Variant report

Variant	rs9919207
Chromosome Location	chr1:227455637-227455638
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:227441285..227444497-chr1:227452902..227455834,3	K562	blood:
2	chr1:227454247..227456630-chr1:227461574..227463571,2	K562	blood:
3	chr1:227453649..227455713-chr1:227502343..227504921,2	K562	blood:

Variant related genes	Relation type
ENSG00000143776	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12078593	1.00[AMR][1000 genomes]
rs12089076	1.00[AMR][1000 genomes]
rs16847822	1.00[AMR][1000 genomes]
rs73088936	1.00[AMR][1000 genomes]
rs73102372	1.00[AMR][1000 genomes]
rs73102384	1.00[AMR][1000 genomes]
rs73102391	1.00[AMR][1000 genomes]
rs73104364	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003656	chr1:227034700-227559665	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv535318	chr1:227034700-227559665	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv534002	chr1:227315186-228047108	Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv873242	chr1:227371906-227579344	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv549271	chr1:227411003-227581017	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227414000-227459200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:227415800-227456800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr1:227431600-227486200	Weak transcription	NHDF-Ad	bronchial
4	chr1:227432000-227459200	Weak transcription	Fetal Lung	lung
5	chr1:227433000-227469000	Weak transcription	Aorta	Aorta
6	chr1:227434200-227455800	Weak transcription	Adipose Nuclei	Adipose
7	chr1:227434600-227468800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:227434800-227458400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:227435000-227457000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr1:227440000-227456600	Weak transcription	HepG2	liver
11	chr1:227440200-227456800	Weak transcription	HUVEC	blood vessel
12	chr1:227443400-227474000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:227445800-227458400	Weak transcription	NHEK	skin
14	chr1:227447000-227456800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr1:227447200-227473600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:227448400-227456400	Weak transcription	Psoas Muscle	Psoas
17	chr1:227448600-227457200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:227449600-227473600	Weak transcription	NH-A	brain
19	chr1:227449800-227465200	Weak transcription	K562	blood
20	chr1:227452400-227456000	Enhancers	Brain Hippocampus Middle	brain
21	chr1:227452800-227463800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:227453000-227468600	Weak transcription	Lung	lung
23	chr1:227453600-227457200	Enhancers	Brain Substantia Nigra	brain
24	chr1:227454200-227470400	Weak transcription	Ovary	ovary
25	chr1:227455000-227457200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr1:227455200-227456000	Enhancers	Brain Cingulate Gyrus	brain
27	chr1:227455200-227457200	Enhancers	Brain Anterior Caudate	brain
28	chr1:227455400-227456200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:227455400-227456600	Enhancers	Left Ventricle	heart
30	chr1:227455400-227456600	Enhancers	Right Ventricle	heart
31	chr1:227455400-227456800	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr1:227455400-227457000	Enhancers	Brain Angular Gyrus	brain
33	chr1:227455600-227456000	Enhancers	Colon Smooth Muscle	Colon
34	chr1:227455600-227456000	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr1:227455600-227456000	Enhancers	Rectal Smooth Muscle	rectum
36	chr1:227455600-227458600	Enhancers	Liver	Liver

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