Variant report

Variant	rs2542592
Chromosome Location	chr2:54030862-54030863
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:54012138..54014028-chr2:54027548..54031166,3	K562	blood:
2	chr2:53993226..53995019-chr2:54030146..54032041,3	K562	blood:
3	chr2:54025483..54027940-chr2:54030196..54032461,2	K562	blood:

Variant related genes	Relation type
ENSG00000143942	Chromatin interaction
ENSG00000115239	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10490468	0.87[CEU][hapmap];0.92[CHB][hapmap];0.90[JPT][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11897282	0.84[CHB][hapmap];0.80[JPT][hapmap];0.84[ASN][1000 genomes]
rs11901698	0.84[CHB][hapmap];0.81[JPT][hapmap]
rs1232	1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs13408029	0.91[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs17045176	0.84[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs17045199	0.87[CEU][hapmap]
rs17045203	0.84[CHB][hapmap];0.80[JPT][hapmap]
rs17520505	0.93[CHB][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs17521008	0.83[ASN][1000 genomes]
rs2287340	0.84[CHB][hapmap]
rs2302797	0.84[CHB][hapmap];0.80[JPT][hapmap];0.84[ASN][1000 genomes]
rs2542572	0.81[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2542573	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2542578	0.90[ASN][1000 genomes]
rs2542580	0.90[ASN][1000 genomes]
rs2542582	0.91[CEU][hapmap];0.92[CHB][hapmap];0.90[JPT][hapmap];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2542583	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2542589	0.92[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2542590	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2542591	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543629	0.92[CHB][hapmap];0.92[ASN][1000 genomes]
rs2692512	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2692513	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2692516	0.92[CEU][hapmap]
rs2692519	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2692521	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2692522	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2692523	0.90[ASN][1000 genomes]
rs2692530	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2692533	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2692534	0.83[CEU][hapmap];0.82[AMR][1000 genomes]
rs2692535	0.82[ASN][1000 genomes]
rs2909262	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2949813	0.92[CHB][hapmap];0.91[JPT][hapmap];0.91[YRI][hapmap];0.96[ASN][1000 genomes]
rs2949814	0.87[ASN][1000 genomes]
rs35772199	0.82[ASN][1000 genomes]
rs3770394	0.84[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs3770395	0.84[ASN][1000 genomes]
rs3770397	0.81[ASN][1000 genomes]
rs3770399	0.84[ASN][1000 genomes]
rs4116709	0.93[CHB][hapmap];0.91[JPT][hapmap];0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs62137573	0.83[ASN][1000 genomes]
rs62137602	0.81[ASN][1000 genomes]
rs62137606	0.84[ASN][1000 genomes]
rs6730006	0.84[ASN][1000 genomes]
rs719127	0.84[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs72901256	0.85[ASN][1000 genomes]
rs7600817	0.84[ASN][1000 genomes]
rs805316	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs805334	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs805338	1.00[CHB][hapmap]
rs805368	0.89[ASN][1000 genomes]
rs805383	0.90[ASN][1000 genomes]
rs805385	0.90[ASN][1000 genomes]
rs805398	0.86[ASN][1000 genomes]
rs805413	0.81[ASN][1000 genomes]
rs805435	0.90[ASN][1000 genomes]
rs805437	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs805446	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs805447	1.00[CHB][hapmap]
rs805449	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003263	chr2:53863287-54055359	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv535720	chr2:53863287-54055359	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv834058	chr2:53900674-54072011	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1009829	chr2:53980562-54051927	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2542592	ACYP2	cis	Muscle Skeletal	GTEx
rs2542592	PSME4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54015200-54038200	Weak transcription	Small Intestine	intestine
2	chr2:54015200-54046200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:54015200-54046200	Weak transcription	Aorta	Aorta
4	chr2:54015200-54051600	Weak transcription	Stomach Mucosa	stomach
5	chr2:54015200-54053800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:54015600-54035600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:54015600-54035800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:54015600-54054600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr2:54015800-54038400	Weak transcription	Fetal Heart	heart
10	chr2:54015800-54054000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:54016000-54031600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr2:54016400-54043000	Weak transcription	Gastric	stomach
13	chr2:54017400-54031000	Weak transcription	Ovary	ovary
14	chr2:54020200-54046200	Weak transcription	Colonic Mucosa	Colon
15	chr2:54020600-54047200	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr2:54020600-54048400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:54020600-54048600	Strong transcription	Osteobl	bone
18	chr2:54021000-54047200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr2:54021000-54047200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:54021000-54047400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr2:54021000-54048000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:54021200-54047200	Strong transcription	Placenta	Placenta
23	chr2:54021200-54047600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:54021400-54047000	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr2:54021400-54047000	Strong transcription	Fetal Thymus	thymus
26	chr2:54021600-54035000	Strong transcription	Liver	Liver
27	chr2:54021600-54046400	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:54021800-54047600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:54022000-54032000	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr2:54022000-54039400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr2:54022000-54044800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:54022000-54047000	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr2:54022000-54047000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:54022000-54047200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr2:54022000-54047600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:54022200-54032000	Strong transcription	Duodenum Mucosa	Duodenum
37	chr2:54022200-54039000	Strong transcription	Fetal Intestine Large	intestine
38	chr2:54022200-54046200	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr2:54022200-54046600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:54022200-54047200	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr2:54023000-54053800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:54024200-54043400	Strong transcription	Dnd41	blood
43	chr2:54024400-54031200	Strong transcription	NHDF-Ad	bronchial
44	chr2:54024400-54035000	Weak transcription	HSMMtube	muscle
45	chr2:54024800-54039600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:54024800-54045400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr2:54025000-54040000	Weak transcription	K562	blood
48	chr2:54025800-54035400	Weak transcription	Pancreas	Pancrea
49	chr2:54025800-54036600	Weak transcription	Spleen	Spleen
50	chr2:54025800-54062000	Weak transcription	Right Ventricle	heart

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