Variant report

Variant	rs28855148
Chromosome Location	chr5:43074984-43074985
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:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43073445..43076704-chr5:43084817..43087387,3	K562	blood:
2	chr5:43073690..43076137-chr5:43481731..43483663,2	MCF-7	breast:
3	chr5:43074046..43076584-chr5:43103613..43105462,2	K562	blood:
4	chr5:43038312..43041170-chr5:43074041..43076906,4	K562	blood:
5	chr5:43036891..43039253-chr5:43074561..43077276,2	MCF-7	breast:
6	chr5:43073926..43078603-chr5:43119856..43123275,4	K562	blood:
7	chr5:43074127..43075857-chr5:43482713..43484989,2	K562	blood:
8	chr5:43074312..43077357-chr5:43077925..43083201,8	K562	blood:
9	chr5:43074261..43076510-chr5:43094818..43096635,2	K562	blood:
10	chr5:43073926..43075436-chr5:43121775..43123514,2	K562	blood:
11	chr5:43061551..43063587-chr5:43074317..43077057,2	K562	blood:
12	chr5:43073404..43075652-chr5:43524042..43526111,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114947.1.1-2	chr5:43071269-43076732	XLOC_004366

No data

Variant related genes	Relation type
ENSG00000172262	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000151881	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10060246	0.81[AFR][1000 genomes]
rs10071264	0.93[AFR][1000 genomes]
rs10076685	0.81[AFR][1000 genomes]
rs11949983	0.81[AFR][1000 genomes]
rs12332667	0.93[AFR][1000 genomes]
rs13353916	0.81[AFR][1000 genomes]
rs2198618	0.89[AFR][1000 genomes]
rs2245687	0.89[AFR][1000 genomes]
rs2444855	0.89[AFR][1000 genomes]
rs2548338	0.89[AFR][1000 genomes]
rs2548387	0.85[AFR][1000 genomes]
rs2603618	0.89[AFR][1000 genomes]
rs2603619	0.89[AFR][1000 genomes]
rs2603621	0.89[AFR][1000 genomes]
rs2603643	0.89[AFR][1000 genomes]
rs2603652	0.83[AFR][1000 genomes]
rs2603654	0.93[AFR][1000 genomes]
rs309907	0.89[AFR][1000 genomes]
rs309949	0.85[AFR][1000 genomes]
rs316415	0.96[AFR][1000 genomes]
rs9292861	0.89[AFR][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	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS 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	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised 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	283 gene(s)	inside rSNPs	diseases
7	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
8	nsv870299	chr5:43053679-43107880	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43068000-43077600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:43068600-43082600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:43069000-43081400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:43069400-43075800	Strong transcription	Fetal Stomach	stomach
5	chr5:43069400-43082800	Weak transcription	Colonic Mucosa	Colon
6	chr5:43069400-43087400	Weak transcription	Stomach Mucosa	stomach
7	chr5:43069600-43075200	Weak transcription	Fetal Heart	heart
8	chr5:43069600-43077000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:43069600-43080400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr5:43069600-43080400	Strong transcription	Fetal Muscle Leg	muscle
11	chr5:43069800-43076000	Weak transcription	GM12878-XiMat	blood
12	chr5:43070000-43105400	Weak transcription	HSMMtube	muscle
13	chr5:43070200-43077600	Strong transcription	Fetal Intestine Small	intestine
14	chr5:43070400-43075000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:43070400-43075200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr5:43070400-43075600	Genic enhancers	Dnd41	blood
17	chr5:43071000-43075600	Strong transcription	Stomach Smooth Muscle	stomach
18	chr5:43071400-43075400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:43071400-43084400	Weak transcription	Fetal Kidney	kidney
20	chr5:43071600-43075000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr5:43071600-43079000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:43071600-43079000	Weak transcription	NH-A	brain
23	chr5:43071600-43080800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr5:43071600-43083800	Weak transcription	HepG2	liver
25	chr5:43071600-43084200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:43071800-43075000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:43071800-43075000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr5:43071800-43075000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:43071800-43075000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr5:43071800-43075000	Weak transcription	Brain Angular Gyrus	brain
31	chr5:43071800-43075000	Weak transcription	Brain Anterior Caudate	brain
32	chr5:43071800-43075000	Weak transcription	Lung	lung
33	chr5:43071800-43075000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr5:43071800-43075000	Weak transcription	HUVEC	blood vessel
35	chr5:43071800-43075000	Weak transcription	NHEK	skin
36	chr5:43071800-43075000	Weak transcription	NHLF	lung
37	chr5:43071800-43075200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr5:43071800-43075200	Weak transcription	Brain Hippocampus Middle	brain
39	chr5:43071800-43075200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr5:43071800-43075200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr5:43071800-43075200	Weak transcription	Pancreas	Pancrea
42	chr5:43071800-43075200	Weak transcription	Psoas Muscle	Psoas
43	chr5:43071800-43075400	Weak transcription	Primary B cells from cord blood	blood
44	chr5:43071800-43075600	Weak transcription	Small Intestine	intestine
45	chr5:43071800-43076200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr5:43071800-43076800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:43071800-43077600	Weak transcription	A549	lung
48	chr5:43071800-43079000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:43071800-43079600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr5:43071800-43080000	Weak transcription	Duodenum Mucosa	Duodenum

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