Variant report

Variant	rs73010663
Chromosome Location	chr1:156364266-156364267
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:156355534..156356071-chr1:156363514..156364451,2	K562	blood:
2	chr1:156361599..156364824-chr1:156368205..156372036,4	K562	blood:
3	chr1:156359850..156362270-chr1:156362434..156364882,2	MCF-7	breast:
4	chr1:156360686..156364321-chr1:156408945..156411695,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHBG-1	chr1:156359954-156365401	ENSG00000237390
2	lnc-C1orf61-1	chr1:156364041-156364558	l_136_chr1:156363527-156364558_testes

No data

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs72994617	1.00[AMR][1000 genomes]
rs73010649	1.00[AMR][1000 genomes]
rs73010652	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010655	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010667	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916198	chr1:155804210-156403997	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	428 gene(s)	inside rSNPs	diseases
2	nsv1011302	chr1:156081561-156532624	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	380 gene(s)	inside rSNPs	diseases
3	nsv915822	chr1:156226286-156651655	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	367 gene(s)	inside rSNPs	diseases
4	esv1793632	chr1:156338992-156366178	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a
5	nsv1005335	chr1:156347358-156905648	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	395 gene(s)	inside rSNPs	diseases
6	nsv1004910	chr1:156347358-157258223	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	430 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:156358600-156367600	Weak transcription	Right Atrium	heart
2	chr1:156358800-156364600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr1:156359600-156364400	Enhancers	Brain Hippocampus Middle	brain
4	chr1:156359800-156365000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:156362000-156369200	Weak transcription	Brain Angular Gyrus	brain
6	chr1:156362800-156365200	Enhancers	Brain Germinal Matrix	brain
7	chr1:156363000-156368800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:156363000-156368800	Weak transcription	Fetal Brain Male	brain
9	chr1:156363000-156369200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:156363200-156369800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:156363200-156371000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:156363400-156369000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr1:156363400-156369000	Weak transcription	Fetal Brain Female	brain
14	chr1:156363600-156368800	Weak transcription	A549	lung
15	chr1:156363600-156369000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:156363800-156365400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:156364000-156364600	Enhancers	Brain Substantia Nigra	brain
18	chr1:156364000-156364800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:156364000-156368200	Weak transcription	Hela-S3	cervix
20	chr1:156364200-156369200	Weak transcription	Brain Inferior Temporal Lobe	brain

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