Variant report

Variant	rs7648
Chromosome Location	chr19:18679379-18679380
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18679003-18679859	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18666965..18674770-chr19:18676405..18685095,25	K562	blood:
2	chr19:18678376..18688390-chr19:18697032..18707656,34	K562	blood:
3	chr19:18671197..18672944-chr19:18678465..18680098,2	K562	blood:
4	chr19:18667097..18671007-chr19:18677068..18684435,17	K562	blood:
5	chr19:18677060..18679563-chr19:18680733..18682964,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP8-1	chr19:18679316-18679601	ENSG00000268983.1

No data

Variant related genes	Relation type
UBA52	TF binding region
ENSG00000268030	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000006016	Chromatin interaction
ENSG00000105700	Chromatin interaction
ENSG00000221983	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10402321	0.85[EUR][1000 genomes]
rs10409392	0.86[CHB][hapmap];0.83[EUR][1000 genomes]
rs10414427	0.85[EUR][1000 genomes]
rs10425018	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1043192	0.81[JPT][hapmap]
rs11086114	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11086116	0.81[ASN][1000 genomes]
rs11667551	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11672297	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12150991	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12608925	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12609505	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1468475	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1862645	0.82[JPT][hapmap]
rs2057649	1.00[CHB][hapmap];0.90[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2058077	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2079015	1.00[CHB][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2079016	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2238650	0.82[JPT][hapmap]
rs2283616	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2302055	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2314664	1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314665	1.00[CHB][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314666	1.00[CHB][hapmap];0.84[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314667	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28451415	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28711754	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3170474	0.85[JPT][hapmap]
rs35867875	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35875334	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36050418	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3761032	0.81[JPT][hapmap]
rs3761034	0.95[CHB][hapmap];0.89[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3761036	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3803917	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4629093	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4808137	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808821	0.91[ASN][1000 genomes]
rs4808839	0.81[JPT][hapmap]
rs55724121	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55888366	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58782998	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59798925	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62137086	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6554	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs709679	0.81[JPT][hapmap]
rs7247557	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7250192	0.81[JPT][hapmap]
rs7250623	0.90[JPT][hapmap]
rs7253088	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7254004	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7256319	0.85[JPT][hapmap]
rs7258480	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8109364	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs916791	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh 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 miRNA target site	71 gene(s)	inside rSNPs	diseases
5	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer 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	60 gene(s)	inside rSNPs	diseases
7	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv911284	chr19:18643036-18684216	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription 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	36 gene(s)	inside rSNPs	diseases
10	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7648	UBA52	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18669800-18682000	Weak transcription	Fetal Brain Male	brain
2	chr19:18669800-18682200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:18670200-18681200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:18670600-18681200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr19:18670600-18682000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:18671000-18681200	Strong transcription	Fetal Intestine Small	intestine
7	chr19:18671000-18681200	Strong transcription	Fetal Stomach	stomach
8	chr19:18671000-18681400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr19:18671200-18680600	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr19:18671200-18680600	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr19:18671200-18680600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:18671200-18680600	Strong transcription	Fetal Brain Female	brain
13	chr19:18671200-18680600	Strong transcription	Fetal Intestine Large	intestine
14	chr19:18671200-18680600	Strong transcription	Fetal Thymus	thymus
15	chr19:18671200-18681200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:18671200-18681200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr19:18671400-18681200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:18671800-18680200	Strong transcription	Brain Hippocampus Middle	brain
19	chr19:18671800-18680600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr19:18671800-18680600	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr19:18672200-18680600	Strong transcription	Brain Germinal Matrix	brain
22	chr19:18672400-18680000	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr19:18672400-18680200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr19:18672400-18680200	Strong transcription	Ovary	ovary
25	chr19:18672400-18680400	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr19:18672400-18680400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:18672400-18680400	Strong transcription	Brain Cingulate Gyrus	brain
28	chr19:18672400-18680400	Strong transcription	Duodenum Mucosa	Duodenum
29	chr19:18672400-18680400	Strong transcription	Stomach Smooth Muscle	stomach
30	chr19:18672400-18680600	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr19:18672400-18680600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
32	chr19:18672400-18680600	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr19:18672400-18680600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr19:18672400-18680600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr19:18672400-18680600	Strong transcription	Brain Anterior Caudate	brain
36	chr19:18672400-18680600	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr19:18672400-18680600	Strong transcription	Gastric	stomach
38	chr19:18672400-18680600	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr19:18672400-18680600	Strong transcription	Thymus	Thymus
40	chr19:18672400-18681000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr19:18672400-18681000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr19:18672400-18681000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr19:18672400-18681000	Strong transcription	Primary T cells from cord blood	blood
44	chr19:18672400-18681200	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr19:18672400-18681200	Strong transcription	H9 Cell Line	embryonic stem cell
46	chr19:18672400-18681200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr19:18672400-18681200	Strong transcription	Dnd41	blood
48	chr19:18672400-18681200	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr19:18672600-18680400	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr19:18672600-18680600	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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