Variant report

Variant	rs7810135
Chromosome Location	chr7:86545305-86545306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:86540771..86562582-chr7:86776173..86789890,50	K562	blood:
2	chr7:86543997..86548928-chr7:86780247..86785232,8	K562	blood:
3	chr7:86543705..86546305-chr7:86790604..86792162,2	K562	blood:
4	chr7:86543872..86545996-chr7:86848026..86850410,2	MCF-7	breast:
5	chr7:86540155..86542887-chr7:86543292..86546028,3	K562	blood:
6	chr7:86535930..86538220-chr7:86544113..86545805,2	K562	blood:
7	chr7:86542363..86546305-chr7:86789977..86792162,3	K562	blood:

Variant related genes	Relation type
ENSG00000135164	Chromatin interaction
ENSG00000200397	Chromatin interaction
ENSG00000224046	Chromatin interaction
ENSG00000135185	Chromatin interaction
ENSG00000164659	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1014634	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10232633	0.88[EUR][1000 genomes]
rs10236047	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10236910	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10257473	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10258008	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.92[TSI][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10263372	1.00[CEU][hapmap]
rs10267763	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10271867	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.92[TSI][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11974622	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.94[MKK][hapmap];0.92[TSI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11976876	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11979332	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11981220	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12111888	1.00[CEU][hapmap]
rs12113681	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12704299	0.91[CHB][hapmap]
rs1476455	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1557665	1.00[CEU][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17161067	1.00[CEU][hapmap]
rs17161070	0.89[EUR][1000 genomes]
rs17161096	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17161098	1.00[CEU][hapmap]
rs17161118	1.00[CEU][hapmap]
rs17697806	0.95[ASN][1000 genomes]
rs17697878	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17697894	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17765493	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2299231	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[GIH][hapmap];0.92[TSI][hapmap];0.88[EUR][1000 genomes]
rs2373361	1.00[CEU][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.86[TSI][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28490267	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28583791	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28635668	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61082072	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6965029	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6965383	1.00[CHB][hapmap]
rs6972489	1.00[CEU][hapmap]
rs73382375	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73382388	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73382401	0.90[EUR][1000 genomes]
rs73384105	0.90[EUR][1000 genomes]
rs7781178	0.91[CHB][hapmap]
rs7781414	0.82[CHB][hapmap]
rs7781782	1.00[CEU][hapmap]
rs7783745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7807203	1.00[CHB][hapmap]
rs7808623	1.00[CEU][hapmap]
rs9640574	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1025277	chr7:86299224-87206007	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv538999	chr7:86299224-87206007	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv532147	chr7:86299225-87121975	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv1015870	chr7:86490491-86802320	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
6	nsv539000	chr7:86490491-86802320	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
7	nsv527889	chr7:86496042-86832603	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	esv1802698	chr7:86539563-86560268	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7810135	STEAP4	cis	cerebellum	SCAN

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86495800-86550000	Weak transcription	Lung	lung
2	chr7:86498400-86576200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:86507000-86553200	Weak transcription	Pancreas	Pancrea
4	chr7:86507400-86561400	Weak transcription	Aorta	Aorta
5	chr7:86508000-86551200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:86508000-86560800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:86508000-86566800	Weak transcription	Brain Anterior Caudate	brain
8	chr7:86516000-86556400	Weak transcription	Fetal Stomach	stomach
9	chr7:86518000-86568800	Weak transcription	Psoas Muscle	Psoas
10	chr7:86518000-86577000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:86521000-86576400	Weak transcription	Hela-S3	cervix
12	chr7:86527000-86577000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:86527200-86575800	Weak transcription	Left Ventricle	heart
14	chr7:86530400-86568400	Weak transcription	Brain Hippocampus Middle	brain
15	chr7:86531200-86568800	Weak transcription	Brain Angular Gyrus	brain
16	chr7:86535600-86547200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr7:86537800-86553800	Weak transcription	Stomach Mucosa	stomach
18	chr7:86539200-86578800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:86539600-86568000	Weak transcription	Fetal Brain Male	brain
20	chr7:86539800-86555400	Weak transcription	Brain Germinal Matrix	brain
21	chr7:86540800-86567400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:86541400-86552400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr7:86541600-86568800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:86541800-86554200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr7:86542400-86546800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr7:86542400-86548000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr7:86542400-86549000	Weak transcription	Brain Substantia Nigra	brain
28	chr7:86542600-86554400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr7:86542800-86547400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:86543200-86568800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr7:86543400-86571400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:86543600-86545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:86543600-86545800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr7:86543600-86546800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:86543600-86546800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr7:86543600-86554200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:86543600-86555600	Weak transcription	K562	blood
38	chr7:86543600-86560800	Weak transcription	HUVEC	blood vessel
39	chr7:86543600-86566600	Weak transcription	Adipose Nuclei	Adipose
40	chr7:86543800-86547600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr7:86544200-86545600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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