Variant report

Variant	rs7032542
Chromosome Location	chr9:97837938-97837939
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97584438..97586291-chr9:97836319..97838508,2	MCF-7	breast:
2	chr9:97836720..97838496-chr9:97862659..97865053,2	MCF-7	breast:
3	chr9:97830414..97832862-chr9:97837020..97839088,2	K562	blood:
4	chr9:97824520..97826312-chr9:97836081..97838714,2	MCF-7	breast:
5	chr9:97836263..97838826-chr9:97847053..97849837,2	MCF-7	breast:
6	chr9:97821527..97823304-chr9:97837475..97839849,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000207617	Chromatin interaction
ENSG00000207563	Chromatin interaction
ENSG00000207864	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs4647559	0.81[AFR][1000 genomes]
rs55708950	0.94[AFR][1000 genomes]
rs55838201	0.94[AFR][1000 genomes]
rs57232080	1.00[AFR][1000 genomes]
rs58038897	1.00[AFR][1000 genomes]
rs59149855	0.94[AFR][1000 genomes]
rs59274098	0.87[AFR][1000 genomes]
rs60070508	1.00[AFR][1000 genomes]
rs7032704	1.00[AFR][1000 genomes]
rs73654505	0.81[AFR][1000 genomes]
rs73654506	1.00[AFR][1000 genomes]
rs73654507	1.00[AFR][1000 genomes]
rs73654508	1.00[AFR][1000 genomes]
rs73654509	1.00[AFR][1000 genomes]
rs73654510	1.00[AFR][1000 genomes]
rs73654511	1.00[AFR][1000 genomes]
rs73654512	0.94[AFR][1000 genomes]
rs73654513	1.00[AFR][1000 genomes]
rs73654514	1.00[AFR][1000 genomes]
rs73654515	0.94[AFR][1000 genomes]
rs73654516	1.00[AFR][1000 genomes]
rs73654517	0.86[AFR][1000 genomes]
rs73654518	0.81[AFR][1000 genomes]
rs73654520	0.81[AFR][1000 genomes]
rs73654521	0.81[AFR][1000 genomes]
rs73654522	0.81[AFR][1000 genomes]
rs73654523	0.81[AFR][1000 genomes]
rs73654525	0.81[AFR][1000 genomes]
rs73654526	0.81[AFR][1000 genomes]
rs73654528	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933919	chr9:97619512-97919344	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
2	nsv1038106	chr9:97793038-97881416	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
3	nsv1038523	chr9:97797032-97923774	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
4	nsv540175	chr9:97797032-97923774	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
5	nsv831656	chr9:97831551-97989980	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97813000-97873000	Weak transcription	K562	blood
2	chr9:97820000-97854200	Weak transcription	Fetal Brain Male	brain
3	chr9:97820400-97840800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:97820400-97843000	Weak transcription	Primary T cells from cord blood	blood
5	chr9:97820600-97875000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr9:97821000-97838400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:97821200-97839000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:97821200-97839600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:97821400-97843200	Weak transcription	Fetal Brain Female	brain
10	chr9:97822800-97845400	Weak transcription	Primary B cells from cord blood	blood
11	chr9:97823600-97845000	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr9:97824800-97844600	Weak transcription	Fetal Thymus	thymus
13	chr9:97825200-97841000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:97825400-97854400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr9:97825800-97839200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:97825800-97843400	Weak transcription	Thymus	Thymus
17	chr9:97825800-97852600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:97826000-97842800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr9:97826200-97843200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr9:97826200-97847400	Weak transcription	HUVEC	blood vessel
21	chr9:97826400-97842800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:97826400-97844200	Weak transcription	GM12878-XiMat	blood
23	chr9:97827000-97839600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:97827800-97841400	Genic enhancers	Liver	Liver
25	chr9:97828200-97838800	Strong transcription	Fetal Intestine Large	intestine
26	chr9:97829200-97838400	Genic enhancers	Brain Hippocampus Middle	brain
27	chr9:97829800-97838000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:97830600-97843200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr9:97830600-97844800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr9:97830800-97838600	Strong transcription	Osteobl	bone
31	chr9:97830800-97840800	Strong transcription	NHEK	skin
32	chr9:97831000-97839000	Genic enhancers	Left Ventricle	heart
33	chr9:97831200-97841200	Genic enhancers	Pancreas	Pancrea
34	chr9:97832000-97838000	Weak transcription	Stomach Mucosa	stomach
35	chr9:97832000-97838400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
36	chr9:97832200-97840800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:97832200-97841000	Enhancers	Fetal Heart	heart
38	chr9:97833000-97838200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:97833000-97838400	Strong transcription	Fetal Intestine Small	intestine
40	chr9:97833200-97839000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:97833200-97839800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
42	chr9:97833200-97840600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:97833400-97838200	Weak transcription	Small Intestine	intestine
44	chr9:97833400-97839200	Genic enhancers	A549	lung
45	chr9:97833800-97838800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:97834200-97838600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:97834400-97838800	Strong transcription	Fetal Stomach	stomach
48	chr9:97834600-97839200	Weak transcription	NHDF-Ad	bronchial
49	chr9:97835200-97838600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:97835400-97838600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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