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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS049-04276
Organism
Homo sapiens
Tissue/cell
Fetal_spinal_cord
Coordinate
chr19:55813530-55814000
Target genes
Number: 29
Name
Ensembl ID
NLRP2
ENSG00000022556
RDH13
ENSG00000160439
TNNT1
ENSG00000105048
TNNI3
ENSG00000129991
DNAAF3
ENSG00000167646
snoU13
ENSG00000239137
SYT5
ENSG00000129990
PTPRH
ENSG00000080031
TMEM86B
ENSG00000180089
PPP6R1
ENSG00000105063
HSPBP1
ENSG00000133265
BRSK1
ENSG00000160469
TMEM150B
ENSG00000180061
SUV420H2
ENSG00000133247
COX6B2
ENSG00000160471
FAM71E2
ENSG00000180043
RPL28
ENSG00000108107
SHISA7
ENSG00000187902
ISOC2
ENSG00000063241
NAT14
ENSG00000090971
SSC5D
ENSG00000179954
SBK2
ENSG00000187550
ZNF784
ENSG00000179922
ZNF580
ENSG00000213015
ZNF581
ENSG00000171425
CCDC106
ENSG00000173581
U2AF2
ENSG00000063244
EPN1
ENSG00000063245
AC010525.2
ENSG00000211571
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
ZNF263
MA0528.1
chr19:55813793-55813814
GAGGGAGGAGGGGCTGGGGGC
+
6.03
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
55813823
55813880
Enhancer Sequence
GTACCTGTGA GTATGGGGTA ACTGGACTCT TGGGTCCCTG GCGGAAATAG GGGAGGGGCC 60
AAAGCAGTAG AAGCGGCTGG GAGGGGTGGG ATGCCAGGGT TCCTGAGAGG CAACGGGCTA 120
GGGACTCGGA CTTATGGGTC CTGGGGGAAG AGGACACAGC TAGAGAAGGA GTCTAGGGGT 180
CAGAGGCAGG AGGGGCTAAG CTAGGAGTCC AGGACTCCCA GGTTTGAGGG AAAAAGGGAC 240
TGGGGGCCTG GACTCCTGGA TCCGAGGGAG GAGGGGCTGG GGGCCTGGAC TTCTGGGTCT 300
GAAGAAGGAG GGGCCGGGGG CCTGGACCCC TCGGTCGGAG GGAAAAGGGG CTGGAGGTCT 360
GGACTCCTGG GTCTGAGATG GGGGGCGAGG TCTGGGGCGT CTGGATTCCT GGGTATGAGA 420
GAGAAGGGGC CGGGGCCTAG ACTCGGATTT CGGGGTCCGG GATCATTGAG 470