Variant report

Variant	rs10898437
Chromosome Location	chr11:85847881-85847882
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:85844022..85845904-chr11:85847037..85849621,3	K562	blood:
2	chr11:85810855..85813680-chr11:85847452..85850001,2	K562	blood:
3	chr11:85838134..85840505-chr11:85845229..85848211,2	K562	blood:
4	chr11:85844772..85849892-chr11:85856973..85861809,6	K562	blood:
5	chr11:85846668..85849486-chr11:85860309..85862549,2	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10792829	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs10898433	0.81[JPT][hapmap]
rs10898436	0.93[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10898441	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11234532	0.81[JPT][hapmap]
rs11234542	0.95[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs11234545	0.94[CHB][hapmap];0.88[JPT][hapmap]
rs11234551	0.85[ASN][1000 genomes]
rs11234552	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234562	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11234564	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.89[MKK][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1513389	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17209931	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs17817153	0.81[JPT][hapmap]
rs4944558	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7480193	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[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	nsv1050948	chr11:85756325-85968665	Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv541117	chr11:85756325-85968665	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv832223	chr11:85845315-86015957	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85843600-85848200	Enhancers	Fetal Intestine Large	intestine
2	chr11:85843800-85848200	Enhancers	Fetal Intestine Small	intestine
3	chr11:85845200-85858600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:85845400-85848000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:85845400-85849400	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr11:85845600-85848000	Enhancers	Brain Angular Gyrus	brain
7	chr11:85845600-85848000	Enhancers	Brain Anterior Caudate	brain
8	chr11:85845600-85848200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:85845800-85848000	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr11:85845800-85859800	Weak transcription	Aorta	Aorta
11	chr11:85846000-85848000	Enhancers	Brain Substantia Nigra	brain
12	chr11:85846000-85851600	Weak transcription	Right Atrium	heart
13	chr11:85846400-85849800	Weak transcription	Liver	Liver
14	chr11:85846400-85851600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:85846400-85862200	Weak transcription	Psoas Muscle	Psoas
16	chr11:85846600-85848200	Enhancers	Duodenum Mucosa	Duodenum
17	chr11:85846600-85848600	Enhancers	K562	blood
18	chr11:85846800-85848000	Enhancers	Small Intestine	intestine
19	chr11:85846800-85849200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr11:85847000-85848000	Enhancers	Adipose Nuclei	Adipose
21	chr11:85847000-85848000	Enhancers	Osteobl	bone
22	chr11:85847200-85848000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:85847200-85848000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:85847200-85848000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:85847200-85848000	Enhancers	Ovary	ovary
26	chr11:85847200-85848200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr11:85847400-85848000	Enhancers	Brain Hippocampus Middle	brain
28	chr11:85847400-85848200	Enhancers	Primary hematopoietic stem cells	blood
29	chr11:85847400-85849400	Weak transcription	Placenta	Placenta
30	chr11:85847400-85855600	Weak transcription	Stomach Mucosa	stomach
31	chr11:85847600-85848000	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr11:85847600-85848000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr11:85847600-85848000	Enhancers	Rectal Smooth Muscle	rectum
34	chr11:85847600-85848000	Active TSS	Stomach Smooth Muscle	stomach
35	chr11:85847800-85848000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:85847800-85848000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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