EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-02102 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr11:267140-268560 
TF binding sites/motifs
Number: 41             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFKB1MA0105.4chr11:267820-267833AGGGGAATCACCG+6.25
ZNF263MA0528.1chr11:267295-267316AAGTGAGGAGGAGGGGGGAGG+6.01
ZNF263MA0528.1chr11:267456-267477GGAGGAGGGGGAGGGGCGAGG+6.04
ZNF263MA0528.1chr11:267553-267574GGAGGAGGGGGAGGGGCGAGG+6.04
ZNF263MA0528.1chr11:267281-267302GGAGGAGTGGGGAGAAGTGAG+6.09
ZNF263MA0528.1chr11:267524-267545GGAGCAAGGAGGGGGGAGGAG+6.09
ZNF263MA0528.1chr11:267545-267566CGAGGAGGGGAGGAGGGGGAG+6.12
ZNF263MA0528.1chr11:267462-267483GGGGGAGGGGCGAGGAGGGAG+6.23
ZNF263MA0528.1chr11:267484-267505GGAGGGGGAGGGAGAGGGGAG+6.27
ZNF263MA0528.1chr11:267353-267374GGAGGAGGGGGAGGAGCGAGG+6.28
ZNF263MA0528.1chr11:267308-267329GGGGGAGGAGCGAAGAGGAGG+6.2
ZNF263MA0528.1chr11:267501-267522GGAGGAGCAACGAGGAGGGGG+6.35
ZNF263MA0528.1chr11:267330-267351GGAGGAGCGAGGGGGAGGAGC+6.4
ZNF263MA0528.1chr11:267559-267580GGGGGAGGGGCGAGGAGGAGG+6.4
ZNF263MA0528.1chr11:267453-267474CGAGGAGGAGGGGGAGGGGCG+6.61
ZNF263MA0528.1chr11:267311-267332GGAGGAGCGAAGAGGAGGGGG+6.69
ZNF263MA0528.1chr11:267340-267361GGGGGAGGAGCGAGGAGGAGG+6.6
ZNF263MA0528.1chr11:267427-267448GGGGGAGGAGCGAGGAGGAGG+6.6
ZNF263MA0528.1chr11:267350-267371CGAGGAGGAGGGGGAGGAGCG+6.79
ZNF263MA0528.1chr11:267298-267319TGAGGAGGAGGGGGGAGGAGC+6.81
ZNF263MA0528.1chr11:267518-267539GGGGGAGGAGCAAGGAGGGGG+6.87
ZNF263MA0528.1chr11:267359-267380GGGGGAGGAGCGAGGAGGGGG+6.88
ZNF263MA0528.1chr11:267376-267397GGGGGAGGAGCGAGGAGGGGG+6.88
ZNF263MA0528.1chr11:267393-267414GGGGGAGGAGCGAGGAGGGGG+6.88
ZNF263MA0528.1chr11:267410-267431GGGGGAGGAGCGAGGAGGGGG+6.88
ZNF263MA0528.1chr11:267550-267571AGGGGAGGAGGGGGAGGGGCG+6.96
ZNF263MA0528.1chr11:267535-267556GGGGGAGGAGCGAGGAGGGGA+6.97
ZNF263MA0528.1chr11:267327-267348GGGGGAGGAGCGAGGGGGAGG+7.1
ZNF263MA0528.1chr11:267476-267497GAGGGAGGGGAGGGGGAGGGA+7.1
ZNF263MA0528.1chr11:267362-267383GGAGGAGCGAGGAGGGGGGAG+7.33
ZNF263MA0528.1chr11:267379-267400GGAGGAGCGAGGAGGGGGGAG+7.33
ZNF263MA0528.1chr11:267396-267417GGAGGAGCGAGGAGGGGGGAG+7.33
ZNF263MA0528.1chr11:267413-267434GGAGGAGCGAGGAGGGGGGAG+7.33
ZNF263MA0528.1chr11:267343-267364GGAGGAGCGAGGAGGAGGGGG+7.3
ZNF263MA0528.1chr11:267430-267451GGAGGAGCGAGGAGGAGGGGG+7.3
ZNF263MA0528.1chr11:267487-267508GGGGGAGGGAGAGGGGAGGAG+7.42
ZNF263MA0528.1chr11:267521-267542GGAGGAGCAAGGAGGGGGGAG+7.56
ZNF263MA0528.1chr11:267481-267502AGGGGAGGGGGAGGGAGAGGG+7.64
ZNF263MA0528.1chr11:267472-267493CGAGGAGGGAGGGGAGGGGGA+7.84
ZNF263MA0528.1chr11:267440-267461GGAGGAGGGGGGGCGAGGAGG+7.85
ZNF263MA0528.1chr11:267538-267559GGAGGAGCGAGGAGGGGAGGA+8.21
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_16128chr11:267513-270474CD4_Naive_Primary_7pool
SE_21864chr11:267477-270412CD8_Naive_7pool
SE_22226chr11:267090-270596CD8_Naive_8pool
SE_52556chr11:267492-273530Small_Intestine
SE_61820chr11:266425-273086Toledo
SE_62809chr11:266595-290841Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11267611268165
Number: 1             
IDChromosomeStartEnd
GH11I000266chr11266649273455
Enhancer Sequence
CAGCTGCTCC CACTGGGTGC CAGGCCCTGT TCTAGGTGCT TGGGAAGTGT CAGTGAGCAA 60
AACAGACAAA TCTCCAGCCC ACATGGAGGG GTGAGGAGCA AGGAGGAGGA GTGAGGAGCA 120
AGGAGGAAGG GCAAGGAGCG AGGAGGAGTG GGGAGAAGTG AGGAGGAGGG GGGAGGAGCG 180
AAGAGGAGGG GGAGGAGCGA GGGGGAGGAG CGAGGAGGAG GGGGAGGAGC GAGGAGGGGG 240
GAGGAGCGAG GAGGGGGGAG GAGCGAGGAG GGGGGAGGAG CGAGGAGGGG GGAGGAGCGA 300
GGAGGAGGGG GGGCGAGGAG GAGGGGGAGG GGCGAGGAGG GAGGGGAGGG GGAGGGAGAG 360
GGGAGGAGCA ACGAGGAGGG GGGAGGAGCA AGGAGGGGGG AGGAGCGAGG AGGGGAGGAG 420
GGGGAGGGGC GAGGAGGAGG CGGGAGGAGC TGGACAGGAC ATCGTGCCAG CCCGAGGGCG 480
GAATGAACTT CAGAGAAGTT TGAGAGCAAA AGGTGCTTTG CTGCTGTTAG ACCCTGAAAT 540
TCCACGGGTC CCTGGACAGT TTTGGGAGCC GGGAGGGTGA AGAGAGTGGA TCAAGCTTCG 600
TGGGGTGGAC CCGGAAGAGA TGGGGCAGTG AATGGTTCTG GGGGACTGCG GGAGCCTCCG 660
GGGAGTGATT TTTTGCCCTG AGGGGAATCA CCGCAGCGGG GACAAGGCTG GGGGAAAACA 720
CTTCCTTCTG CAAGGGCACT GCTGAGCCTC ACTTGCTGGA GCTTGCACTG TGCAACGGTA 780
AATTCACGTT GTGTGCCCTC ACCTGAGCTT CTGATGAGGA CGCTGGAGGG CTTGGCCCTT 840
TGAAGTCCTC ACCTGTCCCT CCTTGGGCTG GGGGTGGTGA CTAGGAGGGG CTGCACGGCT 900
GCTGCCCGGG TTGGTCCCGG CCATCCCAGC TCCCTGGTAA ATAGGCTTCT CAAACTAGGA 960
TACCTGGGCC TTGGGCGTTA CCTGCAAACC CTGTTCCTCG CTCTAGTTCC CCACTTCCAT 1020
CCCTCCTCTT GCCTCAGCCC TTCTCATCTC ACACGCCACA TGGGATCCAC CCTTTTTACG 1080
CATGTGCAGA GCGTGGCCCC TCTCTGATTC CCTTCCCCTC AGGAGAGCCG GACGTCTCCC 1140
TCCCTCACAC CCTCCCCAGC CCCACAGCAG CCCAGGGAGC CTTGCCCGCT CCTCGGCCCC 1200
CCTGGCTCTC CCAGCCACCC AGGCCTCCTG TGTCCTGAGT GGGCCAGCTC CTGCCAGACC 1260
ACGGCCCTGC CCTGCACCTG ACTGCGTCCC CACCGCGGAC CTGCCCCCTC GTTTATTCTC 1320
CTCTCTCCGC TCTGCTCTGT CCTTGGCACT GTTTTTGTTT GTTTTTTGTT TTTGTTTTTT 1380
GAGACGCAGT CTCGCTCTGT CACACAGGCT GGAGTGCAGT 1420