Variant report

Variant	rs9920715
Chromosome Location	chr15:38916906-38916907
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:38900766..38902547-chr15:38915124..38917930,2	MCF-7	breast:
2	chr15:38916571..38918602-chr15:38924024..38925641,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11073341	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11073344	0.82[EUR][1000 genomes]
rs62006173	0.84[ASN][1000 genomes]
rs924005	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949171	chr15:38232548-39033746	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv904085	chr15:38786114-38985513	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1046994	chr15:38806163-39239014	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv525770	chr15:38816833-39084956	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1054651	chr15:38827825-39082844	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv542358	chr15:38827825-39082844	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv904086	chr15:38829198-38931396	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:38910800-38918000	Weak transcription	Left Ventricle	heart
2	chr15:38912800-38917200	Enhancers	Fetal Intestine Large	intestine
3	chr15:38913400-38918200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr15:38913400-38918400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr15:38913400-38918400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr15:38913400-38918600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:38913600-38918000	Weak transcription	Fetal Heart	heart
8	chr15:38913600-38918000	Weak transcription	Dnd41	blood
9	chr15:38913600-38918200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:38913600-38918200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr15:38913600-38918200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr15:38913600-38918400	Weak transcription	Primary T cells from cord blood	blood
13	chr15:38913600-38918400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr15:38913800-38918200	Weak transcription	Thymus	Thymus
15	chr15:38913800-38918400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr15:38913800-38918400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr15:38913800-38918600	Weak transcription	Fetal Kidney	kidney
18	chr15:38913800-38919200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr15:38914200-38918000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr15:38914400-38918000	Weak transcription	Fetal Brain Male	brain
21	chr15:38914600-38917000	Enhancers	Fetal Intestine Small	intestine
22	chr15:38914600-38918400	Weak transcription	Fetal Brain Female	brain
23	chr15:38914800-38922000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:38916000-38918200	Weak transcription	Fetal Thymus	thymus
25	chr15:38916200-38918200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr15:38916400-38918400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr15:38916400-38923000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr15:38916800-38917200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr15:38916800-38918000	Weak transcription	Placenta	Placenta
30	chr15:38916800-38918600	Weak transcription	Fetal Muscle Leg	muscle
31	chr15:38916800-38922800	Weak transcription	GM12878-XiMat	blood

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