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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS187-10040
Organism
Homo sapiens
Tissue/cell
Th1
Coordinate
chr17:7453510-7454110
Target genes
Number: 34
Name
Ensembl ID
GPS2
ENSG00000132522
NEURL4
ENSG00000215041
ACAP1
ENSG00000072818
TNK1
ENSG00000174292
C17orf61
ENSG00000262481
PLSCR3
ENSG00000187838
NLGN2
ENSG00000169992
RP11
ENSG00000262880
TMEM102
ENSG00000181284
FGF11
ENSG00000161958
CHRNB1
ENSG00000170175
SLC35G6
ENSG00000259224
ZBTB4
ENSG00000174282
POLR2A
ENSG00000181222
TNFSF12
ENSG00000239697
TNFSF13
ENSG00000161955
SENP3
ENSG00000161956
EIF4A1
ENSG00000161960
CD68
ENSG00000129226
MPDU1
ENSG00000129255
AC113189.5
ENSG00000233223
SOX15
ENSG00000129194
FXR2
ENSG00000129245
SAT2
ENSG00000141504
ATP1B2
ENSG00000129244
WRAP53
ENSG00000141499
TP53
ENSG00000141510
KDM6B
ENSG00000132510
CYB5D1
ENSG00000182224
CHD3
ENSG00000170004
LSMD1
ENSG00000183011
AC025335.1
ENSG00000179859
C17orf59
ENSG00000196544
AURKB
ENSG00000178999
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
Zfx
MA0146.2
chr17:7453777-7453791
GAGGCCTGGGCCCC
-
6.42
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
7453713
7454046
Enhancer Sequence
TGGTGAGCAT CCCTCTATCC CAACCTCAGG AAGCGGGCAG AGCAAAAACC ATTATCCACA 60
GGGAGAAACT GAGGCACGGA GGGTGAAAGG AGTTCAGAGT CATGCAGCTA ACCAGCCAAG 120
ACTCAAACCT AGGGATTCTC GCCCTCCTCT GAAGCTCCTT CTGTCATATG GATGTGCTCC 180
TTCAGACCCT ACCCCAAACA GGAAGGCAGG GTGGCCATGA GTTAGAAGAA CTACTGGGAT 240
CCTGATGGAG ACTAGGCCTG GCAGTCAGAG GCCTGGGCCC CGGTAGGCAA AGAGACTTAG 300
GAATGGGATG ATGGGGTGGC CGGATGACCA CGTGTCCAAG TCGGCATGCA GTTGTCCTGG 360
CCCCCACCTG TTATCTCGGT GTGATTAATA GCAGCTTCCC GTTTTGCTCT CAGCAGTATC 420
CCAGTGTGGA TGACAAATTA TAGTCACTCT ACTTACTGAG GAAGATGAGG CCTGAGATTC 480
TAAGGCCAGG AGTCTGGACA AGAATAAGGA TGCCAGGGTT CCTGAGAGGG GAATGGGGCT 540
GGGAGAGTTG CTCTGGGACC CCCACTAGGG CCCGCTTTGC TCATCTGTCT TTCCTTGATC 600