Variant report

Variant	rs11633416
Chromosome Location	chr15:40250506-40250507
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:40249478..40251970-chr15:40252584..40255230,2	K562	blood:
2	chr15:40249084..40251970-chr15:40253423..40255230,2	K562	blood:
3	chr15:40244109..40246944-chr15:40248464..40252710,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128829	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10518676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10851392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11631801	0.81[ASN][1000 genomes]
rs11632930	0.83[ASW][hapmap];0.87[CEU][hapmap];0.85[CHD][hapmap];0.92[GIH][hapmap];0.86[LWK][hapmap];0.91[MKK][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes]
rs12324733	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12438989	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12439021	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12439335	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12441927	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12442713	0.88[CEU][hapmap];0.84[GIH][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs12906976	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1656894	0.84[ASN][1000 genomes]
rs2279579	0.81[TSI][hapmap]
rs28617639	0.98[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2934194	0.91[CEU][hapmap];0.90[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];0.86[ASN][1000 genomes]
rs3207297	0.81[TSI][hapmap]
rs34298786	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs480095	0.84[JPT][hapmap]
rs486816	0.84[JPT][hapmap]
rs489424	0.84[JPT][hapmap]
rs494614	0.84[JPT][hapmap]
rs518770	0.84[JPT][hapmap]
rs534757	0.84[JPT][hapmap]
rs552251	0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs55957853	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs56143280	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs562159	0.84[JPT][hapmap]
rs577289	0.84[JPT][hapmap]
rs580836	0.83[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7173315	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72729488	0.92[ASN][1000 genomes]
rs8030025	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.91[TSI][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8030640	1.00[ASW][hapmap];0.91[CEU][hapmap];0.81[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs8030687	0.90[CEU][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs8030980	0.84[GIH][hapmap]
rs8034362	0.83[MEX][hapmap];0.84[TSI][hapmap]
rs8035930	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8042788	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9302104	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11633416	EIF2AK4	cis	cerebellum	SCAN
rs11633416	EIF2AK4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40227200-40268400	Weak transcription	Esophagus	oesophagus
2	chr15:40227400-40283400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:40227800-40268400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:40228200-40323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr15:40230000-40263000	Strong transcription	Fetal Muscle Trunk	muscle
6	chr15:40230200-40255600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr15:40230400-40261600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:40230600-40252400	Weak transcription	Right Atrium	heart
9	chr15:40231000-40268400	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:40231800-40252600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr15:40232000-40261400	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr15:40232000-40262600	Strong transcription	Liver	Liver
13	chr15:40232200-40252400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr15:40232400-40252400	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr15:40232600-40251000	Strong transcription	Left Ventricle	heart
16	chr15:40232600-40251800	Strong transcription	Adipose Nuclei	Adipose
17	chr15:40235000-40263000	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr15:40236000-40255400	Strong transcription	Fetal Lung	lung
19	chr15:40236000-40260000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr15:40236600-40303000	Weak transcription	Small Intestine	intestine
21	chr15:40237800-40255600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:40238000-40277800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr15:40238600-40268200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr15:40238600-40272200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr15:40238800-40273200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:40239200-40259600	Weak transcription	Fetal Brain Male	brain
27	chr15:40239400-40261200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:40239400-40262000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:40239600-40251400	Strong transcription	Osteobl	bone
30	chr15:40239600-40261400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr15:40239800-40262200	Strong transcription	Muscle Satellite Cultured Cells	--
32	chr15:40240000-40251200	Strong transcription	NHDF-Ad	bronchial
33	chr15:40240200-40261000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:40240400-40252000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr15:40240800-40268000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:40241000-40252400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:40241000-40252400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:40241000-40268600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr15:40241200-40272600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:40241400-40256000	Strong transcription	Primary T cells from cord blood	blood
41	chr15:40241400-40260800	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr15:40241400-40262800	Strong transcription	Fetal Intestine Large	intestine
43	chr15:40241800-40259800	Weak transcription	Stomach Mucosa	stomach
44	chr15:40242400-40252800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:40242600-40255600	Strong transcription	Fetal Muscle Leg	muscle
46	chr15:40243000-40250800	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr15:40243200-40254800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr15:40243200-40262600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr15:40243400-40252400	Strong transcription	HUVEC	blood vessel
50	chr15:40243600-40251600	Strong transcription	Fetal Thymus	thymus

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