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

TagContent
EnhancerAtlas ID
HS133-13861 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:80202710-80203850 
Target genes
Number: 54             
NameEnsembl ID
C17orf56ENSG00000167302
RP11ENSG00000263154
BAHCC1ENSG00000171282
ACTG1ENSG00000184009
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
TEX19ENSG00000182459
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
FOXK2ENSG00000141568
WDR45LENSG00000141580
RAB40BENSG00000141542
FN3KRPENSG00000141560
FN3KENSG00000167363
TBCDENSG00000141556
ZNF750ENSG00000141579
B3GNTL1ENSG00000175711
AC139099.3ENSG00000232938
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat4MA0518.1chr17:80202998-80203012TCCCTTCCTGGAAA-6.2
ZNF263MA0528.1chr17:80202897-80202918GGAAGACGGGAAGGAGGAAGA+6
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_01443chr17:80202973-80205606Adrenal_Gland
SE_05640chr17:80198836-80203278Brain_Cingulate_Gyrus
SE_05640chr17:80203484-80204895Brain_Cingulate_Gyrus
SE_09650chr17:80203628-80206038CD14
SE_23259chr17:80203384-80205729Colon_Crypt_1
SE_24820chr17:80203369-80205663Colon_Crypt_3
SE_27039chr17:80203692-80206532Esophagus
SE_34714chr17:80203706-80205421HeLa
SE_41839chr17:80202354-80203085LNCaP
SE_42636chr17:80203422-80205920Lung
SE_47252chr17:80186949-80206249Panc1
SE_48220chr17:80203331-80206149Psoas_Muscle
SE_50338chr17:80203494-80205793Sigmoid_Colon
SE_52974chr17:80203610-80205797Small_Intestine
SE_54984chr17:80192319-80203024Stomach_Smooth_Muscle
SE_54984chr17:80203263-80206952Stomach_Smooth_Muscle
SE_65283chr17:80195707-80206124Pancreatic_islets
Number: 1             
IDChromosomeStartEnd
GH17I082246chr178020364580205825
Enhancer Sequence
TCGGAGCCAA AGCACAGGAG AAGGTCAGCA TGGGGCTGGG GGAGCCGGCC AGGCAGATAC 60
CACAGTGACG GTGCTGGGCA GGGAGGGGAC GCACCGCCAC CGCCTAGCCC CAGTCTAGAC 120
GCCTGCGTCC CCCGCCACGC ACAGGGGCCT CTGTGGCTGG GACACGTGCT CAGCAGAACG 180
AGTGACAGGA AGACGGGAAG GAGGAAGAGG CATGCAAGCA AGGTGCCCGC GGAGCCGGGC 240
TCGGCAGGGT CGAAGGATCC GAGTGGAGCG GAGACGGGTG CTCCTGCCTC CCTTCCTGGA 300
AAGGAACCTG GTGTTTGAAA ATGGGTACCC CTCTCAGGGA AGACATGAAA AGCAGTTCCT 360
GTCAACACAT TTCCAGAGTG TGCACAGTGT GAAAACTGCA GCGGGTCTCC CAGCGGCACA 420
GACCCGACAG AAGCGCAAGC CCCTGCTGGA AGGAGCCGCC GAGCGCGCGT GGCCGCCGAG 480
GAGGGAGCAC AGCGTGGACG CCGGCCATGC ACCGACGGCG GGGAGTGAGT GGGCTGCGGC 540
TGGAGGAGTT AATACAGACG AAGCTGCGTG GACAAGACGG CTGGGCAGAG ACCAAGTGTG 600
AAAAGAAACA CAAAACAAGG ACAGAGATAA ATGAGACAGG AAGAGAGAGG CGACTAGAAA 660
AGCTGGCATG GCAGAGACTG CCCAGAGTGT GGCGCAGCAA GAGCTTAGGA GCCCCCAACA 720
CCAAGCGTGG AGCCACCCAG CTGAGCAGGA CACAGACGCC CCTCCAGGCA CGGCCGACCG 780
CAGACAAGGC AACTCAAGTG CTCGGGGCAC CCGCCTTGCC ACTCCTGCCT CACGGGTGGG 840
CACCCAGGAC AGGAGGAGAG CAACGGCACA CGGAACGCAG TCACGGGGAG GCCACAGGCC 900
AACAGGATGG TCTCCTGGGG TCACTCTGTT CCAAAGCTCT CTGTGGACAG CCTCCCCCCA 960
AGACTGGGCA GCGGACTGCC GCCGCTCTGC ACCCCACAAG AAGAACAGAG CAGAAGAAGC 1020
CTCACTCTAC CTCCAGCACC TGGCATGCAA GCCCAGCCCA CCTGCAAGCT CCCATGGGTG 1080
GGGCATGGTG GCTCCCACCC ACCTGGCGCT GCTGCCTGGC GCCCGCCACG CGCACACTCA 1140