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

TagContent
EnhancerAtlas ID
HS180-47285 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr8:56918810-56919960 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr8:56919291-56919312GGATGGAAAGTGAAACTGTGT-6.24
IRF2MA0051.1chr8:56919295-56919313GGAAAGTGAAACTGTGTG+6.1
POU2F2MA0507.1chr8:56919698-56919711TTATGCAAATGAG-6.44
Pou2f3MA0627.1chr8:56919696-56919712TTTTATGCAAATGAGG+7.38
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_09229chr8:56916924-56920471CD14
SE_10861chr8:56915117-56927850CD20
SE_31281chr8:56917435-56920396Fetal_Thymus
SE_53331chr8:56917300-56920003Spleen
SE_58907chr8:56872805-56941745Ly3
SE_61351chr8:56875318-56932483HBL1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr85691917456919348
chr85691944156919801
Number: 1             
IDChromosomeStartEnd
GH08I056004chr85691727456920309
Enhancer Sequence
AAGAAATTTG TCCTGCTGCA AACAAACACT CACCTTGGTC ACAAGCAAAG CTCAGAAAAT 60
AATAATAGTA ATAATAATTT GCCCTTTTGG AAGGAGTATG ATTGGGTGGG AGACTGTACT 120
CCCAGGGTAT CTAGCTCTTC CTGATACACA TACACACAAA GGGCCCTGTG TGACTGAAGA 180
CTGTCATAGT TTGTGGTACA GCTGTGCTCC TCCCTGTCAC TAGCTATCTG TTCCTTTTCT 240
CTACTGTACC ACATTTTTCT CCTTCTTCTG CTTCTTTACC AACTTGTAGT CTCTGCTGAT 300
TTCTACCCAC TCCAGATGCC ACCTTCTGCT CCCCACCACC TCCTTCTGGT GAGGGCATTG 360
TCCTGACTGG GCTGTGTGCC ATTTGAGGAT GATGCTCTGT CTTAACTATC TCTGCATGTC 420
TCAGAGCTCA GTGCTAGTTC ATGACCCATA GTGAGCACTC AGTGTTTGTT GAAAGGAGGA 480
AGGATGGAAA GTGAAACTGT GTGCCTTCTA AGCAGATCAC CAGCTAATGG GTGTTTACTT 540
TCTTTAACTT AGCGACAGGC CAACACCAAC TATCACATGT AATCTTAGGG TCTGGTTGAG 600
GTCCCTCTCC TCTTCTTATT TCTTTCTTTC ACAAGACTTG TCATTTAATA GCGGATTTTA 660
TTTATTGCTT TCCTTGTACA TAAAAAGATA GGCTTCAGAT TCCCTTCTTC CAATTCTTCT 720
TATCAAGTCG AATTCCCCAA ACAGGGTGGA GCATGTCCAG CCTTTACCAG CATCATCGAG 780
AGTCCTTCAG AGCTAGGAGA ACATACTGGA ACCAGGAAAA AAAAATCTGC TGTGGGGCTA 840
GGGTGACCTA GAAAGCTTTA TCTTCCACTG TGGCTGCATT CTGACCTTTT ATGCAAATGA 900
GGGATCTCCA GGAAGGAAGT GAAAGAGATA TTCCAAACTG AGTGTGCAGG TCCAATTGCT 960
ATTTATATCA TACTGGATGT TAGTCCTCCC ACCACGATCC CAGAATTTCA CCCAAGAAAG 1020
CAGAAGTATA CACAAATCTT TCTTCTGAAA TTTATCCAAG TTATAAGAGC CAGAGCAATG 1080
CTGAGGCCAT ATCATTTTGT GGAGACTAAA ACTCCCAAAT AAAGAGGATG ATACAAATCT 1140
GTCTTTCGCT 1150