Variant report

Variant	rs74024187
Chromosome Location	chr16:70317470-70317471
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:70311320..70313500-chr16:70315118..70317601,2	MCF-7	breast:
2	chr16:70315876..70318226-chr16:70381253..70382948,2	K562	blood:
3	chr16:70302571..70304253-chr16:70316380..70318407,2	K562	blood:
4	chr16:70316535..70319262-chr16:70321753..70323880,3	MCF-7	breast:
5	chr16:70301578..70303718-chr16:70316070..70318288,2	MCF-7	breast:
6	chr16:70316213..70317972-chr16:70332773..70334830,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000090861	Chromatin interaction
ENSG00000260537	Chromatin interaction
ENSG00000157349	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs11537667	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11859191	0.81[AMR][1000 genomes]
rs11859257	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11859730	0.90[AMR][1000 genomes]
rs11859827	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11860870	0.94[AFR][1000 genomes]
rs11860922	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11861097	0.81[AMR][1000 genomes]
rs11862053	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11862150	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11862188	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11866378	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11866451	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970147	0.83[AFR][1000 genomes]
rs16970361	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970609	0.96[AFR][1000 genomes]
rs2869156	1.00[AMR][1000 genomes]
rs3972037	0.89[AMR][1000 genomes]
rs3972075	0.90[AMR][1000 genomes]
rs55657328	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55805938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55819743	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55936739	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55963712	0.81[AMR][1000 genomes]
rs55965002	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55971559	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56043981	0.93[AFR][1000 genomes]
rs56051513	0.90[AMR][1000 genomes]
rs56090000	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56096542	0.91[AFR][1000 genomes]
rs56217164	0.96[AFR][1000 genomes]
rs56234537	0.96[AFR][1000 genomes]
rs57279408	0.96[AFR][1000 genomes]
rs57320283	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57422630	0.83[AFR][1000 genomes]
rs57623576	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58055772	0.83[AFR][1000 genomes]
rs58131227	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58319566	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs58328210	0.86[AFR][1000 genomes]
rs59384897	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59612351	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59769732	1.00[AMR][1000 genomes]
rs59791510	0.93[AFR][1000 genomes]
rs59849898	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59928915	0.86[AFR][1000 genomes]
rs60103946	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60426209	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60463946	1.00[AMR][1000 genomes]
rs60523557	0.93[AFR][1000 genomes]
rs60567469	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs60841206	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61172065	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61391917	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61594809	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6499307	0.81[AMR][1000 genomes]
rs6499309	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7184248	0.91[AFR][1000 genomes]
rs7185665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7186024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7189535	0.81[AMR][1000 genomes]
rs7190921	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7195567	0.93[AFR][1000 genomes]
rs7198871	0.81[AMR][1000 genomes]
rs7204800	0.93[AFR][1000 genomes]
rs7205871	0.91[AFR][1000 genomes]
rs7205990	0.83[AFR][1000 genomes]
rs74024172	0.90[AMR][1000 genomes]
rs74024176	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024177	1.00[AMR][1000 genomes]
rs74024180	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024182	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024183	0.81[AMR][1000 genomes]
rs74024184	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024185	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024191	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024193	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024196	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74024199	0.93[AFR][1000 genomes]
rs74024200	0.93[AFR][1000 genomes]
rs8044699	0.90[AMR][1000 genomes]
rs8045571	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8045769	0.90[AMR][1000 genomes]
rs8046280	0.89[AFR][1000 genomes]
rs8046662	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8051869	0.86[AFR][1000 genomes]
rs8053040	0.93[AFR][1000 genomes]
rs8055675	0.81[AMR][1000 genomes]
rs8056196	0.81[AMR][1000 genomes]
rs8063749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33745	chr16:70116599-70319873	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv833271	chr16:70185694-70353334	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS 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	51 gene(s)	inside rSNPs	diseases
3	nsv1061286	chr16:70253809-70331407	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv906870	chr16:70295061-70323126	Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv906871	chr16:70302333-70375873	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv906872	chr16:70303418-70356746	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70286000-70318600	Strong transcription	Fetal Intestine Large	intestine
2	chr16:70286000-70319000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr16:70286000-70320000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr16:70286000-70320400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr16:70286000-70320400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:70286000-70320400	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr16:70286000-70320400	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr16:70286000-70320400	Strong transcription	Osteobl	bone
9	chr16:70286000-70321400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr16:70286000-70321400	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr16:70286200-70318600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr16:70286200-70319000	Strong transcription	Stomach Smooth Muscle	stomach
13	chr16:70286200-70319600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr16:70286200-70319800	Strong transcription	Fetal Muscle Trunk	muscle
15	chr16:70286200-70320000	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr16:70286200-70320400	Strong transcription	Fetal Muscle Leg	muscle
17	chr16:70286200-70320400	Strong transcription	Skeletal Muscle Male	skeletal muscle
18	chr16:70286200-70320600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr16:70286200-70321200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr16:70286200-70321400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr16:70286200-70321400	Strong transcription	Fetal Stomach	stomach
22	chr16:70286200-70321600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr16:70286400-70317800	Strong transcription	Brain Germinal Matrix	brain
24	chr16:70286400-70318000	Strong transcription	Adipose Nuclei	Adipose
25	chr16:70286400-70319800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr16:70286400-70319800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr16:70286400-70320000	Strong transcription	H9 Cell Line	embryonic stem cell
28	chr16:70286400-70320000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
29	chr16:70286400-70320400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr16:70287200-70321800	Weak transcription	Right Atrium	heart
31	chr16:70287400-70320000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:70288600-70320000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr16:70290200-70321600	Strong transcription	Fetal Intestine Small	intestine
34	chr16:70290600-70320600	Strong transcription	HepG2	liver
35	chr16:70291800-70319600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:70292000-70319800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr16:70292200-70319800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr16:70292200-70319800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:70296400-70319800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr16:70301200-70319800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr16:70306600-70320000	Strong transcription	HMEC	breast
42	chr16:70308400-70318600	Strong transcription	Thymus	Thymus
43	chr16:70308800-70318000	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr16:70308800-70319000	Strong transcription	Left Ventricle	heart
45	chr16:70309600-70319400	Strong transcription	Brain Substantia Nigra	brain
46	chr16:70309800-70319600	Strong transcription	Brain Anterior Caudate	brain
47	chr16:70309800-70319800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr16:70309800-70320400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
49	chr16:70310000-70317600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr16:70310000-70317600	Strong transcription	Fetal Lung	lung

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