Variant report

Variant	rs2033932
Chromosome Location	chr14:105447075-105447076
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr14:105446128-105447119	ECC-1	luminal epithelium:	n/a	chr14:105446676-105446685 chr14:105446968-105446981
2	JUND	chr14:105446211-105447172	SK-N-SH	brain:	n/a	chr14:105446674-105446685 chr14:105446675-105446684 chr14:105446676-105446685 chr14:105446676-105446683 chr14:105446675-105446685 chr14:105446674-105446686
3	STAT3	chr14:105446132-105447113	MCF10A-Er-Src	breast:	n/a	chr14:105446675-105446684
4	SMARCB1	chr14:105446413-105447171	Hela-S3	cervix:	n/a	chr14:105446676-105446685 chr14:105446675-105446684
5	NFIC	chr14:105446277-105447121	SK-N-SH	brain:	n/a	n/a
6	SIN3AK20	chr14:105446281-105447134	HCT-116	colon:	n/a	n/a
7	SMARCC2	chr14:105446439-105447278	Hela-S3	cervix:	n/a	chr14:105446676-105446685 chr14:105446675-105446684
8	SMARCC1	chr14:105446352-105447094	Hela-S3	cervix:	n/a	chr14:105446676-105446685 chr14:105446675-105446684
9	SIN3AK20	chr14:105446080-105447087	MCF-7	breast:	n/a	n/a
10	STAT3	chr14:105446116-105447088	MCF10A-Er-Src	breast:	n/a	chr14:105446675-105446684
11	TCF12	chr14:105446088-105447102	SK-N-SH	brain:	n/a	n/a
12	MXI1	chr14:105443473-105447213	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105444730..105447554-chr14:105478549..105481250,3	MCF-7	breast:
2	chr14:105446908..105449625-chr14:105498780..105501070,3	MCF-7	breast:
3	chr14:105446494..105448202-chr14:105449526..105451372,2	K562	blood:
4	chr14:105445145..105447583-chr14:105504457..105506627,3	MCF-7	breast:
5	chr14:105445649..105448428-chr14:105631488..105633523,2	MCF-7	breast:
6	chr14:105445779..105447281-chr14:105498227..105500995,2	MCF-7	breast:
7	chr14:105446577..105448410-chr14:105484620..105488615,3	MCF-7	breast:
8	chr14:105433937..105458439-chr14:105476653..105492775,70	MCF-7	breast:

Variant related genes	Relation type
AHNAK2	TF binding region
ENSG00000170779	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12883995	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.96[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12884027	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2582574	0.95[CEU][hapmap];0.84[CHB][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2582575	0.92[EUR][1000 genomes]
rs2582577	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2819457	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34995109	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35689208	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150306	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
4	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
5	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
6	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
7	nsv902419	chr14:105381763-105494262	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv1049253	chr14:105384959-105471855	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv542228	chr14:105390569-105459912	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
12	nsv1036224	chr14:105404755-105470333	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv902420	chr14:105410183-105494262	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
14	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
15	nsv1438	chr14:105412728-105457581	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
16	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
17	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
18	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
20	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
21	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
23	esv3325583	chr14:105444107-105448405	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2033932	C14orf79	cis	Artery Tibial	GTEx
rs2033932	C14orf79	cis	Skin Sun Exposed Lower leg	GTEx
rs2033932	C14orf79	cis	Esophagus Mucosa	GTEx
rs2033932	C14orf79	cis	Heart Left Ventricle	GTEx

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105444600-105447400	Weak transcription	HSMMtube	muscle
2	chr14:105444600-105447600	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr14:105444600-105448200	Weak transcription	Brain Substantia Nigra	brain
4	chr14:105444600-105448400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:105444600-105451000	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:105444800-105447800	Enhancers	Pancreas	Pancrea
7	chr14:105445200-105447600	Weak transcription	HSMM	muscle
8	chr14:105445200-105448200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr14:105445200-105448400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr14:105445200-105451800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr14:105445200-105451800	Weak transcription	Right Atrium	heart
12	chr14:105445200-105452200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr14:105445400-105447400	Weak transcription	Spleen	Spleen
14	chr14:105445400-105447600	Enhancers	Stomach Smooth Muscle	stomach
15	chr14:105445400-105447800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:105445400-105448000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr14:105445400-105448200	Weak transcription	Brain Hippocampus Middle	brain
18	chr14:105445400-105449200	Enhancers	A549	lung
19	chr14:105445400-105449400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105445400-105451200	Weak transcription	Adipose Nuclei	Adipose
21	chr14:105445400-105451400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr14:105445400-105451600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr14:105445400-105451600	Weak transcription	Fetal Brain Female	brain
24	chr14:105445600-105448200	Weak transcription	Brain Angular Gyrus	brain
25	chr14:105445600-105448200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr14:105445600-105448400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:105445800-105447200	Flanking Active TSS	Hela-S3	cervix
28	chr14:105445800-105448400	Weak transcription	Esophagus	oesophagus
29	chr14:105446000-105447200	Bivalent Enhancer	HepG2	liver
30	chr14:105446000-105447200	Enhancers	HMEC	breast
31	chr14:105446000-105451800	Enhancers	Fetal Muscle Leg	muscle
32	chr14:105446400-105447200	Weak transcription	Fetal Lung	lung
33	chr14:105446600-105448400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:105446800-105448800	Weak transcription	NHEK	skin
35	chr14:105446800-105452600	Weak transcription	Fetal Heart	heart
36	chr14:105447000-105447200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr14:105447000-105448600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:105447000-105449200	Enhancers	Fetal Muscle Trunk	muscle
39	chr14:105447000-105451200	Weak transcription	Gastric	stomach
40	chr14:105447000-105451200	Weak transcription	Right Ventricle	heart

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