Variant report

Variant	rs568638045
Chromosome Location	chr14:105443652-105443653
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:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105397847..105399946-chr14:105442912..105445708,2	MCF-7	breast:
2	chr14:105441950..105443788-chr14:105450832..105453768,2	K562	blood:
3	chr14:105261681..105264088-chr14:105440432..105444268,3	MCF-7	breast:
4	chr14:105442748..105444564-chr14:105532745..105535377,2	MCF-7	breast:
5	chr14:105441981..105444790-chr14:105863308..105866164,2	MCF-7	breast:
6	chr14:105442006..105443959-chr14:105511075..105512715,25	MCF-7	breast:
7	chr14:105440890..105445623-chr14:105485614..105489562,6	MCF-7	breast:
8	chr14:105329992..105332567-chr14:105443160..105445644,3	MCF-7	breast:
9	chr14:105442175..105444429-chr14:105444520..105447131,2	K562	blood:
10	chr14:105440794..105444073-chr14:105510721..105514386,4	K562	blood:
11	chr14:105265965..105267568-chr14:105442748..105445496,2	MCF-7	breast:
12	chr14:105389558..105391968-chr14:105443207..105445217,2	MCF-7	breast:
13	chr14:105442698..105444680-chr14:105485412..105488707,3	K562	blood:
14	chr14:105441584..105444154-chr14:105510721..105515062,5	K562	blood:
15	chr14:105441376..105443921-chr14:105550710..105553221,2	MCF-7	breast:
16	chr14:105443512..105446839-chr14:105449245..105453481,5	K562	blood:
17	chr14:105441389..105444198-chr14:105485839..105488707,2	K562	blood:
18	chr14:105441966..105444390-chr14:105493852..105497490,3	MCF-7	breast:
19	chr14:105433937..105458439-chr14:105476653..105492775,70	MCF-7	breast:
20	chr14:105442218..105444582-chr14:105521648..105524128,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000185567	Chromatin interaction
ENSG00000226174	Chromatin interaction
ENSG00000166428	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000170779	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000140104	Chromatin interaction
ENSG00000183484	Chromatin interaction
ENSG00000179627	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers 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	114 gene(s)	inside rSNPs	diseases
3	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
4	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
5	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
6	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
7	nsv902419	chr14:105381763-105494262	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv1049253	chr14:105384959-105471855	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv542228	chr14:105390569-105459912	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
12	nsv1036224	chr14:105404755-105470333	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv902420	chr14:105410183-105494262	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
14	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
15	nsv1438	chr14:105412728-105457581	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
16	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
17	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
18	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
20	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
21	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
23	esv3355872	chr14:105443532-105446080	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105433000-105445400	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr14:105434400-105443800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr14:105434600-105444000	Weak transcription	Aorta	Aorta
4	chr14:105436800-105443800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr14:105437400-105444000	Enhancers	Pancreas	Pancrea
6	chr14:105438000-105446800	Enhancers	Lung	lung
7	chr14:105439600-105445400	Enhancers	Spleen	Spleen
8	chr14:105440200-105443800	Enhancers	NHLF	lung
9	chr14:105440200-105444000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:105440400-105444000	Enhancers	Right Ventricle	heart
11	chr14:105440600-105443800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr14:105440600-105444000	Bivalent Enhancer	Stomach Mucosa	stomach
13	chr14:105440800-105443800	Weak transcription	Right Atrium	heart
14	chr14:105441000-105443800	Weak transcription	Left Ventricle	heart
15	chr14:105441400-105443800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
16	chr14:105441600-105443800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:105441600-105443800	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr14:105441600-105444000	Enhancers	Gastric	stomach
19	chr14:105441800-105443800	Enhancers	Brain Angular Gyrus	brain
20	chr14:105441800-105443800	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr14:105441800-105443800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
22	chr14:105441800-105444400	Bivalent Enhancer	Placenta	Placenta
23	chr14:105441800-105446800	Enhancers	Fetal Heart	heart
24	chr14:105442000-105443800	Enhancers	Brain Anterior Caudate	brain
25	chr14:105442000-105443800	Bivalent Enhancer	Fetal Intestine Small	intestine
26	chr14:105442000-105444000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:105442000-105444000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr14:105442000-105444000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr14:105442200-105443800	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr14:105442200-105443800	Flanking Active TSS	A549	lung
31	chr14:105442200-105444000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr14:105442200-105444000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr14:105442200-105444000	Enhancers	Liver	Liver
34	chr14:105442200-105444000	Enhancers	NH-A	brain
35	chr14:105442600-105443800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
36	chr14:105442600-105443800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:105442600-105443800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr14:105442600-105443800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:105442600-105443800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr14:105442600-105444000	Flanking Active TSS	Hela-S3	cervix
41	chr14:105442800-105443800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr14:105442800-105444000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr14:105442800-105444000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
44	chr14:105442800-105444000	Flanking Active TSS	NHEK	skin
45	chr14:105442800-105444400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:105443000-105443800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:105443000-105443800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr14:105443000-105443800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr14:105443000-105443800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
50	chr14:105443000-105443800	Weak transcription	Osteobl	bone

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