EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-13824 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr22:30697330-30699240 
Target genes
TF binding sites/motifs
Number: 6             
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
ZBTB18MA0698.1chr22:30697363-30697376GAACATCTGGATG-7.82
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
GGATAAAGGG GATGGGCGCT CGGGGCATGA GAAGAACATC TGGATGTGGG TTTGAATCTA 60
GCGCTGACCT TAAGCCAACC ACTTCTCAAC TGTAAGATCT GAATAATACC TACTACTGTG 120
CAGAGTTGTC AAAGGAGTCC ATTAGAGAGG GAAAATGTGC TTAGTGTGGG GCCTGACACA 180
GTCTGTGTTC AGTAAGCAAT GGCTTCCTCT CTGCCCCTCC ATCCCAGGAG GATGCTTGAC 240
ACAGAAGCCC AGGACCTCAG CTCACACCTA ACTTCCCCTC ACCTAGAAAC CCCCTTCAAC 300
AGTCCTGCTG GAAGCTCTCA GAGGAGGGAG TACAGAAGCC CTGGCCTTCC TGGGGACCAG 360
TGCAAACAAG AGAAAACTTT CCAAGGGTCA GAGAGAGTCA AGAACCAGGA AGGAGCCAGG 420
CAAACAGGCT GAGGGTGGTG GGGGAAGAGT AGCAGTGGCT GGTCACAGGT GCCAAGTGAG 480
AGCTTCTGGG ACTGCCTAGA AAGGAGGCAG AGGAAGGGGG CTGAAGGGAA CTGCACTAGA 540
CGCAAGGAAG AGTTTCCTGC GGCTATGGGA CAAGGGTCTC CTTAAGGAAG CCAACTTGGG 600
CAGGCTTTGG CAAAGGGATG TGCTTTAGCC CAAAGCCACA GGCCCTTCAG GCTCTCCCAC 660
AGAGCTAAGC TCAGCAAGAG GCAGCCCCAC ATCATCACAG CCCCCATCAT ATTTGGCCTT 720
CTCCAGGAGA GCCCTGGAAC ACTTCGCGGG CAGCAAAGAG CTGGGAGTAC AGCCAGCCTT 780
TCCCACTCTG GCCTCCTCAG CATAAAGGTG CTGGAGGGGG TCATCTCTAC CCTGCCTGCC 840
TTAGGGAGGA TGGTAGGGAC CAGTAAGGAT AAAGCATGGG AAAGTATTCC CAGAAACCAC 900
AGAGGATTAC CATTCTCTGA GGCCAGGCCT TGGGAAAGGA GGTCTCTGAT GAAAGCTGAG 960
TGAGGACACA CCCTTGCCTG CTGAACTCTG TGAGGGCAGG GCCCTGCGGG AAGACAGCAT 1020
TCCAGCCCCA GCCCTGCCTC CCTGCAGGAC CAGAATTCTG TCCTAGACAT GGCTGGGAGT 1080
CTCCGGAAAG GAAGGCACCC TCCCAGCAGG ACTATGTATG AGTCCAGGAG AAGTGTTGGG 1140
TCTGAGCCCA CTTCCTGAAA CAGGTATTAT ACTTCCTGTG CCACGACTTC CTGACCAGAG 1200
GGAGAACTCA AGCCTCCACA GGCAGGAAGA GCCCCGAGGG CAGGGCCCAG TATGGCCACA 1260
GCTGAGATGG CACGAGGGGC ACCCAGTGGA TGGTTCTGGG CTGGAGAGAA GCAGTGAGTT 1320
AGGGCCTCTG GGCACGGTGG ATTGAAGCAC TTCCTCTGGA GGCCTCAGCT GGGCAGGGGC 1380
AGGTCTTGGG CTCTAACCAC AGTGCCAGGA AAGAAAAGGG GAAGTGTCAG CTGCTACTCT 1440
GCTGAGAGGT GCTCCCCGAA GCTCCCCTCT GGAATCCCGA TTTTCAAGAA CACGGAAGGT 1500
CCCTGCCAAC CACCAGTCAC CATAACAGAT TGCTGGAGAG CAAGCTACAG CTCACAGTAA 1560
GAGCCAGAGG AATGATGAGG CAGGGAAACA GAGCCAGAGT CAGGCAGGAA GCAGGTGAGG 1620
AATAACTGTC TTAACATTGT TTTTTAAAAA AGAGATAGGC TGGGTGCAGT GGCTCATGCC 1680
AGTAATTCCA GCACTTTGGG AGGCCAACGC ACATGGATTG CTTGAGCTCA GGAGTTCCAG 1740
ACCGGCCTGG GCAACATGGT GAAACCCCAT CTCTACAAAA AATACAAAAA TTCGCCACGT 1800
GTGGTGACGT GCCTGTGGTC CCAGCTACTT GGGAGGCTGA GGTGGGAGAA TCACTTAACT 1860
CCAGGAGTTC GAGGCTGCAG TGAGCCAAGA TCATACTGCT GCACTACAGC 1910