Variant report

Variant	rs2255410
Chromosome Location	chr15:43831097-43831098
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	15:43807815-43812531..15:43825784-43834250	K562	blood:
2	15:43792489-43802874..15:43825784-43834250	K562	blood:
3	15:43825784-43834250..15:44067689-44069261	Hela-S3	cervix:
4	15:43825784-43834250..15:44034348-44042259	Hela-S3	cervix:
5	15:43782117-43785993..15:43825784-43834250	Hela-S3	cervix:
6	chr15:43828054..43831995-chr15:43833960..43836416,4	K562	blood:

Variant related genes	Relation type
ENSG00000205771	Chromatin interaction
ENSG00000067369	Chromatin interaction
ENSG00000128886	Chromatin interaction
ENSG00000167004	Chromatin interaction
ENSG00000166963	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs1060939	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1079309	0.91[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12905772	0.84[CEU][hapmap]
rs1814538	0.95[JPT][hapmap]
rs1869258	1.00[CEU][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2242069	0.95[JPT][hapmap]
rs2244981	0.91[CEU][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2245715	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2249952	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2251844	0.98[ASN][1000 genomes]
rs2253268	0.91[CEU][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2253708	0.91[JPT][hapmap]
rs2254927	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2255042	0.99[ASN][1000 genomes]
rs2255051	0.95[ASN][1000 genomes]
rs2255440	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2255663	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2264050	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2264876	0.91[JPT][hapmap]
rs2278857	0.87[CEU][hapmap]
rs2412781	0.91[CEU][hapmap]
rs2439831	0.95[JPT][hapmap]
rs2439832	0.95[JPT][hapmap]
rs2439834	0.89[ASN][1000 genomes]
rs2439839	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2439843	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2439845	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2439846	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2439850	0.91[JPT][hapmap]
rs2444032	0.95[JPT][hapmap]
rs2444244	0.94[ASN][1000 genomes]
rs2444250	0.91[JPT][hapmap]
rs2444251	0.91[CEU][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2467736	0.95[JPT][hapmap]
rs2467737	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2467738	0.87[CEU][hapmap];0.91[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2467739	0.95[JPT][hapmap]
rs2467741	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2467742	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2467745	0.91[CEU][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2470130	0.99[ASN][1000 genomes]
rs2470131	0.99[ASN][1000 genomes]
rs2602141	0.91[CEU][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28649346	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2915788	0.95[ASN][1000 genomes]
rs2924369	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2927070	0.80[AMR][1000 genomes]
rs3097773	0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs3809482	0.91[CEU][hapmap]
rs4296223	0.91[CEU][hapmap]
rs4547312	0.87[CEU][hapmap]
rs475486	0.92[ASN][1000 genomes]
rs480108	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs486301	0.98[ASN][1000 genomes]
rs493377	0.91[CEU][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs495175	0.91[JPT][hapmap]
rs496584	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs506120	0.91[CEU][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs518288	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs523156	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs529611	1.00[CEU][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs536313	0.91[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs537115	0.95[JPT][hapmap]
rs542898	0.84[AMR][1000 genomes]
rs548704	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs560191	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs570933	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs572837	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6493083	0.91[CEU][hapmap]
rs689647	0.95[JPT][hapmap]
rs689693	0.82[AMR][1000 genomes]
rs689767	0.88[CEU][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs689781	0.95[JPT][hapmap]
rs689797	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs689826	0.91[JPT][hapmap]
rs689835	0.91[JPT][hapmap]
rs689883	0.97[ASN][1000 genomes]
rs690012	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs690276	0.91[CEU][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes]
rs690316	0.91[JPT][hapmap]
rs690367	0.91[CEU][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs690436	0.95[JPT][hapmap]
rs690446	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs690466	0.91[JPT][hapmap]
rs690472	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs690512	0.88[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes]
rs693510	0.88[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes]
rs694725	0.91[CEU][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs694985	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7163288	0.91[CEU][hapmap]
rs7497780	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9920879	0.91[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534649	chr15:43591116-43851142	Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	esv1846172	chr15:43632138-44116986	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	esv1846701	chr15:43759774-44116986	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv437799	chr15:43784000-43989518	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv832988	chr15:43804641-43976862	Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
6	nsv428304	chr15:43823158-44008580	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	esv2758379	chr15:43823158-44148641	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
8	esv2760028	chr15:43823158-44148641	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
9	nsv427960	chr15:43823158-44148641	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
10	nsv428633	chr15:43823160-44008580	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs2255410	AC011330.5	cis	Thyroid	GTEx
rs2255410	STRCP1	cis	Whole Blood	GTEx
rs2255410	ZSCAN29	cis	Thyroid	GTEx
rs2255410	TGM5	cis	multi-tissue	Pritchard
rs2255410	ZSCAN29	cis	multi-tissue	Pritchard
rs2255410	STRCP1	cis	Esophagus Muscularis	GTEx
rs2255410	TGM7	cis	Esophagus Mucosa	GTEx
rs2255410	AC011330.5	cis	Artery Tibial	GTEx

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43812000-43844400	Weak transcription	Fetal Brain Male	brain
2	chr15:43815400-43833600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr15:43815800-43839400	Weak transcription	Stomach Mucosa	stomach
4	chr15:43818000-43835400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr15:43818000-43852600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr15:43818200-43851600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr15:43822800-43842800	Weak transcription	HSMM	muscle
8	chr15:43823200-43835600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr15:43823600-43837400	Weak transcription	Fetal Lung	lung
10	chr15:43823600-43840000	Weak transcription	Psoas Muscle	Psoas
11	chr15:43823800-43833200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:43823800-43836400	Weak transcription	NHLF	lung
13	chr15:43823800-43852600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr15:43824200-43833400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:43824200-43842800	Weak transcription	HSMMtube	muscle
16	chr15:43824200-43845000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:43824800-43853000	Weak transcription	GM12878-XiMat	blood
18	chr15:43824800-43853200	Weak transcription	Hela-S3	cervix
19	chr15:43826000-43832000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr15:43827200-43849800	Weak transcription	Colonic Mucosa	Colon
21	chr15:43827400-43831400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:43827400-43834200	Weak transcription	Fetal Brain Female	brain
23	chr15:43827400-43839800	Weak transcription	Colon Smooth Muscle	Colon
24	chr15:43827400-43841400	Weak transcription	NHEK	skin
25	chr15:43827400-43842400	Weak transcription	Osteobl	bone
26	chr15:43827400-43852600	Weak transcription	Left Ventricle	heart
27	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr15:43827600-43834200	Weak transcription	Dnd41	blood
29	chr15:43827600-43837000	Weak transcription	Gastric	stomach
30	chr15:43827600-43839200	Weak transcription	Primary T cells from cord blood	blood
31	chr15:43827600-43839200	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr15:43827600-43840400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr15:43827600-43840400	Weak transcription	Fetal Stomach	stomach
34	chr15:43827600-43846800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr15:43827600-43848400	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr15:43827600-43848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr15:43827600-43849000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:43827600-43849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr15:43827600-43851200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr15:43827600-43851400	Weak transcription	Right Ventricle	heart
41	chr15:43827600-43851800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr15:43827600-43852800	Weak transcription	Lung	lung
43	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
44	chr15:43827600-43855400	Weak transcription	Ovary	ovary
45	chr15:43827800-43831200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr15:43827800-43831400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr15:43827800-43833200	Weak transcription	K562	blood
48	chr15:43827800-43834000	Weak transcription	Adipose Nuclei	Adipose
49	chr15:43827800-43834200	Weak transcription	Placenta	Placenta
50	chr15:43827800-43835600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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