Variant report

Variant	rs9863007
Chromosome Location	chr3:121425814-121425815
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12386356	0.93[EUR][1000 genomes]
rs59987610	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60154494	0.81[EUR][1000 genomes]
rs72626328	0.82[EUR][1000 genomes]
rs9637385	0.97[ASN][1000 genomes]
rs9837315	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9841861	0.93[AFR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9849087	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9854863	0.81[EUR][1000 genomes]
rs9856046	0.81[EUR][1000 genomes]
rs9859702	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9861782	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9882312	0.81[EUR][1000 genomes]
rs9968051	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[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	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv432480	chr3:121355723-121629928	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv432482	chr3:121364236-121629634	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv432481	chr3:121364236-121637178	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv829703	chr3:121383290-121534493	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9863007	IQCB1	Cis_1M	lymphoblastoid	RTeQTL
rs9863007	EAF2	Cis_1M	lymphoblastoid	RTeQTL
rs9863007	SLC15A2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121386600-121447200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:121396800-121435600	Weak transcription	Psoas Muscle	Psoas
3	chr3:121399000-121426400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr3:121399000-121440400	Weak transcription	K562	blood
5	chr3:121401200-121429400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:121401200-121434000	Weak transcription	Gastric	stomach
7	chr3:121404000-121432800	Weak transcription	Brain Angular Gyrus	brain
8	chr3:121407400-121429400	Weak transcription	Esophagus	oesophagus
9	chr3:121408200-121428400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:121408600-121427400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:121408600-121428200	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr3:121410400-121435600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr3:121411000-121432000	Weak transcription	NHEK	skin
14	chr3:121411000-121432800	Weak transcription	Fetal Brain Male	brain
15	chr3:121411000-121442400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:121411400-121432800	Weak transcription	Colonic Mucosa	Colon
17	chr3:121411400-121437200	Weak transcription	Small Intestine	intestine
18	chr3:121413400-121446200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:121414200-121428000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr3:121414800-121436200	Weak transcription	Stomach Mucosa	stomach
21	chr3:121415400-121427400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr3:121415600-121428400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr3:121417200-121430800	Weak transcription	Brain Hippocampus Middle	brain
24	chr3:121417200-121435800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:121417400-121426200	Weak transcription	Thymus	Thymus
26	chr3:121417400-121431600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr3:121417600-121430800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:121417600-121431600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr3:121417600-121432000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr3:121417600-121432000	Weak transcription	Fetal Brain Female	brain
31	chr3:121417600-121432800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:121417600-121432800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr3:121417600-121434200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:121417600-121434200	Weak transcription	Aorta	Aorta
35	chr3:121417600-121435200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr3:121417600-121437200	Weak transcription	Spleen	Spleen
37	chr3:121417800-121431600	Weak transcription	HSMMtube	muscle
38	chr3:121418000-121432000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:121418000-121434200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr3:121418000-121435400	Weak transcription	NHLF	lung
41	chr3:121418800-121442000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:121419600-121436200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr3:121419800-121434400	Weak transcription	HUVEC	blood vessel
44	chr3:121420200-121426200	Weak transcription	Fetal Thymus	thymus
45	chr3:121420200-121426200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr3:121420200-121432600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr3:121420200-121433000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr3:121420400-121432000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr3:121420600-121429400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:121420800-121430800	Weak transcription	Fetal Kidney	kidney

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