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

TagContent
EnhancerAtlas ID
HS116-05450 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr10:121438380-121441510 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr10:121438509-121438523ATTCCCATGGGAAT+7.58
EBF1MA0154.3chr10:121438509-121438523ATTCCCATGGGAAT-7.58
IRF1MA0050.2chr10:121441308-121441329CTTTTCTTTTTCTTTTTCTTT+6.02
JUN(var.2)MA0489.1chr10:121439791-121439805CTGAGTCATTTCCT-6.73
MEF2AMA0052.3chr10:121441494-121441506TCTATTTTTAGT-6.27
MEF2BMA0660.1chr10:121441494-121441506TCTATTTTTAGT-6.32
MEF2CMA0497.1chr10:121441493-121441508ATCTATTTTTAGTAG-6.25
Nkx2-5(var.2)MA0503.1chr10:121439012-121439023CTTGAGTGGTT-6.32
Nr2f6(var.2)MA0728.1chr10:121439570-121439585TGAACTCCTGACCTC-6.22
Nr2f6(var.2)MA0728.1chr10:121438715-121438730GAGGTCAAGAGTTCG+6.24
TBX20MA0689.1chr10:121441013-121441024AAGGTGTGAAG+6.32
TBX21MA0690.1chr10:121441013-121441023AAGGTGTGAA+6.02
ZfxMA0146.2chr10:121438691-121438705GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_00555chr10:121439120-121441332Adipose_Nuclei
SE_02770chr10:121438773-121440633Astrocytes
SE_26382chr10:121439312-121440562Duodenum_Smooth_Muscle
SE_26842chr10:121438879-121442586Esophagus
SE_36345chr10:121437622-121442871HMEC
SE_37697chr10:121437223-121442903HSMMtube
SE_38457chr10:121438752-121441379HUVEC
SE_40827chr10:121437269-121438798Left_Ventricle
SE_40827chr10:121438845-121441329Left_Ventricle
SE_42731chr10:121439374-121441341Lung
SE_47241chr10:121435461-121442012Panc1
SE_48147chr10:121437265-121442689Psoas_Muscle
SE_48898chr10:121438319-121438776Right_Atrium
SE_48898chr10:121438861-121441156Right_Atrium
SE_51226chr10:121436976-121442593Skeletal_Muscle
SE_54668chr10:121439219-121441065Stomach_Smooth_Muscle
SE_64548chr10:121437831-121442889NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr10121438822121439316
chr10121439426121439595
chr10121440088121440536
chr10121441361121441509
Number: 1             
IDChromosomeStartEnd
GH10I119677chr10121437435121442729
Enhancer Sequence
CTGACTTAAG AGCCCCCGAG CTGAATTTCT CATGACTGTA TTGAGTTTAA TACTGGTGCC 60
TGACGATGCT GCACAAAAAT ACACCCTGGT GTGCTTGCCA CTGTTAGCCT GCTGAGGAAG 120
GCTGAAGTCA TTCCCATGGG AATCTGCCAA CATCATTCCT GGGTGAACTC ATTTGGGGAG 180
TACAAGCCGA CATGCCACTG ATTCTAGAAA CTCGAACATG TAAATAGGAA AAAAAAAAAA 240
AAATACTAGA CTATTTTAAA AATGAACCAG GCTGGGTGCA GTGGCTCATT CCCGTAATCC 300
CAGCACTTTG GGAGGCCGAG GCGGGTGGAT TACTTGAGGT CAAGAGTTCG AGACCAGCCT 360
GGCAAACATG GTGAAACCCC ACCTCTACTA AAAATACAAA AATTAGCCGG GCGTGGTGGC 420
ATGCACCTAT ACTCCCAGCT ACTTGGGAGG CTGAGGCACG AGAATTGTTT GTACCTGGGA 480
GGCAGATGTT GCAATGAGCC GAGATCACGC CACTATACTG CAGCCTGAGC AACAGAGTGA 540
GACTCGATCT CAAAAAAAAA AAAAAAAAGA ACCAAAGATG ATGTGACCAC TTCTCTTTGG 600
GACTCAATGG ACCTCATACG ACGTTAAGCC TCCTTGAGTG GTTACTGGAT TAGGTTGATA 660
GTATTTTTAT CACTAAACAT CATCAAATAA GTAGCTGTTT AATGTGGTTG GAATATTTTC 720
AATCATCCAA ATGAGACATG CTGTGGGCAT CAGGACGGGA GTTATCTGGC CTGTGTTGGT 780
GGCCCCTGGG CCTTGTGTGG GGAGCAGGGC ATAGAGCTAG CTGTACGCTC TTGGTGACAC 840
AACTGTCTTG GCCCCTGTAG GCATTGGGGG GCTACAGCCA CTGAGCATCT ACCGAGTGTC 900
AGGGCTATTT CCTGCGATGC CTGCTCAGGC CCTCTCTATC TGCTTTTCCA AATCTTCCGA 960
CTCCATTTTT TTTTTTTTTT TTTTTTTGAG ATGGAGTCTT ACTCTGTCGC CCAGGCTGGA 1020
GTGCAGTGAT GCAATCTCAG CTCACTGAAA CCTCTGCCTC CCGGGTTCAA GCGATTGTCC 1080
TGTCTCAGCC TCCCGAGCAG CCGGGATTAT AGGTGTGCGT CACCCCGGCT AATTTTTGTA 1140
TTTTTTAGTA GAGATGGTTT TTTGCCATGT TGGCCAGGCT AGGCTAGTCT TGAACTCCTG 1200
ACCTCAAGTG ATCTGCCCAC CTCGGCCTCC CAAGTGCTGG GATTACAGCT GTGAGCCACC 1260
ATGCCCAGCC TCCAGATCTT CCCACTCTGA GGCCCACCTT GGGTTGAAAC TTTCCCCACC 1320
TGGACCACGC ATTCCTTCTC AGACTCTCCC TTCCCAAAGC TCCTAGCACC CTTCTGTGCA 1380
TTTGCCAAAA CCCAGTTGTT TTCTCAACAT CCTGAGTCAT TTCCTCAGCA AGACAGAATC 1440
CCCGGAGGGG TGGCAGGTTC ATTCCGACAC TTCCTTCTTC CCACATTGTT GTCCAGACCT 1500
GGGCACAGAA GCACCCTGGA TGGTCAGGGA GTGCTTAAAA GTCCCTTCCA CTTAAGATGT 1560
TAGGATTCTA AGGCTAAATT GATGTTCCTG CACAAATAAA TACCTCTTTA GGAGCTGTGA 1620
GTTGAGGGCC AACTCTTTCA CCAACTTTCA TAATTCCCAG ATATGTAATT TATTTAAGTT 1680
AATTTATGTA AGTAATTTCC TCTCTCTGTG CCCTTTGCTC TCATCTGTGA AAGGAGGGCC 1740
TTGCCCAAGG GCCCTCTTGG TGATCTGGAT GTTTCTGGCA GGTCTGCACT TGGCTACTGT 1800
TGTGGTCTCT GCCTTGGTAT TTCTCCCTTA GCAGCCTAGC CAGGAAGCAT AGCGTGGAGC 1860
TCCATTATGG GCTGTGCGGT CCTGCAAGCC CCTGTGTGAG TGTGGCTGGC CGGCCTGCCC 1920
ACTGTCTGTA ACATTATACA AATGTAATCG AATGCCAACG GACAGGATCC AGGGTTGCAG 1980
TTATTTTGGG ATGTGCAGGA GCCTGTGGGA AAACGCTGGA ACATGTCTTA GTCACTTGGG 2040
CAAATACCTT TCTTTCCCTG TTCCAGCGTG TTTTGAACTT TCAGGCAGCA CAAAAAAAGC 2100
TCCAGCAGGC ACACCCACCC TTGGTGATTC CGGTGCCCTT ACACATCCTG TGGCTCTGAA 2160
AAGTGTGAGT GCAGAGGGCT GAGAGCGGGG CTGGGGAAGC CCTAGACACC CACCTATGGA 2220
AAAAATTGTA GCGCTTCCCT CAATACGTAA TTCAAAATAA AAACAACAAA AGAAACGTAA 2280
GGAAGATGTG CAATTCCCAC TTTATACTTT GTTGCTTCCT AAAAATTGTA AAATTTCCTC 2340
CACTCATGCG TATGTGCGCT TGGCCAGGTC CCTGCCTTCC TGGTACTCTG TTGTCCAGCA 2400
CTACCCAGTA AGAACCACTG GAGACCAGGA AGAGCTCCAT CAGTCCCCGC GGAGCATCTG 2460
AGCAGGTGAG GAGGTACAGG ACCACAACAG AGGGCAGCAG AAGCCAGCAA TGGTGCCATC 2520
CTGCGCTTGG TGGAAGGGAT GAGGAGGCAG CCACAGGTCC TCTCGATGGA CAGTGTTGCC 2580
CCCGCACCTC ACACGTGGGC CCAGAGTTCC TGGTGCAACT AGAAGCCAGC CTGAAGGTGT 2640
GAAGGGAGTT GGAAAAAGCA TTCCAGATGG AAAGGGTCTT TTTCTAAAAC ATTTTCTTGC 2700
CTGTCCTTGC CTTCTCTAGC CAGAGCTTTG CCCTAGGATC TGGCCGGCTG CATGGAGGCT 2760
GAGGAAGTTC TCCTCTAGTT TGAAGAGGGG AAATCCTTCT GCCAGCCCCT CACTCACTGT 2820
CTTCCACTTC ATCTCTTTCT CTCTCCAATG GCTCTTTTCT TGTCCTTAGC CTACAGAAAA 2880
CACAAACCAA AAAGAAATGC TTCCTCCTCA CTTTACCCCC TGCCCCCACT TTTCTTTTTC 2940
TTTTTCTTTT TGAGACAGAG TATTGCTCTG TTGCCCAGGC TGGAGTGAAG TAGTGCAATT 3000
TTGGCTCACT GCAACCTCTG CTTCCGAAGT TCAAGCAGTT CTCCCACCTC AGCCTCCCGA 3060
GTAGCTGGAA TTACAGACAT GTGCCACACA CCCAGCTAAA TTAAAAAAAA AAAATCTATT 3120
TTTAGTAGAG 3130