Variant report

Variant	rs72806562
Chromosome Location	chr2:47214477-47214478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47213870..47217482-chr2:47217996..47221953,5	MCF-7	breast:
2	chr2:47214296..47216240-chr2:47260136..47264108,3	MCF-7	breast:
3	chr2:47212569..47215623-chr2:47548901..47551029,3	K562	blood:
4	chr2:47213873..47215501-chr2:47549847..47551396,20	K562	blood:
5	chr2:47214073..47216296-chr2:47255513..47257887,2	MCF-7	breast:
6	chr2:47206562..47208636-chr2:47212925..47215220,2	K562	blood:
7	chr2:47213500..47216240-chr2:47548901..47552350,5	K562	blood:
8	chr2:47141714..47144704-chr2:47213169..47216343,3	MCF-7	breast:
9	chr2:47166662..47168239-chr2:47214409..47216366,2	MCF-7	breast:
10	chr2:47211199..47217347-chr2:47399008..47404700,12	K562	blood:
11	chr2:47214279..47216434-chr2:47222625..47224948,2	MCF-7	breast:
12	chr2:47213903..47214786-chr2:47396818..47397476,2	MCF-7	breast:
13	chr2:47146090..47146882-chr2:47213985..47214715,2	MCF-7	breast:
14	chr2:47213608..47215277-chr2:47549985..47550910,10	MCF-7	breast:
15	chr2:47205847..47208964-chr2:47212925..47215633,5	K562	blood:
16	chr2:47214133..47214774-chr2:47499196..47500160,4	K562	blood:
17	chr2:47214252..47214763-chr2:47524847..47525691,2	K562	blood:
18	chr2:47141281..47143622-chr2:47212443..47214863,2	MCF-7	breast:
19	chr2:47213985..47214817-chr2:47255980..47256485,2	MCF-7	breast:
20	chr2:47209205..47217024-chr2:47399516..47404811,13	MCF-7	breast:
21	chr2:47214206..47214770-chr20:53290236..53290902,2	MCF-7	breast:
22	chr2:47212859..47216615-chr2:47301507..47304672,4	MCF-7	breast:
23	chr2:47213696..47215367-chr2:47239730..47241544,2	MCF-7	breast:
24	chr2:47213933..47214713-chr2:47539627..47540579,3	MCF-7	breast:
25	chr2:47213989..47214766-chr2:47546474..47547462,2	MCF-7	breast:
26	chr2:47164097..47165002-chr2:47213891..47214776,2	MCF-7	breast:
27	chr2:47187898..47188405-chr2:47213880..47214767,2	K562	blood:
28	chr2:47212899..47215171-chr2:47549795..47551134,10	MCF-7	breast:
29	chr2:47211854..47216258-chr2:47229137..47232912,5	K562	blood:
30	chr2:47212912..47216047-chr2:47549012..47553411,7	MCF-7	breast:
31	chr2:47210303..47217706-chr2:47402135..47406405,13	MCF-7	breast:
32	chr2:47214273..47214840-chr2:47276289..47276999,3	K562	blood:
33	chr2:47213957..47214845-chr2:47348299..47348953,3	MCF-7	breast:
34	chr2:47214229..47214810-chr2:47548565..47549556,2	MCF-7	breast:
35	chr2:47212292..47217234-chr2:47401238..47405508,6	K562	blood:
36	chr2:47212036..47214586-chr2:47495464..47497856,2	MCF-7	breast:
37	chr2:47213916..47214788-chr2:47499094..47500691,5	MCF-7	breast:
38	chr2:47213839..47216114-chr2:47390613..47392812,2	K562	blood:
39	chr2:47213914..47214545-chr2:47245154..47245890,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000068724	Chromatin interaction
ENSG00000143933	Chromatin interaction
ENSG00000180398	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13399571	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036022	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036033	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17480869	1.00[ASN][1000 genomes]
rs17480988	1.00[ASN][1000 genomes]
rs17481037	1.00[ASN][1000 genomes]
rs17481209	1.00[ASN][1000 genomes]
rs17540157	1.00[ASN][1000 genomes]
rs17540219	1.00[ASN][1000 genomes]
rs17540462	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3814035	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55641002	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55805005	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55824224	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56186415	0.87[ASN][1000 genomes]
rs58637066	1.00[ASN][1000 genomes]
rs58674434	1.00[ASN][1000 genomes]
rs59785154	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60732316	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6726941	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6727430	1.00[ASN][1000 genomes]
rs6727529	1.00[ASN][1000 genomes]
rs6751599	1.00[ASN][1000 genomes]
rs6751621	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6754795	1.00[ASN][1000 genomes]
rs6755001	1.00[ASN][1000 genomes]
rs72806525	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72806536	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72806537	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72806538	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72806541	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72806558	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72806571	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7564728	1.00[ASN][1000 genomes]
rs7576915	1.00[ASN][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	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv457352	chr2:47004788-47325973	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv581749	chr2:47004788-47325973	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS 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	37 gene(s)	inside rSNPs	diseases
4	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
5	nsv524970	chr2:47162739-47302095	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1000377	chr2:47189386-47344029	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv581750	chr2:47207665-47229953	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv525197	chr2:47210747-47297973	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47169800-47214600	Weak transcription	Fetal Kidney	kidney
2	chr2:47196600-47227800	Strong transcription	Dnd41	blood
3	chr2:47200800-47216400	Genic enhancers	Fetal Thymus	thymus
4	chr2:47202000-47214800	Genic enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:47208000-47217400	Enhancers	Stomach Mucosa	stomach
6	chr2:47208200-47214600	Weak transcription	Fetal Brain Female	brain
7	chr2:47208400-47214800	Enhancers	HUVEC	blood vessel
8	chr2:47208600-47216000	Enhancers	Brain Substantia Nigra	brain
9	chr2:47208600-47219200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr2:47209400-47217200	Genic enhancers	NHLF	lung
11	chr2:47209600-47214600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr2:47209600-47215200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:47209600-47217400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:47209600-47218200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr2:47209800-47214800	Enhancers	Primary hematopoietic stem cells	blood
16	chr2:47210000-47215200	Enhancers	Brain Anterior Caudate	brain
17	chr2:47210200-47214600	Genic enhancers	Primary T cells fromperipheralblood	blood
18	chr2:47210200-47214600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr2:47210200-47215200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr2:47210200-47215800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr2:47210400-47214800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:47210600-47215600	Weak transcription	Psoas Muscle	Psoas
23	chr2:47210600-47215600	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr2:47210600-47216600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr2:47210800-47215800	Enhancers	Spleen	Spleen
26	chr2:47211000-47214600	Genic enhancers	Thymus	Thymus
27	chr2:47211000-47214800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:47211000-47215800	Enhancers	Brain Hippocampus Middle	brain
29	chr2:47211400-47214800	Genic enhancers	Osteobl	bone
30	chr2:47211400-47215600	Enhancers	Esophagus	oesophagus
31	chr2:47211400-47217600	Enhancers	Right Atrium	heart
32	chr2:47211600-47214600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr2:47211600-47214800	Enhancers	HMEC	breast
34	chr2:47211800-47214600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr2:47211800-47214600	Enhancers	Lung	lung
36	chr2:47211800-47215600	Enhancers	Colonic Mucosa	Colon
37	chr2:47211800-47215800	Enhancers	HSMMtube	muscle
38	chr2:47211800-47218000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:47211800-47218000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:47212000-47214800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:47212000-47215000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:47212000-47217200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:47212000-47217200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr2:47212000-47217600	Enhancers	Rectal Smooth Muscle	rectum
45	chr2:47212200-47214800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr2:47212200-47218200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:47212400-47214600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr2:47212400-47214800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:47212400-47215600	Enhancers	NHDF-Ad	bronchial
50	chr2:47212400-47217000	Enhancers	Fetal Heart	heart

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