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

TagContent
EnhancerAtlas ID
HS040-03346 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr1:223902460-223904790 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TP53MA0106.3chr1:223903596-223903614TGCTTGCCAGGGCATGTT+6.17
TP53MA0106.3chr1:223903596-223903614TGCTTGCCAGGGCATGTT-6.32
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00224chr1:223891886-223912166Adipose_Nuclei
SE_01908chr1:223903739-223904850Aorta
SE_02306chr1:223899487-223903687Astrocytes
SE_04026chr1:223903291-223905474Brain_Anterior_Caudate
SE_05036chr1:223902343-223904766Brain_Cingulate_Gyrus
SE_05972chr1:223899184-223905867Brain_Hippocampus_Middle
SE_09681chr1:223899395-223907924CD14
SE_19702chr1:223899422-223907008CD4p_CD25-_Il17p_PMAstim_Th17
SE_23408chr1:223902389-223903605Colon_Crypt_1
SE_23408chr1:223904046-223904670Colon_Crypt_1
SE_24051chr1:223902436-223903004Colon_Crypt_2
SE_24051chr1:223903089-223903543Colon_Crypt_2
SE_24051chr1:223903970-223904550Colon_Crypt_2
SE_25230chr1:223902434-223903064Colon_Crypt_3
SE_26209chr1:223899230-223905388Duodenum_Smooth_Muscle
SE_26925chr1:223899336-223904834Esophagus
SE_31491chr1:223898405-223906097Gastric
SE_33950chr1:223900271-223904290HCC1954
SE_34545chr1:223899419-223904575HCT-116
SE_34979chr1:223899218-223904777HeLa
SE_36294chr1:223899426-223904613HMEC
SE_37129chr1:223899390-223911201HSMMtube
SE_38254chr1:223899363-223904539HUVEC
SE_38957chr1:223902403-223904692IMR90
SE_42269chr1:223902366-223906841Lung
SE_44530chr1:223900206-223905349NHDF-Ad
SE_44904chr1:223902263-223903610NHLF
SE_44904chr1:223903924-223904809NHLF
SE_45872chr1:223899383-223910101Osteoblasts
SE_50365chr1:223899342-223907084Sigmoid_Colon
SE_51879chr1:223902338-223905051Skeletal_Muscle_Myoblast
SE_53249chr1:223902420-223905033Small_Intestine
SE_55958chr1:223898795-223906601u87
SE_63671chr1:223902338-223906710HSMM
SE_64794chr1:223900231-223904926NHEK
SE_65644chr1:223902687-223903954Pancreatic_islets
SE_65644chr1:223904002-223904652Pancreatic_islets
SE_67677chr1:223898795-223906601u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr1223904365223904567
chr1223903033223903347
chr1223902800223903000
chr1223903000223903425
chr1223903915223904781
Enhancer Sequence
AATACCTACT ATATGCTGGG CACAATGCAT ATGGTTTCTG CTTCTGAAGA CTTACTTCTG 60
AGGCTAGTGA GGGGACAGAG ACAGGTCCCC CAACAGTTGG AAATGCCTGT GGGACTTCCA 120
GATGAGGATG TAGAGGTCTA GAGATGATCT AGCGCCACTG CTTAGGGCAG GCGGGCTGTG 180
CACTGCACAA CTAAGGAAGA GTGTGACTTT TACGATCCCC ATTTGCCAGT TGAAGAAATT 240
GAGGCTTGGG AAGGTTAAAT ACTTGCTCAG AGTCAAGTGG ATATAGGGCA TAGATCCAGG 300
ACTGTGTGTA GTCTGTGCAT GTTGAGCCTA CCCCTTATGG CTGCGCTCTC TGCCTCCTTC 360
CTACCTTCTC AAATGCTGCT GAGGTCAGGC AAGGGGAGCA CAGTTGTTTC CGCTGGATTT 420
GAACACTAGC AAGTCATTGG TGAGTTTAGC AGAGCAATTT CAATGGAAAG GTGAGAGTAG 480
AAGCCAGATT GTTGTAGACT CCAGAGTAAA GGAACTGGAA ATTAAGAACA TGATCAACTT 540
ATTTAAGAAG GACCCCCGGG AAGAGAGGAG AACTGATAGG TAGAGTAGGA CCTGGACTTT 600
GAGAGCCTGT GTTTTTTTCA TATGAGAACA ACTTGAATGT GTCATATGTT GAATCACCAG 660
GAAGAAGGGA TTAAAGATAA AGGCAGGGAG GGGGCAGTGA AACAGGATCC CTGAGGAAGT 720
GAGAATACGG GTTGTGGGCA GGGGAGGGGA GCAGGTTAGC CTTGCAGCAG GAGGAGCTGC 780
TCTTCCTCGG AGAGAGGATT TCACAACACT GGCAAGAGTG GCTCCAGTGC CTGGAGCGGG 840
GATTAAAGCA GTAAGTCCAG TGGGGTCCAA GGGCCATGCA GGGGTACAGT GAGGAGAAAG 900
CAGGTGTGAT CCGGGTGGCA CATCAGATCC TTCCAGCAAC CAGTCTGTTA GGAGCAAGGG 960
CAGATGTTGT GAGCCCCTAT GTTTCCCCCA AGAAAATCAA ACCTCTGAGA GGTTTCTCAC 1020
TTGCTTATCT TCAGCTGGCC GAACTCAGCC TCAAACCCAT ATGTCCTGTC TCCAAGTTCA 1080
GTGACTGTTA TCATCAACTT CTTCAACAGT AATAATAATA GATCACATTT ATGGAGTGCT 1140
TGCCAGGGCA TGTTTACATC ATTATCTCAT TTAACACTCA GAACAATCCT CTGTGGTGGG 1200
TGTTTTCATC GTTCCCATTT TGCAGGTGAA AAAACTGAGA CTTCAAAAGG TTAAGTGACT 1260
TCCCAGGGTC CTACGACCTA CATAATAAGT GGCAGAGCCA GGATTCAAAC CTAGGTTATC 1320
AGAATAATGC AGCAAAGCCC AAACCCTCAG CCCCTTTTCA CTGACTGGTA AGACCCATAT 1380
TTAATTCGAT GCCCTACATG CCGTGCACAA GTTTCAGTTT TCTGAAGCAT CGCTTAGATG 1440
CTTAGGTGTT TAGCACCACT CTGAACTCTG ACTTTTCTAG AGAGGCTGCT AAAGGCATTA 1500
GAAAGTTTCT GAAGTATAAT GGAAAAACCC TGCTGGAGTA AGTGCCTGGC ACACTCAGGA 1560
TTATCAGTGT GATTCTTTAT AATAAACAGG CTCCCAGCAC CAAGCCCAAT CTATTCCATC 1620
AGCTGGATAA GAGCTCTCTG GCAGGCCTTG GGCCAAGCTG GCTTCCTTTG CCTCAGCAGA 1680
AGAGCATTCT GATTCTCTCT GCCATCCCCA AAACTGACAG GAGCAGAGAG AAACAAGGCA 1740
GAGGCATGAA GGGAATGTCC TCTGCGGCAG ATGGTGCTTC CGGAAGAGCT CCCACAATCT 1800
GAGCTAGAAT GAACAGGGGC TAGATCCAAG TCTCATATAG GCATACTTCT GCTTGACAGA 1860
GTGGGCATGC CGAGGGCCGT TGGGTGGAGG CAGGCGTGTG CAACCCAAGC AGACATGAGA 1920
CGCAGCTCCT TCAAGGCAAG GTTGCCTGAG CCCAGAGAGG CTCAAATTTG TGCCCCAACT 1980
TCCTCTGTGG CTTTTGGGTG GGGCTCTTCA GAATCGAAAC ACACTCAGAG GGCTGCTGAA 2040
AGGGCTAAGA AGTGTTCAAG GTTGGCTTCC ATCAGGCTGC TCATGACAAT GGCCCCTGAG 2100
GTTTTAACAC CCTTGAACGC TTGGTACTAA ATCAATTAGA GGCAGGGCAG GAGCAGAAAG 2160
AGTTGGCGCA TTTGATCAGT AAGTTCCAAT GCCAGTGCTG TCTATTATCT GTGAACTGTG 2220
TTAACTTTGG ACACGTCACT TCACCTTTTT GAGCTGTTTC CTCGTCTGTA AAAGGGGGAT 2280
AATACCCATT CCATGAGGTA AAGCTTTGAG CACAGTCTCT GATGTAAGCA 2330