EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-00418 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:21587250-21589830 
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
GACAGAGGCC GGTCTTGGTT TTCAGATACC AGATGATCTT TCTTGTGATA AAGACTGAAG 60
TTGGATGGAA ACTCAAAAGG CTCATTCATT ATGAATTTAC TTTTTGCTTC CTCCTTGGAG 120
GGGCTAGGCA CGTTCACCAG GCTTACAGCC AACTCCTGGG GCCGTTTTCC ACCGCCCTTG 180
CCAACTCCAG CAAGCAGCAT CTCCCTCCTG CAGTGGCTTC TCAGACCTTA CCCCAGACAC 240
CCGGAGATTC TGTTCCCTTC TCCCTCACCT CAGTGCCCTG GTCCAGATGC CACCTGCTAA 300
AGGCAATGCT CCGGTGGGTG CACCTGGTGA AGATGACCGC TTCCTGCCAC TCAGGTCCAC 360
AAGGGACCCA CTATATACTG GGGCTCTGTG CATGAGCCTT CTTCTCAGAG CCCTGCTCCA 420
GGCCATGCCA GATACTCTAA ACCCCTCAAT TCCATCTGTC CCTCTTGCCT CCTCTGGGAA 480
ACTCACTGCT CCAGACACAT TCCCTCATTT CATGTTCATT TCTCTCTGGC CCTGAAGCCC 540
CTTCCTTTGC CTCCTTCAAA GATCCCTCAA ACCCCAGCTC CTTCACAAAG ACTTTCCTGG 600
CAGAACTGTA TCCATCCACC CTCTGACCAG ATACTAGATG CTTACTCTAT GCTAGGCCCT 660
GTGTAAGCTG TGGGACACAA GAGAAAACAT CCCTGTCCCC AAGGAGCTTC TGCATGGGAC 720
CCTGTTAAAA TCCTACTCAA CCTCAAGGCC TCTACGGGGA CATCTTTTTG ATGAAGGCTC 780
TCCTAAGATG TTCATTCCCA AAGGCCCTCA CCGCTCTGCA TACCTGTGTC CACCATTAGA 840
CCGTGAGCTC CTTGGGACAG AAAGCGGGTC TTATTTATGC CTATAAAATT CAGAGCCCAG 900
CCCTGTGCCT GGCACCCAGC AGAAACTCAA AGAAATGACC ACAAGACACG ACAGTGCTAT 960
GAACAACGCA CGTGGCTATG GAACACAGAG AAAAGTCACT CCCTTCGGAG GGGTGGGGAG 1020
AAGAGGGGTC TCCAGAGGGC GTTCCATTTG AGCTGGTTCT GAAAGCTGAA GTTGTTCACC 1080
AGGTGGAAGG GAGGGGAGAG GCCACTGGGT TGCGCGGAGC AGGACAGGAC AGTGTGGGGA 1140
CAAGCGGGGA TGCCTGAAAG GGCAGGCGGA CTGCTTGGAG AAAAGAAAGC TGTCTGGCGT 1200
AGTCACTTGG AGCAAAGGAC ATGAGTCACT TCCTGGCCAG TCTTTCATCA GCTTTCCCAG 1260
CCTCACCCCG AGAGCTCCCT GCCCCCCGAT CCTCACCATA AATAGCACCA TGGCTTTCAC 1320
TGATCAGAGC ATCGAGCCCC GGTCTTGCTG ACCTCAGGGT GATGGCCCTG AAAGGGGGAC 1380
GGGACCAGCT TGGGGCTAGT CTGAAGGAAG ACACAGAGAC AAGAGAGCCC CTTGAGAGAC 1440
AGGGTCAGGG GCCTGAACGA GGGGCTATGG AGGGTTCGTA CAGCCCTGGA GACCATGGGC 1500
TACTGGGTTG CTAAGTGCTG GAAACACCTG CATGTCCCCC AGGCACCACG GCAGCTCTGA 1560
GAAGAGGACT CTGTGAGGGG AGGGCGGAAA TGGGGAAGCT GGGATACAGA AGATCAGGGA 1620
GAGCAAAAGG GGAGTGCCTC GCCCCTCCCA GGGGCCTCGT TCCTATGGCA ACACTCCCAA 1680
TGAAGCTCTT GGAAGAAAAA GCAGGAGAAT CGTCATTGCT CCCCAGGCCT CAGATGCAGC 1740
GTCTCACCCT CCACATCTGG CTCCGGCCAA AGCCCTGAAA TGCCAGGGCC AGCGCTGGGG 1800
AAGGCACTCT GTGTGCTCTG GCCCATGAGT GAGCCTGGCA TCTCCCTCCC CCAAGGCCAC 1860
AAAGATAAGA GGCCTAAAGA ACAGCTCCCA GGAGCAGCCT GGCTGTGCTA ATCACAGCGA 1920
GTTCCGAGGC CCTCTTCCCT AACACCTGTC TGCAAGCCCC AAATTATCAC CGGGAGGGAG 1980
AAGGAATGCC TCCTTCAGAC ACAGCCTCCC TTGCTCCTTC GCTGAGAGGC TGCCACAGGC 2040
CAGGTTCAAA CTCCATTCCT TTGGCCCCCA CCACCTGGGT GCCACGCTCA CTTGCTTTCC 2100
CACATTGTTT ACAAAGTTCC TTTTGCCTGG CAACCGCCAG GCCGGGTGTG GGGGACAGTG 2160
GGCAACATAA CTGGAGGCCT GTCCACGTGA GGCATGCAGC GTGGTGAGTG AGGCAAACGG 2220
CAGCCAAGGA CTCGCGGGAG CATCTGATTA CGCACGGGGT GAACGCTGTG AGAACATCCC 2280
AGAGGCCTTG AAGGGGAGGG CGGGAGGAGA CCAGGGAAGC CAAGCAAGGC CCCGGGGAAG 2340
CTTCGTTTGA GCTTCGGGCT GAAGGATGAA CTCAATGTGG AGTAGAAGCA GGGGCTGTGC 2400
CTGGGCTGCC CCTCCGCCAT TCCATGTCTT AGTGGTCCCT GCAGCCCCAG AACCAGCCCT 2460
GGATAGGGAC CTAGTAGGCC CCTAGCAACA GGTGGTGGCT GCAAGAACAG AGCCCAGTGT 2520
CCCTTTCTGG AGAGGAAGGA CATCTGGAAG ATGAGAGGGT GATGAGGCCG GATGCCCACC 2580