Variant report

Variant	rs2724556
Chromosome Location	chr4:152341717-152341718
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:152337823..152339848-chr4:152340887..152343384,2	K562	blood:
2	chr4:152334377..152337765-chr4:152341477..152345908,4	K562	blood:

Extended variants
information (count: 92 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10028035	0.86[EUR][1000 genomes]
rs10454251	0.83[EUR][1000 genomes]
rs10857260	0.81[EUR][1000 genomes]
rs11099815	0.86[EUR][1000 genomes]
rs11099816	0.80[EUR][1000 genomes]
rs11099819	0.80[EUR][1000 genomes]
rs11729923	0.82[EUR][1000 genomes]
rs11735957	0.81[EUR][1000 genomes]
rs11932398	0.83[EUR][1000 genomes]
rs12647555	0.83[EUR][1000 genomes]
rs1596290	0.83[EUR][1000 genomes]
rs1838043	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1899550	0.82[EUR][1000 genomes]
rs2034061	0.81[EUR][1000 genomes]
rs2709812	0.86[EUR][1000 genomes]
rs2709813	0.85[EUR][1000 genomes]
rs2709814	0.82[EUR][1000 genomes]
rs2709815	0.85[EUR][1000 genomes]
rs2709816	0.81[EUR][1000 genomes]
rs2709817	0.82[EUR][1000 genomes]
rs2709818	0.83[EUR][1000 genomes]
rs2709819	0.83[EUR][1000 genomes]
rs2709820	0.83[EUR][1000 genomes]
rs2709821	0.86[EUR][1000 genomes]
rs2709822	0.85[EUR][1000 genomes]
rs2709823	0.88[EUR][1000 genomes]
rs2709825	0.85[EUR][1000 genomes]
rs2709826	0.86[EUR][1000 genomes]
rs2709827	0.86[EUR][1000 genomes]
rs2709828	0.86[EUR][1000 genomes]
rs2709829	0.86[EUR][1000 genomes]
rs2709831	0.84[EUR][1000 genomes]
rs2709832	0.84[EUR][1000 genomes]
rs2709833	0.84[EUR][1000 genomes]
rs2709834	0.85[EUR][1000 genomes]
rs2709838	0.85[EUR][1000 genomes]
rs2709842	0.85[EUR][1000 genomes]
rs2709844	0.85[EUR][1000 genomes]
rs2724547	0.85[EUR][1000 genomes]
rs2724550	0.85[EUR][1000 genomes]
rs2724551	0.86[EUR][1000 genomes]
rs2724553	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2724555	0.88[EUR][1000 genomes]
rs2724558	0.81[EUR][1000 genomes]
rs2724563	0.86[EUR][1000 genomes]
rs2724564	0.86[EUR][1000 genomes]
rs2724565	0.82[EUR][1000 genomes]
rs2724567	0.86[EUR][1000 genomes]
rs2724568	0.86[EUR][1000 genomes]
rs2724571	0.85[EUR][1000 genomes]
rs2724574	0.82[EUR][1000 genomes]
rs2724577	0.86[EUR][1000 genomes]
rs2724578	0.85[EUR][1000 genomes]
rs2724580	0.85[EUR][1000 genomes]
rs28549769	0.83[EUR][1000 genomes]
rs28622593	0.85[EUR][1000 genomes]
rs28666858	0.81[EUR][1000 genomes]
rs4235219	0.85[EUR][1000 genomes]
rs4263379	0.83[EUR][1000 genomes]
rs4266275	0.86[EUR][1000 genomes]
rs4479686	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4696088	0.85[EUR][1000 genomes]
rs4696089	0.82[EUR][1000 genomes]
rs4696092	0.83[EUR][1000 genomes]
rs6843639	0.82[EUR][1000 genomes]
rs6845648	0.85[EUR][1000 genomes]
rs6851814	0.85[EUR][1000 genomes]
rs7657670	0.86[EUR][1000 genomes]
rs7657747	0.82[EUR][1000 genomes]
rs7658169	0.86[EUR][1000 genomes]
rs7676059	0.82[EUR][1000 genomes]
rs7676493	0.81[EUR][1000 genomes]
rs7676922	0.84[EUR][1000 genomes]
rs7677131	0.86[EUR][1000 genomes]
rs7678823	0.85[EUR][1000 genomes]
rs7680013	0.83[EUR][1000 genomes]
rs7680236	0.83[EUR][1000 genomes]
rs7682770	0.82[EUR][1000 genomes]
rs7682837	0.81[EUR][1000 genomes]
rs7684462	0.86[EUR][1000 genomes]
rs7698816	0.86[EUR][1000 genomes]
rs9994482	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1025192	chr4:152202627-152498890	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer 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	24 gene(s)	inside rSNPs	diseases
4	nsv537307	chr4:152202627-152498890	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv880624	chr4:152280646-152549112	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv432643	chr4:152335395-152417635	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv2611953	chr4:152340150-152342335	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3466395	chr4:152340328-152341939	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3500697	chr4:152340389-152341996	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2051581	chr4:152340510-152341768	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2724556	FAM160A1	cis	Whole Blood	GTEx

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152332000-152347600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr4:152338400-152341800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:152338400-152362000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:152338600-152342200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:152338600-152342400	Enhancers	HMEC	breast
6	chr4:152339800-152351800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:152340000-152342200	Enhancers	HUVEC	blood vessel
8	chr4:152340000-152349600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr4:152340200-152341800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:152340400-152343000	Enhancers	NHEK	skin
11	chr4:152340600-152341800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:152340600-152341800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:152340600-152341800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:152340600-152344000	Weak transcription	Small Intestine	intestine
15	chr4:152340600-152347000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:152340600-152353000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr4:152340800-152341800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:152340800-152342800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr4:152341200-152342400	Enhancers	Psoas Muscle	Psoas
20	chr4:152341400-152342200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:152341400-152345800	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr4:152341600-152341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:152341600-152341800	Enhancers	NH-A	brain
24	chr4:152341600-152342000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:152341600-152342000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:152341600-152342000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:152341600-152342000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr4:152341600-152342200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:152341600-152342200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr4:152341600-152342200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr4:152341600-152342200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:152341600-152342400	Enhancers	HSMM	muscle
33	chr4:152341600-152342600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:152341600-152342800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr4:152341600-152343200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:152341600-152343200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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