EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-00367 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr1:21587390-21590090 
Target genes
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:21588469-21588480CATGAGTCACT-6.14
JUN(var.2)MA0489.1chr1:21588470-21588484ATGAGTCACTTCCT-7.12
RFX1MA0509.2chr1:21588907-21588923CGTTCCTATGGCAACA-6.04
RFX1MA0509.2chr1:21588907-21588923CGTTCCTATGGCAACA+6.07
RFX2MA0600.2chr1:21588907-21588923CGTTCCTATGGCAACA+6.34
RFX2MA0600.2chr1:21588907-21588923CGTTCCTATGGCAACA-6.41
RFX5MA0510.2chr1:21588907-21588923CGTTCCTATGGCAACA-6.55
RFX5MA0510.2chr1:21588907-21588923CGTTCCTATGGCAACA+6.71
SCRT1MA0743.1chr1:21589732-21589747TAGCAACAGGTGGTG+6.21
SCRT2MA0744.1chr1:21589732-21589745TAGCAACAGGTGG+6.28
ZNF263MA0528.1chr1:21587786-21587807GCCCCTTCCTTTGCCTCCTTC-6.12
Number of super-enhancer constituents: 18             
IDCoordinateTissue/cell
SE_00105chr1:21586822-21590872Adipose_Nuclei
SE_00854chr1:21585915-21590867Adrenal_Gland
SE_01887chr1:21585859-21590888Aorta
SE_05944chr1:21586051-21591007Brain_Hippocampus_Middle
SE_29228chr1:21587440-21590639Fetal_Intestine_Large
SE_31433chr1:21587266-21590892Gastric
SE_35152chr1:21585886-21590992HeLa
SE_38063chr1:21586453-21590827HUVEC
SE_41030chr1:21586788-21590937Left_Ventricle
SE_42174chr1:21585877-21590904Lung
SE_45257chr1:21586444-21590604NHLF
SE_46896chr1:21587759-21589841Ovary
SE_47523chr1:21588012-21589939Pancreas
SE_48583chr1:21586247-21589944Right_Atrium
SE_52874chr1:21586846-21589919Small_Intestine
SE_53334chr1:21587315-21590662Spleen
SE_56415chr1:21587102-21589962u87
SE_65263chr1:21585851-21593514Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12158817621588724
chr12158882921589430
chr12158813521589698
Number: 1             
IDChromosomeStartEnd
GH01I021259chr12158602521590811
Enhancer Sequence
GCTTACAGCC AACTCCTGGG GCCGTTTTCC ACCGCCCTTG CCAACTCCAG CAAGCAGCAT 60
CTCCCTCCTG CAGTGGCTTC TCAGACCTTA CCCCAGACAC CCGGAGATTC TGTTCCCTTC 120
TCCCTCACCT CAGTGCCCTG GTCCAGATGC CACCTGCTAA AGGCAATGCT CCGGTGGGTG 180
CACCTGGTGA AGATGACCGC TTCCTGCCAC TCAGGTCCAC AAGGGACCCA CTATATACTG 240
GGGCTCTGTG CATGAGCCTT CTTCTCAGAG CCCTGCTCCA GGCCATGCCA GATACTCTAA 300
ACCCCTCAAT TCCATCTGTC CCTCTTGCCT CCTCTGGGAA ACTCACTGCT CCAGACACAT 360
TCCCTCATTT CATGTTCATT TCTCTCTGGC CCTGAAGCCC CTTCCTTTGC CTCCTTCAAA 420
GATCCCTCAA ACCCCAGCTC CTTCACAAAG ACTTTCCTGG CAGAACTGTA TCCATCCACC 480
CTCTGACCAG ATACTAGATG CTTACTCTAT GCTAGGCCCT GTGTAAGCTG TGGGACACAA 540
GAGAAAACAT CCCTGTCCCC AAGGAGCTTC TGCATGGGAC CCTGTTAAAA TCCTACTCAA 600
CCTCAAGGCC TCTACGGGGA CATCTTTTTG ATGAAGGCTC TCCTAAGATG TTCATTCCCA 660
AAGGCCCTCA CCGCTCTGCA TACCTGTGTC CACCATTAGA CCGTGAGCTC CTTGGGACAG 720
AAAGCGGGTC TTATTTATGC CTATAAAATT CAGAGCCCAG CCCTGTGCCT GGCACCCAGC 780
AGAAACTCAA AGAAATGACC ACAAGACACG ACAGTGCTAT GAACAACGCA CGTGGCTATG 840
GAACACAGAG AAAAGTCACT CCCTTCGGAG GGGTGGGGAG AAGAGGGGTC TCCAGAGGGC 900
GTTCCATTTG AGCTGGTTCT GAAAGCTGAA GTTGTTCACC AGGTGGAAGG GAGGGGAGAG 960
GCCACTGGGT TGCGCGGAGC AGGACAGGAC AGTGTGGGGA CAAGCGGGGA TGCCTGAAAG 1020
GGCAGGCGGA CTGCTTGGAG AAAAGAAAGC TGTCTGGCGT AGTCACTTGG AGCAAAGGAC 1080
ATGAGTCACT TCCTGGCCAG TCTTTCATCA GCTTTCCCAG CCTCACCCCG AGAGCTCCCT 1140
GCCCCCCGAT CCTCACCATA AATAGCACCA TGGCTTTCAC TGATCAGAGC ATCGAGCCCC 1200
GGTCTTGCTG ACCTCAGGGT GATGGCCCTG AAAGGGGGAC GGGACCAGCT TGGGGCTAGT 1260
CTGAAGGAAG ACACAGAGAC AAGAGAGCCC CTTGAGAGAC AGGGTCAGGG GCCTGAACGA 1320
GGGGCTATGG AGGGTTCGTA CAGCCCTGGA GACCATGGGC TACTGGGTTG CTAAGTGCTG 1380
GAAACACCTG CATGTCCCCC AGGCACCACG GCAGCTCTGA GAAGAGGACT CTGTGAGGGG 1440
AGGGCGGAAA TGGGGAAGCT GGGATACAGA AGATCAGGGA GAGCAAAAGG GGAGTGCCTC 1500
GCCCCTCCCA GGGGCCTCGT TCCTATGGCA ACACTCCCAA TGAAGCTCTT GGAAGAAAAA 1560
GCAGGAGAAT CGTCATTGCT CCCCAGGCCT CAGATGCAGC GTCTCACCCT CCACATCTGG 1620
CTCCGGCCAA AGCCCTGAAA TGCCAGGGCC AGCGCTGGGG AAGGCACTCT GTGTGCTCTG 1680
GCCCATGAGT GAGCCTGGCA TCTCCCTCCC CCAAGGCCAC AAAGATAAGA GGCCTAAAGA 1740
ACAGCTCCCA GGAGCAGCCT GGCTGTGCTA ATCACAGCGA GTTCCGAGGC CCTCTTCCCT 1800
AACACCTGTC TGCAAGCCCC AAATTATCAC CGGGAGGGAG AAGGAATGCC TCCTTCAGAC 1860
ACAGCCTCCC TTGCTCCTTC GCTGAGAGGC TGCCACAGGC CAGGTTCAAA CTCCATTCCT 1920
TTGGCCCCCA CCACCTGGGT GCCACGCTCA CTTGCTTTCC CACATTGTTT ACAAAGTTCC 1980
TTTTGCCTGG CAACCGCCAG GCCGGGTGTG GGGGACAGTG GGCAACATAA CTGGAGGCCT 2040
GTCCACGTGA GGCATGCAGC GTGGTGAGTG AGGCAAACGG CAGCCAAGGA CTCGCGGGAG 2100
CATCTGATTA CGCACGGGGT GAACGCTGTG AGAACATCCC AGAGGCCTTG AAGGGGAGGG 2160
CGGGAGGAGA CCAGGGAAGC CAAGCAAGGC CCCGGGGAAG CTTCGTTTGA GCTTCGGGCT 2220
GAAGGATGAA CTCAATGTGG AGTAGAAGCA GGGGCTGTGC CTGGGCTGCC CCTCCGCCAT 2280
TCCATGTCTT AGTGGTCCCT GCAGCCCCAG AACCAGCCCT GGATAGGGAC CTAGTAGGCC 2340
CCTAGCAACA GGTGGTGGCT GCAAGAACAG AGCCCAGTGT CCCTTTCTGG AGAGGAAGGA 2400
CATCTGGAAG ATGAGAGGGT GATGAGGCCG GATGCCCACC TAAGGTTTCC TTTTTTTATA 2460
TTTATTTTTT TTTTTTTTGA GACAGAGTCT CGCTCTGTCA CTAGGCTGGA GCGCAGGGGC 2520
GCAATCTCGG CTCACTGCAA CCTCCACCTC CTGGGTTCAA GTGATTCTCC TGCCTCAGCC 2580
TCCCGAGTAG CTGGGACTAC AGGCGTGTAC CACCACGCCT GGCTAATTTT TGTATTTTTA 2640
GTAGAGACTG GGTTTCACCA TGTTGGCCAG GATGGTCTCA ATCTCTTGAC GTGTGATCTG 2700