Variant report

Variant	rs4832028
Chromosome Location	chr2:86440963-86440964
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:86439896..86442073-chr2:86446226..86448627,3	MCF-7	breast:
2	chr2:86420942..86422450-chr2:86438729..86441369,2	MCF-7	breast:
3	chr2:86360704..86363436-chr2:86439912..86441950,2	K562	blood:
4	chr2:86425789..86431197-chr2:86439712..86443537,8	K562	blood:
5	chr2:86440455..86442755-chr2:86456199..86458575,2	K562	blood:
6	chr2:86420399..86424157-chr2:86440260..86444660,8	K562	blood:
7	chr2:86420399..86424157-chr2:86440260..86443835,4	K562	blood:
8	chr2:86436600..86438656-chr2:86439163..86441997,2	MCF-7	breast:
9	chr2:86439775..86441344-chr2:86445094..86448007,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000132313	Chromatin interaction
ENSG00000273080	Chromatin interaction
ENSG00000132305	Chromatin interaction
ENSG00000208772	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10187875	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10779967	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11127015	0.91[ASN][1000 genomes]
rs11127017	0.82[CEU][hapmap]
rs11127025	0.88[EUR][1000 genomes]
rs11682376	0.88[EUR][1000 genomes]
rs11695402	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs11885520	0.83[ASN][1000 genomes]
rs11890563	0.91[ASN][1000 genomes]
rs11891096	0.91[ASN][1000 genomes]
rs11895453	0.91[ASN][1000 genomes]
rs12473739	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13353	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13420958	0.91[ASN][1000 genomes]
rs1424516	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1469982	0.91[ASN][1000 genomes]
rs1559513	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1863054	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs1863064	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs1863065	0.82[CEU][hapmap]
rs2059353	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2161896	0.84[EUR][1000 genomes]
rs2288117	0.91[ASN][1000 genomes]
rs2367205	1.00[CEU][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2367231	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs311561	0.91[ASN][1000 genomes]
rs311570	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs311580	0.91[ASN][1000 genomes]
rs311581	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs311582	0.91[ASN][1000 genomes]
rs311583	0.91[ASN][1000 genomes]
rs311584	0.91[ASN][1000 genomes]
rs34892520	0.83[ASN][1000 genomes]
rs3810828	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3821016	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs4832027	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4832034	0.88[EUR][1000 genomes]
rs4832239	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4832254	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4832255	0.82[CEU][hapmap]
rs4832256	0.82[CEU][hapmap]
rs4832258	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4832259	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs4832266	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs4832275	0.82[CEU][hapmap]
rs58077381	0.91[ASN][1000 genomes]
rs6547666	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6715623	0.91[ASN][1000 genomes]
rs6720431	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6723248	0.91[ASN][1000 genomes]
rs6730604	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs6734695	0.82[CEU][hapmap]
rs6754021	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6756213	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs6758535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6760209	0.88[EUR][1000 genomes]
rs72847853	0.91[ASN][1000 genomes]
rs7340327	0.91[ASN][1000 genomes]
rs7419344	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7558040	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7565645	1.00[JPT][hapmap]
rs7576102	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs7583021	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7592211	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7606188	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs889911	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs918856	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs929916	0.91[ASN][1000 genomes]
rs9677675	0.91[ASN][1000 genomes]
rs979940	1.00[JPT][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751903	chr2:86253542-86505453	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv531380	chr2:86253552-86469217	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv1007474	chr2:86281967-86505453	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv997563	chr2:86281967-86506132	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv1008924	chr2:86282722-86499402	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv999956	chr2:86285944-86505453	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv1012768	chr2:86285944-86506132	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv1003207	chr2:86286314-86496732	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1000441	chr2:86286314-86508168	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv535808	chr2:86286314-86508168	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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 miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv1004442	chr2:86286480-86506132	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	nsv916616	chr2:86289130-86509326	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv458563	chr2:86292341-86507688	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv582370	chr2:86292341-86507688	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv1009140	chr2:86294939-86506132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv582371	chr2:86296566-86507688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv531381	chr2:86301091-86478346	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv1001157	chr2:86301440-86508168	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer 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
20	nsv458574	chr2:86385728-86507688	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
21	nsv582372	chr2:86385728-86507688	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4832028	MRPL35	cis	Artery Tibial	GTEx
rs4832028	MRPL35	cis	Esophagus Muscularis	GTEx
rs4832028	MRPL35	cis	Nerve Tibial	GTEx
rs4832028	MRPL35	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86427200-86444200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:86427200-86450200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:86427400-86448200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:86429400-86441600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr2:86429600-86448200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:86430800-86441800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:86431600-86441200	Strong transcription	Fetal Brain Female	brain
8	chr2:86431600-86441600	Strong transcription	Thymus	Thymus
9	chr2:86431600-86441800	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr2:86431600-86443000	Strong transcription	Primary T cells from cord blood	blood
11	chr2:86431800-86441400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:86432200-86442400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr2:86432400-86441000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:86432400-86441600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:86432400-86441600	Strong transcription	Fetal Muscle Leg	muscle
16	chr2:86432400-86441800	Strong transcription	Adipose Nuclei	Adipose
17	chr2:86432400-86441800	Strong transcription	Fetal Thymus	thymus
18	chr2:86432400-86442000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr2:86432600-86441200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:86432600-86441600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr2:86432600-86441600	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr2:86432600-86441800	Strong transcription	Dnd41	blood
23	chr2:86432600-86442000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:86432600-86442000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:86432800-86441200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:86432800-86441800	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr2:86432800-86441800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:86432800-86441800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:86432800-86442000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr2:86432800-86442400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr2:86433000-86441600	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr2:86433000-86441800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr2:86433200-86441200	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr2:86433200-86441200	Strong transcription	Brain Germinal Matrix	brain
35	chr2:86433200-86441200	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:86433200-86441600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr2:86433200-86441800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:86433200-86441800	Strong transcription	A549	lung
39	chr2:86433400-86441600	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:86433400-86442000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:86433400-86442000	Strong transcription	Left Ventricle	heart
42	chr2:86433600-86441200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:86433600-86441400	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:86433600-86441600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:86433600-86441600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:86433600-86441600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr2:86433600-86441600	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr2:86433600-86441800	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr2:86433600-86441800	Strong transcription	Brain Cingulate Gyrus	brain
50	chr2:86433600-86443400	Strong transcription	Skeletal Muscle Female	skeletal muscle

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