HOME
BROWSE
DOWNLOAD
LINKS
HELP
EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-14435
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr19:581590-582300
Target genes
Number: 39
Name
Ensembl ID
WDR18
ENSG00000065268
HCN2
ENSG00000099822
FGF22
ENSG00000070388
RNF126
ENSG00000070423
FSTL3
ENSG00000070404
PALM
ENSG00000099864
AC004449.6
ENSG00000261204
ARID3A
ENSG00000116017
R3HDM4
ENSG00000198858
MED16
ENSG00000175221
PTBP1
ENSG00000011304
LPPR3
ENSG00000129951
CFD
ENSG00000197766
PPAP2C
ENSG00000141934
MIER2
ENSG00000105556
C2CD4C
ENSG00000183186
SHC2
ENSG00000129946
TPGS1
ENSG00000141933
CDC34
ENSG00000099804
BSG
ENSG00000172270
GRIN3B
ENSG00000116032
C19orf6
ENSG00000182087
CNN2
ENSG00000064666
ABCA7
ENSG00000064687
HMHA1
ENSG00000180448
POLR2E
ENSG00000099817
GPX4
ENSG00000167468
SBNO2
ENSG00000064932
STK11
ENSG00000118046
C19orf26
ENSG00000099625
ATP5D
ENSG00000099624
C19orf24
ENSG00000228300
MUM1
ENSG00000160953
AC005330.1
ENSG00000240846
AC005329.7
ENSG00000248015
DAZAP1
ENSG00000071626
C19orf25
ENSG00000119559
REEP6
ENSG00000115255
MEX3D
ENSG00000181588
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
Zfx
MA0146.2
chr19:581999-582013
CGGGGCGAGGCCTG
+
6.67
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
581834
581994
Enhancer Sequence
GGTGAGCCGT CTGCCCTCCT GCCCACATGC CCTGCTCTCG GGGTGGCCCA GGGCCACTCC 60
TGGTCCGTCC CTGCCAGCCC CACCGCTGAC CCAGAGCTTG GAACTGAGGA GCCCCAGGCA 120
GGGAGTTGAT GGGACCCCGA AAGAAAGTGT GGGATGGAGG GTCTAGCCCC GGGCAGCTGC 180
GGCTCAGTGG GCAGCGGGAC CCCGGGAGGA GGAGGCGGCA CCTCCGCCCC ACAGCCTCAC 240
CCGGCCCTTC CCTCCCGCTC ACTTGGCTGC AAGCCAGTGT CCTCCGTGGT GAGCCGGCCC 300
TTGCTGCTCT GCATGATCAG GCTCGGGAAC CTGAGGTCAG CCATGCTGTG CTCCGGCAGC 360
CCCTGCCTGC CTCCTCGCGG AGCCCTTCTG CCCCTTGGGC TGCGTGTGCC GGGGCGAGGC 420
CTGTGTGGGG CCTGTGATGG CAGCTCCTGG AAAACGCTGT GGGGCAGGGG TGAGGCCCAC 480
GAGGCCATGG GGACAGCTCA CCATGGGGAG CACACCTGCA GGTGGGGAGG GCTGCCTTTC 540
CCCACAGCAC TCAGAAGATG CACGTGGCCG GGGCTGATGA GCTGCCCCGA GCCACCCCTG 600
GGGGTCACTG AGGGCAGGGC TGGCAGCACA GATGCCCCTG CTCGGGGCCT GAGTGGGGCC 660
AGTGCTGACA GGCTGTCCTC TCGTCCTCTT TTTCATGGCG GCGGTCCTTC 710