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

TagContent
EnhancerAtlas ID
HS180-01220 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:33463240-33464320 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr1:33463749-33463764TGGCCTTTGGCCTCC-6.67
ZEB1MA0103.3chr1:33463958-33463969CCCACCTGCCC+6.14
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_00738chr1:33462028-33465022Adipose_Nuclei
SE_09317chr1:33461979-33465482CD14
SE_19886chr1:33462395-33464231CD4p_CD25-_Il17p_PMAstim_Th17
SE_35956chr1:33462426-33463603HMEC
SE_37722chr1:33462131-33464726HSMMtube
SE_38650chr1:33461796-33465504HUVEC
SE_42882chr1:33462381-33465190Lung
SE_46598chr1:33461959-33465296Osteoblasts
SE_53906chr1:33462344-33465122Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13346369033463885
Number: 1             
IDChromosomeStartEnd
GH01I032996chr13346213233465154
Enhancer Sequence
GTGGGAGGGA ACTGCAAATT AGTGGGCCTT GAGTCAGACA GATCAGAGTT TTGGCTCCAG 60
ACCTCCCTTA CTGGCCAGAT GACCTGAAAC AAGTCATCTC GTACTTGGTA ACACTCTTCC 120
TGTGCTGCTT CAGGAAGCTG GTTCTCTAGA ACCTCATGTT CAAACTGCAA CTCAGGGATG 180
CCTTCCCTGT CTGTGCAGGG AGGTCAGCTG ATTGGTATGA TCACATCTTT AGCATCTGTC 240
TTCCCAGCCA GACTGAGGGC TCCCAGCAAG AATTTTGTCT GGCCTGTTCT CCAGAGGCCA 300
ACATGGGGCC TGGCCCATAG GTGCTCCCTG TTTCTGTATC ACCTACAAGT TCTTTCAGTC 360
TTGGCTGCCT CACTAGGCTG CTGGAGAAAC CCAGAAGGTA GACGATGAGA CCCACAAGTA 420
TGAGGCATTT GGAATGCATG GGCTACCCTG TGAAGAACTT TACCGGAGGT TGAAAGGGGG 480
CAGAGTGCCC TGAACAGGAA GGCACAGGGT GGCCTTTGGC CTCCAGGGAA GGGAAGGAAG 540
TATGAGACAC AGGAAGAAAT GCAAGCAGCA GGAGGAAGAG CGTTACCAAG CTGGGACTCC 600
AGAGGCTCGA GGCCCTCTCC AGTGCCTGTG AAGCCTGTAT GCGGGCTCTG CTCCTTGTAG 660
CCTTGGAGAC TTGAGCTGTG GCTCAGGAAC TTGGCACTCA GTCCAGTCCC TGCTGCCTCC 720
CACCTGCCCT GTAGCCCCAT CTCCTTGCAC TCACATTCCT TCCCACCATC TGCCACATGG 780
AGCTCACCCT TTTCTCAACA CCTGGTCTTT TCTGTCTCCC GACCACTGTG GAGGTTGTTC 840
CCTCAATAGG AATGCACATC CCCTTCTCTA CCTGGAAGAT GTAGTAGCTC CACGTCCTTC 900
CTATAGGGAA GCCATCCAGG ACACTGCAGG CAGTCAGTTG CTCTCTCCAT GGAGCCCTGC 960
AGCTCCTTGG GCATCCTTCT CGCTATGCAG TGCAGTACTT CCTTCTCTCT ATGCAGTGCA 1020
GCACTTATCA CACTAGGTTG ATGGCTGGTT TTCCTGTCTG TCTCGCTCCA CACCCCCCCT 1080