Variant report

Variant	rs4368077
Chromosome Location	chr14:37639504-37639505
allele	C/G
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	JUND	chr14:37639452-37639816	HepG2	liver:	n/a	chr14:37639621-37639631 chr14:37639620-37639631 chr14:37639620-37639632 chr14:37639622-37639630 chr14:37639623-37639630 chr14:37639621-37639630 chr14:37639622-37639631
2	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
3	JUND	chr14:37639444-37639935	K562	blood:	n/a	chr14:37639621-37639631 chr14:37639620-37639631 chr14:37639620-37639632 chr14:37639622-37639630 chr14:37639623-37639630 chr14:37639621-37639630 chr14:37639622-37639631

No.	Distal block	Cell Line	Cell type
1	chr14:37439762..37441841-chr14:37637700..37639770,2	K562	blood:
2	chr14:37131202..37132825-chr14:37638068..37640984,2	K562	blood:
3	chr14:37638241..37643981-chr14:37665773..37670423,8	MCF-7	breast:
4	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:
5	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:

Variant related genes	Relation type
SLC25A21-AS1	TF binding region
ENSG00000151338	Chromatin interaction
ENSG00000198807	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12879089	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12883863	1.00[ASN][1000 genomes]
rs12889779	0.82[ASN][1000 genomes]
rs12893236	1.00[ASN][1000 genomes]
rs12897482	1.00[ASN][1000 genomes]
rs17554224	0.90[ASN][1000 genomes]
rs2899854	0.97[ASN][1000 genomes]
rs34164918	1.00[ASN][1000 genomes]
rs34503846	0.97[ASN][1000 genomes]
rs35127962	1.00[ASN][1000 genomes]
rs35130743	0.87[ASN][1000 genomes]
rs35281444	1.00[ASN][1000 genomes]
rs35412613	0.92[ASN][1000 genomes]
rs35424693	1.00[ASN][1000 genomes]
rs35799924	0.98[ASN][1000 genomes]
rs36057482	0.98[ASN][1000 genomes]
rs36112910	0.92[ASN][1000 genomes]
rs4344641	1.00[ASN][1000 genomes]
rs4522325	1.00[ASN][1000 genomes]
rs61988260	0.89[ASN][1000 genomes]
rs61988282	1.00[ASN][1000 genomes]
rs61988284	1.00[ASN][1000 genomes]
rs61988286	1.00[ASN][1000 genomes]
rs61988287	1.00[ASN][1000 genomes]
rs61988312	0.85[ASN][1000 genomes]
rs61988340	0.82[ASN][1000 genomes]
rs7145475	0.98[ASN][1000 genomes]
rs7151191	0.84[ASN][1000 genomes]
rs8006144	1.00[ASN][1000 genomes]
rs8007653	0.85[ASN][1000 genomes]
rs8018493	1.00[ASN][1000 genomes]
rs8019652	1.00[ASN][1000 genomes]
rs8021181	1.00[ASN][1000 genomes]
rs8022156	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1050174	chr14:37556357-37664143	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1043410	chr14:37556357-37671059	Enhancers Weak transcription Active TSS Flanking Active TSS 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	11 gene(s)	inside rSNPs	diseases
4	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv915783	chr14:37607836-38002966	Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1036854	chr14:37609535-38013533	Active TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv542045	chr14:37609535-38013533	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv901635	chr14:37623177-37782273	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	esv3528451	chr14:37631483-37771365	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	esv3527359	chr14:37631504-37771435	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	esv3370191	chr14:37631508-37771354	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	esv3527360	chr14:37631521-37771311	Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	esv3528462	chr14:37631535-37771345	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	esv3528473	chr14:37631543-37771255	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	esv3527361	chr14:37631554-37771408	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	esv3528484	chr14:37631599-37771228	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	esv3527363	chr14:37631608-37771230	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	esv3310838	chr14:37636091-37639750	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
19	esv3310839	chr14:37636091-37639750	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37638400-37640800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr14:37638400-37641000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:37638600-37639600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr14:37638600-37639600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:37638600-37640400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr14:37638600-37640400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr14:37638600-37640800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:37638600-37641000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:37638600-37641000	Weak transcription	Pancreas	Pancrea
10	chr14:37638800-37639600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr14:37638800-37640400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:37638800-37640800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr14:37638800-37640800	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:37639000-37639600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:37639000-37639800	Weak transcription	Small Intestine	intestine
16	chr14:37639000-37640800	Weak transcription	Fetal Heart	heart
17	chr14:37639000-37643400	Active TSS	K562	blood
18	chr14:37639200-37640200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:37639200-37642400	Active TSS	Duodenum Mucosa	Duodenum
20	chr14:37639400-37640000	Enhancers	HUES48 Cell Line	embryonic stem cell

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