Variant report

Variant	rs804823
Chromosome Location	chr6:37587459-37587460
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:37568344..37572932-chr6:37584973..37589083,4	K562	blood:
2	chr6:37576514..37579539-chr6:37585884..37588412,3	K562	blood:
3	chr6:37587258..37590079-chr6:37590589..37593405,2	K562	blood:
4	chr6:37581243..37582863-chr6:37586444..37588975,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1342979	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs804842	1.00[AMR][1000 genomes]
rs9470658	1.00[AMR][1000 genomes]
rs9470659	1.00[AMR][1000 genomes]
rs9470664	1.00[AMR][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	esv2752124	chr6:37416219-37680622	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription 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 miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1024016	chr6:37567651-37981590	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv602955	chr6:37581200-37599962	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37584400-37590600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:37585800-37588000	Enhancers	Brain Germinal Matrix	brain
3	chr6:37586000-37587800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:37586000-37588800	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr6:37586000-37588800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr6:37586200-37587600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr6:37586200-37587800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:37586200-37589200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:37586200-37592400	Weak transcription	Right Atrium	heart
10	chr6:37586400-37587600	Enhancers	Fetal Brain Female	brain
11	chr6:37586400-37587800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:37586400-37588000	Enhancers	K562	blood
13	chr6:37586400-37588400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:37586400-37588400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr6:37586600-37587800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:37586600-37587800	Enhancers	NH-A	brain
17	chr6:37586600-37588200	Enhancers	Fetal Thymus	thymus
18	chr6:37586600-37592400	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:37586600-37593800	Enhancers	Primary B cells from cord blood	blood
20	chr6:37586800-37587600	Bivalent Enhancer	Fetal Stomach	stomach
21	chr6:37586800-37587600	Enhancers	GM12878-XiMat	blood
22	chr6:37586800-37587800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr6:37587000-37587600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr6:37587000-37587800	Enhancers	Primary T cells from cord blood	blood
25	chr6:37587000-37588000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:37587000-37588000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:37587000-37588000	Enhancers	Spleen	Spleen
28	chr6:37587000-37588200	Enhancers	Primary hematopoietic stem cells	blood
29	chr6:37587000-37592600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:37587200-37587600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:37587200-37588200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:37587200-37588200	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr6:37587200-37590600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:37587200-37592800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:37587400-37587800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr6:37587400-37588000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:37587400-37588400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:37587400-37589000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr6:37587400-37590400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:37587400-37590600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:37587400-37590600	Weak transcription	HMEC	breast
42	chr6:37587400-37592000	Weak transcription	Fetal Brain Male	brain

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