Variant report

Variant	rs10849855
Chromosome Location	chr12:121651373-121651374
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:121645581..121650866-chr12:121650989..121654547,8	K562	blood:

Variant related genes	Relation type
ENSG00000135124	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10774587	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10849856	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10849858	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11065479	0.89[AMR][1000 genomes]
rs11065486	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1169720	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1169727	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1180051	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1182945	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1629287	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1653622	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1653623	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1718117	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2071271	0.87[ASN][1000 genomes]
rs2393849	0.90[ASN][1000 genomes]
rs2393850	0.88[ASN][1000 genomes]
rs25643	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2567978	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2567980	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2567993	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2567994	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2668235	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2668252	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2686362	0.93[AMR][1000 genomes]
rs2686363	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2686387	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2686388	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2942063	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58232824	0.90[ASN][1000 genomes]
rs6489799	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs725135	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7298368	0.87[ASN][1000 genomes]
rs930186	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs930187	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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	29 gene(s)	inside rSNPs	diseases
3	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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	25 gene(s)	inside rSNPs	diseases
5	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv1050519	chr12:121552964-121756420	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
7	nsv899564	chr12:121641509-121689798	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv899565	chr12:121641509-121698785	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121648800-121652200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr12:121648800-121652200	Weak transcription	Fetal Heart	heart
3	chr12:121648800-121652400	Weak transcription	HSMM	muscle
4	chr12:121648800-121655800	Weak transcription	Aorta	Aorta
5	chr12:121648800-121660400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:121648800-121661400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:121648800-121666600	Weak transcription	Ovary	ovary
8	chr12:121649000-121651400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr12:121649000-121651400	Weak transcription	Small Intestine	intestine
10	chr12:121649000-121651800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:121649000-121651800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr12:121649000-121651800	Weak transcription	Liver	Liver
13	chr12:121649000-121651800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr12:121649000-121651800	Weak transcription	Left Ventricle	heart
15	chr12:121649000-121651800	Weak transcription	NHLF	lung
16	chr12:121649000-121652000	Weak transcription	A549	lung
17	chr12:121649000-121652000	Weak transcription	Hela-S3	cervix
18	chr12:121649000-121652000	Weak transcription	HepG2	liver
19	chr12:121649000-121652000	Weak transcription	HUVEC	blood vessel
20	chr12:121649000-121652000	Weak transcription	NHEK	skin
21	chr12:121649000-121652200	Weak transcription	Primary T cells from cord blood	blood
22	chr12:121649000-121652200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr12:121649000-121652200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:121649000-121652200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:121649000-121652200	Weak transcription	HMEC	breast
26	chr12:121649000-121652200	Weak transcription	HSMMtube	muscle
27	chr12:121649000-121652200	Weak transcription	K562	blood
28	chr12:121649000-121652200	Weak transcription	Osteobl	bone
29	chr12:121649000-121652400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:121649000-121652400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:121649000-121652400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:121649000-121652400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:121649000-121652400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:121649000-121652400	Weak transcription	Right Atrium	heart
35	chr12:121649000-121652400	Weak transcription	NH-A	brain
36	chr12:121649000-121652800	Weak transcription	Colon Smooth Muscle	Colon
37	chr12:121649000-121653800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:121649000-121654000	Weak transcription	Gastric	stomach
39	chr12:121649000-121654800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr12:121649000-121655000	Weak transcription	Fetal Kidney	kidney
41	chr12:121649000-121655000	Weak transcription	Lung	lung
42	chr12:121649000-121656600	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr12:121649000-121659800	Weak transcription	Thymus	Thymus
44	chr12:121649000-121660000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr12:121649000-121660400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:121649000-121660600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:121649000-121660600	Weak transcription	Brain Germinal Matrix	brain
48	chr12:121649000-121661200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:121649000-121661200	Weak transcription	Esophagus	oesophagus
50	chr12:121649000-121665000	Weak transcription	Placenta Amnion	Placenta Amnion

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