Variant report

Variant	rs36064568
Chromosome Location	chr16:30646970-30646971
allele	A/G
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:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr16:30638067..30640591-chr16:30646061..30647718,3	K562	blood:
2	chr16:30446409..30448380-chr16:30645519..30647162,2	MCF-7	breast:
3	chr16:30637395..30641819-chr16:30644073..30647444,4	MCF-7	breast:
4	chr16:30425764..30431777-chr16:30643606..30648792,10	MCF-7	breast:
5	chr16:30405528..30407554-chr16:30645343..30647105,2	MCF-7	breast:
6	chr16:30536523..30540644-chr16:30645221..30648194,5	MCF-7	breast:
7	chr16:30455807..30458356-chr16:30645639..30647441,2	K562	blood:
8	chr16:30437361..30442565-chr16:30644593..30648400,5	MCF-7	breast:
9	chr16:30645938..30648105-chr16:30662242..30664418,2	K562	blood:
10	chr16:30440125..30441909-chr16:30644218..30647208,2	K562	blood:
11	chr16:30611646..30614130-chr16:30645104..30647330,2	K562	blood:
12	chr16:30456814..30458698-chr16:30645372..30647261,2	MCF-7	breast:
13	chr16:30619502..30621875-chr16:30644431..30647056,2	K562	blood:
14	chr16:30388120..30390013-chr16:30644572..30647101,3	K562	blood:
15	chr16:30646175..30649628-chr16:30709431..30711629,3	K562	blood:
16	chr16:30417175..30420189-chr16:30644712..30648071,3	MCF-7	breast:
17	chr16:30627523..30629109-chr16:30644539..30647168,2	MCF-7	breast:
18	chr16:30439875..30443880-chr16:30644269..30648773,5	MCF-7	breast:
19	chr16:30644455..30647507-chr16:30709405..30711853,4	MCF-7	breast:
20	chr16:30645018..30647863-chr17:56736329..56737954,2	MCF-7	breast:
21	chr16:30643767..30647614-chr16:30667017..30672688,11	MCF-7	breast:
22	chr16:30644081..30647716-chr16:30660195..30665578,9	MCF-7	breast:
23	chr16:30580526..30584022-chr16:30644027..30647188,4	MCF-7	breast:
24	chr16:30567925..30573022-chr16:30645244..30647249,4	MCF-7	breast:
25	chr16:30594953..30598897-chr16:30644540..30647635,4	MCF-7	breast:
26	chr16:30645016..30649381-chr16:30667944..30672183,8	MCF-7	breast:
27	chr16:30594602..30599221-chr16:30645132..30650024,7	K562	blood:
28	chr16:30429524..30432595-chr16:30644365..30647909,3	MCF-7	breast:
29	chr16:30448830..30450569-chr16:30645154..30647301,2	MCF-7	breast:
30	chr16:30625207..30628170-chr16:30644709..30647482,2	MCF-7	breast:
31	chr16:30535592..30540399-chr16:30644319..30649503,5	K562	blood:
32	chr16:30620535..30622152-chr16:30645217..30647880,3	MCF-7	breast:
33	chr16:30644135..30648252-chr16:30660557..30664970,6	K562	blood:
34	chr16:30459949..30461970-chr16:30646123..30648226,2	K562	blood:
35	chr16:30644633..30647330-chr16:30647891..30651993,5	MCF-7	breast:
36	chr16:30595417..30597147-chr16:30644762..30647524,2	MCF-7	breast:
37	chr16:30645887..30647845-chr16:30759708..30761310,2	MCF-7	breast:
38	chr16:30614887..30616635-chr16:30644253..30647134,2	MCF-7	breast:
39	chr16:30597245..30598925-chr16:30644612..30647515,2	MCF-7	breast:
40	chr16:30644157..30647888-chr16:30708038..30710957,4	MCF-7	breast:
41	chr16:30620386..30623143-chr16:30645358..30647531,3	MCF-7	breast:
42	chr16:30437251..30438885-chr16:30644712..30647395,2	MCF-7	breast:
43	chr16:30386731..30390013-chr16:30644584..30647173,3	K562	blood:
44	chr16:30454647..30458430-chr16:30643646..30647468,4	MCF-7	breast:
45	chr16:30453201..30454916-chr16:30646669..30649201,2	K562	blood:
46	chr16:30645346..30647310-chr3:64328079..64330992,2	MCF-7	breast:
47	chr16:30645725..30647722-chr16:30647789..30649558,2	MCF-7	breast:
48	chr16:30484187..30486380-chr16:30645587..30647332,2	MCF-7	breast:
49	chr16:30644676..30647831-chr16:30651672..30654361,3	K562	blood:
50	chr16:30641739..30648234-chr16:30659002..30664628,9	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000180096	Chromatin interaction
ENSG00000260167	Chromatin interaction
ENSG00000005844	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000239791	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000199787	Chromatin interaction
ENSG00000260678	Chromatin interaction
ENSG00000179965	Chromatin interaction
ENSG00000180209	Chromatin interaction
ENSG00000180035	Chromatin interaction
ENSG00000156873	Chromatin interaction
ENSG00000197162	Chromatin interaction
ENSG00000169951	Chromatin interaction
ENSG00000156853	Chromatin interaction
ENSG00000260869	Chromatin interaction
ENSG00000169957	Chromatin interaction
ENSG00000179918	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000260113	Chromatin interaction
ENSG00000229809	Chromatin interaction
ENSG00000179958	Chromatin interaction
ENSG00000156860	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12918327	0.92[ASN][1000 genomes]
rs28728333	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28841118	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34699226	0.86[ASN][1000 genomes]
rs35661204	0.80[ASN][1000 genomes]
rs4485386	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55875685	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6565195	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6565196	0.81[EUR][1000 genomes]
rs67693285	0.94[ASN][1000 genomes]
rs7184055	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7185620	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7186852	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7187071	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7187802	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7188789	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7191389	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7191761	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7194347	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7197475	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7204632	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7499339	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9925025	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9927137	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905727	chr16:30564526-30689696	Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
7	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
8	nsv905728	chr16:30642867-30928970	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	171 gene(s)	inside rSNPs	diseases
9	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30644800-30647000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr16:30644800-30647000	Active TSS	Fetal Brain Female	brain
3	chr16:30645000-30647000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr16:30645000-30647000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:30645000-30647000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr16:30645000-30647000	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr16:30645000-30647000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr16:30645000-30647000	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr16:30645000-30647000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr16:30645000-30647000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr16:30645200-30647000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr16:30645200-30647000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr16:30645200-30647000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:30645200-30647000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr16:30645200-30647000	Active TSS	GM12878-XiMat	blood
16	chr16:30645200-30647000	Active TSS	HSMMtube	muscle
17	chr16:30645200-30647000	Active TSS	NH-A	brain
18	chr16:30645200-30647200	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr16:30645800-30647000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr16:30646000-30647000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr16:30646000-30647000	Flanking Active TSS	HUVEC	blood vessel
22	chr16:30646200-30647000	Flanking Active TSS	Stomach Smooth Muscle	stomach
23	chr16:30646400-30647000	Enhancers	Primary B cells from peripheral blood	blood
24	chr16:30646400-30647000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr16:30646400-30647000	Enhancers	Liver	Liver
26	chr16:30646400-30647000	Flanking Active TSS	Fetal Heart	heart
27	chr16:30646400-30647000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr16:30646400-30647000	Flanking Active TSS	Dnd41	blood
29	chr16:30646400-30651000	Weak transcription	Stomach Mucosa	stomach
30	chr16:30646600-30647000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr16:30646600-30647000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr16:30646600-30647000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr16:30646600-30647000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr16:30646600-30647000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr16:30646600-30647000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr16:30646600-30647000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr16:30646600-30647000	Enhancers	Rectal Smooth Muscle	rectum
38	chr16:30646600-30647000	Flanking Active TSS	A549	lung
39	chr16:30646600-30647000	Flanking Active TSS	HMEC	breast
40	chr16:30646600-30647000	Flanking Active TSS	K562	blood
41	chr16:30646600-30647000	Flanking Active TSS	NHEK	skin
42	chr16:30646600-30647000	Flanking Active TSS	Osteobl	bone
43	chr16:30646600-30647200	Enhancers	Fetal Muscle Trunk	muscle
44	chr16:30646600-30647200	Flanking Active TSS	Hela-S3	cervix
45	chr16:30646600-30647400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr16:30646800-30647000	Enhancers	Primary B cells from cord blood	blood
47	chr16:30646800-30647000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr16:30646800-30647000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr16:30646800-30647000	Active TSS	Brain Hippocampus Middle	brain
50	chr16:30646800-30647000	Enhancers	Colon Smooth Muscle	Colon

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