Variant report

Variant	rs73404246
Chromosome Location	chr11:5731516-5731517
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	11:5033143-5038367..11:5721056-5732713	GM12878	blood:
2	11:4957178-4961904..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
3	11:4988858-5002113..11:5721056-5732713	Hela-S3	cervix:
4	11:5087036-5092291..11:5721056-5732713	K562	blood:
5	11:5488942-5494633..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
6	11:5586716-5591774..11:5721056-5732713	GM12878	blood:

Variant related genes	Relation type
ENSG00000273085	Chromatin interaction
ENSG00000230484	Chromatin interaction
ENSG00000225003	Chromatin interaction
ENSG00000227023	Chromatin interaction
ENSG00000233646	Chromatin interaction
ENSG00000224300	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16932813	1.00[AMR][1000 genomes]
rs16936199	1.00[AMR][1000 genomes]
rs73404237	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404276	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv896939	chr11:5497799-5809548	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv553241	chr11:5506034-6203685	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
4	nsv1041568	chr11:5585716-5765688	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv1053414	chr11:5612989-6030212	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv530216	chr11:5614439-6468232	Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv553273	chr11:5639873-5871831	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv1036389	chr11:5695451-6177680	Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
9	nsv540943	chr11:5695451-6177680	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
10	nsv553277	chr11:5722948-6010075	Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
11	esv1843296	chr11:5730377-5970717	Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	esv2758255	chr11:5730377-5970717	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
13	esv2759801	chr11:5730377-6007613	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5712400-5731800	Weak transcription	NH-A	brain
2	chr11:5712400-5732400	Weak transcription	Pancreas	Pancrea
3	chr11:5712400-5732400	Weak transcription	Stomach Mucosa	stomach
4	chr11:5712600-5732000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:5712600-5732600	Weak transcription	Colonic Mucosa	Colon
6	chr11:5713000-5734600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr11:5713600-5734800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr11:5713600-5745800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:5714000-5732600	Weak transcription	Brain Substantia Nigra	brain
10	chr11:5715200-5733000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:5717400-5732400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr11:5717400-5734400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:5717600-5732600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:5718000-5734600	Weak transcription	HUVEC	blood vessel
15	chr11:5720000-5732600	Weak transcription	Brain Hippocampus Middle	brain
16	chr11:5720200-5731800	Weak transcription	Small Intestine	intestine
17	chr11:5720200-5731800	Weak transcription	NHLF	lung
18	chr11:5720200-5732600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr11:5720400-5732800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr11:5722000-5732800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:5722600-5732600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr11:5722600-5733000	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr11:5723000-5731800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr11:5723000-5733000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:5723400-5731600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:5723400-5733800	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr11:5723800-5733000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:5724400-5732400	Strong transcription	Primary T cells from cord blood	blood
29	chr11:5725400-5732800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:5725400-5733600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:5726200-5732600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr11:5726600-5732400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr11:5726800-5731800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:5727000-5732400	Strong transcription	Ovary	ovary
35	chr11:5727200-5732800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:5727400-5732800	Strong transcription	HSMM	muscle
37	chr11:5727600-5731800	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr11:5727600-5732800	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr11:5728000-5732400	Weak transcription	HMEC	breast
40	chr11:5729200-5731600	Strong transcription	Primary hematopoietic stem cells	blood
41	chr11:5729600-5732200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr11:5729800-5732200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr11:5729800-5733000	Strong transcription	GM12878-XiMat	blood
44	chr11:5730400-5732200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr11:5730400-5732400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:5730400-5732400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr11:5730400-5732600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr11:5730400-5732600	Weak transcription	Gastric	stomach
49	chr11:5730400-5733600	Weak transcription	NHDF-Ad	bronchial
50	chr11:5730400-5736000	Weak transcription	Rectal Smooth Muscle	rectum

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