Variant report

Variant	rs7158432
Chromosome Location	chr14:56393578-56393579
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10151450	1.00[CHB][hapmap]
rs11158067	0.91[ASN][1000 genomes]
rs17090816	1.00[MEX][hapmap]
rs41528447	1.00[TSI][hapmap]
rs57532344	1.00[EUR][1000 genomes]
rs7144818	1.00[CHB][hapmap]
rs8016445	1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv34106	chr14:56346245-56550642	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1043948	chr14:56393578-56423793	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56380800-56394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:56387200-56395800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:56389200-56393800	Weak transcription	Gastric	stomach
4	chr14:56391200-56393800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr14:56391400-56395200	Enhancers	Stomach Mucosa	stomach
6	chr14:56391800-56395000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:56391800-56395800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:56391800-56395800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr14:56391800-56396200	Enhancers	Fetal Intestine Large	intestine
10	chr14:56391800-56396200	Enhancers	Fetal Intestine Small	intestine
11	chr14:56392400-56394000	Enhancers	HepG2	liver
12	chr14:56392400-56395200	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr14:56392600-56393800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:56392600-56394800	Enhancers	Pancreas	Pancrea
15	chr14:56392600-56396000	Enhancers	Duodenum Mucosa	Duodenum
16	chr14:56392600-56396200	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr14:56392800-56393600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr14:56392800-56394200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr14:56392800-56394800	Enhancers	Small Intestine	intestine
20	chr14:56392800-56395800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:56393000-56394000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr14:56393000-56394600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:56393200-56393800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:56393200-56394200	Weak transcription	Colonic Mucosa	Colon
25	chr14:56393400-56393800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:56393400-56394000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr14:56393400-56394600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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