Variant report

Variant	rs7551520
Chromosome Location	chr1:212805326-212805327
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:212803388..212806406-chr1:212807371..212811389,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BATF3-2	chr1:212800569-212805905	XLOC_001195

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11571532	1.00[ASN][1000 genomes]
rs11571536	1.00[ASN][1000 genomes]
rs11571538	1.00[ASN][1000 genomes]
rs11571552	1.00[ASN][1000 genomes]
rs17019442	1.00[ASN][1000 genomes]
rs35777725	1.00[ASN][1000 genomes]
rs3890801	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55854080	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56023947	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6540751	1.00[ASN][1000 genomes]
rs6656504	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6670396	1.00[ASN][1000 genomes]
rs6682816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72756370	1.00[ASN][1000 genomes]
rs72756371	1.00[ASN][1000 genomes]
rs74138596	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74138599	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74138600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74138601	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv549139	chr1:212332294-212876902	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	nsv1013110	chr1:212555764-212948092	Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
3	nsv535287	chr1:212555764-212948092	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
4	esv2757770	chr1:212648143-212843103	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	77 gene(s)	inside rSNPs	diseases
5	esv2758996	chr1:212648143-212843103	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	77 gene(s)	inside rSNPs	diseases
6	nsv428588	chr1:212705588-212862875	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212793600-212810600	Weak transcription	Esophagus	oesophagus
2	chr1:212794400-212812200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:212802600-212822800	Weak transcription	Fetal Kidney	kidney
4	chr1:212803200-212808200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:212803400-212807600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:212803400-212807800	Weak transcription	Osteobl	bone
7	chr1:212803600-212807800	Weak transcription	Fetal Intestine Large	intestine
8	chr1:212803600-212808200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr1:212803800-212805600	Enhancers	Primary hematopoietic stem cells	blood
10	chr1:212803800-212808600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:212803800-212808800	Weak transcription	Left Ventricle	heart
12	chr1:212803800-212808800	Weak transcription	Right Atrium	heart
13	chr1:212803800-212808800	Weak transcription	Right Ventricle	heart
14	chr1:212804000-212807800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr1:212804000-212808600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:212804200-212806600	Weak transcription	GM12878-XiMat	blood
17	chr1:212804200-212808600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr1:212804400-212805400	Weak transcription	Adipose Nuclei	Adipose
19	chr1:212804400-212808200	Weak transcription	Thymus	Thymus
20	chr1:212804400-212808200	Weak transcription	Spleen	Spleen
21	chr1:212804600-212808400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:212804800-212807800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:212804800-212807800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:212805000-212806400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:212805000-212807800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:212805000-212810400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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