Variant report

Variant	rs2529192
Chromosome Location	chr7:101387262-101387263
allele	C/T
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:101383707..101389205-chr7:101455835..101460728,14	MCF-7	breast:
2	chr7:101386443..101387267-chr7:101458731..101459463,4	K562	blood:
3	chr7:101374945..101377549-chr7:101385778..101388199,3	K562	blood:
4	chr7:101386153..101388465-chr7:101446824..101448422,2	MCF-7	breast:
5	chr7:101383858..101388453-chr7:101455921..101461745,10	K562	blood:
6	chr7:101386587..101387369-chr7:101458812..101459637,3	MCF-7	breast:
7	chr7:101385593..101388435-chr7:101388835..101390401,2	K562	blood:
8	chr7:101342072..101344254-chr7:101386656..101389051,3	MCF-7	breast:
9	chr7:101375406..101379067-chr7:101385960..101390621,6	MCF-7	breast:
10	chr7:101374945..101377506-chr7:101385778..101388397,3	K562	blood:
11	chr7:101384444..101389414-chr7:101389757..101394090,5	MCF-7	breast:
12	chr7:101385593..101388435-chr7:101388835..101390929,3	K562	blood:
13	chr7:101358883..101362441-chr7:101383235..101387377,4	MCF-7	breast:
14	chr7:101381459..101384895-chr7:101386139..101388176,3	K562	blood:
15	chr7:101383224..101388686-chr7:101455921..101460973,10	K562	blood:

No data

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2529193	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2529194	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2529198	0.83[ASN][1000 genomes]
rs2529200	0.82[ASN][1000 genomes]
rs2529202	0.80[AMR][1000 genomes]
rs2529236	0.89[AMR][1000 genomes]
rs2690935	0.82[ASN][1000 genomes]
rs2690936	0.83[ASN][1000 genomes]
rs2690941	0.83[ASN][1000 genomes]
rs954757	0.81[ASN][1000 genomes]
rs954758	0.82[ASN][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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv1021797	chr7:101342353-101466957	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv539046	chr7:101342353-101466957	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
8	nsv1024319	chr7:101368299-101668159	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv539047	chr7:101368299-101668159	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101385600-101388000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:101386000-101387400	Enhancers	Stomach Mucosa	stomach
3	chr7:101386200-101387400	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr7:101386400-101387400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr7:101386400-101387400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr7:101386400-101387400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr7:101386400-101387400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:101386400-101387400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:101386400-101387400	Bivalent Enhancer	Fetal Brain Male	brain
10	chr7:101386400-101387400	Active TSS	Right Atrium	heart
11	chr7:101386400-101387400	Active TSS	Thymus	Thymus
12	chr7:101386400-101387800	Active TSS	H9 Cell Line	embryonic stem cell
13	chr7:101386400-101387800	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr7:101386600-101387400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:101386600-101387400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:101386600-101387400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:101386600-101387400	Active TSS	Brain Angular Gyrus	brain
18	chr7:101386600-101387400	Active TSS	Fetal Kidney	kidney
19	chr7:101386600-101387400	Flanking Active TSS	Placenta	Placenta
20	chr7:101386600-101387600	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr7:101386600-101387800	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr7:101386600-101387800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr7:101386800-101387400	Enhancers	Spleen	Spleen
24	chr7:101387000-101387400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
25	chr7:101387000-101387400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr7:101387000-101387400	Enhancers	Liver	Liver
27	chr7:101387000-101387400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr7:101387000-101387400	Flanking Active TSS	Colonic Mucosa	Colon
29	chr7:101387000-101387400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr7:101387000-101387400	Enhancers	Esophagus	oesophagus
31	chr7:101387000-101387400	Enhancers	Fetal Lung	lung
32	chr7:101387000-101387400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr7:101387000-101387400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr7:101387000-101387400	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr7:101387000-101387600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr7:101387000-101387600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:101387000-101387600	Enhancers	Pancreas	Pancrea
38	chr7:101387000-101387600	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr7:101387000-101387600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr7:101387200-101387400	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:101387200-101387400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:101387200-101387400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:101387200-101387400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:101387200-101387400	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:101387200-101387400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:101387200-101387400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:101387200-101387400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr7:101387200-101387400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr7:101387200-101387400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:101387200-101387400	Enhancers	Primary T helper cells PMA-I stimulated	--

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