Variant report

Variant	rs10882618
Chromosome Location	chr10:97315717-97315718
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	chr10:97315253..97317391-chr10:97320414..97322052,2	K562	blood:
2	chr10:97314309..97316972-chr10:97319111..97320746,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000095637	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10786218	0.82[CEU][hapmap];0.85[EUR][1000 genomes]
rs10786221	0.91[ASN][1000 genomes]
rs10882614	0.90[JPT][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882616	0.93[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11188355	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11188357	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11188359	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12219483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12411861	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12416299	0.83[CEU][hapmap];0.85[EUR][1000 genomes]
rs1536445	0.90[ASN][1000 genomes]
rs17458865	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs17537576	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs55873943	0.94[EUR][1000 genomes]
rs56353860	1.00[EUR][1000 genomes]
rs61869973	0.85[EUR][1000 genomes]
rs61869974	0.85[EUR][1000 genomes]
rs61869975	0.84[EUR][1000 genomes]
rs61869976	0.86[EUR][1000 genomes]
rs61870045	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61870046	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61870048	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61870049	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61870050	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61870051	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61870052	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7069574	0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7085647	0.83[CEU][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1808679	chr10:97266478-97316855	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv552022	chr10:97308114-97328227	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97305200-97318600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr10:97305200-97319000	Weak transcription	HSMM	muscle
3	chr10:97308000-97318600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:97310400-97318400	Weak transcription	Fetal Kidney	kidney
5	chr10:97310800-97316800	Weak transcription	Ovary	ovary
6	chr10:97310800-97317800	Weak transcription	Pancreas	Pancrea
7	chr10:97311000-97316800	Weak transcription	Gastric	stomach
8	chr10:97311000-97318600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:97311200-97317000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr10:97311400-97316800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr10:97311400-97316800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr10:97311400-97316800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr10:97311400-97317000	Weak transcription	Brain Angular Gyrus	brain
14	chr10:97311400-97317200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr10:97311400-97318400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr10:97311600-97317400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr10:97312600-97317000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr10:97313000-97316800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:97313000-97316800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr10:97313000-97317200	Weak transcription	Spleen	Spleen
21	chr10:97313000-97318600	Weak transcription	Stomach Mucosa	stomach
22	chr10:97313400-97316800	Weak transcription	Fetal Brain Female	brain
23	chr10:97313400-97316800	Weak transcription	Fetal Muscle Leg	muscle
24	chr10:97313400-97317800	Weak transcription	Lung	lung
25	chr10:97313400-97318200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr10:97313600-97317000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr10:97313800-97316800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr10:97313800-97316800	Weak transcription	K562	blood
29	chr10:97313800-97317200	Weak transcription	Fetal Intestine Small	intestine
30	chr10:97313800-97318400	Weak transcription	Placenta	Placenta
31	chr10:97314000-97317600	Weak transcription	Fetal Stomach	stomach
32	chr10:97314800-97315800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:97314800-97316000	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr10:97314800-97318200	Enhancers	Left Ventricle	heart
35	chr10:97315000-97315800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:97315000-97315800	Enhancers	Brain Cingulate Gyrus	brain
37	chr10:97315000-97316000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr10:97315000-97316000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr10:97315000-97316000	Enhancers	Brain Hippocampus Middle	brain
40	chr10:97315000-97316000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr10:97315000-97316000	Flanking Active TSS	Rectal Smooth Muscle	rectum
42	chr10:97315000-97316000	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr10:97315000-97316200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr10:97315000-97316200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr10:97315000-97316200	Enhancers	Fetal Heart	heart
46	chr10:97315000-97316800	Weak transcription	Liver	Liver
47	chr10:97315000-97316800	Enhancers	Brain Anterior Caudate	brain
48	chr10:97315200-97315800	Genic enhancers	HepG2	liver
49	chr10:97315200-97316000	Active TSS	Colon Smooth Muscle	Colon
50	chr10:97315200-97316200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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