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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS098-27099
Organism
Homo sapiens
Tissue/cell
HSMM
Coordinate
chr19:10568780-10569780
Target genes
Number: 35
Name
Ensembl ID
SNORA70
ENSG00000200237
UBL5
ENSG00000198258
PIN1
ENSG00000127445
C19orf66
ENSG00000130813
ANGPTL6
ENSG00000130812
PPAN
ENSG00000243207
P2RY11
ENSG00000244165
EIF3G
ENSG00000130811
DNMT1
ENSG00000130816
S1PR2
ENSG00000175898
MRPL4
ENSG00000105364
ICAM1
ENSG00000090339
ICAM4
ENSG00000105371
ICAM5
ENSG00000105376
ZGLP1
ENSG00000220201
FDX1L
ENSG00000167807
RAVER1
ENSG00000161847
ICAM3
ENSG00000076662
TYK2
ENSG00000105397
MIR1181
ENSG00000221566
CDC37
ENSG00000105401
PDE4A
ENSG00000065989
KEAP1
ENSG00000079999
ATG4D
ENSG00000130734
KRI1
ENSG00000129347
CDKN2D
ENSG00000129355
AP1M2
ENSG00000129354
SLC44A2
ENSG00000129353
ILF3
ENSG00000129351
QTRT1
ENSG00000213339
DNM2
ENSG00000079805
TMED1
ENSG00000099203
C19orf38
ENSG00000214212
CARM1
ENSG00000142453
LDLR
ENSG00000130164
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
STAT3
MA0144.2
chr19:10568869-10568880
TTTCCCAGAAG
-
6.62
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
10568855
10569056
Enhancer Sequence
GGGTGGGGGC TCAGTAGGGG CAGGGCTGGA GGGGGTGGTC TCCTGGGACC CTGAGAAGGA 60
CTGGGCATTG GGTTATGTCT TAGGCCAGGT TTCCCAGAAG CAGAGCTTGA GATGAGGGTT 120
TGAGCCCATC TTGAGGCAAG CATGCTGGCT CTTTGTACCT CTGTATCATT CATTGCTTGG 180
GGGCCGTCCC CAGGGCTGGA CGTATCACCT CTTGCATGTA GCTCCTGTTG GGACTAGTCT 240
TCTGGAAATG CAGGCAGCTG TGAGCCTTAG CAGGCAACAC TCCCAGCTGC AGAGGGATTG 300
GTGTACACAG CAGTGACGCT AATCCAGACT GTGCCCCCAT AGTGTCCCCA ACAGTCCAGA 360
CCGGTGTTTC ACTCCTAGCT CTTCCAGGGG ACAGCGGCAG TGGAAGTGAT CCATCTTTGG 420
TGGCTCACTC AGCTGAGGCT TATTGTAACC CTCTTTGAGC CACCTCCTCC AGTGAATCTT 480
CCATTCAGTC ACCTGGCCTT TAGTTATTTA TTTTTATTTA TTTATTTATT TTGAGATGGA 540
GACTCGCTCT GTTGCCCAGG TTGGAGTGCA GTAGTGTGAT CTCGGCTCAA GGCAACCTCC 600
ACCTCCTGGG TTCAAGCAAT ACTCCTGCCT CACCCTCCTG ACTAGCCGGG ACTAAAGGCC 660
TGTGCCAGCA CACCTGGCTA ATTTTTGTAT TTTTAGTAGA AATGGGGTTT CACCATGTTG 720
ACCAGGCTGG TCTCGAACTC CTGGCCTCAA GTGATCCACC CGCCTTAGCC TCACAAAGTG 780
CTGGGATTGC AGGCGTGAGC CACTGCACCT GGCCAACTGG TGTTTATTAA GCAGCTACTA 840
TGTGCTGGCC CTTTTCTGAA TTTTGGAGAG ACATGGAAAA TAAGCCCTTC TTCCTTTCTC 900
CCCTGGGGCT CGTGAACAGC TTAGCTAAGA GGCTGAGCTG TGCTGGGGCC AGTCGTGCTG 960
GGTTCCTATC CTAGCTTTGC CACTTATGAG CTGCATGATC 1000