EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS184-05959 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr11:72496850-72497990 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr11:72496929-72496950TTCTCCCCCACCCCCTCCTCA-7.36
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_05866chr11:72497802-72502258Brain_Hippocampus_Middle
SE_09492chr11:72497802-72500679CD14
SE_23353chr11:72484971-72499602Colon_Crypt_1
SE_24028chr11:72496591-72499607Colon_Crypt_2
SE_27728chr11:72483650-72501497Fetal_Intestine
SE_28682chr11:72492797-72501545Fetal_Intestine_Large
SE_31502chr11:72482095-72499735Gastric
SE_40268chr11:72497836-72499724K562
SE_47934chr11:72497422-72497852Pancreas
SE_50857chr11:72485443-72499721Sigmoid_Colon
SE_65258chr11:72495555-72499786Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr117249755972497879
Enhancer Sequence
CCTACTCACC ATCTAGTTCG ACAGATGATG GCTGCCTTGA TCTCCCCTCT GGGAGATGAT 60
AGGGTCCCAC CCCTACCCCT TCTCCCCCAC CCCCTCCTCA GGGGTAACCC TGCCTGCCAG 120
TTTTGATGGA GCAAATTCAC AGGTTGTGCA GGGCAACAAG GCAGTGTCCT GGCACTGTTC 180
TAGAAGATTA GGCAGTGACC TGTGTGATGT CACCAGGAAG CAGTGACATG GAGGAGGAGT 240
TCCAGAGACC CTCAGGGTGC AGCAGGCCGG GCGCGGTGGC TCACACCTGT AATCCCAGCA 300
CTTAGAGAAG CCAAAGCAGG CAGACTGCAT GAGGCTAAGA GCTCAAGACC TGGCTGGGTA 360
ACATGGTGAA ACCCCGTCTC TACTAAAAAT TTAAAAATTA GCTGGGCGTG GTGGTGCACA 420
CCTGAGGTCT CAGCTAGTCA GAAGGCTGAG GCAAGAGGAT GGCTTGAGCC CGGGAGATCA 480
AGGCTGCAGT GAGCTGAGAT GTTGCCACAG CACTCCAGCC TGGGTGACAG AGCAAGACTC 540
TGTCTCCAGT TAAAAAAAAA AAGGAAAAAA AAGGTTCAGC ACCAAGAACT CTGAGGCCCC 600
CAGGGCTGGC TCGGCCTTGA GAGGGATGTG TCCTTCACAG TGGCGATAGG TGTTCCATCC 660
CAGTCCCACC TGGAGCCGGA TCTAAGTGTT TGCCCAGGGT GGGTCTCATA CCTTGCTGGG 720
CCTCACTGAG CAAACAGCTC ACACCTGCCC TTAGGGAGCT GCTGGAGCCT CAGGGAGCCA 780
CACTGTAGTG CGCAGCCTCA AAGTCAGTGC AGGTCAGGGT CACCCCCACC TGCACTTCTC 840
CTAATGTCCT GTCACAGTCC CATACAGAAA CACTCCACCT TGGTATTACA CAGGGCCAGA 900
CCTACACAGC TACACACACT TGATCATGCC AGGCCACACA TGGCACCAAA GTGGAGTTGC 960
CAGATAAAAT ACAGGACGAC AGCCAGGTGC AGTGGCTCAC ACCTGTAATC ACACCTATAA 1020
TTCCAGTGCT TTGAGATGCT AAGGTGGGAA GACTGCTTGA GGCCAGGAGT TGGAGACCAG 1080
CTTAGGGAAC ATAGTGAGAC GCCATCTCTA CAAAAAAATG TAAAACTTAG CTGGGCATGG 1140