Variant report

Variant	rs552955932
Chromosome Location	chr13:67434808-67434809
allele	A/G
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	nsv1041133	chr13:66723731-67530595	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv523360	chr13:67322714-67520344	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1051576	chr13:67322747-67520255	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv900405	chr13:67347245-67446835	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1042756	chr13:67352439-67445867	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv430580	chr13:67352439-67468100	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv562136	chr13:67355618-67485147	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1051623	chr13:67377549-67465276	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv455933	chr13:67392298-67437316	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv562137	chr13:67392298-67437316	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv900406	chr13:67434161-67532205	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv900407	chr13:67434161-67603745	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67431800-67436000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr13:67432600-67435400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:67433200-67435200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:67433200-67435200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:67433200-67435200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr13:67433200-67435400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr13:67433200-67435400	Enhancers	Brain Substantia Nigra	brain
8	chr13:67433400-67435400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:67433400-67435400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:67433400-67435400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr13:67433400-67435400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr13:67433400-67436600	Enhancers	Brain Hippocampus Middle	brain
13	chr13:67433800-67435600	Enhancers	Brain Angular Gyrus	brain
14	chr13:67433800-67435600	Enhancers	Brain Cingulate Gyrus	brain
15	chr13:67433800-67435800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr13:67433800-67438600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr13:67434000-67435000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr13:67434000-67435200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:67434000-67435400	Enhancers	Brain Anterior Caudate	brain
20	chr13:67434200-67435000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr13:67434200-67435000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr13:67434200-67435000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:67434200-67435200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr13:67434200-67435200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr13:67434200-67435200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr13:67434200-67435400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:67434200-67435400	Enhancers	A549	lung
28	chr13:67434400-67435000	Enhancers	Adipose Nuclei	Adipose
29	chr13:67434400-67435200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:67434400-67435200	Enhancers	Fetal Stomach	stomach
31	chr13:67434400-67435200	Enhancers	Psoas Muscle	Psoas
32	chr13:67434400-67435400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:67434400-67435400	Enhancers	Fetal Heart	heart
34	chr13:67434400-67435400	Enhancers	Fetal Muscle Leg	muscle
35	chr13:67434400-67435600	Enhancers	Right Atrium	heart
36	chr13:67434600-67435000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr13:67434600-67435000	Enhancers	Fetal Kidney	kidney
38	chr13:67434600-67435000	Enhancers	Left Ventricle	heart
39	chr13:67434600-67435000	Enhancers	HUVEC	blood vessel
40	chr13:67434600-67435400	Enhancers	Colon Smooth Muscle	Colon
41	chr13:67434600-67438400	Weak transcription	Brain Germinal Matrix	brain
42	chr13:67434800-67435000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:67434800-67435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr13:67434800-67435400	Enhancers	Right Ventricle	heart
45	chr13:67434800-67435800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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