Variant report

Variant	rs4078149
Chromosome Location	chr14:104691649-104691650
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11628649	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4906423	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs68036376	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7142792	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7144831	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7160242	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs72717026	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050479	chr14:104500427-104805738	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active 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	42 gene(s)	inside rSNPs	diseases
2	nsv902331	chr14:104523839-104849219	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv1044920	chr14:104528663-104803058	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv470674	chr14:104545284-104710505	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv902345	chr14:104554044-104865071	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	esv1826669	chr14:104554461-105065941	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv1047665	chr14:104577600-104787620	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1049810	chr14:104577600-105060539	Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv542214	chr14:104600431-104694456	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1041696	chr14:104614589-104798502	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
11	nsv1048001	chr14:104632614-104895474	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv456436	chr14:104657760-104769149	Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv566032	chr14:104657760-104769149	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv566033	chr14:104666821-104747384	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv902356	chr14:104686346-104758887	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	esv2095024	chr14:104691397-104691880	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104687000-104692200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr14:104688600-104692600	Enhancers	Spleen	Spleen
3	chr14:104689400-104691800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:104689400-104691800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:104689800-104692400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr14:104689800-104692600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr14:104690200-104692600	Weak transcription	Lung	lung
8	chr14:104690400-104691800	Enhancers	Fetal Intestine Large	intestine
9	chr14:104690400-104691800	Enhancers	Stomach Mucosa	stomach
10	chr14:104690400-104692800	Weak transcription	Left Ventricle	heart
11	chr14:104690400-104696000	Weak transcription	Fetal Heart	heart
12	chr14:104690600-104692200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr14:104691000-104691800	Enhancers	Fetal Intestine Small	intestine
14	chr14:104691000-104692200	Enhancers	Pancreas	Pancrea
15	chr14:104691000-104692800	ZNF genes & repeats	Placenta	Placenta
16	chr14:104691000-104698200	Weak transcription	Fetal Brain Male	brain
17	chr14:104691200-104692400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr14:104691200-104693200	Enhancers	Fetal Muscle Trunk	muscle
19	chr14:104691400-104691800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr14:104691400-104692200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr14:104691400-104692400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr14:104691400-104692400	Weak transcription	Gastric	stomach
23	chr14:104691400-104692800	Enhancers	Primary B cells from peripheral blood	blood
24	chr14:104691400-104692800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:104691400-104693000	Enhancers	Hela-S3	cervix
26	chr14:104691400-104693400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:104691400-104693600	Enhancers	Fetal Muscle Leg	muscle
28	chr14:104691600-104691800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr14:104691600-104692000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:104691600-104692400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:104691600-104692400	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr14:104691600-104692600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr14:104691600-104692800	Weak transcription	Colonic Mucosa	Colon
34	chr14:104691600-104693400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr14:104691600-104697400	Weak transcription	Ovary	ovary
36	chr14:104691600-104698000	Weak transcription	Fetal Lung	lung

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