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

TagContent
EnhancerAtlas ID
HS101-18131 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr17:25858930-25860040 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HSF1MA0486.2chr17:25859758-25859771TTCTGGAAGGTTC+6.19
NR2C2MA0504.1chr17:25859266-25859281AAAGGTCAGAGGGCA+6.91
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_04008chr17:25857858-25860526Brain_Anterior_Caudate
SE_05395chr17:25858844-25860581Brain_Cingulate_Gyrus
SE_06005chr17:25857301-25860608Brain_Hippocampus_Middle
SE_07581chr17:25857685-25860654Brain_Hippocampus_Middle_150
SE_08498chr17:25858489-25859973Brain_Inferior_Temporal_Lobe
SE_28195chr17:25857184-25860227Fetal_Intestine
SE_28854chr17:25855956-25860462Fetal_Intestine_Large
SE_39279chr17:25857442-25860510IMR90
SE_47492chr17:25857923-25859109Pancreas
SE_47492chr17:25859123-25860114Pancreas
SE_54042chr17:25856364-25860556Spleen
SE_65525chr17:25859016-25860140Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172585943525859718
Number: 1             
IDChromosomeStartEnd
GH17I027528chr172585509725864442
Enhancer Sequence
TAGGGAACCA GCGTTACCAG CTAGACCACT CGCTCACAGC AGGTTGAACC CAGGACTTCT 60
GCCATCCAGT ATGGGGGAAA GAGTGCTGGA CAGAACCAGG AGACCGTCCT GGCACTGCCT 120
TCTACTTTGT GTGAGTTTGA CTAAGTCGTT GTCCCTCTCT GGGCCTCAGT TTCCTCATCA 180
GTTTTTCATC TATTTCTGTG AGATGACCTT AGGCCCTTCT TGTCTTAGAA CATCCAAGGA 240
TTTTGTAATT TAAAGGCATT TCAGACATCT GAAGATGGGT CTGGTCCTGC TAATAATCCT 300
CACTGGTTGA CGTGGTCCTT AGATGGGGCC AATTGCAAAG GTCAGAGGGC AGGAGATGCA 360
GAGCCCTGTG GGGTTTGCCC GGTTTTTCTC AGTGCGGGTG AGCTATCCTC CACCTGGAGG 420
GTTATGGTAG CTGGGTCACC TGGGAACAGG CCGTGGGAGA ACTGGCCTCC TTGGGAATGT 480
GTTGTCCTGC GCGGCAGAGC ACTTTCAGGT ACGGGCTGCT CTGTGAGGCC ACCCTGTGCT 540
CCAGCCCGCA GCACTTGAGA CTGACTTGCC CTGAGGTTTG TGTGAGCGAA ATCGGGTCTT 600
ATGCAACAGT GAGTGCGTGC ATCTCCGCTT CGAGCTGTTA CATCAGAAAG CTAAACACAG 660
AGAGCCCTTG CAACTGGAGA ACTAGCAGGA GGCCCTCGCT CTGGTTCTTT GTCAGCGGGT 720
GGGACGGGGT AGGATGTGGC TTACAGGCAG CTGTGGAGGA GAGGACTGTG CTAGGAAAGA 780
GGTTGGAGCT GGTGGACTCT CTCCCAGGCG CTGCTTTTCC AACAGGCTTT CTGGAAGGTT 840
CTGGCCTCCT TCTGATCAGG TGGCAGAGCA TCCCTGGGGC TCCTCACCAG TATTCGTGTG 900
CTCTGGGTCA GTGATGTCTC CATCTGCATC ACTGCTGGTG GAGCACAGTG GGAAAGGTCA 960
GCCTTCAAAC TGTGGAAGGT CAGACCCAGC GCCTCAAGCC TGGAGGGGCA GCGTGGGGCA 1020
TCAGCCTCTT ATGAGTTTAA GTTGGCTCTG ACACATACCA GCTGGGTGAC GTTGGGTTGG 1080
CTTCCTGACC CTCTGAGTCC TTTTTTATAA 1110