Variant report

Variant	rs1020179
Chromosome Location	chr14:105393275-105393276
allele	C/T
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	IRF4	chr14:105392786-105393310	GM12878	blood:	n/a	n/a
2	EBF1	chr14:105392874-105393286	GM12878	blood:	n/a	n/a
3	ELF1	chr14:105392838-105393476	GM12878	blood:	n/a	n/a
4	EBF1	chr14:105392553-105393550	GM12878	blood:	n/a	n/a
5	NFIC	chr14:105392719-105393389	GM12878	blood:	n/a	n/a
6	SP1	chr14:105392792-105393290	GM12878	blood:	n/a	n/a
7	EP300	chr14:105392887-105393276	GM12878	blood:	n/a	chr14:105393072-105393086
8	MEF2C	chr14:105392747-105393279	GM12878	blood:	n/a	chr14:105392992-105393001 chr14:105392990-105393001 chr14:105392987-105393008 chr14:105392991-105393002
9	FOXM1	chr14:105392741-105393341	GM12878	blood:	n/a	n/a
10	STAT5A	chr14:105392481-105393382	GM12878	blood:	n/a	n/a
11	RELA	chr14:105392883-105393278	GM18951	blood:	n/a	n/a
12	RUNX3	chr14:105392558-105393517	GM12878	blood:	n/a	n/a
13	ELF1	chr14:105392659-105393662	GM12878	blood:	n/a	n/a
14	EP300	chr14:105392841-105393489	GM12878	blood:	n/a	chr14:105393072-105393086
15	SPI1	chr14:105392535-105393485	GM12878	blood:	n/a	chr14:105393077-105393086
16	RELA	chr14:105392693-105393305	GM19193	blood:	n/a	n/a
17	ZNF143	chr14:105392893-105393348	GM12878	blood:	n/a	chr14:105393278-105393296
18	NFATC1	chr14:105392836-105393277	GM12878	blood:	n/a	n/a
19	POU2F2	chr14:105392738-105393382	GM12878	blood:	n/a	chr14:105393086-105393093 chr14:105393078-105393100
20	POU2F2	chr14:105392766-105393420	GM12891	blood:	n/a	chr14:105393086-105393093 chr14:105393078-105393100
21	CUX1	chr14:105392960-105393334	GM12878	blood:	n/a	n/a
22	TBL1XR1	chr14:105392820-105393373	GM12878	blood:	n/a	n/a
23	TCF12	chr14:105392889-105393441	GM12878	blood:	n/a	chr14:105393404-105393414
24	RELA	chr14:105392773-105393290	GM10847	blood:	n/a	n/a
25	MAZ	chr14:105392702-105393389	GM12878	blood:	n/a	n/a
26	PML	chr14:105392718-105393353	GM12878	blood:	n/a	n/a
27	POLR2A	chr14:105392089-105393339	GM19193	blood:	n/a	n/a
28	BHLHE40	chr14:105392796-105393418	GM12878	blood:	n/a	n/a
29	CHD2	chr14:105392827-105393412	GM12878	blood:	n/a	n/a
30	MTA3	chr14:105392799-105393357	GM12878	blood:	n/a	n/a
31	BCLAF1	chr14:105392803-105393399	GM12878	blood:	n/a	chr14:105393266-105393279 chr14:105393077-105393086
32	BCLAF1	chr14:105392732-105393342	GM12878	blood:	n/a	chr14:105393266-105393279 chr14:105393077-105393086
33	PAX5	chr14:105392705-105393437	GM12878	blood:	n/a	chr14:105393077-105393086
34	MEF2A	chr14:105392813-105393412	GM12878	blood:	n/a	chr14:105392992-105393001 chr14:105392990-105393001 chr14:105392987-105393008 chr14:105392991-105393002
35	POU2F2	chr14:105392757-105393316	GM12891	blood:	n/a	chr14:105393086-105393093 chr14:105393078-105393100
36	MXI1	chr14:105392888-105393420	GM12878	blood:	n/a	n/a
37	POLR2A	chr14:105393205-105393292	GM12878	blood:	n/a	n/a
38	PAX5	chr14:105393055-105393337	GM12892	blood:	n/a	chr14:105393077-105393086
39	USF2	chr14:105392973-105393382	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:105392860-105393300	GM12878	blood:	n/a	chr14:105393266-105393279 chr14:105393077-105393086
41	POLR2A	chr14:105393082-105393326	GM12878	blood:	n/a	n/a
42	POU2F2	chr14:105392795-105393332	GM12878	blood:	n/a	chr14:105393086-105393093 chr14:105393078-105393100
43	RCOR1	chr14:105392731-105393384	GM12878	blood:	n/a	n/a
44	MTA3	chr14:105390644-105393638	GM12878	blood:	n/a	n/a
45	MEF2C	chr14:105392667-105393339	GM12878	blood:	n/a	chr14:105392992-105393001 chr14:105392990-105393001 chr14:105392987-105393008 chr14:105392991-105393002
46	RUNX3	chr14:105392652-105393530	GM12878	blood:	n/a	n/a
47	CEBPB	chr14:105392767-105393371	GM12878	blood:	n/a	n/a
48	MEF2A	chr14:105392624-105393392	GM12878	blood:	n/a	chr14:105392992-105393001 chr14:105392990-105393001 chr14:105392987-105393008 chr14:105392991-105393002
49	NFIC	chr14:105392842-105393349	GM12878	blood:	n/a	n/a
50	EBF1	chr14:105392588-105393388	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105387983..105391489-chr14:105392006..105395629,4	MCF-7	breast:
2	chr14:105391507..105394096-chr14:105419228..105421927,2	MCF-7	breast:
3	chr14:105391640..105393998-chr14:105436679..105438519,2	MCF-7	breast:
4	chr14:105392936..105394714-chr14:105435765..105438591,2	MCF-7	breast:
5	chr14:105387917..105389579-chr14:105391282..105393689,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHNAK2-1	chr14:105393063-105393552	expReg_chr14_7322_-

Variant related genes	Relation type
PLD4	TF binding region
ENSG00000185567	Chromatin interaction
ENSG00000166428	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1020178	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2582527	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2582528	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2819423	1.00[AMR][1000 genomes]
rs2819431	1.00[AMR][1000 genomes]
rs2841270	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841273	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs748358	1.00[AMR][1000 genomes]
rs894037	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv456456	chr14:105285159-105412541	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv566099	chr14:105285159-105412541	Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers 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	38 gene(s)	inside rSNPs	diseases
8	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
9	nsv566139	chr14:105347296-105417147	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105390800-105393600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
2	chr14:105390800-105393600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:105390800-105393600	Flanking Active TSS	GM12878-XiMat	blood
4	chr14:105390800-105393600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr14:105390800-105394000	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr14:105391000-105394000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr14:105391000-105395400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:105391200-105393600	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr14:105391200-105393600	Enhancers	Adipose Nuclei	Adipose
10	chr14:105391200-105393600	Active TSS	Brain Hippocampus Middle	brain
11	chr14:105391200-105394200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr14:105391600-105394200	Enhancers	Fetal Thymus	thymus
13	chr14:105391600-105395000	Enhancers	Fetal Intestine Small	intestine
14	chr14:105391600-105398600	Weak transcription	Gastric	stomach
15	chr14:105391800-105394200	Enhancers	Spleen	Spleen
16	chr14:105392200-105394200	Enhancers	Fetal Muscle Leg	muscle
17	chr14:105392200-105395800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:105392600-105393600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
19	chr14:105392600-105393800	Weak transcription	Fetal Intestine Large	intestine
20	chr14:105392600-105394400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr14:105392600-105394600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:105392800-105393400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:105392800-105393600	Enhancers	Placenta	Placenta
24	chr14:105392800-105393800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:105392800-105393800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:105393000-105393600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:105393000-105393600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:105393000-105394200	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr14:105393200-105393400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr14:105393200-105393400	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr14:105393200-105393600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
32	chr14:105393200-105393600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:105393200-105394000	Enhancers	Esophagus	oesophagus
34	chr14:105393200-105394200	Enhancers	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links