Variant report

Variant	rs73719739
Chromosome Location	chr6:5194232-5194233
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
2	chr6:5191188..5195166-chr6:5259406..5262990,4	K562	blood:

Variant related genes	Relation type
ENSG00000214113	Chromatin interaction
ENSG00000145982	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs17139744	1.00[AMR][1000 genomes]
rs17139831	1.00[AMR][1000 genomes]
rs55728654	1.00[AMR][1000 genomes]
rs55951971	1.00[AMR][1000 genomes]
rs56080716	1.00[AMR][1000 genomes]
rs56358324	1.00[AMR][1000 genomes]
rs56670098	1.00[AMR][1000 genomes]
rs57147800	1.00[AMR][1000 genomes]
rs59218577	1.00[AMR][1000 genomes]
rs59361101	1.00[AMR][1000 genomes]
rs59668620	1.00[AMR][1000 genomes]
rs61473991	1.00[AMR][1000 genomes]
rs73363037	1.00[AMR][1000 genomes]
rs73718025	1.00[AMR][1000 genomes]
rs73718034	1.00[AMR][1000 genomes]
rs73718037	1.00[AMR][1000 genomes]
rs73718042	1.00[AMR][1000 genomes]
rs73718073	1.00[AMR][1000 genomes]
rs73718079	1.00[AMR][1000 genomes]
rs73718080	1.00[AMR][1000 genomes]
rs73718081	1.00[AMR][1000 genomes]
rs73718082	1.00[AMR][1000 genomes]
rs73718083	1.00[AMR][1000 genomes]
rs73718084	1.00[AMR][1000 genomes]
rs73718085	1.00[AMR][1000 genomes]
rs73719720	1.00[AMR][1000 genomes]
rs73719730	1.00[AMR][1000 genomes]
rs73719732	1.00[AMR][1000 genomes]
rs73719735	1.00[AMR][1000 genomes]
rs73719736	1.00[AMR][1000 genomes]
rs73719737	1.00[AMR][1000 genomes]
rs73719753	1.00[AMR][1000 genomes]
rs73719755	1.00[AMR][1000 genomes]
rs73719757	1.00[AMR][1000 genomes]
rs73719758	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1034681	chr6:5070351-5387176	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv538113	chr6:5070351-5387176	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1018152	chr6:5077025-5387176	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv600873	chr6:5089278-5400658	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1017821	chr6:5114609-5213200	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv538114	chr6:5114609-5213200	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1030254	chr6:5132261-5431585	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
11	nsv1034463	chr6:5137959-5345678	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv1022336	chr6:5145194-5200687	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
13	nsv1018984	chr6:5145194-5200801	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1021646	chr6:5157795-5367254	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv538115	chr6:5157795-5367254	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv1029609	chr6:5187633-5397254	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5176200-5201200	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:5176200-5203600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:5176200-5239600	Weak transcription	Thymus	Thymus
4	chr6:5177800-5205200	Weak transcription	Aorta	Aorta
5	chr6:5179200-5207600	Weak transcription	Primary B cells from cord blood	blood
6	chr6:5180000-5201000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:5180200-5212200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr6:5180600-5195800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:5180600-5205000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:5180600-5205800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:5180600-5208200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:5181200-5204600	Weak transcription	Esophagus	oesophagus
13	chr6:5182000-5196200	Weak transcription	Pancreas	Pancrea
14	chr6:5182000-5213600	Weak transcription	Gastric	stomach
15	chr6:5182200-5200000	Weak transcription	Left Ventricle	heart
16	chr6:5186400-5195800	Weak transcription	K562	blood
17	chr6:5186400-5205000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:5186600-5196200	Weak transcription	Fetal Stomach	stomach
19	chr6:5186600-5200400	Weak transcription	Right Ventricle	heart
20	chr6:5186600-5202600	Weak transcription	Primary T cells from cord blood	blood
21	chr6:5189000-5213200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr6:5189400-5205400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:5191000-5202400	Weak transcription	Dnd41	blood
24	chr6:5191000-5206600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr6:5191200-5196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:5191200-5201400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:5191200-5202400	Weak transcription	HMEC	breast
28	chr6:5191600-5201400	Weak transcription	NHEK	skin
29	chr6:5191600-5202400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:5191600-5202800	Weak transcription	Hela-S3	cervix
31	chr6:5191600-5204600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:5191800-5200800	Weak transcription	HSMMtube	muscle
33	chr6:5191800-5201800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:5191800-5204800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:5191800-5204800	Weak transcription	HSMM	muscle
36	chr6:5191800-5206000	Weak transcription	NHLF	lung
37	chr6:5191800-5206400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr6:5192000-5203800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:5192000-5205800	Weak transcription	A549	lung
40	chr6:5192200-5201400	Weak transcription	Fetal Intestine Small	intestine
41	chr6:5192600-5194600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr6:5192800-5213000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:5193000-5196000	Weak transcription	HepG2	liver
44	chr6:5193000-5201600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr6:5193000-5202600	Weak transcription	Placenta	Placenta
46	chr6:5193000-5204200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr6:5193000-5205200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr6:5193200-5204600	Weak transcription	Lung	lung
49	chr6:5193200-5212400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:5193400-5196200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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