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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS182-21337
Organism
Homo sapiens
Tissue/cell
Spleen
Coordinate
chr8:144643590-144643910
Target genes
Number: 36
Name
Ensembl ID
LY6E
ENSG00000160932
GPIHBP1
ENSG00000182851
ZFP41
ENSG00000181638
GLI4
ENSG00000250571
RP13
ENSG00000253716
ZNF696
ENSG00000185730
TOP1MT
ENSG00000184428
C8orf51
ENSG00000254389
RHPN1
ENSG00000158106
MAFA
ENSG00000182759
ZC3H3
ENSG00000014164
7SK
ENSG00000221399
RP11
ENSG00000254144
GSDMD
ENSG00000104518
C8orf73
ENSG00000204839
NAPRT1
ENSG00000147813
TIGD5
ENSG00000179886
EEF1D
ENSG00000104529
PYCRL
ENSG00000104524
TSTA3
ENSG00000104522
ZNF623
ENSG00000183309
ZNF707
ENSG00000181135
CCDC166
ENSG00000255181
MAPK15
ENSG00000181085
FAM83H
ENSG00000180921
SCRIB
ENSG00000180900
PUF60
ENSG00000179950
EPPK1
ENSG00000227184
PLEC
ENSG00000178209
GRINA
ENSG00000178719
PARP10
ENSG00000178685
EXOSC4
ENSG00000178896
GPAA1
ENSG00000197858
CYC1
ENSG00000179091
MAF1
ENSG00000179632
SHARPIN
ENSG00000179526
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
EWSR1-FLI1
MA0149.1
chr8:144643769-144643787
CCAGCCTCCCTTCCTGCC
-
6.09
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr8
144643707
144643860
Enhancer Sequence
CAGGTGAGAG CCGAGAGCCC CCAGCATGGG GTGTCCGGTG GGAAAAGCAC ACTCCCTGGG 60
CAGTTGAGGC CTTCTCCTCA TGTTCTCAGG GCACAGGGAG GCCGGGCAGC CCCCTGAGGC 120
GGTGGGCACC CCCCATACAC ACACAAGGGG CAACACAGGA CAGCTGACCC TGGGCCTCCC 180
CAGCCTCCCT TCCTGCCCTG GGCTGCCAGT GTTGGCAGTG GTGAGCGGGG CTGTGACGGC 240
CTGGGGAAGG CCTCAGCCCT CTCTGGCTCA GACACCCTTC CCCGGCACTG ACCAGCCCTG 300
CCCTCCCATG CCCCTGCCCA 320