Variant report

Variant	rs11836509
Chromosome Location	chr12:25380071-25380072
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10743548	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771175	0.84[AMR][1000 genomes]
rs10771176	0.84[AMR][1000 genomes]
rs10771183	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10842503	0.88[ASN][1000 genomes]
rs10842515	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10842516	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10842517	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11047878	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11047879	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11047885	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11047903	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11047904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11047908	0.90[ASN][1000 genomes]
rs11047914	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1137282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12367971	0.84[AMR][1000 genomes]
rs17388573	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17389103	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3924650	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4368021	0.91[EUR][1000 genomes]
rs4606562	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61761150	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61762422	0.81[ASN][1000 genomes]
rs7133640	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7298444	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7303373	0.84[AMR][1000 genomes]
rs7309670	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7960917	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7964623	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7965763	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7968023	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7973450	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7973623	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7977616	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7980769	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7980834	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898922	chr12:25274593-25408047	Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv898923	chr12:25357680-25397282	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv898924	chr12:25357680-25398972	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv557798	chr12:25359841-25397282	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv898925	chr12:25367669-25398972	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv898926	chr12:25367669-25408047	Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25348600-25402200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:25348600-25403200	Weak transcription	Spleen	Spleen
3	chr12:25349000-25386000	Weak transcription	Left Ventricle	heart
4	chr12:25349000-25402400	Weak transcription	Right Ventricle	heart
5	chr12:25349400-25388200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr12:25349400-25388600	Weak transcription	NHLF	lung
7	chr12:25349400-25393800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr12:25349400-25396000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr12:25349400-25401800	Weak transcription	Fetal Brain Male	brain
10	chr12:25349400-25402600	Weak transcription	Brain Germinal Matrix	brain
11	chr12:25349600-25389000	Weak transcription	Brain Angular Gyrus	brain
12	chr12:25349600-25394600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:25349600-25402600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr12:25349600-25402600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr12:25349600-25402600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr12:25349600-25402600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr12:25349800-25386200	Weak transcription	Hela-S3	cervix
18	chr12:25349800-25390200	Weak transcription	K562	blood
19	chr12:25350000-25402800	Weak transcription	Ovary	ovary
20	chr12:25354000-25402400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:25354400-25402200	Weak transcription	Pancreas	Pancrea
22	chr12:25354600-25389000	Weak transcription	HSMMtube	muscle
23	chr12:25355800-25396000	Weak transcription	Small Intestine	intestine
24	chr12:25356600-25402600	Weak transcription	Fetal Heart	heart
25	chr12:25360200-25380200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:25360800-25388600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr12:25360800-25389200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr12:25360800-25402200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:25361000-25383800	Weak transcription	NHEK	skin
30	chr12:25361000-25388000	Weak transcription	A549	lung
31	chr12:25361000-25388600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr12:25361000-25388800	Weak transcription	Esophagus	oesophagus
33	chr12:25361000-25395800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr12:25361000-25402600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr12:25361000-25402600	Weak transcription	Fetal Brain Female	brain
36	chr12:25361200-25388400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr12:25361200-25389200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr12:25362000-25402400	Weak transcription	HepG2	liver
39	chr12:25362600-25380200	Weak transcription	Primary T cells from cord blood	blood
40	chr12:25363400-25388000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr12:25365200-25393800	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:25367800-25388200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:25369600-25388200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr12:25370000-25380200	Weak transcription	Fetal Intestine Large	intestine
45	chr12:25372400-25381000	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr12:25372400-25402800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr12:25373000-25393800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr12:25373400-25388200	Weak transcription	GM12878-XiMat	blood
49	chr12:25374200-25381400	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr12:25374200-25383800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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