Variant report

Variant	rs651905
Chromosome Location	chr1:155641975-155641976
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	FOXA1	chr1:155641594-155641993	HepG2	liver:	n/a	chr1:155641765-155641780
2	MAFK	chr1:155641469-155642063	GM12878	blood:	n/a	chr1:155641726-155641742 chr1:155641729-155641745 chr1:155641729-155641744 chr1:155641727-155641741 chr1:155641724-155641744 chr1:155641732-155641746

No.	Distal block	Cell Line	Cell type
1	chr1:155632359..155634916-chr1:155641249..155643126,2	MCF-7	breast:
2	chr1:155641405..155643309-chr1:155647135..155648981,2	K562	blood:
3	chr1:155640302..155642809-chr1:155644583..155646250,2	MCF-7	breast:

Variant related genes	Relation type
YY1AP1	TF binding region
ENSG00000163374	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs2136918	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs2175390	0.97[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2686266	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs348187	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs348195	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs348198	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs487216	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4971094	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4971096	0.90[AFR][1000 genomes]
rs4971098	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs525240	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs536192	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs589431	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs601103	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs602905	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs662116	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6675983	0.92[AFR][1000 genomes]
rs7524742	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
2	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
3	esv3431739	chr1:155514331-155664183	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription 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	61 gene(s)	inside rSNPs	diseases
4	esv3388968	chr1:155532335-155658278	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv1002390	chr1:155553423-155706930	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv428246	chr1:155558197-155785831	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers 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	43 gene(s)	inside rSNPs	diseases
7	nsv436522	chr1:155559513-155674249	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	esv3360339	chr1:155562157-155683127	Active TSS Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv547965	chr1:155563152-155688600	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats 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 target site	41 gene(s)	inside rSNPs	diseases
10	esv3381327	chr1:155582853-155718436	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	esv3436971	chr1:155618172-155733386	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
12	esv3338099	chr1:155618190-155733359	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers 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	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155627000-155657600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:155627200-155648200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:155627200-155651600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:155627200-155654000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:155627600-155650200	Strong transcription	GM12878-XiMat	blood
6	chr1:155627600-155650600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:155627600-155653600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:155627800-155650600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:155628000-155647600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:155628000-155648000	Strong transcription	Primary hematopoietic stem cells	blood
11	chr1:155628000-155650400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:155628000-155650400	Strong transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:155628000-155650400	Strong transcription	Stomach Smooth Muscle	stomach
14	chr1:155628000-155650600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:155628000-155650600	Strong transcription	Primary B cells from peripheral blood	blood
16	chr1:155628000-155650600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr1:155628000-155650600	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr1:155628000-155650800	Strong transcription	Primary T cells from cord blood	blood
19	chr1:155628000-155650800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:155628000-155650800	Strong transcription	Placenta	Placenta
21	chr1:155628000-155651600	Strong transcription	Adipose Nuclei	Adipose
22	chr1:155628000-155652000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:155628000-155652000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:155628000-155653800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:155628000-155654600	Strong transcription	Fetal Thymus	thymus
26	chr1:155628200-155643200	Strong transcription	Brain Hippocampus Middle	brain
27	chr1:155628200-155645400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr1:155628200-155645600	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr1:155628200-155647000	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:155628200-155649600	Strong transcription	Brain Cingulate Gyrus	brain
31	chr1:155628200-155649800	Strong transcription	Osteobl	bone
32	chr1:155628200-155650200	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:155628200-155650200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:155628200-155650200	Strong transcription	Fetal Intestine Large	intestine
35	chr1:155628200-155650400	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr1:155628200-155650400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr1:155628200-155650400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:155628200-155650600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
39	chr1:155628200-155650600	Strong transcription	Brain Inferior Temporal Lobe	brain
40	chr1:155628200-155650800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr1:155628200-155650800	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:155628200-155650800	Strong transcription	Duodenum Mucosa	Duodenum
43	chr1:155628200-155651000	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr1:155628200-155651000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:155628200-155651200	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:155628200-155651200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:155628200-155653200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:155628400-155645200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:155628400-155647200	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr1:155628400-155648200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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