EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-34311 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr9:33138930-33141300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
NFYBMA0502.1chr9:33140242-33140257CTGATTGGCCAGTGG-6
RARA(var.2)MA0730.1chr9:33141277-33141294AGGTCACCTTGAGGTCA+7.71
RREB1MA0073.1chr9:33138936-33138956CCCCAACACACACACTAACG+6.46
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00330chr9:33138866-33141700Adipose_Nuclei
SE_00992chr9:33138818-33140399Adrenal_Gland
SE_00992chr9:33140510-33141415Adrenal_Gland
SE_10229chr9:33134720-33146706CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33136393-33139356CD3
SE_12090chr9:33140249-33142158CD3
SE_14891chr9:33140511-33142287CD4_Memory_Primary_7pool
SE_18081chr9:33140148-33141844CD4p_CD25-_CD45ROp_Memory
SE_18665chr9:33135758-33139718CD4p_CD25-_Il17-_PMAstim_Th
SE_18665chr9:33140056-33142210CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33140372-33141391CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33134255-33146063CD56
SE_22416chr9:33135220-33146719CD8_primiary
SE_26031chr9:33139672-33141321Duodenum_Smooth_Muscle
SE_26859chr9:33139260-33140484Esophagus
SE_26859chr9:33140490-33141363Esophagus
SE_27770chr9:33139911-33141110Fetal_Intestine
SE_29800chr9:33139312-33141840Fetal_Muscle
SE_31534chr9:33139337-33140430Gastric
SE_31534chr9:33140552-33141138Gastric
SE_32659chr9:33135226-33145795GM12878
SE_40894chr9:33138811-33142004Left_Ventricle
SE_41831chr9:33139282-33140314LNCaP
SE_42236chr9:33137933-33140413Lung
SE_42236chr9:33140421-33142021Lung
SE_44340chr9:33139198-33141245NHDF-Ad
SE_45447chr9:33139306-33141157NHLF
SE_45731chr9:33138938-33141879Osteoblasts
SE_46917chr9:33138775-33140378Ovary
SE_46917chr9:33140576-33141301Ovary
SE_47814chr9:33139478-33140178Pancreas
SE_48426chr9:33138706-33140393Psoas_Muscle
SE_48426chr9:33140480-33141409Psoas_Muscle
SE_48738chr9:33136686-33140472Right_Atrium
SE_48738chr9:33140483-33141323Right_Atrium
SE_50176chr9:33134918-33140478Sigmoid_Colon
SE_50176chr9:33140489-33142097Sigmoid_Colon
SE_51651chr9:33138989-33141643Skeletal_Muscle
SE_52621chr9:33139293-33140398Small_Intestine
SE_52621chr9:33140511-33141315Small_Intestine
SE_53402chr9:33139080-33142103Spleen
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr93313893033139314
chr93313932133140496
chr93314069633141208
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA CATACACACA CACACACGCC 60
CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA ACCCACAGAA GCCGATCGAG 120
CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC TGCAAACTTG CCCTGTGATA 180
TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT CTGGGTACCT ACTGTGTGCC 240
AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG ACAAGACAAA TCCTGCCTTC 300
CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA AATTACCCTG GTTTAAGGAT 360
GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT TTATCACTGA ACAGCCTCTT 420
CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG CACAACCCCC ATCATGCTTC 480
CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT TGCCAATCTG GCAATTTTTT 540
CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA CAACAGACAG CAGCCCCAGA 600
CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG AGGCCTCCTG AATGCCCTGC 660
ACACCTCCTG CCATACTGCA GGGACCATGC TCTGCTACAC ACCTGGCTCT GTCCCAGTGA 720
GAAACTCCAG AGAGCTCAGA CTCCAGGAAG GCAACGACTA CCTCTGTTCA GAATCATGCA 780
GACCTGCGAC CAGGTTTCAG AGCCACTGCC TGGGGTGGTG GGGAGAAGCT CTGGGAGGAG 840
GCAGAGGGCT GAGGGCTTCA TGACAGGCCT CAAGCCGAGC CAAGGCGCCC TTGCTGTGCG 900
GCGCATGGCG TGTGCTACCA CAGGCTCTCG GCCCCGCTGG GCTGGCTTGT GTGTTTTCTT 960
GGCTCTGGAA GCTGGGAGGC AGGGTTACGT AAGCAGATGA GCAGATGTAA GCTGTCCTCG 1020
GCTCCCCCAG CTCAAGCCCC GCCACGTGGG CCTCTCGGCT GGGAGTCCAG GTCATGGCCT 1080
TGCATGTAAG TCGCTCAATA ACTTCAATGT GTGAGCTCAA TTCAGACAAA TTCCACTGCT 1140
CCCCTGCCTG GCACAGCAAA CCCAAACACA TACATGCCCC TCCATCAAAG GCCCTGCTAA 1200
TCTAAGCCAA CACCAGCACG GACTCCTGAC TGGTTTTCAT GCTGGCTGAA GCACTAGTTC 1260
AATCCTTTAG CCTCAGCAAA ATAGGCTGAA ACATCTAGTC ACTGTTTGTC AACTGATTGG 1320
CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT GCTTTATTGT GACAATGTTT CACTAGCCCA 1380
GGAATGAAAT CACAGAAGTA AAGACCATGT AGGTGTTTTT TAATTAAACT AAAGGTAATC 1440
AAAGTATAGG AATGCCCTTT CTTCCAAGAT TAAGTGCTTC TTACTCTTTG AATATTAAAA 1500
TGTCCTTTCT CTTATGAAAT CATCATAGAT TTTCATGCTG GACTGATTTT TAAAATTTAA 1560
TTTAAAAAAA AAATCCTTCC TTGGCAGCCA TGGGTCAGGC CTCTAAGTTT GTTTTGAAAA 1620
TTCTCTGGAC AGGAAATCCA AGTATTCAGG AAACATTTGG GAACACGTGG AACTAGGCAG 1680
TGCCTAGAAC TCTGTGATTC TGAGAGCTGG GATACTGGAA TTTCTTCCTG GGTCTCAGAC 1740
CTGACAGTAC ACTGCACAGC CCCTCTTCAC AAATCAGCTC CCCCACCAGT GCTGTTCCAC 1800
AGGCTCATGT GGATGGGCCG CTTCTCTCTG TACCAATCTT CCAAAGGCCA GGTGCGCACC 1860
GCAAGCTGAG CCAGGCATTA CCACCAAATT CCCCAGCTTG AGAAAAGATT TGCTTGCAGC 1920
ATTCTCGTGA AATCACGGTG CCCCTTGAGG CCCCTTGGGC TAGAAATGAG AAGCACCATT 1980
TACTGTACGT GGCTCACCCG TCATTCTGGG AAGAGCACAA GCTCTCTAAG TCTGCAAGGG 2040
CTTCAGTCTA ACAAATCTAA CAGCTGCCTG GCCTTAGCTC AAACACCACC CTCCCAGGAA 2100
GCCTTCCCAG ACCACTCAAG GTTGGTTCTT AAGCATTTCA CCCACTTCCC CTAAGCATTC 2160
ACAGCACCAC ATCCATTCAT ATTCAAACAT GTACCCAGTT AGTATGTATC ATGTGCCAGG 2220
TGGTATAGGG CATGCAGGGG TTGGTAGGGG AGTGGGCGGC AGGGTGAGCA AGTAAAGAAG 2280
AGGTCTTTGA GGCTGGGCAT GGTGGCTCAT GTCTGTAATC CCAGCACTTT GGGAGGCTGA 2340
GACAGGCAGG TCACCTTGAG GTCAGGGGCT 2370