Variant report

Variant	rs3181256
Chromosome Location	chr14:24800879-24800880
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:24800860-24801010	NHEK	skin:	n/a	n/a
2	MYBL2	chr14:24800874-24802346	HepG2	liver:	n/a	n/a
3	POLR2A	chr14:24800400-24801095	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr14:24800848-24802400	HUVEC	blood vessel:	n/a	n/a
5	ZNF263	chr14:24800274-24801733	HEK293-T-REx	kidney:	n/a	n/a
6	MAX	chr14:24800815-24802487	HepG2	liver:	n/a	chr14:24801678-24801685 chr14:24801677-24801686 chr14:24801676-24801687 chr14:24801677-24801687 chr14:24801676-24801687 chr14:24801676-24801686 chr14:24801677-24801686 chr14:24801675-24801688 chr14:24801166-24801176
7	CTCF	chr14:24800820-24800970	SAEC	small airway:	n/a	n/a
8	ZNF263	chr14:24800144-24801331	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24799476..24801488-chr14:24903490..24905098,2	K562	blood:
2	chr14:24796879..24804920-chr14:24831628..24840088,12	MCF-7	breast:
3	chr14:24789439..24822082-chr14:24898039..24913135,99	MCF-7	breast:
4	chr14:24709884..24713728-chr14:24799730..24804763,6	MCF-7	breast:
5	chr14:24791358..24808812-chr14:24895309..24913599,55	K562	blood:
6	chr14:24682382..24684800-chr14:24800505..24802328,2	K562	blood:
7	chr14:24768871..24772362-chr14:24798723..24803416,4	MCF-7	breast:
8	chr14:24781460..24810019-chr14:24892340..24914262,110	MCF-7	breast:
9	chr14:24800598..24804207-chr14:24909756..24912911,5	K562	blood:
10	chr14:24800528..24803981-chr14:24898784..24901810,5	K562	blood:

Variant related genes	Relation type
ADCY4	TF binding region
ENSG00000100441	Chromatin interaction
ENSG00000092330	Chromatin interaction
ENSG00000254505	Chromatin interaction
ENSG00000100445	Chromatin interaction
ENSG00000254692	Chromatin interaction
ENSG00000196943	Chromatin interaction
ENSG00000139899	Chromatin interaction
ENSG00000157379	Chromatin interaction
ENSG00000100968	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1109153	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12436417	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7147370	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv564060	chr14:24776401-24809795	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24786200-24801600	Weak transcription	Left Ventricle	heart
2	chr14:24787000-24801200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr14:24788400-24801000	Weak transcription	Gastric	stomach
4	chr14:24793800-24801000	Weak transcription	Right Ventricle	heart
5	chr14:24794800-24801200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr14:24794800-24801200	Weak transcription	K562	blood
7	chr14:24795000-24801200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr14:24795600-24801600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:24796800-24801000	Weak transcription	Colonic Mucosa	Colon
10	chr14:24796800-24801600	Weak transcription	Right Atrium	heart
11	chr14:24796800-24801600	Weak transcription	Osteobl	bone
12	chr14:24797000-24801000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:24797000-24801000	Weak transcription	Liver	Liver
14	chr14:24797000-24801000	Weak transcription	Lung	lung
15	chr14:24797000-24801000	Weak transcription	Pancreas	Pancrea
16	chr14:24797000-24801000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr14:24797000-24801000	Weak transcription	Dnd41	blood
18	chr14:24797000-24801400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr14:24797000-24801400	Weak transcription	HUVEC	blood vessel
20	chr14:24797800-24801600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr14:24798000-24801000	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr14:24798400-24801000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr14:24798400-24801000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr14:24799000-24801600	Weak transcription	Stomach Mucosa	stomach
25	chr14:24799200-24801000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr14:24799200-24801200	Weak transcription	Primary T cells from cord blood	blood
27	chr14:24799400-24801000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr14:24799400-24801200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr14:24799400-24801200	Weak transcription	NHDF-Ad	bronchial
30	chr14:24799600-24801000	Weak transcription	Placenta	Placenta
31	chr14:24800000-24801200	Weak transcription	Adipose Nuclei	Adipose
32	chr14:24800200-24801600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr14:24800400-24801000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr14:24800400-24801000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr14:24800400-24801000	Bivalent Enhancer	HepG2	liver
36	chr14:24800400-24801200	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr14:24800400-24801600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:24800400-24801600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr14:24800400-24801600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr14:24800400-24802200	Genic enhancers	Spleen	Spleen
41	chr14:24800600-24801200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr14:24800600-24801200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:24800600-24801600	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr14:24800800-24801000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr14:24800800-24801000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr14:24800800-24801200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr14:24800800-24801400	Enhancers	Primary B cells from cord blood	blood
48	chr14:24800800-24801400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr14:24800800-24801600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:24800800-24801600	Enhancers	Primary hematopoietic stem cells	blood

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