Variant report

Variant	rs10903357
Chromosome Location	chr10:1101535-1101536
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:1101242-1104708	IMR90	lung:	n/a	n/a
2	SPI1	chr10:1101517-1101915	HL-60	blood:	n/a	n/a
3	CHD1	chr10:1100666-1103912	IMR90	lung:	n/a	chr10:1103297-1103307
4	POLR2A	chr10:1101523-1103113	PBDE	blood:	n/a	n/a
5	POLR2A	chr10:1101450-1103158	GM18505	blood:	n/a	n/a
6	IRF1	chr10:1101305-1102967	K562	blood:	n/a	chr10:1101389-1101400 chr10:1102285-1102294 chr10:1101388-1101400
7	POLR2A	chr10:1101270-1101775	GM12878	blood:	n/a	n/a
8	POLR2A	chr10:1101489-1101618	HUVEC	blood vessel:	n/a	n/a
9	POLR2A	chr10:1099971-1103106	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr10:1099924-1103110	K562	blood:	n/a	n/a
11	ZNF384	chr10:1101511-1101758	GM12878	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:833990..835898-chr10:1099433..1102164,2	K562	blood:
2	chr10:1031887..1035944-chr10:1099515..1103666,8	MCF-7	breast:
3	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
4	chr10:1034367..1036220-chr10:1101305..1103834,2	MCF-7	breast:
5	chr10:1033196..1035740-chr10:1100283..1103390,4	K562	blood:
6	chr10:1031711..1035740-chr10:1100728..1103796,4	K562	blood:
7	chr10:1101227..1103442-chr17:57918099..57920735,2	MCF-7	breast:
8	chr10:1024931..1026734-chr10:1099565..1101968,2	MCF-7	breast:
9	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
10	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
11	chr10:1100725..1104850-chr10:1118585..1122154,6	K562	blood:
12	chr10:1101511..1104003-chr10:3108866..3111744,3	MCF-7	breast:
13	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
14	chr10:1100859..1106350-chr10:1117983..1126025,11	MCF-7	breast:

No data

Variant related genes	Relation type
WDR37	TF binding region
ENSG00000107937	Chromatin interaction
ENSG00000107929	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000067064	Chromatin interaction
ENSG00000205740	Chromatin interaction
ENSG00000047056	Chromatin interaction
ENSG00000067057	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10903355	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10903359	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10903372	0.86[CHB][hapmap];0.90[MEX][hapmap]
rs11250239	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11250246	0.84[ASN][1000 genomes]
rs11250250	1.00[ASW][hapmap];0.95[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];0.92[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11250253	1.00[ASW][hapmap];0.95[CEU][hapmap];0.93[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11250254	0.94[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11250263	0.88[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap]
rs11250266	1.00[ASW][hapmap];0.90[CEU][hapmap];0.93[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];1.00[YRI][hapmap]
rs11253564	0.84[CEU][hapmap]
rs1285	0.85[CEU][hapmap];0.87[GIH][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2170142	0.83[CEU][hapmap]
rs2279257	0.84[CEU][hapmap]
rs2306403	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2306404	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs2306406	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs2306408	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs2387217	1.00[ASW][hapmap];0.95[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.87[GIH][hapmap];0.92[JPT][hapmap];0.90[LWK][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3765102	0.84[CEU][hapmap]
rs58551457	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs61830994	0.85[AMR][1000 genomes]
rs6560711	0.90[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap]
rs68128658	0.81[AMR][1000 genomes]
rs7071250	0.84[CEU][hapmap]
rs7075695	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.90[GIH][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7094916	0.84[CEU][hapmap]
rs7101191	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs7915650	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs7916430	0.86[CHB][hapmap];0.90[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
3	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS 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 target site	34 gene(s)	inside rSNPs	diseases
8	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv1050577	chr10:986723-1277854	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv540409	chr10:986723-1277854	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
14	nsv949405	chr10:1010464-1376105	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv1048254	chr10:1016006-1146595	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
16	nsv1040178	chr10:1024910-1126104	Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	nsv540410	chr10:1024910-1126104	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
18	nsv894722	chr10:1058837-1274538	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
19	nsv1046220	chr10:1064024-1188998	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
20	nsv894723	chr10:1073684-1259485	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
21	nsv5532	chr10:1079499-1101700	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
22	nsv894724	chr10:1084942-1116294	Flanking Active TSS Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10903357	WDR37	cis	parietal	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1095800-1102000	Weak transcription	Spleen	Spleen
2	chr10:1096000-1101800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr10:1096000-1101800	Weak transcription	Gastric	stomach
4	chr10:1096800-1101600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:1096800-1101800	Weak transcription	Esophagus	oesophagus
6	chr10:1099200-1101800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr10:1099400-1101600	Weak transcription	Ovary	ovary
8	chr10:1100000-1101600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:1100000-1101600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr10:1100000-1101600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr10:1100000-1101800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:1100000-1101800	Weak transcription	Lung	lung
13	chr10:1100000-1103800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr10:1100200-1101600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr10:1100200-1101600	Enhancers	Fetal Heart	heart
16	chr10:1100200-1101600	Weak transcription	Left Ventricle	heart
17	chr10:1100200-1101600	Weak transcription	Pancreas	Pancrea
18	chr10:1100400-1101600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:1100400-1101600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:1100400-1101600	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr10:1100400-1101600	Enhancers	Brain Cingulate Gyrus	brain
22	chr10:1100400-1101600	Flanking Active TSS	NHEK	skin
23	chr10:1100600-1101600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:1100600-1101600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr10:1100600-1101600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr10:1100600-1101600	Flanking Active TSS	HUVEC	blood vessel
27	chr10:1100800-1101600	Enhancers	Primary T cells fromperipheralblood	blood
28	chr10:1100800-1101600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr10:1100800-1101600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr10:1100800-1101600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr10:1100800-1101600	Enhancers	Brain Angular Gyrus	brain
32	chr10:1100800-1101600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr10:1100800-1101600	Enhancers	Fetal Stomach	stomach
34	chr10:1100800-1101600	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr10:1100800-1101600	Enhancers	Thymus	Thymus
36	chr10:1100800-1101600	Flanking Active TSS	Hela-S3	cervix
37	chr10:1100800-1101600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr10:1100800-1101800	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr10:1100800-1101800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr10:1100800-1101800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr10:1100800-1101800	Flanking Active TSS	Liver	Liver
42	chr10:1100800-1102000	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr10:1100800-1104400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr10:1101000-1101600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr10:1101000-1101600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:1101000-1101600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
47	chr10:1101000-1101600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr10:1101000-1101600	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr10:1101000-1101600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr10:1101000-1101600	Flanking Active TSS	K562	blood

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