Variant report

Variant	rs7537172
Chromosome Location	chr1:212388696-212388697
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:212386087..212387745-chr1:212388194..212390712,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10157725	1.00[ASN][1000 genomes]
rs11800208	1.00[EUR][1000 genomes]
rs11803526	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12739715	1.00[ASN][1000 genomes]
rs1342151	1.00[MEX][hapmap]
rs17018697	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17018717	1.00[EUR][1000 genomes]
rs17018767	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs17018784	1.00[EUR][1000 genomes]
rs17018792	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1873299	1.00[EUR][1000 genomes]
rs1908141	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs35030678	1.00[ASN][1000 genomes]
rs4369290	1.00[EUR][1000 genomes]
rs55764484	1.00[EUR][1000 genomes]
rs56410034	1.00[EUR][1000 genomes]
rs57461449	1.00[EUR][1000 genomes]
rs58031667	1.00[EUR][1000 genomes]
rs58388470	1.00[EUR][1000 genomes]
rs58972361	1.00[ASN][1000 genomes]
rs59665922	1.00[EUR][1000 genomes]
rs59988047	1.00[EUR][1000 genomes]
rs61331273	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6656320	1.00[ASN][1000 genomes]
rs6657771	1.00[MEX][hapmap]
rs6676652	1.00[EUR][1000 genomes]
rs6687793	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6701982	1.00[EUR][1000 genomes]
rs71646161	1.00[ASN][1000 genomes]
rs73078491	1.00[EUR][1000 genomes]
rs73078499	1.00[EUR][1000 genomes]
rs73078520	1.00[EUR][1000 genomes]
rs73078526	1.00[EUR][1000 genomes]
rs73078531	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73078536	1.00[EUR][1000 genomes]
rs74138106	1.00[ASN][1000 genomes]
rs74138110	1.00[ASN][1000 genomes]
rs74140412	1.00[ASN][1000 genomes]
rs7515005	1.00[CHB][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7530958	1.00[EUR][1000 genomes]
rs7533954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7534244	0.87[AMR][1000 genomes]
rs7534621	1.00[EUR][1000 genomes]
rs7536393	1.00[EUR][1000 genomes]
rs7536704	1.00[EUR][1000 genomes]
rs7538315	1.00[CHB][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7551910	1.00[ASN][1000 genomes]
rs884208	1.00[EUR][1000 genomes]
rs9804026	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	nsv999738	chr1:212218618-212513690	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	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

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212368800-212391000	Weak transcription	Thymus	Thymus
2	chr1:212379600-212391600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:212381800-212391200	Weak transcription	Right Atrium	heart
4	chr1:212382800-212388800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:212382800-212391000	Weak transcription	Stomach Mucosa	stomach
6	chr1:212383000-212393000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:212383400-212394600	Weak transcription	Left Ventricle	heart
8	chr1:212386200-212388800	Enhancers	Fetal Intestine Small	intestine
9	chr1:212386400-212391200	Weak transcription	Fetal Kidney	kidney
10	chr1:212387200-212389000	Enhancers	Fetal Intestine Large	intestine
11	chr1:212387200-212389000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr1:212387200-212389000	Enhancers	K562	blood
13	chr1:212387600-212389000	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr1:212387600-212391200	Weak transcription	Spleen	Spleen
15	chr1:212387800-212390800	Weak transcription	Adipose Nuclei	Adipose
16	chr1:212388000-212390800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr1:212388200-212388800	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr1:212388200-212389000	Enhancers	Colonic Mucosa	Colon
19	chr1:212388600-212391000	Weak transcription	Fetal Thymus	thymus
20	chr1:212388600-212392400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:212388600-212393000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:212388600-212393200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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