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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-29519
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chr16:2867970-2868670
Target genes
Number: 30
Name
Ensembl ID
RNPS1
ENSG00000205937
CCNF
ENSG00000162063
C16orf59
ENSG00000162062
TBC1D24
ENSG00000162065
RP11
ENSG00000260272
ATP6V0C
ENSG00000185883
AMDHD2
ENSG00000162066
CEMP1
ENSG00000205923
PDPK1
ENSG00000140992
CTD
ENSG00000261093
AC141586.5
ENSG00000215154
PDPK2
ENSG00000205918
ERVK13
ENSG00000260565
KCTD5
ENSG00000167977
PRSS27
ENSG00000172382
SRRM2
ENSG00000167978
TCEB2
ENSG00000103363
PRSS21
ENSG00000007038
ZG16B
ENSG00000162078
PRSS30P
ENSG00000172460
LA16c
ENSG00000262482
PKMYT1
ENSG00000127564
CLDN9
ENSG00000213937
CLDN6
ENSG00000184697
THOC6
ENSG00000131652
HCFC1R1
ENSG00000103145
CCDC64B
ENSG00000162069
MMP25
ENSG00000008516
IL32
ENSG00000008517
U1
ENSG00000252561
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
HSF1
MA0486.2
chr16:2868182-2868195
TTCCAGAATGTTC
+
6.54
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr16
2868619
2868669
Enhancer Sequence
AGTGGGGGTG CGAACGGAGG GGTGCGGGGA CGGGCAGGAA CAGGGCTGGA GGGAGTGCCA 60
CCGAACTTTA CCTCTGGTCT GATGCCAGAC TTGGGCGTGA AAGTTGTGCG TGGATGCGGC 120
CTGGTGTTCT CCTGAGCCCC AGGCTGTGCT GCAGCCGGTT ACACCCACTC CAGTTCCCTT 180
TGGGTCTCCT GGAGGGAACC CTGTTCAGGT TATTCCAGAA TGTTCTTCCA GAACATTTCC 240
ACACACTTTT GGGTATTCTC TCCCTTTTTC TTTCAACCCA AAGTTCACCA CTGACCATCC 300
CACCCTCATC CCCCCTCCTG GTGGACGGTG CGGTACAGTG TGGGGCACTG AGCCAAGGCC 360
AGCACCCCCG GGCCGCTGTG TGGACTCCAT CCTGCCAATC CCACATTGGC GTGGTGCATC 420
TCCCCATTCC TCCTTGGGCT GCATGGGGGT GCCCCTGGAG GCCTTGGCTC AATGCAAGGC 480
TCCTTGGGAC AGCTCTGGGA GGTGACAAGA CCCCACCCTT CTGCTGCAGG AGCAGGTCCT 540
AGGACTTTGG TTGTGGTCTG TCTGGGCTCC TTCATTTCTG CAGGGGACCC TGGGTGTTAG 600
CAAGTAGCAG CAACACCACA GTTTCCCCTC CTGCACTGGA CCCCAGTTGT GCTCAGGTAG 660
CCAGCCCTCC ATCCAGGGCC CCTGACTGCT CTCTTCTCTT 700