Variant report

Variant	rs58877025
Chromosome Location	chr6:26284445-26284446
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:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26283746..26285627-chr8:37553252..37556026,2	MCF-7	breast:
2	chr6:26283829..26285786-chr6:26519588..26522507,3	K562	blood:
3	chr6:26284169..26287182-chr6:27098843..27102282,9	MCF-7	breast:
4	chr6:26283512..26285254-chr6:26544162..26546329,2	K562	blood:
5	chr6:26283501..26285151-chr6:26542189..26543890,2	K562	blood:
6	chr6:26282374..26290542-chr6:27772727..27779446,9	MCF-7	breast:
7	chr20:52192767..52194510-chr6:26283656..26285528,2	MCF-7	breast:
8	chr6:26283553..26288411-chr6:27099109..27103890,9	K562	blood:
9	chr6:26282883..26285080-chr6:27774991..27777594,2	MCF-7	breast:
10	chr6:26283501..26289776-chr6:27108470..27116413,14	K562	blood:
11	chr6:26283488..26285487-chr6:27802901..27805712,2	MCF-7	breast:
12	chr6:26282779..26285012-chr6:26536372..26539326,2	K562	blood:
13	chr5:91194593..91196093-chr6:26282424..26284564,2	MCF-7	breast:
14	chr1:28973827..28976562-chr6:26282453..26285142,2	K562	blood:
15	chr6:26283014..26285478-chr6:27796832..27799433,3	K562	blood:
16	chr1:41949707..41951692-chr6:26284096..26286311,2	MCF-7	breast:
17	chr6:26284431..26286748-chr6:26538592..26541230,2	K562	blood:
18	chr6:26283774..26285764-chr6:27791060..27793861,2	MCF-7	breast:
19	chr6:26284256..26286912-chr6:27114805..27118000,3	K562	blood:
20	chr6:26283233..26285164-chr6:26541195..26542791,2	MCF-7	breast:
21	chr17:41380482..41382083-chr6:26284329..26287201,2	MCF-7	breast:
22	chr6:26283553..26287733-chr6:27097522..27103890,12	K562	blood:
23	chr6:26280754..26288136-chr6:27109918..27116629,16	MCF-7	breast:
24	chr17:13840444..13843165-chr6:26283532..26285209,2	MCF-7	breast:
25	chr6:26283604..26286375-chr6:27859105..27861545,3	K562	blood:
26	chr6:26284286..26286997-chr6:26519588..26522057,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000196331	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000236383	Chromatin interaction
ENSG00000127129	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000197914	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000183779	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000228223	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs60202454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6900192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6900610	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6901096	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6924986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73393494	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73395344	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73395352	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7746636	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7749338	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
6	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
7	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
8	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
9	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
10	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
11	nsv601173	chr6:26239404-26322524	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	184 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	chr6:26274400-26284600	Weak transcription	Ovary	ovary
2	chr6:26282800-26284600	Enhancers	Spleen	Spleen
3	chr6:26282800-26284800	Enhancers	Lung	lung
4	chr6:26282800-26287200	Active TSS	H1 Cell Line	embryonic stem cell
5	chr6:26283000-26286800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:26283400-26284600	Enhancers	Fetal Heart	heart
7	chr6:26283400-26284600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr6:26283400-26284800	Enhancers	Pancreas	Pancrea
9	chr6:26283400-26285200	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr6:26283400-26285600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr6:26283400-26285800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:26283400-26286800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:26283400-26286800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:26283400-26286800	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr6:26283400-26287200	Active TSS	H9 Cell Line	embryonic stem cell
16	chr6:26283400-26287200	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr6:26283400-26287200	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr6:26283600-26284600	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr6:26283600-26284800	Enhancers	Stomach Mucosa	stomach
20	chr6:26283600-26286800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:26283600-26287000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr6:26283600-26287000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:26283600-26287200	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr6:26283600-26287200	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr6:26283600-26287200	Active TSS	Thymus	Thymus
26	chr6:26283800-26284600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
27	chr6:26283800-26284600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr6:26283800-26284600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr6:26283800-26284800	Flanking Active TSS	Fetal Thymus	thymus
30	chr6:26283800-26285200	Active TSS	Osteobl	bone
31	chr6:26283800-26285400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:26283800-26286800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:26283800-26286800	Active TSS	Aorta	Aorta
34	chr6:26283800-26286800	Active TSS	NHLF	lung
35	chr6:26283800-26287000	Active TSS	Fetal Intestine Large	intestine
36	chr6:26283800-26287000	Active TSS	K562	blood
37	chr6:26283800-26287200	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr6:26283800-26287200	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr6:26284000-26284600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr6:26284000-26284600	Flanking Active TSS	Fetal Muscle Trunk	muscle
41	chr6:26284000-26284600	Flanking Active TSS	Fetal Muscle Leg	muscle
42	chr6:26284000-26284600	Flanking Active TSS	Placenta	Placenta
43	chr6:26284000-26284600	Flanking Active TSS	Psoas Muscle	Psoas
44	chr6:26284000-26284600	Flanking Active TSS	Right Ventricle	heart
45	chr6:26284000-26284600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr6:26284000-26285000	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr6:26284000-26285000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr6:26284000-26285000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
49	chr6:26284000-26285000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr6:26284000-26285200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

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