Variant report

Variant	rs17415857
Chromosome Location	chr2:54765040-54765041
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:54764232..54766337-chr2:54769153..54772806,3	K562	blood:
2	chr2:54763693..54765544-chr2:54775882..54778958,3	MCF-7	breast:
3	chr2:54764181..54766561-chr2:54813594..54815881,2	K562	blood:
4	chr2:54760402..54763033-chr2:54763448..54765136,2	MCF-7	breast:
5	chr2:54764431..54771229-chr2:54784220..54787609,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000115306	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10181201	0.82[CEU][hapmap]
rs13405115	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs17343918	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17344134	0.83[EUR][1000 genomes]
rs17344169	0.83[EUR][1000 genomes]
rs17344176	0.83[EUR][1000 genomes]
rs17344287	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17344308	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17344343	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17415829	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17416130	0.83[EUR][1000 genomes]
rs17416291	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17416364	1.00[CEU][hapmap]
rs17521468	0.83[EUR][1000 genomes]
rs17521510	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17580255	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17580855	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17580876	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1804472	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs3796015	0.91[EUR][1000 genomes]
rs41281495	0.83[EUR][1000 genomes]
rs41281497	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4258834	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs4440005	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56077523	1.00[AFR][1000 genomes]
rs57810131	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58143357	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59228485	1.00[ASN][1000 genomes]
rs61480394	1.00[ASN][1000 genomes]
rs6755737	0.83[EUR][1000 genomes]
rs72911560	1.00[ASN][1000 genomes]
rs72911563	1.00[ASN][1000 genomes]
rs72915032	1.00[ASN][1000 genomes]
rs73932786	1.00[ASN][1000 genomes]
rs73932787	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998277	chr2:54710337-54849648	Genic enhancers Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv2731	chr2:54745069-54790057	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv528848	chr2:54758305-54777576	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54740400-54770200	Weak transcription	Esophagus	oesophagus
2	chr2:54744000-54777600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:54744400-54769600	Weak transcription	Spleen	Spleen
4	chr2:54747200-54769800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:54748400-54768000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:54748400-54776800	Weak transcription	Pancreas	Pancrea
7	chr2:54750800-54769800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:54752200-54767600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:54752200-54777800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:54753800-54768200	Strong transcription	Fetal Muscle Leg	muscle
11	chr2:54754400-54767800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:54754800-54767800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:54755000-54767600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:54756800-54767600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:54757000-54767800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr2:54757000-54776800	Weak transcription	Brain Germinal Matrix	brain
17	chr2:54757400-54766200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr2:54757400-54771000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr2:54758200-54778200	Weak transcription	Placenta	Placenta
20	chr2:54758600-54772600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr2:54760200-54768800	Genic enhancers	Left Ventricle	heart
22	chr2:54760400-54769600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr2:54760600-54765200	Weak transcription	Colon Smooth Muscle	Colon
24	chr2:54760600-54766000	Weak transcription	Small Intestine	intestine
25	chr2:54760600-54767000	Weak transcription	NH-A	brain
26	chr2:54760800-54767800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr2:54761000-54767000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:54761000-54769400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:54761200-54768800	Strong transcription	HSMM	muscle
30	chr2:54761400-54766000	Weak transcription	Lung	lung
31	chr2:54761600-54767200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:54761600-54773200	Weak transcription	Fetal Brain Male	brain
33	chr2:54761800-54766000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:54761800-54769600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr2:54762000-54766000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:54762000-54766800	Weak transcription	Right Ventricle	heart
37	chr2:54762000-54775400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:54762200-54765800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:54762200-54770400	Weak transcription	Fetal Kidney	kidney
40	chr2:54762200-54772800	Weak transcription	Aorta	Aorta
41	chr2:54762200-54772800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr2:54762200-54773800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:54762400-54766000	Weak transcription	Brain Anterior Caudate	brain
44	chr2:54762400-54770800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr2:54762400-54772600	Weak transcription	Liver	Liver
46	chr2:54762600-54767000	Weak transcription	Brain Substantia Nigra	brain
47	chr2:54762600-54767200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr2:54762600-54767400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:54762800-54772600	Weak transcription	NHDF-Ad	bronchial
50	chr2:54763000-54767400	Weak transcription	HUVEC	blood vessel

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