Variant report

Variant	rs11810682
Chromosome Location	chr1:45768960-45768961
allele	A/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:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45767756..45770451-chr1:45964648..45967377,2	K562	blood:
2	chr1:45765046..45767711-chr1:45767729..45769778,4	K562	blood:
3	chr1:45768281..45771138-chr1:45796764..45802126,5	MCF-7	breast:
4	chr1:45761061..45765465-chr1:45766442..45769712,4	MCF-7	breast:
5	chr1:45768003..45772070-chr1:45964648..45967315,5	K562	blood:
6	chr1:45276358..45278669-chr1:45768111..45770170,2	K562	blood:
7	chr1:45767877..45774853-chr1:45802459..45807372,12	K562	blood:
8	chr1:45768778..45770892-chr1:45955419..45957288,2	MCF-7	breast:
9	chr1:45239714..45242119-chr1:45768024..45770641,2	K562	blood:
10	chr1:45196186..45198352-chr1:45768360..45771059,2	MCF-7	breast:
11	chr1:45768057..45769740-chr1:45781016..45782971,2	K562	blood:
12	chr1:45279599..45282542-chr1:45767964..45769557,2	K562	blood:
13	chr1:45476357..45485239-chr1:45761850..45773601,48	K562	blood:
14	chr1:45767832..45771484-chr1:45985093..45988810,5	K562	blood:
15	chr1:45262923..45267744-chr1:45767225..45772183,8	K562	blood:
16	chr1:45300157..45303159-chr1:45767947..45769819,5	K562	blood:
17	chr1:45184077..45189466-chr1:45767737..45771248,11	K562	blood:
18	chr1:45756933..45758729-chr1:45768463..45770390,2	K562	blood:
19	chr1:45284161..45290157-chr1:45766666..45771483,12	K562	blood:
20	chr1:45768203..45769814-chr1:45799672..45801687,2	K562	blood:
21	chr1:45300157..45301709-chr1:45767947..45769590,2	K562	blood:
22	chr1:45767853..45771862-chr1:45786144..45789985,4	K562	blood:
23	chr1:45194559..45197105-chr1:45768008..45770693,4	K562	blood:
24	chr1:45768158..45770163-chr1:45795401..45797079,2	K562	blood:
25	chr1:45283674..45286034-chr1:45767652..45771171,5	MCF-7	breast:
26	chr1:45396788..45398380-chr1:45768568..45771235,2	K562	blood:
27	chr1:45264001..45267369-chr1:45768099..45771014,4	K562	blood:
28	chr1:45265368..45267824-chr1:45766487..45769933,3	MCF-7	breast:
29	chr1:45479863..45480810-chr1:45768917..45770306,5	K562	blood:
30	chr1:45193680..45198999-chr1:45768008..45771912,9	K562	blood:
31	chr1:45185975..45188981-chr1:45767504..45771091,13	K562	blood:
32	chr1:45735419..45737073-chr1:45768258..45770509,2	K562	blood:
33	chr1:45276358..45279263-chr1:45768111..45771018,3	K562	blood:
34	chr1:45282609..45288514-chr1:45767803..45773154,13	K562	blood:
35	chr1:45768289..45770936-chr1:45808529..45810402,2	K562	blood:
36	chr1:45766405..45769697-chr1:46047969..46051126,5	K562	blood:
37	chr1:45476265..45486633-chr1:45761064..45774272,63	K562	blood:
38	chr1:45768110..45772204-chr1:45801230..45805942,7	MCF-7	breast:
39	chr1:45768160..45769888-chr1:45781471..45784355,3	K562	blood:
40	chr1:45767776..45771231-chr1:45801954..45807210,10	K562	blood:
41	chr1:45477751..45479652-chr1:45767630..45769422,3	MCF-7	breast:
42	chr1:45763746..45766388-chr1:45768053..45771001,2	MCF-7	breast:
43	chr1:45271760..45274543-chr1:45767824..45769471,2	K562	blood:
44	chr1:45476329..45477906-chr1:45768337..45771148,2	MCF-7	breast:
45	chr1:45768893..45771768-chr1:45791455..45796830,6	MCF-7	breast:
46	chr1:45767740..45770966-chr1:46047969..46050912,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000199377	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000236624	Chromatin interaction
ENSG00000117425	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000070759	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000188396	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000253039	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000222009	Chromatin interaction
ENSG00000132763	Chromatin interaction
ENSG00000186603	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs59517508	1.00[ASN][1000 genomes]
rs72478599	0.93[ASN][1000 genomes]
rs72890555	1.00[ASN][1000 genomes]
rs7521364	0.89[ASN][1000 genomes]
rs9429064	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1014509	chr1:45687523-45887501	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv997548	chr1:45733596-45955845	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv534942	chr1:45733596-45955845	Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv482356	chr1:45750459-45915545	Enhancers Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45766800-45769000	Weak transcription	Stomach Mucosa	stomach
2	chr1:45768400-45769800	Active TSS	H1 Cell Line	embryonic stem cell
3	chr1:45768400-45770000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:45768400-45770000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:45768400-45770200	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr1:45768400-45770200	Active TSS	Brain Substantia Nigra	brain
7	chr1:45768400-45770400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr1:45768600-45769000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:45768600-45769000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr1:45768600-45769000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:45768600-45769000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:45768600-45769000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:45768600-45769000	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr1:45768600-45769000	Flanking Active TSS	Colonic Mucosa	Colon
15	chr1:45768600-45769000	Enhancers	Fetal Brain Male	brain
16	chr1:45768600-45769000	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr1:45768600-45769000	Flanking Active TSS	Fetal Muscle Leg	muscle
18	chr1:45768600-45769000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr1:45768600-45769000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr1:45768600-45769000	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr1:45768600-45769000	Flanking Active TSS	Dnd41	blood
22	chr1:45768600-45769000	Flanking Active TSS	HMEC	breast
23	chr1:45768600-45769200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr1:45768600-45769200	Flanking Active TSS	Primary B cells from cord blood	blood
25	chr1:45768600-45769200	Flanking Active TSS	Fetal Thymus	thymus
26	chr1:45768600-45769600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:45768600-45769800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:45768600-45769800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:45768600-45769800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:45768600-45769800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:45768600-45769800	Active TSS	Rectal Smooth Muscle	rectum
32	chr1:45768600-45769800	Active TSS	Hela-S3	cervix
33	chr1:45768600-45769800	Active TSS	Monocytes-CD14+_RO01746	blood
34	chr1:45768600-45770000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:45768600-45770000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:45768600-45770000	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr1:45768600-45770000	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr1:45768600-45770000	Active TSS	Brain Anterior Caudate	brain
39	chr1:45768600-45770000	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr1:45768600-45770000	Active TSS	Fetal Brain Female	brain
41	chr1:45768600-45770000	Active TSS	Fetal Lung	lung
42	chr1:45768600-45770000	Active TSS	Left Ventricle	heart
43	chr1:45768600-45770000	Active TSS	A549	lung
44	chr1:45768600-45770000	Active TSS	NHDF-Ad	bronchial
45	chr1:45768600-45770000	Active TSS	NHLF	lung
46	chr1:45768600-45770200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:45768600-45770200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:45768600-45770200	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr1:45768600-45770200	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr1:45768600-45770200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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