Variant report

Variant	rs73294095
Chromosome Location	chr17:37811007-37811008
allele	C/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	CTCF	chr17:37810920-37811070	GM06990	blood:	n/a	n/a
2	CTCF	chr17:37810940-37811090	GM12872	blood:	n/a	n/a
3	CTCF	chr17:37810960-37811110	GM12874	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:37792606..37795177-chr17:37810755..37812742,3	MCF-7	breast:
2	chr17:37809503..37812375-chr17:37822536..37826640,4	K562	blood:

Variant related genes	Relation type
STARD3	TF binding region
ENSG00000131748	Chromatin interaction
ENSG00000141744	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1050293	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs15968	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934958	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934959	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934960	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934961	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934962	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934963	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934965	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934966	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2941510	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941511	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941513	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941514	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941515	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941516	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941523	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2952139	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2952149	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2952150	0.92[EUR][1000 genomes]
rs57837184	0.91[AFR][1000 genomes]
rs59522915	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294088	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294092	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73296106	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73296109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73308323	0.82[AFR][1000 genomes]
rs73308326	0.91[AFR][1000 genomes]
rs73308333	0.82[AFR][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	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
11	esv1792029	chr17:37797757-37886460	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv908213	chr17:37807698-37839493	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37795000-37814000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr17:37795000-37823800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr17:37795200-37814000	Weak transcription	Aorta	Aorta
4	chr17:37795200-37814600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr17:37795400-37818000	Weak transcription	Fetal Kidney	kidney
6	chr17:37798200-37813800	Weak transcription	GM12878-XiMat	blood
7	chr17:37799800-37812400	Weak transcription	Psoas Muscle	Psoas
8	chr17:37799800-37819600	Weak transcription	Osteobl	bone
9	chr17:37800000-37812800	Weak transcription	NHLF	lung
10	chr17:37800000-37814000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr17:37800000-37815200	Weak transcription	HUVEC	blood vessel
12	chr17:37800000-37818600	Weak transcription	Hela-S3	cervix
13	chr17:37800000-37820000	Weak transcription	NH-A	brain
14	chr17:37800200-37816800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr17:37800400-37814000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr17:37800600-37816200	Weak transcription	NHEK	skin
17	chr17:37801000-37814600	Weak transcription	Primary B cells from cord blood	blood
18	chr17:37801800-37817000	Weak transcription	A549	lung
19	chr17:37803400-37814200	Strong transcription	Thymus	Thymus
20	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr17:37804000-37812600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr17:37807200-37811200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr17:37807200-37811200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr17:37807400-37811200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr17:37807800-37811200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr17:37808200-37812200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr17:37808400-37819200	Weak transcription	Small Intestine	intestine
28	chr17:37808800-37811200	Flanking Active TSS	Brain Hippocampus Middle	brain
29	chr17:37809000-37811400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
30	chr17:37809000-37811800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr17:37809200-37816200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr17:37809400-37813400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr17:37809400-37813800	Weak transcription	Fetal Lung	lung
34	chr17:37809600-37811800	Weak transcription	Fetal Brain Female	brain
35	chr17:37809600-37814200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr17:37809800-37811200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:37809800-37811200	Genic enhancers	Lung	lung
38	chr17:37809800-37811400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr17:37809800-37811400	Strong transcription	Fetal Muscle Leg	muscle
40	chr17:37809800-37811600	Strong transcription	Dnd41	blood
41	chr17:37809800-37812000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr17:37809800-37812600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr17:37809800-37812600	Strong transcription	Stomach Smooth Muscle	stomach
44	chr17:37809800-37816400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr17:37809800-37819400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr17:37810000-37811400	Genic enhancers	Primary T cells fromperipheralblood	blood
47	chr17:37810000-37811400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
48	chr17:37810000-37811600	Genic enhancers	Brain Inferior Temporal Lobe	brain
49	chr17:37810000-37812000	Weak transcription	Gastric	stomach
50	chr17:37810000-37812200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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