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

TagContent
EnhancerAtlas ID
HS133-13797 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:79815480-79817050 
Target genes
Number: 54             
NameEnsembl ID
CTDENSG00000226137
BAIAP2ENSG00000175866
AATKENSG00000181409
RP11ENSG00000262115
AZI1ENSG00000141577
AC027601.1ENSG00000260005
C17orf56ENSG00000167302
C17orf89ENSG00000224877
SLC38A10ENSG00000157637
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
C17orf62ENSG00000178927
NARFENSG00000141562
FOXK2ENSG00000141568
RAB40BENSG00000141542
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GRHL1MA0647.1chr17:79816391-79816403AGAACCGGTTTT-6.07
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_00970chr17:79816430-79818673Adrenal_Gland
SE_15245chr17:79815930-79818769CD4_Memory_Primary_7pool
SE_19571chr17:79815950-79820127CD4p_CD25-_Il17p_PMAstim_Th17
SE_23250chr17:79816043-79818576Colon_Crypt_1
SE_23797chr17:79816391-79818542Colon_Crypt_2
SE_24729chr17:79816237-79819941Colon_Crypt_3
SE_26662chr17:79815242-79820051Esophagus
SE_31589chr17:79816008-79819974Gastric
SE_41652chr17:79816124-79818625LNCaP
SE_42720chr17:79816249-79820348Lung
SE_45366chr17:79816710-79820125NHLF
SE_47521chr17:79816225-79817441Pancreas
SE_50418chr17:79816096-79820108Sigmoid_Colon
SE_52468chr17:79815210-79820391Small_Intestine
SE_53575chr17:79815920-79820198Spleen
SE_57575chr17:79816430-79818538VACO_503
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177981550879815942
chr177981607379816158
Enhancer Sequence
CCACCTGACT CCCGCGCCTC CTAACTTATC CCAGGCGTTT CGGGAGTTCT CGCCAATGGC 60
CCACCCTCCA TGCCTCCCAG ACCAGGAAGA AGATGACACA CTTTTATGCC ACCAAAGGCG 120
GTCAACTGAC AGGAAAGAAA CTTCCTCCTC CTGGGAGACT GAGGCTAAGG AATGATGCCT 180
CTCCTTTTTC CCTCCTAGAA CTTGACTCCC TGGTCCGAAT CGGGAAAACC CCATTCAGAT 240
GTAGAAGGAT TCCACCAGTG CTAACAAGAC GGTCACCAGT GACAAGTGGA TTTAGGAGTG 300
CTCATCTCAT CTGCAAACCT GAGTGTTAGT GACAGAACCA CGGTGACTTT GGACAGAGCA 360
CTTCCCGTTC CAAAAGTGAA CATGAGTAAA AAATGAGAAC ATCAATCACG CCTGTAATCC 420
TAGCACTCTA GGAGGCCGAG ACGGGTGGAT CACGAGGTCA CGATCGAGAC CATCCTGGCC 480
AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT AGCCAGGCGT GGTGGTGCAC 540
ACCTGTAGCC CCAGCTACTC AAGAGGCTGA GGCAGGAGAA TCACTTGTAC CCGGGAGGCA 600
GAGGTTGCAG TGAGCAGAGA TCGCACCACT GCACGACAGA GCGAGACTGT CTCAAAAAAA 660
AAAAAAAAAA AAAAAAAAGG AAACATCAAA ACAGCCAAGT GAGAGGCAAC CACAGAGCTG 720
CTGCCACTAG AACAGGACAG GGCACACCTG CTTAAGGGGA CAAAAGGAAA CATCAAAACA 780
GCCAAGTGAG AGGCAACCAC GGAGTTGCTG CCACTAGAAC AGGACAGGGC ACACCTGCTT 840
AAGGGGAGAA CCCTGCTAAC ACTGGAATGA GCTGCTTTCG GGCTACCCAC CATGAGCATC 900
TGACATGCCA CAGAACCGGT TTTATAGACG AGTTTTCTTT TGCCACCGTC ACTGATCTGG 960
CTACACAGGG GCTCGGCCTC CACTACGGCA GCTTCAGAGG CGGCAGACGA GCAGCTGAGG 1020
GCCCGTGCTA CAGACGGAGC AGGGCGGGCT TGGATTCGAG GTCTGCTACC GACAGGCTCG 1080
ATGCTGTTAC TCAGCTGCTC TAAGCCTCAG CCCTTTGTCT GGGAAAAGCC CGCCTCACAG 1140
AGAGGATGCG AGGAGAAATC ACGCAAGCAC GTGACGCGGC AGCTGGCACG CTACACACGA 1200
CAGCTAGCAG GTGTCACCCC GAGAGCTACA GCCATGCTGC TGCTCCTAGG AACAGGGGGC 1260
AGCACAAACA GCCCATGTGG CCAGAAAGGC ACCAGTCTCC CTCTCCTCGC TGGTCAGTCT 1320
CCAAACAGAC CTCAGCCAGC CGCCCCCAGG ATGGCACCAG ACAAGACAGG TTCTCCATTC 1380
GAAGGTTCTT CCAGGATGAA AACTCCTCAC AAGACCCTCA GGGCACAAGT GGACAGAGAA 1440
CCCGGCCTGA GGAACGGGAT CCCTCCAAGC CTCTGGAACC CGGCCTCCCC ACCGCTCAGA 1500
CAGCTGCCCC TGCCCTTCCA AGTCGGCAGG CCAGTCCCTC TCTAAAGACA GTTCAAGGGC 1560
AGTGCCACAG 1570