EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-21727 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr20:351640-354640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6051520chr20351944hg19
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:354010-354028GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr20:352764-352782AAAAGGAAGGCAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr20:354002-354020GAAAAGAGGGAAGGAAGG+7.36
EWSR1-FLI1MA0149.1chr20:352788-352806GGAAGGAAGGAAGGTCAG+7.43
EWSR1-FLI1MA0149.1chr20:352772-352790GGCAGGAAGGCAGGCAGG+7.44
EWSR1-FLI1MA0149.1chr20:352780-352798GGCAGGCAGGAAGGAAGG+7.74
EWSR1-FLI1MA0149.1chr20:354006-354024AGAGGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr20:354018-354036GGAAGGAAGGGAGGGAGG+8.13
EWSR1-FLI1MA0149.1chr20:352768-352786GGAAGGCAGGAAGGCAGG+8.19
EWSR1-FLI1MA0149.1chr20:352776-352794GGAAGGCAGGCAGGAAGG+8.42
EWSR1-FLI1MA0149.1chr20:352784-352802GGCAGGAAGGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr20:354014-354032GGAAGGAAGGAAGGGAGG+9.42
MEF2CMA0497.1chr20:354268-354283GGGATAAAAATAGCA+6.34
NFE2L1MA0089.2chr20:351815-351830CCTGCTGAGTCACAG-6.03
NFE2L1MA0089.2chr20:352804-352819AGGTGACTCAGCAAT+6.89
Nfe2l2MA0150.2chr20:351817-351832TGCTGAGTCACAGTC-6.55
ZNF263MA0528.1chr20:354007-354028GAGGGAAGGAAGGAAGGAAGG+6.24
ZNF263MA0528.1chr20:354011-354032GAAGGAAGGAAGGAAGGGAGG+6.76
ZNF263MA0528.1chr20:354019-354040GAAGGAAGGGAGGGAGGGAAA+6.97
ZNF263MA0528.1chr20:354015-354036GAAGGAAGGAAGGGAGGGAGG+7.19
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_15234chr20:349357-357936CD4_Memory_Primary_7pool
SE_21243chr20:349857-354719CD8_Memory_7pool
SE_34190chr20:350231-354605HCC1954
SE_35196chr20:349088-355405HeLa
SE_39865chr20:350235-356875K562
SE_56861chr20:351592-352091VACO_400
SE_56861chr20:352106-353254VACO_400
SE_56861chr20:353349-353789VACO_400
SE_57497chr20:351576-351999VACO_503
SE_57497chr20:352033-353210VACO_503
SE_64879chr20:352146-354815NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr20353974354548
chr20352488352859
chr20352123352173
chr20352269353175
chr20353462354638
Number: 1             
IDChromosomeStartEnd
GH20I000368chr20349178357150
Enhancer Sequence
GGCCTGGCTT CAGGACTGGA GCTGCTTTAC CTTAAAGGGC CTGTCGGACC ACATGTACCA 60
TCCCACATCC CAGACCAGCT CTGCACTCAG AGACTGTCCC TCTCTCCCTG CCCTGACTCA 120
GCACCTGCCT GGCCTATCCC CAGTGGTCCT GCCTGACTCT ACCTCCAGCT CCCACCCTGC 180
TGAGTCACAG TCAGGCTGGT CAGGGGGCTG TCCCATGTTC AGTCCAGCCC CTCAGCCTTC 240
CTCGACCTGG GGGGGTATGG GGAGCAGCCC AGAGGGGAGG GGAGCAGGTG CCAAGCTCTT 300
GATTCCTGTG CCTGAGCACT GCCCTGTTGA GACCAGAGAG AGAATCTATG GCTAGGGTAT 360
CTGGGGCTAC AGTTGGGGTT TATCTGGGGC CTGGGGTCAC ACATGATGGA TTAGAGCTAA 420
ATCTATCTCC AGGGTTATAA CTCAATCAGG AGCTAGAATT CAAATTCAGT TTATGGATCA 480
TGTGGGGAAA AAGTGACCAA GACACCGTTC AGTTTGGGAC CTGTGTCGGC GTTAGCTGTG 540
GCTACGGCCC AGGGCTTAGT GATCACAGGT CAGACCATGT TCAAGGTTTC AGGCCAGAGT 600
GCAGTTGAAG TGCAAAGTCA GGCAATAGGG TTCACCCTAG GACCACAGTC AAGGATCTGG 660
GTCAGTTAGT GTCCAGGGCA CTGGCCTTGT CTCCTCTTCT TTGGGAGAGA AGCCAGGTGG 720
ATGAGTTGGA TCTAAATGTC CTGAGGAGCA ACTTCCAGCT CAAGTTCCTT CACCCAGGCG 780
GCCTAAGCCC TCTCAGCACT GGCCCCAAAG CCTTCCTTCA TCCCTCAACT TCCTCCATCA 840
CTCCCTGACA GCCTGGCCTT GCTCAGTGTC CCTCGCAAGG CTGAACAGTC CTCATTCTGG 900
CACCTCAGGG GACAGGGTAG GGGTGGGGAC TATGGGACAG GGCTCAGTGC TGGACCCAGG 960
AGGGCGCCTT GCGCAAGGTT TTCTGATGCA ACTGGCTGAG TGCTTCAGCA TTCCACCCCC 1020
ACCCCCCAAG CTTTTCTCAG AAAGGCAAGG CCTGGGCAGT TATCCAGACT GAACATATAA 1080
TCCCCTTCCT TCTCTGGCCT TTGATGGCTT CAGGACCTGC AGGCAAAAGG AAGGCAGGAA 1140
GGCAGGCAGG AAGGAAGGAA GGTCAGGTGA CTCAGCAATG CGTCCAGCAC TGGGAGCTGG 1200
CAGATCTGGG GCTCCCTCAT CCTCCAGCTG AGAGGCGAGA AAGAGAATCA GGATCCCTGG 1260
AAGTTTGGAG ATCCTAACCC CTTATACATA CAAAGCAGCA ATTATGTGCC TAAGCCCAGG 1320
GAGAGACCTG TAGCTGCCCA AGGTCAGAGG CAAGGTCAGA ACCAGACCAG CTGTCTTCAG 1380
CCCATGGCTA TGATCTAGCT ATTTCCACTA CACAGAAAGA GAGAACCCTT CACCCTTGAG 1440
GAGGACACGG GACTTCCCCA GGAACCTCCC GTCAATCCTG TTGAGGCTCC TGAAATGGTG 1500
GAATGACGTG GACTTTGGAA CCACGCAGAC CTGGGTTTAA ATCCCAGGCC AGGCACGGTG 1560
GCTCATGACT GTAATCCCAA CACTTTGGGA GGCTGAGGCA GGCAGATCAC TTGTGGTCAG 1620
GAGTTTGAGA CCAGCCTGGC CAACATGGTA AAACCCCATC TCTACTAAAA ATACAAAAAC 1680
TAGCCAGGCG TGGTGGCACA CGCCTGTAAT CCCAGCTACT CAGGAGGCAG AAGCGTGAGA 1740
ATCGCTTGAA CCCGGGAGGC GGAGGTTGCA GTGGGCTGAG ATCATGCCAC CGCACTCCTA 1800
GGTGAGAGTG AGACTCCGTC TCAAAAAGCC ACACTGGCTA GCTGTGTAAC GCTGGGCAGG 1860
TTACTTTCAC TCTTTGACAC TGGATTTGCT CACTTGCAAA GTGGGCGTAA ATGCATCCTT 1920
AGCTCACAGG GCTGTGGTGA GGCTGACATG AGGAAGCACT GGAAGGCACA GCTTAGGCTC 1980
CACATGGGCC ACTCTCAGGA AGTGTGTCCC CACCTCCCCC TTTATCCTCA GCTCTCACTG 2040
GGTGTGTTTG CTGGGGAAGG AGGTGCAGCA GCCCTGGGGC CTTGGAAATA ATAATAGCCA 2100
CTCACCCTCC AGTGCTTACC ATGTGCTGGG AACTCTCCTA AGCGTGAACT TAACCTGTAT 2160
TAGCCCATTT AACCCTCCAT TTAATCCAAT AACAGTTCCC AGGCCAGGCA TGGTGGTGCA 2220
TGCCCATAGT CCCAGCTACT CAGGAAGCTG AGGCGGGAGT ATCGCTTGAG CCTGGGAGGT 2280
TGAGGCTACA GTGAGTCATG ATCACCCTAC TGCACTGCAG CCTGGGCAAC AGAGTGAGAT 2340
CTTCTCTCAA AAGAAAAGAA AAGAAAAGAG GGAAGGAAGG AAGGAAGGGA GGGAGGGAAA 2400
TCCCAATGAC AATAAGCAGT TCAATAACCC TACAGGAAAA CACTGTCATC AATCCCACTT 2460
TATAGATAGG GCTGTGGGTC TGAGTAGCTA AGTGACTTTG TCCAAGACAG TGGACAAGAG 2520
ACCACACGGA TTTTGAGCCA GGCCAGCTGG CTCTGAATCC CACTGTCTCC TCCCTCCTTA 2580
AACTAGTGAT GTCACTGCTC TGAGCCCTGG TTTCCTCATC TGTCTCCAGG GATAAAAATA 2640
GCAGCTTCAT GGGGAAGTTT GAGGATGACA CAAGATGACG TAAGGGAGGT CCCCACACAG 2700
GGCTCCACCC ACAGGCATGA GAAGAGCCTT TCTCAGGAAG AATCCCAGGC CGCCCCTGGG 2760
GCAACCGCCG GGCTGGCCTT CCTGCCTCTC CTTAGGCCCA GCCTAGCGTG ATCTGGATGG 2820
TGAGAGATTT CTGCAAAGCC CCCAGGGGCC TCCAGAGAAG GGAGGTGCCC GGTCTCCTAG 2880
ATAAGGGCTC CCAGAGAGGA TCACAGCCCT GGAGTTGCCA TTCTTGAATC ACCCACTGTC 2940
TTCCCCAAGT TGATTGGTCT GAATCCATGT ACTTATTTTT TATATTAGTT CCATAATGTC 3000