Variant report

Variant	rs11573596
Chromosome Location	chr1:45288956-45288957
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:45284835-45290143	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr1:45288728-45289158	HepG2	liver:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45246681..45259677-chr1:45281336..45290057,25	MCF-7	breast:
2	chr1:45186219..45188640-chr1:45288842..45291625,2	MCF-7	breast:
3	chr1:45282320..45290015-chr1:45470338..45482903,45	K562	blood:
4	chr1:45238319..45262026-chr1:45262351..45301953,358	K562	blood:
5	chr1:45193443..45200768-chr1:45280884..45289784,25	MCF-7	breast:
6	chr1:45172916..45175274-chr1:45288943..45290612,2	K562	blood:
7	chr1:45178001..45208867-chr1:45262751..45305400,520	K562	blood:
8	chr1:45281186..45291350-chr1:45463934..45483092,44	K562	blood:
9	chr1:45178748..45209946-chr1:45262890..45299284,515	K562	blood:

No data

Variant related genes	Relation type
RNU5E-6P	TF binding region
PTCH2	TF binding region
ENSG00000142937	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000142945	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000202031	Chromatin interaction
ENSG00000234093	Chromatin interaction
ENSG00000142959	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000207421	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11581172	1.00[YRI][hapmap]
rs174638	0.87[AFR][1000 genomes]
rs196764	0.87[AFR][1000 genomes]
rs263957	0.87[AFR][1000 genomes]
rs263963	0.87[AFR][1000 genomes]
rs263968	0.87[AFR][1000 genomes]
rs263972	0.87[AFR][1000 genomes]
rs263974	0.87[AFR][1000 genomes]
rs263976	0.87[AFR][1000 genomes]
rs263983	0.87[AFR][1000 genomes]
rs263984	0.87[AFR][1000 genomes]
rs35710243	0.87[AFR][1000 genomes]
rs418302	0.87[AFR][1000 genomes]
rs425780	0.87[AFR][1000 genomes]
rs430057	0.87[AFR][1000 genomes]
rs547476	0.87[AFR][1000 genomes]
rs662660	0.87[AFR][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	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
3	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
4	nsv1014894	chr1:45139123-45397943	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	414 gene(s)	inside rSNPs	diseases
5	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
6	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
7	nsv461406	chr1:45218542-45293518	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
8	nsv546145	chr1:45218542-45293518	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
9	nsv870815	chr1:45233638-45318752	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
10	nsv546146	chr1:45258141-45318752	Genic enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	109 gene(s)	inside rSNPs	diseases
11	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 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	chr1:45285600-45292400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:45286200-45301800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:45286400-45292000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr1:45286400-45308400	Weak transcription	Aorta	Aorta
5	chr1:45286600-45289000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:45286600-45289000	Strong transcription	Fetal Brain Female	brain
7	chr1:45286600-45291600	Weak transcription	Placenta	Placenta
8	chr1:45286600-45291800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:45286600-45291800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:45286600-45291800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:45286600-45292000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr1:45286600-45292000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:45286600-45292000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr1:45286600-45292000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:45286600-45292200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:45286600-45292200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:45286600-45299400	Weak transcription	Primary B cells from cord blood	blood
18	chr1:45286600-45301600	Weak transcription	Right Atrium	heart
19	chr1:45286600-45301800	Weak transcription	Brain Angular Gyrus	brain
20	chr1:45286800-45289600	Weak transcription	Fetal Heart	heart
21	chr1:45286800-45291200	Weak transcription	Fetal Intestine Large	intestine
22	chr1:45286800-45291800	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr1:45286800-45291800	Weak transcription	Liver	Liver
24	chr1:45286800-45301600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr1:45287000-45289600	Strong transcription	Brain Germinal Matrix	brain
26	chr1:45287000-45291600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:45287000-45292000	Strong transcription	Fetal Stomach	stomach
28	chr1:45287000-45292000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr1:45287000-45292200	Weak transcription	Esophagus	oesophagus
30	chr1:45287000-45301800	Weak transcription	Thymus	Thymus
31	chr1:45287200-45291400	Weak transcription	HepG2	liver
32	chr1:45287200-45291600	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr1:45287200-45291600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr1:45287200-45291800	Weak transcription	Adipose Nuclei	Adipose
35	chr1:45287200-45291800	Weak transcription	Colonic Mucosa	Colon
36	chr1:45287200-45291800	Weak transcription	Fetal Muscle Leg	muscle
37	chr1:45287200-45291800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr1:45287200-45291800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr1:45287200-45291800	Weak transcription	Spleen	Spleen
40	chr1:45287200-45292000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:45287200-45292000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr1:45287200-45292200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:45287200-45292400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr1:45287200-45293800	Weak transcription	Fetal Lung	lung
45	chr1:45287200-45295000	Weak transcription	Brain Substantia Nigra	brain
46	chr1:45287200-45307400	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:45287400-45289200	Strong transcription	Fetal Intestine Small	intestine
48	chr1:45287400-45291600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:45287400-45291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:45287400-45291800	Weak transcription	Lung	lung

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