Variant report

Variant	rs7537853
Chromosome Location	chr1:76547305-76547306
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	chr1:76538798..76540470-chr1:76545089..76547752,3	K562	blood:
2	chr1:76540930..76543846-chr1:76546687..76549468,2	K562	blood:

Variant related genes	Relation type
ENSG00000184005	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10493581	0.86[ASN][1000 genomes]
rs1144344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1146661	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1146662	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12401785	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17098034	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28675110	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	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv870968	chr1:76490234-76552475	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv871862	chr1:76525783-76598209	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76541200-76551200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:76541600-76548000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:76541600-76550000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:76541800-76547400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:76542000-76547400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:76542200-76553200	Weak transcription	Fetal Intestine Large	intestine
7	chr1:76542400-76550000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr1:76542800-76572000	Weak transcription	Primary B cells from cord blood	blood
9	chr1:76545200-76548600	Enhancers	Brain Hippocampus Middle	brain
10	chr1:76545200-76548800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:76545400-76551400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr1:76545600-76548000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:76545600-76548000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr1:76545600-76548600	Enhancers	Brain Substantia Nigra	brain
15	chr1:76545600-76549000	Weak transcription	Lung	lung
16	chr1:76545600-76552200	Weak transcription	Fetal Intestine Small	intestine
17	chr1:76545600-76558200	Weak transcription	Left Ventricle	heart
18	chr1:76545800-76547400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:76545800-76548000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr1:76545800-76550600	Enhancers	Fetal Lung	lung
21	chr1:76546000-76548000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:76546200-76547600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr1:76546200-76547800	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:76546200-76550600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:76546400-76547400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:76546400-76547600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr1:76546400-76547600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:76546400-76548800	Enhancers	Brain Cingulate Gyrus	brain
29	chr1:76546400-76549000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr1:76546600-76547400	Enhancers	Fetal Kidney	kidney
31	chr1:76546600-76547600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:76546600-76548400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:76546600-76549200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:76546800-76547800	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:76546800-76548000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:76546800-76548800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:76547000-76547400	Weak transcription	Brain Anterior Caudate	brain
38	chr1:76547000-76547400	Weak transcription	Fetal Stomach	stomach
39	chr1:76547000-76549000	Weak transcription	Fetal Muscle Leg	muscle
40	chr1:76547200-76547600	Enhancers	Brain Angular Gyrus	brain
41	chr1:76547200-76548000	Enhancers	Fetal Brain Female	brain

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