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

TagContent
EnhancerAtlas ID
HS045-39063 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr2:238570090-238573360 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:238570110-238570128GACTCCCTCCTTCCTTCC-6.31
MEF2AMA0052.3chr2:238571316-238571328GCTATTTATAGT-6.11
MEF2BMA0660.1chr2:238571316-238571328GCTATTTATAGT-6.74
SP8MA0747.1chr2:238571480-238571492GACACGCCCACC+6.02
ZNF263MA0528.1chr2:238572669-238572690GGAGGAGCAGGGTGAAGGGTG+6.06
ZNF263MA0528.1chr2:238572666-238572687GAGGGAGGAGCAGGGTGAAGG+6.33
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_01566chr2:238568879-238571154Aorta
SE_01566chr2:238571303-238573686Aorta
SE_23331chr2:238571349-238572688Colon_Crypt_1
SE_23963chr2:238571497-238572221Colon_Crypt_2
SE_24998chr2:238569122-238570436Colon_Crypt_3
SE_24998chr2:238570520-238573269Colon_Crypt_3
SE_25815chr2:238570466-238572445Duodenum_Smooth_Muscle
SE_26722chr2:238570190-238571204Esophagus
SE_26722chr2:238571408-238572780Esophagus
SE_29646chr2:238570702-238573032Fetal_Muscle
SE_31908chr2:238568844-238571159Gastric
SE_31908chr2:238571335-238571973Gastric
SE_31908chr2:238572010-238572953Gastric
SE_40633chr2:238570413-238573764Left_Ventricle
SE_42111chr2:238568829-238571135Lung
SE_42111chr2:238571181-238573276Lung
SE_44921chr2:238570901-238572414NHLF
SE_45786chr2:238570567-238572579Osteoblasts
SE_48071chr2:238568749-238573479Psoas_Muscle
SE_48757chr2:238572029-238573322Right_Atrium
SE_49604chr2:238572197-238573233Right_Ventricle
SE_51094chr2:238569466-238573270Skeletal_Muscle
SE_54582chr2:238569703-238573611Stomach_Smooth_Muscle
SE_58523chr2:238563966-238621920Ly1
SE_59868chr2:238570692-238624050Ly4
SE_65656chr2:238569477-238570566Pancreatic_islets
SE_65656chr2:238570576-238573536Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr2238571237238571811
chr2238572069238572172
chr2238572122238572400
Number: 1             
IDChromosomeStartEnd
GH02I237660chr2238568862238573173
Enhancer Sequence
TGGCCGGGCT GCCCTCCCCA GACTCCCTCC TTCCTTCCAG ATGTGAGCAA ATCCCTTTCC 60
TTCCACCTCG CTCTCGGCCC CTGGTTCACC TTCTGTTCCT GCCCAGGGCA AACTGCCCTA 120
TGTGCATCTC TGTCCTCATC CATGAAACCA TCCTTGTCCT CACTGTCGAT GGAATTTTTC 180
AGTGATACCT AACATCTGTC CCAGAGCCAT GCACGTTCCG AAAGCACATT CCAGGGGGAC 240
AGTTGTGTCC CTGGTGCAAC ACGGGAGTGG GCACACATTC TCTGTGCTGT GCATGGGGAC 300
AGCTCCAGGA AGAGAGAGGG CACTGTTTTC CTGTTTCCTG AGTCAATCCG CTGTAGTTCT 360
GTGGCCCAGC TGAGTGGCAT AGGCTCTCCT GACCCAGGTA CCTATCAGCC CCCAAAATAG 420
GTGTTGCCAT GATTCCTTTG GACAAAATGT AAAATCTGGC TGAAGACTGA GTCCTCGTGC 480
ACCTAGCGTG ACCCATGACA GCATGCAGGT GTTGGTCTGT AGGGATGCCA TAACAAAGTG 540
CCACAAACTG GGTGACTTAA AATAACAGAA CTGTATTCTC TCACAGTTCC GGAGACCGGA 600
AGTCCAAAGT CGAGGTATTG GGCCAGGTGG GTTCCTTCTG GAGGCTCTGA GGGGAAGGTG 660
TTCCAGGCGT CTCTCCAGCT TCTGGTGCTG CTGGCAGCCC TCGGCCCTCT GGCTTGTAGA 720
CACATCACAC CAGGCTCTGC CTCCGTCTCC ACGTGGCCCC CTCCCTGGGT ATTTGTGTCT 780
CTGTGTGCAA ATTTCTGTTT CCTTATAAGA AAGTCATTGA ATGAGGGCCC ACCCTAATCT 840
AGTACGACCT CATCTTAACT TGATTGTACA CGCAAAAAGC CTATGTCCAA ATAAGGCCCC 900
ATCCACGGGT TCTGGGTGGA CATGAACTTT TGGGGGATGT TACTGAACGC AGTGCAGGGT 960
TCTTACATTC TCACCATCAC GTATATGATT TTATTCTTCA GGGTGCTAAG GTGTGGTGTG 1020
TGCCATGTGC TCTTAACCCC TTAGAAAAGA TAAGGACAAT TTTTTTTTCA GGTCCAATGT 1080
CTGAATGTAT TTTTTTTCTT TCTCTTAGGA TTTGAAGATA TATAACAATA TGTCATAAAC 1140
TGACCTGAAA TCCTTGTTTG TTCCGCAGCG AAATCCATTA ATAATCCCTA TAACTGGGAC 1200
AGTTTTATGT TCCCATTCTC GGTGTGGCTA TTTATAGTGA AACCTCACTT TCCCTGTGTT 1260
GGTTAACATT AAAAACTGGA ACTGCTTCTG AGGTAGGAGG CGGGACTTGA CTCCAGAGGC 1320
GGGGCTTGGA CACTGGGCCA GATTGAGGAC TAGCTAAAAC AGGCCCGGTG GGGAAAGCAG 1380
TCTTCAATCA GACACGCCCA CCAGCGCTAT GTCAATTTAC CGTTGCCATG ACGGCACCCA 1440
GGCATTACCG CTCCTTTCCA CGGCAATGAC CCAGTGATTA CTACCTCTTC CTTGCATAAA 1500
CCGCTCCTTA ATCTGCATGC AATTACAAGT GAGTATAAAC AGGACTGCAA AACTGCCCTG 1560
AGGTGCTGCT CTCTGCCTGC GGGGTAGCCC TGCCCTGCGG GAGCCGGCAG GGAGCTGGAA 1620
CACTGACACT TCAGTAAAGC TGTTTTCTTC TACCTATGAC TTGCCCTTGA ATTCTTTCCT 1680
GAGCAAGGCC AAGAACCCAG ATGGGCTAAG CTCCACTTTA GGGCTCGCCT GCCCTGCATC 1740
AGTTTAACTA AACTATTAGA ATTTTTAGTT TAAAAGAAAT GAGTAAGATT GTGAGCATTC 1800
TGTGAGATGC GGAGTGAAAG AAGGTGCTGT AGTCTGAACG TTTGTGTCTC CCCTAAATTC 1860
ATGTATAGAA ATCCTAACCA CCAAGCTGAC TGTATTAGGA GGTGGGAGCT TTTAGGAGGT 1920
GATTAGGGCA TGAGAGTAAA TGAGATTAGT GCCCTTATAA AACAAACCCG GGGAGTTCTT 1980
TCCCCCCCCA TCCCGCCATG TGAGGACACA ATGGGAAGGG GGCCCTCACC CCTTCTATGA 2040
ACAAGAAAGG GGGCCCTCCC CAGACACTGA ATCTGCTGGC ACCTTGATCT TGGGCTTCAC 2100
AGCCTCTGGA ACTGGGGGAA GTTAATTTCT GTTGTTTATA AGCCACCTAG TCTATGCCCT 2160
TCTGCTACAG CAGCCTAAAC AGCTCAGCCT TAATGGACGA GGCACATGGA ATGACTTCCG 2220
GGCCTCTGAC AGGGTGCTTG GGGAGGATGG TGTGATGTTG CGTTATCACT CACAGACACT 2280
GTGGAACTGA CTGGGTTGGT GGAGCGGGGA CCCGGGGAAG AGTTCAGTTC TGTTCTGGGA 2340
ATGTTGCCTT GAGGCAGCTG AGCACTACCC ACAGGGAAAG GTCTGGCAAA GGTTCACGTG 2400
CATTCGCCTG GGCCATAGGG GAGAGGGGAG CCGTCAGCGG TCAGGGTGGT CAAAGCCACA 2460
TAGTTGCATG AGGTCTCCTA AGTAGGTCAG TGGAGCAGAG TACCCAGGGT GGAGCCCCGG 2520
GAACCTCAGA AACAAGGAAG GGGTGAGCAG AGGAAGGGTC GCCCTCAGGG CACTGGGAGG 2580
GAGGAGCAGG GTGAAGGGTG GGGGCAGAGG GGAAACAGCC ATGTCCATGC TGCAGAGAGA 2640
CCCAAGGGAG ACCCGGGGAA GAATGTCACT TGCACCTTGC AAAAGGGAGG GTCCTGGCGG 2700
CCTCAGCCAG AGCCGTTTTA GTGAAGTCAT GGGGAGAAGG ACCACAGAGG CTTAGTCCTG 2760
GCTGGGGCCG CAGTGGGACT GGCAGTGGAG AGGAGGGGGC CCAAGCCAGG GAGATTGAGT 2820
TCTTGGCAAA GAGGCCGGCG GCGTTCTCCA CTGCGTTTCC ATCCGCAGGT GCGCCTGCCG 2880
CCTGGCCTGT CCACAGTGTG CTGGTTGCTG GTATTCAGTT CTGGATTGTA CCTCTGACTG 2940
GACTGAGGTC CATCAGCAAA TGACGGGGCC TCGGCGGTGT GGCAGTGTGT TCAGCTGCTG 3000
GCATGCCGCC TCGGGAACAG AAAAGTCACG TTGTTGTGTA TGCGGGTAAC AGCTCCAGGG 3060
AGGCGTGAAG AGAACTTCCT GGCAAGGAGT GCTGCTCCAA GACTGAATGG ACTTTTTTTG 3120
AAGTGCAAGG GTCTGGCCTC TGGAAGGGTG TTTTTGCTGC CACCTTTGAA CTTCTCTGTG 3180
AGTTTTTAAA TTTTGAGCAA ATCGCCTTTT ATAATCATTC TATATGTACT TTTTCTACCC 3240
AACGGCTGCA TAGTGTTCTC TTCCCACAGC 3270