Variant report

Variant	rs16969894
Chromosome Location	chr15:78776456-78776457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:78775973..78778928-chr15:78790506..78793354,2	K562	blood:
2	chr15:78728533..78731605-chr15:78775460..78778377,3	K562	blood:

Variant related genes	Relation type
ENSG00000136381	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10851906	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11072763	0.88[EUR][1000 genomes]
rs11072766	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12101809	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2036529	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2036533	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2568483	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2568485	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2568488	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2568490	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2568493	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2568497	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2568499	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2656055	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2656056	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2656069	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2656070	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2656071	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2656072	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2656073	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2656074	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28480606	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28511883	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28602670	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2869032	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2869045	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2915695	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2938671	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2938674	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2958719	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35031105	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4887053	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7174190	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7174348	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs924840	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs958025	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9672608	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
2	esv1806890	chr15:78744695-78786064	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16969894	IREB2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78732200-78799400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:78741200-78781800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78751000-78793200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr15:78754000-78789400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:78754400-78787600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr15:78754600-78793400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr15:78754800-78793800	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr15:78755000-78787000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr15:78755000-78787000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr15:78755000-78793800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr15:78755000-78794400	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr15:78755200-78779000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:78755200-78783800	Strong transcription	Primary B cells from peripheral blood	blood
14	chr15:78755200-78787000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:78755200-78792600	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr15:78755200-78793400	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr15:78755200-78793600	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr15:78755200-78793800	Strong transcription	Fetal Thymus	thymus
19	chr15:78755200-78794000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr15:78755200-78794600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr15:78755400-78779000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr15:78755400-78783200	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr15:78755400-78791400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr15:78755400-78791400	Strong transcription	Fetal Muscle Trunk	muscle
25	chr15:78755400-78791800	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr15:78755400-78792600	Strong transcription	Fetal Muscle Leg	muscle
27	chr15:78755400-78793600	Strong transcription	Liver	Liver
28	chr15:78756000-78783600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr15:78756000-78792800	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr15:78756000-78793600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:78757000-78789600	Weak transcription	Stomach Mucosa	stomach
32	chr15:78758400-78778200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:78758800-78776800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:78759000-78793000	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr15:78759800-78793800	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:78760800-78787000	Weak transcription	Aorta	Aorta
37	chr15:78761800-78792000	Strong transcription	Duodenum Mucosa	Duodenum
38	chr15:78762200-78791600	Strong transcription	Fetal Intestine Large	intestine
39	chr15:78766000-78799200	Weak transcription	Fetal Heart	heart
40	chr15:78766800-78776600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr15:78767800-78785800	Strong transcription	Fetal Lung	lung
42	chr15:78767800-78792600	Strong transcription	Primary T cells from cord blood	blood
43	chr15:78767800-78794200	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr15:78769400-78776800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr15:78769400-78780000	Strong transcription	Fetal Stomach	stomach
46	chr15:78769600-78776600	Strong transcription	Fetal Intestine Small	intestine
47	chr15:78769600-78777000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr15:78770200-78778000	Weak transcription	Brain Angular Gyrus	brain
49	chr15:78771000-78778000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr15:78771000-78778600	Weak transcription	Esophagus	oesophagus

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