Variant report

Variant	rs7101191
Chromosome Location	chr10:1105019-1105020
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
2	chr10:976791..979037-chr10:1103503..1105214,2	K562	blood:
3	chr10:975998..978434-chr10:1103106..1105638,3	MCF-7	breast:
4	chr10:1100859..1106350-chr10:1117983..1126025,11	MCF-7	breast:
5	chr10:1103509..1105162-chr10:1115825..1118791,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000067064	Chromatin interaction
ENSG00000047056	Chromatin interaction
ENSG00000107929	Chromatin interaction
ENSG00000229869	Chromatin interaction

Extended variants
information (count: 51 )
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];0.83[EUR][1000 genomes]
rs10903357	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]
rs10903359	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10903372	0.86[CHB][hapmap];0.89[MEX][hapmap]
rs11250239	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11250246	0.85[ASN][1000 genomes]
rs11250250	1.00[ASW][hapmap];0.95[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];0.88[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];0.92[ASN][1000 genomes]
rs11250253	1.00[ASW][hapmap];0.95[CEU][hapmap];0.93[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.84[AMR][1000 genomes];0.92[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];0.88[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];0.94[MEX][hapmap];1.00[YRI][hapmap]
rs11253564	0.84[CEU][hapmap]
rs1285	0.85[CEU][hapmap];0.84[GIH][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2170142	0.83[CEU][hapmap]
rs2279257	0.84[CEU][hapmap]
rs2306403	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[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];0.92[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];0.91[GIH][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7094916	0.84[CEU][hapmap]
rs7915650	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs7916430	0.86[CHB][hapmap];0.89[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 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	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
rs7101191	WDR37	cis	parietal	SCAN

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1103600-1105200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr10:1103600-1105800	Weak transcription	Gastric	stomach
3	chr10:1103600-1108200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr10:1103600-1109000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:1103600-1109600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:1103600-1110400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:1103600-1119400	Weak transcription	Aorta	Aorta
8	chr10:1103600-1119600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:1103800-1105200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr10:1103800-1107000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr10:1103800-1107600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:1103800-1108600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr10:1103800-1108800	Weak transcription	Fetal Stomach	stomach
14	chr10:1103800-1109400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr10:1103800-1118200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr10:1104000-1105200	Genic enhancers	Primary monocytes fromperipheralblood	blood
17	chr10:1104000-1105400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr10:1104000-1105800	Weak transcription	Fetal Intestine Small	intestine
19	chr10:1104000-1109400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr10:1104200-1105800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:1104200-1106800	Weak transcription	Lung	lung
22	chr10:1104200-1107000	Weak transcription	Thymus	Thymus
23	chr10:1104200-1107400	Weak transcription	Fetal Thymus	thymus
24	chr10:1104200-1107600	Weak transcription	NH-A	brain
25	chr10:1104200-1107800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:1104200-1108000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr10:1104200-1108200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr10:1104200-1108200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr10:1104200-1108400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:1104200-1108600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr10:1104200-1109000	Weak transcription	Fetal Brain Female	brain
32	chr10:1104200-1109200	Weak transcription	Placenta	Placenta
33	chr10:1104200-1109400	Weak transcription	Brain Substantia Nigra	brain
34	chr10:1104200-1109400	Weak transcription	Colonic Mucosa	Colon
35	chr10:1104200-1116800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:1104200-1116800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr10:1104200-1118000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr10:1104200-1118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr10:1104200-1118200	Weak transcription	Brain Angular Gyrus	brain
40	chr10:1104200-1119200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr10:1104200-1119200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr10:1104200-1119600	Weak transcription	Fetal Lung	lung
43	chr10:1104200-1119600	Weak transcription	Psoas Muscle	Psoas
44	chr10:1104200-1119600	Weak transcription	Rectal Smooth Muscle	rectum
45	chr10:1104400-1105200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:1104400-1105800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr10:1104400-1105800	Weak transcription	Pancreas	Pancrea
48	chr10:1104400-1105800	Weak transcription	Right Atrium	heart
49	chr10:1104400-1106000	Weak transcription	Right Ventricle	heart
50	chr10:1104400-1106200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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