Variant report

Variant	rs2136709
Chromosome Location	chr9:15431384-15431385
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:15422069..15423659-chr9:15430578..15433740,3	K562	blood:
2	chr9:15420595..15424773-chr9:15424796..15433036,11	MCF-7	breast:
3	chr9:15429263..15431513-chr9:15449169..15450709,2	K562	blood:
4	chr9:15422138..15423750-chr9:15430824..15433204,2	K562	blood:

Variant related genes	Relation type
ENSG00000164975	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10756663	0.83[AMR][1000 genomes]
rs1983207	0.83[AMR][1000 genomes]
rs2382529	0.83[AMR][1000 genomes]
rs4741498	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517975	chr9:15286446-15534070	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1030287	chr9:15332709-15458001	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv831520	chr9:15404866-15444447	Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
7	nsv892628	chr9:15420805-15528290	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 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	chr9:15423600-15434400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:15423600-15439000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:15424000-15443400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:15424000-15443600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr9:15425000-15431800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr9:15425000-15437000	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:15425400-15433600	Weak transcription	Fetal Kidney	kidney
8	chr9:15425400-15439000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr9:15425800-15431400	Strong transcription	HUVEC	blood vessel
10	chr9:15425800-15433800	Weak transcription	HSMMtube	muscle
11	chr9:15425800-15434000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr9:15426200-15441800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:15426400-15433000	Weak transcription	NHLF	lung
14	chr9:15426400-15433600	Weak transcription	Primary T cells from cord blood	blood
15	chr9:15426400-15433600	Weak transcription	Thymus	Thymus
16	chr9:15426400-15434000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr9:15426400-15435400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:15426400-15436000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:15426400-15439000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:15426400-15439800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:15426400-15441800	Weak transcription	Spleen	Spleen
22	chr9:15426400-15442800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr9:15426400-15443600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:15426400-15443600	Weak transcription	Gastric	stomach
25	chr9:15426400-15468200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:15426600-15433600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr9:15426600-15433600	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:15426600-15433600	Weak transcription	Stomach Smooth Muscle	stomach
29	chr9:15426600-15434000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:15426600-15434000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr9:15426600-15442400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr9:15426600-15443400	Weak transcription	Fetal Heart	heart
33	chr9:15426800-15433000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:15426800-15433000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr9:15426800-15433200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr9:15426800-15433200	Weak transcription	NHDF-Ad	bronchial
37	chr9:15426800-15433400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr9:15426800-15433600	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr9:15426800-15433600	Weak transcription	HMEC	breast
40	chr9:15426800-15433600	Weak transcription	Osteobl	bone
41	chr9:15426800-15434200	Weak transcription	Fetal Brain Male	brain
42	chr9:15427000-15433600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:15427000-15433800	Weak transcription	Fetal Lung	lung
44	chr9:15427000-15436000	Weak transcription	Fetal Brain Female	brain
45	chr9:15427000-15443400	Weak transcription	NHEK	skin
46	chr9:15427800-15431600	Weak transcription	K562	blood
47	chr9:15427800-15433600	Weak transcription	Placenta	Placenta
48	chr9:15428000-15432600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr9:15428400-15433600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr9:15428600-15432200	Strong transcription	Primary B cells from cord blood	blood

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