Variant report

Variant	rs7733529
Chromosome Location	chr5:68534781-68534782
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:68534182..68537947-chr5:68660840..68664102,4	K562	blood:
2	chr5:68533315..68535936-chr5:68536358..68538976,2	K562	blood:
3	chr5:68528908..68532551-chr5:68533389..68536013,4	MCF-7	breast:
4	chr5:68511993..68513624-chr5:68533582..68536463,2	MCF-7	breast:
5	chr5:68530055..68532156-chr5:68533925..68536230,3	K562	blood:
6	chr5:68529704..68533341-chr5:68533925..68536755,6	K562	blood:

Variant related genes	Relation type
ENSG00000085231	Chromatin interaction
ENSG00000134056	Chromatin interaction
ENSG00000134058	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10940206	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12651858	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12656423	0.89[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs12656449	0.94[EUR][1000 genomes]
rs12656918	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12657418	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2054977	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2069433	0.85[ASN][1000 genomes]
rs3934529	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4443380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4976158	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59515371	0.94[EUR][1000 genomes]
rs60113639	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60824482	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73121291	0.80[ASN][1000 genomes]
rs73125214	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73125295	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73127319	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73127323	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73127331	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018151	chr5:68377118-68667581	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv1035004	chr5:68405526-68670101	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv3378789	chr5:68438275-68540725	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv1795469	chr5:68534233-68565285	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7733529	CCDC125	cis	Muscle Skeletal	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68531200-68584200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:68531400-68537400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:68531400-68605000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:68531600-68554600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:68531800-68534800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:68531800-68535800	Weak transcription	Right Ventricle	heart
7	chr5:68531800-68538800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:68531800-68545800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr5:68531800-68552200	Weak transcription	Colonic Mucosa	Colon
10	chr5:68531800-68552200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:68531800-68554600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr5:68531800-68556000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:68531800-68556800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:68532000-68535000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:68532200-68551400	Weak transcription	Psoas Muscle	Psoas
16	chr5:68532200-68553400	Weak transcription	Fetal Heart	heart
17	chr5:68532400-68534800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr5:68532400-68535000	Enhancers	HMEC	breast
19	chr5:68532400-68535800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr5:68532400-68536800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr5:68532400-68537000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:68532400-68537200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:68532400-68539600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr5:68532400-68551600	Weak transcription	Ovary	ovary
25	chr5:68532400-68558600	Weak transcription	Brain Substantia Nigra	brain
26	chr5:68532400-68558800	Weak transcription	Brain Angular Gyrus	brain
27	chr5:68532400-68563600	Weak transcription	Fetal Brain Male	brain
28	chr5:68532400-68574600	Weak transcription	Spleen	Spleen
29	chr5:68532600-68536000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:68532600-68537000	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr5:68532800-68535400	Strong transcription	Fetal Stomach	stomach
32	chr5:68532800-68540800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr5:68533000-68534800	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr5:68533000-68535200	Strong transcription	Primary hematopoietic stem cells	blood
35	chr5:68533000-68535600	Strong transcription	Fetal Kidney	kidney
36	chr5:68533000-68536000	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr5:68533000-68537000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr5:68533000-68537000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:68533000-68538400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:68533000-68539200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:68533200-68534800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:68533200-68536600	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr5:68533200-68536800	Strong transcription	Primary B cells from cord blood	blood
44	chr5:68533200-68536800	Strong transcription	Fetal Intestine Small	intestine
45	chr5:68533200-68538000	Strong transcription	Fetal Thymus	thymus
46	chr5:68533200-68538400	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr5:68533200-68539200	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr5:68533200-68545800	Weak transcription	Adipose Nuclei	Adipose
49	chr5:68533200-68576800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr5:68533400-68534800	Strong transcription	Thymus	Thymus

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