Variant report

Variant	rs62577670
Chromosome Location	chr9:115644784-115644785
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr9:115644663-115644859	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr9:115644699-115644847	SK-N-SH_RA	brain:	n/a	n/a
3	CTCF	chr9:115644700-115644850	HEK293	kidney:	n/a	n/a
4	CTCF	chr9:115644700-115644850	HBMEC	blood vessel:	n/a	n/a
5	CTCF	chr9:115644737-115644831	MCF-7	breast:	n/a	n/a
6	CTCF	chr9:115644640-115644790	BE2_C	brain:	n/a	n/a
7	RAD21	chr9:115644727-115644883	GM12878	blood:	n/a	n/a
8	CTCF	chr9:115644700-115644850	SAEC	small airway:	n/a	n/a
9	CTCF	chr9:115644680-115644830	GM12874	blood:	n/a	n/a
10	CTCF	chr9:115644740-115644890	GM12869	blood:	n/a	n/a
11	CTCF	chr9:115644723-115644875	MCF-7	breast:	n/a	n/a
12	CTCF	chr9:115644700-115644850	GM12865	blood:	n/a	n/a
13	CTCF	chr9:115644680-115644830	NHEK	skin:	n/a	n/a
14	CTCF	chr9:115644700-115644850	GM12871	blood:	n/a	n/a
15	CTCF	chr9:115644680-115644830	WI-38	lung:	n/a	n/a
16	CTCF	chr9:115644672-115644883	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr9:115644700-115644850	HepG2	liver:	n/a	n/a
18	CTCF	chr9:115644700-115644850	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr9:115644660-115644810	GM12867	blood:	n/a	n/a
20	CTCF	chr9:115644682-115644910	K562	blood:	n/a	n/a
21	CTCF	chr9:115644700-115644850	GM12868	blood:	n/a	n/a
22	CTCF	chr9:115644700-115644850	GM12873	blood:	n/a	n/a
23	CTCF	chr9:115644700-115644850	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr9:115644740-115644890	RPTEC	kidney:	n/a	n/a
25	CTCF	chr9:115644720-115644870	SAEC	small airway:	n/a	n/a
26	CTCF	chr9:115644740-115644890	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr9:115644764-115644817	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:115644740-115644890	GM12867	blood:	n/a	n/a
29	CTCF	chr9:115644700-115644850	GM12864	blood:	n/a	n/a
30	CTCF	chr9:115644740-115644890	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr9:115644720-115644870	GM12874	blood:	n/a	n/a
32	CTCF	chr9:115644720-115644870	GM12872	blood:	n/a	n/a
33	CTCF	chr9:115644680-115644830	HCT-116	colon:	n/a	n/a
34	CTCF	chr9:115644720-115644870	HMF	breast:	n/a	n/a
35	CTCF	chr9:115644680-115644830	HMEC	breast:	n/a	n/a
36	CTCF	chr9:115644680-115644830	BJ	skin:	n/a	n/a
37	CTCF	chr9:115644700-115644850	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr9:115644700-115644850	NHEK	skin:	n/a	n/a
39	CTCF	chr9:115644720-115644870	HCT-116	colon:	n/a	n/a
40	CTCF	chr9:115644703-115644888	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:115644755-115644865	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr9:115644740-115644890	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr9:115644760-115644910	GM12864	blood:	n/a	n/a
44	CTCF	chr9:115644660-115644810	GM06990	blood:	n/a	n/a
45	CTCF	chr9:115644700-115644850	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr9:115644612-115644945	HepG2	liver:	n/a	n/a
47	CTCF	chr9:115644640-115644790	K562	blood:	n/a	n/a
48	CTCF	chr9:115644760-115644910	RPTEC	kidney:	n/a	n/a
49	CTCF	chr9:115644720-115644870	GM12865	blood:	n/a	n/a
50	RAD21	chr9:115644581-115644983	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:115606728..115607289-chr9:115644336..115645178,2	MCF-7	breast:
2	chr9:115607030..115607606-chr9:115644620..115645220,2	MCF-7	breast:
3	chr9:115634993..115639011-chr9:115640065..115646725,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000271631	TF binding region

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10981530	0.80[EUR][1000 genomes]
rs10981531	0.80[EUR][1000 genomes]
rs10981533	0.85[EUR][1000 genomes]
rs16917440	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925078	1.00[AFR][1000 genomes]
rs41280193	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41280195	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60824158	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62576438	0.80[EUR][1000 genomes]
rs62576455	0.92[EUR][1000 genomes]
rs62576456	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62577669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62577673	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73536648	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription 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	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv893733	chr9:115397206-115712068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	esv2422302	chr9:115550339-115656433	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv1047000	chr9:115610445-115884038	ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115615600-115646400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:115624200-115652600	Weak transcription	Fetal Heart	heart
3	chr9:115625800-115645200	Weak transcription	Thymus	Thymus
4	chr9:115626400-115650800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr9:115627000-115647000	Weak transcription	Colonic Mucosa	Colon
6	chr9:115627600-115646800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:115630600-115646400	Weak transcription	Fetal Lung	lung
8	chr9:115630600-115647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:115630800-115646400	Weak transcription	Placenta	Placenta
10	chr9:115631200-115646400	Weak transcription	Fetal Kidney	kidney
11	chr9:115631800-115646400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:115631800-115652200	Weak transcription	Gastric	stomach
13	chr9:115632200-115644800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr9:115633000-115645800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr9:115633000-115646400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr9:115633000-115652600	Weak transcription	Left Ventricle	heart
17	chr9:115633200-115646400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:115633200-115652400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr9:115633200-115652400	Weak transcription	Right Ventricle	heart
20	chr9:115633400-115646800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr9:115633400-115648200	Weak transcription	Esophagus	oesophagus
22	chr9:115633400-115649200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr9:115633800-115652600	Weak transcription	Liver	Liver
24	chr9:115634600-115646400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr9:115634800-115646400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr9:115634800-115651800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr9:115635000-115650800	Weak transcription	Fetal Thymus	thymus
28	chr9:115635600-115649000	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr9:115636000-115648600	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr9:115636600-115646400	Weak transcription	NHDF-Ad	bronchial
31	chr9:115638200-115647000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr9:115638600-115650000	Weak transcription	Fetal Brain Female	brain
33	chr9:115640400-115644800	Weak transcription	Psoas Muscle	Psoas
34	chr9:115640800-115647000	Weak transcription	Primary T cells from cord blood	blood
35	chr9:115641000-115646400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr9:115642200-115644800	Strong transcription	Fetal Stomach	stomach
37	chr9:115643000-115645600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr9:115643200-115652600	Weak transcription	Brain Anterior Caudate	brain
39	chr9:115643200-115652800	Weak transcription	Ovary	ovary
40	chr9:115643400-115645400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr9:115643400-115646400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:115643400-115651600	Weak transcription	Primary B cells from cord blood	blood
43	chr9:115643400-115652400	Weak transcription	Brain Substantia Nigra	brain
44	chr9:115643600-115646400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr9:115643600-115650000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr9:115643600-115650400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr9:115643600-115652200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:115643600-115652600	Weak transcription	Brain Angular Gyrus	brain
49	chr9:115643800-115646000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:115643800-115650000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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