Variant report

Variant	rs192192327
Chromosome Location	chr14:66157815-66157816
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
4	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
5	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
6	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking 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	8 gene(s)	inside rSNPs	diseases
8	nsv902026	chr14:66061020-66171541	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3530654	chr14:66157550-66158352	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3530655	chr14:66157563-66158354	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3530653	chr14:66157648-66158250	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
12	esv3530656	chr14:66157662-66158246	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66100600-66160000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:66137000-66189000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr14:66138000-66177400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr14:66147600-66176000	Weak transcription	Stomach Mucosa	stomach
5	chr14:66147800-66170200	Weak transcription	Primary B cells from cord blood	blood
6	chr14:66153800-66160200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:66154000-66170000	Weak transcription	Brain Hippocampus Middle	brain
8	chr14:66156000-66160000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr14:66156000-66161200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:66156000-66163400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr14:66156000-66179600	Weak transcription	Primary B cells from peripheral blood	blood
12	chr14:66156200-66160200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:66156200-66172600	Weak transcription	Primary T cells from cord blood	blood
14	chr14:66157800-66158200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr14:66157800-66158200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr14:66157800-66158200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr14:66157800-66158200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:66157800-66158200	ZNF genes & repeats	Dnd41	blood
19	chr14:66157800-66160000	Weak transcription	Fetal Intestine Small	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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