Variant report

Variant	rs28622038
Chromosome Location	chr19:44004514-44004515
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:43977180..43982299-chr19:44003653..44008245,6	K562	blood:
2	chr19:43967644..43971432-chr19:44003665..44007669,4	K562	blood:

Variant related genes	Relation type
ENSG00000124466	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10408863	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10413072	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420249	0.82[EUR][1000 genomes]
rs11083711	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4803634	0.81[EUR][1000 genomes]
rs57686229	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs66849333	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055872	chr19:43173614-44075193	Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv544009	chr19:43173614-44075193	Enhancers ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1067126	chr19:43260649-44075194	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv544015	chr19:43260649-44075194	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv1057657	chr19:43302497-44076564	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv1059631	chr19:43316978-44075054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv544030	chr19:43316978-44075054	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	40 gene(s)	inside rSNPs	diseases
8	nsv532820	chr19:43807486-44080610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv1056721	chr19:43808474-44095077	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
11	nsv1058162	chr19:43846238-44055058	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	esv2762041	chr19:43986023-44014457	Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43979600-44005800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:43980000-44005600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr19:43980000-44005600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr19:43980000-44006200	Weak transcription	HMEC	breast
5	chr19:43980800-44007400	Weak transcription	HSMM	muscle
6	chr19:43981200-44007200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr19:43981400-44007200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr19:43982800-44006800	Weak transcription	K562	blood
9	chr19:43983600-44005800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr19:43993000-44005600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr19:43993000-44007200	Weak transcription	A549	lung
12	chr19:43993600-44005800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr19:43993600-44006200	Weak transcription	GM12878-XiMat	blood
14	chr19:43993600-44007400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr19:43994200-44007200	Weak transcription	Primary B cells from cord blood	blood
16	chr19:43996000-44006400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:43997400-44007000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:43997600-44004800	Strong transcription	Primary T cells from cord blood	blood
19	chr19:43997600-44006200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:43998000-44007200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr19:43998200-44006200	Weak transcription	Dnd41	blood
22	chr19:43998400-44006000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:43998400-44006800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr19:43998600-44005800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:43999600-44005600	Weak transcription	Fetal Brain Female	brain
26	chr19:43999600-44005800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr19:43999600-44006200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:43999600-44007600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr19:43999800-44007600	Weak transcription	HSMMtube	muscle
30	chr19:44000000-44005600	Weak transcription	NHLF	lung
31	chr19:44000000-44007000	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr19:44000000-44007000	Weak transcription	NHDF-Ad	bronchial
33	chr19:44000000-44007200	Weak transcription	Adipose Nuclei	Adipose
34	chr19:44000000-44007400	Weak transcription	Brain Angular Gyrus	brain
35	chr19:44000000-44008000	Weak transcription	Small Intestine	intestine
36	chr19:44001400-44005600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr19:44001400-44006800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr19:44001400-44007000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr19:44001400-44007000	Weak transcription	Colon Smooth Muscle	Colon
40	chr19:44001400-44007200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr19:44001400-44007600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr19:44001600-44005800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr19:44001600-44006000	Weak transcription	Osteobl	bone
44	chr19:44001600-44006800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr19:44001600-44006800	Weak transcription	Brain Hippocampus Middle	brain
46	chr19:44001600-44007400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr19:44001800-44005400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr19:44001800-44006000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr19:44001800-44007000	Weak transcription	Brain Substantia Nigra	brain
50	chr19:44001800-44007400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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