EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS080-17526 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr19:45221500-45222970 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs79638902chr1945221767hg19
rs73037426chr1945222789hg19
TF binding sites/motifs
Number: 27             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:45221677-45221698AAAAAAAAAAGGAAAGTGAGA-6.12
ZNF263MA0528.1chr19:45222336-45222357AGAGGAGCATGGAGGAGGGGG+6.08
ZNF263MA0528.1chr19:45222167-45222188GGAGGTGGGAGAGAGAGAAAA+6.32
ZNF263MA0528.1chr19:45222262-45222283GAAGAAGGAGGTGGAGGAGGT+6.49
ZNF263MA0528.1chr19:45222146-45222167AGAGCAGGGAGGAGGGAAGGG+6.53
ZNF263MA0528.1chr19:45222193-45222214AAAGGAGGAAAGAGAAGGGAG+6.54
ZNF263MA0528.1chr19:45222164-45222185GGGGGAGGTGGGAGAGAGAGA+6.59
ZNF263MA0528.1chr19:45222153-45222174GGAGGAGGGAAGGGGGAGGTG+6.62
ZNF263MA0528.1chr19:45222311-45222332GGAGAAGAAAGAGGAAGGAGA+6.67
ZNF263MA0528.1chr19:45222305-45222326GGAAGAGGAGAAGAAAGAGGA+6.89
ZNF263MA0528.1chr19:45222259-45222280GGAGAAGAAGGAGGTGGAGGA+6.95
ZNF263MA0528.1chr19:45222308-45222329AGAGGAGAAGAAAGAGGAAGG+6.95
ZNF263MA0528.1chr19:45222299-45222320TGGGGAGGAAGAGGAGAAGAA+7.09
ZNF263MA0528.1chr19:45222280-45222301GGTGGAGGAGGAGGAGGGATG+7.12
ZNF263MA0528.1chr19:45222289-45222310GGAGGAGGGATGGGGAGGAAG+7.1
ZNF263MA0528.1chr19:45222293-45222314GAGGGATGGGGAGGAAGAGGA+7.29
ZNF263MA0528.1chr19:45222265-45222286GAAGGAGGTGGAGGAGGTGGA+7.34
ZNF263MA0528.1chr19:45222216-45222237GGAGGAGGGTGGAGGAGGGAG+7.3
ZNF263MA0528.1chr19:45222223-45222244GGTGGAGGAGGGAGAAAAGGG+7.44
ZNF263MA0528.1chr19:45222286-45222307GGAGGAGGAGGGATGGGGAGG+7.46
ZNF263MA0528.1chr19:45222283-45222304GGAGGAGGAGGAGGGATGGGG+7.72
ZNF263MA0528.1chr19:45222302-45222323GGAGGAAGAGGAGAAGAAAGA+7.84
ZNF263MA0528.1chr19:45222268-45222289GGAGGTGGAGGAGGTGGAGGA+7.86
ZNF263MA0528.1chr19:45222271-45222292GGTGGAGGAGGTGGAGGAGGA+8.42
ZNF263MA0528.1chr19:45222226-45222247GGAGGAGGGAGAAAAGGGGAA+8.59
ZNF263MA0528.1chr19:45222277-45222298GGAGGTGGAGGAGGAGGAGGG+8.87
ZNF263MA0528.1chr19:45222274-45222295GGAGGAGGTGGAGGAGGAGGA+9.35
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_23197chr19:45221566-45222864Colon_Crypt_1
SE_23877chr19:45221674-45222170Colon_Crypt_2
SE_23877chr19:45222271-45222660Colon_Crypt_2
SE_26699chr19:45221482-45222244Esophagus
SE_31568chr19:45221350-45222937Gastric
SE_34750chr19:45221155-45223153HeLa
SE_47531chr19:45221530-45222127Pancreas
SE_47531chr19:45222206-45222953Pancreas
SE_53360chr19:45220837-45222992Spleen
SE_56197chr19:45221543-45222371u87
SE_62704chr19:45221152-45271677Tonsil
SE_65330chr19:45221160-45223183Pancreatic_islets
Number: 1             
IDChromosomeStartEnd
GH19I044717chr194522095845223023
Enhancer Sequence
CACTTCAACT TCTGCCTCCC GGGTTCAAGC TATTCTCGTG CCTCAGCCTC CCGAGTAGCT 60
GAGATTATAG GCGCCTGCCA CCACGCCCGG AAAGCAGAAT TTTTAACAAA GGGTCTAGGG 120
AATTTTTGTT AGCTGGGAAA TTGGGGGACT CAGATGCAGA GACTGTTTGA CAAAAAAAAA 180
AAAAAAAGGA AAGTGAGACA CCACAAAGAA GAGGAGGTGA CTTGCCCAAA GTTACTCAGC 240
CAGAAAGGAG CAGGGCCAGG ATTTGGCCCA GAGAGGAGCA GGAACTAGTC CAGGGTCACG 300
GAGCAGGTTT CAGATGAGGG CTGAGACTGG CGCCCTTCAC TGTCCCGAGC AGGTCCGCAG 360
TGGCTCCTCG CCTCCCCCAT TAAGCCACGA AGCTCTGGTG GCGCCGGGGG CCCTCAGGTT 420
CCACCAGCCG TGGGTGGGGA GGCAGACTAT ACCCCTCTCA GCCCCAATCC CTTCCCCCTC 480
ACCCAAGCTG CCTTTTCTCA AATAACCACA CTGGGGAGGG CAGGGAGTCG GGGTGACCTT 540
GAGGCCAGAA TACACAATGG CCCAGTCCCT CTCTGGAGCC CTGCCAGGGA GAGGAAGGAA 600
GCCTGCCCTG TTTTTTTCCA TGGACTGGAA TGTTGATTCA GGATGGAGAG CAGGGAGGAG 660
GGAAGGGGGA GGTGGGAGAG AGAGAAAAAA AAAAAAGGAG GAAAGAGAAG GGAGTAGGAG 720
GAGGGTGGAG GAGGGAGAAA AGGGGAACAG GGCAAAAAGG GAGAAGAAGG AGGTGGAGGA 780
GGTGGAGGAG GAGGAGGGAT GGGGAGGAAG AGGAGAAGAA AGAGGAAGGA GACAGAAGAG 840
GAGCATGGAG GAGGGGGTGC CAAGGCCAGA CTTTGGGAAC CAAGGAATGA GCCCCATCAG 900
CTTCAGCCCA TCCTGACACA CAGTGTGGAG AATGCAGAGT CCAGAGAGGG CACCCCAAAT 960
CTGCAAGGTT GCACAGGACC AGTGCAGCCA AAGGGCCTCA CCTGTGCGGC TGCCTCCTGC 1020
CTGTGGAGGC AGGAGCTCCC TGAGTCCTCA CAGAGACCTT CAGACGCAGG TGTCATGTTG 1080
CATGTTTCTC AGAAGAGGAG ACTGAGGCGC CCAGAGGTAA AGCCACATTT CCTGGAGCAT 1140
CTCCCCTTCG GATCGGACTC CAGGGTCCTT ACAATGGTCT GCAGGCCTGC CCGCCCGTCA 1200
TTCCCTTCAT CATCTCCTCT CCTTCACTCA CTGCAGCCAC CTGGCCTCCT GGCTATTGTT 1260
TGAACAAATC AAGCAACTCC TTCCTCGGGG CCTTTGCACT GGCTGTTCCC GCTGCCAGGA 1320
ATTTCCTTCC CTCAGACACC TGCATCACTC CAGTCAGGTC TCTGCTCAGA TGTCACCTCC 1380
TCAGAGGGGT CCCCTGTACA CCCAAAGTTG TCTGGCTTTA TTCTTCACAG CATTTATCAC 1440
TTACACAACT AACCCAACTT TACATTTTAT 1470