Variant report

Variant	rs62328372
Chromosome Location	chr4:120166809-120166810
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:120131927..120134724-chr4:120165743..120168558,4	K562	blood:
2	chr4:120132009..120134724-chr4:120165743..120167609,3	K562	blood:
3	chr4:120131912..120135684-chr4:120163783..120168921,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000178636	Chromatin interaction
ENSG00000145390	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11935130	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12645079	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12645965	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12647635	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12649811	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12650267	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17049968	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17642800	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1858285	0.85[ASN][1000 genomes]
rs28421394	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28848291	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28864107	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35372126	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4833614	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4834768	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4834769	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55732167	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56072232	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56344202	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62328369	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62328371	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62328373	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62328374	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62328376	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62328377	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62328379	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62328398	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62328407	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62328426	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv948802	chr4:119844269-120208926	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	esv2763386	chr4:120143861-120186968	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv461632	chr4:120158734-120180790	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv461633	chr4:120158734-120180790	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv595332	chr4:120158734-120180790	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs62328372	FABP2	cis	Heart Left Ventricle	GTEx
rs62328372	FABP2	cis	Whole Blood	GTEx

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120134800-120170000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:120135000-120170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:120135000-120195800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:120135200-120176200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:120135200-120176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:120135400-120194600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr4:120135600-120173800	Weak transcription	Brain Anterior Caudate	brain
8	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
9	chr4:120140600-120167400	Weak transcription	Colonic Mucosa	Colon
10	chr4:120141000-120192400	Weak transcription	Hela-S3	cervix
11	chr4:120143000-120167200	Weak transcription	Placenta	Placenta
12	chr4:120143000-120176200	Weak transcription	Esophagus	oesophagus
13	chr4:120143800-120167000	Weak transcription	Fetal Intestine Large	intestine
14	chr4:120146000-120178600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr4:120148200-120213600	Weak transcription	Fetal Muscle Leg	muscle
16	chr4:120152200-120167200	Weak transcription	Pancreas	Pancrea
17	chr4:120155200-120167000	Weak transcription	NH-A	brain
18	chr4:120155400-120167200	Weak transcription	Aorta	Aorta
19	chr4:120155400-120167200	Weak transcription	Fetal Thymus	thymus
20	chr4:120155400-120167400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr4:120155400-120169800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr4:120155400-120169800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr4:120155400-120169800	Weak transcription	Ovary	ovary
24	chr4:120155400-120176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:120155400-120176400	Weak transcription	Right Ventricle	heart
26	chr4:120155600-120169800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:120155600-120173800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr4:120155600-120176400	Weak transcription	Brain Substantia Nigra	brain
29	chr4:120155600-120186000	Weak transcription	Fetal Heart	heart
30	chr4:120156200-120167200	Weak transcription	Psoas Muscle	Psoas
31	chr4:120156800-120167200	Weak transcription	Fetal Intestine Small	intestine
32	chr4:120156800-120167200	Weak transcription	Fetal Stomach	stomach
33	chr4:120157000-120170000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr4:120157600-120167000	Weak transcription	HepG2	liver
35	chr4:120157600-120176800	Weak transcription	Primary B cells from cord blood	blood
36	chr4:120157800-120167200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:120158000-120167000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr4:120158000-120167200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr4:120158000-120167200	Weak transcription	Lung	lung
40	chr4:120158200-120167000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr4:120158200-120167000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:120158800-120167000	Weak transcription	Primary T cells from cord blood	blood
43	chr4:120159200-120167200	Weak transcription	Gastric	stomach
44	chr4:120159400-120200800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr4:120159400-120201600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr4:120159400-120206200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr4:120159600-120167000	Weak transcription	Left Ventricle	heart
48	chr4:120159600-120170000	Weak transcription	K562	blood
49	chr4:120159600-120200800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr4:120159800-120167000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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