Variant report

Variant	rs341052
Chromosome Location	chr11:72344541-72344542
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:72333492..72335782-chr11:72342126..72344876,2	K562	blood:
2	chr11:72343339..72345279-chr11:72353249..72356170,2	K562	blood:
3	chr11:72339617..72343114-chr11:72344003..72346053,4	K562	blood:
4	chr11:72310660..72312266-chr11:72342413..72344790,2	MCF-7	breast:
5	chr11:72334834..72339078-chr11:72340923..72346253,6	K562	blood:
6	chr11:72324136..72326937-chr11:72343059..72344870,2	K562	blood:
7	chr11:72309197..72311837-chr11:72341889..72344712,2	K562	blood:
8	chr11:71930243..71933219-chr11:72343934..72345638,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000186642	Chromatin interaction
ENSG00000272036	Chromatin interaction
ENSG00000255808	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10793036	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs11235551	0.86[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs11235556	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11235557	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11235558	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11235559	0.93[CHB][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12146545	0.81[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12276767	0.89[ASN][1000 genomes]
rs12362256	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12363065	0.93[CHB][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12576058	0.93[CHB][hapmap]
rs12797368	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12797791	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12804316	0.91[CHB][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1391888	0.85[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs163694	0.94[CHB][hapmap]
rs1872126	0.93[CHB][hapmap]
rs189332	0.93[CHB][hapmap];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2035467	0.80[CEU][hapmap];0.94[CHB][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2037030	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs341051	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs341053	0.93[CHB][hapmap]
rs341060	0.83[ASN][1000 genomes]
rs341061	0.93[CHB][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs341062	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs341086	0.86[JPT][hapmap]
rs342322	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3758934	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3758935	0.84[EUR][1000 genomes]
rs3758936	0.84[EUR][1000 genomes]
rs3781913	0.93[CHB][hapmap];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3781916	0.80[CEU][hapmap];0.93[CHB][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3825009	0.85[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs401801	0.81[CHB][hapmap];0.86[ASN][1000 genomes]
rs455611	0.99[ASN][1000 genomes]
rs456405	0.83[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs458275	1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs458575	0.86[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs4943939	0.86[JPT][hapmap]
rs56133505	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61895572	0.89[ASN][1000 genomes]
rs7105428	0.86[ASN][1000 genomes]
rs7119321	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs900613	0.86[CHB][hapmap]
rs90409	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs907853	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs907854	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs907856	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs907857	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs907858	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs932074	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs932075	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1806140	chr11:72268466-72546175	Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	77 gene(s)	inside rSNPs	diseases
2	esv1832864	chr11:72270965-72389125	Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
3	nsv832207	chr11:72272750-72469122	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
4	nsv523601	chr11:72281884-72430935	Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1042182	chr11:72294042-72348491	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
6	nsv825991	chr11:72320642-72385221	Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
7	esv3394774	chr11:72320884-72694077	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	esv1793754	chr11:72335673-72348106	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72334800-72350200	Enhancers	Left Ventricle	heart
2	chr11:72335400-72346600	Enhancers	Brain Angular Gyrus	brain
3	chr11:72335600-72344600	Enhancers	Rectal Smooth Muscle	rectum
4	chr11:72335600-72349400	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr11:72335800-72349000	Enhancers	Fetal Brain Male	brain
6	chr11:72335800-72350600	Enhancers	Brain Hippocampus Middle	brain
7	chr11:72336000-72345000	Enhancers	Fetal Muscle Leg	muscle
8	chr11:72336000-72350400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr11:72337800-72348200	Weak transcription	Gastric	stomach
10	chr11:72338400-72348200	Weak transcription	Ovary	ovary
11	chr11:72339000-72350600	Enhancers	Brain Cingulate Gyrus	brain
12	chr11:72339600-72345000	Genic enhancers	Spleen	Spleen
13	chr11:72339800-72345800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr11:72340200-72344600	Enhancers	Psoas Muscle	Psoas
15	chr11:72340200-72345000	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr11:72340200-72349400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:72340400-72349400	Enhancers	Fetal Brain Female	brain
18	chr11:72341400-72346200	Enhancers	Right Ventricle	heart
19	chr11:72341600-72349400	Enhancers	Brain Anterior Caudate	brain
20	chr11:72342200-72344600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr11:72342400-72344800	Enhancers	Fetal Heart	heart
22	chr11:72342400-72345000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:72342400-72345200	Enhancers	K562	blood
24	chr11:72342600-72346000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr11:72342600-72349400	Enhancers	HUVEC	blood vessel
26	chr11:72343000-72344600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr11:72343000-72345600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:72343400-72346400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr11:72343400-72348200	Weak transcription	Liver	Liver
30	chr11:72343400-72350200	Enhancers	Right Atrium	heart
31	chr11:72343400-72351000	Weak transcription	Esophagus	oesophagus
32	chr11:72343600-72344600	Enhancers	Fetal Muscle Trunk	muscle
33	chr11:72343600-72344600	Enhancers	HSMMtube	muscle
34	chr11:72343600-72345200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr11:72343600-72346200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:72343600-72347000	Enhancers	Placenta	Placenta
37	chr11:72343600-72347400	Enhancers	Brain Germinal Matrix	brain
38	chr11:72343600-72348600	Weak transcription	Pancreas	Pancrea
39	chr11:72343600-72349600	Bivalent Enhancer	Fetal Stomach	stomach
40	chr11:72343600-72350800	Weak transcription	Brain Substantia Nigra	brain
41	chr11:72343600-72351000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr11:72343800-72348000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:72344000-72345000	Enhancers	Colon Smooth Muscle	Colon
44	chr11:72344200-72345200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr11:72344200-72345400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr11:72344200-72347600	Weak transcription	Hela-S3	cervix
47	chr11:72344400-72344600	Enhancers	Fetal Intestine Large	intestine
48	chr11:72344400-72344600	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr11:72344400-72345400	Bivalent Enhancer	Adipose Nuclei	Adipose
50	chr11:72344400-72346600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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