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

TagContent
EnhancerAtlas ID
HS116-21930 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr22:20903300-20905720 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr22:20905650-20905661GGGCGGGAAGG+6.62
GATA2MA0036.3chr22:20903414-20903425TTCTTATCTGT+6.14
Gata1MA0035.3chr22:20903414-20903425TTCTTATCTGT+6.62
SPICMA0687.1chr22:20904262-20904276TACTTCCCCTTGTT-6.23
SPICMA0687.1chr22:20905700-20905714TGCTTCCTGTTTTT-6
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00966chr22:20903540-20907807Adrenal_Gland
SE_02184chr22:20903570-20907980Aorta
SE_04597chr22:20903183-20908048Brain_Anterior_Caudate
SE_05425chr22:20903182-20909943Brain_Cingulate_Gyrus
SE_06221chr22:20902991-20910126Brain_Hippocampus_Middle
SE_08018chr22:20902869-20910055Brain_Inferior_Temporal_Lobe
SE_12414chr22:20903165-20907601CD3
SE_14430chr22:20902445-20908068CD4_Memory_Primary_7pool
SE_15690chr22:20903014-20907417CD4_Memory_Primary_8pool
SE_16601chr22:20902939-20907578CD4_Naive_Primary_8pool
SE_18628chr22:20902613-20908055CD4p_CD25-_Il17-_PMAstim_Th
SE_20611chr22:20902676-20907646CD56
SE_22152chr22:20902964-20907868CD8_Naive_8pool
SE_22532chr22:20902593-20913247CD8_primiary
SE_36960chr22:20902709-20913524HSMMtube
SE_41024chr22:20903441-20907986Left_Ventricle
SE_43192chr22:20903216-20907966Lung
SE_44170chr22:20902716-20909601NHDF-Ad
SE_44919chr22:20903603-20908906NHLF
SE_45715chr22:20902734-20910273Osteoblasts
SE_48421chr22:20903406-20912990Psoas_Muscle
SE_48978chr22:20903696-20907980Right_Atrium
SE_51756chr22:20903473-20909780Skeletal_Muscle_Myoblast
SE_53780chr22:20902969-20909178Spleen
SE_56041chr22:20903306-20907264u87
SE_63544chr22:20903416-20910302HSMM
SE_65524chr22:20903348-20907761Pancreatic_islets
SE_67959chr22:20903306-20907264u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr222090380020904604
chr222090343520904266
Number: 1             
IDChromosomeStartEnd
GH22I020548chr222090293820913464
Enhancer Sequence
TGGTCTTAAA CTCCTGGCCT CAAGGGACCC TCCTGCCTTG GCTTCCCAAA ATGTTGGAAT 60
AATAGATGTG AGCCTCCACG ATTGGCCTCT ATGGAGTTTT TTAAGGTTTC TGTTTTCTTA 120
TCTGTAAACT GGATGTGTTA GTAGTACCTG CCTCTGGGTG GTTGGGAGAA ATCAAGGCGA 180
TAATGCATGT GAATTGATGA CTCCTGTGTC TGGCACTGTA AAGTGCCAAG TGCTAGCTGT 240
TACTGTCATG ATGTTCATTG TTTATGGTTT GTAATACTCA GCCTCAGGTA CAGCTGGACA 300
CTTATATTTT GATAGCCAGC AGGGGAGCTG GAGCAGACCA AGTGAAGATA GGGAGTTTCC 360
TGACTCTTTA GCCCTTTTTT CTGCAGCAGT TCTAGGGGAG TTGGTGTGCT TTGGAGCAGA 420
AAGGGGCATA ATAATCTGTC CATCTGGATG GGGGTGGGGG TGGATGGTGA GGAGTCAGGA 480
GTGAAAGAGC CCAGCCAGGG GGATCAGAGG CGCAGTTTCA GATCCAGGGC TTTCTCCCCT 540
GGAAAGGAGT TGTTGTGGTT GACCCATTGC GTTCAGCCCC TAGATGTTCC TAGATAAACC 600
TGCCTTTGGG GGAATGTAGG AAGTATCATC GCCCACAAGA AAGCTCCTTG GCTGGCAGCA 660
TGACAGCTTC CTGTGCTTGT TTCTCACATC AGGCGTCCCC TCCCTCCCCG CTCCCCACTA 720
AGCCTCCTCA CGCTGGTCTG GTAGCAGAGC TGGAGCAGAT GGCAGTGGCT GCGCCTACTG 780
TGGGTCAGGA GTGGTGCTGG GCACTGCAGG ATGATGATGC CTGCCCACTG CATTCCAGGT 840
GCTGGGCTGG CAGTGGGTCT TGCTCAGCCC TGGTGTTATG CAGAAGGGCT TTGGTGACAT 900
GGTCCTGAGC CTTGTTTGAG TGTCTTATGT CTAAGTAAAA GTATCTTGTT GCTTTTGAAA 960
CCTACTTCCC CTTGTTTTAC CTTTTATGGA TGTGGAGAAA ACAAATTCAT TTAAAGTATC 1020
GCAGACCTAA AAAATGGTCC AGGGCCTTAG GAGCTGTGAG GTGTTGACCT GGCTGGCCCC 1080
CAGGCCCTTC TCCCCTCATA CATGGCCACC TTGCTTCTGT TCCTGAGTGT CCTCAGGTTC 1140
CCACACCTCC ATTGCCCCCA TTCTCATACC ACTGTCCTTC AGGGACAGGC TGCCTGTGGG 1200
CCCCCTTCAC ACGCACATCA GCTTTCCTAT CAGTAATTGA TGGGGATAGC CGGAAGCTGG 1260
GCGTGTTGAC AGAACTGCCT TGGTGTCCCC TTGTTCTGGC CAGGCCTCGC TGCTTATCCC 1320
AGCTTTTCCT CTCCCCTGGG CCTTTCTTCT TCATGTTGTC CTGTGCTAAT TCCCCGAGCT 1380
GAAAAAAAGA AGTGGGGTAG AGTTTGGAGA TAGATGTGGG ATGATAAAGA TTTCAAAAGT 1440
GTCTTTGTAT TTTTACACTC ATCTGAGACC ACTTTTCATC ATCCTTCCCT CTGCCCTGCC 1500
ATCTTATGAG TGTAGTGGAT GGACTCTGAG TGTCACAGTG ACTCAGGAGG AAGGTTGGGT 1560
GAGCAGGGCA CGGAGCCGGG GCTTTGCCCC TTCCAGGCTG CCCTGCCAGA AGGATGGGCA 1620
CTTCAGCAGA AGACAAGGAT GCTTCTCTGA AATAAGACTT TACCTCAGAC ATCCGTGTAT 1680
TGACCACAAG ACCAACTCAC AGTAGTGATT TCCCTGAAAC ACTTGGGAGT GAGTGTCCTT 1740
GGGGCCAAAG AGGACAATGG GTGGGAGGCA GCCCCTGCCA GACAATCTCA GAAACACAGC 1800
AGCTTGCATA TAGCGGGCCT TGGCAGCCAG TGGCCTTCAC CTCACCTGAG AGTGGGCTTC 1860
ACCCTCTGCC TTGCCTGTGC GTAAATGGAG ATGAACACAG ATTCTCCCGG AAAGCGCAGC 1920
CAGGGGAGGG CCGCCCAGAT TTTCAGCAGA TACTGCGTCA TCAGTGAAAA GGCAGCAACA 1980
GGCTGGGCTG AGAAATGAAA GCCCTTCTTT ACAGATAGTG CAAAGACACA GCGGCCCACC 2040
CACGGCTGCC TCTGACAGGC CTTGTGCCCT CAGGCCAGCG CCTCATCACC CCCAACCTGC 2100
CTGTCCCCTT TGTGATGAAG AGAGGGCACT CAAGATGGCT CCCAGCTCTC TCAGCTGAGT 2160
GCCTTTCCAT CAGGGGAGAG GAGTGGCCGT TGGAGGCTCT CTGTCCCCTT CTTGTTTCTT 2220
TGTGCCTGTT ATTGGCCAGC CTAGCTGAGC ACTGACGGCT CTCTTCCGAG AGGCGGATTC 2280
CAGAGGAGGC CGAGCAAGCG TCTGAATCTG CCTTGCAGGA TGGGCTTCAG CTCGGTGCCA 2340
GCAGGCGAGG GGGCGGGAAG GGGGAGTCCG ATGACTGCGC TTCTTCATCT GGTATTAAAC 2400
TGCTTCCTGT TTTTACTTTT 2420