Variant report

Variant	rs1055144
Chromosome Location	chr7:25871109-25871110
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:25862249..25865211-chr7:25870561..25873090,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPA2B1-4	chr7:25870914-25871179	XLOC_006383
2	lnc-HNRNPA2B1-4	chr7:25870839-25871179	XLOC_006383
3	lnc-HNRNPA2B1-4	chr7:25870914-25871197	XLOC_006383
4	lnc-HNRNPA2B1-4	chr7:25870917-25871179	NONHSAT119604

Extended variants
information (count: 44 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10225976	0.96[ASN][1000 genomes]
rs10238703	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10241634	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10241659	0.91[ASN][1000 genomes]
rs10242536	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10245353	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10260677	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10262483	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10267498	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10271088	0.92[ASN][1000 genomes]
rs10271460	0.91[ASN][1000 genomes]
rs10274306	0.91[ASN][1000 genomes]
rs10282436	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10951112	0.94[EUR][1000 genomes]
rs11770186	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12666961	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1451382	0.90[ASN][1000 genomes]
rs1451385	0.83[CEU][hapmap]
rs2391168	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28392961	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs28473292	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28858973	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2893220	0.91[ASN][1000 genomes]
rs2893221	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35766302	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4141278	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs41469349	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4722530	0.95[EUR][1000 genomes]
rs56376645	0.94[ASN][1000 genomes]
rs57246313	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60643312	0.94[ASN][1000 genomes]
rs61140461	0.91[ASN][1000 genomes]
rs62447896	0.90[ASN][1000 genomes]
rs73093663	0.81[AFR][1000 genomes]
rs7782246	0.91[ASN][1000 genomes]
rs7782292	0.91[ASN][1000 genomes]
rs7798002	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7798130	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7798431	0.89[ASN][1000 genomes]
rs966042	0.84[ASW][hapmap];0.83[LWK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs9987000	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv830928	chr7:25820147-25965014	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Waist-hip ratio	20935629	GWAS catalog

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1055144	CCDC126	cis	parietal	SCAN
rs1055144	SKAP2	cis	cerebellum	SCAN

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25868800-25873400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:25869000-25872000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr7:25869000-25874000	Enhancers	Fetal Stomach	stomach
4	chr7:25869200-25871200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:25869200-25871200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:25869200-25873000	Enhancers	Fetal Lung	lung
7	chr7:25869400-25871200	Enhancers	Colon Smooth Muscle	Colon
8	chr7:25869400-25871600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:25869400-25872200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:25869400-25872200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:25869400-25872400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:25869400-25872400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:25869400-25872400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr7:25869600-25871400	Weak transcription	Psoas Muscle	Psoas
15	chr7:25869600-25871600	Enhancers	Ovary	ovary
16	chr7:25869600-25873600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:25869600-25881800	Weak transcription	Right Atrium	heart
18	chr7:25869800-25872200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr7:25869800-25872400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:25869800-25872400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:25870000-25872000	Enhancers	Rectal Smooth Muscle	rectum
22	chr7:25870000-25872400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:25870000-25873200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:25870000-25873200	Enhancers	Fetal Kidney	kidney
25	chr7:25870200-25871400	Enhancers	Brain Substantia Nigra	brain
26	chr7:25870200-25871600	Enhancers	Stomach Smooth Muscle	stomach
27	chr7:25870200-25872200	Enhancers	Brain Germinal Matrix	brain
28	chr7:25870200-25873200	Enhancers	Brain Anterior Caudate	brain
29	chr7:25870400-25871400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:25870400-25872000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr7:25870600-25871400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:25870600-25872000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr7:25870600-25873000	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr7:25870600-25874000	Enhancers	Fetal Heart	heart
35	chr7:25870800-25871200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:25870800-25871200	Enhancers	K562	blood
37	chr7:25870800-25871800	Enhancers	Fetal Intestine Small	intestine
38	chr7:25870800-25872200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:25870800-25872400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:25871000-25871600	Enhancers	Brain Hippocampus Middle	brain
41	chr7:25871000-25871600	Bivalent Enhancer	HepG2	liver
42	chr7:25871000-25872000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:25871000-25872400	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr7:25871000-25872600	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr7:25871000-25872800	Enhancers	Brain Angular Gyrus	brain
46	chr7:25871000-25872800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:25871000-25872800	Enhancers	HUVEC	blood vessel
48	chr7:25871000-25873000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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