Variant report

Variant	rs7702848
Chromosome Location	chr5:95183265-95183266
allele	C/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	CTCF	chr5:95182069-95183294	SK-N-SH	brain:	n/a	chr5:95182878-95182891 chr5:95182876-95182894 chr5:95182871-95182892 chr5:95182877-95182893 chr5:95182883-95182890
2	CTCF	chr5:95183220-95183370	AG09319	gingival:	n/a	n/a
3	RAD21	chr5:95182242-95183303	SK-N-SH	brain:	n/a	chr5:95182878-95182892 chr5:95182874-95182893 chr5:95182883-95182892
4	CTCF	chr5:95181941-95183437	A549	lung:	n/a	chr5:95182878-95182891 chr5:95182876-95182894 chr5:95182871-95182892 chr5:95182877-95182893 chr5:95182883-95182890
5	CHD1	chr5:95182249-95183453	IMR90	lung:	n/a	n/a
6	SMC3	chr5:95182071-95183443	SK-N-SH	brain:	n/a	chr5:95182878-95182892
7	CTCF	chr5:95183260-95183410	NHDF-neo	bronchial:	n/a	n/a
8	CTCF	chr5:95183200-95183350	NHEK	skin:	n/a	n/a
9	CTCF	chr5:95182432-95183295	HCT-116	colon:	n/a	chr5:95182878-95182891 chr5:95182876-95182894 chr5:95182871-95182892 chr5:95182877-95182893 chr5:95182883-95182890
10	CTCF	chr5:95183200-95183350	GM12865	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:94979741..94980745-chr5:95182392..95183367,12	K562	blood:
2	chr5:95116355..95117924-chr5:95182403..95183379,13	MCF-7	breast:
3	chr5:95001354..95003054-chr5:95181008..95183990,2	K562	blood:
4	chr5:95116312..95117533-chr5:95181736..95183486,9	MCF-7	breast:
5	chr5:94979762..94980497-chr5:95182499..95183331,2	MCF-7	breast:
6	chr5:94999746..95000533-chr5:95182399..95183335,3	K562	blood:
7	chr5:94984590..94987808-chr5:95181177..95184579,4	K562	blood:
8	chr5:94979759..94980687-chr5:95182790..95183359,3	MCF-7	breast:
9	chr5:95182879..95183392-chr5:95194256..95194971,2	K562	blood:
10	chr5:95066232..95068400-chr5:95182417..95184649,2	MCF-7	breast:
11	chr5:95115987..95117779-chr5:95182285..95183519,12	K562	blood:

Variant related genes	Relation type
C5orf27	TF binding region
ENSG00000272021	TF binding region
ENSG00000250240	Chromatin interaction
ENSG00000164292	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10044151	1.00[CHB][hapmap]
rs10055875	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10067941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10079710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12520664	0.98[ASN][1000 genomes]
rs2161312	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2546196	0.98[ASN][1000 genomes]
rs3797207	0.88[CEU][hapmap];0.94[CHD][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs41470049	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6420125	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6556887	0.93[ASN][1000 genomes]
rs6556888	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6882301	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6883552	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6884979	0.94[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7703084	0.93[ASN][1000 genomes]
rs7708375	0.98[ASN][1000 genomes]
rs7716279	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7719227	1.00[JPT][hapmap];0.98[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	nsv830409	chr5:95006686-95204496	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015180	chr5:95134357-95286446	Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1019566	chr5:95180352-95300677	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr5:95171800-95185800	Weak transcription	Pancreas	Pancrea
2	chr5:95177800-95192200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:95178400-95188400	Weak transcription	Stomach Mucosa	stomach
4	chr5:95179000-95186200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:95179000-95206000	Weak transcription	Spleen	Spleen
6	chr5:95179200-95184200	Weak transcription	HSMM	muscle
7	chr5:95179200-95185800	Weak transcription	Lung	lung
8	chr5:95179400-95183600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:95179400-95184600	Weak transcription	NH-A	brain
10	chr5:95179400-95184600	Weak transcription	NHDF-Ad	bronchial
11	chr5:95179600-95184400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:95179800-95185200	Weak transcription	Left Ventricle	heart
13	chr5:95180000-95186000	Weak transcription	Right Atrium	heart
14	chr5:95180200-95184600	Weak transcription	Adipose Nuclei	Adipose
15	chr5:95182000-95185200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr5:95182200-95183400	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr5:95182600-95183600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:95182600-95186200	Weak transcription	NHLF	lung
19	chr5:95182800-95183800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:95182800-95184200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:95182800-95184200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:95182800-95184200	Weak transcription	Osteobl	bone
23	chr5:95182800-95184400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:95182800-95184400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:95182800-95185800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:95182800-95185800	Weak transcription	Placenta	Placenta
27	chr5:95182800-95185800	Weak transcription	HepG2	liver
28	chr5:95182800-95186000	Enhancers	Liver	Liver
29	chr5:95182800-95191000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr5:95182800-95191000	Weak transcription	Brain Substantia Nigra	brain
31	chr5:95182800-95191200	Weak transcription	Psoas Muscle	Psoas
32	chr5:95182800-95191800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr5:95182800-95192200	Weak transcription	Esophagus	oesophagus
34	chr5:95183000-95184400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr5:95183000-95185000	Enhancers	Fetal Heart	heart

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