EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS133-13787 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:79622110-79623520 
Target genes
Number: 53             
NameEnsembl ID
CHMP6ENSG00000176108
CTDENSG00000263218
BAIAP2ENSG00000175866
AATKENSG00000181409
RP11ENSG00000262115
AZI1ENSG00000141577
AC027601.1ENSG00000260005
C17orf56ENSG00000167302
C17orf89ENSG00000224877
SLC38A10ENSG00000157637
LINC00482ENSG00000185168
BAHCC1ENSG00000171282
ACTG1ENSG00000184009
FSCN2ENSG00000186765
C17orf70ENSG00000185504
TSPAN10ENSG00000182612
NPLOC4ENSG00000182446
PDE6GENSG00000185527
CCDC137ENSG00000185298
C17orf90ENSG00000204237
HGSENSG00000185359
ARL16ENSG00000214087
RP13ENSG00000262049
MRPL12ENSG00000262814
SLC25A10ENSG00000183048
AC174470.1ENSG00000215621
FAM195BENSG00000225663
P4HBENSG00000185624
ARHGDIAENSG00000141522
ANAPC11ENSG00000141552
ALYREFENSG00000183684
NPBENSG00000183979
PCYT2ENSG00000185813
SIRT7ENSG00000187531
MAFGENSG00000197063
PYCR1ENSG00000183010
ASPSCR1ENSG00000169696
STRA13ENSG00000169689
LRRC45ENSG00000169683
RAC3ENSG00000169750
DCXRENSG00000169738
RFNGENSG00000169733
GPS1ENSG00000169727
DUS1LENSG00000169718
FASNENSG00000169710
CCDC57ENSG00000176155
SLC16A3ENSG00000141526
AC132872.1ENSG00000184551
CSNK1DENSG00000141551
SECTM1ENSG00000141574
HEXDCENSG00000169660
C17orf101ENSG00000181396
NARFENSG00000141562
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35763415chr1779622370hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HSF1MA0486.2chr17:79622694-79622707GAAAGTTCTGGAA-6.29
MYCNMA0104.4chr17:79623260-79623272GCCCACGTGGCC+6.27
MYCNMA0104.4chr17:79623260-79623272GCCCACGTGGCC-6.27
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr177962283079623001
chr177962255579622720
chr177962211279623200
Enhancer Sequence
GTTTATTGCT TTCTGCCTCT TGTCTGTGCT TTGCAGTTGG GGTGCTGTCA GTTCCCTTCA 60
CCCACTCACG GAGGCATCCC TGAGCCCCTC AGCACCATGA CGGGCACCCC GCAGTGCTGA 120
TGGAGAATGA CCCACAAAAT GGGGGGCAGG GTCCCCAGGC ACGGCGCCCC TGGGAAAGGG 180
GCCTGTCTCA GAGACTTGGT GCTGAGCTGT GAAGCCCTGC GTTCCCCAAC CCCACTTCAT 240
AGAGGGACAA GCTGGGGCTT GGGGACGGAG GGTGCCGGGC ATGTGTTCCC CCTGCTGGGG 300
GAATCACCAG GCCCTCTCTG TGTCTGGAGT CAGCTCGGGG AGCAGGGTCA CCCGCCTGGC 360
GTGGCGTGGC GTGGCTGAAG GGCCTCGGCC GCTCTGGACG AGATCAGTGT CCCTGCACTG 420
CTGCACAGGG TGGCCTCTCC TCCTCCTCTC CCTACAGCCT CTCCCCAGAT GCCCTAAGCC 480
CCAGTGACCT GGGCCAAGGG CAGTTCAGCT TCCCCTAAGC CTATTAACAG CAGAGGGGAA 540
TTCCTAATCT CCCATCGAGC TGCTGTCAGC TGCACATGCT GCCGGAAAGT TCTGGAAGGA 600
GGCACATGAC ACAGACAGGA GGGGCTGCTT GCCCGCACTG GATGCCCCAG GGACCACCTC 660
TTGGGGTCCC CTTTCCTGCC CCTGGTCTTT TTGGCTGGGA TTCCTGACTC CAGCCCTGGG 720
CTACTACCAG CTGTTTGCCG AGCTTCAGGC GTGAGAGTGA TCAGAAAGCA AGGGCAGGTG 780
GCCCATTTTG GGGACGCGGG CTCTGCAAGG GGTGCTGGGC ACCTGGGATT GGGGTGGACC 840
CTGCCATGGC ACCTTCCCTC ACTAAGGTTC AGCCTCTGTC CCCGGGACTG GGACCAGCAC 900
CAGCCTGTGC AAAACCAGCA CTCAGGAGCC CGGTGGTCCC AGCTGCTCAG ATCCCATGGC 960
ACCCAATCCT CATATCCTAG ATAGCACAGG CCCCGTCCAG CTGCTTCTCC AGCCCTGGGA 1020
CATGGGCTGT CCTGGGCAGC TCTGGGCCCT GATGGAGCTC CAACCATCAG ATGCCATCCA 1080
TGTGGAAACC GCTGCCTGCG CTGCCCTGGC CCGACCCAGC CTGTGACTGG CGTCCACTCA 1140
GGTCAGCTGA GCCCACGTGG CCTGAGGTTC CCAGACCATC ACTGGCCTGG GGATGGTGGA 1200
AGCACTGGTT ACCATGGGGG AGCAGAGGAG GAGGTTGGCT GGGAGTCCCC TCTGAATAAC 1260
AGGGTGGCGG GTAGGCATCT GCAGACCCAG ACCTCAGCCA CGGTGGTAAA AGCCTGTCAG 1320
CTCCCTCTGC CCCTTGGGTG ATGAGCAGAC CCCCACTGAC TCACTGGGGG AAGTGGCTGC 1380
CAGGAAAGAC AGCGGGGTTG GCCACTACTC 1410