Variant report

Variant	rs4714000
Chromosome Location	chr6:36637597-36637598
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:36633841..36635669-chr6:36637312..36639563,2	K562	blood:
2	chr6:36524196..36527132-chr6:36635202..36638000,2	MCF-7	breast:
3	chr6:36637280..36638995-chr6:36645495..36647593,2	K562	blood:

Variant related genes	Relation type
ENSG00000124762	Chromatin interaction

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

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

rs_ID	r²[population]
rs1321312	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1969701	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1977172	0.82[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3176330	0.96[ASN][1000 genomes]
rs3176331	0.89[CHB][hapmap];0.83[CHD][hapmap];0.87[GIH][hapmap];0.93[JPT][hapmap];0.83[TSI][hapmap];0.89[ASN][1000 genomes]
rs3829966	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3829967	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3829968	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4135234	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4135237	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4135239	0.97[ASN][1000 genomes]
rs4713997	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6457936	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902994	0.85[ASN][1000 genomes]
rs6907801	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6926780	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7452626	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs762623	0.89[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.97[ASN][1000 genomes]
rs9380585	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9380586	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[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	nsv1031191	chr6:36588974-36718015	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv538201	chr6:36588974-36718015	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv602946	chr6:36633160-36641478	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
4	nsv602947	chr6:36637597-36641157	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4714000	ITPR3	cis	parietal	SCAN

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36631000-36644000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:36632000-36638800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr6:36633200-36640200	Enhancers	HepG2	liver
4	chr6:36633600-36637800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:36633800-36637800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:36634200-36637800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:36634600-36638000	Enhancers	Fetal Muscle Leg	muscle
8	chr6:36634800-36638200	Enhancers	Fetal Muscle Trunk	muscle
9	chr6:36635000-36637800	Enhancers	HSMMtube	muscle
10	chr6:36635200-36643800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:36635400-36639600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr6:36635400-36644000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr6:36635400-36645600	Weak transcription	Small Intestine	intestine
14	chr6:36635600-36644000	Weak transcription	Hela-S3	cervix
15	chr6:36635800-36637600	Weak transcription	Fetal Kidney	kidney
16	chr6:36635800-36639800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:36636000-36640800	Enhancers	Fetal Intestine Small	intestine
18	chr6:36636200-36637600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr6:36636400-36643800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:36636400-36643800	Weak transcription	NH-A	brain
21	chr6:36636800-36641000	Enhancers	Fetal Intestine Large	intestine
22	chr6:36637000-36637800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:36637000-36638000	Weak transcription	Ovary	ovary
24	chr6:36637000-36638600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr6:36637000-36643800	Weak transcription	Osteobl	bone
26	chr6:36637200-36637600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:36637200-36638200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:36637200-36638400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:36637200-36641600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:36637200-36641600	Weak transcription	GM12878-XiMat	blood
31	chr6:36637200-36643600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:36637200-36643800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:36637200-36643800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:36637200-36643800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:36637200-36643800	Weak transcription	HSMM	muscle
36	chr6:36637400-36637800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:36637400-36639800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:36637400-36642600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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