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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS197-08625
Organism
Homo sapiens
Tissue/cell
ZR75-30
Coordinate
chr17:4710520-4711060
Target genes
Number: 28
Name
Ensembl ID
SPNS2
ENSG00000183018
RP11
ENSG00000262519
SMTNL2
ENSG00000188176
ALOX15
ENSG00000161905
PELP1
ENSG00000141456
ARRB2
ENSG00000141480
MED11
ENSG00000161920
CXCL16
ENSG00000161921
VMO1
ENSG00000182853
GLTPD2
ENSG00000182327
PSMB6
ENSG00000142507
PLD2
ENSG00000129219
MINK1
ENSG00000141503
ATP6V0CP1
ENSG00000230201
CHRNE
ENSG00000108556
GP1BA
ENSG00000185245
RNF167
ENSG00000108523
SLC25A11
ENSG00000108528
ENO3
ENSG00000108515
PFN1
ENSG00000108518
SPAG7
ENSG00000091640
RP5
ENSG00000262429
CAMTA2
ENSG00000108509
INCA1
ENSG00000196388
KIF1C
ENSG00000129250
AC109333.10
ENSG00000227495
SLC52A1
ENSG00000132517
USP6
ENSG00000129204
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