Variant report

Variant	rs17653133
Chromosome Location	chr15:38921861-38921862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:38909645..38913032-chr15:38921609..38923824,3	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs16967103	0.83[EUR][1000 genomes]
rs16967104	0.84[EUR][1000 genomes]
rs16967112	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16967120	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17574546	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17651741	1.00[CHD][hapmap];0.87[TSI][hapmap]
rs17652674	0.84[EUR][1000 genomes]
rs4614699	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55762999	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55791667	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56083426	0.82[EUR][1000 genomes]
rs56165729	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56249992	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56279249	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59659806	0.86[EUR][1000 genomes]
rs60455438	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60924694	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61109886	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61573680	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7164418	0.81[EUR][1000 genomes]
rs7171171	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7173588	0.81[EUR][1000 genomes]
rs72729306	0.83[EUR][1000 genomes]
rs72729314	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72729320	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72729321	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72729322	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs883625	0.87[EUR][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

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs17653133	RASGRP1	cis	Esophagus Mucosa	GTEx
rs17653133	C15orf41	cis	cerebellum	SCAN
rs17653133	ARHGAP11A	cis	parietal	SCAN
rs17653133	C15orf54	cis	parietal	SCAN
rs17653133	RASGRP1	Cis_1M	lymphoblastoid	RTeQTL
rs17653133	RASGRP1	cis	normal skin	skin_eQTL
rs17653133	RASGRP1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:38914800-38922000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:38916400-38923000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr15:38916800-38922800	Weak transcription	GM12878-XiMat	blood
4	chr15:38918800-38923200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr15:38919200-38922800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:38919200-38923400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr15:38919400-38922000	Weak transcription	Thymus	Thymus
8	chr15:38919400-38922800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr15:38919400-38923200	Weak transcription	Primary T cells from cord blood	blood
10	chr15:38919400-38923200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr15:38919400-38923200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr15:38919400-38923400	Weak transcription	Dnd41	blood
13	chr15:38919400-38923600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr15:38919400-38923600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr15:38919400-38923800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr15:38919600-38923400	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr15:38920200-38922000	Weak transcription	Fetal Thymus	thymus
18	chr15:38920200-38924000	Weak transcription	Fetal Brain Female	brain
19	chr15:38921600-38922400	Enhancers	Fetal Brain Male	brain
20	chr15:38921800-38922000	Enhancers	Primary T helper cells PMA-I stimulated	--

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