Variant report

Variant	rs869016
Chromosome Location	chr2:112659110-112659111
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:112658476..112659217-chr2:112777886..112778574,2	MCF-7	breast:
2	chr2:112640266..112649080-chr2:112649576..112660203,14	MCF-7	breast:
3	chr2:112657825..112659209-chr2:112806011..112807065,8	MCF-7	breast:
4	chr2:112651539..112654934-chr2:112657187..112660968,3	K562	blood:

Variant related genes	Relation type
ENSG00000153107	Chromatin interaction
ENSG00000236307	Chromatin interaction

Extended variants
information (count: 135 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs10166564	0.95[CEU][hapmap];0.83[CHB][hapmap];0.86[EUR][1000 genomes]
rs10171174	0.82[EUR][1000 genomes]
rs10173553	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs10175316	0.96[ASN][1000 genomes]
rs10177803	0.86[EUR][1000 genomes]
rs10180345	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs10186291	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs10187041	0.81[EUR][1000 genomes]
rs10188642	0.84[EUR][1000 genomes]
rs10189399	0.84[EUR][1000 genomes]
rs10199083	0.86[EUR][1000 genomes]
rs10199616	0.95[CEU][hapmap];0.84[CHB][hapmap];0.86[EUR][1000 genomes]
rs10207820	0.95[CEU][hapmap];0.83[CHB][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10210692	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs11123024	0.83[ASN][1000 genomes]
rs11123035	0.97[ASN][1000 genomes]
rs11123073	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs1113418	0.80[ASN][1000 genomes]
rs1131244	0.84[EUR][1000 genomes]
rs11673958	0.80[ASN][1000 genomes]
rs11676037	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs11680354	0.80[EUR][1000 genomes]
rs11681295	0.85[ASN][1000 genomes]
rs11683409	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs11683421	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs11683819	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs11690939	0.84[EUR][1000 genomes]
rs11887259	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs12711677	0.92[ASN][1000 genomes]
rs12992449	0.97[ASN][1000 genomes]
rs13385764	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs13386914	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13391947	0.97[ASN][1000 genomes]
rs13394651	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs13397063	0.97[ASN][1000 genomes]
rs13399108	0.84[EUR][1000 genomes]
rs1400322	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1400323	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1516627	0.95[CEU][hapmap];0.83[CHB][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1516628	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs1516639	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1516640	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1554214	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs1554215	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs1607059	0.95[CEU][hapmap];0.84[CHB][hapmap];0.87[EUR][1000 genomes]
rs1607060	1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[ASN][1000 genomes]
rs17042094	0.81[ASN][1000 genomes]
rs17042095	0.80[ASN][1000 genomes]
rs1996322	0.84[EUR][1000 genomes]
rs1996323	0.84[EUR][1000 genomes]
rs1996325	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs1996326	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs1996327	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs1996328	0.95[CEU][hapmap];0.89[CHB][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1996329	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs1996330	0.85[ASN][1000 genomes]
rs2001200	0.82[ASN][1000 genomes]
rs2230515	0.84[EUR][1000 genomes]
rs2311813	0.97[ASN][1000 genomes]
rs2312226	0.92[ASN][1000 genomes]
rs28637361	0.85[ASN][1000 genomes]
rs2871922	0.95[CEU][hapmap];0.83[CHB][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34067354	0.81[ASN][1000 genomes]
rs34648366	0.80[ASN][1000 genomes]
rs35776963	0.82[ASN][1000 genomes]
rs3761700	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs3761701	0.95[CEU][hapmap];0.83[CHB][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3811636	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs3811637	0.84[EUR][1000 genomes]
rs3811638	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs4290663	0.97[ASN][1000 genomes]
rs4303721	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs4305289	0.81[EUR][1000 genomes]
rs4353657	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs4374383	0.91[CEU][hapmap]
rs4468823	0.95[CEU][hapmap];0.89[CHB][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4500955	0.87[CEU][hapmap]
rs4511729	0.84[EUR][1000 genomes]
rs4519530	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs4524124	0.80[CEU][hapmap];0.80[EUR][1000 genomes]
rs4525705	0.81[EUR][1000 genomes]
rs4627569	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs4632346	0.80[ASN][1000 genomes]
rs4643544	0.81[EUR][1000 genomes]
rs4848901	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs4848918	0.84[EUR][1000 genomes]
rs4848923	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs4848933	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs55757240	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56822761	0.88[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs59219838	0.84[ASN][1000 genomes]
rs6541971	0.95[CEU][hapmap];0.83[CHB][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6541998	0.86[CEU][hapmap]
rs66477683	0.87[EUR][1000 genomes]
rs66486378	0.87[EUR][1000 genomes]
rs67063370	0.85[ASN][1000 genomes]
rs6709662	0.81[EUR][1000 genomes]
rs6710591	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs6711146	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs6711987	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs6725192	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs6726639	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs6739294	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs6742470	0.82[ASN][1000 genomes]
rs6755970	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs68087924	0.87[EUR][1000 genomes]
rs7425877	0.80[EUR][1000 genomes]
rs7564225	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs7571009	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs7571120	0.91[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs7571447	0.97[ASN][1000 genomes]
rs7579906	0.95[CEU][hapmap];0.84[CHB][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7588459	0.84[EUR][1000 genomes]
rs7592909	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs7601798	0.83[ASN][1000 genomes]
rs7604639	0.95[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs7605527	0.87[EUR][1000 genomes]
rs868500	0.94[ASN][1000 genomes]
rs870762	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs884448	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs908518	0.95[CEU][hapmap];0.89[CHB][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803356	chr2:111899783-112662597	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv428402	chr2:111899783-112662597	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1801950	chr2:111899783-112746937	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv2757825	chr2:111899783-112746937	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	esv2759083	chr2:111899783-112746937	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv874863	chr2:112591224-113157344	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv874864	chr2:112617280-113104142	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
8	nsv874865	chr2:112623098-113049274	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
9	nsv961869	chr2:112645626-112660962	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
10	nsv1013218	chr2:112645633-112908416	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv998028	chr2:112649472-112734015	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv582701	chr2:112649472-112740597	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv526647	chr2:112651316-112738562	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv582702	chr2:112651316-112738562	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112655200-112659400	Active TSS	Right Atrium	heart
2	chr2:112655600-112659200	Active TSS	Stomach Smooth Muscle	stomach
3	chr2:112657000-112662600	Weak transcription	Spleen	Spleen
4	chr2:112657000-112663400	Weak transcription	Dnd41	blood
5	chr2:112657000-112663600	Weak transcription	Small Intestine	intestine
6	chr2:112657400-112660600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:112657400-112661200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:112657400-112661600	Weak transcription	Right Ventricle	heart
9	chr2:112657400-112662200	Weak transcription	Gastric	stomach
10	chr2:112657400-112662600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:112657400-112664400	Weak transcription	Pancreas	Pancrea
12	chr2:112657600-112660000	Weak transcription	Left Ventricle	heart
13	chr2:112657800-112661000	Weak transcription	Fetal Kidney	kidney
14	chr2:112657800-112662200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr2:112657800-112662400	Weak transcription	Brain Angular Gyrus	brain
16	chr2:112658000-112660000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:112658000-112662400	Weak transcription	Fetal Muscle Leg	muscle
18	chr2:112658200-112659200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr2:112658400-112660600	Weak transcription	Fetal Intestine Small	intestine
20	chr2:112658400-112663800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr2:112658600-112659200	Enhancers	Fetal Stomach	stomach
22	chr2:112658600-112660200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:112658600-112661400	Weak transcription	Fetal Heart	heart
24	chr2:112658600-112663600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:112658800-112659200	Enhancers	Colon Smooth Muscle	Colon
26	chr2:112658800-112660000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr2:112658800-112660400	Weak transcription	K562	blood
28	chr2:112658800-112660600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:112658800-112660800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:112658800-112660800	Weak transcription	Brain Substantia Nigra	brain
31	chr2:112658800-112661200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr2:112658800-112661200	Weak transcription	Aorta	Aorta
33	chr2:112658800-112661400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:112658800-112662400	Weak transcription	Lung	lung
35	chr2:112658800-112663400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr2:112658800-112663800	Weak transcription	Ovary	ovary
37	chr2:112658800-112665000	Enhancers	Liver	Liver
38	chr2:112659000-112659200	Enhancers	Brain Hippocampus Middle	brain
39	chr2:112659000-112659200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr2:112659000-112659400	Active TSS	Brain Anterior Caudate	brain
41	chr2:112659000-112659800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:112659000-112660000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr2:112659000-112660000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr2:112659000-112660600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr2:112659000-112660800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr2:112659000-112660800	Weak transcription	Fetal Intestine Large	intestine
47	chr2:112659000-112661000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:112659000-112661000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr2:112659000-112661200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:112659000-112661400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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