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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS182-22088
Organism
Homo sapiens
Tissue/cell
Spleen
Coordinate
chr9:130550970-130551450
Target genes
Number: 34
Name
Ensembl ID
SLC2A8
ENSG00000136856
ZNF79
ENSG00000196152
RPL12
ENSG00000197958
LRSAM1
ENSG00000148356
FAM129B
ENSG00000136830
STXBP1
ENSG00000136854
C9orf117
ENSG00000160401
RP11
ENSG00000248666
TTC16
ENSG00000167094
PTRH1
ENSG00000187024
TOR2A
ENSG00000160404
SH2D3C
ENSG00000095370
CDK9
ENSG00000136807
FPGS
ENSG00000136877
ENG
ENSG00000106991
AK1
ENSG00000106992
ST6GALNAC6
ENSG00000160408
ST6GALNAC4
ENSG00000136840
PIP5KL1
ENSG00000167103
DPM2
ENSG00000136908
FAM102A
ENSG00000167106
SLC25A25
ENSG00000148339
NAIF1
ENSG00000171169
PTGES2
ENSG00000148334
LCN2
ENSG00000148346
C9orf16
ENSG00000171159
DNM1
ENSG00000106976
CIZ1
ENSG00000148337
GOLGA2
ENSG00000167110
COQ4
ENSG00000167113
TRUB2
ENSG00000167112
SLC27A4
ENSG00000167114
TMSB4XP4
ENSG00000223551
URM1
ENSG00000167118
TF binding sites/motifs
Number: 2
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
TFAP4
MA0691.1
chr9:130551158-130551168
ATCAGCTGTT
-
6.02
ZNF263
MA0528.1
chr9:130551019-130551040
AGAGGAGGAGTGGGGAGTAGA
+
6.32
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr9
130551005
130551386
Enhancer Sequence
GGTACGGGGC CCCGGTCCCC ACGGGGTGCA GAGATCGAGG TCCCCCGGCA GAGGAGGAGT 60
GGGGAGTAGA ATGGAAGGAG CGCTCCTCTC TGGAAGGGAG GCTGGTTTGG TGACAGGGCC 120
TGTCTTGGGG TGGGGAGTGT GTGGGAGAAA AAAACACCTG ACACAGGCTG TGCGCCAGTC 180
TCGGTTCCAT CAGCTGTTCT GTGGCCTTGG GCAGAACATC TGAGTCAGCG CTGGGTTTCT 240
CTTCTGTGAA CCAGAAATGT GACGTGTATC AGGGTTGGAG CCCATATTCC AGGTGATGTG 300
GGTGGAAGGA CCTGGCACGT GGTATGTGCC AATCCATAGC GGGCACTGCT TCTGGGAGGG 360
GTCGAGTAGC AGTCTGGGAG CCTCCGAGTG GAGCAGGTAT TTTAGTCCTT TTAGGCCTTT 420
ATGAAGGGAT AAGCCACGCA CCTCCTGACC GGACTCCATA TTCTCTCAAC GCCCCCTCCC 480