Variant report

Variant	rs10034163
Chromosome Location	chr4:57855684-57855685
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:57855657-57855940	K562	blood:	n/a	n/a
2	POLR2A	chr4:57855633-57856117	K562	blood:	n/a	n/a
3	RCOR1	chr4:57855587-57856014	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:57841254..57846591-chr4:57852896..57857451,6	MCF-7	breast:
2	chr4:57854152..57858062-chr4:57860294..57862898,3	K562	blood:

Variant related genes	Relation type
ENSG00000238579	TF binding region
ENSG00000047315	Chromatin interaction
ENSG00000084092	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10002269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10018580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10018619	0.85[EUR][1000 genomes]
rs10033214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11930475	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11940411	0.92[EUR][1000 genomes]
rs11947717	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13125046	0.82[EUR][1000 genomes]
rs13133792	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13145285	0.92[EUR][1000 genomes]
rs1568260	0.86[EUR][1000 genomes]
rs17087332	0.88[EUR][1000 genomes]
rs17087382	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17181222	0.83[EUR][1000 genomes]
rs34278765	0.86[EUR][1000 genomes]
rs34749389	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35706166	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71601666	0.86[EUR][1000 genomes]
rs71601672	0.92[EUR][1000 genomes]
rs7440152	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7659855	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7684271	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9991234	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv868815	chr4:57114268-58084688	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv1012125	chr4:57668229-57865803	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	esv1799567	chr4:57853485-57857771	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57846000-57881000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:57846200-57861600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:57846200-57861800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:57846600-57861200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:57846800-57900000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:57847000-57861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:57847600-57856000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr4:57848000-57861400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:57848400-57860800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr4:57848400-57875200	Weak transcription	Stomach Mucosa	stomach
11	chr4:57848600-57900000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr4:57849000-57900000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:57849200-57869000	Strong transcription	Primary B cells from peripheral blood	blood
14	chr4:57849200-57886200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:57849400-57857600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:57849600-57884600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr4:57849800-57857000	Strong transcription	Fetal Intestine Small	intestine
18	chr4:57849800-57861400	Weak transcription	Psoas Muscle	Psoas
19	chr4:57850000-57855800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:57850400-57856000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr4:57850400-57858200	Strong transcription	Primary B cells from cord blood	blood
22	chr4:57850400-57858600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:57850600-57870200	Strong transcription	GM12878-XiMat	blood
24	chr4:57850600-57899400	Strong transcription	Fetal Thymus	thymus
25	chr4:57850800-57859400	Strong transcription	Fetal Stomach	stomach
26	chr4:57850800-57899400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr4:57851000-57860600	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:57851000-57861200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr4:57851000-57899200	Strong transcription	Primary T cells from cord blood	blood
30	chr4:57851000-57899400	Strong transcription	Duodenum Mucosa	Duodenum
31	chr4:57851200-57858400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr4:57851200-57859200	Strong transcription	Fetal Muscle Leg	muscle
33	chr4:57851200-57897200	Strong transcription	Fetal Intestine Large	intestine
34	chr4:57851400-57858200	Strong transcription	Thymus	Thymus
35	chr4:57851400-57894800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:57851600-57857400	Strong transcription	HepG2	liver
37	chr4:57851600-57859400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:57851600-57859800	Strong transcription	Fetal Muscle Trunk	muscle
39	chr4:57851600-57861400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:57851600-57861400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:57851600-57864400	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr4:57851600-57899400	Strong transcription	Placenta	Placenta
43	chr4:57851800-57856600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr4:57851800-57857200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:57851800-57857800	Strong transcription	Brain Anterior Caudate	brain
46	chr4:57851800-57858000	Strong transcription	Colon Smooth Muscle	Colon
47	chr4:57851800-57858000	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr4:57851800-57858200	Strong transcription	NHLF	lung
49	chr4:57851800-57858200	Strong transcription	Osteobl	bone
50	chr4:57851800-57858600	Strong transcription	Dnd41	blood

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