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

TagContent
EnhancerAtlas ID
HS007-10061 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr20:31068800-31071160 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GSCMA0648.1chr20:31069191-31069201GCTAATCCCC+6.02
INSM1MA0155.1chr20:31069643-31069655TGTCAGGGGTCA+6.18
KLF5MA0599.1chr20:31069757-31069767GGGGCGGGGC-6.02
NOTOMA0710.1chr20:31070150-31070160GCTAATTAGC+6.02
NOTOMA0710.1chr20:31070150-31070160GCTAATTAGC-6.02
RREB1MA0073.1chr20:31069710-31069730CCCCCAAACACCTCTCCCCA+6.11
ZNF263MA0528.1chr20:31070332-31070353GGTGGAGGGAGGAGAGAGAGG+7.06
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_01118chr20:31068829-31069943Adrenal_Gland
SE_03291chr20:31068751-31069389Brain_Angular_Gyrus
SE_04048chr20:31067134-31071090Brain_Anterior_Caudate
SE_04930chr20:31057146-31071030Brain_Cingulate_Gyrus
SE_05885chr20:31047540-31074914Brain_Hippocampus_Middle
SE_06864chr20:31067757-31074247Brain_Hippocampus_Middle_150
SE_07969chr20:31057244-31071007Brain_Inferior_Temporal_Lobe
SE_17373chr20:31066829-31071268CD4p_CD25-_CD45RAp_Naive
SE_23164chr20:31059880-31071430Colon_Crypt_1
SE_23809chr20:31067267-31069846Colon_Crypt_2
SE_24726chr20:31059872-31072878Colon_Crypt_3
SE_25428chr20:31066518-31071431DND41
SE_27760chr20:31059930-31074602Fetal_Intestine
SE_28710chr20:31060148-31074579Fetal_Intestine_Large
SE_30561chr20:31067789-31070956Fetal_Muscle
SE_31615chr20:31067935-31073566Gastric
SE_38064chr20:31066677-31074444HUVEC
SE_42465chr20:31066614-31070981Lung
SE_47565chr20:31068861-31069764Pancreas
SE_50168chr20:31059715-31074357Sigmoid_Colon
SE_52531chr20:31059835-31074536Small_Intestine
SE_53462chr20:31068073-31074508Spleen
SE_54992chr20:31067889-31071101Stomach_Smooth_Muscle
SE_65380chr20:31066398-31071131Pancreatic_islets
SE_69043chr20:31067433-31069755H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr203107040031070925
Enhancer Sequence
CAGGAAGGGC TGAGACACAG CCAATCACCT ACCACACTGG AGGCATTCTC GCTCTCTCTC 60
CCTCACACTC ACTCACACGC ACACTGTGTC TGTCAGAAGC GTATTCCCAT CTACATGTGG 120
TCCTCTGTTG TCCCTGCTGT CATAGACACC TGGATGCTGG AAGTGAGCAT TTCCCACACC 180
TTCCCACTGT ATATCAAGTG GAAAACAGGC TTTTGTTCCT AAGCAAAGGC ACCTGGCTGC 240
TCCCCATCAG CATTCCTCAC CACGAGGGCC TCGCTGGTAC CCTCAGACCC TGCCATTAAT 300
GGGGGTTTCT TTAAAAGTGA AGCTGGAGAG AGGAGCTTCA GCAGACAGGG ATCTTCCAGC 360
CAAAAGGAAG GCTGGAAGGG AGCCGCTGTG AGCTAATCCC CTGCAGGGCT GTCCTTCCAA 420
GAAAGGAACC CAGACAACAC AGAAAAAGTT CTTGAGCAAT TCCCAGGCGG TCCAGCTCCA 480
CAGAGCCCCA GGGTAGGGGC CGCAGGAAAA GTTCCCCAAA GGCGTCTTCT CAGCTGGGAG 540
GAAGGCCGTC TTCTCAGCTG GGAGGAAGGC CGCAGTGAGC TCTGTTCCCA CTGTGCGGCA 600
GGAAGGTGCT GAATAGGGTG GTGTCGCCCA GCTCAAGAGG TGCTGTCTTA AAACCCTGCT 660
CTATAAAGCA AGCCCAGCCT GAGCCTGGAT TAGACAGGAG CTTGATATTA TTCAAGGACA 720
CATTTAGGCC CTAATGGCTT TCCAATGAAG GGGTAATTTA CTACCCGGGG GGCTAAACTA 780
CCACAGGGCC TGGGCCATAA ACGGGCCTTT TCCCCAGACC AACTCAGTCC AGAATCCGGC 840
CTGTGTCAGG GGTCAAGACA GGGGCCTGGT CCCATCACAC AGATGGCTCT CCCCAGAAGA 900
GCCATGAGGT CCCCCAAACA CCTCTCCCCA CACCCCCTTT GGTGTGTGTG AGTTGGTGGG 960
GCGGGGCGGG GGGGGGGGAG CAGGCTGGGG TTGCCAGCTG ATTCTGGGAT AAGTAGGGCT 1020
TTATCTCAAG GGAGAATCTA TTTCAAGCCA CAATCCTTCT CAGAAAGAGG AGGAAATCAC 1080
AGAGTCCAAA CACCATTTCA GGTGAAATCA GGAGGTTATT CATCTCCCCT CAGAGCAGAC 1140
AGAAAGGAAA ATCAATGTTT TAGAGGGGGA AAAAAGGTTC CATTTGAATT AATGGGTTTG 1200
TGGCTTCTCC ATTGATCTGA GCCTCTTCAC ACTTTCTTTT TGTGCTTTTG TGCTCTTGGG 1260
GAGAGGGGAG GGAGTAGGGA ATGGGGAGGA GGGGGTGGGC CTCCCATAAG GAAAAGGACG 1320
GTCTAACCTT AACCTTTCTA CAGGAATAAT GCTAATTAGC GAGGCTTAAT GAGAACTTCC 1380
CCCAGGAAGC GCAGCCCGGT AGGGGCGGCC GGACTCGGGC AAACGCAGCT CCGGGTGGGA 1440
GCAGGGTCAC TTCTGCTCCC GAGCGGCTGG AATAAAAATG CGGATTGCAC TCCCCCCTCC 1500
TCCCTATCCA AAGTGTCCAG CCTTGAAGAC AAGGTGGAGG GAGGAGAGAG AGGGCGGAGG 1560
TGTAAATCCA ACTTAACCCC TGCGCGCGCC CTCGAGGCGG CCGGCTGCCC CCGCCCCGCC 1620
GTGTCCCCTC ATTAAGGAAG GCCCCTTCGC CAGGGGCCGC CAACGCCCGC GGCTTCCGGT 1680
CAGACGGTGC ACCTGAGAGG GACACCCCGT CCCCTCCCGG GAGGGACCCG GGCCTGCTGA 1740
AGTGGGCTCA ACTCTGCAAA CCGCGTCTCA ACTCCCCGCG CCGCGCCGGG GAACCCCTCC 1800
CTGACACTCA ACGCTTCCCG TCCTCACATC CCCAAACACA GTCCACTTCC CTTCTCGTGG 1860
CGGCCGCGGC AACCCGAGCC CGGCCCCCGC CCCGCCGCCA GAGAACGCCT CCCTCGCCGG 1920
GACGCGGTGC CGAGCCCGCT GCACACCGAG CGGCCGTGGC ACAATACCGC GGCGCTGCGC 1980
GCACAATCAC CGCCCCCCAG GACCCGCGGC GCGCACCCCG GGAGTGGGGT GCGCCCCGCG 2040
ACCCTGGGCG CTCAGGGCCA GACACACCTC TTGGGCGCCC CGCGGCCCCC ACAGTGCAGC 2100
CTTCATCGCC CCCCCTCCAC TCTCGGGCAC ACTCACCCGC CCCCCGCCCC AGCCCACTCG 2160
GCCCAGGGCG CAGCCGCTCC CCCGCGCCCC CTCCCTCAGC CCCGGCAAAG GAAGCTCCCC 2220
CTGCGCCCCC CTCCCCAGAA CCGCCCCCAG CCCCTCGCCC CCCTAACCGC AGCTCAACGG 2280
CCGGCGGCAG CAGCCGGAGA AGGGGGGCGG CGGCCCGGGC CCCGGAAACG GCCCGATCGC 2340
CGGGATCCGG GCCGGACTCC 2360