Variant report

Variant	rs374080063
Chromosome Location	chr4:96118006-96118007
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv594907	chr4:95975470-96170439	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	esv3325370	chr4:96117229-96119277	Strong transcription Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3450367	chr4:96117552-96118490	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv280124	chr4:96118004-96118007	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96098000-96127000	Weak transcription	Right Atrium	heart
2	chr4:96100000-96143000	Weak transcription	Fetal Kidney	kidney
3	chr4:96103600-96123000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:96105800-96123200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr4:96110600-96133800	Weak transcription	Gastric	stomach
6	chr4:96110600-96134000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:96112600-96125600	Weak transcription	Ovary	ovary
8	chr4:96112600-96127200	Weak transcription	Fetal Intestine Small	intestine
9	chr4:96112800-96122200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:96112800-96125400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:96115400-96134000	Weak transcription	Aorta	Aorta
12	chr4:96115800-96122000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:96115800-96132800	Weak transcription	Right Ventricle	heart
14	chr4:96116000-96121400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr4:96116200-96123600	Weak transcription	Brain Substantia Nigra	brain
16	chr4:96116800-96118400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr4:96116800-96118600	Weak transcription	Fetal Stomach	stomach
18	chr4:96116800-96123400	Weak transcription	Brain Hippocampus Middle	brain
19	chr4:96116800-96124800	Weak transcription	Brain Angular Gyrus	brain
20	chr4:96117000-96118800	Weak transcription	Fetal Lung	lung
21	chr4:96117000-96119600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:96117000-96123000	Weak transcription	Brain Anterior Caudate	brain
23	chr4:96117200-96119200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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