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

TagContent
EnhancerAtlas ID
HS145-10306 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr17:57922950-57924070 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
POU2F2MA0507.1chr17:57923113-57923126TGTATTTGCATAT+6.41
RELMA0101.1chr17:57923757-57923767GGAAATCCCC-6.02
TCF3MA0522.2chr17:57923328-57923338AACACCTGCT+6.02
Number of super-enhancer constituents: 51             
IDCoordinateTissue/cell
SE_00167chr17:57921765-57927189Adipose_Nuclei
SE_02295chr17:57922055-57924540Astrocytes
SE_10048chr17:57913237-57927649CD14
SE_12351chr17:57923038-57924493CD3
SE_12872chr17:57922965-57923614CD34_Primary_RO01480
SE_13390chr17:57922525-57924465CD34_Primary_RO01536
SE_14102chr17:57922759-57924444CD34_Primary_RO01549
SE_14484chr17:57921937-57924651CD4_Memory_Primary_7pool
SE_17196chr17:57922962-57924565CD4p_CD225int_CD127p_Tmem
SE_18111chr17:57922085-57925043CD4p_CD25-_CD45ROp_Memory
SE_18274chr17:57913216-57925634CD4p_CD25-_Il17-_PMAstim_Th
SE_19224chr17:57913069-57924613CD4p_CD25-_Il17p_PMAstim_Th17
SE_23233chr17:57922872-57924653Colon_Crypt_1
SE_24435chr17:57922972-57924603Colon_Crypt_2
SE_25771chr17:57921970-57927112Duodenum_Smooth_Muscle
SE_27082chr17:57922837-57925640Esophagus
SE_27746chr17:57920340-57927032Fetal_Intestine
SE_28673chr17:57920322-57927067Fetal_Intestine_Large
SE_30688chr17:57922705-57924636Fetal_Muscle
SE_31691chr17:57922855-57928410Gastric
SE_32541chr17:57921468-57927090GM12878
SE_33772chr17:57913056-57927377HCC1954
SE_34288chr17:57912088-57927293HCT-116
SE_34651chr17:57912951-57927107HeLa
SE_35896chr17:57913277-57924923HMEC
SE_37171chr17:57913355-57925459HSMMtube
SE_38158chr17:57913267-57924576HUVEC
SE_38933chr17:57921923-57924658IMR90
SE_43382chr17:57912648-57925582MCF-7
SE_44187chr17:57913075-57925500NHDF-Ad
SE_44824chr17:57922283-57924609NHLF
SE_45686chr17:57913234-57925367Osteoblasts
SE_47118chr17:57902074-57938709Panc1
SE_47932chr17:57922938-57923586Pancreas
SE_47932chr17:57923628-57924624Pancreas
SE_50387chr17:57922852-57924685Sigmoid_Colon
SE_51624chr17:57921832-57925543Skeletal_Muscle
SE_51976chr17:57922249-57924611Skeletal_Muscle_Myoblast
SE_52483chr17:57922815-57925637Small_Intestine
SE_54204chr17:57922884-57925577Spleen
SE_55059chr17:57922569-57925554Stomach_Smooth_Muscle
SE_55921chr17:57922042-57924676u87
SE_57301chr17:57923190-57924603VACO_400
SE_58037chr17:57922960-57923567VACO_9m
SE_58037chr17:57923747-57924506VACO_9m
SE_59128chr17:57902596-57931450Ly3
SE_61214chr17:57902066-57937473HBL1
SE_62339chr17:57902123-57931675Tonsil
SE_63783chr17:57922249-57924625HSMM
SE_64271chr17:57913695-57925402NHEK
SE_67474chr17:57922042-57924676u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr175792299957923843
Enhancer Sequence
GAGAAAGCAC ATCATGTATT TTAAACTTTA GAAGCAACTG AGTCATTAGT GTCTGGTGGA 60
CAGGAGCTAG GGATCCTATC CCTTCCCAAC AAGGCCAAGA GTTCACCTGA GGTAATGCAT 120
TTGCCTTGGG GGCGAGGCCT TGAATTGCAG CAAATAACCT GTGTGTATTT GCATATTTAA 180
CCAGTACTCT TAAGAAGGAT TATACAAAAA CCTGTTCCAG ACAGCTGCTT ACTCATTGCC 240
TTTAAAATTG CGTGGTGCTG GGATTGGCAG GTGCCAACTG TTTGCTCATT CTCTTTGACC 300
CACTAGCCTT GCAGTTTGCT GTGTGGGTGT TGATACTCCT AAATTAAAGC AGGGAAGGGG 360
TGGTTTTAGA TGGCTTTTAA CACCTGCTCT CCACCCAAGC ACCCTGGATT CATTTGATAT 420
CTGGATTCTA ATTCTGTAGT CAGGAGACTG GCCCAAACTG TGGCCCAGAG AGAAGTGAGT 480
CAGTTGCAAG TGGCTAGCTG ACTCTATGGG AACAGAAATA AAATGCAGCT TAGAGAGTTT 540
GTCAGCCAAA TCCACAAATG TGTGGCTTTT TGAAACATTG GACATCTGTT CCTCTTAATT 600
TAAAATAAAC TTTTTTTTTT TTTTTTTTTA AGCACAAAGT TGCTTGGCTC CTTGTTTCTT 660
TGTGTCAGCA GCAGTTGCTG CTCTAATTTA GGAACCCTAG GATCTGATTT AGGACATTTG 720
GAATCTTTAA GGCACATTCG ATCTAGAAAG TGGAACTGAA TTGCTTTGGG AAGGCAAGAG 780
GATGATTTTA CAGTATAGGG TTTGTGTGGA AATCCCCTTC AGCAGTAATC AACCCAGGTG 840
TCCAACCTGT TTGTTAACCA TTTCCAAATG ACTCAGAGGA CCTAGAGGGA GGGCTTGAAC 900
ACACTCCAGC ACTGTTTCTA CAATTTAGCC TTTATTTGCA TTGGAAACCA CATTCCTGAA 960
TTCTTGAGGG GGCAGGCTCT GGCTTATTCT GGGCAACTGA CTTCAAGTGG GACCCCTGAG 1020
CTACCTATGT AAGCAAAGAG TCAGCCATCT CTGGAGAGTT ACCAGGGAGG AGGATCTTTC 1080
TGTGAACTTG CTTTGATGAC CTCCACCCAA AGCCCTTTGA 1120