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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-18770
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr17:4710520-4711060
Target genes
Number: 34
Name
Ensembl ID
MYBBP1A
ENSG00000132382
RP11
ENSG00000262519
SMTNL2
ENSG00000188176
ALOX15
ENSG00000161905
AC091153.4
ENSG00000235085
PELP1
ENSG00000141456
ARRB2
ENSG00000141480
MED11
ENSG00000161920
CXCL16
ENSG00000161921
ZMYND15
ENSG00000141497
TM4SF5
ENSG00000142484
VMO1
ENSG00000182853
GLTPD2
ENSG00000182327
PSMB6
ENSG00000142507
PLD2
ENSG00000129219
MINK1
ENSG00000141503
ATP6V0CP1
ENSG00000230201
C17orf107
ENSG00000205710
CHRNE
ENSG00000108556
GP1BA
ENSG00000185245
RNF167
ENSG00000108523
SLC25A11
ENSG00000108528
ENO3
ENSG00000108515
PFN1
ENSG00000108518
SPAG7
ENSG00000091640
RP5
ENSG00000262429
AC004771.1
ENSG00000203562
CAMTA2
ENSG00000108509
INCA1
ENSG00000196388
KIF1C
ENSG00000129250
AC109333.10
ENSG00000227495
AC012146.7
ENSG00000234327
ZNF232
ENSG00000167840
ZNF594
ENSG00000180626
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
SP2
MA0516.2
chr17:4710845-4710862
CGGGGGGCGGGACTGGG
-
6.18
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
4710730
4710800
Enhancer Sequence
GTGAGGGGGC CGGGAAGGGG CGCGCGGGGG TCCCGGGTCT CGGAAATCGG GCGGGGACGG 60
AACGGGCTCG GGCTGCGGGG CCTCCAGACT CAGTCGCACG CTCAGATTTC GGGATTTCTA 120
CCCCCGGCTG GGATCGCGTA ACTTCCTCAT TCCCGCCTGG ACCCCTGCCC CCGGCCCGCC 180
TGGCCTGGCG TGAGCCCCGT AGCCGCGCGC TCTCCGGACC ACCCAGGGCC GCTTCCCCGC 240
GCAGCTGCTG CGCCGCCCCA GGTCGGAGCC TTCCGGGCCT GGCTGGGTGT TCCCCGGGGC 300
TCTGGTTACG GGACGGGGCG GGGGGCGGGG GGCGGGACTG GGATTGTGGA TGAAGGACTA 360
AGGTAGGGGA TGGGGGCTCG AAGGGGTCGG TGGGGCGTTG CAAACTGGTC AGGCGTCATC 420
CGCGGGCGGT CAGGAGGCCG TGGGGGAAGA GGAGGATCTG GAAGAGATGG AGGACCTGCG 480
GGAGTTAGGA TGGGGGGCGG GTTCTGCAGG ACAGCTCGCC TCCCTGAGGC TTCCCAATGT 540