Variant report

Variant	rs6756326
Chromosome Location	chr2:180122162-180122163
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	chr2:180120526..180124742-chr2:180127021..180129947,5	K562	blood:

Variant related genes	Relation type
ENSG00000187231	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10170520	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10174774	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10186198	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10205390	0.81[AFR][1000 genomes]
rs10205999	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10439299	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10930858	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158872	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11884516	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11894870	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11898291	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12997314	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13026497	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13383965	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13391602	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13418701	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1907421	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2289992	0.82[EUR][1000 genomes]
rs4585064	0.83[EUR][1000 genomes]
rs58887763	0.80[EUR][1000 genomes]
rs6433757	0.82[EUR][1000 genomes]
rs6433760	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6433761	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6433764	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6433769	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6707081	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6734121	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6736098	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6742739	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7562730	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7579536	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7585600	0.83[EUR][1000 genomes]
rs7608882	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949133	chr2:179711376-180124327	Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1004693	chr2:179933683-180265288	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv834471	chr2:179974303-180123027	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv834472	chr2:180091670-180220448	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6756326	SESTD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180091800-180127200	Weak transcription	Fetal Lung	lung
2	chr2:180102800-180127800	Weak transcription	Psoas Muscle	Psoas
3	chr2:180110200-180124200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:180112400-180126200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:180112600-180125000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr2:180112600-180126800	Weak transcription	Hela-S3	cervix
7	chr2:180115400-180127600	Weak transcription	NHLF	lung
8	chr2:180116200-180124400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:180116800-180124400	Enhancers	HepG2	liver
10	chr2:180117400-180126200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:180117800-180124400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:180117800-180126400	Weak transcription	Small Intestine	intestine
13	chr2:180118000-180125200	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:180118200-180122400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:180118200-180122800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:180118200-180124800	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr2:180118600-180126200	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr2:180118800-180127600	Weak transcription	HSMM	muscle
19	chr2:180118800-180128200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:180119200-180124400	Weak transcription	Primary B cells from cord blood	blood
21	chr2:180119400-180123400	Weak transcription	Brain Substantia Nigra	brain
22	chr2:180119400-180128200	Weak transcription	Pancreas	Pancrea
23	chr2:180119600-180126200	Weak transcription	Brain Anterior Caudate	brain
24	chr2:180120000-180127400	Weak transcription	Brain Angular Gyrus	brain
25	chr2:180120200-180127200	Weak transcription	Fetal Kidney	kidney
26	chr2:180120200-180127600	Weak transcription	Fetal Stomach	stomach
27	chr2:180120400-180122600	Weak transcription	Adipose Nuclei	Adipose
28	chr2:180120400-180125000	Weak transcription	Right Atrium	heart
29	chr2:180120400-180126800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:180121200-180122800	Enhancers	Primary B cells from peripheral blood	blood
31	chr2:180121200-180124400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:180121400-180123200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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