EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS113-00490 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr1:21587780-21589970 
Target genes
Number: 7             
NameEnsembl ID
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
CCTGAAGCCC CTTCCTTTGC CTCCTTCAAA GATCCCTCAA ACCCCAGCTC CTTCACAAAG 60
ACTTTCCTGG CAGAACTGTA TCCATCCACC CTCTGACCAG ATACTAGATG CTTACTCTAT 120
GCTAGGCCCT GTGTAAGCTG TGGGACACAA GAGAAAACAT CCCTGTCCCC AAGGAGCTTC 180
TGCATGGGAC CCTGTTAAAA TCCTACTCAA CCTCAAGGCC TCTACGGGGA CATCTTTTTG 240
ATGAAGGCTC TCCTAAGATG TTCATTCCCA AAGGCCCTCA CCGCTCTGCA TACCTGTGTC 300
CACCATTAGA CCGTGAGCTC CTTGGGACAG AAAGCGGGTC TTATTTATGC CTATAAAATT 360
CAGAGCCCAG CCCTGTGCCT GGCACCCAGC AGAAACTCAA AGAAATGACC ACAAGACACG 420
ACAGTGCTAT GAACAACGCA CGTGGCTATG GAACACAGAG AAAAGTCACT CCCTTCGGAG 480
GGGTGGGGAG AAGAGGGGTC TCCAGAGGGC GTTCCATTTG AGCTGGTTCT GAAAGCTGAA 540
GTTGTTCACC AGGTGGAAGG GAGGGGAGAG GCCACTGGGT TGCGCGGAGC AGGACAGGAC 600
AGTGTGGGGA CAAGCGGGGA TGCCTGAAAG GGCAGGCGGA CTGCTTGGAG AAAAGAAAGC 660
TGTCTGGCGT AGTCACTTGG AGCAAAGGAC ATGAGTCACT TCCTGGCCAG TCTTTCATCA 720
GCTTTCCCAG CCTCACCCCG AGAGCTCCCT GCCCCCCGAT CCTCACCATA AATAGCACCA 780
TGGCTTTCAC TGATCAGAGC ATCGAGCCCC GGTCTTGCTG ACCTCAGGGT GATGGCCCTG 840
AAAGGGGGAC GGGACCAGCT TGGGGCTAGT CTGAAGGAAG ACACAGAGAC AAGAGAGCCC 900
CTTGAGAGAC AGGGTCAGGG GCCTGAACGA GGGGCTATGG AGGGTTCGTA CAGCCCTGGA 960
GACCATGGGC TACTGGGTTG CTAAGTGCTG GAAACACCTG CATGTCCCCC AGGCACCACG 1020
GCAGCTCTGA GAAGAGGACT CTGTGAGGGG AGGGCGGAAA TGGGGAAGCT GGGATACAGA 1080
AGATCAGGGA GAGCAAAAGG GGAGTGCCTC GCCCCTCCCA GGGGCCTCGT TCCTATGGCA 1140
ACACTCCCAA TGAAGCTCTT GGAAGAAAAA GCAGGAGAAT CGTCATTGCT CCCCAGGCCT 1200
CAGATGCAGC GTCTCACCCT CCACATCTGG CTCCGGCCAA AGCCCTGAAA TGCCAGGGCC 1260
AGCGCTGGGG AAGGCACTCT GTGTGCTCTG GCCCATGAGT GAGCCTGGCA TCTCCCTCCC 1320
CCAAGGCCAC AAAGATAAGA GGCCTAAAGA ACAGCTCCCA GGAGCAGCCT GGCTGTGCTA 1380
ATCACAGCGA GTTCCGAGGC CCTCTTCCCT AACACCTGTC TGCAAGCCCC AAATTATCAC 1440
CGGGAGGGAG AAGGAATGCC TCCTTCAGAC ACAGCCTCCC TTGCTCCTTC GCTGAGAGGC 1500
TGCCACAGGC CAGGTTCAAA CTCCATTCCT TTGGCCCCCA CCACCTGGGT GCCACGCTCA 1560
CTTGCTTTCC CACATTGTTT ACAAAGTTCC TTTTGCCTGG CAACCGCCAG GCCGGGTGTG 1620
GGGGACAGTG GGCAACATAA CTGGAGGCCT GTCCACGTGA GGCATGCAGC GTGGTGAGTG 1680
AGGCAAACGG CAGCCAAGGA CTCGCGGGAG CATCTGATTA CGCACGGGGT GAACGCTGTG 1740
AGAACATCCC AGAGGCCTTG AAGGGGAGGG CGGGAGGAGA CCAGGGAAGC CAAGCAAGGC 1800
CCCGGGGAAG CTTCGTTTGA GCTTCGGGCT GAAGGATGAA CTCAATGTGG AGTAGAAGCA 1860
GGGGCTGTGC CTGGGCTGCC CCTCCGCCAT TCCATGTCTT AGTGGTCCCT GCAGCCCCAG 1920
AACCAGCCCT GGATAGGGAC CTAGTAGGCC CCTAGCAACA GGTGGTGGCT GCAAGAACAG 1980
AGCCCAGTGT CCCTTTCTGG AGAGGAAGGA CATCTGGAAG ATGAGAGGGT GATGAGGCCG 2040
GATGCCCACC TAAGGTTTCC TTTTTTTATA TTTATTTTTT TTTTTTTTGA GACAGAGTCT 2100
CGCTCTGTCA CTAGGCTGGA GCGCAGGGGC GCAATCTCGG CTCACTGCAA CCTCCACCTC 2160
CTGGGTTCAA GTGATTCTCC TGCCTCAGCC 2190