Variant report

Variant	rs34693097
Chromosome Location	chr15:31253984-31253985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:31253672-31255135	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:31252830..31256274-chr15:31263661..31267030,3	K562	blood:
2	chr15:31242525..31245070-chr15:31253686..31255271,2	K562	blood:
3	chr15:31253352..31256135-chr15:31282312..31285268,3	K562	blood:
4	chr15:31253352..31256135-chr15:31282609..31285268,3	K562	blood:

Variant related genes	Relation type
MTMR10	TF binding region
ENSG00000166912	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1043742	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11293	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11629793	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11634216	0.83[EUR][1000 genomes]
rs11634761	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11637469	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11638409	0.83[EUR][1000 genomes]
rs11639169	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12906054	0.83[EUR][1000 genomes]
rs1425292	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1474380	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2140734	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34095794	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34294266	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34331396	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34909055	0.88[EUR][1000 genomes]
rs3512	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35239376	0.83[EUR][1000 genomes]
rs35256769	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35396566	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35607976	0.85[EUR][1000 genomes]
rs35784593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3817498	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61997079	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61997138	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61997139	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61997140	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7168641	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7176569	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8031584	0.83[EUR][1000 genomes]
rs8032942	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8034856	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs890159	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427955	chr15:30467980-31273174	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv531138	chr15:30653877-31609679	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv916936	chr15:30921917-31337510	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv525795	chr15:30936285-31324531	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS 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	35 gene(s)	inside rSNPs	diseases
5	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1046874	chr15:31008133-31294654	Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
8	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv832951	chr15:31131239-31304469	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	28 gene(s)	inside rSNPs	diseases
10	nsv1039037	chr15:31140415-31277268	Strong transcription ZNF genes & repeats Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv542309	chr15:31140415-31277268	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv1036018	chr15:31140415-31544888	Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
13	nsv521842	chr15:31140700-31272670	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	nsv903834	chr15:31179534-31293774	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	esv33507	chr15:31183324-31471023	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers 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	35 gene(s)	inside rSNPs	diseases
16	nsv832952	chr15:31204426-31333998	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31200600-31254800	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr15:31225400-31255800	Strong transcription	Fetal Intestine Large	intestine
3	chr15:31225800-31256000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr15:31226000-31255800	Strong transcription	Fetal Stomach	stomach
5	chr15:31226000-31258800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr15:31226200-31269200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr15:31226400-31260800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr15:31226600-31254400	Strong transcription	Fetal Thymus	thymus
9	chr15:31226600-31255200	Strong transcription	Duodenum Smooth Muscle	Duodenum
10	chr15:31227000-31269600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr15:31227200-31255800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:31227200-31258800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr15:31228400-31254400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr15:31228400-31254600	Strong transcription	Thymus	Thymus
15	chr15:31228600-31258800	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr15:31229000-31254800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr15:31229200-31261000	Strong transcription	Primary B cells from peripheral blood	blood
18	chr15:31230400-31258800	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr15:31233400-31269200	Strong transcription	Liver	Liver
20	chr15:31236600-31255000	Strong transcription	Rectal Smooth Muscle	rectum
21	chr15:31237200-31269600	Strong transcription	Primary B cells from cord blood	blood
22	chr15:31238200-31254600	Strong transcription	Fetal Lung	lung
23	chr15:31238600-31255200	Strong transcription	Fetal Kidney	kidney
24	chr15:31240400-31255000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr15:31241400-31254600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:31242000-31282800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr15:31242200-31254600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr15:31242400-31255800	Strong transcription	Fetal Intestine Small	intestine
29	chr15:31243000-31254400	Strong transcription	Primary hematopoietic stem cells	blood
30	chr15:31243200-31254800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr15:31243200-31267600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:31245000-31276400	Weak transcription	Brain Germinal Matrix	brain
33	chr15:31246600-31254400	Weak transcription	Right Atrium	heart
34	chr15:31246800-31254400	Weak transcription	Fetal Heart	heart
35	chr15:31247000-31254200	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr15:31247000-31270200	Weak transcription	K562	blood
37	chr15:31247200-31254400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:31247400-31260600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr15:31247600-31261000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr15:31247800-31258800	Strong transcription	Stomach Smooth Muscle	stomach
41	chr15:31248200-31254600	Strong transcription	Primary T cells from cord blood	blood
42	chr15:31248200-31255200	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr15:31248400-31254200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr15:31248400-31254600	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr15:31248800-31255000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr15:31248800-31259800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:31248800-31283000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr15:31249000-31254400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:31249000-31269600	Strong transcription	HUVEC	blood vessel
50	chr15:31249000-31270200	Weak transcription	Stomach Mucosa	stomach

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