Variant report

Variant	rs13109916
Chromosome Location	chr4:56951236-56951237
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs35798357	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1005845	chr4:56522075-56980357	Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv999328	chr4:56942917-57041586	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1007114	chr4:56942917-57055381	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv999639	chr4:56942917-57401310	Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv1014045	chr4:56942917-57404511	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56945200-56951800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:56945400-56952200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:56945600-56965200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:56947000-56951800	Weak transcription	Fetal Intestine Small	intestine
5	chr4:56947200-56951600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr4:56947600-56952200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr4:56947800-56957000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:56948800-56972200	Weak transcription	Fetal Stomach	stomach
9	chr4:56949000-56965200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:56949600-56951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:56949600-56951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:56949600-56952200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:56950800-56951400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:56950800-56952800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:56950800-56952800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr4:56951000-56951400	Enhancers	Fetal Brain Male	brain
17	chr4:56951000-56951400	Enhancers	HUVEC	blood vessel
18	chr4:56951000-56951600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:56951000-56952600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:56951000-56952800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:56951000-56952800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:56951000-56952800	Enhancers	Fetal Kidney	kidney
23	chr4:56951000-56953000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:56951000-56953200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:56951000-56953200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:56951000-56953600	Enhancers	Brain Germinal Matrix	brain
27	chr4:56951200-56951400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:56951200-56951400	Enhancers	Brain Anterior Caudate	brain
29	chr4:56951200-56951400	Enhancers	Ovary	ovary
30	chr4:56951200-56951400	Enhancers	Right Atrium	heart
31	chr4:56951200-56951600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:56951200-56951600	Enhancers	Stomach Mucosa	stomach
33	chr4:56951200-56952000	Enhancers	Fetal Brain Female	brain
34	chr4:56951200-56952000	Flanking Active TSS	Hela-S3	cervix
35	chr4:56951200-56952200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr4:56951200-56952600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr4:56951200-56952800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:56951200-56952800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:56951200-56953000	Enhancers	H1 Cell Line	embryonic stem cell

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