Variant report

Variant	rs11981205
Chromosome Location	chr7:13983369-13983370
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs56041031	0.90[ASN][1000 genomes]
rs62454585	0.85[ASN][1000 genomes]
rs73679047	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1020310	chr7:13839681-14015794	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538738	chr7:13839681-14015794	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv887698	chr7:13841798-14056075	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1020543	chr7:13851470-14021121	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv887700	chr7:13948517-14042702	Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv887701	chr7:13955324-13988170	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13933800-13983600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:13960200-13983600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:13960200-13987400	Weak transcription	K562	blood
4	chr7:13960200-13988200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:13960400-13985200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:13960400-13989000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:13960800-13985400	Weak transcription	NH-A	brain
8	chr7:13961400-13985000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:13963200-13985200	Weak transcription	Osteobl	bone
10	chr7:13969400-13985400	Weak transcription	Brain Hippocampus Middle	brain
11	chr7:13971400-13986400	Weak transcription	Lung	lung
12	chr7:13971400-13991600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr7:13971600-13989800	Weak transcription	Liver	Liver
14	chr7:13973400-13989000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:13973400-13990000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:13973800-13985000	Weak transcription	NHLF	lung
17	chr7:13974200-13983600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:13974200-13986000	Weak transcription	Fetal Kidney	kidney
19	chr7:13974200-13987400	Weak transcription	Fetal Heart	heart
20	chr7:13975000-13985400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:13975600-13988200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:13975600-14003600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:13975600-14003600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:13975600-14013800	Weak transcription	Left Ventricle	heart
25	chr7:13978800-13985200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:13978800-14004600	Weak transcription	Fetal Lung	lung
27	chr7:13979000-13983600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:13979000-13985200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:13979200-13984000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:13979200-13984400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:13979200-13988800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:13979200-13998000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr7:13979600-13989000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr7:13981800-13985200	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:13982400-13984600	Weak transcription	NHDF-Ad	bronchial

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