Variant report

Variant	rs269260
Chromosome Location	chr7:140332062-140332063
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:140326135..140327836-chr7:140331660..140333245,2	K562	blood:
2	chr7:140330889..140333777-chr7:140334738..140338747,3	K562	blood:
3	chr7:140326135..140328395-chr7:140330259..140333160,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10227869	1.00[EUR][1000 genomes]
rs10270838	1.00[ASN][1000 genomes]
rs11973083	1.00[EUR][1000 genomes]
rs11982424	1.00[EUR][1000 genomes]
rs11983453	1.00[EUR][1000 genomes]
rs269251	1.00[EUR][1000 genomes]
rs269252	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs269253	1.00[EUR][1000 genomes]
rs55816014	1.00[EUR][1000 genomes]
rs56711326	1.00[EUR][1000 genomes]
rs56942922	1.00[ASN][1000 genomes]
rs57565761	1.00[EUR][1000 genomes]
rs57916123	1.00[ASN][1000 genomes]
rs57960333	1.00[EUR][1000 genomes]
rs58118476	1.00[EUR][1000 genomes]
rs59489402	1.00[EUR][1000 genomes]
rs60480710	1.00[EUR][1000 genomes]
rs60901124	1.00[EUR][1000 genomes]
rs61333130	1.00[EUR][1000 genomes]
rs61369053	1.00[ASN][1000 genomes]
rs61737088	1.00[EUR][1000 genomes]
rs61737090	1.00[EUR][1000 genomes]
rs6943180	1.00[ASN][1000 genomes]
rs6952059	1.00[EUR][1000 genomes]
rs6957365	1.00[EUR][1000 genomes]
rs6964971	1.00[EUR][1000 genomes]
rs6964982	1.00[EUR][1000 genomes]
rs6971144	1.00[ASN][1000 genomes]
rs6972562	1.00[EUR][1000 genomes]
rs6979290	1.00[EUR][1000 genomes]
rs73483908	1.00[ASN][1000 genomes]
rs73491595	1.00[EUR][1000 genomes]
rs73498495	1.00[ASN][1000 genomes]
rs73498497	1.00[ASN][1000 genomes]
rs73498501	1.00[ASN][1000 genomes]
rs73500409	1.00[ASN][1000 genomes]
rs73500413	1.00[ASN][1000 genomes]
rs73500418	1.00[ASN][1000 genomes]
rs73500424	1.00[ASN][1000 genomes]
rs73500426	1.00[ASN][1000 genomes]
rs73502154	1.00[EUR][1000 genomes]
rs73736617	1.00[EUR][1000 genomes]
rs73736622	1.00[EUR][1000 genomes]
rs73736632	1.00[EUR][1000 genomes]
rs73736633	1.00[EUR][1000 genomes]
rs7789961	1.00[ASN][1000 genomes]
rs7795017	1.00[EUR][1000 genomes]
rs7796944	1.00[ASN][1000 genomes]
rs7804236	1.00[EUR][1000 genomes]
rs7811087	1.00[ASN][1000 genomes]
rs9942679	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831157	chr7:140241339-140426876	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS 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 miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1021133	chr7:140270797-140338653	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv1029128	chr7:140293389-140335570	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140326400-140334800	Weak transcription	Spleen	Spleen
2	chr7:140326600-140335400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:140326600-140335400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:140326600-140335400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:140326600-140335800	Weak transcription	Fetal Intestine Small	intestine
6	chr7:140326600-140337400	Weak transcription	Gastric	stomach
7	chr7:140326600-140339600	Weak transcription	Esophagus	oesophagus
8	chr7:140326800-140334800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:140326800-140335200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:140326800-140335400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:140326800-140335400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:140327000-140335200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:140327000-140335200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr7:140327000-140335200	Weak transcription	Brain Substantia Nigra	brain
15	chr7:140327000-140335400	Weak transcription	Brain Anterior Caudate	brain
16	chr7:140327000-140337000	Weak transcription	Fetal Kidney	kidney
17	chr7:140327000-140338000	Weak transcription	NH-A	brain
18	chr7:140327800-140335600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:140327800-140338200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:140328200-140334400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:140328200-140334800	Weak transcription	Ovary	ovary
22	chr7:140328200-140335200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:140328200-140335200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:140328200-140335200	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:140328200-140335200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr7:140328200-140335200	Weak transcription	Right Ventricle	heart
27	chr7:140328200-140335400	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:140328200-140335400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr7:140328800-140337600	Weak transcription	Liver	Liver
30	chr7:140329400-140337400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:140329600-140334800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:140329600-140335200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:140329600-140337600	Weak transcription	Fetal Brain Female	brain
34	chr7:140330000-140334400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:140330200-140332400	Enhancers	Adipose Nuclei	Adipose
36	chr7:140330600-140332200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:140330600-140332400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:140330600-140332400	Enhancers	Fetal Stomach	stomach
39	chr7:140330600-140332600	Genic enhancers	Fetal Muscle Trunk	muscle
40	chr7:140330800-140332400	Strong transcription	Fetal Lung	lung
41	chr7:140330800-140332400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr7:140330800-140332400	Enhancers	NHDF-Ad	bronchial
43	chr7:140331000-140332200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:140331000-140332400	Enhancers	HSMMtube	muscle
45	chr7:140331000-140332600	Enhancers	Stomach Smooth Muscle	stomach
46	chr7:140331200-140332200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:140331200-140332200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:140331200-140332200	Bivalent Enhancer	HSMM	muscle
49	chr7:140331200-140332400	Enhancers	Left Ventricle	heart
50	chr7:140331200-140332400	Enhancers	NHLF	lung

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