EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-20896 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr20:48983020-48984900 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6067417chr2048983697hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:48983073-48983091CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983077-48983095CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983081-48983099CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983061-48983079CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr20:48983043-48983061CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr20:48983085-48983103CCTTCCTTCCTTCCTTTT-7.95
EWSR1-FLI1MA0149.1chr20:48983065-48983083CCTCCCTCCCTTCCTTCC-8.13
EWSR1-FLI1MA0149.1chr20:48983069-48983087CCTCCCTTCCTTCCTTCC-9.42
IRF1MA0050.2chr20:48983319-48983340ACACAGTTTCATTTTCACCTT+6.64
MyogMA0500.1chr20:48984003-48984014GACAGCTGCTG+6.14
Stat6MA0520.1chr20:48983524-48983539GTTTTCCAGAGAAAA+6.07
Tcf12MA0521.1chr20:48984003-48984014GACAGCTGCTG+6.02
ZNF263MA0528.1chr20:48983056-48983077CTTCCCCTCCCTCCCTCCCTT-6.14
ZNF263MA0528.1chr20:48983081-48983102CCTTCCTTCCTTCCTTCCTTT-6.16
ZNF263MA0528.1chr20:48983043-48983064CCCTCCCTCCCTCCTTCCCCT-6.46
ZNF263MA0528.1chr20:48983042-48983063TCCCTCCCTCCCTCCTTCCCC-6.61
ZNF263MA0528.1chr20:48983069-48983090CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr20:48983073-48983094CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983077-48983098CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983039-48983060GTCTCCCTCCCTCCCTCCTTC-7.12
ZNF263MA0528.1chr20:48983065-48983086CCTCCCTCCCTTCCTTCCTTC-7.19
ZNF263MA0528.1chr20:48983061-48983082CCTCCCTCCCTCCCTTCCTTC-7.38
ZNF263MA0528.1chr20:48983052-48983073CCTCCTTCCCCTCCCTCCCTC-7.65
ZNF263MA0528.1chr20:48983048-48983069CCTCCCTCCTTCCCCTCCCTC-7.73
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_28491chr20:48982335-48987321Fetal_Intestine
SE_31629chr20:48983043-48983874Gastric
SE_33764chr20:48982789-48984100HCC1954
SE_42215chr20:48984303-48987016Lung
SE_52401chr20:48982681-48987083Small_Intestine
SE_53316chr20:48982599-48984069Spleen
SE_56118chr20:48982851-48984157u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204898308348983800
Number: 1             
IDChromosomeStartEnd
GH20I050365chr204898243148987174
Enhancer Sequence
CTTATAATTG ACTATAAAAG TCTCCCTCCC TCCCTCCTTC CCCTCCCTCC CTCCCTTCCT 60
TCCTTCCTTC CTTCCTTCCT TTTGTTCCCT TCTGCTTTCT AAGGATATGC CTGGTGTTTG 120
GCAAGCATTG CATGAATTAC ATTAGGAAAT AACTTTTGTA ACAAACCCAT TTAACAACCA 180
TTCTTTGTTC CCCGCCTCCT GATAATGCTC AGAGCCACAG CAACAGCCTT TGCCCAACTC 240
CATGTCATTA ACCCTTGATC TTTTCCTGCT GAATAGCAGA TTGCTTTCCG GGGCTGGCAA 300
CACAGTTTCA TTTTCACCTT CCTGCTGATG GAACTGCCCT GGCTCTGTGC CAGATGGCTG 360
TTTACATAAG AAATGATTTG ATTATATTGC ACAGCCAATG GCAGCCTTTC TCAGAATAAA 420
GAAGCCAGAA ACATATAATC AAAGCCATTA ACTGTGTACA AAGAAACGCA GCCCACTCTA 480
AATTTCCCAC CAACCATAAT CACAGTTTTC CAGAGAAAAA TAAGAACAGG GTTATGGTTC 540
CCTACTAAAA ACGTGTTAGG GGAAAGACTT TTAAAAGGAA ATTGTGGTAT AGCTCAGTTG 600
CACTCTCAGA TCAACCCTTG AGCCTTGACT CCAATCCCAG CTCTGTAACT CACTGTCCTT 660
GTGACCTTGG AAAAGTCGTT TACTGCCAAA AGCCTCCGTT TCTTTATTGT AAAATGGCTA 720
TAATAGTAAT ATCAACCTCA GAGGTTTACG AGAGGATTAA GTGAGATAGT GCATAAGAAC 780
ACTTTCTCAG TCAGAATGTT TTCAGCCGCA AGGAGCAGAA CACTTGACTA AAGGAGGGAA 840
AAAAAAGCTA GAGGACTTAT AATTTTATTT AACAGGGTTG TTTCATTTGG AGGCATAAAG 900
ATGTAACCAG TGATTCACAT TCTTTTCTTC TTCCTGCTAT GCCATTCTCA GCAATTTATG 960
GACATGTCTC CTCATGGTTT CAAGACAGCT GCTGTGGCTC CAGGCATCAC ACTGGGACAT 1020
GATAAAATCA AGCAAAGAGG AGGAGGGCAT TTTTTCCCCT GTGTCTCCTT TCATGATGGA 1080
GAAAATTGTT CCCAAATTTC CCCCCTGCAG ATCTGCAGAC TTCTTATTGG CCAAGATGGC 1140
GTTACATCTA TAATTCCAAA CCAGTCACTG ATGGAGGAAT GAGAATGACT GCAGTTGGCT 1200
TGGACCTATA ACTCACTCTG AAGCCGGGGC GAGGAATAGC CACCGTCCCT GAGCTCCTGA 1260
GTAGATGCAC AACCAACAAA ACTGAATCCC GTCAGCGAAG GAGTCATGGG TGGGCAACCC 1320
GTGCTGTGTC TACCATAAGC ACAACTCCTG GTGCTCATGA GGTGCCCCCA AAGGCTGGCA 1380
TTTGGCAAGC TCAAGACTGG GAGTCCACAC AGTGCTCCAG GTGGGAGGAT CACAACCGCG 1440
ATTGGCCAGG GAGTCCCTCT GGGTGCCAGA CCCCTGTATG CAAAGCCCCA CTCAGCATCT 1500
CCACTTGATT GGCTTATGGG AACCTCAAAT CCAACACACT ATATTTGAAC TCATCATATT 1560
TCCTCCCCAC TGGCCTCCTC TGTTGGTACC CACCTTGCTC AAGCCAGAAG CTGGCTGGTC 1620
CTCAGGAGTC CCTGCTTTCC TTCCCCATCT GTGCCCACGT CTCTCCAGCT CTGCCATCAT 1680
CTTCCACCTG GACACCAACC AAGCCCCCGC TCTCCCTGCT GCTGTGTGGG CATCAACAGC 1740
CTATGCTGTT CCCTCTGAAC GGAACTCTTC CCGCTCCTGT TTCCCTGTCA CCTTGCTCAG 1800
GAAAGCTCTT CTGATCCCCC CAAGTTGAAT CCCTCATTAC AAACCTCACA TCCTGACATA 1860
CATCTCTCCA TTGCCCTGAT 1880