Variant report

Variant	rs16842355
Chromosome Location	chr4:8476497-8476498
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:8472049..8473735-chr4:8474244..8476711,2	K562	blood:
2	chr4:8442292..8444495-chr4:8476315..8478872,2	MCF-7	breast:
3	chr4:8471024..8473735-chr4:8474244..8476611,2	K562	blood:
4	chr4:8475299..8477901-chr4:8499421..8502393,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000087008	Chromatin interaction
ENSG00000155275	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10938716	0.94[ASN][1000 genomes]
rs10938717	0.94[ASN][1000 genomes]
rs13105415	0.94[ASN][1000 genomes]
rs13105907	0.98[ASN][1000 genomes]
rs13106582	0.92[ASN][1000 genomes]
rs13111630	0.94[ASN][1000 genomes]
rs13120514	0.94[ASN][1000 genomes]
rs13120605	0.98[ASN][1000 genomes]
rs13121817	0.98[ASN][1000 genomes]
rs13122276	0.98[ASN][1000 genomes]
rs13129077	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13132875	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13141535	0.98[ASN][1000 genomes]
rs13147943	0.96[ASN][1000 genomes]
rs34053441	0.83[ASN][1000 genomes]
rs34465110	0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs34681013	0.86[AFR][1000 genomes]
rs34935132	0.88[ASN][1000 genomes]
rs35769879	0.86[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs36122693	0.94[ASN][1000 genomes]
rs3775895	0.84[ASN][1000 genomes]
rs3796763	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3806811	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56786736	0.98[ASN][1000 genomes]
rs60080531	0.98[ASN][1000 genomes]
rs6811968	0.96[ASN][1000 genomes]
rs6813502	0.96[ASN][1000 genomes]
rs6816430	0.96[ASN][1000 genomes]
rs6832505	0.86[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6832668	0.96[ASN][1000 genomes]
rs73089514	0.94[ASN][1000 genomes]
rs7670021	0.94[ASN][1000 genomes]
rs7697154	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002794	chr4:8110083-8490934	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv829854	chr4:8402921-8506407	Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8447000-8480200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:8447200-8480200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr4:8447400-8482200	Strong transcription	Primary T cells from cord blood	blood
4	chr4:8459800-8478800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:8463800-8478800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:8465200-8482200	Strong transcription	Brain Germinal Matrix	brain
7	chr4:8465400-8480200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:8467600-8482200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr4:8467800-8480400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:8468000-8478600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:8468400-8479600	Weak transcription	Psoas Muscle	Psoas
12	chr4:8470600-8479000	Weak transcription	Fetal Brain Male	brain
13	chr4:8471200-8476800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr4:8471200-8477400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr4:8471200-8480600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr4:8471400-8477200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:8471400-8477400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:8471400-8477400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr4:8471400-8479600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:8471400-8480200	Weak transcription	HMEC	breast
21	chr4:8471600-8477200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr4:8471600-8477800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr4:8471800-8477200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:8471800-8477600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr4:8471800-8477600	Weak transcription	A549	lung
26	chr4:8471800-8479600	Weak transcription	NHEK	skin
27	chr4:8471800-8480000	Weak transcription	GM12878-XiMat	blood
28	chr4:8471800-8480800	Weak transcription	HepG2	liver
29	chr4:8471800-8483200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:8472000-8477000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr4:8472000-8480200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr4:8472200-8477400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:8472200-8480800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr4:8472400-8477400	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr4:8472400-8479800	Weak transcription	Primary B cells from cord blood	blood
36	chr4:8472600-8480000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr4:8472800-8476800	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr4:8473200-8477000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:8473400-8476600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:8473400-8477000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr4:8473400-8477200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:8473400-8477200	Weak transcription	Dnd41	blood
43	chr4:8473400-8477600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:8473600-8476600	Genic enhancers	Fetal Muscle Trunk	muscle
45	chr4:8473600-8476800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:8473600-8477400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:8473600-8477600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr4:8473600-8477600	Weak transcription	Brain Angular Gyrus	brain
49	chr4:8473600-8501400	Weak transcription	Brain Substantia Nigra	brain
50	chr4:8473800-8476800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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