EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS104-53475 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr7:518850-520340 
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6MA0463.2chr7:519750-519766CCTTCCTAGAAAGCGG-6.36
EWSR1-FLI1MA0149.1chr7:518860-518878AGGAGGAGGGAAGGAGGG+6.03
EWSR1-FLI1MA0149.1chr7:518902-518920AGGAGGAGGGAAGGAGGG+6.03
EWSR1-FLI1MA0149.1chr7:518852-518870GGAAGGGAAGGAGGAGGG+6.11
EWSR1-FLI1MA0149.1chr7:518894-518912GGAAGGGAAGGAGGAGGG+6.11
EWSR1-FLI1MA0149.1chr7:518906-518924GGAGGGAAGGAGGGAAGA+6.96
EWSR1-FLI1MA0149.1chr7:518868-518886GGAAGGAGGGAAGGAGGA+7.61
EWSR1-FLI1MA0149.1chr7:518864-518882GGAGGGAAGGAGGGAAGG+7.85
ZNF263MA0528.1chr7:518881-518902GAGGAAGGAGGAGGGAAGGGA+6.1
ZNF263MA0528.1chr7:518907-518928GAGGGAAGGAGGGAAGAGGGG+6.25
ZNF263MA0528.1chr7:518915-518936GAGGGAAGAGGGGAGGAGGGA+6.43
ZNF263MA0528.1chr7:518891-518912GAGGGAAGGGAAGGAGGAGGG+7.09
ZNF263MA0528.1chr7:518865-518886GAGGGAAGGAGGGAAGGAGGA+7.19
ZNF263MA0528.1chr7:518880-518901GGAGGAAGGAGGAGGGAAGGG+7.36
ZNF263MA0528.1chr7:518869-518890GAAGGAGGGAAGGAGGAAGGA+7.44
ZNF263MA0528.1chr7:518877-518898GAAGGAGGAAGGAGGAGGGAA+7.86
ZNF263MA0528.1chr7:518858-518879GAAGGAGGAGGGAAGGAGGGA+7.89
ZNF263MA0528.1chr7:518900-518921GAAGGAGGAGGGAAGGAGGGA+7.89
ZNF263MA0528.1chr7:518911-518932GAAGGAGGGAAGAGGGGAGGA+8.28
ZNF263MA0528.1chr7:518861-518882GGAGGAGGGAAGGAGGGAAGG+8.35
ZNF263MA0528.1chr7:518887-518908GGAGGAGGGAAGGGAAGGAGG+8.38
ZNF263MA0528.1chr7:518903-518924GGAGGAGGGAAGGAGGGAAGA+8.47
ZNF263MA0528.1chr7:518884-518905GAAGGAGGAGGGAAGGGAAGG+8.51
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_65447chr7:519986-521265Pancreatic_islets
SE_68824chr7:519586-521122H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7518964519189
Number: 1             
IDChromosomeStartEnd
GH07I000479chr7519587521265
Enhancer Sequence
AGGGAAGGGA AGGAGGAGGG AAGGAGGGAA GGAGGAAGGA GGAGGGAAGG GAAGGAGGAG 60
GGAAGGAGGG AAGAGGGGAG GAGGGATTGG TATGGTCAGT ATTTTTTATT TGTCCGTCTG 120
ATGGCCAGGT AGTGGTGTCT GATTGCGGCT TTACTTTATG TCCTCCTAAT GGCAACTGGT 180
GTGAAACATC CTTCCATTCG CTCCCGTGCT GTCAGCGGAT CTTCTTTGAT GAAACGTTAG 240
CTGATGTGGG AACAGCTACT CTGCCAGGCT CTGTGCCAGG CTCTGAAAAT CTGTGACAGA 300
GGCACATAAG ACATCCTTGC TCTCTTCATG GTGTTTACAA CCTCATGGGA GAGGCAAACA 360
CATAAATAAA CCTGGTGCCT CGAAGGTTTG GAAACAGAGC AACAGAGCTT TGGAAAGGGC 420
TGGGTGGGCC GCTCCTTCCC TTGTTGCCCC CTGCACACGA GACCCAGCAA AGCTCCAACT 480
CCTCGTCTGG GAACTGAGGG TGATACGGCA CCAACTGCGT CAGCGGCCCA GTCCACAGCA 540
CCAGGGGCTG GGAAGAGCTT TGTAAAACTT TGCTACCGTT GCCTCCACCA CCATCAGCTG 600
GAGGGTCACA GAAGGCGACC CCAGAGCCGG AGCCGGAGCC AAGCCTCAGC CACGAGTCAG 660
CCTCTGCCGG CTCTGAGGAC CCCCAGAGAG GGTGCCCCTC CCCAGTCATG GTTTCCAGGC 720
AGTGACGCAG GGTGGTCTGC ACCAGGCACC CTTTTCCAAG GATTTCAAGT TAGGTTTGTT 780
TTCCAGAAAG CCAGTACTGG GGCCAAGCCA GCTCCAGGTG AGACAGGCGC TGGGGGTGCT 840
GGGCTGGCCA CTCACATCCA CCCTCCCCCG GCCAGCGGGC AGGGAAGACC CCCCAACCTC 900
CCTTCCTAGA AAGCGGCCCC ATCTAAGAGA AGCCTTGAAA TCGGAGCGTC AGGAAAGGAG 960
TGTGGGGCTC AGCCCAGAGC TTTGTCAGCC TCACCAACAC GGGGTCCATC CAGAAGGCTC 1020
CCGGCCTCCC CGGCCCTTCC TGGCTTTTAG TCACTGCCGA GCTTGTGAGC ACTTGTGTGC 1080
TCCGGTGAAA CGGCCGAGGG CAAGAGCCCT GGGGGGCAGG GGCGCTGTTC TCAGTTCCTG 1140
GAGGCAGCAG AGTGGGAGGA AGAGGCCCTG AGATGCCGTC TCAGTGCCCC CACCCCCAGC 1200
TTAGGAGAGA GATTACCTGG CCAGGGCCAT CTGAGCAGCA AGATAGAGAA CCTCTCTCCC 1260
TCAGACCTAG GAAACAACAT TTGGGGTGCA ATCGCCCAGG GAACCCAAAA AGGAGCCCCG 1320
GGAGGTCCCA GCCCTAGACT CACACTGACA GGTGCTTCTC CAAAGGAGGG GGCTTGTGGG 1380
TGGGGGGCAG CCATGCAGAT GGGCCCAACA GCCCCTGGGA GCCAAGGCAG GGGCAGCTCA 1440
GGCAGGCAGG GCAAGGAGCG AGCGCAGGCC GAGGATCAGG GTGGGGCAGC 1490