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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS092-00019
Organism
Homo sapiens
Tissue/cell
HFF
Coordinate
chr1:1180760-1181890
Target genes
Number: 41
Name
Ensembl ID
RP11
ENSG00000242590
ISG15
ENSG00000187608
AGRN
ENSG00000188157
SDF4
ENSG00000078808
B3GALT6
ENSG00000176022
FAM132A
ENSG00000184163
RP5
ENSG00000260179
UBE2J2
ENSG00000160087
SCNN1D
ENSG00000162572
PUSL1
ENSG00000169972
ACAP3
ENSG00000131584
CPSF3L
ENSG00000127054
GLTPD1
ENSG00000224051
TAS1R3
ENSG00000169962
DVL1
ENSG00000107404
MXRA8
ENSG00000162576
AURKAIP1
ENSG00000175756
CCNL2
ENSG00000221978
RP4
ENSG00000224870
MRPL20
ENSG00000242485
ANKRD65
ENSG00000235098
VWA1
ENSG00000179403
ATAD3C
ENSG00000215915
ATAD3B
ENSG00000160072
ATAD3A
ENSG00000197785
TMEM240
ENSG00000205090
AL645728.2
ENSG00000215791
SSU72
ENSG00000160075
AL645728.1
ENSG00000215014
C1orf233
ENSG00000228594
MIB2
ENSG00000197530
MMP23B
ENSG00000189409
CDK11B
ENSG00000248333
SLC35E2B
ENSG00000189339
MMP23A
ENSG00000215914
CDK11A
ENSG00000008128
RP1
ENSG00000227775
SLC35E2
ENSG00000215790
NADK
ENSG00000008130
GNB1
ENSG00000078369
CALML6
ENSG00000169885
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
KLF5
MA0599.1
chr1:1180990-1181000
GCCCCGCCCC
+
6.02
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
1180764
1180856
Enhancer Sequence
AGCCTATCTG GGGGCTGAGA GCCAGAGGCA ACAGAGAGCA GGCTGCAGGA GAACCGCCCA 60
ACCCTGGAAG CCTGGAGGGC CAGCCTGAGC ACACACCTCA CAGCCCTCCA GCCGGCACCC 120
TTTGAGGGAG GCCCGCCACC CTGCAGGGTC TCTGGAGGAG TGGCCCTGGG CAGTGGGGTG 180
CCCCCTCCCT TCCAGGGGGA CTGGCCCGGA CTGCTGAAGA CCCCCCCACT GCCCCGCCCC 240
TGCCAGCACT GCCAGCCTGG CCCTAGCGCC GGGAACCAGC CCACTCTTCC TGAGCTGGCA 300
GAGCCGCGGC CTCAACCCTC CTCAGCCTTC CCATCTGGGA AACGGGACCT CGGGCTCCAG 360
CGGGGCCGCG TGGGCTGAGA GGCAGCCGGG CTGGCTGCAG CAGAGACGCC CTCGGGAGGA 420
GGGAGACCAG CATCAAAGGT GTGAGGGCCG GGGATGGGGG CTGCTCTGGC AACTGCGGCT 480
CCCCTCCCAG TCCTGGGGCC CACGACGGCG GCAGCAAGAC CTGCCCTCCA AGACCCCTGG 540
AGAGACCCTG AGCAGGAGAG AGGAAGCCCA GGGTTGAGGT GGGCTTGGGG CCTTCTGTCT 600
TTGTGAGGAC GCCCGGCCTG ACTGGGGCCC CAGGACTTAA CCCGCAAGAG GGGGTGCTAG 660
CTACACAGGA CCCCCAGAAA GCACAAGGGA CAGGCTCGCC ATGGCGTCTC CAGCCGCAGG 720
AGTCATGGGG CGCTGGACTC CCAAGGGGTC TGGTGAACCA TCCAGCAAGC AGCCGGAACC 780
ACCCCACCCC CGCCCCCAAA TCAGCAATTA ACCTAATAGC AACAGGTTCC TCAGAGCGCG 840
GCAGGCCCAC GCTTCAAAGG GTTAACTGCG GCCCCCAACC GCGGGAAGCC CCCTTCACCC 900
ACCCACCCCA GGCCAGCTGG GGGCCAGGTC TCCGCTGCAG AGGAGGAGAG GGCTTCCCAG 960
AGGCCGGCCT GGCTGGGCTG CAGCAGATTC TCAAGGCGGG ACCGTGGCCG AGGCCTCGAA 1020
AAGGGCGACC CGGAGGCAGA GCCGGCAGGG ACAGAGCCTG CTGGGGGAGG ACGCCCCAGA 1080
GCCCCAGCTC CGAAGCTGCC CCGCGAGGGC CCACGTGCGT CCCGGCCGCG 1130