Variant report

Variant	rs433030
Chromosome Location	chr4:2815632-2815633
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	POLR2A	chr4:2815406-2816239	HL-60	blood:	n/a	n/a
2	BCL3	chr4:2814900-2815797	GM12878	blood:	n/a	n/a
3	ZNF263	chr4:2813465-2815744	HEK293-T-REx	kidney:	n/a	chr4:2813988-2813997
4	BCL3	chr4:2815229-2815713	GM12878	blood:	n/a	n/a
5	MTA3	chr4:2813221-2816423	GM12878	blood:	n/a	n/a
6	POLR2A	chr4:2815241-2816487	GM12878	blood:	n/a	n/a
7	RUNX3	chr4:2815481-2816257	GM12878	blood:	n/a	chr4:2815970-2815987
8	POU2F2	chr4:2815114-2815649	GM12891	blood:	n/a	chr4:2815417-2815430
9	POU2F2	chr4:2815149-2815675	GM12878	blood:	n/a	chr4:2815417-2815430
10	NFATC1	chr4:2815141-2815793	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:2815418-2816325	GM12878	blood:	n/a	chr4:2816097-2816113 chr4:2816089-2816105
12	STAT5A	chr4:2814412-2816129	GM12878	blood:	n/a	chr4:2814848-2814856
13	POLR2A	chr4:2815313-2816045	GM12892	blood:	n/a	n/a
14	EBF1	chr4:2815530-2816163	GM12878	blood:	n/a	chr4:2815996-2816007
15	POLR2A	chr4:2815136-2815908	GM12892	blood:	n/a	n/a
16	NFATC1	chr4:2815218-2815755	GM12878	blood:	n/a	n/a
17	RUNX3	chr4:2814703-2816204	GM12878	blood:	n/a	chr4:2815970-2815987

No.	Distal block	Cell Line	Cell type
1	chr4:2815555..2818329-chr4:2819380..2822501,3	MCF-7	breast:
2	chr4:2811128..2813446-chr4:2813847..2818794,5	MCF-7	breast:
3	chr4:2815294..2817110-chr4:2817843..2820313,2	K562	blood:

Variant related genes	Relation type
SH3BP2	TF binding region
ENSG00000087266	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs13113803	0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs13137906	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1751848	0.83[CHD][hapmap]
rs1784148	0.95[CHB][hapmap];0.91[CHD][hapmap];0.83[JPT][hapmap];0.91[ASN][1000 genomes]
rs1784149	0.95[CHB][hapmap];0.83[JPT][hapmap];0.91[ASN][1000 genomes]
rs2269484	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2269485	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2282770	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2282771	0.96[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3213501	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.90[TSI][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34993433	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs370470	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs385715	1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs393635	0.86[ASN][1000 genomes]
rs397292	1.00[CHB][hapmap];0.86[CHD][hapmap];0.89[ASN][1000 genomes]
rs402855	0.90[ASN][1000 genomes]
rs407770	0.89[ASN][1000 genomes]
rs419096	0.89[ASN][1000 genomes]
rs421714	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs422734	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs426192	0.81[EUR][1000 genomes]
rs426904	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs445160	0.97[ASN][1000 genomes]
rs450080	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.94[TSI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6820967	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs743691	0.87[CHB][hapmap]
rs9685721	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948659	chr4:1828867-2815632	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv470002	chr4:2701098-2836628	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv878445	chr4:2704046-2831383	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv878447	chr4:2723531-2831383	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv516797	chr4:2723531-2836628	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv878448	chr4:2723531-2846799	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
9	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
10	nsv878449	chr4:2744480-2831383	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1002517	chr4:2747905-2822017	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
13	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv878452	chr4:2789184-2830076	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv1010533	chr4:2792848-2873441	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	nsv461162	chr4:2794320-2846799	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	nsv593436	chr4:2794320-2846799	Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs433030	ADD1	cis	lymphoblastoid	seeQTL

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2803400-2819200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:2811000-2816000	Enhancers	Brain Substantia Nigra	brain
3	chr4:2811800-2819400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:2813200-2816000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:2813400-2815800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr4:2813400-2816000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:2813400-2817200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:2813800-2818800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:2813800-2819000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr4:2814000-2815800	Enhancers	HepG2	liver
11	chr4:2814200-2817200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:2814200-2817400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:2814800-2816600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
14	chr4:2814800-2819000	Weak transcription	Fetal Lung	lung
15	chr4:2814800-2819200	Weak transcription	NH-A	brain
16	chr4:2814800-2819400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:2815000-2816000	Enhancers	Left Ventricle	heart
18	chr4:2815000-2816000	Enhancers	Stomach Mucosa	stomach
19	chr4:2815000-2816200	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr4:2815000-2816400	Flanking Active TSS	GM12878-XiMat	blood
21	chr4:2815200-2815800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
22	chr4:2815200-2815800	Enhancers	Fetal Muscle Leg	muscle
23	chr4:2815200-2816000	Enhancers	Fetal Muscle Trunk	muscle
24	chr4:2815200-2816000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
25	chr4:2815200-2816200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr4:2815200-2816600	Enhancers	Primary hematopoietic stem cells	blood
27	chr4:2815200-2817400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:2815200-2817400	Genic enhancers	Gastric	stomach
29	chr4:2815200-2817400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
30	chr4:2815200-2817600	Genic enhancers	Placenta	Placenta
31	chr4:2815200-2817800	Genic enhancers	Primary monocytes fromperipheralblood	blood
32	chr4:2815200-2818800	Weak transcription	Fetal Intestine Large	intestine
33	chr4:2815200-2819000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:2815200-2819200	Weak transcription	Small Intestine	intestine
35	chr4:2815200-2819200	Weak transcription	NHLF	lung
36	chr4:2815400-2815800	Enhancers	Esophagus	oesophagus
37	chr4:2815400-2815800	Enhancers	Fetal Heart	heart
38	chr4:2815400-2815800	Weak transcription	Psoas Muscle	Psoas
39	chr4:2815400-2815800	Weak transcription	Right Ventricle	heart
40	chr4:2815400-2816000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:2815400-2816000	Active TSS	Colonic Mucosa	Colon
42	chr4:2815400-2816000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr4:2815400-2816000	Strong transcription	Pancreas	Pancrea
44	chr4:2815400-2816200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr4:2815400-2816200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr4:2815400-2816600	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
47	chr4:2815400-2817000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:2815400-2817000	Genic enhancers	Liver	Liver
49	chr4:2815400-2817200	Strong transcription	Fetal Intestine Small	intestine
50	chr4:2815400-2817400	Enhancers	Fetal Thymus	thymus

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