Variant report

Variant	rs7068359
Chromosome Location	chr10:21607779-21607780
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFIC	chr10:21606674-21608388	SK-N-SH	brain:	n/a	chr10:21607877-21607905 chr10:21607889-21607905 chr10:21607888-21607905
2	NFIC	chr10:21607547-21608205	ECC-1	luminal epithelium:	n/a	chr10:21607877-21607905 chr10:21607889-21607905 chr10:21607888-21607905
3	NFIC	chr10:21607588-21608203	ECC-1	luminal epithelium:	n/a	chr10:21607877-21607905 chr10:21607889-21607905 chr10:21607888-21607905
4	NFIC	chr10:21607618-21608127	SK-N-SH	brain:	n/a	chr10:21607877-21607905 chr10:21607889-21607905 chr10:21607888-21607905
5	CTCF	chr10:21607720-21607870	GM12868	blood:	n/a	n/a
6	TCF12	chr10:21606801-21608289	SK-N-SH	brain:	n/a	n/a
7	ZNF263	chr10:21607661-21608061	HEK293-T-REx	kidney:	n/a	chr10:21607832-21607853

Variant related genes	Relation type
RNU6-15P	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12246574	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12264555	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35732149	1.00[ASN][1000 genomes]
rs56988582	1.00[ASN][1000 genomes]
rs66527303	1.00[ASN][1000 genomes]
rs7076249	1.00[CEU][hapmap]
rs7092209	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7094045	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72793050	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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv2761579	chr10:21554557-21612760	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21605200-21607800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:21605400-21607800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:21605400-21608000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr10:21606000-21608800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:21606600-21608800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:21606800-21607800	Enhancers	NHDF-Ad	bronchial
7	chr10:21606800-21607800	Enhancers	Osteobl	bone
8	chr10:21606800-21608000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:21606800-21608200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr10:21606800-21608400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr10:21606800-21608400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr10:21606800-21608400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr10:21606800-21608800	Enhancers	A549	lung
14	chr10:21607000-21607800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:21607000-21607800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr10:21607000-21607800	Enhancers	HSMM	muscle
17	chr10:21607000-21608000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr10:21607000-21608000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr10:21607000-21608000	Enhancers	Fetal Stomach	stomach
20	chr10:21607000-21608000	Enhancers	Fetal Thymus	thymus
21	chr10:21607000-21608000	Enhancers	Right Atrium	heart
22	chr10:21607000-21608200	Enhancers	Fetal Muscle Leg	muscle
23	chr10:21607000-21608400	Enhancers	NH-A	brain
24	chr10:21607000-21608400	Enhancers	NHLF	lung
25	chr10:21607200-21607800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr10:21607200-21607800	Weak transcription	Adipose Nuclei	Adipose
27	chr10:21607200-21608000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr10:21607200-21608000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr10:21607200-21608200	Enhancers	Fetal Heart	heart
30	chr10:21607200-21608400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr10:21607200-21608400	Enhancers	Ovary	ovary
32	chr10:21607200-21608600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr10:21607200-21608600	Enhancers	Fetal Kidney	kidney
34	chr10:21607400-21607800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:21607400-21608000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr10:21607600-21607800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr10:21607600-21607800	Enhancers	K562	blood
38	chr10:21607600-21608000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr10:21607600-21608000	Enhancers	Lung	lung
40	chr10:21607600-21608400	Enhancers	Fetal Lung	lung
41	chr10:21607600-21608400	Enhancers	Fetal Muscle Trunk	muscle
42	chr10:21607600-21608400	Enhancers	Right Ventricle	heart
43	chr10:21607600-21608800	Enhancers	HUVEC	blood vessel

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