Variant report

Variant	rs11102521
Chromosome Location	chr1:113238487-113238488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:113237535-113239993	A549	lung:	n/a	n/a
2	POLR2A	chr1:113238093-113238626	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:113159779..113171222-chr1:113238237..113251191,41	K562	blood:
2	chr1:113214866..113222565-chr1:113237012..113253952,54	K562	blood:
3	chr1:113160176..113163931-chr1:113238020..113242018,6	K562	blood:
4	chr1:113214002..113222947-chr1:113236890..113251579,47	MCF-7	breast:

Variant related genes	Relation type
MOV10	TF binding region
ENSG00000235299	Chromatin interaction
ENSG00000155363	Chromatin interaction
ENSG00000116489	Chromatin interaction
ENSG00000007341	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10399919	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11102519	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12060267	1.00[AMR][1000 genomes]
rs12069740	1.00[AMR][1000 genomes]
rs12073750	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12074157	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12077330	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12087862	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12095563	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17030592	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4424506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57573777	1.00[AMR][1000 genomes]
rs58634778	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59053530	1.00[AMR][1000 genomes]
rs61203550	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72982599	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72984503	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72984509	1.00[AMR][1000 genomes]
rs72984515	1.00[AMR][1000 genomes]
rs72986505	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72986535	1.00[AMR][1000 genomes]
rs9919308	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv13370	chr1:112693290-113246263	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer 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	166 gene(s)	inside rSNPs	diseases
4	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
5	nsv533295	chr1:113167645-113589588	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
6	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
9	esv997362	chr1:113234820-113243297	Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113218600-113240800	Weak transcription	Right Atrium	heart
2	chr1:113219000-113242200	Weak transcription	NHDF-Ad	bronchial
3	chr1:113219000-113243800	Weak transcription	Fetal Brain Male	brain
4	chr1:113222000-113243000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:113228400-113239000	Strong transcription	Fetal Intestine Small	intestine
6	chr1:113228600-113242800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:113228600-113242800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr1:113229000-113242200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr1:113229200-113248000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:113229600-113243200	Strong transcription	Dnd41	blood
11	chr1:113230200-113239400	Strong transcription	Fetal Intestine Large	intestine
12	chr1:113230200-113239800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:113230200-113240200	Weak transcription	Fetal Heart	heart
14	chr1:113230200-113240600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:113230200-113240800	Strong transcription	Adipose Nuclei	Adipose
16	chr1:113230200-113241200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:113230200-113242600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:113230200-113243000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:113230200-113243200	Strong transcription	Primary T cells from cord blood	blood
20	chr1:113230400-113240400	Strong transcription	HepG2	liver
21	chr1:113230400-113240600	Strong transcription	Stomach Smooth Muscle	stomach
22	chr1:113230400-113241200	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr1:113230600-113240800	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr1:113230600-113241000	Strong transcription	Gastric	stomach
25	chr1:113230600-113241400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:113230600-113242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:113230600-113242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:113230600-113242200	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr1:113230600-113242600	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr1:113230800-113239800	Strong transcription	Liver	Liver
31	chr1:113230800-113240000	Strong transcription	Duodenum Mucosa	Duodenum
32	chr1:113230800-113241400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr1:113231200-113241400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:113231400-113241800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr1:113231600-113241200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:113231600-113243000	Weak transcription	Psoas Muscle	Psoas
37	chr1:113231600-113243200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr1:113231800-113238800	Strong transcription	Placenta Amnion	Placenta Amnion
39	chr1:113231800-113239200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:113231800-113239800	Strong transcription	HMEC	breast
41	chr1:113231800-113240000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:113231800-113240400	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr1:113231800-113242400	Strong transcription	Osteobl	bone
44	chr1:113231800-113242600	Strong transcription	Fetal Lung	lung
45	chr1:113232000-113240400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:113232000-113241000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:113232000-113241000	Strong transcription	Hela-S3	cervix
48	chr1:113232000-113241400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:113232000-113242400	Strong transcription	Fetal Stomach	stomach
50	chr1:113232000-113242600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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