EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-09937 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr17:74247130-74249810 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr17:74247150-74247161AAATCACAGCT+6.14
Hnf4aMA0114.3chr17:74247841-74247857AGGTTCAAAGTCCTAC+6.19
IRF1MA0050.2chr17:74248745-74248766ATTTTCTCTCTCTTTCACTTT+6.21
IRF1MA0050.2chr17:74248751-74248772TCTCTCTTTCACTTTTTTTTT+7.63
Nr2f6(var.2)MA0728.1chr17:74247509-74247524TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr17:74248049-74248070CTTTCTTCCTTTTCCTCCTCA-7.04
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_11415chr17:74247580-74249549CD20
SE_15056chr17:74247576-74249126CD4_Memory_Primary_7pool
SE_15056chr17:74249138-74250044CD4_Memory_Primary_7pool
SE_18937chr17:74247402-74249906CD4p_CD25-_Il17-_PMAstim_Th
SE_19565chr17:74247575-74249815CD4p_CD25-_Il17p_PMAstim_Th17
SE_21340chr17:74248712-74249921CD8_Memory_7pool
SE_23599chr17:74247703-74248615Colon_Crypt_1
SE_24131chr17:74247750-74248058Colon_Crypt_2
SE_24131chr17:74248072-74248530Colon_Crypt_2
SE_27367chr17:74247623-74248919Esophagus
SE_28090chr17:74247720-74249008Fetal_Intestine
SE_29152chr17:74247624-74248997Fetal_Intestine_Large
SE_31864chr17:74247673-74248817Gastric
SE_31864chr17:74249094-74249622Gastric
SE_32663chr17:74247575-74249525GM12878
SE_43246chr17:74247582-74249663Lung
SE_47749chr17:74247791-74248535Pancreas
SE_48284chr17:74246270-74250806Psoas_Muscle
SE_50371chr17:74247468-74249790Sigmoid_Colon
SE_52552chr17:74247474-74249789Small_Intestine
SE_53757chr17:74247335-74249794Spleen
SE_55588chr17:74247785-74248788Thymus
SE_60322chr17:74239092-74270751Ly4
SE_60510chr17:74247565-74275632DHL6
SE_62440chr17:74241844-74272934Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr177424907974249712
chr177424719074247386
chr177424756774249035
chr177424822274248574
Number: 1             
IDChromosomeStartEnd
GH17I076250chr177424672674249804
Enhancer Sequence
CAGAAACCAT CAAATGCTGC AAATCACAGC TTCCTCCCAT TCTCCAGAGC CAGTTTACCA 60
GCATACCCCT GGTCTTAGGT TTCTTCTAAT CCCCCAGAAG GGCTGGGTAC ATTGCTTCCC 120
ATATAGAAAG TGCTCACTAA ATGAATGACT ATTTAGTTGT TGTTGTTGTT GTTGTTTTGA 180
GACGGAGTCT CCCTCTGTAG CCCAGGCTGA TGTGCAATGG CGCAATCTTG ACTCACTGCA 240
ACCTCTGCCT CCCAGGTTCA AGTGATTCTC CTGCCTCAGC CTCCCGAATA GCTGGGATTA 300
CAGGTGAATG CCACCATGCC CAGCTAATTT TTGTATTTTT AGTAGAGATA GGGTTTCACC 360
ATGCTGGTAA GGCTGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCTGCC TTGGCCTCCC 420
AAAGTGCTGG GATTATAGGC GTGAACCACC GAGCCCAGCC AAGAATAGTC ATTTTTGAGC 480
AATGACTCTG TCCAAGCACT TTGGAATGCG TTGTCACCCG AGCTGGAGTG CAGTGGTGTG 540
ATCACAGTTC ACTGCAGTCT CAACCTCCTG GGCTCAAGCG ATCCTCCCAC CTGAGCCTCA 600
TTTAATCTTC AAAACAACCC TAAGAGATAA GTATTATTGT TCCCACTTCC CAGATGAGGA 660
AACTGGAACT CAAGTAGGCA CAGGGAGCAG GAACTGGCCC CAGGTTCTTC CAGGTTCAAA 720
GTCCTACATT TTACCCATGG ATCATCATCT CACCAGCCTC TGTGGGGAAA GCCTGCCTGG 780
GTGCCAGCCC TACTGCCCAC CAAGCTAGCG GAGTGATTCT CCCAGGGTGG TGCCAGTGAC 840
AAAGGGCAAT GCATGGGGAC GTCTCCATCA TTGTCACACC ACCACCTCCA CCTTCACTGT 900
GCCTCTCTCT AGGTTTAATC TTTCTTCCTT TTCCTCCTCA CTTCCCTCTG TATTATCAAT 960
CTCCTTCCTG TATCGGGACT ATTTCCTCAA CAGGCCCGGG GAAGCTCTTG TCTATGGAAG 1020
TCCTCTTTGG CCTTAAGCTT CCCTCTAAGA GCTCCAGCAG ATGAGTAACC TGTCCTCCTG 1080
CAAACACTGC CATGAAGTGC GTAGGCAGCT GCCTGCCTTC AGGGCTGGAT GGACACCCTG 1140
TTTCCTTGCT CAATCCCTTC TGATGACTGG ACTCTGTACA CAGTGTGGTC AGTGGGTCAG 1200
CTCTGATCTG GAAGCTCCCA AAGGCAGGAC ACAAGATTTT CTCTGACTGT TCCCAGGCCC 1260
CAGGGCGTGT TGGGCACGGG AGCGTGTGGC ACGGATGTTG TTCGTGATGA GGCATATTCT 1320
AGTGGTTTCC CAATTCGGTT GTGTACAACC CAGTGCTCTA GTGTTCAGTA AATACTTCCT 1380
TCCTCTTTAG GCAGAACACT GGCTCTGTGT TTTATTAACA GCACCTCATG CCTGGCCCAA 1440
AGAATGATTT GTGTGGCTTG GGCTGTTGGG GTCAGAAATG GCATTCATTC ATCATTCACT 1500
CTGGAGGTGC TGTGTTTCTG AAGGAGAAGG GGACCTATCC TGGCAAACAA ATCAGGGGCT 1560
TTATGGTAAA CAAACTCCTC TCTTCCCAGC ACTTGTTTCT TGCTCTCTGT TTTTGATTTT 1620
CTCTCTCTTT CACTTTTTTT TTTTTTTCAC TATACCCGGG CTTCCTGAGT TCCTGACAAT 1680
TTCTAAAGCC TCAAGCATGA TCTCATCAGA AACTCTGGCT TCTTTTAACA TTTCTTTCCC 1740
TTCTGCTGAG TCCTAGTCCA TTTAAATTTC CTCTGTGACT CTGGGAATTT TTTTTCCTTG 1800
AGACACAGTC TCGCTCTTGT TGCCCAGGCT GGAAGTGCAA TGGGCTGATC TCAGCTCACT 1860
GCAATCTCTG CCTCCCAAGT TAAAGCGATT CTCCTGCCTC AGTCTCCCAA GTAGCTGGGA 1920
CTACAGGCAT GCACCACCAT GCCCGGCTGA TTTTGTATTT TTAACAGAGA CGGGGTTTCA 1980
CCATATTGGT CAGACTGACC TCAAACTCCT GACCTCAAAT GATCCGCCCA CCTCGGCCTC 2040
CCAAAGTGCT GAGATTACAG GCGTGAGCCA CCGCGCCCAG CCGGACTCTG GGATTTAAAG 2100
ATAACCAAGT GAAAATAGGT TCATCCTCTT TGACTCACAG CCTGGCTGCC TGTGGAGGCA 2160
ATGAGGAGCT GACATTCACC TGACCCCCGT CCTCTACTTT CGGGTATGCA GAGGCTCTCT 2220
TTTGCTGCCC GCGTCAAGTT AGAAGAGGCC ACATGATTCT TCGGGACAGT GAACCATGAA 2280
CAAAGGTGTA CTGCAGTCAT GTGTTGCTTA AAGACCCGTA TACGCTCCGA GAAATGCGTC 2340
ATTAGGCGAT TCTGTCGTCG TGTGAACATT CTAGAGTGTA CTCACACACA CCTAAATGGG 2400
CTAGCCTACC ACACACCTAG GCCATGTGGC ATAGCCATTG CTCCCAGGCT ACAAACCTAT 2460
CCAGCATGTT ACTATACTAA ATACTGTAGG GAATTGTAGC ACAGTGGTGA AGTATTTGTC 2520
CATCTAAACA TAGAAAAGCA CTTTGGGAGG CCAAGGCGGG CAGATGACTT GAGGTCAGGA 2580
ATTTGAGACC AGCCTGGCTA ACATGGTGAA ACCCTATCTC TACTAAAAAT ACAAAAATTA 2640
GCCAGGCATG GTGGCAGGTG CCTGTAATCC CAGCTACTCA 2680