EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS103-00210 
Organism
Homo sapiens 
Tissue/cell
HUES64 
Coordinate
chr1:21587470-21590370 
TF binding sites/motifs
Number: 12             
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
ZEB1MA0103.3chr1:21590176-21590187GGGCAGGTGGG-6.14
ZNF263MA0528.1chr1:21587786-21587807GCCCCTTCCTTTGCCTCCTTC-6.12
Number of super-enhancer constituents: 21             
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_46896chr1:21590051-21590692Ovary
SE_47523chr1:21588012-21589939Pancreas
SE_47523chr1:21590077-21590815Pancreas
SE_48583chr1:21586247-21589944Right_Atrium
SE_48583chr1:21589973-21590853Right_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
TCAGACCTTA CCCCAGACAC CCGGAGATTC TGTTCCCTTC TCCCTCACCT CAGTGCCCTG 60
GTCCAGATGC CACCTGCTAA AGGCAATGCT CCGGTGGGTG CACCTGGTGA AGATGACCGC 120
TTCCTGCCAC TCAGGTCCAC AAGGGACCCA CTATATACTG GGGCTCTGTG CATGAGCCTT 180
CTTCTCAGAG CCCTGCTCCA GGCCATGCCA GATACTCTAA ACCCCTCAAT TCCATCTGTC 240
CCTCTTGCCT CCTCTGGGAA ACTCACTGCT CCAGACACAT TCCCTCATTT CATGTTCATT 300
TCTCTCTGGC CCTGAAGCCC CTTCCTTTGC CTCCTTCAAA GATCCCTCAA ACCCCAGCTC 360
CTTCACAAAG ACTTTCCTGG CAGAACTGTA TCCATCCACC CTCTGACCAG ATACTAGATG 420
CTTACTCTAT GCTAGGCCCT GTGTAAGCTG TGGGACACAA GAGAAAACAT CCCTGTCCCC 480
AAGGAGCTTC TGCATGGGAC CCTGTTAAAA TCCTACTCAA CCTCAAGGCC TCTACGGGGA 540
CATCTTTTTG ATGAAGGCTC TCCTAAGATG TTCATTCCCA AAGGCCCTCA CCGCTCTGCA 600
TACCTGTGTC CACCATTAGA CCGTGAGCTC CTTGGGACAG AAAGCGGGTC TTATTTATGC 660
CTATAAAATT CAGAGCCCAG CCCTGTGCCT GGCACCCAGC AGAAACTCAA AGAAATGACC 720
ACAAGACACG ACAGTGCTAT GAACAACGCA CGTGGCTATG GAACACAGAG AAAAGTCACT 780
CCCTTCGGAG GGGTGGGGAG AAGAGGGGTC TCCAGAGGGC GTTCCATTTG AGCTGGTTCT 840
GAAAGCTGAA GTTGTTCACC AGGTGGAAGG GAGGGGAGAG GCCACTGGGT TGCGCGGAGC 900
AGGACAGGAC AGTGTGGGGA CAAGCGGGGA TGCCTGAAAG GGCAGGCGGA CTGCTTGGAG 960
AAAAGAAAGC TGTCTGGCGT AGTCACTTGG AGCAAAGGAC ATGAGTCACT TCCTGGCCAG 1020
TCTTTCATCA GCTTTCCCAG CCTCACCCCG AGAGCTCCCT GCCCCCCGAT CCTCACCATA 1080
AATAGCACCA TGGCTTTCAC TGATCAGAGC ATCGAGCCCC GGTCTTGCTG ACCTCAGGGT 1140
GATGGCCCTG AAAGGGGGAC GGGACCAGCT TGGGGCTAGT CTGAAGGAAG ACACAGAGAC 1200
AAGAGAGCCC CTTGAGAGAC AGGGTCAGGG GCCTGAACGA GGGGCTATGG AGGGTTCGTA 1260
CAGCCCTGGA GACCATGGGC TACTGGGTTG CTAAGTGCTG GAAACACCTG CATGTCCCCC 1320
AGGCACCACG GCAGCTCTGA GAAGAGGACT CTGTGAGGGG AGGGCGGAAA TGGGGAAGCT 1380
GGGATACAGA AGATCAGGGA GAGCAAAAGG GGAGTGCCTC GCCCCTCCCA GGGGCCTCGT 1440
TCCTATGGCA ACACTCCCAA TGAAGCTCTT GGAAGAAAAA GCAGGAGAAT CGTCATTGCT 1500
CCCCAGGCCT CAGATGCAGC GTCTCACCCT CCACATCTGG CTCCGGCCAA AGCCCTGAAA 1560
TGCCAGGGCC AGCGCTGGGG AAGGCACTCT GTGTGCTCTG GCCCATGAGT GAGCCTGGCA 1620
TCTCCCTCCC CCAAGGCCAC AAAGATAAGA GGCCTAAAGA ACAGCTCCCA GGAGCAGCCT 1680
GGCTGTGCTA ATCACAGCGA GTTCCGAGGC CCTCTTCCCT AACACCTGTC TGCAAGCCCC 1740
AAATTATCAC CGGGAGGGAG AAGGAATGCC TCCTTCAGAC ACAGCCTCCC TTGCTCCTTC 1800
GCTGAGAGGC TGCCACAGGC CAGGTTCAAA CTCCATTCCT TTGGCCCCCA CCACCTGGGT 1860
GCCACGCTCA CTTGCTTTCC CACATTGTTT ACAAAGTTCC TTTTGCCTGG CAACCGCCAG 1920
GCCGGGTGTG GGGGACAGTG GGCAACATAA CTGGAGGCCT GTCCACGTGA GGCATGCAGC 1980
GTGGTGAGTG AGGCAAACGG CAGCCAAGGA CTCGCGGGAG CATCTGATTA CGCACGGGGT 2040
GAACGCTGTG AGAACATCCC AGAGGCCTTG AAGGGGAGGG CGGGAGGAGA CCAGGGAAGC 2100
CAAGCAAGGC CCCGGGGAAG CTTCGTTTGA GCTTCGGGCT GAAGGATGAA CTCAATGTGG 2160
AGTAGAAGCA GGGGCTGTGC CTGGGCTGCC CCTCCGCCAT TCCATGTCTT AGTGGTCCCT 2220
GCAGCCCCAG AACCAGCCCT GGATAGGGAC CTAGTAGGCC CCTAGCAACA GGTGGTGGCT 2280
GCAAGAACAG AGCCCAGTGT CCCTTTCTGG AGAGGAAGGA CATCTGGAAG ATGAGAGGGT 2340
GATGAGGCCG GATGCCCACC TAAGGTTTCC TTTTTTTATA TTTATTTTTT TTTTTTTTGA 2400
GACAGAGTCT CGCTCTGTCA CTAGGCTGGA GCGCAGGGGC GCAATCTCGG CTCACTGCAA 2460
CCTCCACCTC CTGGGTTCAA GTGATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGACTAC 2520
AGGCGTGTAC CACCACGCCT GGCTAATTTT TGTATTTTTA GTAGAGACTG GGTTTCACCA 2580
TGTTGGCCAG GATGGTCTCA ATCTCTTGAC GTGTGATCTG CCCACTTCAG CCTCCCCAAA 2640
TGCTGGGATT ACAGGCGTGA GCCACCATGC TTGGCCAAGA TTCCCTTTTT TTTTTTAAAG 2700
GAAATCGGGC AGGTGGGGCA GGAGTGGACA GGATGAGGGG GCCCCGCCAG GAGTTGGTGT 2760
TCATGCCCCC TCTGTGTGTG TCATCAGTAT CCCCACTGCC AATGCTGGCT GGGGCAGGAG 2820
CCCTGGTAGA AGGTACGGTT CCTCTTCCTC CCCCTGGTTC CAGGAGCCCA CGGGGACAAC 2880
CCACGGCACA CTCTCCCACC 2900