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

TagContent
EnhancerAtlas ID
HS048-06686 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr11:60896510-60897720 
Target genes
Number: 5             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr11:60896690-60896703TCCAGCTGTCCCT+6.16
ZNF263MA0528.1chr11:60897524-60897545GGAAGAGCGGGAGAGGGAAGG+6.06
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_16005chr11:60896728-60897732CD4_Naive_Primary_7pool
SE_16912chr11:60896783-60897359CD4p_CD225int_CD127p_Tmem
SE_17368chr11:60895921-60898285CD4p_CD25-_CD45RAp_Naive
SE_18251chr11:60896129-60898222CD4p_CD25-_Il17-_PMAstim_Th
SE_19177chr11:60896797-60898036CD4p_CD25-_Il17p_PMAstim_Th17
SE_22975chr11:60896373-60897673CD8_primiary
SE_29266chr11:60896859-60900777Fetal_Intestine_Large
SE_31646chr11:60896810-60899794Gastric
SE_42023chr11:60896719-60898728LNCaP
SE_62235chr11:60737625-60898192Tonsil
SE_65694chr11:60895981-60900818Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr116089682060897215
Number: 1             
IDChromosomeStartEnd
GH11I061128chr116089639760900548
Enhancer Sequence
AGCAAAGAGC ACAGGGTGGG ACACGCGGGC TGACCAGCTG AGGCAGCTCA TGATGGTCCT 60
TTCTTAGAAA GTCAGCCCCT CCGTGCCCCC TGCCACCACT CTGGCACCAA CCCAAGGCAG 120
GTGACCTGAC TATGCGCCTA GAGGGAGATT TGCAGCCTCT TCCTACAAAG CCAAATTGCT 180
TCCAGCTGTC CCTGATGTCC TGTGTCCTCA GCCTTGGACA CCTGCAAGGC AAAGCCAGAG 240
TTCAGCTGGG GGTGAAGGGC AGTAAACGTT TGACCAGAGC CCAGAGACTC TCAGCTCTGT 300
CCTCGGGAGG CACTTCTGGC ACCACCAAGG CAGGGGGAAG GAGCCCCTGC AGCCTCTGAA 360
ATCCAACCGA CCCAGTCCAA GTCCCACCTC CTCCTAAGGC TGTGCAACCC GCTCACCGAA 420
CCACCTGCCC TGTGGTTTCC TCCCATTTAA ACTGGGGATG AAAGGGCTGT TGCGAGGACT 480
CCAGGACATA ATGCGCCTGA AAGCACAGTA CAGCCTGCAG CCATAGCGAC TTCAGGGCAT 540
CTCTAGGCAT CCTCCACAGG TGGCCGCCCG GTCACCTTGC GGGGAAGGAG AGGCGGAGGG 600
CTGACATGAG GGACTGTTAG AAGCCTGGTC TTCAGACTCC CTCCAAGCTG CCCTTCCTGC 660
TGAGCTGAAG ACGCCCTCCC TGGCCTCGGG ATAGGCAGCT CAGCAGCAGA GGCGACGCTG 720
GGGAGGGAGG CAGGCTGGGC CAAGGCCTAG AAGACTGTTG GTGCCGCAGC CAGTTTAGCG 780
GCCTGCTGTT CCTCTGAGCC CATCCTGCAA GCCCAGGTTA GAATTAGATG GCTCACAGAC 840
AGGCCCACAC GCCGACATCC CGCCAGCCCG GCAGGTGGCA GGAACGCAGC ACCTCCCGAG 900
CAGGCTGAGG ACCAGACGCC CCCTCGTGGC ATCCTGTGGC CTTGCATGCC ATTGCTCTCA 960
GTCCAGGACC AGGCAAACGT AGGCTCCAAT AGGAAAACGG CTAAGAAAGA AAGCGGAAGA 1020
GCGGGAGAGG GAAGGTAAAT ACTCCCAGGG CCAGCCCTGG GGCGAGCGGG CAAGGGAGGG 1080
CTGACATCCA GACGGATGGG GCTTTGGGAT GTGAATCACA GAGGCCCCTC CAGAGAGCAC 1140
GATCTGAAGG CTGCAGAAGA GTTCAAGGCA CCCACATGCA GCCACGTCTT CACTCAAACC 1200
CAGCAACACC 1210