivalent Enhancer	Fetal Muscle Leg	muscle
21	chr15:74097800-74101800	Weak transcription	Brain Angular Gyrus	brain
22	chr15:74097800-74102000	Weak transcription	Brain Hippocampus Middle	brain
23	chr15:74097800-74110200	Weak transcription	Brain Germinal Matrix	brain

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