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

TagContent
EnhancerAtlas ID
HS145-15802 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr22:30697620-30699070 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFIAMA0670.1chr22:30697797-30697807GGTGCCAAGT+6.02
RUNX1MA0002.2chr22:30698223-30698234AAACCACAGAG-6.14
SPI1MA0080.4chr22:30698742-30698756GAAAAGGGGAAGTG+6.64
SPIBMA0081.2chr22:30698744-30698756AAAGGGGAAGTG+6.07
ZNF263MA0528.1chr22:30697829-30697850AAAGGAGGCAGAGGAAGGGGG+6.86
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00207chr22:30696033-30714616Adipose_Nuclei
SE_01017chr22:30697528-30699059Adrenal_Gland
SE_01933chr22:30698201-30702501Aorta
SE_03076chr22:30697273-30698942Bladder
SE_06187chr22:30696247-30703814Brain_Hippocampus_Middle
SE_11435chr22:30693586-30712890CD20
SE_12307chr22:30697444-30699157CD3
SE_15119chr22:30696526-30703994CD4_Memory_Primary_7pool
SE_16208chr22:30697107-30699229CD4_Naive_Primary_7pool
SE_18199chr22:30696796-30709288CD4p_CD25-_CD45ROp_Memory
SE_19840chr22:30697181-30699157CD4p_CD25-_Il17p_PMAstim_Th17
SE_22773chr22:30696696-30709496CD8_primiary
SE_23721chr22:30697471-30699113Colon_Crypt_1
SE_25730chr22:30696761-30709491DND41
SE_26571chr22:30696437-30709562Esophagus
SE_31521chr22:30697029-30703752Gastric
SE_34216chr22:30697102-30703879HCC1954
SE_39484chr22:30697242-30699103Jurkat
SE_41271chr22:30696285-30703529Left_Ventricle
SE_41665chr22:30697626-30698975LNCaP
SE_42270chr22:30696389-30702599Lung
SE_47044chr22:30697038-30698916Ovary
SE_47736chr22:30697890-30698326Pancreas
SE_47736chr22:30698345-30698991Pancreas
SE_48841chr22:30696485-30699248Right_Atrium
SE_50213chr22:30696873-30703874Sigmoid_Colon
SE_53095chr22:30697322-30699159Small_Intestine
SE_55187chr22:30697421-30699335Thymus
SE_63164chr22:30696999-30708171Tonsil
SE_66498chr22:30697242-30699103Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223069804930698990
Number: 1             
IDChromosomeStartEnd
GH22I030300chr223069653430717414
Enhancer Sequence
CCCCTTCAAC AGTCCTGCTG GAAGCTCTCA GAGGAGGGAG TACAGAAGCC CTGGCCTTCC 60
TGGGGACCAG TGCAAACAAG AGAAAACTTT CCAAGGGTCA GAGAGAGTCA AGAACCAGGA 120
AGGAGCCAGG CAAACAGGCT GAGGGTGGTG GGGGAAGAGT AGCAGTGGCT GGTCACAGGT 180
GCCAAGTGAG AGCTTCTGGG ACTGCCTAGA AAGGAGGCAG AGGAAGGGGG CTGAAGGGAA 240
CTGCACTAGA CGCAAGGAAG AGTTTCCTGC GGCTATGGGA CAAGGGTCTC CTTAAGGAAG 300
CCAACTTGGG CAGGCTTTGG CAAAGGGATG TGCTTTAGCC CAAAGCCACA GGCCCTTCAG 360
GCTCTCCCAC AGAGCTAAGC TCAGCAAGAG GCAGCCCCAC ATCATCACAG CCCCCATCAT 420
ATTTGGCCTT CTCCAGGAGA GCCCTGGAAC ACTTCGCGGG CAGCAAAGAG CTGGGAGTAC 480
AGCCAGCCTT TCCCACTCTG GCCTCCTCAG CATAAAGGTG CTGGAGGGGG TCATCTCTAC 540
CCTGCCTGCC TTAGGGAGGA TGGTAGGGAC CAGTAAGGAT AAAGCATGGG AAAGTATTCC 600
CAGAAACCAC AGAGGATTAC CATTCTCTGA GGCCAGGCCT TGGGAAAGGA GGTCTCTGAT 660
GAAAGCTGAG TGAGGACACA CCCTTGCCTG CTGAACTCTG TGAGGGCAGG GCCCTGCGGG 720
AAGACAGCAT TCCAGCCCCA GCCCTGCCTC CCTGCAGGAC CAGAATTCTG TCCTAGACAT 780
GGCTGGGAGT CTCCGGAAAG GAAGGCACCC TCCCAGCAGG ACTATGTATG AGTCCAGGAG 840
AAGTGTTGGG TCTGAGCCCA CTTCCTGAAA CAGGTATTAT ACTTCCTGTG CCACGACTTC 900
CTGACCAGAG GGAGAACTCA AGCCTCCACA GGCAGGAAGA GCCCCGAGGG CAGGGCCCAG 960
TATGGCCACA GCTGAGATGG CACGAGGGGC ACCCAGTGGA TGGTTCTGGG CTGGAGAGAA 1020
GCAGTGAGTT AGGGCCTCTG GGCACGGTGG ATTGAAGCAC TTCCTCTGGA GGCCTCAGCT 1080
GGGCAGGGGC AGGTCTTGGG CTCTAACCAC AGTGCCAGGA AAGAAAAGGG GAAGTGTCAG 1140
CTGCTACTCT GCTGAGAGGT GCTCCCCGAA GCTCCCCTCT GGAATCCCGA TTTTCAAGAA 1200
CACGGAAGGT CCCTGCCAAC CACCAGTCAC CATAACAGAT TGCTGGAGAG CAAGCTACAG 1260
CTCACAGTAA GAGCCAGAGG AATGATGAGG CAGGGAAACA GAGCCAGAGT CAGGCAGGAA 1320
GCAGGTGAGG AATAACTGTC TTAACATTGT TTTTTAAAAA AGAGATAGGC TGGGTGCAGT 1380
GGCTCATGCC AGTAATTCCA GCACTTTGGG AGGCCAACGC ACATGGATTG CTTGAGCTCA 1440
GGAGTTCCAG 1450