Variant report

Variant	rs7517360
Chromosome Location	chr1:10052214-10052215
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	chr1:10039534..10042218-chr1:10050029..10052647,2	K562	blood:

Variant related genes	Relation type
ENSG00000173614	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10779734	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11121510	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11121512	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11828	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12140009	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12140015	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12140058	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1220389	0.86[ASN][1000 genomes]
rs1220397	0.81[ASN][1000 genomes]
rs1220399	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1220400	0.87[ASN][1000 genomes]
rs1220402	0.88[ASN][1000 genomes]
rs1220420	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1220421	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1220424	0.88[ASN][1000 genomes]
rs1234694	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1628143	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1660733	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2890358	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2919694	0.84[ASN][1000 genomes]
rs3003376	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3003377	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3003378	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3013783	0.84[ASN][1000 genomes]
rs3013784	0.90[ASN][1000 genomes]
rs3013788	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3123522	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58528460	0.82[ASN][1000 genomes]
rs6541073	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6661806	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6664631	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6678023	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6680076	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7517806	0.89[ASN][1000 genomes]
rs7517812	0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7539191	0.91[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	esv3385337	chr1:9105242-10082223	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	549 gene(s)	inside rSNPs	diseases
2	esv3417409	chr1:9683992-10241703	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv3372906	chr1:9838995-10052992	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv1012469	chr1:9925714-10147796	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1012301	chr1:9963962-10118393	Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv534853	chr1:9963962-10118393	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv1001742	chr1:9971776-10116767	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7517360	LZIC	Cis_1M	lymphoblastoid	RTeQTL
rs7517360	LZIC	cis	multi-tissue	Pritchard

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10032800-10057000	Weak transcription	Psoas Muscle	Psoas
2	chr1:10037200-10054600	Weak transcription	Fetal Brain Female	brain
3	chr1:10039600-10053600	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:10042600-10053800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:10042800-10053000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:10042800-10055600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:10042800-10056600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:10042800-10057200	Weak transcription	Gastric	stomach
9	chr1:10044600-10054800	Weak transcription	Fetal Intestine Large	intestine
10	chr1:10044800-10056000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:10045200-10053200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:10045400-10056600	Weak transcription	Brain Angular Gyrus	brain
13	chr1:10045400-10057000	Weak transcription	Brain Substantia Nigra	brain
14	chr1:10045600-10056600	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:10045600-10056600	Weak transcription	Fetal Heart	heart
16	chr1:10046200-10057000	Weak transcription	Ovary	ovary
17	chr1:10046400-10054800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr1:10047200-10052400	Weak transcription	Fetal Stomach	stomach
19	chr1:10049000-10054200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:10049600-10052400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:10049600-10054000	Enhancers	Adipose Nuclei	Adipose
22	chr1:10050000-10052600	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:10050800-10052600	Weak transcription	Right Atrium	heart
24	chr1:10050800-10053000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr1:10050800-10056600	Weak transcription	Right Ventricle	heart
26	chr1:10051200-10052800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:10051400-10055400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:10051600-10052400	Enhancers	Spleen	Spleen
29	chr1:10051600-10052800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:10051600-10053400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr1:10051600-10056600	Weak transcription	Placenta	Placenta
32	chr1:10051800-10053000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:10051800-10054000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr1:10051800-10056800	Weak transcription	Liver	Liver
35	chr1:10052000-10053400	Enhancers	Primary B cells from cord blood	blood
36	chr1:10052200-10052600	Enhancers	Left Ventricle	heart

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