Variant report

Variant	rs203435
Chromosome Location	chr4:16236539-16236540
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:16230982..16233844-chr4:16235259..16238422,3	MCF-7	breast:
2	chr4:16228310..16230197-chr4:16235714..16237466,2	MCF-7	breast:
3	chr4:16234324..16237129-chr4:16262058..16264893,2	K562	blood:
4	chr4:16235269..16243012-chr4:16245014..16252154,9	K562	blood:

Variant related genes	Relation type
ENSG00000169762	Chromatin interaction
ENSG00000263327	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10006159	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1025897	0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13133263	0.81[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13634	0.94[JPT][hapmap]
rs1712492	0.88[JPT][hapmap]
rs203434	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs317873	0.88[JPT][hapmap]
rs6812660	0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs961449	0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.81[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	nsv1004821	chr4:16055996-16830629	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537046	chr4:16055996-16830629	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537047	chr4:16182060-16375787	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv878720	chr4:16222046-16242215	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv537048	chr4:16226406-16375787	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16229400-16241000	Weak transcription	Aorta	Aorta
2	chr4:16229600-16237600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:16229600-16254000	Weak transcription	Ovary	ovary
4	chr4:16229600-16254800	Weak transcription	Psoas Muscle	Psoas
5	chr4:16229800-16241400	Weak transcription	Primary T cells from cord blood	blood
6	chr4:16229800-16259800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:16230000-16237000	Weak transcription	Fetal Brain Female	brain
8	chr4:16230000-16238000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:16230000-16244200	Weak transcription	Pancreas	Pancrea
10	chr4:16230000-16244800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:16230000-16244800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr4:16230600-16244200	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:16232200-16244000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr4:16232600-16238200	Enhancers	Fetal Brain Male	brain
15	chr4:16233800-16237800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr4:16234000-16237600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr4:16234000-16237800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:16234000-16238000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr4:16234000-16239800	Weak transcription	Stomach Mucosa	stomach
20	chr4:16234000-16252000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:16234000-16252400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr4:16234000-16255000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:16234200-16237000	Weak transcription	Brain Substantia Nigra	brain
24	chr4:16234200-16237400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:16234200-16244800	Weak transcription	Right Atrium	heart
26	chr4:16234200-16254400	Weak transcription	NHDF-Ad	bronchial
27	chr4:16234200-16257400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr4:16234200-16264800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:16234400-16236600	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:16234400-16237600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:16234400-16247200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr4:16234400-16247800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:16234400-16247800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr4:16234400-16252200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:16234400-16261600	Weak transcription	Brain Cingulate Gyrus	brain
36	chr4:16234600-16239200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr4:16234600-16246600	Weak transcription	Adipose Nuclei	Adipose
38	chr4:16234800-16239600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:16234800-16243600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr4:16234800-16253800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr4:16235000-16252200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:16235200-16239200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:16235400-16272800	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr4:16235600-16236600	Weak transcription	Brain Germinal Matrix	brain
45	chr4:16235600-16237400	Enhancers	Primary B cells from peripheral blood	blood
46	chr4:16235600-16247200	Weak transcription	Brain Anterior Caudate	brain
47	chr4:16235600-16261600	Weak transcription	Fetal Kidney	kidney
48	chr4:16235800-16236800	Enhancers	Primary B cells from cord blood	blood
49	chr4:16235800-16237000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr4:16236000-16237000	Enhancers	Monocytes-CD14+_RO01746	blood

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