Variant report

Variant	rs7591191
Chromosome Location	chr2:77236613-77236614
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-4	chr2:77236150-77236917	ENSG00000234653.1
2	lnc-MRPL19-4	chr2:77236150-77236914	NR_110284

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10048661	0.82[ASN][1000 genomes]
rs10184102	0.81[ASN][1000 genomes]
rs10520175	0.90[ASN][1000 genomes]
rs11889881	0.99[ASN][1000 genomes]
rs11899047	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13384774	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13388164	0.96[ASN][1000 genomes]
rs13396539	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13403143	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13414012	0.82[ASN][1000 genomes]
rs1446719	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17013534	0.91[ASN][1000 genomes]
rs17013535	0.91[ASN][1000 genomes]
rs17013563	0.95[ASN][1000 genomes]
rs17013580	0.99[ASN][1000 genomes]
rs28896632	0.81[ASN][1000 genomes]
rs41375150	0.91[ASN][1000 genomes]
rs55765941	0.82[ASN][1000 genomes]
rs57522758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59645157	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61335199	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834266	chr2:77120236-77287504	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv949670	chr2:77125218-77712607	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv519950	chr2:77213103-77256291	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv997284	chr2:77233426-77303198	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1007408	chr2:77235194-77255152	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77232000-77245600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:77232600-77238200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:77232800-77238000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:77233600-77237200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:77233800-77236800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:77233800-77237000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr2:77233800-77237000	Enhancers	HUVEC	blood vessel
8	chr2:77234000-77237600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:77234200-77239000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:77234400-77238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:77234600-77237000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr2:77234600-77237600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:77235000-77237800	Enhancers	Fetal Brain Male	brain
14	chr2:77235200-77236800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:77235600-77236800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:77235600-77236800	Enhancers	Brain Anterior Caudate	brain
17	chr2:77235600-77237000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:77235800-77237000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr2:77235800-77237000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:77236000-77239600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:77236200-77237000	Enhancers	NH-A	brain
22	chr2:77236400-77236800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:77236400-77236800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr2:77236400-77237400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:77236400-77239600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:77236400-77240200	Weak transcription	Fetal Lung	lung
27	chr2:77236600-77237000	Enhancers	Hela-S3	cervix
28	chr2:77236600-77238200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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