Variant report

Variant	rs17677434
Chromosome Location	chr2:145219688-145219689
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:145196931..145199466-chr2:145218622..145221129,2	K562	blood:
2	chr2:145207858..145210614-chr2:145217823..145220494,2	K562	blood:
3	chr2:145218002..145220863-chr2:145221709..145223384,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZEB2-1	chr2:145218679-145221645	NONHSAT074762

Variant related genes	Relation type
ENSG00000213410	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12996983	0.85[TSI][hapmap]
rs17678182	1.00[ASN][1000 genomes]
rs17738837	0.86[MEX][hapmap]
rs35355807	1.00[ASN][1000 genomes]
rs62169201	1.00[ASN][1000 genomes]
rs67375672	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72858498	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532755	chr2:144631279-145270874	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription 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	10 gene(s)	inside rSNPs	diseases
2	nsv1006344	chr2:144657716-145334899	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv535951	chr2:144657716-145334899	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1067624	chr2:144657717-145425705	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv531413	chr2:144657717-145425705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv532756	chr2:144746353-145315596	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv1008032	chr2:144840552-145234229	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv997624	chr2:144906679-145294503	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
9	nsv535952	chr2:144906679-145294503	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
10	nsv532757	chr2:144922143-145263446	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
11	nsv916172	chr2:144970681-145425713	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
12	nsv948474	chr2:145035890-145436665	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers 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 target site	14 gene(s)	inside rSNPs	diseases
13	nsv535953	chr2:145099512-145336083	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
14	nsv535954	chr2:145128008-145311097	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
15	nsv535955	chr2:145143961-145298714	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
16	nsv535956	chr2:145178224-145311097	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
17	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
18	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
19	nsv535958	chr2:145190081-145285400	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
20	nsv531662	chr2:145219415-145422833	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145206800-145253400	Weak transcription	Lung	lung
2	chr2:145209200-145221000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:145210600-145219800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr2:145211400-145221000	Enhancers	Fetal Heart	heart
5	chr2:145211400-145231000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:145213400-145221600	Enhancers	Fetal Brain Male	brain
7	chr2:145214000-145221800	Enhancers	NHDF-Ad	bronchial
8	chr2:145215000-145227400	Weak transcription	A549	lung
9	chr2:145215200-145235200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr2:145216000-145220400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:145216200-145220600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:145216200-145221800	Genic enhancers	Fetal Lung	lung
13	chr2:145216400-145220600	Enhancers	Fetal Brain Female	brain
14	chr2:145216400-145220800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:145216400-145221400	Genic enhancers	Primary monocytes fromperipheralblood	blood
16	chr2:145216600-145221200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:145216600-145233800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr2:145216800-145221000	Genic enhancers	Monocytes-CD14+_RO01746	blood
19	chr2:145217400-145219800	Genic enhancers	Fetal Muscle Leg	muscle
20	chr2:145217400-145220200	Genic enhancers	Primary hematopoietic stem cells	blood
21	chr2:145217400-145223600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:145217800-145220600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:145217800-145220600	Weak transcription	Primary B cells from cord blood	blood
24	chr2:145217800-145220800	Enhancers	HSMM	muscle
25	chr2:145217800-145222400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr2:145217800-145224200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:145217800-145224600	Genic enhancers	K562	blood
28	chr2:145218000-145224400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr2:145218000-145225200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr2:145218200-145220000	Enhancers	NH-A	brain
31	chr2:145218200-145230200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr2:145218400-145219800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:145218400-145219800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:145218800-145219800	Strong transcription	Fetal Muscle Trunk	muscle
35	chr2:145218800-145220000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:145218800-145220200	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr2:145218800-145220800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:145218800-145221000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:145219000-145219800	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr2:145219000-145219800	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr2:145219000-145219800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:145219000-145219800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:145219000-145220400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:145219000-145220600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:145219200-145219800	Enhancers	Fetal Stomach	stomach
46	chr2:145219200-145223000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr2:145219200-145224400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr2:145219200-145227400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:145219200-145228200	Weak transcription	HUVEC	blood vessel
50	chr2:145219400-145219800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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