EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-12159 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr10:123900000-123902680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10788251chr10123901964hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr10:123902504-123902523TGTCCAGCAGGGGGCACTC+7.86
EWSR1-FLI1MA0149.1chr10:123900962-123900980AGAAGGAAGGGAGGAGGG+7.05
JUN(var.2)MA0489.1chr10:123900572-123900586AGGAGGTGACTCAG+6.25
Klf1MA0493.1chr10:123900933-123900944AGGGTGTGGCC-6.32
NFE2L1MA0089.2chr10:123900575-123900590AGGTGACTCAGCAGG+6.09
Stat6MA0520.1chr10:123900194-123900209GACTTCCTGAGAACA+6.39
ZNF263MA0528.1chr10:123900681-123900702GGGGGAGGAGGAGGAGGGTCA+6.63
ZNF263MA0528.1chr10:123900690-123900711GGAGGAGGGTCAGGAGGGAAG+7
ZNF263MA0528.1chr10:123900687-123900708GGAGGAGGAGGGTCAGGAGGG+8.5
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_01992chr10:123898386-123902743Aorta
SE_26436chr10:123897974-123902520Duodenum_Smooth_Muscle
SE_27133chr10:123898102-123903528Esophagus
SE_29718chr10:123899157-123903043Fetal_Muscle
SE_32286chr10:123899977-123901358Gastric
SE_32286chr10:123901643-123902699Gastric
SE_35263chr10:123899003-123902454HeLa
SE_37106chr10:123897698-123903945HSMMtube
SE_38152chr10:123898042-123902922HUVEC
SE_40692chr10:123896279-123903555Left_Ventricle
SE_42242chr10:123898109-123903575Lung
SE_44550chr10:123898721-123902566NHDF-Ad
SE_45030chr10:123899658-123902417NHLF
SE_47305chr10:123896062-123903196Panc1
SE_48163chr10:123898340-123903773Psoas_Muscle
SE_48687chr10:123896405-123903534Right_Atrium
SE_49530chr10:123898671-123901312Right_Ventricle
SE_49530chr10:123901619-123902591Right_Ventricle
SE_51475chr10:123897946-123902902Skeletal_Muscle
SE_54572chr10:123897762-123902908Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10123900798123900950
Number: 1             
IDChromosomeStartEnd
GH10I122138chr10123898049123903387
Enhancer Sequence
AGGCATCCCA GATGTTTAGC CCCAGGCTAG CTTTCCGCCA GAGGAAGACA GCAAGATAAC 60
TCTAGCAGGT GGAATGAGAC TACAGAATGT GCGGACCCCA TATCAGTGCC CTGCTCTCTC 120
TGGGCTGGGT TTGGCAGCTG TCTGGAAGGT TCTGCAAAGG CCTGGGATTG GTCCTGGGCA 180
TTTGTTCAGG GCCCGACTTC CTGAGAACAA TGTCTTTAAG AGGAGTCACT GCTGGTCACG 240
GGAGGCTTGA ACGCAGATGG GAGCTGACTG GGGTTGTTGG TGAGGAGCTG GCTGCCGGCT 300
GCCCCTACCT GCTTACTCGC TTTGCTTGAG CAACATTGCC CTCTGGCAGC TCAGGGGGAG 360
TTCAAGGGAC CTTGACTAGG CTCCTGGAGG ACCAGCTTCC GAATGCCGTG GAAAGTCAGG 420
GAGGGCTTTA CTCAGTGGAA GGACCTGATC AGAACTTGAG TTGGGTCATT CTGGTGGCTG 480
TGGGGCCTTG GATCTGAGGG GACAAAACGG AAAGCAGGCA CAGCAGGATA GCCCAGGAGT 540
CCTGCTCAGA GAGGGCAGAT TCCAGAAGGA GAAGGAGGTG ACTCAGCAGG AAGGGGTGAT 600
GAGGGGCATG GGAATGAGAG AACTGGAAGT CAGTGCCAGG GCCTGGCGGG CTGATGGTGC 660
CACTACCTTG CTGGGAAAAT TGGGGGAGGA GGAGGAGGGT CAGGAGGGAA GAGGAGAAGT 720
TCTGTTGGGC CCAGGAGGTG TCTGTGGGGG CCCATGTGTT AGCGCTTGGG CTTGGATGGT 780
GAGTCACTGA GTGTTTCCTC GTGGGAGCCT GACCTCCTCG GCCCCTGGGT ATGAGCCAAC 840
AGGCGGTGGA AGGAGGGGGG CGCCTTTCTT AAATGAGCTG TTGAGTCACA CTTGTTTGAT 900
GCCTTTGGCT AACGGGACCC AGCCAGCGCA GGAAGGGTGT GGCCATGGCA GTTGGGACCA 960
ACAGAAGGAA GGGAGGAGGG AGCAGCCAGG TGGCCCCTCA GGAACAGGAG CAGCTGTGGG 1020
TGTTAAGGGC AGGCGGGGGA GCTTGGTGAG TGAGCCTTGG TTGTGCTGCC CCAGGGTGTT 1080
CTCAGAGATG GGGCAGGTGT AGCCTTGGGC ATCTGCATCA GATCCCAGGG CTGTCAGCTG 1140
TCACAGAGCT GGCTTTGTTG TGATTAGCAG CGGGCCACAG ATCTAAGGTA GCATCTCCCC 1200
CCCACCCGCC ACTGTTTTCT AAGACAGAGA TCCTTCCTTG CAGTTTGATA AACAGTACCC 1260
TTAAATCACA GAACCACAAA CAATACCACC TTTCCACAAT TTGCATTAAA CTAAGTAAAA 1320
TCTTGGTGGG ATGTGTGTGG TGGAGGGGGG AGCACAGCAG TGTAATTTCT TGAGAAAGCG 1380
AAGTTAGACT AGTAGTTTGC GTTTGTAAGT GGTCCATTTG CCGATTATGA GTACATGTCA 1440
GCCTCCAAAG TGCAAAATAG CTCTCTTAAG GAGCTTAAAT GCCTCTGGTA GTTTGCATTA 1500
TTCATTTTGA GTCATTCTTT TACAAAATGA TTAATTTTAG CCACTGCCCA AATTGTTGCA 1560
AATAATAGTT TGACAAAGGA GGCCAGTCAC TCCATCTGTG AATCCACTTT GCTGTTTTGC 1620
TGGGTTTCCT CCAAGCACTT GTAATTTTTG TTCCCCCGTG GATTGGTCTG CTCTGGGCTT 1680
TCCTAGGTCG TTATTTCTTG GGCTCTGTTT TCCTCTGTGG AGCCCCGAGG GAGCAGGCAG 1740
CATGGGTTCC AGCCCTGGCT CTGCTCCCAC ACTTGGTTGC AGCCAGTTGG ACACTTGGCG 1800
GTATCCCCTC TGCCTGCTGT GGGCGGCCTG GCCCAGGGTT GCGATCCTGC GGTGGATGTG 1860
GCAGATGTGG CCCCTGTCCT CGTGGAGCTC TGAGGCCAGG ACGGTGAGGG GCTGGGAAGT 1920
GCCTGCTGGA CCTGCAGAAT CTGCTAAGCT GTGACCAGAC TTATGGGCAA GACTGAGTCC 1980
TCTGTCCAGT GTACAGTGTG GGTGCCTATG GCAGCTGCCC TTCAGACCAG GGTGCTAGCC 2040
TGTCAGGTGG ACCTCGAAGA GATGGAGTGA GCAGACATAG CAGCCCAGAG GCCCACGCAC 2100
CCTGGACTCC TGCAATCTGG GAGCTCCCTG GAGGTGTTTA CCCGCAGAGG GAAGCAGTGA 2160
TCCCTCACTG CAAGGGCTGT GACGCCACAA ACCCCAGCTA CCACCTCAGG CTGGGTTTCA 2220
GGCCGTCTGT GCTGAGTCTT GTATTCCAGC CTGGCTACCC CAAGACACCT TCAGCCTGGC 2280
CAGTCCCACT GTGGACCAGA GCAGGGATGG CTGGAGAGGC TGGGAGGGTA CCACCCTGAA 2340
AGCTGTTCCC AGGCTTTAGT CTGTGGAGGC CGTTGCTAGC CTTGCTTTTT GCCAGTGGGG 2400
AAAATCAGAA CCTCTTCTGC ACTGCAAGCC TGTGCCTTTT GGCTTTTGTG GGGAGTGGTC 2460
TCCAGTGCTA CCCCCGGAGG CCCCGCACGC TGTGGTTCCC TGGCTGTCCA GCAGGGGGCA 2520
CTCGTTCCCT ACTCGAGGGC CACACTCCGT CTCTGAAACT CATTCCTCCC CCAGGACACG 2580
GGTGGCCCAA CTGGTCCCGG GGCAGGTTCC CGAATTTCCC ATCATCCTTT TCCCCTGGAT 2640
TTTTCTCAGC CTTGGGATTT GCGGGCAAAG CCTGGGGAAT 2680