Variant report

Variant	rs10518870
Chromosome Location	chr15:57017888-57017889
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:56999178..57001451-chr15:57017169..57019734,2	K562	blood:

Variant related genes	Relation type
ENSG00000137871	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11630168	0.84[CEU][hapmap]
rs11638497	0.83[EUR][1000 genomes]
rs11638580	0.83[EUR][1000 genomes]
rs11638707	0.88[CEU][hapmap];0.82[MEX][hapmap];0.83[TSI][hapmap]
rs11856558	0.82[CEU][hapmap]
rs11857706	0.80[CEU][hapmap]
rs12442189	0.88[CEU][hapmap];0.86[MEX][hapmap];0.83[TSI][hapmap]
rs12591502	0.90[CEU][hapmap]
rs12592389	0.84[CEU][hapmap]
rs12595822	0.84[EUR][1000 genomes]
rs12898521	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs12900244	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs12900441	0.80[EUR][1000 genomes]
rs12901887	0.92[CEU][hapmap];0.95[CHB][hapmap]
rs12903283	0.86[MEX][hapmap]
rs12903336	0.80[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs12903862	0.90[MEX][hapmap]
rs12905514	0.88[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.83[EUR][1000 genomes]
rs12906591	0.81[EUR][1000 genomes]
rs12910459	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12911381	0.92[CEU][hapmap];0.86[MEX][hapmap]
rs12912666	0.84[CEU][hapmap]
rs12913361	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs12913960	0.81[EUR][1000 genomes]
rs1424694	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs17238845	0.80[CEU][hapmap];0.86[MEX][hapmap]
rs1979467	0.80[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs1994081	0.84[CEU][hapmap]
rs2170463	0.85[MEX][hapmap]
rs2279298	0.88[CEU][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs2279299	0.84[CEU][hapmap]
rs28620278	0.88[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs3803457	0.80[CEU][hapmap];0.86[MEX][hapmap]
rs4774244	0.88[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs4774886	0.88[CEU][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap]
rs521904	0.82[EUR][1000 genomes]
rs538382	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs553421	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs62022931	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62022933	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62022934	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6493885	0.80[EUR][1000 genomes]
rs7162317	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs7168178	0.84[CEU][hapmap]
rs795032	0.81[EUR][1000 genomes]
rs8025391	0.84[CEU][hapmap]
rs8043223	0.84[CEU][hapmap]

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	esv3422474	chr15:56867190-57244330	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv569576	chr15:57012816-57126917	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56958400-57019200	Weak transcription	Fetal Intestine Small	intestine
2	chr15:56971000-57023400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:56992400-57021800	Weak transcription	Right Ventricle	heart
4	chr15:56992600-57022600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:56993000-57024000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:56993400-57021600	Weak transcription	Fetal Brain Male	brain
7	chr15:56994000-57023800	Weak transcription	Fetal Kidney	kidney
8	chr15:56995800-57022200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:56996000-57021800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr15:56996400-57021600	Weak transcription	HSMMtube	muscle
11	chr15:56996400-57022600	Weak transcription	NH-A	brain
12	chr15:56996800-57022600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:56997200-57022800	Weak transcription	Gastric	stomach
14	chr15:56997200-57023800	Weak transcription	Fetal Stomach	stomach
15	chr15:56998400-57021200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr15:56998800-57021800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr15:56998800-57023400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr15:56998800-57023800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr15:56999400-57023400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:57009200-57021400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:57009400-57022800	Weak transcription	Right Atrium	heart
22	chr15:57009400-57024400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:57011000-57022200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:57011200-57022600	Weak transcription	Fetal Heart	heart
25	chr15:57011400-57021200	Weak transcription	Brain Substantia Nigra	brain
26	chr15:57011400-57021400	Weak transcription	Adipose Nuclei	Adipose
27	chr15:57011400-57021800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:57011600-57018400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr15:57011600-57021000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr15:57011600-57022600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:57011600-57023400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr15:57011600-57024400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr15:57011600-57024400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr15:57011800-57019200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr15:57011800-57022600	Weak transcription	HMEC	breast
36	chr15:57011800-57024000	Weak transcription	Aorta	Aorta
37	chr15:57012400-57022600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr15:57012400-57022600	Weak transcription	Osteobl	bone
39	chr15:57012400-57025000	Weak transcription	Spleen	Spleen
40	chr15:57012600-57022600	Weak transcription	NHEK	skin
41	chr15:57012600-57023000	Weak transcription	NHLF	lung
42	chr15:57012600-57023400	Weak transcription	Psoas Muscle	Psoas
43	chr15:57013000-57022800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr15:57013200-57022600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr15:57013400-57024200	Weak transcription	Ovary	ovary
46	chr15:57014000-57022400	Weak transcription	Brain Germinal Matrix	brain
47	chr15:57014200-57022800	Weak transcription	K562	blood
48	chr15:57014800-57019200	Weak transcription	A549	lung
49	chr15:57015400-57022600	Weak transcription	HUVEC	blood vessel
50	chr15:57015800-57018600	Enhancers	Colon Smooth Muscle	Colon

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