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

TagContent
EnhancerAtlas ID
HS182-03021 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr10:105396200-105398840 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Twist2MA0633.1chr10:105396772-105396782AACATATGGT-6.02
ZNF263MA0528.1chr10:105396520-105396541CCCCCCACTCCTTCCTCTCCC-6.03
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01123chr10:105396629-105399110Adrenal_Gland
SE_01834chr10:105396073-105399207Aorta
SE_03619chr10:105397040-105397726Brain_Angular_Gyrus
SE_04829chr10:105394742-105399247Brain_Cingulate_Gyrus
SE_05806chr10:105394193-105399268Brain_Hippocampus_Middle
SE_07764chr10:105394691-105399325Brain_Inferior_Temporal_Lobe
SE_09008chr10:105397695-105397960Brain_Mid_Frontal_Lobe
SE_27093chr10:105396256-105399138Esophagus
SE_28404chr10:105397256-105398037Fetal_Intestine
SE_29224chr10:105397265-105398147Fetal_Intestine_Large
SE_29876chr10:105396214-105398785Fetal_Muscle
SE_32187chr10:105396343-105396965Gastric
SE_32187chr10:105397287-105398438Gastric
SE_41304chr10:105396080-105399222Left_Ventricle
SE_42617chr10:105396080-105399038Lung
SE_44236chr10:105396072-105399222NHDF-Ad
SE_44930chr10:105396879-105399251NHLF
SE_45960chr10:105396020-105401233Osteoblasts
SE_46694chr10:105396524-105396983Ovary
SE_46694chr10:105397030-105398994Ovary
SE_49112chr10:105397083-105399004Right_Atrium
SE_50307chr10:105396178-105398920Sigmoid_Colon
SE_52745chr10:105397177-105398930Small_Intestine
SE_65658chr10:105396742-105398330Pancreatic_islets
SE_65658chr10:105398501-105399024Pancreatic_islets
SE_69111chr10:105394693-105399105H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr10105398400105398835
chr10105397000105397820
chr10105396220105397591
chr10105397600105398554
chr10105398566105398625
Number: 1             
IDChromosomeStartEnd
GH10I103635chr10105395645105399046
Enhancer Sequence
CTGAGGCACA GATTGACATA CACAGAGAGA CAGAGGGAAA TGAAAGAGTG AGCCAGACAG 60
AGCAAGAGGC CAGGAGAGGG ACCAGGGCCT TAGACTCTCC AGGAATGGGG GAGCCTGACT 120
GAGGGCGGCA GGAAGTGACG GGCACTCCCA GGCCACTGCT GTCCCCAGGG TGACTAGGCC 180
ACAATGGCCT CCTTAAGGAG GGAGAATAAT GAGCTCGTTA GGGCCAGAGT CAGGCCAGCT 240
GCACACAATT AGGATGTTAA TTAAGTCCTC TGAGGTCACA GCTCAGCCTA GGACAAAACA 300
GCTGGTGGGG GGAGGGGAGA CCCCCCACTC CTTCCTCTCC CTCTGAAATC CTCTCGTCCT 360
CCCGCTCTGA CTCCCAAACC TCCCAGCCCT GTTCAGCCCA GGATTGAGCC CAAGGATGCT 420
TCTTAATCCC TTCTTCCTAG ACAGACCTCG GTTAGGATCC TAGCTTTACC ACTCACTGTT 480
GGCGTGACCT GAGATAGGTC ACTGGCCCTC TCTGAGCCTC ACTGGCACAC CAGAGTAATA 540
CTAAGTACCT GGGGATGCCC AGTGGCATCA GGAACATATG GTGTATGCAA TACCCAGAGA 600
TTTTCACCAG CAAGTATTTC CCGAGCACCT GGTACGGGCC AGGTCCTGTT CCAGGCACGA 660
GGACACTGCA GTGAACAACA CGCATCCGGG ACTCATGCTC TACTCCCCCA TCACCCAGGC 720
ATGGCACACG CGGGGTTCGA TTGCCGCCTG TGCCCTGGCC CTGAGGCCTG CTGGAGAAGG 780
CTGGGCTTCA GGCTCTGGGC ACAAACCCAG AGGATTTCAA GGCAGGATGA GACTCAGAGC 840
TTGGAGTTTG GAAAAACCCA GGAGGCTTTA GATGACTTCC AGGCTTCATG TTTTCCTTCC 900
CCGTGAGTTA CTCTTGGTCC TTCACATCTG GCTTAACACC AGGTAATTCA GAGCTCAGAA 960
TGTGGGCTGC ACTCATTCCA TGCCCAGGCC TATGTAAGGG TTTTGGTATC CAGGTGGGGA 1020
AGGGTGCATG GTGGAGCTAG GAAAAGAGGA AGACAGGCCC TGCCTCAAAC TCCTCCTCAT 1080
ATAGGCTCGG GGTGGGTGAA CAGCAGCAGC CCACTTCCAG AACCCTCAGC CAGCACCCTG 1140
ACCTGCTTCT CAAAGCACCT CTATTCATGA TTTAAACCTG AGCTCAGACC TTGACCCTTT 1200
GGAAGGGTGA TCTTCCTAGG CATTCCAAGT TCTTTGCTTG GTGCGGGTTT GGAGAAGGGA 1260
ATAGGGCATT TGCGAGCTCC AAGTGGCGAC GGGTGGGGAG ACACTGAGAG GAAGAAAGGG 1320
CTGAGGGCAT CCTGGCCAGG CGCATGGCAC CAGCGCTGCC TACCTACCCA TACCACACCC 1380
AGCACAAGGC TGGGCCCAAG TGAGTGCTGC TGTCCTGGAC CCAGCCTGAC CCCTTTCCCA 1440
TGACCTCCAG GCAGAGCTAA GGCTTCTGCC TTTGTGGAAC CAGAGAAGCT GGAAATGCAG 1500
GCTGTCTGCG AGTGCTGTGC CTTTAAGACC AGTGAAAGGC TGCCCACCCT CGGCCAGGCC 1560
TCCCCTGGTC AGAAAGCCCT GTCACTGCAG CTCTTGCCAA GACACGCGCC TCCATGGTCC 1620
AAAGCAAACA GGAGCGAGCG AGAAACTCCT CCAGTCCCTC CTGCGTGCAC CCACACAGCC 1680
CCTGCCTTCA TGAGCCACTC AGCGGGTCCT ACCTGTGCCC ACCCTGCTCC GTTGCCCAGG 1740
GCCTTCCCTC CCCTAGACGG GCTCTGAGGC CACCAGGGAC CCAGAACCTC CCCTGGGCAC 1800
CTGGGGCCTG GATTCCAAGA CCATTAGCAC AGGCTGCTAC GTCACCATTT GGAAGGCTCC 1860
GTGGAGTCCG TGTCAAGACA GCCTGGGCTG CTGCCACCTT CCCACTCAGC TCCAGCCTGC 1920
CCACCTCACC GAACAGGCCC AGAAGCCAGT GCTAGGCTGG GTCCCCGCCA AGCCCACAGG 1980
GCTCTGGTGT GTCTGAGCAG ACCAAGGTCA TGGGTGAGGC ACCCAGAAGG AGGCCTGACT 2040
AACAAGCAAC GCAGGCAGAG AGGGACACAT GGTTAAATGA CAGGTAGCGG AGAATGGTTT 2100
CCAGCGAGGG CGCCAGAGCC AGGCTGCCTG GGATTGAGGC CCAGCTCTGC TACTTGCCAG 2160
CTGCATGAAT TTGGGCAATT GCCTCAATTT TCTCATCTGC AAAACCGACC CAAAGTACCC 2220
ACATCTCAGT GTTGTTACGA GGATTAGAGG AGCTAATCCT TGAAAAGCCT TCAGAATAGT 2280
GCCTGATTGG AATCAGAATA GTGCCTTCAG ACGAGCACAA GTCGCAAAGC GCTGACATGA 2340
AGTGAAATTC TAAAGAAGGA ACCAAGACCT CAATGCGCCT GGGTGACTGG GGCCAGGGAT 2400
GGCCAGGGAA GCAGGTAGGT CTTGGGTGTC TGGAGTTTCA GGGGGAGAGA GAGACCCTCG 2460
TGGTGTCAGT GTCATTTACC CTTGACCTCA GAAGGTCTCT ACTGAAAACA TGTGGGTCTG 2520
ATTCTGTGCC TGGCACGGGT GGGGGTCGGA GACAGGTTGA GGTGGAGATT ATAAGATGGC 2580
ATGAGGCCTC TCCAGGAGCT GCAGAGCAGT GGATGGATGA GAAGGGCGGC TGCTTGCAGG 2640