Variant report

Variant	rs421714
Chromosome Location	chr4:2806727-2806728
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr4:2806309-2807021	GM12878	blood:	n/a	chr4:2806930-2806942
2	EBF1	chr4:2806482-2806736	GM12878	blood:	n/a	n/a
3	POLR2A	chr4:2806726-2806869	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2805467..2811002-chr4:2816486..2823721,11	MCF-7	breast:
2	chr4:2804056..2806985-chr4:2932653..2936211,3	K562	blood:
3	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
4	chr4:2802222..2807121-chr4:2932653..2939222,7	K562	blood:
5	chr4:2805238..2807617-chr4:2936403..2938042,3	K562	blood:
6	chr4:2804665..2806753-chr4:2851605..2853395,2	MCF-7	breast:
7	chr4:2806060..2809541-chr4:2819791..2822068,4	MCF-7	breast:

No data

Variant related genes	Relation type
SH3BP2	TF binding region
ENSG00000249673	Chromatin interaction
ENSG00000087269	Chromatin interaction
ENSG00000109736	Chromatin interaction
ENSG00000087266	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10011310	0.94[AMR][1000 genomes]
rs13113803	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13137906	0.89[ASN][1000 genomes]
rs1784148	0.88[ASN][1000 genomes]
rs1784149	0.88[ASN][1000 genomes]
rs2269484	0.82[ASN][1000 genomes]
rs2269485	0.89[ASN][1000 genomes]
rs2282770	0.89[ASN][1000 genomes]
rs2282771	0.89[ASN][1000 genomes]
rs3213501	0.91[ASN][1000 genomes]
rs34993433	0.91[ASN][1000 genomes]
rs370470	0.94[ASN][1000 genomes]
rs385715	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs393635	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs397292	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs402855	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs407770	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs419096	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs422734	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs426904	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs433030	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs445160	0.97[ASN][1000 genomes]
rs450080	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6820967	0.96[ASN][1000 genomes]
rs9685721	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	nsv1005116	chr4:2633935-2812340	Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	nsv878446	chr4:2710644-2810634	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2796200-2813800	Enhancers	Left Ventricle	heart
2	chr4:2796600-2814600	Enhancers	Stomach Mucosa	stomach
3	chr4:2798400-2809600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:2801800-2809800	Enhancers	Fetal Intestine Large	intestine
5	chr4:2802800-2808400	Weak transcription	Brain Angular Gyrus	brain
6	chr4:2802800-2808800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:2802800-2810200	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr4:2803000-2808600	Enhancers	Fetal Muscle Leg	muscle
9	chr4:2803000-2810600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:2803200-2807200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:2803200-2811600	Enhancers	Right Ventricle	heart
12	chr4:2803200-2813400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:2803400-2807000	Weak transcription	A549	lung
14	chr4:2803400-2807200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:2803400-2807200	Enhancers	Adipose Nuclei	Adipose
16	chr4:2803400-2807200	Enhancers	Colonic Mucosa	Colon
17	chr4:2803400-2807200	Weak transcription	Ovary	ovary
18	chr4:2803400-2807200	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr4:2803400-2807400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:2803400-2807600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:2803400-2807600	Weak transcription	Brain Germinal Matrix	brain
22	chr4:2803400-2808200	Weak transcription	HSMMtube	muscle
23	chr4:2803400-2808400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:2803400-2808400	Weak transcription	Thymus	Thymus
25	chr4:2803400-2808600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:2803400-2808600	Enhancers	Duodenum Mucosa	Duodenum
27	chr4:2803400-2808600	Weak transcription	Osteobl	bone
28	chr4:2803400-2811600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:2803400-2812800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr4:2803400-2819200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr4:2803600-2807000	Weak transcription	Fetal Brain Female	brain
32	chr4:2803600-2807200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:2803600-2807400	Weak transcription	Rectal Smooth Muscle	rectum
34	chr4:2803600-2808200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:2803600-2808200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:2803600-2808600	Enhancers	GM12878-XiMat	blood
37	chr4:2803600-2808600	Weak transcription	NH-A	brain
38	chr4:2803600-2809000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr4:2803600-2812600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr4:2803600-2813000	Weak transcription	Primary T cells from cord blood	blood
41	chr4:2803600-2813200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:2803600-2813400	Enhancers	Primary B cells from cord blood	blood
43	chr4:2803800-2806800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:2803800-2807000	Weak transcription	HUVEC	blood vessel
45	chr4:2803800-2807600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr4:2803800-2807600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:2803800-2808600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr4:2803800-2813000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:2804200-2811400	Weak transcription	HepG2	liver
50	chr4:2804400-2807400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood

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