Variant report

Variant	rs10141933
Chromosome Location	chr14:21949950-21949951
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr14:21949512-21949988	HepG2	liver:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21942911..21947036-chr14:21948493..21952401,7	MCF-7	breast:
2	chr14:21949379..21951265-chr14:21955547..21957612,2	K562	blood:
3	chr14:21948837..21951421-chr14:21953212..21956640,4	MCF-7	breast:
4	chr14:21945001..21948392-chr14:21948946..21951939,4	K562	blood:
5	chr14:21923120..21925863-chr14:21948762..21952189,3	MCF-7	breast:
6	chr14:21949289..21951385-chr14:21959586..21961238,2	MCF-7	breast:

No data

Variant related genes	Relation type
RAB2B	TF binding region
ENSG00000092203	Chromatin interaction
ENSG00000100888	Chromatin interaction
ENSG00000129472	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10142478	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10143000	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1045842	0.87[EUR][1000 genomes]
rs11156996	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1263788	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1263790	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1263792	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1263795	0.81[AMR][1000 genomes]
rs1263797	1.00[ASN][1000 genomes]
rs1263798	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1794219	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1999139	0.89[EUR][1000 genomes]
rs3762160	0.80[ASN][1000 genomes]
rs3762162	0.83[ASN][1000 genomes]
rs6571843	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6571844	0.86[ASN][1000 genomes]
rs6571845	0.85[ASN][1000 genomes]
rs6571856	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7151259	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157961	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7159433	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8005163	0.85[ASN][1000 genomes]
rs8013109	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	esv3518898	chr14:21805983-22077584	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	esv3518899	chr14:21805983-22077584	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv1054013	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv541991	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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	31 gene(s)	inside rSNPs	diseases
9	nsv530011	chr14:21876973-21985341	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	esv2422459	chr14:21931624-22169502	Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
11	esv994931	chr14:21947144-21956367	Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10141933	TOX4	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21946000-21960600	Weak transcription	Small Intestine	intestine
2	chr14:21946200-21955600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:21946200-21955600	Weak transcription	Gastric	stomach
4	chr14:21946200-21955600	Weak transcription	Left Ventricle	heart
5	chr14:21946200-21955600	Weak transcription	Ovary	ovary
6	chr14:21946200-21955600	Weak transcription	Thymus	Thymus
7	chr14:21946200-21977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:21946400-21952000	Weak transcription	Lung	lung
9	chr14:21946400-21952600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:21946400-21952800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:21946400-21955400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:21946400-21955600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr14:21946400-21958000	Weak transcription	Pancreas	Pancrea
14	chr14:21946400-21958800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:21946400-21960800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:21946400-21971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:21946600-21950400	Weak transcription	Primary B cells from cord blood	blood
18	chr14:21946600-21954600	Weak transcription	HSMMtube	muscle
19	chr14:21946600-21954800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr14:21946600-21954800	Weak transcription	K562	blood
21	chr14:21946600-21955000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:21946600-21955000	Weak transcription	Fetal Thymus	thymus
23	chr14:21946600-21955400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr14:21946600-21955400	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr14:21946600-21955600	Weak transcription	Brain Germinal Matrix	brain
26	chr14:21946600-21955600	Weak transcription	Colonic Mucosa	Colon
27	chr14:21946600-21955600	Weak transcription	Fetal Muscle Leg	muscle
28	chr14:21946600-21955600	Weak transcription	Psoas Muscle	Psoas
29	chr14:21946600-21955600	Weak transcription	Right Ventricle	heart
30	chr14:21946600-21955600	Weak transcription	Spleen	Spleen
31	chr14:21946600-21955800	Weak transcription	Fetal Brain Female	brain
32	chr14:21946600-21958000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr14:21946600-21960400	Weak transcription	Stomach Mucosa	stomach
34	chr14:21946600-21960800	Weak transcription	Aorta	Aorta
35	chr14:21946800-21950200	Weak transcription	NHLF	lung
36	chr14:21946800-21950400	Weak transcription	NHDF-Ad	bronchial
37	chr14:21946800-21954600	Weak transcription	Brain Hippocampus Middle	brain
38	chr14:21946800-21954800	Weak transcription	Osteobl	bone
39	chr14:21946800-21955000	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr14:21946800-21955400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr14:21946800-21955600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr14:21946800-21955600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr14:21946800-21955600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:21946800-21955600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr14:21946800-21955600	Weak transcription	A549	lung
46	chr14:21946800-21955600	Weak transcription	GM12878-XiMat	blood
47	chr14:21946800-21955600	Weak transcription	NHEK	skin
48	chr14:21946800-21956200	Weak transcription	NH-A	brain
49	chr14:21946800-21956400	Weak transcription	Hela-S3	cervix
50	chr14:21946800-21956800	Weak transcription	H1 Cell Line	embryonic stem cell

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