Variant report

Variant	rs1792122
Chromosome Location	chr11:121459522-121459523
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	GATA1	chr11:121459423-121460137	PBDE	blood:	n/a	chr11:121459819-121459827
2	TEAD4	chr11:121459417-121459972	K562	blood:	n/a	n/a
3	SPI1	chr11:121459409-121459929	HL-60	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120975216..120977193-chr11:121456635..121459591,2	K562	blood:

Variant related genes	Relation type
SORL1	TF binding region

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10892758	0.85[CEU][hapmap]
rs10892759	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1503422	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1503423	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1619545	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1620003	0.84[CEU][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1625828	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1629493	0.86[EUR][1000 genomes]
rs1699098	0.82[EUR][1000 genomes]
rs1699099	0.81[EUR][1000 genomes]
rs1699103	1.00[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1699106	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1699108	1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1784923	0.88[ASN][1000 genomes]
rs1784931	0.84[CEU][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1790213	0.86[YRI][hapmap];0.81[AFR][1000 genomes]
rs1792113	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1792125	1.00[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs639648	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs640479	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7112853	0.87[ASN][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	nsv975233	chr11:121359656-121574786	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv527072	chr11:121448090-121486552	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv34768	chr11:121452651-121534938	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121416600-121471800	Strong transcription	Primary T cells from cord blood	blood
2	chr11:121431000-121466400	Weak transcription	Ovary	ovary
3	chr11:121435200-121464800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:121440600-121485000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr11:121443400-121464600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:121443800-121461600	Weak transcription	Pancreas	Pancrea
7	chr11:121448400-121461200	Weak transcription	Gastric	stomach
8	chr11:121448800-121495600	Weak transcription	Stomach Mucosa	stomach
9	chr11:121449800-121465800	Weak transcription	Adipose Nuclei	Adipose
10	chr11:121450000-121460200	Weak transcription	Brain Germinal Matrix	brain
11	chr11:121450200-121460800	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr11:121450200-121461600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:121450200-121461800	Weak transcription	Fetal Brain Male	brain
14	chr11:121450600-121460600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:121451000-121462600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr11:121451200-121461600	Weak transcription	Fetal Kidney	kidney
17	chr11:121451200-121464000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:121451200-121488200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:121451400-121469600	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr11:121451400-121470000	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr11:121452000-121460000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:121452000-121466400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:121453000-121460200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:121453000-121470800	Strong transcription	HepG2	liver
25	chr11:121453200-121504200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr11:121453400-121462000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:121453400-121491200	Weak transcription	Small Intestine	intestine
28	chr11:121453400-121505400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr11:121453600-121462000	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr11:121453600-121469800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
31	chr11:121453800-121465800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:121454000-121503800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:121454200-121461200	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr11:121454400-121459800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:121454400-121459800	Weak transcription	Aorta	Aorta
36	chr11:121454400-121469600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr11:121454400-121504000	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr11:121454800-121459600	Weak transcription	HMEC	breast
39	chr11:121454800-121503600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr11:121455200-121461800	Strong transcription	Dnd41	blood
41	chr11:121455600-121461200	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr11:121455600-121503800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:121455800-121469800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:121456000-121460400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
45	chr11:121456200-121461600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:121456400-121462200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
47	chr11:121456400-121465600	Strong transcription	NHEK	skin
48	chr11:121456600-121459600	Genic enhancers	Primary hematopoietic stem cells	blood
49	chr11:121456600-121462000	Strong transcription	Stomach Smooth Muscle	stomach
50	chr11:121456600-121464000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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