Variant report

Variant	rs12504979
Chromosome Location	chr4:99546654-99546655
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10020677	0.92[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11097625	0.84[ASN][1000 genomes]
rs11097626	0.84[ASN][1000 genomes]
rs11937119	0.84[ASN][1000 genomes]
rs11938081	0.85[JPT][hapmap];0.89[ASN][1000 genomes]
rs11941870	0.84[ASN][1000 genomes]
rs11941880	0.84[ASN][1000 genomes]
rs11946198	0.81[CHB][hapmap];0.90[CHD][hapmap];0.84[ASN][1000 genomes]
rs12507537	0.84[ASN][1000 genomes]
rs12509046	0.87[CHB][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs12509170	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12512885	0.84[ASN][1000 genomes]
rs2178216	0.85[CEU][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28531755	0.82[ASN][1000 genomes]
rs3941	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs4699356	0.90[CHD][hapmap];0.84[ASN][1000 genomes]
rs4699660	0.82[ASN][1000 genomes]
rs4699661	0.87[CHB][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs4699662	0.83[ASN][1000 genomes]
rs6532752	0.84[ASN][1000 genomes]
rs6819238	0.90[CHD][hapmap];0.84[ASN][1000 genomes]
rs6832517	0.80[JPT][hapmap];0.81[ASN][1000 genomes]
rs6848644	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7682381	0.83[ASN][1000 genomes]
rs9684705	0.84[ASN][1000 genomes]
rs9686007	0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594940	chr4:99542475-99573350	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99535600-99554200	Enhancers	Brain Substantia Nigra	brain
2	chr4:99539000-99547200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:99539200-99547200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr4:99539200-99547200	Weak transcription	Right Atrium	heart
5	chr4:99539200-99547600	Weak transcription	Gastric	stomach
6	chr4:99539200-99547600	Weak transcription	Left Ventricle	heart
7	chr4:99539200-99547600	Weak transcription	Right Ventricle	heart
8	chr4:99539200-99547800	Weak transcription	Fetal Stomach	stomach
9	chr4:99540000-99547400	Weak transcription	Fetal Lung	lung
10	chr4:99541800-99546800	Weak transcription	Fetal Brain Female	brain
11	chr4:99542000-99547200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:99542000-99547200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:99542000-99547200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:99542200-99547600	Weak transcription	Fetal Brain Male	brain
15	chr4:99542400-99547200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr4:99543200-99547200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:99543400-99547200	Enhancers	NHDF-Ad	bronchial
18	chr4:99543400-99547200	Enhancers	NHLF	lung
19	chr4:99543400-99549400	Enhancers	Brain Hippocampus Middle	brain
20	chr4:99543400-99550000	Enhancers	Brain Cingulate Gyrus	brain
21	chr4:99543600-99547200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:99543800-99548200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr4:99543800-99550000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr4:99544000-99550000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:99544000-99552400	Weak transcription	Thymus	Thymus
26	chr4:99544200-99547200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr4:99544200-99547400	Enhancers	Osteobl	bone
28	chr4:99544400-99547800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:99544400-99548400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr4:99544400-99551200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:99544600-99547200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:99544600-99547200	Weak transcription	Primary B cells from cord blood	blood
33	chr4:99544600-99547800	Weak transcription	Brain Germinal Matrix	brain
34	chr4:99544800-99546800	Enhancers	Primary T cells from cord blood	blood
35	chr4:99544800-99547400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:99544800-99548600	Weak transcription	Small Intestine	intestine
37	chr4:99544800-99549000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:99544800-99550000	Enhancers	NH-A	brain
39	chr4:99545000-99546800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr4:99545000-99548200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr4:99545000-99549000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:99545000-99550000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:99545200-99546800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr4:99545200-99547200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr4:99545200-99547400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:99545400-99547000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:99545800-99546800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr4:99545800-99546800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr4:99545800-99547000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:99545800-99547800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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