Variant report

Variant	rs16957444
Chromosome Location	chr16:75264506-75264507
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75263332..75265712-chr16:75269441..75271613,2	K562	blood:
2	chr16:75260323..75263123-chr16:75264222..75267022,3	K562	blood:
3	chr16:75263871..75266298-chr16:75266366..75267894,2	K562	blood:
4	chr16:75262796..75265611-chr16:75265904..75267442,2	MCF-7	breast:
5	chr16:75181385..75183781-chr16:75264084..75265885,2	K562	blood:
6	chr16:75259171..75262723-chr16:75263223..75268032,5	MCF-7	breast:
7	chr16:75244083..75246522-chr16:75263997..75266825,2	MCF-7	breast:
8	chr16:75259599..75261544-chr16:75263829..75267105,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000050820	Chromatin interaction
ENSG00000184517	Chromatin interaction
ENSG00000240338	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1049303	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11545087	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11644299	0.80[EUR][1000 genomes]
rs11645877	0.80[EUR][1000 genomes]
rs11859224	0.83[EUR][1000 genomes]
rs16957329	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17673911	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56902145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57145526	0.85[AFR][1000 genomes]
rs57376763	0.93[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs57935818	0.85[AFR][1000 genomes]
rs59475255	0.93[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs59633007	0.85[AFR][1000 genomes]
rs59720502	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59769904	0.93[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs61400279	0.93[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs730367	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061095	chr16:74519718-75407020	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv532560	chr16:74692406-75411912	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
3	nsv916502	chr16:74845880-75732365	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
4	nsv1056082	chr16:75004990-75295847	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv833282	chr16:75154171-75330634	Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv516504	chr16:75223491-75306402	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv523405	chr16:75227969-75342846	Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	esv1806781	chr16:75235390-75307470	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv906909	chr16:75236154-75316074	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
10	esv1792587	chr16:75237936-75305783	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
11	nsv906910	chr16:75251299-75316074	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
12	nsv906911	chr16:75252526-75296247	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv906912	chr16:75252526-75320827	Flanking Active TSS Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	esv1813349	chr16:75257361-75302684	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
15	nsv931939	chr16:75261354-75765025	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75254000-75267600	Weak transcription	Fetal Brain Male	brain
2	chr16:75254600-75268000	Weak transcription	GM12878-XiMat	blood
3	chr16:75256400-75266600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr16:75256600-75267600	Weak transcription	Fetal Heart	heart
5	chr16:75256600-75267600	Weak transcription	Right Atrium	heart
6	chr16:75259400-75267400	Weak transcription	Psoas Muscle	Psoas
7	chr16:75260000-75267800	Weak transcription	Stomach Mucosa	stomach
8	chr16:75260600-75264800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr16:75260800-75266600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr16:75260800-75267600	Strong transcription	Fetal Intestine Small	intestine
11	chr16:75260800-75278000	Weak transcription	Small Intestine	intestine
12	chr16:75261000-75267000	Strong transcription	Fetal Stomach	stomach
13	chr16:75261000-75267200	Strong transcription	NHLF	lung
14	chr16:75261000-75267600	Strong transcription	Brain Inferior Temporal Lobe	brain
15	chr16:75261000-75267600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr16:75261000-75268000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr16:75261000-75268000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr16:75261200-75264800	Strong transcription	Brain Cingulate Gyrus	brain
19	chr16:75261200-75268000	Strong transcription	Muscle Satellite Cultured Cells	--
20	chr16:75261400-75264800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr16:75261400-75265000	Strong transcription	Brain Germinal Matrix	brain
22	chr16:75261400-75267600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr16:75261400-75267800	Strong transcription	NHDF-Ad	bronchial
24	chr16:75261400-75268000	Strong transcription	Esophagus	oesophagus
25	chr16:75261400-75268000	Strong transcription	Gastric	stomach
26	chr16:75261400-75268000	Strong transcription	HUVEC	blood vessel
27	chr16:75261400-75271800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr16:75261400-75272400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:75261600-75264600	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr16:75261600-75264800	Strong transcription	HMEC	breast
31	chr16:75261600-75267400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr16:75261600-75267600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr16:75261600-75267600	Strong transcription	Adipose Nuclei	Adipose
34	chr16:75261600-75268000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr16:75261600-75268000	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr16:75261600-75268000	Strong transcription	NHEK	skin
37	chr16:75261800-75264800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr16:75261800-75267200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:75261800-75267400	Strong transcription	Brain Anterior Caudate	brain
40	chr16:75261800-75267600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr16:75261800-75267600	Strong transcription	Colonic Mucosa	Colon
42	chr16:75261800-75267600	Strong transcription	Fetal Intestine Large	intestine
43	chr16:75261800-75267800	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr16:75261800-75268000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr16:75261800-75268000	Strong transcription	HepG2	liver
46	chr16:75261800-75268000	Weak transcription	K562	blood
47	chr16:75261800-75272200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:75262000-75264800	Genic enhancers	Pancreas	Pancrea
49	chr16:75262000-75267200	Strong transcription	Stomach Smooth Muscle	stomach
50	chr16:75262000-75267400	Strong transcription	Liver	Liver

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