Variant report

Variant	rs534118799
Chromosome Location	chr5:37152375-37152376
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers 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 target site	28 gene(s)	inside rSNPs	diseases
4	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	esv1802391	chr5:36958598-37242600	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
10	nsv597823	chr5:37111565-37430365	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
11	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
12	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
13	nsv1025988	chr5:37115142-37586211	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv537727	chr5:37115142-37586211	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv830265	chr5:37152221-37312233	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37082800-37169200	Weak transcription	Spleen	Spleen
2	chr5:37105800-37156200	Weak transcription	NHLF	lung
3	chr5:37112200-37198200	Weak transcription	Small Intestine	intestine
4	chr5:37113600-37222200	Weak transcription	Psoas Muscle	Psoas
5	chr5:37113800-37157000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr5:37114600-37165400	Weak transcription	HMEC	breast
7	chr5:37118600-37153600	Weak transcription	Pancreas	Pancrea
8	chr5:37122000-37156000	Weak transcription	Brain Substantia Nigra	brain
9	chr5:37133200-37169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:37134200-37171200	Weak transcription	Colonic Mucosa	Colon
11	chr5:37136200-37197200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr5:37136800-37170000	Weak transcription	Esophagus	oesophagus
13	chr5:37137400-37174000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:37137600-37169000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr5:37138000-37156000	Weak transcription	Aorta	Aorta
16	chr5:37138000-37157000	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:37138400-37155200	Weak transcription	Brain Angular Gyrus	brain
18	chr5:37138400-37156800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:37138400-37196800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr5:37138600-37153400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:37138600-37179600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr5:37138800-37156800	Weak transcription	HUVEC	blood vessel
23	chr5:37143000-37153400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr5:37143400-37189600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:37143600-37156000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr5:37143600-37157200	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:37143800-37152800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr5:37143800-37153400	Weak transcription	HepG2	liver
29	chr5:37143800-37169200	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr5:37144000-37153200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:37144000-37154800	Weak transcription	Gastric	stomach
32	chr5:37144000-37156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr5:37144200-37156400	Weak transcription	Fetal Brain Male	brain
34	chr5:37144400-37153400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:37144400-37153800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr5:37144400-37156000	Weak transcription	Lung	lung
37	chr5:37144400-37171400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:37144800-37152400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:37145600-37158800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:37146400-37174000	Weak transcription	GM12878-XiMat	blood
41	chr5:37146800-37152400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:37147200-37158600	Strong transcription	Dnd41	blood
43	chr5:37147200-37200600	Strong transcription	HSMM	muscle
44	chr5:37147400-37158600	Strong transcription	Adipose Nuclei	Adipose
45	chr5:37147600-37158400	Strong transcription	Stomach Smooth Muscle	stomach
46	chr5:37147800-37157400	Strong transcription	Fetal Intestine Large	intestine
47	chr5:37147800-37158600	Strong transcription	Fetal Lung	lung
48	chr5:37148000-37153800	Strong transcription	Placenta	Placenta
49	chr5:37148000-37156800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:37148000-37182000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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