Variant report

Variant	rs403186
Chromosome Location	chr5:16527431-16527432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:16465063..16466907-chr5:16527277..16528831,2	K562	blood:
2	chr5:16527152..16530063-chr5:16533839..16538809,7	K562	blood:
3	chr5:16521375..16523909-chr5:16526389..16530359,4	K562	blood:
4	chr5:16522409..16525329-chr5:16526389..16528895,4	K562	blood:
5	chr5:16417923..16420482-chr5:16527282..16529023,2	K562	blood:
6	chr5:16471300..16474284-chr5:16525885..16528906,3	K562	blood:

Variant related genes	Relation type
ENSG00000173545	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16868758	1.00[CHD][hapmap]
rs16868760	1.00[CHD][hapmap]
rs334483	1.00[ASW][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.90[MKK][hapmap];0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334484	1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334493	0.87[ASW][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.90[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs431440	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs437407	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.90[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs441908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv881187	chr5:16514269-16654960	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16509600-16528800	Weak transcription	Brain Hippocampus Middle	brain
2	chr5:16516000-16540800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr5:16519800-16531400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr5:16521600-16539600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:16522200-16528800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:16522400-16529000	Weak transcription	Stomach Mucosa	stomach
7	chr5:16522400-16567400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr5:16522600-16528400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr5:16522600-16530000	Weak transcription	Right Atrium	heart
10	chr5:16523400-16540800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr5:16523600-16533800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr5:16523600-16535400	Weak transcription	Pancreas	Pancrea
13	chr5:16523800-16528600	Weak transcription	Fetal Intestine Large	intestine
14	chr5:16523800-16539000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr5:16523800-16540800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr5:16524200-16528600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr5:16524200-16528600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr5:16524400-16529600	Weak transcription	Psoas Muscle	Psoas
19	chr5:16524400-16529800	Weak transcription	Brain Substantia Nigra	brain
20	chr5:16524600-16531800	Weak transcription	Small Intestine	intestine
21	chr5:16524600-16533800	Weak transcription	Right Ventricle	heart
22	chr5:16525000-16528600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr5:16525000-16528600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr5:16525000-16529800	Weak transcription	Brain Angular Gyrus	brain
25	chr5:16525000-16540800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr5:16525000-16542000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr5:16525200-16528600	Weak transcription	Fetal Brain Female	brain
28	chr5:16525200-16540400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr5:16525600-16539200	Weak transcription	Gastric	stomach
30	chr5:16525800-16528200	Weak transcription	Fetal Brain Male	brain
31	chr5:16525800-16528400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:16525800-16528600	Weak transcription	Fetal Muscle Leg	muscle
33	chr5:16525800-16528600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr5:16526200-16528600	Weak transcription	Fetal Intestine Small	intestine
35	chr5:16526200-16529800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr5:16526400-16537400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr5:16526600-16528600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr5:16526600-16528800	Weak transcription	Fetal Heart	heart
39	chr5:16527200-16533800	Weak transcription	Primary T cells from cord blood	blood
40	chr5:16527200-16534400	Weak transcription	Thymus	Thymus
41	chr5:16527400-16528600	Weak transcription	Left Ventricle	heart

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