Variant report

Variant	rs73892528
Chromosome Location	chr21:17141092-17141093
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:17100962..17103706-chr21:17140698..17142890,2	MCF-7	breast:
2	chr21:17101984..17103858-chr21:17138166..17141099,3	K562	blood:
3	chr21:17104587..17106311-chr21:17139989..17141909,2	K562	blood:
4	chr21:17135749..17138458-chr21:17138787..17142045,4	K562	blood:

Variant related genes	Relation type
ENSG00000155313	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs56292282	0.90[AFR][1000 genomes]
rs57732471	0.90[AFR][1000 genomes]
rs59764941	0.81[AFR][1000 genomes]
rs73892511	1.00[AFR][1000 genomes]
rs73892531	1.00[AFR][1000 genomes]
rs73892551	0.90[AFR][1000 genomes]
rs73892557	0.81[AFR][1000 genomes]
rs73892558	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762093	chr21:16948663-17145770	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1064683	chr21:16954570-17145758	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv459099	chr21:16956866-17145011	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv587076	chr21:16956866-17145011	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1062105	chr21:16956885-17141961	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv544380	chr21:16956885-17141961	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1059500	chr21:16957752-17145758	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	esv1815433	chr21:17106192-17167353	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17115400-17145400	Weak transcription	Fetal Thymus	thymus
2	chr21:17116600-17145400	Weak transcription	Esophagus	oesophagus
3	chr21:17122600-17142800	Weak transcription	Hela-S3	cervix
4	chr21:17125800-17153400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr21:17126800-17147600	Weak transcription	Placenta	Placenta
6	chr21:17127000-17147400	Weak transcription	HSMMtube	muscle
7	chr21:17127000-17152800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr21:17127200-17153400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr21:17127400-17146200	Weak transcription	NHDF-Ad	bronchial
10	chr21:17127400-17147800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr21:17127400-17153400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr21:17127600-17145200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr21:17127800-17141600	Weak transcription	HMEC	breast
14	chr21:17127800-17152800	Weak transcription	Fetal Intestine Large	intestine
15	chr21:17130800-17156800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr21:17132800-17153400	Weak transcription	Spleen	Spleen
17	chr21:17133800-17145800	Weak transcription	Colon Smooth Muscle	Colon
18	chr21:17133800-17149400	Weak transcription	Small Intestine	intestine
19	chr21:17134000-17143600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr21:17134000-17143600	Weak transcription	Gastric	stomach
21	chr21:17134000-17147600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr21:17134000-17152400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr21:17134000-17153400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr21:17134200-17142200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr21:17134200-17143400	Weak transcription	Right Atrium	heart
26	chr21:17134200-17143600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr21:17134200-17153000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr21:17134200-17153400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr21:17134200-17154000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr21:17134400-17143600	Weak transcription	Lung	lung
31	chr21:17134400-17153200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr21:17134600-17143800	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr21:17135000-17145000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr21:17135000-17152600	Weak transcription	Primary T cells from cord blood	blood
35	chr21:17135000-17153000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr21:17135000-17153400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr21:17135000-17153600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr21:17135200-17142400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr21:17135200-17153000	Weak transcription	Fetal Muscle Leg	muscle
40	chr21:17135400-17153200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr21:17135600-17153200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr21:17135800-17147200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr21:17136000-17145400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr21:17136600-17141800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr21:17136600-17148400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr21:17136600-17153200	Weak transcription	Thymus	Thymus
47	chr21:17137000-17141400	Strong transcription	Primary hematopoietic stem cells	blood
48	chr21:17137200-17142800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr21:17137600-17144200	Strong transcription	GM12878-XiMat	blood
50	chr21:17137600-17145400	Weak transcription	Fetal Stomach	stomach

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